Cargando…

Establishing the Role of Iridoids as Potential Kirsten Rat Sarcoma Viral Oncogene Homolog G12C Inhibitors Using Molecular Docking; Molecular Docking Simulation; Molecular Mechanics Poisson–Boltzmann Surface Area; Frontier Molecular Orbital Theory; Molecular Electrostatic Potential; and Absorption, Distribution, Metabolism, Excretion, and Toxicity Analysis

The RAS gene family is one of the most frequently mutated oncogenes in human cancers. In KRAS, mutations of G12D and G12C are common. Here, 52 iridoids were selected and docked against 8AFB (KRAS G12C receptor) using Sotorasib as the standard. As per the docking interaction data, 6-O-trans-p-coumaro...

Descripción completa

Detalles Bibliográficos
Autores principales: Alamri, Mubarak A., Alawam, Abdullah S., Alshahrani, Mohammed Merae, Kawsar, Sarkar M. A., Prinsa, Saha, Supriyo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10343556/
https://www.ncbi.nlm.nih.gov/pubmed/37446713
http://dx.doi.org/10.3390/molecules28135050
_version_ 1785072764984492032
author Alamri, Mubarak A.
Alawam, Abdullah S.
Alshahrani, Mohammed Merae
Kawsar, Sarkar M. A.
Prinsa
Saha, Supriyo
author_facet Alamri, Mubarak A.
Alawam, Abdullah S.
Alshahrani, Mohammed Merae
Kawsar, Sarkar M. A.
Prinsa
Saha, Supriyo
author_sort Alamri, Mubarak A.
collection PubMed
description The RAS gene family is one of the most frequently mutated oncogenes in human cancers. In KRAS, mutations of G12D and G12C are common. Here, 52 iridoids were selected and docked against 8AFB (KRAS G12C receptor) using Sotorasib as the standard. As per the docking interaction data, 6-O-trans-p-coumaroyl-8-O-acetylshanzhiside methyl ester (dock score: −9.9 kcal/mol), 6′-O-trans-para-coumaroyl geniposidic acid (dock score: −9.6 kcal/mol), 6-O-trans-cinnamoyl-secologanoside (dock score: −9.5 kcal/mol), Loganic acid 6′-O-beta-d-glucoside (dock score: −9.5 kcal/mol), 10-O-succinoylgeniposide (dock score: −9.4), Loganic acid (dock score: −9.4 kcal/mol), and Amphicoside (dock score: −9.2 kcal/mol) showed higher dock scores than standard Sotorasib (dock score: −9.1 kcal/mol). These common amino acid residues between iridoids and complexed ligands confirmed that all the iridoids perfectly docked within the receptor’s active site. The 100 ns MD simulation data showed that RMSD, RMSF, radius of gyration, and SASA values were within range, with greater numbers of hydrogen bond donors and acceptors. MM/PBSA analysis showed maximum binding energy values of −7309 kJ/mol for 6-O-trans-p-coumaroyl-8-O-acetylshanzhiside methyl ester. FMO analysis showed that 6-O-trans-p-coumaroyl-8-O-acetylshanzhiside methyl ester was the most likely chemically reactive molecule. MEP analysis data highlighted the possible electrophilic and nucleophilic attack regions of the best-docked iridoids. Of all the best-docked iridoids, Loganic acid passed Lipinski, Pfizer, and GSK filters with a similar toxicity profile to Sotorasib. Thus, if we consider these iridoids to be KRAS G12C inhibitors, they will be a boon to mankind.
format Online
Article
Text
id pubmed-10343556
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-103435562023-07-14 Establishing the Role of Iridoids as Potential Kirsten Rat Sarcoma Viral Oncogene Homolog G12C Inhibitors Using Molecular Docking; Molecular Docking Simulation; Molecular Mechanics Poisson–Boltzmann Surface Area; Frontier Molecular Orbital Theory; Molecular Electrostatic Potential; and Absorption, Distribution, Metabolism, Excretion, and Toxicity Analysis Alamri, Mubarak A. Alawam, Abdullah S. Alshahrani, Mohammed Merae Kawsar, Sarkar M. A. Prinsa Saha, Supriyo Molecules Article The RAS gene family is one of the most frequently mutated oncogenes in human cancers. In KRAS, mutations of G12D and G12C are common. Here, 52 iridoids were selected and docked against 8AFB (KRAS G12C receptor) using Sotorasib as the standard. As per the docking interaction data, 6-O-trans-p-coumaroyl-8-O-acetylshanzhiside methyl ester (dock score: −9.9 kcal/mol), 6′-O-trans-para-coumaroyl geniposidic acid (dock score: −9.6 kcal/mol), 6-O-trans-cinnamoyl-secologanoside (dock score: −9.5 kcal/mol), Loganic acid 6′-O-beta-d-glucoside (dock score: −9.5 kcal/mol), 10-O-succinoylgeniposide (dock score: −9.4), Loganic acid (dock score: −9.4 kcal/mol), and Amphicoside (dock score: −9.2 kcal/mol) showed higher dock scores than standard Sotorasib (dock score: −9.1 kcal/mol). These common amino acid residues between iridoids and complexed ligands confirmed that all the iridoids perfectly docked within the receptor’s active site. The 100 ns MD simulation data showed that RMSD, RMSF, radius of gyration, and SASA values were within range, with greater numbers of hydrogen bond donors and acceptors. MM/PBSA analysis showed maximum binding energy values of −7309 kJ/mol for 6-O-trans-p-coumaroyl-8-O-acetylshanzhiside methyl ester. FMO analysis showed that 6-O-trans-p-coumaroyl-8-O-acetylshanzhiside methyl ester was the most likely chemically reactive molecule. MEP analysis data highlighted the possible electrophilic and nucleophilic attack regions of the best-docked iridoids. Of all the best-docked iridoids, Loganic acid passed Lipinski, Pfizer, and GSK filters with a similar toxicity profile to Sotorasib. Thus, if we consider these iridoids to be KRAS G12C inhibitors, they will be a boon to mankind. MDPI 2023-06-28 /pmc/articles/PMC10343556/ /pubmed/37446713 http://dx.doi.org/10.3390/molecules28135050 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Alamri, Mubarak A.
Alawam, Abdullah S.
Alshahrani, Mohammed Merae
Kawsar, Sarkar M. A.
Prinsa
Saha, Supriyo
Establishing the Role of Iridoids as Potential Kirsten Rat Sarcoma Viral Oncogene Homolog G12C Inhibitors Using Molecular Docking; Molecular Docking Simulation; Molecular Mechanics Poisson–Boltzmann Surface Area; Frontier Molecular Orbital Theory; Molecular Electrostatic Potential; and Absorption, Distribution, Metabolism, Excretion, and Toxicity Analysis
title Establishing the Role of Iridoids as Potential Kirsten Rat Sarcoma Viral Oncogene Homolog G12C Inhibitors Using Molecular Docking; Molecular Docking Simulation; Molecular Mechanics Poisson–Boltzmann Surface Area; Frontier Molecular Orbital Theory; Molecular Electrostatic Potential; and Absorption, Distribution, Metabolism, Excretion, and Toxicity Analysis
title_full Establishing the Role of Iridoids as Potential Kirsten Rat Sarcoma Viral Oncogene Homolog G12C Inhibitors Using Molecular Docking; Molecular Docking Simulation; Molecular Mechanics Poisson–Boltzmann Surface Area; Frontier Molecular Orbital Theory; Molecular Electrostatic Potential; and Absorption, Distribution, Metabolism, Excretion, and Toxicity Analysis
title_fullStr Establishing the Role of Iridoids as Potential Kirsten Rat Sarcoma Viral Oncogene Homolog G12C Inhibitors Using Molecular Docking; Molecular Docking Simulation; Molecular Mechanics Poisson–Boltzmann Surface Area; Frontier Molecular Orbital Theory; Molecular Electrostatic Potential; and Absorption, Distribution, Metabolism, Excretion, and Toxicity Analysis
title_full_unstemmed Establishing the Role of Iridoids as Potential Kirsten Rat Sarcoma Viral Oncogene Homolog G12C Inhibitors Using Molecular Docking; Molecular Docking Simulation; Molecular Mechanics Poisson–Boltzmann Surface Area; Frontier Molecular Orbital Theory; Molecular Electrostatic Potential; and Absorption, Distribution, Metabolism, Excretion, and Toxicity Analysis
title_short Establishing the Role of Iridoids as Potential Kirsten Rat Sarcoma Viral Oncogene Homolog G12C Inhibitors Using Molecular Docking; Molecular Docking Simulation; Molecular Mechanics Poisson–Boltzmann Surface Area; Frontier Molecular Orbital Theory; Molecular Electrostatic Potential; and Absorption, Distribution, Metabolism, Excretion, and Toxicity Analysis
title_sort establishing the role of iridoids as potential kirsten rat sarcoma viral oncogene homolog g12c inhibitors using molecular docking; molecular docking simulation; molecular mechanics poisson–boltzmann surface area; frontier molecular orbital theory; molecular electrostatic potential; and absorption, distribution, metabolism, excretion, and toxicity analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10343556/
https://www.ncbi.nlm.nih.gov/pubmed/37446713
http://dx.doi.org/10.3390/molecules28135050
work_keys_str_mv AT alamrimubaraka establishingtheroleofiridoidsaspotentialkirstenratsarcomaviraloncogenehomologg12cinhibitorsusingmoleculardockingmoleculardockingsimulationmolecularmechanicspoissonboltzmannsurfaceareafrontiermolecularorbitaltheorymolecularelectrostaticpotentialandabsorpti
AT alawamabdullahs establishingtheroleofiridoidsaspotentialkirstenratsarcomaviraloncogenehomologg12cinhibitorsusingmoleculardockingmoleculardockingsimulationmolecularmechanicspoissonboltzmannsurfaceareafrontiermolecularorbitaltheorymolecularelectrostaticpotentialandabsorpti
AT alshahranimohammedmerae establishingtheroleofiridoidsaspotentialkirstenratsarcomaviraloncogenehomologg12cinhibitorsusingmoleculardockingmoleculardockingsimulationmolecularmechanicspoissonboltzmannsurfaceareafrontiermolecularorbitaltheorymolecularelectrostaticpotentialandabsorpti
AT kawsarsarkarma establishingtheroleofiridoidsaspotentialkirstenratsarcomaviraloncogenehomologg12cinhibitorsusingmoleculardockingmoleculardockingsimulationmolecularmechanicspoissonboltzmannsurfaceareafrontiermolecularorbitaltheorymolecularelectrostaticpotentialandabsorpti
AT prinsa establishingtheroleofiridoidsaspotentialkirstenratsarcomaviraloncogenehomologg12cinhibitorsusingmoleculardockingmoleculardockingsimulationmolecularmechanicspoissonboltzmannsurfaceareafrontiermolecularorbitaltheorymolecularelectrostaticpotentialandabsorpti
AT sahasupriyo establishingtheroleofiridoidsaspotentialkirstenratsarcomaviraloncogenehomologg12cinhibitorsusingmoleculardockingmoleculardockingsimulationmolecularmechanicspoissonboltzmannsurfaceareafrontiermolecularorbitaltheorymolecularelectrostaticpotentialandabsorpti