| Literature DB >> 12577518 |
Ola A el-Sayed1, Fatma M el-Bieh, Shada I el-Aqeel, Badr A al-Bassam, Maher E Hussein.
Abstract
Two series of 4-aminopyrimido[4,5-b]quinoline derivatives substituted in the 2-position 6a-c and/or in 1-position 9a-e have been prepared by facile routes starting from 2-amino-3-cyanoquinoline 2,2-chloro-3-cyanoquinoline 4 and 2-arylamino-3-cyanoquinolines 8a-d. The reactions involved simple fusion with thiourea or urea and, in some cases, with guanidine. The prepared compounds were in vitro tested for antimicrobial activities against some selected Gram-positive, Gram-negative bacteria and fungi. The products containing the thio-function were the most active followed by those containing the imino-function while the carbonyl containing derivatives were without significant antimicrobial effect.Entities:
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Year: 2002 PMID: 12577518
Source DB: PubMed Journal: Boll Chim Farm ISSN: 0006-6648