Literature DB >> 6617846

Synthesis and antimicrobial activity of monoalkylcarbamic and thiocarbamic esters of 3-mercapto-1,2,4-benzothiadiazine-1,1-dioxide and of its Bz-derivatives.

M Di Bella, G Gamberini, A Tait, U Fabio, G P Quaglio.   

Abstract

A new series of monoalkylcarbamic esters of 3-mercapto-1,2,4-benzothiadiazine-1,1-dioxide (I) and of its 6-chloro- and 5,7-dichloroderivatives [compounds (II leads to XVI)] and a series of monoalkylthiocarbamic esters of (I) [compounds (XVII leads to XIX)] were synthesized and evaluated in vitro for antimicrobial activity. All the substances studied have been found to possess an inhibiting action on one or more strains of mycetes of the genus Candida and on some strains of Gram-positive bacteria belonging to the genus Staphylococcus. Moreover, some compounds have shown a bacteriostatic effect on a strain belonging to the genus Streptococcus. None of the substances tested was active on Gram-negative schizomycetes.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6617846     DOI: 10.1002/chin.198352237

Source DB:  PubMed          Journal:  Farmaco Sci        ISSN: 0430-0920


  2 in total

1.  3-(6-Bromo-4-oxo-4H-chromen-3-yl)-3,4-dihydro-2H-1,2,4-benzothia-diazine-1,1-dione.

Authors:  Mariya Al-Rashida; Saeed Ahmad Nagra; Islam Ullah Khan; George Kostakis; Ghulam Abbas
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-11-06

2.  3-(6-Fluoro-4-oxo-4H-chromen-3-yl)-3,4-dihydro-2H-1,2,4-benzothia-diazine-1,1-dione.

Authors:  Mariya Al-Rashida; Saeed Ahmad Nagra; Islam Ullah Khan; George Kostakis; Ghulam Abbas
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-10-02
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.