Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/64938
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dc.contributor.authorEdiriweera, Meran Keshawa-
dc.contributor.authorAnandappa, Joshua Miguel-
dc.contributor.authorZhang, Baohua-
dc.date.accessioned2024-11-28T10:00:47Z-
dc.date.issued2024-11-
dc.identifier.issn0975-0959 (Online), 0301-1208 (Print)en
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/64938-
dc.description17-24en_US
dc.description.abstractHMG-CoA reductase (HMGCR) plays a key role as the rate-limiting enzyme in cholesterol biosynthesis. Fatty acid amides possess a range of biochemical and physiological functions. In an attempt to identify potential inhibitors of HMGCR, three fatty acid amides - namely stearamide, oleamide, and butyramide were investigated. Results demonstrated that these amides inhibited the activity of HMGCR, with stearamide being the most potent, followed by oleamide and butyramide. Stearamide appears to demonstrate a competitive mode of inhibition for HMGCR. Notably, these fatty acid amides interacted with key amino acid residues in the catalytic region of HMGCR through hydrogen bonding and hydrophobic interactions. These findings highlight the necessity for further research to delve into the effects of fatty acid amides on HMGCR inhibition in both in vitro and in vivo.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJBB Vol.62(1) [January 2025]en_US
dc.subjectButyramideen_US
dc.subjectCholesterol biosynthesis inhibitionen_US
dc.subjectEnzyme assaysen_US
dc.subjectOleamideen_US
dc.subjectStearamideen_US
dc.titleThe HMG-CoA reductase inhibitory potential of fatty acid amidesen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijbb.v62i1.13885en_US
Appears in Collections:IJBB Vol.62(01) [January 2025]
IJBB Vol.62(01) [January 2025]

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