Chemical Structure : GW843682X
CAS No.: 660868-91-7
货号: PC-42779Not For Human Use, Lab Use Only.
GW843682X is a potent and selective inhibitor of PLK1 (IC5=2.2 nM) and PLK3 (IC50=9 nM).
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | ¥980 | In stock | |
25 mg | ¥1480 | In stock | |
50 mg | ¥2380 | In stock | |
100 mg | Get quote |
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GW843682X is a potent and selective inhibitor of PLK1 (IC5=2.2 nM) and PLK3 (IC50=9 nM).
GW843682X displays >1,000-fold lower than cell CDK-2/cyclin A, CDK1/cyclin A and aurora A.
GW843682X induces a transient G2-M arrest, mitotic spindle defects, and a multinucleate phenotype.
分子量 | 477.4562 | |
分子式 | C22H18F3N3O4S | |
外观性状 | Solid | |
储存条件 |
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|
Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
2-Thiophenecarboxamide, 5-(5,6-dimethoxy-1H-benzimidazol-1-yl)-3-[[2-(trifluoromethyl)phenyl]methoxy]- |
1. Lansing TJ, et al. Mol Cancer Ther. 2007 Feb;6(2):450-9.
2. Nihal M, et al. Cell Cycle. 2011 Apr 15;10(8):1303-11.
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