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- CH 223191 301326-22-7

- CH 223191 301326-22-7
CH 223191 301326-22-7
产品描述 描述 CH 223191 is a potent and specific aryl hydrocarbon receptor (AhR) antagonist with IC50 of 30 nM.
纯度 >98%储存/保存方法 Store at -20℃ for three years(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.基本信息 别名 CH-223191;CH223191外观 Yellow to orange powder可溶性/溶解性 Ethanol :3.3 mg/mL (10 mM)
DMSO :33.3 mg/mL (100 mM)生物活性 靶点 AhRIn vitro(体外研究) CH-223191 blocks TCDD-mediated nuclear translocation and DNA binding of AhR, and also causes the inhibition of TCDD-induced cytochrome P450 enzyme activity. In human glioblastoma cells, CH-223191downregulates the TGF-beta/Smad pathway, and reduces clonogenic survival and invasiveness. In SK-N-SH human-derived neuronal cells, CH223191 counteracts the TCDD-induced suppression of neuronal acetylcholinesterase expression. In endothelial cells, CH-223191 potentiates ICAM-1 expression and prevents RelB nuclear translocation.In vivo(体内研究) CH-223191 (10 mg/kg/day, p.o.) potently prevents TCDD-caused cytochrome P450 induction, liver toxicity, and wasting syndrome in mice.研究领域 研究领域 EpigeneticsTranscriptionDomain FamiliesHLH / Leucine ZipperHelix-Turn-HelixNeuroscienceDevelopmentNeuroscienceProcessesDrug DiscoverySmall Molecule DrugLead Compound DiscoveryCH 223191 301326-22-7温馨提示:本产品仅作科研实验使用,不支持临床等研究
