Literature DB >> 9821214

Novel compounds, 1,3-selenazine derivatives, as antibacterial agents against Escherichia coli and Staphylococcus aureus.

M Koketsu1, H Ishihara, M Hatsu.   

Abstract

The antibacterial activities of several kinds of novel 4H-5,6-dihydro-1,3-selenazine derivatives against Escherichia coli and Staphylococcus aureus were investigated. 4-Hydroxy-4-methyl-2-p-tolyl-4H-5,6-dihydro-1,3-selenazine (TS-1), 4-ethyl-4-hydroxy-2-p-tolyl-4H-5,6-dihydro-1,3-selenazine (TS-2), and 4-hydroxy-4-methyl-2-pentyl-4H-5,6-dihydro-1,3-selenazine (PS-1) exhibited strong inhibitory activity against E. coli, and TS-1, TS-2, PS-1, 4-hydroxy-4-methyl-2-pentyl-6-propyl-4H-5,6-dihydro-1,3-selenazine (PS-6) and 4-hydroxy-4-methyl-2-pentyl-6-phenyl-4H-5,6-dihydro-1,3-selenazine (PS-8) also showed inhibitory activity against S. aureus. 4H-5,6-dihydro-1,3-thiazines and 1,3-selenazole had no inhibitory activities against both bacteria. TS-1, TS-2, and PS-1 exhibited marked antibacterial activities against both Gram-negative and Gram-positive bacteria.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9821214

Source DB:  PubMed          Journal:  Res Commun Mol Pathol Pharmacol        ISSN: 1078-0297


  3 in total

1.  Toward pyridine-fused selenium-containing antioxidants.

Authors:  Tahli Fenner; Carl H Schiesser
Journal:  Molecules       Date:  2004-05-31       Impact factor: 4.411

Review 2.  Isoselenocyanates: a powerful tool for the synthesis of selenium-containing heterocycles.

Authors:  Dinesh Ramesh Garud; Mamoru Koketsu; Hideharu Ishihara
Journal:  Molecules       Date:  2007-03-17       Impact factor: 4.411

3.  Inhibition of bacterial α-, β- and γ-class carbonic anhydrases with selenazoles incorporating benzenesulfonamide moieties.

Authors:  Andrea Angeli; Mariana Pinteala; Stelian S Maier; Sonia Del Prete; Clemente Capasso; Bogdan C Simionescu; Claudiu T Supuran
Journal:  J Enzyme Inhib Med Chem       Date:  2019-12       Impact factor: 5.051

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.