Design and Synthesis of Echitamine-inspired Hybrid Analogues Containing Thiazolidinediones as Potential Pancreatic Lipase Inhibitors

Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/13590

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DC Field	Value	Language
dc.contributor.author	Paul, Atish Tulshiram	-
dc.date.accessioned	2024-01-02T04:51:34Z	-
dc.date.available	2024-01-02T04:51:34Z	-
dc.date.issued	2022-11	-
dc.identifier.uri	https://www.ingentaconnect.com/content/ben/lddd/2022/00000019/00000011/art00003	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/13590	-
dc.description.abstract	Obesity is a multifactorial metabolic disease characterised by excessive accumulation of triglycerides. The prevalence and morbidity rates associated with obesity are increasing tremendously, posing a significant risk to society. Pancreatic lipase (PL) is a key enzyme responsible for the digestion of dietary triglycerides; hence its inhibition is considered an attractive target in obesity.	en_US
dc.language.iso	en	en_US
dc.publisher	Bentham Science	en_US
dc.subject	Pharmacy	en_US
dc.subject	Obesity	en_US
dc.subject	Enzyme inhibition	en_US
dc.subject	Fluorescence spectroscopy	en_US
dc.subject	Molecular docking	en_US
dc.subject	Pancreatic lipase	en_US
dc.subject	Thiazolidinediones (TZDs)	en_US
dc.title	Design and Synthesis of Echitamine-inspired Hybrid Analogues Containing Thiazolidinediones as Potential Pancreatic Lipase Inhibitors	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Pharmacy

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