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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis, in vitro antimicrobial and in vivo antitumor evaluation of novel pyrimidoquinolines and its nucleoside derivatives.
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Synthesis, in vitro antimicrobial and in vivo antitumor evaluation of novel pyrimidoquinolines and its nucleoside derivatives.

机译:新型嘧啶并喹啉及其核苷衍生物的合成,体外抗微生物和体内抗肿瘤评价。

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摘要

Seven series of pyrimidoquinoline derivatives have been synthesized, tetrazolo[4',3':-1,2]pyrimido[4,5-b]quinoline (3), 2-aminopyrimido[4,5-b]quinoline (4), triazolo[4',3':1,2]-pyrimidoquinoline (5a,b, 10), imidazolo[3',2':1,2]pyrimido[4,5-b]-quinoline (8a,b), 6-chloro-2-methylthiopyrimido[4,5-b]quinoline (12), acetylated nucleosides (16, 17a,b) and deacetylated nucleosides (18, 19a,b). Some of the novel pyrimidoquinoline derivatives possess highly activity toward the bacteria and fungi species. The new quinolines derivatives were evaluated for their anticancer activity toward human cancer cell lines by the National Cancer Institute (NCI). Most of them had excellent growth inhibition activity, having LD(50) values in the low micromolar to nanomolar concentration range.
机译:已经合成了七个系列的嘧啶基喹啉衍生物,四唑并[4',3':-1,2]嘧啶基[4,5-b]喹啉(3),2-氨基嘧啶基[4,5-b]喹啉(4), triazolo [4',3':1,2]-嘧啶喹啉(5a,b,10),咪唑并[3',2':1,2,pyrimido [4,5-b]-喹啉(8a,b), 6-氯-2-甲基硫代嘧啶并[4,5-b]喹啉(12),乙酰化核苷(16、17a,b)和脱乙酰化核苷(18、19a,b)。一些新颖的嘧啶并喹啉衍生物对细菌和真菌种类具有很高的活性。美国国家癌症研究所(NCI)对新的喹啉衍生物对人癌细胞的抗癌活性进行了评估。它们中的大多数具有优异的生长抑制活性,在低微摩尔至纳摩尔浓度范围内具有LD(50)值。

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