期刊
JOURNAL OF MOLECULAR STRUCTURE
卷 1142, 期 -, 页码 261-266出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.molstruc.2017.04.067
关键词
Crystal structure; Isostructural crystal packing; 2[1H]-pyrimidinethione; 2[1H]-pyrimidineselenone; Antibacterials; Antifungals
Four new crystal structures of sulfur and selenium analogues of 2[1H]-pyrimidinone derivatives were determined with the use of X-ray diffraction method. The molecular geometry and intermolecular interactions of the investigated molecules were analyzed in order to find the structural features and geometrical parameters, which can be responsible for antimicrobial activities. The influence of chalcogen substituents (sulfur and selenium) on the crystal packing was also studied. The main differences in the molecular structures exist in mutual arrangement of two aromatic rings. The intermolecular interactions in all investigated compounds are similar. Furthermore, the in vitro antibacterial and antifungal activities for these compounds were evaluated. Preliminary investigations have identified two highly potent antibacterial compounds containing selenium atom, which display selectivity towards staphylococci and micrococci. This selectivity was not observed for a control compound used as a drug, namely vancomycin. These compounds possess also good antifungal activity. This is the first report of biological activities of 2 [1H]-pyrimidineselenone derivatives. (C) 2017 Elsevier B.V. All rights reserved.
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