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首页-小分子抑制剂&激动剂-Epigenetics-HDAC-GSK-3117391
GSK-3117391

Chemical Structure : GSK-3117391

CAS No.: 1018673-42-1

GSK-3117391 (ESM-HDAC391;CHR-5154;GSK3117391;CHR5154)

货号: PC-63389Not For Human Use, Lab Use Only.

GSK-3117391 (ESM-HDAC391, CHR-5154) is an orally active, myeloid-targeted histone deacetylase (HDAC) inhibitor with IC50 of 55 nM in a HeLa cell nuclear extract fluorometric assay, potently inhibits Class I, Class IIb and Class IV members (HDAC 1/2/3/8, HDAC6/10, and HDAC 11, respectively), with Class IIa enzymes (HDAC4/5/7/9) unaffected.

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

生物&药学活性

GSK-3117391 (ESM-HDAC391, CHR-5154) is an orally active, myeloid-targeted histone deacetylase (HDAC) inhibitor with IC50 of 55 nM in a HeLa cell nuclear extract fluorometric assay, potently inhibits Class I, Class IIb and Class IV members (HDAC 1/2/3/8, HDAC6/10, and HDAC 11, respectively), with Class IIa enzymes (HDAC4/5/7/9) unaffected.
GSK-3117391 (ESM-HDAC391, CHR-5154) increases global acetylation in monocytes in human whole blood with EC50 of 158 nM, with marked selectivity over other leucocyte populations.
GSK-3117391 (ESM-HDAC391, CHR-5154) inhibits TNFα production in LPS-stimulated blood (IC50=174 nM).
GSK-3117391 (ESM-HDAC391, CHR-5154) shows rapid conversion to acid metabolite HDAC189 in carboxylesterase-1-expressing cells.
GSK-3117391 (ESM-HDAC391, CHR-5154) is a novel targeted inhibitor demonstrating sustained potent mechanistic engagement and antiinflammatory activity.

物理化学性质&存储条件

分子量 389.496
分子式 C21H31N3O4
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

cyclopentyl (S)-2-cyclohexyl-2-((6-(3-(hydroxyamino)-3-oxopropyl)pyridin-3-yl)amino)acetate

参考文献

1. Rebecca C Furze, et al. Br J Clin Pharmacol. 2022 Jun 2. doi: 10.1111/bcp.15428.

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