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新型嘧啶并喹啉及其核苷衍生物的合成、体外抗菌和体内抗肿瘤活性评价。

Synthesis, in vitro antimicrobial and in vivo antitumor evaluation of novel pyrimidoquinolines and its nucleoside derivatives.

机构信息

Photochemistry Department, National Research Centre, 12622 Dokki, Cairo, Egypt.

出版信息

Eur J Med Chem. 2011 Jan;46(1):21-30. doi: 10.1016/j.ejmech.2010.09.071. Epub 2010 Oct 8.

Abstract

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.

摘要

已经合成了七系列嘧啶并喹啉衍生物,包括四唑并[4',3':-1,2]嘧啶并[4,5-b]喹啉(3)、2-氨基嘧啶并[4,5-b]喹啉(4)、三唑并[4',3':1,2]-嘧啶并喹啉(5a,b, 10)、咪唑并[3',2':1,2]嘧啶并[4,5-b]-喹啉(8a,b)、6-氯-2-甲硫基嘧啶并[4,5-b]喹啉(12)、乙酰化核苷(16, 17a,b)和去乙酰化核苷(18, 19a,b)。其中一些新型嘧啶并喹啉衍生物对细菌和真菌具有高度活性。这些新的喹啉衍生物通过美国国立癌症研究所(NCI)评估了其对人类癌细胞系的抗癌活性。它们中的大多数具有优异的生长抑制活性,LD(50) 值在低微摩尔至纳摩尔浓度范围内。

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