中文名 | Fadraciclib |
英文名 | Fadraciclib |
别名 | 化合物CYC065 |
英文别名 | CDK259 CYC065 CYC-065 CPD1574 CYC-065 CYC 065 Fadraciclib CYC065 base 1070790-89-4 CYC065, CDK259 CYC065 free base 2-Pentanol, 3-[[6-[[(4,6-dimethyl-3-pyridinyl)methyl]amino]-9-(1-methylethyl)-9H-purin-2-yl]amino]-, (2R,3S)- |
CAS | 1070790-89-4 |
化学式 | C21H31N7O |
分子量 | 397.52 |
密度 | 1.25±0.1 g/cm3(Predicted) |
沸点 | 618.3±65.0 °C(Predicted) |
溶解度 | 溶于DMSO,不溶于水 |
酸度系数 | 14.62±0.20(Predicted) |
存储条件 | -20℃ |
产品用途 | Fadraciclib, also known as CYC065, is an orally bioavailable inhibitor of cyclin dependent kinases 2, 5 and 9 (CDK2/5/9) with potential antineoplastic and chemoprotective activities. CYC065 selectively binds to and inhibits the activity of CDK2, 5 and 9, which leads to inhibition of CDK2, 5 and 9-dependent cellular pathways, downregulation of genes involved in the pro-survival pathway, prevention of the activation of DNA double-strand break repair pathways, and induction of both cell cycle arrest and apoptosis. This inhibits the proliferation of CDK2/5/9-overexpressing tumor cells. In addition, CYC065 protects hematopoietic stem and progenitor cells (HSPCs), prevents myelosuppression, and preserves the function of the bone marrow. |
参考资料 展开查看 | 1. Cocco E, et al. Dual CCNE1/PIK3CA targeting is synergistic in CCNE1-amplified/PIK3CA-mutated uterine serous carcinomas in vitro and in vivo. Br J Cancer. 2016 Jul 26;115(3):303-11.2. Sumana Devata, et al. Molecular markers and venous thromboembolism (VTE) in acute myelogenous leukemia (AML) |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 2.516 ml | 12.578 ml | 25.156 ml |
5 mM | 0.503 ml | 2.516 ml | 5.031 ml |
10 mM | 0.252 ml | 1.258 ml | 2.516 ml |
5 mM | 0.05 ml | 0.252 ml | 0.503 ml |
微信搜索化工百科或扫描下方二维码,添加化工百科小程序,随时随地查信息!