IN SILICO DOCKING STUDIES OF PHYTOSTEROL COMPOUNDS SELECTED FROM Ficus religiosa AS POTENTIAL CHEMOPREVENTIVE AGENT

Traditional medicine has employed Ficus reliosa (Moraceae) to treat a wide range of diseases such as central nervous system disorder, infectious disease, endocrine system, respiratory system, etc. This study aimed to evaluate phytosterol constituents that may serve as lead-drug such as 28-Isofucoste...

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Veröffentlicht in:Rasāyan journal of chemistry 2022, Vol.15 (2), p.1080-1084
Hauptverfasser: Syahputra, H.D., M. Masfria, Hasibuan, P.A.Z, Iksen, I.
Format: Artikel
Sprache:eng
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Zusammenfassung:Traditional medicine has employed Ficus reliosa (Moraceae) to treat a wide range of diseases such as central nervous system disorder, infectious disease, endocrine system, respiratory system, etc. This study aimed to evaluate phytosterol constituents that may serve as lead-drug such as 28-Isofucosterol, Stigmasterol, Sitosterol, and Campesterol towards their pharmacokinetic properties and chemopreventive activity to regulate nuclear receptor factor 2 (Nrf2) uptake bound by Kelch-like Activating Protein (Keap1). Structures were studied to evaluate their respective bioactivity using Milliprot followed by a docking study with Autodock Tools for macromolecule obtained from Protein Data Bank in 2FLU PDB file name. Chemopreventive activity from Sitosterol, Stigmasterol, Campesterol and 28-Isofucosterol in each respective bioactivity towards nuclear receptor target : 0.72; 0.74; 0.71; 0.91. A computational study performed by Autodock Tools against Keap1 targeted macromolecule covalent binding toward threonine 609 to obtain inhibition results. As respective Inhibition constant obtained (pM) : 522.97; 286.75; 620.16; 369.55. Free energy obtained (kcal/mol) : -8.57; -13.02; -12.56; -12.87. Hence the results revealed from the study showed that phytosterol compound from Ficus religiosa proven to be useful as a chemopreventive agent to promote antioxidant gene activity through regulation of Nrf2 factor by competing for receptor site with Keap1 during stressed conditions.
ISSN:0974-1496
0974-1496
DOI:10.31788/RJC.2022.1526801