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新型萘并[2,1-b]-1,4,5-氧杂或硫杂二氮杂卓类化合物的合成:潜在的抗菌和抗癌药物

Synthesis of novel naphtho[2,1-b]-1,4,5-oxa- or thiadiazepines as potential antimicrobial and anticancer agents.

作者信息

Khalil M A, Habib N S

机构信息

Pharmaceutical Chemistry Department, Faculty of Pharmacy, University of Alexandria, Egypt.

出版信息

Arch Pharm (Weinheim). 1990 Aug;323(8):471-4. doi: 10.1002/ardp.19903230806.

DOI:10.1002/ardp.19903230806
PMID:2278512
Abstract

Two novel series of quinone derivatives have been synthesized. Thus, condensation of 2-ethoxycarbonylmethylthio-; 3-ethoxycarbonylmethylthio-2-methyl- and 3-ethoxycarbonylmethoxy-2-methyl derivatives of 1,4-naphthoquinone with substituted phenylhydrazines afforded the corresponding hydrazones, while cyclization of the same quinones with the same substituted hydrazines in glacial acetic acid gave the corresponding naphtho[2,1-b]-1,4,5-oxa- or thiadiazepine derivatives. The antimicrobial and anticancer activities of the synthesized compounds were studied.

摘要

已经合成了两个新型的醌衍生物系列。因此,1,4-萘醌的2-乙氧羰基甲基硫代、3-乙氧羰基甲基硫代-2-甲基和3-乙氧羰基甲氧基-2-甲基衍生物与取代苯肼缩合得到相应的腙,而相同的醌与相同的取代肼在冰醋酸中环化得到相应的萘并[2,1-b]-1,4,5-恶二氮杂卓或噻二氮杂卓衍生物。研究了合成化合物的抗菌和抗癌活性。

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