Synthesis and Biological Evaluation of Novel Antifolate Analogs as Potential Anticancer Treatment

被引:0
|
作者
Stoicescu, Dan F. [1 ]
Rotaru, Maria [1 ]
机构
[1] Univ Bucharest, Dept Analyt Chem, Fac Chem, Bucharest 050663, Romania
关键词
Antifolate inhibitors; Antitumor activity; Cancer therapy; Classic antifolates; Dihydrofolate reductase; Folyl polyglutamate synthetase; Chemical synthesis; Leukemia; Methotrexate; Multitarget antifolate; Non-classic antifolates; Polyglutamates; Thymidylate synthase; Tumor resistance; 2-(2-{4-[(2,4-diamino-pteridin-6-ylmethyl)-amino]-phenyl}-2-oxo-ethyl) pentanedioic acid; 2-(2-{4-[(2,4-diamino-pteridin-6-ylmethyl)-methyl-amino]-phenyl}-2-oxo-ethyl) pentanedioic acid; ANTIOPPORTUNISTIC INFECTION AGENTS; THYMIDYLATE SYNTHASE; DIHYDROFOLATE-REDUCTASE; ENZYME-INHIBITION; PHASE-I; METHOTREXATE; RESISTANCE; AMINOPTERIN; SYNTHETASE; ANTITUMOR;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A novel process for the preparation of two ketomethylenic antifolates, 2-(2-{4-[(2,4-diamino-pteridin-6-ylmethyl)-amino]-phenyl}-2-oxo-ethyl) pentanedioic acid and 2-(2-{4-[(2,4- diamino-pteridin-6-ylmethyl)-methyl-amino]-phenyl}-2-oxo-ethyl) pentanedioic acid is described herein. Both compounds were compared with methotrexate as inhibitors of human dihydrofolate reductase and thymidylate synthase. The in-vitro and in-vivo results suggest that these novel antifolate inhibitors could potentially constitute effective therapeutic molecules in the treatment of certain cancers and might present a lower toxicity profile than methotrexate.
引用
收藏
页码:364 / 372
页数:9
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