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首页-小分子抑制剂&激动剂-Epigenetics-Histone Methyltransferase (HMTase)-BAY-598
BAY-598

Chemical Structure : BAY-598

CAS No.: 906919-67-2

BAY-598 (BAY598;BAY 598)

货号: PC-60420Not For Human Use, Lab Use Only.

BAY-598 (BAY598) is a potent, selective, and cell-active, substrate-competitive inhibitor of SMYD2 with IC50 of 27±7 nM in the biochemical SPA assay.

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5 mg ¥1280 In stock
10 mg ¥1880 In stock
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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

BAY-598 (BAY598) is a potent, selective, and cell-active, substrate-competitive inhibitor of SMYD2 with IC50 of 27±7 nM in the biochemical SPA assay.
BAY-598 displays >100-fold selectivity over other HMTases (SMYD3, SUV420H1, SUV420H2, etc.) and other non-epigenetic targets.
BAY-598 inhibits the methylation of p53K370 in cells with IC50 <1 uM, has properties that are compatible with in vivo experiments.

物理化学性质&存储条件

分子量 525.3
分子式 C22H20Cl2F2N6O3
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,Z)-N-(1-(N'-cyano-N-(3-(difluoromethoxy)phenyl)carbamimidoyl)-3-(3,4-dichlorophenyl)-4,5-dihydro-1H-pyrazol-4-yl)-N-ethyl-2-hydroxyacetamide

参考文献

1. Eggert E, et al. J Med Chem. 2016 May 26;59(10):4578-600.

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