Cytotoxic 4′-aminochalcones and related compounds

被引:0
|
作者
Dimmock, JR
Jha, A
Zello, GA
Allen, TM
Santos, CL
Balzarini, J
De Clercq, E
Manavathu, EK
Stables, JP
机构
[1] Univ Saskatchewan, Coll Pharm & Nutr, Saskatoon, SK S7N 5C9, Canada
[2] Univ Alberta, Dept Pharmacol, Edmonton, AB T6G 2M7, Canada
[3] Rega Inst, Louvain, Belgium
[4] Wayne State Univ, Dept Med, Detroit, MI 48202 USA
[5] NINDS, Bethesda, MD 20892 USA
来源
PHARMAZIE | 2003年 / 58卷 / 04期
关键词
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of 4'-aminochalcones 1 and related maleamic acids 2 and Schiff bases 3 were designed and synthesized as candidate cytotoxic agents. The atomic charges on different atoms of representative compounds were calculated. Evaluation of the enones 1-3 against human Molt 4/C8 and CEM T-lymphocytes as well as murine P388 and L1210 leukemic cells revealed that approximately 40% of the IC(50) values generated were less than 10 muM. In some cases cytotoxicity was correlated with the Hammett sigma values of the aryl substituents and less frequently with the aryl Hansch pi values. Evidence was obtained that in general these compounds displayed selective toxicity for certain malignant cells and were well tolerated in mice. This study has revealed various directions whereby the project may be amplified in the future with a view to finding compounds with increased cytotoxicity to tumour cells.
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页码:227 / 232
页数:6
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