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AZ82 是一种具有选择性和高效性的驱动蛋白样蛋白 KIFC1 抑制剂,抑制 PCa 细胞胞质和细胞核中 KIFC1 的表达,诱导前列腺癌细胞多极有丝分裂和细胞凋亡。
AZ82 是一种具有选择性和高效性的驱动蛋白样蛋白 KIFC1 抑制剂,抑制 PCa 细胞胞质和细胞核中 KIFC1 的表达,诱导前列腺癌细胞多极有丝分裂和细胞凋亡。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 915 | 现货 |
产品描述 | AZ82 is a selective and potent inhibitor of the kinesin-like protein KIFC1, inhibits KIFC1 expression in the cytoplasm and nucleus of PCa cells, and induces multipolar mitosis and apoptosis in prostate cancer cells. |
靶点活性 | HSET/KIFC1:43 nM (Ki), HSET/KIFC1:300 nM, HSET/KIFC1:43 nM (ki) |
体外活性 | AZ82 specifically induce multipolar spindles in BT-549 cells, but not in cancer cells with normal centrosome numbers, such as HeLa [1]. AZ82 binds specifically to KIFC1/MT complex but not to KIFC1 or MT alone. Treatment with AZ82 caused centrosome declustering in BT-549 breast cancer cells with amplified centrosomes. AZ82 inhibits both processes for mant-ATP binding/releasing (IC50: 0.90 μM/1.26 μM) [2]. |
别名 | AZ-82, AZ 82 |
分子量 | 560.63 |
分子式 | C28H31F3N4O3S |
CAS No. | 1449578-65-7 |
Smiles | CCCc1cc(sc1C)C(=O)N[C@H](Cc1ccc(nc1)-c1cccc(OC(F)(F)F)c1)C(=O)N[C@@H]1CCNC1 |
密度 | 1.32 g/cm3 (Predicted) |
存储 | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 100 mg/mL (178.37 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
DMSO
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