In Silico Identification of Canthin-6-one as a Pancreatic Lipase Inhibitory Anti-Obesity Drug Lead from Hibiscus Sabdariffa

Authors

  • O. S. AJALA
  • P. U. OKECHUKWU
  • D. O. INNOCENT-UGWU
  • O. H. DADA

DOI:

https://doi.org/10.4314/

Keywords:

Pancreatic Lipase inhibition, In-silico studies, Computer Assisted Drug Discovery, Hibiscus sabdariffa, Anti-obesity agents

Abstract

Background:  The therapeutic use of the only Pancreatic Lipase (PL) - inhibiting anti-obesity drug available in clinical practice, orlistat, is bedevilled with unbearable side effects, necessitating the discovery of new and better-tolerated ones. Hibiscus sabdariffa, a folkloric anti-obesity plant is a plausible repertoire from which such agents could be sought.

Objective: The main objective of this work was to evaluate in silico the phytochemicals of Hibiscus sabdariffa for a possible identification of potential leads for PL inhibitory anti-obesity drug discovery..

Methods: Phytoligands from H. sabdariffa were subjected to a series of in silico evaluations including site directed docking, MM/GBSA calculations, SwissADME drug-likeness screening, Protox II-based toxicity evaluations and a 20 ns molecular dynamics (MD) simulation.

Results: MM/GBSA ranking of docked phytoligands and SwissADME evaluations produced three PL inhibitor hits. One of them, canthin-6-one, demonstrated minimal end-organ toxicity with a 1200 mg/kg LD50; its PL complex generated stability-implying root mean square deviation (RMSD), root mean square fluctuation (RMSF), radius of gyration (Rg) and solvent accessible surface area (SASA) plots, after the 20 ns MD simulation.

Conclusion: Hibiscus sabdariffa-based canthin-6-one has demonstrated, in silico, high human PL binding affinity, impressive drug-likeness/toxicity profiles and stability-implying MD simulation parameters. It is therefore, herein, recommended as lead for further in vitro, in vivo and molecular modification studies for possible development into a clinical PL inhibitory anti-obesity drug.

A – 2D and B – 3D simulations of supramolecular interactions at the active site of the colipase- free human Pancreatic Lipase in complex with canthin-6-one

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Published

2024-07-09

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Full Length Articles

How to Cite

In Silico Identification of Canthin-6-one as a Pancreatic Lipase Inhibitory Anti-Obesity Drug Lead from Hibiscus Sabdariffa. (2024). Nigerian Journal of Pharmaceutical Research, 20(1), 57-68. https://doi.org/10.4314/

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