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Mesoionic purinone analogs IV: Synthesis and in vitro antibacterial properties of mesoionic thiazolo[3,2‐a]pyrimidin‐5,7‐diones and mesoionic 1,3,4‐thiadiazolo[3,2‐a]pyrimidin‐5,7‐diones

  • SUNY Buffalo

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

65 Scopus citations

Abstract

Derivatives of two members of a new and unusual class of heterocycles, termed mesoionic purinone analogs, were synthesized and examined for in vitro antibacterial activity. Mesoionic thiazolo[3,2‐a]pyrimidin‐5,7‐diones and mesoionic 1,3,4‐thiadiazolo[3,2‐a]pyrimidin‐5,7‐diones, which are isoconjugate with xanthine, were found to exhibit antibacterial activity against both Gram‐negative and Gram‐positive organisms. Several mesoionic 1,3,4‐thiadiazolo[3,2‐a]pyrimidin‐5,7‐diones possess significant levels of activity against Proteus vulgaris and Staphylococcus aureus.

Original languageEnglish
Title of host publicationJournal of Pharmaceutical Sciences
Pages1785-1789
Number of pages5
Volume62
Edition11
DOIs
StatePublished - Nov 1973

Keywords

  • Antibacterial activity—synthesis and screening of mesoionic thiazolo (or 1,3,4‐thiadiazolo) [3,2‐a]pyrimidin‐5,7‐diones
  • Mesoionic purinone analogs—synthesis and antibacterial properties of mesoionic thiazolo (or 1,3,4‐thiadiazolo) [3,2‐a]‐pyrimidin‐5,7‐diones
  • Mesoionic thiazolo (and 1,3,4‐thiadiazolo) [3,2‐a]pyrimidin‐5,7‐diones—synthesis and antibacterial screening
  • Xanthine(mesoionic) analogs—synthesis and antibacterial properties of mesoionic thiazolo (and 1,3,4‐thiadiazolo) [3,2‐a]pyrimidin‐5,7‐diones

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