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<article xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="1.3" article-type="research-article"><front><journal-meta><journal-id journal-id-type="issn">2089-0257</journal-id><journal-title-group><journal-title>Jurnal Entomologi Indonesia</journal-title></journal-title-group><issn pub-type="epub">2089-0257</issn><issn pub-type="ppub">1829-7722</issn><publisher><publisher-name>Perhimpunan Entomologi Indonesia</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.5994/jei.20.3.223</article-id><article-categories><subj-group subj-group-type="toc-heading"><subject>PENDAHULUAN</subject></subj-group><subj-group subj-group-type="toc-heading"><subject>BAHAN DAN METODE</subject><subj-group subj-group-type="toc-heading"><subject>Pembiakan maggot BSF</subject></subj-group><subj-group subj-group-type="toc-heading"><subject>Pembuatan simplisia, analisis proksimat, dan ekstraksi bertingkat tepung</subject></subj-group><subj-group subj-group-type="toc-heading"><subject>Analisis LC-MS/MS</subject></subj-group><subj-group subj-group-type="toc-heading"><subject>Preparasi dan analisis stabilitas ligan</subject></subj-group><subj-group subj-group-type="toc-heading"><subject>Preparasi dan analisis stabilitas reseptor</subject></subj-group><subj-group subj-group-type="toc-heading"><subject>Analisis bioavailabilitas dan toksisitas ligan</subject></subj-group><subj-group subj-group-type="toc-heading"><subject>Penambatan molekuler</subject></subj-group></subj-group><subj-group subj-group-type="toc-heading"><subject>HASIL</subject><subj-group subj-group-type="toc-heading"><subject>Simplisia dan identifikasi senyawa bioaktif ekstrak maggot BSF</subject></subj-group><subj-group subj-group-type="toc-heading"><subject>Prediksi bioavailabilitas dan toksisitas</subject></subj-group><subj-group subj-group-type="toc-heading"><subject>Penapisan virtual senyawa aktif berpotensi antioksidan dan antiinflamasi</subject></subj-group></subj-group><subj-group subj-group-type="toc-heading"><subject>PEMBAHASAN</subject></subj-group><subj-group subj-group-type="toc-heading"><subject>KESIMPULAN</subject></subj-group></article-categories><title-group><article-title>Potensi ekstrak maggot lalat tentara hitam Hermetia illucens (Linnaeus) dalam regulasi mekanisme antioksidan selular dan antiradang: Kajian in silico</article-title><subtitle>The potential of black soldier fly Hermetia illucens (Linnaeus) maggot extracts in the regulation of cellular antioxidant and anti-inflammatory mechanisms: In silico study</subtitle></title-group><contrib-group><contrib contrib-type="author"><name><surname>Sulistiyani</surname></name><address><country>Indonesia</country><email>sulistiyani@apps.ipb.ac.id</email></address><xref ref-type="aff" rid="AFF-1"/></contrib><contrib contrib-type="author"><name><surname>Firdaus</surname><given-names>Muhamad Fajar</given-names></name><address><country>Indonesia</country><email>fajar_xd@apps.ipb.ac.id</email></address><xref ref-type="aff" rid="AFF-1"/></contrib><contrib contrib-type="author"><name><surname>Sigiro</surname><given-names>Ria Heni</given-names></name><address><country>Indonesia</country><email>ria_heni1@apps.ipb.ac.id</email></address><xref ref-type="aff" rid="AFF-1"/></contrib><contrib contrib-type="author"><name><surname>Nawangsih</surname><given-names>Abdjad Asih</given-names></name><address><country>Indonesia</country><email>ryuntania@apps.ipb.ac.id</email></address><xref ref-type="aff" rid="AFF-4"/></contrib><contrib contrib-type="author"><name><surname>Purwanto</surname><given-names>Ukhradiya Magharaniq Safira</given-names></name><address><country>Indonesia</country><email>irabikg8@apps.ipb.ac.id</email></address><xref ref-type="aff" rid="AFF-1"/></contrib><contrib contrib-type="author"><name><surname>Andrianto</surname><given-names>Dimas</given-names></name><address><country>Indonesia</country><email>dimasandrianto@apps.ipb.ac.id</email></address><xref ref-type="aff" rid="AFF-1"/></contrib><aff id="AFF-1">Departemen Biokimia, Fakutas Matematika dan Ilmu Pengetahuan Alam, IPB University, Indonesia</aff><aff id="AFF-4">Departemen Proteksi Tanaman, Fakultas Pertanian, IPB University, Indonesia</aff></contrib-group><pub-date date-type="pub" iso-8601-date="2024-1-3" publication-format="electronic"><day>3</day><month>1</month><year>2024</year></pub-date><volume>20</volume><issue>3</issue><fpage>223</fpage><history><date date-type="received" iso-8601-date="2022-11-25"><day>25</day><month>11</month><year>2022</year></date><date date-type="accepted" iso-8601-date="2023-11-30"><day>30</day><month>11</month><year>2023</year></date></history><permissions><copyright-statement>Copyright (c) 2023 Sulistiyani, Muhamad Fajar Firdaus, Ria Heni Sigiro, Abdjad Asih Nawangsih, Ukhradiya Magharaniq Safira Purwanto, Dimas Andrianto</copyright-statement><license license-type="open-access"><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref><license-p>This work is licensed under a Creative Commons Attribution 4.0 International License.Authors who publish with this journal agree to the following terms:

Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution 4.0 International License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
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Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access).</license-p></license></permissions><self-uri xlink:href="https://jurnal.pei-pusat.org/index.php/jei/article/view/750">https://jurnal.pei-pusat.org/index.php/jei/article/view/750</self-uri><abstract><p>The potential of black soldier fly (<italic>Hermetia illucens </italic>(Linnaeus), BSF) maggots as the source of biopharmaca, has not been extensively studied. This research aimed to identify bioactive compunds in BSF maggot extract that potentially activate antioxidant signaling mechanism. BSF maggots fed with vegetable waste were extracted based on maceration method with water, methanol, and acetone as solvents. Forty bioactive compounds were identified by <italic>liquid chromatography-mass spectrometry</italic>: 15 were in the aqueous extract, 13 were from methanolic extract, and 12 were in the acetone extract. Most of those compounds (90%) were having high bioavailability score (= 0.55 or more) and relatively low toxicity (500 mg/Kg&lt;LD50&lt;5000mg/Kg BW). Molecular docking predicted that there were 26 bioactive compounds potential to activate cellular antioxidant signaling through activation of NRF2 transcription factor, better than the commercial NRF2 activator. The aqueous extract compound with PubChem CID: 73775828 was the best one that inhibited NRF2 signaling by binding to Keap-1 protein (PDB ID: 6FFM) with Gibbs free energy (Î”G) = -6.08 Kcal/mol and dissociation constant (Kd) = 3.58 í— 10-5 µM. Whereas inhibition of inflammation via NF-kappa B signaling was shown by an aqueous extract compound verpacamide A which bound inhibitor NF-kappa B kinase (IKK2) (PDB ID: 4KIK) with Î”G = -5.024 kcal/mol; Kd = 0.207 í— 103 µM. This potency was better than that of aspirin. In conclusion, BSF maggot extracts are source of biopharmaca with potential cellular antioxidant and anti-inflammatory activity.</p></abstract><kwd-group><kwd>molecular docking</kwd><kwd>NF-kappa B kinase inhibitor</kwd><kwd>NRF2 activator</kwd><kwd>vegetable waste</kwd></kwd-group></article-meta></front><body><sec><title>PENDAHULUAN</title><p><italic>Hermetia illucens</italic> (Linnaeus) atau yang lebih dikenal dengan sebutan black soldier fly (BSF) merupakan salah satu serangga asal Benua Amerika yang telah dikembangkan sebagai teknologi biokonversi limbah organik menjadi produk pupuk kompos <xref ref-type="bibr" rid="BIBR-7">(Čičková et al., 2015)</xref>. Pemanfaatan tersebut makin populer karena serangga ini bukan hama sehingga relatif aman jika ditinjau dari segi kesehatan manusia <xref ref-type="bibr" rid="BIBR-25">(Li et al., 2011)</xref>. Larva (<italic>maggot</italic>) BSF banyak digunakan sebagai pakan ternak karena kandungan nutrisi yang baik antara lain protein 44,26%, lemak 29,65%, dan beberapa mineral Mn, Zn, Cu, P, Ca, Mg, Na, dan K <xref ref-type="bibr" rid="BIBR-50">(Wardana, 2016)</xref>. Selain protein dan lemak, <italic>maggot</italic> BSF mengandung pula komponen biologis aktif yang bersifat antioksidan, antimikroba, dan modulator kekebalan pada hewan <xref ref-type="bibr" rid="BIBR-29">(Mlcek et al., 2014)</xref><xref ref-type="bibr" rid="BIBR-22">(Lee et al., 2018)</xref><xref ref-type="bibr" rid="BIBR-43">(Silva et al., 2018)</xref><xref ref-type="bibr" rid="BIBR-47">(Vogel et al., 2018)</xref><xref ref-type="bibr" rid="BIBR-38">(Rabani et al., 2019)</xref>. Minyak maggot BSF, terutama asam laurat, menunjukkan aktivitas antibakteri <xref ref-type="bibr" rid="BIBR-53">(Zeitz et al., 2015)</xref>(Schiavone et al. 2017). Zat bioaktif potensial dari ekstrak air <italic>maggot</italic> BSF mampu meningkatkan ekspresi peptida antimikroba (<italic>antimicrobial peptide</italic>, AMP) <xref ref-type="bibr" rid="BIBR-33">(Muller et al., 2017)</xref>. Penelitian <xref ref-type="bibr" rid="BIBR-18">(Kim et al., 2020)</xref> menunjukkan bahwa kapasitas antioksidan total (berdasarkan kemampuan reduksi Cu<sup>2+</sup> menjadi Cu<sup>+</sup>) dari minyak maggot BSF sebesar 1,32 mmol/l lebih tinggi dibandingkan dengan minyak jagung dan minyak kelapa.</p><p>Ekstrak <italic>maggot</italic> dari larva <italic>Lucilla seriata Meigen</italic> (sejenis lalat rumah) dilaporkan mampu menekan peradangan dan stres oksidatif dalam studi menggunakan kultur sel makrofag RAW246.7 dan studi in vivo menggunakan hewan model mencit untuk penyakit radang usus besar (<italic>colitis</italic>) <xref ref-type="bibr" rid="BIBR-48">(Wang et al., 2019)</xref>. Mekanisme ekstrak larva lalat tersebut dilaporkan memengaruhi regulasi ekspresi <italic>nuclear factor-erythroid-2 related factor</italic> (NRF2) <xref ref-type="bibr" rid="BIBR-49">(Wang et al., 2021)</xref>. Faktor transkripsi NRF2 ini pada gilirannya mengendalikan ekspresi gen berbagai enzim antioksidan, seperti glutation peroksidase, katalase, dan superoksida dismutase (SOD) <xref ref-type="bibr" rid="BIBR-45">(Tong et al., 2006)</xref><xref ref-type="bibr" rid="BIBR-14">(He et al., 2020)</xref>. <italic>Maggot</italic> BSF juga mengandung senyawa flavonoid <xref ref-type="bibr" rid="BIBR-41">(Shumo et al., 2019)</xref>. Senyawa flavonoid, seperti kuersetin, kaempferol, dan lainnya dilaporkan memiliki sifat anti-inflamasi dengan menghambat <italic>nuclear factor-kappa B</italic> (NF-kB) secara <italic>in vivo</italic> dan <italic>in vitro</italic> <xref ref-type="bibr" rid="BIBR-8">(Choy et al., 2019)</xref>. Hal ini membuka peluang pengembangan <italic>maggot</italic> BSF sebagai sumber bahan alami untuk kesehatan hewan atau manusia khususnya dalam menanggulangi penyakit degeneratif/noninfeksius akibat stres oksidatif.</p><p>Potensi ekstrak <italic>maggot</italic> BSF, khususnya yang diberi pakan limbah pertanian, dalam pengendalian aktivitas NRF2 terkait stres oksidatif maupun persinyalan NF-kB dalam peradangan masih terbatas. Oleh karena itu, penelitian ini bertujuan mengidentifikasi senyawa dalam ekstrak maggot BSF yang berpotensi mengaktifkan mekanisme persinyalan antioksidan seluler melalui penghambatan asosiasi NRF2 dengan protein regulator negatifnya, yaitu <italic>Kelch-like ECH associated protein 1 </italic>(Keap-1), dan penghambatan aktivitas enzim inhibitor NF-kB kinase (IKK2) yang berperan dalam regulasi persinyalan radang via aktivasi NF-kB. Hipotesis dari penelitian ini adalah terdapatnya senyawa aktif yang dapat menghambat asosiasi NRF2 dengan protein Keap-1 terkait respons antioksidan dan yang menghambat enzim IKK2 terkait antiperadangan. Informasi tentang senyawa aktif pada ekstrak <italic>maggot</italic> BSF yang menghambat asosiasi Keap-1/NRF2 dan aktivitas enzim IKK2 secara molekuler menjadi dasar kajian untuk mendukung pemanfaatan <italic>maggot</italic> BSF sebagai sumber antioksidan dan antiinflamasi alami.</p></sec><sec><title>BAHAN DAN METODE</title><p>Penelitian dilaksanakan di Rumah Maggot dusun Gunung Batu, Desa Sindangjaya, Cipanas, Kabupaten Cianjur dan di Laboratorium Biokimia, Departemen Biokimia, Fakultas Matematika dan Ilmu Pengetahuan Alam, IPB University. Analisis senyawa metabolit menggunakan instrument LC-MS/MS yang terdapat di Pusat Laboratorium Forensik (Sentul, Bogor). Penelitian dimulai dari bulan Januari sampai Agustus 2022.</p><sec><title>Pembiakan maggot BSF</title><p>Larva (<italic>maggot</italic>) diperbanyak dari lalat BSF yang dikembangbiakkan dalam kandang berukuran 2 m × 3 m dengan rerata temperatur ruangan 14–17 °C <xref ref-type="fig" rid="figure-1">Gambar 1</xref>. Setelah lalat BSF bertelur (± membutuhkan waktu 2 minggu), telur ditetaskan di bak penampungan (3–4 hari). Selanjutnya, maggot dipelihara dengan pemberian substrat limbah pertanian berupa cacahan sisa sayur- mayur, seperti tomat, seledri, pakcoy, kembang kol, brokoli, dan wortel dan sisa parutan kelapa selama 18–21 hari hingga fase pra-pupa <xref ref-type="fig" rid="fig-59025e83">Gambar 2</xref>.</p></sec><sec><title>Pembuatan simplisia, analisis proksimat, dan ekstraksi bertingkat tepung <italic>maggot</italic> BSF</title><p>Maggot BSF dibekukan dalam freezer selama 24 jam, lalu dikering-anginkan pada suhu ruang (27–28 °C). Sebanyak 1,237 g <italic>maggot</italic> BSF dikeringkan dalam oven 60 ℃ selama 24 jam lalu diserbukkan dan diperoleh tepung simplisia sebanyak 202,32 g. Analisis proksimat tepung <italic>maggot</italic> BSF dilakukan di Laboratorium Terpadu, Departemen Ilmu dan Teknologi Pangan, IPB University. Selanjutnya, simplisia diekstraksi secara maserasi bertingkat menggunakan 3 macam pelarut, yaitu aseton, metanol, dan akuades <xref ref-type="bibr" rid="BIBR-51">(Yantina, 2016)</xref>. Semua filtrat hasil maserasi dipekatkan dengan <italic>rotary vacuum evaporator</italic> pada suhu 50 ℃.</p></sec><sec><title>Analisis LC-MS/MS</title><p>Ekstrak maggot BSF dianalisis menggunakan ultra performance liquid chromatography (UPLC) dan tandem mass spectrometry (MS/MS) sesuai metode <xref ref-type="bibr" rid="BIBR-31">(Muchammad, 2019)</xref>. Kromatografi menggunakan kolom jenis C18 HSS berukuran 1,8 μm 2,1 x 100 mm), suhu kolom 50 ℃ dengan fase geraknya air + ammonium format 5 mM- acetonitril (A) + 0,05% asam format (B), dan laju alir: 0,2 ml/menit selama 23 menit. Sampel yang telah disaring dengan filter 0,2 μm diinjeksi sebanyak 5 μl. Sistem MS yang digunakan, ialah electrospray ionization (positive mode) dengan rentang analisis 50–1200 m/z, suhu sumber 100 ℃, suhu desolvasi 350 ℃, cone gas flow 0 l/jam, desolvation gas flow: 793 l/jam, collision energy: 4 volt (energi rendah), dan rampt collision energy: 25–60 volt (energi tinggi).</p><fig id="figure-1"><label>Gambar 1</label><caption><p>Kondisi kandang<italic> maggot black soldier</italic> <italic>fly</italic> (BSF). A: area perkembangan BSF dewasa dan penetasan telur; B: tempat BSF dewasa meletakkan telur; dan C: lalat BSF dewasa.<italic>(The black soldier fly maggot (BSF) cage. A: area for egg hatching and developmental into mature BSF; B: place where the adult BSF lays eggs; C: adult BSF.)</italic></p></caption><graphic xlink:href="https://jurnal.pei-pusat.org/index.php/jei/article/download/750/565/7426" mimetype="image" mime-subtype="png"><alt-text>Image</alt-text></graphic></fig><fig id="fig-59025e83"><label>Gambar 2</label><caption><p><italic>Maggot</italic> <italic>black soldier fly</italic> berumur 18–21 hari.<italic>(Black soldier fly maggots of 18–21 days-old.)</italic></p></caption><graphic xlink:href="https://jurnal.pei-pusat.org/index.php/jei/article/download/750/565/7428" mimetype="image" mime-subtype="png"><alt-text>Image</alt-text></graphic></fig></sec><sec><title>Preparasi dan analisis stabilitas ligan</title><p>Struktur tiga dimensi (3D) ligan diperoleh dari PubChem dengan situs <ext-link ext-link-type="uri" xlink:href="https://pubchem.ncbi.nlm.nih.gov/">https://pubchem.ncbi.nlm. nih.gov/</ext-link> berformat (*sdf). Preparasi dilakukan terhadap ligan bawaan (PubChem CID 134823961) hasil kristalografi protein Keap-1 (PDB ID: 6FFM) dan ligan alami yang tertambat pada enzim IKK2 (PDB ID: 4KIK) berupa senyawa sintetik staurosporine (KSA700) <xref ref-type="bibr" rid="BIBR-26">(Liu et al., 2013)</xref>. Untuk ligan pembanding digunakan KI696 (inhibitor Nrf2/Keap-1 komersial) (CID 118170767), dimetil fumarat (antiinflamasi Tecfidera®), TPCA-1 (Presscot et al.2018), aspirin <xref ref-type="bibr" rid="BIBR-11">(Frelin et al., 2003)</xref>, dan wedelolakton <xref ref-type="bibr" rid="BIBR-2">(Ali et al., 2016)</xref>. Ligan uji yang dipakai berasal dari senyawa ekstrak maggot (H. illucens), yaitu 5 macam ligan dari penelusuran pustaka, yaitu luteolin, apegenin, kuersetin, rutin, kaempferol <xref ref-type="bibr" rid="BIBR-41">(Shumo et al., 2019)</xref>, dan 40 ligan uji yang didapatkan dari hasil LC-MS/MS ekstrak maggot BSF. Struktur 3D ligan uji dan pembanding dioptimasi geometrinya pada perangkat lunak YASARA structure Version 19.9.17. Selanjutnya, disimpan dalam format (*pdb) <xref ref-type="bibr" rid="BIBR-17">(Jain &amp; Nicholls, 2008)</xref>.</p></sec><sec><title>Preparasi dan analisis stabilitas reseptor</title><p>Analisis in silico menggunakan struktur 3D dua macam reseptor, yaitu protein Keap-1 (PDB ID: 6FFM) dan enzim IKK2 (PDB ID: 4KIK). Struktur 3D reseptor diunduh pada situs web Protein Data Bank menggunakan kode akses 6FFM untuk protein Keap-1 (<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.2210/pdb6ffm/pdb">https://doi.org/10.2210/pdb6ffm/ pdb</ext-link>) dan 4KIK untuk enzim IKK2 (<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.2210/pdb4kik/pdb">https:// doi.org/10.2210/pdb4kik/pdb</ext-link>) dalam format (*pdb). Struktur 3D reseptor tersebut kemudian dibersihkan dari molekul air dan ligan alami yang masih menempel pada strukturnya, atom hidrogen polar ditambahkan menggunakan perangkat lunak YASARA Structure, selanjutnya disimpan dalam bentuk format (*pdb) <xref ref-type="bibr" rid="BIBR-21">(Krieger &amp; Vriend, 2015)</xref>.</p></sec><sec><title>Analisis bioavailabilitas dan toksisitas ligan</title><p>Analisis bioavailabilitas terhadap seluruh senyawa (ligan) uji dan kontrol/pembanding dilakukan dalam bentuk canonical SMILES pada laman situs web pkCSM (<ext-link ext-link-type="uri" xlink:href="http://biosig.unimelb.edu.au/pkcsm/prediction">http://biosig.unimelb.edu.au/pkcsm/prediction</ext-link>) dan laman situs web SwissADME (<ext-link ext-link-type="uri" xlink:href="http://www.swissadme.ch">http://www.swissadme.ch</ext-link>). Hasil analisis dapat langsung terlihat pada masing- masing laman situs web <xref ref-type="bibr" rid="BIBR-9">(Daina et al., 2017)</xref><xref ref-type="bibr" rid="BIBR-37">(Pires et al., 2015)</xref>. Bioavailabilitas semua senyawa yang teridentifikasi diprediksi secara in silico menggunakan parameter fisikokimiawi, yakni bobot molekul, donor, dan akseptor hidrogen, logP, serta refraktivitas molar ligan sesuai aturan <xref ref-type="bibr" rid="BIBR-24">(Lipinski et al., 2012)</xref>.</p><p>Toksisitas ligan uji dianalisis menggunakan situs web ProTox-II <xref ref-type="bibr" rid="BIBR-5">(Banerjee et al., 2018)</xref>. Prediksi dilakukan dengan mengunggah struktur Canonical SMILES ligan pada bagian Tox-Prediction di laman <ext-link ext-link-type="uri" xlink:href="https://tox-new.charite.de/protox_II">https://tox-new.charite.de/protox_II</ext-link>. Hasil analisis ditampilkan pada laman prediction result dalam parameter absorpsi, distribusi, metabolisme, dan ekskresi (ADME) yang mencakup topology polar surface area (TPSA), kelarutan air, absorpsi gastro intestinal (GI), log kp, dan skor bioavailabilitas sesuai standar ADME.</p></sec><sec><title>Penambatan molekuler</title><p><bold>Validasi metode. </bold>Setelah ligan alami dipreparasi, dilakukan penambatan molekuler untuk validasi gridbox dan kemudian root mean square deviation (RMSD) dihitung menggunakan perangkat lunak AutoDockTools-1.5.7 (Hilman 2010 dengan modifikasi) atau YASARA Structure <xref ref-type="bibr" rid="BIBR-21">(Krieger &amp; Vriend, 2015)</xref>. Ukuran gridbox terbaik digunakan untuk penapisan virtual.</p><p><bold>Penapisan virtual dan analisis energi bebas Gibbs.</bold> Penapisan virtual untuk menentukan potensi sebagai antioksidan (inhibitor protein Keap-1) menggunakan perangkat lunak Autodock 4.2.6, sedangkan potensi antiinflamasi (inhibitor enzim IKK2) ditentukan dengan YASARA Structure. Hasil penapisan virtual berupa file dalam format (*txt). Hasil penambatan molekul dianalisis melalui parameter energi bebas Gibbs (ΔG/ energi bebas pengikatan), yakni menganalisis afinitas pengikatan dan konstanta disosiasi (Kd) ligan dan reseptor <xref ref-type="bibr" rid="BIBR-10">(Durai et al., 2017)</xref><xref ref-type="bibr" rid="BIBR-3">(Ali et al., 2020)</xref>. Visualisasi 3D dilakukan menggunakan perangkat lunak PyMOL.</p></sec></sec><sec><title>HASIL</title><sec><title>Simplisia dan identifikasi senyawa bioaktif ekstrak maggot BSF</title><p>Hasil analisis proksimat menunjukkan bahwa tepung maggot BSF memiliki bobot kering sebesar 91,61%, kadar abu 8,41%, protein kasar 34,70%, serat kasar 7,56%, lemak kasar 40,91%, dan beta-N 0,03%. Hasil analisis LC-MS/MS terhadap ekstrak maggot BSF didapatkan 41 senyawa, namun terdeteksi 40 senyawa yang terdiri atas 15 senyawa ekstrak air <xref ref-type="table" rid="table-d5287621">Tabel 1</xref>, 13 senyawa ekstrak aseton<xref ref-type="table" rid="table-3c2c2c8a">Tabel 2</xref>, dan 12 senyawa ekstrak metanol <xref ref-type="table" rid="table-d6c27840">Tabel 3</xref>. Secara umum golongan senyawa yang terbanyak adalah senyawa alkaloid (70%) dan sisanya beragam senyawa derivat lipid dan alkohol rantai panjang.</p></sec><sec><title>Prediksi bioavailabilitas dan toksisitas</title><p>Skor bioavailabilitas menunjukkan bahwa untuk semua ligan nilainya berkisar 0,17–0,85 dengan mayoritas skor bioavailabilitas = 0,55 <xref ref-type="table" rid="table-dfc17c3b">Tabel 4</xref>, artinya semua senyawa memiliki skor bioavailabilitas di atas 0,10 sehingga diprediksi dapat menjadi kandidat antioksidan dan obat anti-inflamasi yang efektif jika memenuhi syarat keamanan melalui prediksi toksisitas. Meskipun demikian, berdasarkan karakteristik fisikokimiawi terdapat satu senyawa yang tidak memenuhi persyaratan karena melanggar lebih dari 2 aturan Lipinski, yaitu suatu senyawa alkaloid pada ekstrak air dengan formula C39H75N5O9 (PubChem ID 22819456). Senyawa ini juga termasuk salah satu dari 3 senyawa yang tidak memenuhi standar ADME karena tidak memenuhi standar TPSA (226,77 Å²), tidak larut air, absorpsi GI rendah, dan log kp negatif (-6,84 cm/s). Dua senyawa lainnya adalah satu senyawa alkaloid pada ekstrak aseton (C27H47N3O6S, PubChem ID11082109) dengan TPSA = 279,75 Å², absoprsi GI rendah, sangat larut air, dan log kp sangat negatif (-14,47 cm/s) dan satu senyawa alkohol rantai panjang pada ekstrak metanol (C24H48O3, PubChem ID16320 5262) memiliki TPSA = 142,21 Å², cukup larut dengan air, absorpsi GI rendah, dan log kp negatif (-6,99 cm/s).</p><p>Toksisitas senyawa ekstrak maggot BSF diprediksi melalui parameter kardiotoksisitas berupa inhibisi kanal kalium Human Ether-à-go- go-Related Gene (hERG) jantung, karsinogenitas, dan toksisitas oral akut. Terdapat total 16 senyawa terkonfirmasi sebagai senyawa toksik karena tidak lolos uji kardiotoksisitas dan karsinogenitas, yaitu masing-masing 6 senyawa pada ekstrak air dan 5 senyawa pada ekstrak aseton, serta 5 senyawa pada ekstrak metanol<xref ref-type="table" rid="table-dfc17c3b">Tabel 4</xref>. Sementara itu, analisis toksisitas berdasarkan toksisitas oral akut (LD<sub>50</sub>) memperlihatkan bahwa semua senyawa yang teridentifikasi tidak ada yang masuk kategori sangat toksik. Mayoritas senyawa ekstrak maggot BSF masuk kategori III/toksisitas rendah, dengan persentase pada ekstrak air, aseton, dan metanol berturut-turut adalah 73%, 75%, dan 69%<xref ref-type="table" rid="table-dfc17c3b">Tabel 4</xref>. Terdapat masing-masing 2 senyawa dalam ekstrak air dan aseton dengan toksisitas sedang/kategori II, sedangkan pada ekstrak metanol selebihnya adalah senyawa tidak toksik/kategori IV (LD<sub>50</sub> ≥ 5000 mg/kg). Prediksi toksisitas sejumlah kontrol menunjukkan bahwa beberapa ligan kontrol, yaitu KI690, dimethyl fumarate (DMF), dan aspirin masuk kategori toksisitas sedang (Data tidak ditampilkan).</p><table-wrap id="table-d5287621"><label>Tabel 1</label><caption><p>Kandungan senyawa bioaktif ekstrak air<italic> maggot black soldier fly</italic><italic>(Bioactive compounds in water extract of black soldier fly maggot)</italic></p></caption><table frame="box" rules="all"><thead><tr><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>No.</p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Waktu retensi (menit)</p><p><italic>(Retention time/Rt) (minute)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Bobot terhitung <italic>(Calculated</italic></p><p><italic>mass)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Golongan senyawa <italic>(Compound group)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Rumus kimia</p><p><italic>(Chemical formula)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Nama senyawa/PubChem CID</p><p><italic>(Compound name/PubChem CID)</italic></p></th></tr></thead><tbody><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>1.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">2,512</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>120,0813</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C8 H9 N</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>N-ethenylaniline</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>2.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">1,633</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>137,0463</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C5 H4 N4 O</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Isoxazolo[5,4-D]pyrimidin-4-amine</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>3.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">3,517</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>188,0712</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C11 H9 N O2</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>1-Naphthyl carbamate</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">9,844</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>216,1964</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C12 H25 N O2</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Butoctamide</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>5.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">11,581</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>244,2277</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C14 H29 N O2</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>N-(2-Hydroxyethyl) dodecanamide</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>6.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">1,985</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>254,1617</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C11 H19 N5 O2</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Verpacamide A</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>7.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">15,644</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>439,3787</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Wax</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C27 H50 O4</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>91722024</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>8.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">15,694</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>439,3801</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C28 H46 N4</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>101885348</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>9.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">16,046</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>465,3944</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Sterol</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C29 H52 O4</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>146760</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>10.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">18,063</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>467,4114</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C30 H50 N4</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>142527989</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>11.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">10,723</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>478,2441</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Naphthalenone</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C25 H35 N O8</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>73775828</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>12.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">18,394</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>493,4257</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Sterol</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C31 H56 O4</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>53318176</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>13.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">15,033</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>537,4519</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Wax</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C33 H60 O5</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>134768022</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>14.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">15,251</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>537,4532</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C34 H56 N4 O</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>58770928</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>15.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">17,753</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>758,5643</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Acyl Amine</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C39 H75 N5 O9</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>22819456</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>16.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">4,571</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>1097,6557</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C47 H80 N22 O9</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p><italic>Unknown</italic></p></td></tr></tbody></table></table-wrap><table-wrap id="table-3c2c2c8a"><label>Tabel 2</label><caption><p>Kandungan senyawa bioaktif ekstrak aseton <italic>maggot black soldier fly</italic><italic>(Bioactive compounds in acetone extract of black soldier fly maggot)</italic></p></caption><table frame="box" rules="all"><thead><tr><th colspan="1" rowspan="1" style="" align="left" valign="top">No.</th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Waktu retensi (menit)</p><p><italic>(Retention time/Rt) (minute)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Bobot terhitung <italic>(Calculated mass)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Golongan senyawa <italic>(Compound</italic></p><p><italic>group)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Rumus kimia</p><p><italic>(Chemical formula)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Nama senyawa/PubChem CID</p><p><italic>(Compound name/PubChem CID)</italic></p></th></tr></thead><tbody><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">1.</td><td colspan="1" rowspan="1" style="" align="left" valign="top">1,261</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>108,0813</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C7 H9 N</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>1-(prop-2-en-1-yl)-1H-pyrrole</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">2.</td><td colspan="1" rowspan="1" style="" align="left" valign="top">7,785</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>138,0919</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C8 H11 N O</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>N-(2-furylmethyl) cyclopropanamine</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">3.</td><td colspan="1" rowspan="1" style="" align="left" valign="top">1,407</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>138,1283</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C9 H15 N</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>N-(prop-2-yn-1-yl) cyclohexanamine</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">4.</td><td colspan="1" rowspan="1" style="" align="left" valign="top">9,141</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>170,0606</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Benzofuran</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C11 H8 N O</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Benzofuro[3,2-b]pyridine</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">5.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>13,409</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>184,0722</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C7 H9 N3 O3</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>2,3-Dihydro-2-ethyl-6- nitroimidazo(2,1-b)oxazole</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">6.</td><td colspan="1" rowspan="1" style="" align="left" valign="top">4,705</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>188,1439</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C13 H17 N</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>2,2,4,6-Tetramethyl-1,2-</p><p>dihydroquinoline</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">7.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>18,176</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>226,2171</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C14 H27 NO</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>395324</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">8.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>10,794</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>227,2011</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Wax</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">C14 H26 O2</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Citronellyl butyrate</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">9.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>11,384</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>286,2746</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Sphingolipid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C17 H35 N O2</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C17 Sphingosine</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">10.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>13,535</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>307,2637</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Fatty acid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C20 H35 O2</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>5,8,14-Eicosatrienoic acid</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">11.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>15,096</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>326,3059</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C20 H39 N O2</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>n-Oleoylethanolamine</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">12.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>16,130</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>328,3216</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C20 H41 N O2</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>N-(2-Hydroxyethyl)</p><p>octadecanamide</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">13</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>12,572</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>542,3264</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C27 H47 N3O6 S</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>11082109</p></td></tr></tbody></table></table-wrap><table-wrap id="table-d6c27840"><label>Tabel 3</label><caption><p>Kandungan senyawa bioaktif ekstrak metanol <italic>maggot black soldier fly</italic><italic>(Bioactive compounds in methanolic extract of black soldier fly maggot)</italic></p></caption><table frame="box" rules="all"><thead><tr><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>No.</p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Waktu retensi (menit)</p><p><italic>(Retention time/Rt) (minute)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Bobot terhitung <italic>(Calculated mass)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Golongan senyawa <italic>(Compound</italic></p><p><italic>group)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Rumus kimia</p><p><italic>(Chemical formula)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Nama senyawa/PubChem CID</p><p><italic>(Compound name/PubChem CID)</italic></p></th></tr></thead><tbody><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>1.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>1,520</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>148,1126</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C10 H13 N</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Actinidine</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>2.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>10,288</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>184,0722</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C7 H9 N3 O3</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>72494</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>3.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>8,789</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>240,2327</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C15 H29 N O</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Tetradecyl isocyanate</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>11,673</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>244,2277</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C14 H29 N O2</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>8899</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>5.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>15,117</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>265,2531</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Long-chain alcohol</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C18 H32 O</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>6436081</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>6.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>9,844</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>357,2866</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C18 H36 N4 O3</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Lauroyl arginine</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>7.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>12,087</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>366,3484</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C22 H43 N3 O</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>101975560</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>8.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>14,640</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>385,3682</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Long-chain alcohol</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C24 H48 O3</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>163205262</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>9.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>16,264</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>396,3478</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C24 H45 N O3</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Semiplenamide E</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>10.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>12,552</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>413,3492</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C22 H44 N4 O3</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Palmitoyl arginine</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>11.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>13,585</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>522,3615</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C22 H47 N7 O7</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>101235998</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>12.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>17,205</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>550,6291</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Alkaloid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C38 H79 N</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>3-hexadecyl-N- propylnonadecan-1-amine</p></td></tr></tbody></table></table-wrap><table-wrap id="table-dfc17c3b"><label>Tabel 4</label><caption><p>Bioavailabilitas dan analisis toksisitas ekstrak maggot<italic> black soldier fly</italic><italic>(Bioavailability and toxicity analyses of black soldier fly maggot extracts)</italic></p></caption><table frame="box" rules="all"><thead><tr><th colspan="1" rowspan="1" style="" align="left" valign="top">No.</th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Nama/Kode senyawa</p><p><italic>(Compund name/Code)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Skor bioavailabilitas</p><p><italic>(Bioavailability score)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Inhibisi hERG</p><p><italic>(hERG inhibition)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Karsinogenitas</p><p><italic>(Carcinogenicity)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Toksisitas oral akut <italic>(Acute oral toxicity)</italic> (LD50)</p></th></tr></thead><tbody><tr><td colspan="6" rowspan="1" style="" align="left" valign="top"><p>Ekstrak air <italic>(Water extract)</italic></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">1.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>58770928**</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,17</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Kuat <italic>(Strong)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">2.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>142527989**</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Kuat <italic>(Strong)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>II</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">3.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>73775828</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">4.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>53318176</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">5.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>1-Naphthyl carbamate**</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>K</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">6.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Verpacamide A</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">7.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>146760</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">8.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>101885348**</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Kuat <italic>(Strong)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>II</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">9.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>1415476**</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>K</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">10.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>91722024</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>IV</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">11.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>134768022</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,17</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>IV</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">12.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>8899</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">13.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Butoctamide</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">14.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>N-ethenylaniline</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">15.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>22819456**</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,17</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Kuat (<italic>Strong)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="6" rowspan="1" style="" align="left" valign="top"><p>Ekstrak aseton <italic>(Acetone extract)</italic></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">16.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C17 Sphingosine**</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Kuat (<italic>Strong)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">17.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>5,8,14-Eicosatrienoic acid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,85</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>IV</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">18.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>2,2,4,6-Tetramethyl-1,2-</p><p>dihydroquinoline</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">19.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Benzofuro[3,2-b]pyridine</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">20.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>3-(tert-Butylamino)-1,7,7- trimethylbicyclo[2.2.1] heptan-2-ol</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">21.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>N-(2-Hydroxyethyl)</p><p>octadecanamide</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">22.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Citronellyl butyrate</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">23.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>11082109**</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Kuat (<italic>Strong)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">24.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>2,3-Dihydro-2-ethyl- 6-nitroimidazo(2,1-b) oxazole**</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>K</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">25.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>N-(prop-2-yn-1-yl) cyclohexanamine</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>II</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">26.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>N-(2-furylmethyl) cyclopropanamine</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">27.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>n-Oleoylethanolamine**</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>K</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>IV</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">28.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>1-(prop-2-en-1-yl)-1H-</p><p>pyrrole**</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">0,55</td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>K</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>II</p></td></tr><tr><td colspan="6" rowspan="1" style="" align="left" valign="top"><p>Ekstrak metanol <italic>(Methanol extract)</italic></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">29.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Tetradecyl isocyanate</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>0,55</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">30.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>1-(1-Lauroylamino</p><p>ethyl)-2-pentyl-2- imidazoline**</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>0,55</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">Kuat (<italic>Strong)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">31.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>3-hexadecyl-N- propylnonadecan-1- amine**</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>0,17</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">Kuat (<italic>Strong)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">32.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>9,12,15-Octadecatrien-1- ol, (9Z,12Z,15Z)-**</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>0,55</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">Kuat (<italic>Strong)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>IV</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">33.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>2,3-Dihydro-2-ethyl- 6-nitroimidazo(2,1-b) oxazole**</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>0,55</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>K</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">34.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Palmitoyl arginine</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>0,55</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">35.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>163205262</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>0,55</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>IV</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">36.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Actinidine</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>0,55</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">37.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Semiplenamide E**</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>0,55</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>K</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">38.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>N-(2-Hydroxyethyl)</p><p>dodecanamide</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>0,55</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">39.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Lauroyl arginine</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>0,55</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>III</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">40.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>101235998</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>0,17</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">Lemah <italic>(Weak)</italic></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>NK</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>IV</p></td></tr></tbody></table><table-wrap-foot><p>Kategori I: LD<sub>50</sub> ≤ 50 mg/kg; II: 50 mg/kg &lt; LD<sub>50</sub> ≤ 500 mg/kg; III: 500 mg/kg &lt; LD50 ≤ 5000 mg/kg; IV: 5000 mg/kg; K: Karsinogenik; NK: Non-karsinogenik. Tanda** menunjukkan ligan/senyawa yang tidak lolos prediksi bioavailibilitas dan toksisitas<italic>. (Category I: LD</italic><italic><sub>50</sub></italic><italic> ≤ 50 mg/kg; II: 50 mg/kg &lt; LD</italic><italic><sub>50</sub></italic><italic> ≤ 500 mg/kg; III: 500 mg/kg &lt; LD50 ≤ 5000 mg/kg; IV: 5000 mg/kg; K: Carcinogenic; NK: Non-carcinogenic. The ** mark indicates ligands/compounds that do not pass bioavailability and toxicity predictions).</italic></p></table-wrap-foot></table-wrap></sec><sec><title>Penapisan virtual senyawa aktif berpotensi antioksidan dan antiinflamasi</title><p>Penapisan virtual terhadap 26 ligan uji yang lolos uji toksisitas <xref ref-type="table" rid="table-1f5f0802">Tabel 6</xref> dengan metode penambatan molekuler terhadap protein Keap-1 menunjukkan bahwa inhibitor NRF2/Keap-1 KI696 adalah senyawa paling berpotensi meng- aktifkan mekanisme antioksidan selular, bahkan lebih baik dari ligan hasil kristalografi, dengan nilai energi bebas Gibbs (ΔG) tertinggi, yakni sebesar -8,07 kkal/mol dan nilai konstanta disosiasi (Kd) = 2,56 × 10<sup>-5</sup> µM (Tabel 5). Visualisasi secara 3-D memprediksi posisi KI696 yang berikatan memenuhi area sisi aktif protein Keap-1 sehingga berpotensi akan menghalangi asosiasi Keap-1 dengan NRF2 <xref ref-type="fig" rid="fig-7d23a746">Gambar 3</xref>. Sementara itu, senyawa DMF yang merupakan anti-inflamasi komersil dapat menghambat aktivasi NRF2 dengan menghasilkan ΔG yang relatif lebih kecil (-3,74 kkal/mol) dan Kd yang lebih besar (5,32 × 10<sup>-5</sup> µM). Hal ini terlihat dari posisi ligan yang menempati sisi aktif protein Keap-1 di bagian tengah sisi aktif saja <xref ref-type="fig" rid="fig-7d23a746">Gambar 3</xref>. Semua senyawa flavonoid yang menjadi ligan pembanding terbukti berpotensi sebagai antioksidan (ΔG antara -5,35 hingga -4,05 kkal/mol dan nilai Kd antara 4,05 × 10<sup>-5</sup> hingga 5,05 × 10<sup>-5</sup> µM). Sementara, semua ligan uji dari ekstrak air, aseton, dan metanol menunjukkan potensi sebagai antioksidan yang lebih baik daripada DMF <xref ref-type="table" rid="table-1f5f0802">Tabel 6</xref>, kecuali satu senyawa alkaloid dari ekstrak metanol (PubChem ID 101235998) yang bernilai ΔG lebih kecil daripada DMF. Gambar 4 memperlihatkan visualisasi 3-D dari senyawa paling potensial sebagai inhibitor Keap-1, yaitu suatu senyawa naphtalenone dalam ekstrak air maggot BSF, yaitu methyl 2-[[(1S,2R,4aS,5R,8aS)-2-acetyloxy-5- [(2E)-2-[(4S)-4-hydroxy-2-oxooxolan-3-ylidene] ethyl]-1,4a-dimethyl-6-methylidene 3,4,5,7,8,8a- hexa hydro- 2H- naphthalene-1-carbonyl] amino] acetate (Pubchem ID73775828).</p><p>Adapun potensi antiinflamasi yang diprediksi melalui penambatan molekuler ligan uji pada enzim IKK2 menunjukkan bahwa ligan alami IKK2, yaitu staurosporine (KSA700) memiliki nilai ΔG yang tertinggi, yaitu sebesar -9.054 kkal/mol dan nilai Kd sangat kecil (0,00023 ×10<sup>3</sup> µM<xref ref-type="table" rid="table-8ca483e0">Tabel 7</xref> . Gambar 5A memperlihatkan visualisasi 3-D dari posisi KSA700 yang berikatan memenuhi area sisi aktif enzim IKK2 sehingga berpotensi akan menghalangi asosiasi enzim IKK2 dengan NF- kappaB. Sementara, kontrol aspirin bernilai ΔG lebih rendah, yaitu -4.284 kkal/mol dan Kd sebesar 0,724 × 10<sup>3</sup> µM, sedangkan kaemferol, kuersetin, dan apigenin bahkan masih lebih berpotensi sebagai antiinflamasi daripada aspirin. Adapun analisis terhadap 26 ligan uji dari ekstrak BSF menunjukkan bahwa ligan dari ekstrak air yang paling berpotensi antiinflamasi, yaitu naphthyl carbamate (ΔG = -6,945 kkal/mol; Kd = 0,008 × 10<sup>3</sup> µM)<xref ref-type="fig" rid="fig-fecdd213">Gambar 5</xref>, diikuti oleh verpacamide A (ΔG = -5,024 kkal/mol; Kd = 0,207 × 10<sup>3</sup> µM)<xref ref-type="table" rid="table-54125da3">Tabel 8</xref>. Senyawa lainnya walau menghasilkan ikatan energi negatif, namun dari nilai Kd yang sangat besar dapat diduga bahwa tidak terdapat interaksi yang kuat antara senyawa tersebut dan enzim IKK2 sehingga bukan antiinflamasi yang potensial<xref ref-type="table" rid="table-54125da3">Tabel 8</xref>.</p><table-wrap id="table-f8f97a78"><label>Tabel 5</label><caption><p>Hasil penambatan molekuler ligan kontrol dan pembanding pada protein Keap-1<italic>(</italic>Bioavailability and toxicity analyses of black soldier fly maggot extracts<italic>)</italic></p></caption><table frame="box" rules="all"><thead><tr><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>No.</p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Nama senyawa</p><p><italic>(Compund name)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Energi bebas Gibbs (Kkal/mol)</p><p><italic>(Gibbs free energy) (Kcal/mol)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Konstanta disosiasi <italic>(Constant of dissociation)</italic> (µM)</p></th></tr></thead><tbody><tr><td colspan="4" rowspan="1" style="" align="left" valign="top"><p>Ligan kontrol <italic>(Control ligand)</italic></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>1.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>N-[4-[(5R)-3-sulfanyl-1,2-oxazolidin-5- yl]phenyl]acetamide</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-5,61</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">3,88 × 10<sup>-5</sup></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>2.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>KI696</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">-8,07</td><td colspan="1" rowspan="1" style="" align="left" valign="top">2,56 × 10<sup>-5</sup></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>3.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Dimethyl fumarate</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-3,74</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">5,32 × 10<sup>-5</sup></td></tr><tr><td colspan="4" rowspan="1" style="" align="left" valign="top"><p>Ligan pembanding <italic>(Reference ligand)</italic></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>1.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Luteolin</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-5,35</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,05 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">2.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Apigenin</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top">-5,25</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,12 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>3.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Kuersetin</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-4,64</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,57 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Kaempferol</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-4,61</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,59 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>5.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Rutin</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-4,05</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>5,05 × 10<sup>-5</sup></p></td></tr></tbody></table><table-wrap-foot><p>No. 1: ligan hasil kristalografi; No. 2: inhibitor NRF2/Keap-1; No. 3: anti-inflamasi Tecfidera®<italic>(No. 1: ligand from crystallography; No.2: NRF2/Keap-1 inhibitor; No.3: anti-inflammatory Tecfidera®)</italic></p></table-wrap-foot></table-wrap><fig id="fig-7d23a746"><label>Gambar 3</label><caption><p>Visualisasi 3-dimensi interaksi reseptor Keap-1 dengan ligan pembanding. A: KI696 dan B: DMF.<italic>(Three-dimesion visualization of Keap-1 reseptor interation with A: KI696 and B: DMF as comparative ligands.)</italic></p></caption><graphic xlink:href="https://jurnal.pei-pusat.org/index.php/jei/article/download/750/565/7430" mimetype="image" mime-subtype="png"><alt-text>Image</alt-text></graphic></fig><table-wrap id="table-1f5f0802"><label>Tabel 6</label><caption><p>Hasil penambatan molekuler ekstrak maggot <italic>black soldier fly</italic> pada protein Keap-1<italic>(Molecular docking of black soldier fly maggot extract with Keap-1 protein)</italic></p></caption><table frame="box" rules="all"><thead><tr><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>No*</p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Nama senyawa</p><p><italic>(Compund name)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Energi bebas Gibbs (Kkal/mol)</p><p><italic>(Gibbs free energy) (Kcal/mol)</italic></p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Konstanta disosiasi (µM)</p><p><italic>(Constant of dissociation)</italic></p></th></tr></thead><tbody><tr><td colspan="4" rowspan="1" style="" align="left" valign="top"><p>Ekstrak air <italic>(Water extract)</italic></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>3.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>73775828</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-6,08</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>3,58 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>53318176</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-6,06</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>3,60 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>5.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>1-Naphtyl carbamate</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-5,44</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>3,99× 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>6.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Verpacamide A</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-5,40</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,02 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>7.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>146760</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-5,23</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,14 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>10.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>91722024</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-4,81</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,44 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>11.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>134768022</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-4,61</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,59 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>12.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>8899</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-4,41</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,75 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>13</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Butoctamide</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-4,35</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,80 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>14.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>N-ethenylaniline</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-4,32</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,82 × 10<sup>-5</sup></p></td></tr><tr><td colspan="4" rowspan="1" style="" align="left" valign="top"><p>Ekstrak aseton <italic>(Acetone extract)</italic></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>16.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C17 Sphingosine</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-6,03</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>3,61× 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>17.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>5,8,14-Eicosatrienoic acid</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-5,65</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>3,85 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>18.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>2,2,4,6-Tetramethyl-1,2-dihydroquinoline</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-5,38</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,03 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>19.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Benzofuro[3,2-b]pyridine</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-5,22</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,14 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>20.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>3-(tert-Butylamino)-1,7,7- trimethylbicyclo[2.2.1]heptan-2-ol</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-5,20</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,16 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>21.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>N-(2-Hydroxyethyl)octadecanamide</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-5,18</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,17 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>22.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Citronellyl butyrate</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-5,13</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,21 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>25.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>N-(prop-2-yn-1-yl)cyclohexanamine</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-4,71</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,52 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>26.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>N-(2-furylmethyl)cyclopropanamine</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>- 4,45</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,72 × 10<sup>-5</sup></p></td></tr><tr><td colspan="4" rowspan="1" style="" align="left" valign="top"><p>Ekstrak metanol <italic>(Methanol extract)</italic></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>29.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Tetradecyl isocyanate</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-5,24</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,13 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>34.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Palmitoyl arginine</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-4,96</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,33 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>35.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>(E)-12,12-dihexoxydodec-3-en-1-ol</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-4,91</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,37 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>36.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Actinidine</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-4,77</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,47 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>38.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>N-(2-Hydroxyethyl)dodecanamide</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-4,71</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,52 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>39.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Lauroyl arginine</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-4,46</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4,71 × 10<sup>-5</sup></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>40.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>101235998</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>-3,42</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>5,61 × 10<sup>-5</sup></p></td></tr></tbody></table><table-wrap-foot><p>*: nomor senyawa disesuaikan dengan nomor pada <xref ref-type="table" rid="table-dfc17c3b">Tabel 4</xref>. <italic>(*: compound number adjusted to the number in</italic><xref ref-type="table" rid="table-dfc17c3b">Tabel 4</xref><italic>).</italic></p></table-wrap-foot></table-wrap><fig id="fig-d2d8b5b8"><label>Gambar 4</label><caption><p>Visualisasi 3-dimensi interaksi antara reseptor Keap-1 dan ligan uji Naphta- lenone 73775828.<italic>(Three-dimension visualization of Keap-1 interaction with test ligand Naphtalenone 73775828.)</italic></p></caption><graphic xlink:href="https://jurnal.pei-pusat.org/index.php/jei/article/download/750/565/7429" mimetype="image" mime-subtype="png"><alt-text>Image</alt-text></graphic></fig></sec></sec><sec><title>PEMBAHASAN</title><table-wrap id="table-8ca483e0"><label>Tabel 7</label><caption><p>Hasil penambatan molekuler ligan kontrol dan pembanding pada enzim IKK<italic>(Molecular docking of control ligands on the IKK enzyme)</italic></p></caption><table frame="box" rules="all"><thead><tr><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>No.</p></th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Nama senyawa</p><p><italic>(Compund name)</italic></p></th><th colspan="1" rowspan="1" style="" align="center" valign="top"><p>Energi bebas Gibbs (Kkal/mol) (<italic>Gibbs free energy</italic>) (<italic>Kcal/mol</italic>)</p></th><th colspan="1" rowspan="1" style="" align="center" valign="top"><p>Konstanta disosiasi (<italic>Constant of dissociation</italic>) <bold>(</bold>µM × 10<sup>3</sup>)</p></th></tr></thead><tbody><tr><td colspan="4" rowspan="1" style="" align="left" valign="top"><p>Ligan kontrol <italic>(Control ligand)</italic></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>1.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>KSA700</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>-9,054</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>0,00023</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>2.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Wedelolakton</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>-5,463</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>0,098</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>3.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Aspirin</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>-4,284*</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>0,724</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>TPCA-1</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>-4,112</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>0,967</p></td></tr><tr><td colspan="4" rowspan="1" style="" align="left" valign="top"><p>Ligan pembanding (<italic>Reference ligand</italic>)</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>1.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Kaempferol</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>-6,450</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>0,018</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">2.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Kuersetin</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>-5,969</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>0,042</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>3.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Luteolin</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>-4,986</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>0,221</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>4.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Apigenin</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>-3,503</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>2,71</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>5.</p></td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Rutin</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>+8,780</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>0</p></td></tr></tbody></table><table-wrap-foot><p>No. 1: ligan hasil alami; No. 2 dan No. 4: inhibitor enzim IKK; No. 3: anti-inflamasi komersil.<italic>(No. 1: natural ligand; No. 2 and 4: IKK enzyme inhibitor; No. 3: commercial anti-inflammatory)</italic></p></table-wrap-foot></table-wrap><fig id="fig-fecdd213"><label>Gambar 5</label><caption><p>Visualisasi 3-dimensi interaksi reseptor enzim IKK2 dengan ligan alami staurosporine (KSA700) (A) dan ligan uji <italic>naphtyl carbamate</italic> (B).(Three-dimension visualization of the interaction of the IKK2 enzyme receptor with the natural ligand staurosporine (KSA700) (A); and test ligand naphtyl carbamate (B).)</p></caption><graphic xlink:href="https://jurnal.pei-pusat.org/index.php/jei/article/download/750/565/7427" mimetype="image" mime-subtype="png"><alt-text>Image</alt-text></graphic></fig><table-wrap id="table-54125da3"><label>Tabel 8</label><caption><p>Hasil penambatan molekuler ekstrak maggot<italic> black soldier fly </italic>pada enzim IKK<italic>(Molecular docking of black soldier flymaggot extracts on the IKK enzyme)</italic></p></caption><table frame="box" rules="all"><thead><tr><th colspan="1" rowspan="1" style="" align="left" valign="top">No*</th><th colspan="1" rowspan="1" style="" align="left" valign="top"><p>Nama senyawa</p><p><italic>(Compund name)</italic></p></th><th colspan="1" rowspan="1" style="" align="center" valign="top"><p>Energi bebas Gibbs (Kkal/mol) (<italic>Gibbs free energy</italic>) (<italic>Kcal/mol</italic>)</p></th><th colspan="1" rowspan="1" style="" align="center" valign="top"><p>Konstanta disosiasi (<italic>Constant of dissociation</italic>) (µM ×10<sup>3</sup>)</p></th></tr></thead><tbody><tr><td colspan="4" rowspan="1" style="" align="left" valign="top"><p>Ekstrak air <italic>(Water extract)</italic></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">5.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Naphthyl Carbamate</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top">-6,94</td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>0,008</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">6.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Verpacamide A</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>-5,024</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>0,207</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">7.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>N-ethenylaniline</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top">-1,22</td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>127</p></td></tr><tr><td colspan="4" rowspan="1" style="" align="left" valign="top"><p>Ekstrak aseton <italic>(Acetone extract)</italic></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">25.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>N-(2-Hydroxyethyl) Dodecanamide</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>-0,297</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>605</p></td></tr><tr><td colspan="4" rowspan="1" style="" align="left" valign="top"><p>Ekstrak metanol <italic>(Methanol extract)</italic></p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">28.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>C17 Sphingosine</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>-2,484</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>15,1</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">31.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>Benzofuropyridin</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>-3,737</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>1,82</p></td></tr><tr><td colspan="1" rowspan="1" style="" align="left" valign="top">37.</td><td colspan="1" rowspan="1" style="" align="left" valign="top"><p>N-(prop-2-yn-1-yl) Cyclohexanamine</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>-3,617</p></td><td colspan="1" rowspan="1" style="" align="center" valign="top"><p>2,23</p></td></tr></tbody></table><table-wrap-foot><p>No*: nomor senyawa disesuaikan dengan nomor pada<xref ref-type="table" rid="table-dfc17c3b">Tabel 4</xref>. <italic>(No*: compound number adjusted to the number in</italic><italic><xref ref-type="table" rid="table-dfc17c3b">Tabel 4</xref></italic><italic> ).</italic></p></table-wrap-foot></table-wrap><p>Maggot yang dihasilkan dari pembiakan di Sindangjaya cenderung berwarna dominan gelap disebabkan maggot sudah memasuki tahap awal pupa (pre-pupa), yaitu 18–25 hari sejak telur menetas. Simplisia tepung maggot yang diberi substrat limbah pertanian ini menunjukkan nilai kandungan protein kasar yang sedikit lebih rendah dan lemak yang lebih tinggi daripada maggot pra- pupa yang diberi limbah dapur <xref ref-type="bibr" rid="BIBR-35">(Patiassana et al., 2020)</xref>, namun relatif masih dalam kisaran yang sama dengan beberapa penelitian yang memberikan pakan ayam komersial, sisa sayuran, hingga sisa ikan sebagai substrat maggot BSF <xref ref-type="bibr" rid="BIBR-4">(Andari et al., 2021)</xref><xref ref-type="bibr" rid="BIBR-19">(Kinasih et al., 2018)</xref>. Beberapa faktor yang dapat berkontribusi terhadap perbedaan kadar protein dan kadar lemak tersebut, salah satunya dari jenis substrat yang diberikan (Meneguz et al. 2018), dalam riset ini berupa sisa aneka sayuran yang tinggi seratnya. Pada umumnya substrat buah dan sayuran yang sejenis (homogen) akan menghasil maggot BSF dengan kadar protein dan lemak yang relatif rendah (&lt;15%) <xref ref-type="bibr" rid="BIBR-42">(Siddiqui et al., 2022)</xref>. Selain itu juga, pengaruh kondisi lingkungan dan temperatur yang relatif cukup dingin di Desa Sindangjaya (ketinggian ±1100 m dpl, suhu ruangan 14–20 °C). Temperatur ruang yang rendah (15 °C) dilaporkan menyebabkan pertumbuhan maggot BSF menjadi perlahan <xref ref-type="bibr" rid="BIBR-40">(Shumo et al., 2019)</xref>, padahal terdapat perbedaan komposisi nutrisi maggot BSF pada umur yang berbeda <xref ref-type="bibr" rid="BIBR-15">(Hsiao et al., 2022)</xref>. Pada penelitian ini, kadar lemak yang diidentifikasi tergolong tinggi. Hal ini sesuai dengan hasil yang dilaporkan <xref ref-type="bibr" rid="BIBR-26">(Liu et al., 2013)</xref>. Berdasarkan hal tersebut, disimpulkan bahwa substrat sisa sayuran yang bersifat heterogen tidak mempengaruhi produksi lemak yang diperlukan metamorphosis BSF. Sebanyak 70% senyawa bioaktif dalam penelitian ini adalah alkaloid, sementara sisanya adalah turunan senyawa lipid dan alkohol rantai panjang, sesuai dengan yang dilaporkan <xref ref-type="bibr" rid="BIBR-27">(Lu et al., 2022)</xref> dan <xref ref-type="bibr" rid="BIBR-15">(Hsiao et al., 2022)</xref>.</p><p>Adanya kandungan flavonoid dalam ekstrak maggot BSF dengan substrat limbah dapur telah dilaporkan oleh <xref ref-type="bibr" rid="BIBR-41">(Shumo et al., 2019)</xref>. Sebaliknya, pada ekstrak maggot BSF dalam riset ini tidak teridentifikasi adanya senyawa flavonoid. Hal ini kemungkinan disebabkan oleh perbedaan jenis substrat yang dominan hijauan sehingga metabolisme maggot BSF menghasilkan lebih banyak alkaloid. Studi lain pada serangga sejenis menunjukkan adanya alkaloid, flavonoid, dan steroid di antara komponen bioaktif lain yang dihasilkan <xref ref-type="bibr" rid="BIBR-32">(Musundire et al., 2014)</xref><xref ref-type="bibr" rid="BIBR-6">(Cheseto et al., 2015)</xref>.</p><p>Dalam kaitannya dengan aspek keamanan suatu senyawa kandidat obat, analisis toksisitas diperlukan untuk mengetahui efek senyawa tersebut. Pada penelitian ini, analisis toksisitas diprediksi berdasarkan database. Hasil analisis toksisitas in silico menunjukkan bahwa terdapat 2 senyawa yang tidak konsisten hasilnya ketika menggunakan aplikasi perangkat lunak yang berbeda, yaitu C17 sphingosine dan 1-Naphtyl carbamate. Senyawa C17 sphingosine dalam ekstrak aseton dengan ProTox-II <xref ref-type="bibr" rid="BIBR-5">(Banerjee et al., 2018)</xref> diprediksi toksik sebagai inhibitor kuat kanal kalium hERG, sedangkan dengan admetSAR (Guan et al. 2018) menunjukkan senyawa ini tidak toksik sebagai inhibitor kanal hERG lemah. Namun demikian, suatu mikotoksin kuat analog C17 dihydrosphingosine dilaporkan terdapat pada kerang laut yang terkontaminasi oleh mikrofungi <xref ref-type="bibr" rid="BIBR-28">(Marrouchi et al., 2013)</xref> sehingga prediksi toksisitas dengan ProTox-II lebih konsisten. Senyawa 1-Naphtyl carbamate dalam ekstrak air yang diprediksi nonkarsinogenik dengan admetSAR ternyata karsinogenik melalui ProTox-II. Hal ini konsisten karena naphtyl carbamate termasuk golongan pestisida kuat dengan aktivitas antikolinesterase <xref ref-type="bibr" rid="BIBR-34">(Patel &amp; Sangeeta, 2018)</xref> sehingga terdapatnya senyawa ini besar kemungkinan sebagai akibat dari cemaran yang berasal dari substrat limbah pertanian.</p><p>Melalui penelitian ini diidentifikasi berbagai senyawa aktif dalam ekstrak maggot BSF yang dapat menghambat asosiasi NRF2 dengan protein Keap-1 sehingga akan mengaktifkan respons antioksidan selular. Dalam menjalankan perannya sebagai regulator respon antioksidan selular, aktivitas NRF2 dikendalikan oleh protein Kelch-like ECH-associated protein 1 (Keap-1) <xref ref-type="bibr" rid="BIBR-20">(Kobayashi et al., 2013)</xref>. Disosiasi protein Keap-1 dari NRF2 akan menstimulasi ekspresi beragam gen antioksidan sehingga mengaktifkan mekanisme persinyalan antioksidan selular. Oleh karena itu, ligan uji yang dapat berikatan dengan Keap-1 pada lokasi tertambatnya ligan kontrol diprediksi akan mencegah asosiasi Keap-1 dengan NRF2 sehingga persinyalan lintasan antioksidan dapat terus berjalan tanpa hambatan dari Keap-1 protein. Dalam penelitian ini, senyawa naphtalenone dalam ekstrak air memiliki potensi penghambatan Keap-1 terbesar; kelompok senyawa sejenis pada jamur (fungi) telah dilaporkan berpotensi farma- kologis <xref ref-type="bibr" rid="BIBR-16">(Ibrahim et al., 2022)</xref>. Terdapat juga satu senyawa golongan benzofuran dalam ekstrak aseton, yang dilaporkan banyak terdapat dalam berbagai tumbuhan <xref ref-type="bibr" rid="BIBR-30">(Miao et al., 2019)</xref> dengan beragam potensi bioaktif. Kelompok benzofuran adalah senyawa dengan potensi bioaktif yang cukup ampuh, antara lain sebagai anti-tumor, antibakteri, antioksidan, dan antiviral. Sejalan dengan ini, pemanfaatan ekstrak metanol dari maggot beberapa jenis serangga (Musca domestica Linnaeus, Lucilia sericata (Meigen), Chrysomya albiceps (Wiedemann)) sebagai sumber biofarmaka telah dilaporkan sebelumnya terkait aktivitas antioksidan dan antikanker <xref ref-type="bibr" rid="BIBR-13">(Hasaballah et al., 2019)</xref>.</p><p>Potensi sebagai antiinflamasi dengan cara menghambat enzim IKK2 hanya dimiliki oleh 2 ligan dari ekstrak air, yaitu Naphthyl carbamate dan verpacamide A. Penghambatan enzim IKK2 menjadi kunci pengendalian aktivitas persinyalan Nuclear Factor kappa B (NF-ƙB) dalam mekanisme peradangan, yakni suatu faktor transkripsi yang bertugas menginduksi berbagai ekspresi gen yang terlibat dalam proses inflamasi <xref ref-type="bibr" rid="BIBR-39">(Serasanambati &amp; Chilakapati, 2016)</xref>. Mengingat naphtyl carbamate adalah cemaran pestisida/insektisida dari lingkungan maka hanya verpacamide A yang berpotensi antiinflamasi pada ekstrak maggot BSF ini. Senyawa yang sama telah ditemukan pada spons laut Axinella vaceleti <xref ref-type="bibr" rid="BIBR-46">(Vergne et al., 2006)</xref>.</p><p>Protein NRF2 merupakan elemen kunci dalam sistem pertahanan seluler melawan stres oksidatif <xref ref-type="bibr" rid="BIBR-52">(Yu &amp; Xiao, 2021)</xref>. Saat dalam keadaan normal, NRF2 berinteraksi dengan Keap-1 sebagai pengatur negatif NRF2, membentuk kompleks Keap1-NRF2 yang berujung pada degradasi proteasom dan ubikitinasi NRF2. Namun, saat terjadi stres oksidatif, Keap1 menjadi tidak aktif, menghentikan ubikitinasi NRF2 dan memungkinkan NRF2 untuk berpindah ke inti sel dan membentuk heterodimer dengan small musculoapo-neuroticfibrosarcoma (sMAF), yang mengikat elemen respons antioksidan (antioxidant response element, ARE) <xref ref-type="bibr" rid="BIBR-23">(Lee &amp; Hu, 2020)</xref><xref ref-type="bibr" rid="BIBR-43">(Silva et al., 2018)</xref>. Pengaktifan sinyal NRF2 melalui Keap-1 menjadi salah satu target yang efektif dalam mencegah stres oksidatif (antioksidan) <xref ref-type="bibr" rid="BIBR-1">(Abed et al., 2015)</xref>.</p><p>Inflamasi (peradangan) muncul karena produksi berlebihan senyawa proinflamasi, salah satunya NF-κB. Sinyal NF-κB dipengaruhi oleh dua protein kunci, yaitu inhibitor of NFkB (IκB) dan kompleks enzim IκB kinase (IKK). Ketika dalam keadaan tidak aktif, NF-κB berikatan dengan protein IκB di dalam sitoplasma. Namun, saat terjadi inflamasi, enzim IkB Kinase menjadi aktif, mengakibatkan fosforilasi IκB dan aktivasi NF-κB. Proses aktivasi NF-κB meliputi pelepasan protein IκB, translokasi ke inti sel, pengikatan DNA, dan transaktivasi <xref ref-type="bibr" rid="BIBR-36">(Patwardhan et al., 2016)</xref>. Aktivasi NF-κB memicu produksi senyawa- senyawa proinflamatori yang memicu inflamasi. Enzim IKK adalah kompleks multiprotein yang terdiri atas dua subunit kinase, yaitu IKKα dan IKKβ. IKKβ (IKK2) memiliki peran yang lebih signifikan dalam jalur kanonikal, terutama dalam merespons proinflamasi <xref ref-type="bibr" rid="BIBR-44">(Solt &amp; May, 2008)</xref>. Penelitian ini diharapkan dapat menjadi salah satu referensi pemanfaatan maggot BSF sebagai alternatif sumber antioksidan alami sehingga dapat meningkatkan nilai jual maggot BSF bagi masyarakat.</p></sec><sec><title>KESIMPULAN</title><p>Sebanyak 26 senyawa aktif yang terkandung dalam ekstrak maggot BSF memiliki potensi sebagai antioksidan melalui penghambatan protein Keap-1 yang diduga dapat asosiasinya dengan faktor transkripsi NRF2. Senyawa naphtalenone, yaitu methyl 2-[[(1S,2R,4aS,5R,8aS)-2-acetyloxy- 5-[(2E)-2-[(4S)-4-hydroxy-2-oxooxolan-3-ylidene] ethyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a- hexa hydro- 2H- naphthalene-1-carbonyl] amino] acetate, dari ekstrak air maggot BSF dengan potensi terbaik sebagai inhibitor Keap-1 sehingga akan mengaktifkan persinyalan antioksidan via jalur NRF2. 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