| Literature DB >> 21485702 |
Jerzy Cieplik1, Marcin Stolarczyk, Janusz Pluta, Olaf Gubrynowicz, Iwona Bryndal, Tadeusz Lis, Marcin Mikulewicz.
Abstract
The paper presents the synthesis of 1,2,3,7-tetraaryl-1,2,3,4-tetrahydropyrimido[4,5-d]pyrimidines. The structures of the obtained compounds were confirmed by crystallographic and spectroscopic analyses, and their antibacterial activity was tested on 9 selected strains, comparing chemical structure changes with increased microbiological activity. It was confirmed that aromatic residues in the hydrogenated pyrimidine ring constitute a significant element influencing antibacterial activity. Electronegative radicals increase microbiological activity, but decrease solubility of the compounds. Therefore, substituents should be selected in a manner ensuring a balanced effect. The presented crystal structure of 6f includes two stereoisomers, which we decided to isolate and compare the microbiological properties in further studies.Entities:
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Year: 2011 PMID: 21485702
Source DB: PubMed Journal: Acta Pol Pharm ISSN: 0001-6837 Impact factor: 0.330