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首页-小分子抑制剂&激动剂-Cell Cycle/DNA Damage-Checkpoint Kinase (Chk)-AZD-7762
AZD-7762

Chemical Structure : AZD-7762

CAS No.: 860352-01-8

AZD-7762 (AZD7762;AZD 7762)

货号: PC-42769Not For Human Use, Lab Use Only.

AZD-7762 (AZD7762) is a potent and selective inhibitor of Chk1/2 with IC50 of 5 nM.

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5 mg ¥780 In stock
10 mg ¥1180 In stock
25 mg ¥1880 In stock
50 mg ¥2980 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

AZD-7762 (AZD7762) is a potent and selective inhibitor of Chk1/2 with IC50 of 5 nM.
AZD-7762 shows less potent against CAM, Yes, Fyn, Lyn, Hck and Lck.
AZD-7762 enhances the radiosensitivity of mutated p53 tumor cell lines and HT29 xenografts.

物理化学性质&存储条件

分子量 362.4218
分子式 C17H19FN4O2S
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-Thiophenecarboxamide, 3-[(aminocarbonyl)amino]-5-(3-fluorophenyl)-N-(3S)-3-piperidinyl-

参考文献

1. Zabludoff SD, et al. Mol Cancer Ther. 2008 Sep;7(9):2955-66.

2. Mitchell JB, et al. Clin Cancer Res. 2010 Apr 1;16(7):2076-84.

3. Morgan MA, et al. Cancer Res. 2010 Jun 15;70(12):4972-81.

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