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首页-小分子抑制剂&激动剂-JAK/STAT Signaling-JAK-ZM39923
ZM39923

Chemical Structure : ZM39923

CAS No.: 273727-89-2

ZM39923 (ZM-39923)

货号: PC-43113Not For Human Use, Lab Use Only.

ZM39923 is a potent, selective JAK3 inhibitor with pIC50 of 7.1, also potently inhibits human tissue transglutaminase (TGM2, hTG2) with IC50 of 10 nM.

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

生物&药学活性

ZM39923 is a potent, selective JAK3 inhibitor with pIC50 of 7.1, also potently inhibits human tissue transglutaminase (TGM2, hTG2) with IC50 of 10 nM.
ZM39923 is less potent for EGFR, JAK1 and CDK4 with pIC50 of 5.6, 4.4 and < 5.0, no activity fgor JAK2.
ZM39923 alteres TGM2 activity in polyglutamine-expressing Drosophila model of neurodegeneration and is found to improve survival.
ZM39923 significantly attenuates CCR7-induced Jak3 phosphorylation in metastatic SCCHN cells.

物理化学性质&存储条件

分子量 331.4507
分子式 C23H25NO
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

1-Propanone, 3-[(1-methylethyl)(phenylmethyl)amino]-1-(2-naphthalenyl)-

参考文献

1. Lai TS, et al. Chem Biol. 2008 Sep 22;15(9):969-78.

2. Zhang Z, et al. Oncol Lett. 2017 May;13(5):3191-3197.

3. Luo C, et al. Drug Discov Today. 2004 Mar 15;9(6):268-75.

4. Brown GR, et al. Bioorg Med Chem Lett. 2000 Mar 20;10(6):575-9.

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