Drug intelligence / Profile preview

V023-9340

Development stage
Preclinical
Lead developer
Guilin Medical University
01

Overview

V023-9340: sourced facts only. name: "Notably, compound V023-9340, which possesses a 4-aminophenylacetamide scaffold, emerged as the most potent FXR antagonist with an IC50 value of 4.27 μM." [PMID:38043493]; target: "Notably, compound V023-9340, which possesses a 4-aminophenylacetamide scaffold, emerged as the most potent FXR antagonist with an IC50 value of 4.27 μM." [PMID:38043493]; developer: "Guangxi Key Laboratory of Drug Discovery and Optimization, College of Pharmacy, Guilin Medical University, Guilin 541199, China." [PMID:38043493]; stage: "In vivo, V023-9340 demonstrated selective accumulation in the intestine, substantially ameliorating high-fat diet (HFD)-induced NASH in mice by mitigating hepatic steatosis and inflammation." [PMID:38043493]

02

Targets

FXR (Farnesoid x-activated receptor)

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