Drug intelligence / Profile preview

HX531

Development stage
Preclinical
Lead developer
Kureha
Modality
Small Molecules
Administration
Oral
01

Overview

HX531 is a potent and selective small molecule antagonist of the Retinoid X Receptors (RXRs), including the alpha (RXRα), beta (RXRβ), and gamma (RXRγ) isoforms. Originally developed to investigate the physiological roles of RXRs, HX531 has become a standard research tool for studying lipid metabolism, glucose homeostasis, and inflammatory responses. In the context of metabolic diseases, HX531 has demonstrated the ability to suppress diet-induced obesity and improve insulin sensitivity in animal models. More recently, research presented at ECCO 2024 highlighted its potential in treating Crohn's disease-like gut inflammation by blocking RXRα-mediated transcription of pro-inflammatory chemokines like CXCL1 in Paneth cells. While primarily utilized as a laboratory reagent, its efficacy in preclinical models of inflammatory bowel disease (IBD) suggests its potential as a lead compound for future therapeutic development.

Other names
4-(2-[5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl]-1,3-dithiolan-2-yl)benzoic acid
02

Targets

RXRB (Retinoid X receptor beta)RXRA (Retinoid X receptor alpha)RXRG (RXRγ)

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