Syntheses and evaluation of benzodiazaborine compounds against M. tuberculosis H37Rv in vitro
摘要:
The synthesis of six benzo[e]diazaborine compounds and thier in vitro evaluation against M. tuberculosis H37Rv is described. The compounds 1,2-dihydro-1-hydroxy-2-phenyl-2,4,1 -benzo[e]diazaborin-3 (4H)-one, 4, and 1,2-dihydro-1-hydroxy-2-(3-pyridyl)-2,4,1-benzo[e]diazaborin-3(4H)-thione, (5), showed the greatest inhibitory activity. (C) 1998 Elsevier Science Ltd. All rights reserved.