CAS NO: | 136194-77-9 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
1mg | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
生物活性 | Go6976 is a Protein Kinase C (PKC) inhibitor, with anIC50of 20 nM. | ||||||||||||||||
IC50& Target | IC50: 20 nM (PKC)[1]. | ||||||||||||||||
体外研究 (In Vitro) | Go6976 is a potent inhibitor of PKC in vitro (IC50is 20 nM. This compound is structurally related to staurosporine, which is the most potent PKC inhibitor[1]. UCN-01 is originally identified as a PKC inhibitor. Surprisingly, Go6976 is found to abrogate S and G2arrest. Dose-response studies reveal that 30 nM Go6976 is sufficient to cause abrogation of S-phase arrest in 6 h and abrogation of G2arrest followed by lethal mitosis in 24 h. Incubation of cells with 100 nM Go6976 is sufficient to cause complete abrogation of S and G2arrest at 6 and 24 h, respectively, which is only slightly less potent than in bovine serum. Incubation of cells with UCN-01 or Go6976 alone do not decrease viability compared with control at the concentrations used. Incubation of cells with 5 ng/mL SN38 result in cytostasis, and addition of 50 nM UCN-01 or 100 nM Go6976 to arrested MDA-MB-231 cells cause a dramatic decrease in viable cell number by 96 h[2]. | ||||||||||||||||
分子量 | 378.43 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C24H18N4O | ||||||||||||||||
CAS 号 | 136194-77-9 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 50 mg/mL(132.12 mM;Need ultrasonic) 配制储备液
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以下溶剂前显示的百
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