AT-7519 |CAS:844442-38-2 Probechem Biochemicals

Chemical Structure : AT-7519

CAS No.: 844442-38-2

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AT-7519 (AT 7519;AT7519)

货号: PC-45911Not For Human Use, Lab Use Only.

AT-7519 (AT7519) is a potent, selective CDK2 inhibitor with IC50 of 47 nM, also inhibits CDK1/4/5 with IC50 of 190/67/18 nM and shows selectivity over some kinases (Aurora A, IR kinase, MEK, PDK1, c-Abl, IC50>10 uM).

规格	价格	库存
25 mg	￥1980	In stock
100 mg	￥4980	In stock
200 mg		Get quote
1 g		Get quote

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生物&药学活性

AT-7519 (AT7519) is a potent, selective CDK2 inhibitor with IC50 of 47 nM, also inhibits CDK1/4/5 with IC50 of 190/67/18 nM and shows selectivity over some kinases (Aurora A, IR kinase, MEK, PDK1, c-Abl, IC50>10 uM).
AT-7519 has antiproliferative activity against HCT116 cells with IC50 of 82 nM.
AT-7519 exhibits good profile against cytochrome P450 isoforms (<30% inhibition at 10 uM for 1A2, 2D6, 3A4, 2C9, 2C19).

物理化学性质&存储条件

分子量	382.2445
分子式	C16H17Cl2N5O2
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	1H-Pyrazole-3-carboxamide, 4-[(2,6-dichlorobenzoyl)amino]-N-4-piperidinyl-

参考文献

1. Wyatt PG, et al. J Med Chem. 2008 Aug 28;51(16):4986-99.

2. Squires MS, et al. Mol Cancer Ther. 2009 Feb;8(2):324-32.

3. Dolman ME, et al. Clin Cancer Res. 2015 Nov 15;21(22):5100-9.

AT-7519 (AT 7519;AT7519)

生物&药学活性

物理化学性质&存储条件

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AT-7519 (AT 7519;AT7519)

生物&药学活性

物理化学性质&存储条件

参考文献

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