Literature DB >> 14622999

The synthesis and antibacterial activity of 1,3,4-thiadiazole phenyl oxazolidinone analogues.

Lisa M Thomasco1, Robert C Gadwood, Elizabeth A Weaver, Jason M Ochoada, Charles W Ford, Gary E Zurenko, Judith C Hamel, Douglas Stapert, Judy K Moerman, Ronda D Schaadt, Betty H Yagi.   

Abstract

Replacement of the morpholine C-ring of linezolid 1 with a 1,3,4-thiadiazolyl ring leads to oxazolidinone analogues 5 having potent antibacterial activity against both gram-positive and gram-negative organisms. Conversion of the C5 acetamide group to a thioacetamide further increases the potency of these compounds.

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Year:  2003        PMID: 14622999     DOI: 10.1016/j.bmcl.2003.07.018

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  3 in total

1.  N-[(3-Methyl-5-phen-oxy-1-phenyl-pyrazol-4-yl)carbon-yl]-N'-(5-propyl-1,3,4-thia-diazol-2-yl)thio-urea.

Authors:  Yan-Rong Sun; Gang Liu; Chen-Jiang Liu; Yan-Ping Li
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-01-09

2.  Synthesis, biological evaluation, and molecular modeling of 3,5-substituted-N1-phenyl-N4,N4-di-n-butylsulfanilamides as antikinetoplastid antimicrotubule agents.

Authors:  Tesmol G George; Molla M Endeshaw; Rachel E Morgan; Kiran V Mahasenan; Dawn A Delfín; Mitali S Mukherjee; Adam J Yakovich; Jean Fotie; Chenglong Li; Karl A Werbovetz
Journal:  Bioorg Med Chem       Date:  2007-06-27       Impact factor: 3.641

3.  5-(3-Nitro-benz-yl)-1,3,4-thia-diazol-2-amine.

Authors:  Samir A Carvalho; Larisse O de Feitosa; Edson F da Silva; Edward R T Tiekink; James L Wardell; Solange M S V Wardell
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-11-25
  3 in total

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