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首页-小分子抑制剂&激动剂-Cell Cycle/DNA Damage-Cyclin-dependent Kinase (CDK)-Voruciclib
Voruciclib

Chemical Structure : Voruciclib

CAS No.: 1000023-04-0

Voruciclib (P1446A-05;P 1446A)

货号: PC-61031Not For Human Use, Lab Use Only.

Voruciclib (P1446A-05) is a potent, selective and orally bioavailable CDK9 inhibitor with Ki of 0.63 nM and 1.68 nM for CDK9/cyclinT2 and CDK9/cyclinT1, respectively.

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

生物&药学活性

Voruciclib (P1446A-05) is a potent, selective and orally bioavailable CDK9 inhibitor with Ki of 0.63 nM and 1.68 nM for CDK9/cyclinT2 and CDK9/cyclinT1, respectively.
Voruciclib (P1446A-05)  also inhibits CDK6/cyclin D1, CDK4/cyclin D1, CDK1/cyclin B and CDK1/cyclin A with Ki of 3-10 nM, shows weak activity against MAK and ICK (Ki>250 nM).
Voruciclib (P1446A-05)  exhibits more selective target profile than flavopiridol, represses MCL-1 protein expression in preclinical models of DLBCL.
Voruciclib (P1446A-05)  causes tumor cell apoptosis and tumor growth inhibition combined with venetoclax in vivo.

物理化学性质&存储条件

分子量 469.841
分子式 C22H19ClF3NO5
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

2-[2-Chloro-4-(trifluoromethyl)phenyl]-5,7-dihydroxy-8-[(2R,3S)-2-(hydroxymethyl)-1-methyl-3-pyrrolidinyl]-4H-1-benzopyran-4-one

参考文献

1. Dey J, et al. Sci Rep. 2017 Dec 21;7(1):18007.

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