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含桥头氮原子的潜在生物活性氮杂和硫氮杂多环化合物的制备:某些吡咯并[1,2,3 - de]-1,4 - 苯并噻嗪的合成及抗菌活性

Preparation of potentially bioactive aza and thiaza polycyclic compounds containing a bridgehead nitrogen atom synthesis and antimicrobial activity of some pyrrolo[1,2,3-de]-1,4-benzothiazines.

作者信息

Armenise D, Trapani G, Arrivo V, Morlacchi F

机构信息

Dipartimento Farmaco-Chimico, Facoltà di Farmacia, Università degli Studi di Bari, Italy.

出版信息

Farmaco. 1991 Sep;46(9):1023-32.

PMID:1807288
Abstract

The synthesis of the 2,3-dihydro-pyrrolo[1,2,3-de]-1,4-benzothiazine 1a and 11b, 12-dihydro-isoquino[1,2-c]-1,4-benzothiazine 8 has been accomplished by using a Bischler type cyclization of the N-(2,2-diethoxyethyl)-3,4-dihydro-2H-1,4-benzothiazines 3a and 3d, respectively. The new compounds 1a and 8 together with the known pyrrolobenzothiazines 1b,c and some their derivatives and intermediates of preparation were tested in vitro for their antimicrobial activity. Compound 1b was the most active against the Gram-positive Bacillus subtilis. Compound 7b showed interesting antifungal activity when tested against Saccharomyces cerevisiae.

摘要

通过分别对N-(2,2-二乙氧基乙基)-3,4-二氢-2H-1,4-苯并噻嗪3a和3d进行Bischler型环化反应,已完成2,3-二氢-吡咯并[1,2,3- de]-1,4-苯并噻嗪1a和11b、12-二氢-异喹啉并[1,2-c]-1,4-苯并噻嗪8的合成。新化合物1a和8以及已知的吡咯并苯并噻嗪1b、c及其一些衍生物和制备中间体进行了体外抗菌活性测试。化合物1b对革兰氏阳性枯草芽孢杆菌活性最强。化合物7b在针对酿酒酵母进行测试时显示出有趣的抗真菌活性。

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