化学
活力测定
程序性细胞死亡
细胞培养
造血
白血病
效力
细胞毒性
立体化学
动力学
体外
细胞凋亡
细胞生长
药理学
生物化学
干细胞
细胞生物学
生物
免疫学
遗传学
量子力学
物理
作者
Shama Nasim,Mónica L. Guzmán,Craig T. Jordan,Peter A. Crooks
标识
DOI:10.1016/j.bmcl.2011.06.027
摘要
4-Benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione (TDZD-8) was previously identified as an antileukemic agent exhibiting no evident toxicity toward normal hematopoietic cells. An SAR study has been carried out to examine the effect of varying the C-2 and C-4- substituents on the thiadiazolidinone ring of TDZD-8 on antileukemic activity. These studies resulted in the identification of more druglike analogs that exhibited comparable potency to TDZD-8 in killing acute myelogenous leukemia (AML) cells in culture. Surprisingly, the cell death kinetics induced by several of these novel analogs on MV-411 cells were extremely fast, with commitment to death occurring within 30 min. At a concentration of 10 μM, 3f (LD(50)=3.5 μM) completely eradicated cell viability of MV-411 cells within 2h, while analog 3e (LD(50)=2.0 μM) decimated cell viability within 30 min at a concentration of 10 μM and effectively abolished cell viability at 5 μM within 1-2h.
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