Anti-atherosclerosis potential activity from Alphitobius diaperinus: a molecular docking study on NLRP3 receptor
This study aimed to analyze the potential activity anti-atherosclerosis of Alphitobius diaperinus larvae using molecular docking. The target receptor used was NLRP3, with β-sitosterol and campesterol as the test ligands, and simvastatin as the control ligand. The results showed that the binding aff...
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Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
Politeknik Negeri Jember
2025-02-01
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Series: | Jurnal Ilmu Peternakan Terapan |
Subjects: | |
Online Access: | https://publikasi.polije.ac.id/jipt/article/view/5814 |
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Summary: | This study aimed to analyze the potential activity anti-atherosclerosis of Alphitobius diaperinus larvae using molecular docking. The target receptor used was NLRP3, with β-sitosterol and campesterol as the test ligands, and simvastatin as the control ligand. The results showed that the binding affinity energies of β-sitosterol and campesterol were more negative than simvastatin, with values of -9.3, -9.3, and -8.6 kcal/mol, respectively. The inhibition constants of β-sitosterol and campesterol were lower than that of simvastatin, with values of 0.213, 0.213, and 0.494 μM, respectively. The percentage of binding site similarity with the native ligand for β-sitosterol and campesterol was 60%, while simvastatin showed 0%. Molecular probability analysis using Lipinski's rules revealed that simvastatin met all five criteria, whereas β-sitosterol and campesterol met four criteria. The LD50 analysis indicated that simvastatin fell under category III, while β-sitosterol and campesterol were in category I. All three molecules β-sitosterol, campesterol, and simvastatin were found to be non-carcinogenic. The conclusion of this study was β-sitosterol and campesterol from A. diaperinus larvae have potential as anti-atherosclerosis candidates.
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ISSN: | 2828-4348 2579-9479 |