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夫拉平度盐酸盐Flavopiridol Hydrochloride 是一种 CDK 的广谱抑制剂,与 ATP 竞争性地抑制 CDK1,CDK2 和 CDK4 的活性,IC50 值分别为 30, 170, 100 nM。
物化属性
熔点:169.5-170℃
沸点:603.6°C at 760 mmHg
闪光点:318.8°C
比旋光度:24D -1.73 to -3.9°
储存条件:2-8°C
PSA:94.14000
LOGP:4.04450
[1]. Mahoney E, et al. ER stress and autophagy: new discoveries in the mechanism of action and drug resistance of the cyclin-dependent kinase inhibitor flavopiridol.Blood. 2012 Aug 9;120(6):1262-1273.
[2]. Keskin H, et al. Complex effects of flavopiridol on the expression of primary response genes. Cell Div. 2012 Mar 29;7:11.
[3]. Kim KS, et al.Thio- and oxoflavopiridols, cyclin-dependent kinase 1-selective inhibitors: synthesis and biological effects. J Med Chem. 2000 Nov 2;43(22):4126-34.
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