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首页-小分子抑制剂&激动剂-Nuclear Receptor/Transcription Factor-PPAR-SR10221
SR10221

Chemical Structure : SR10221

CAS No.: 1415321-64-0

SR10221 (SR 10221)

货号: PC-49401Not For Human Use, Lab Use Only.

SR10221 is a potent, selective PPARγ inverse agonist with IC50 of 13 nM in biochemical peptide recruitment assays, represses downstream PPARγ target genes leading to growth inhibition in bladder cancer cell lines.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

SR10221 is a potent, selective PPARγ inverse agonist with IC50 of 13 nM in biochemical peptide recruitment assays, represses downstream PPARγ target genes leading to growth inhibition in bladder cancer cell lines.

物理化学性质&存储条件

分子量 561.119
分子式 C33H37ClN2O4
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(S)-2-(5-((5-(((S)-1-(4-(tert-butyl)phenyl)ethyl)carbamoyl)-2,3-dimethyl-1H-indol-1-yl)methyl)-2-chlorophenoxy)propanoic acid

参考文献

1. Sean Irwin, et al. J Biol Chem. 2022 Sep 28;298(11):102539.

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