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首页-小分子抑制剂&激动剂-Epigenetics-Bromodomain-BAY1238097
BAY1238097

Chemical Structure : BAY1238097

CAS No.: 1564268-08-1

BAY1238097 (BAY 1238097, BAY-1238097)

货号: PC-62283Not For Human Use, Lab Use Only.

BAY 1238097 is a novel BET bromodomain inhibitor with IC50 of 50 nM, inhibits the interaction between BRD4, BRD3 or BRD2 and H4 with IC50 values of 63 nM, 609 nM and 2430 nM in the NanoBRET assay.

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5 mg ¥1380 In stock
10 mg ¥2180 In stock
25 mg ¥3880 In stock
50 mg ¥5980 In stock
100 mg Get quote

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

生物&药学活性

BAY1238097 is a novel BET bromodomain inhibitor with IC50 of 50 nM, inhibits the interaction between BRD4, BRD3 or BRD2 and H4 with IC50 values of 63 nM, 609 nM and 2430 nM in the NanoBRET assay.
BAY1238097 shows selectivity of the compound for BRD4.
BAY1238097 strongly reduces c-Myc transcript and protein levels in MOLM-13 (AML) and MOLP-8 (MM) cell lines.
BAY1238097 exhibits strong efficacy in the AML models THP-1, MOLM-13 and KG-1.

物理化学性质&存储条件

分子量 451.571
分子式 C25H33N5O3
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)-7,8-dimethoxy-N,4-dimethyl-1-(4-(4-methylpiperazin-1-yl)phenyl)-4,5-dihydro-3H-benzo[d][1,2]diazepine-3-carboxamide

参考文献

1. Bernasconi E, et al. Br J Haematol. 2017 Jun 27. doi: 10.1111/bjh.14803.

2. Patent WO2014026997A1.

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