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Synthesis and properties of mesoionic pyrimido[1,2‐b]pyridazine‐2,4‐diones and mesoionic pyridazino[2,3‐a]‐s‐triazine‐2,4‐diones: Mesoionic analogs structurally related to fervenulin

  • SUNY Buffalo

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

Derivatives of two new and unusual classes of heterocycles, possessing structural similarities to the broad spectrum antibiotic fervenulin, were synthesized and examined for in vitro antimicrobial activity. Only three of 17 mesoionic pyrimido[1,2‐b]pyridazine‐2,4‐diones exhibited evidence of antimicrobial activity while seven of eight mesoionic pyridazino[2,3‐a]‐s‐triazine‐2,4‐diones were active against one or more microorganisms. Susceptibility toward attack by nucleophiles of both mesoionic pyridazino[2,3‐a]‐s‐triazine‐2,4‐diones and fervenulin was observed.

Original languageEnglish
Pages (from-to)1505-1510
Number of pages6
JournalJournal of Pharmaceutical Sciences
Volume65
Issue number10
DOIs
StatePublished - Oct 1976

Keywords

  • Antimicrobial activity—substituted pyrimido[1,2‐b]pyridazines and pyridazino[2,3‐a]‐s‐triazines
  • Heterocycles—substituted pyrimido[1,2‐b]pyridazines and pyridazino[2,3‐a]‐s‐triazines synthesized, screened for antimicrobial activity
  • Mesoionic compounds—substituted pyrimido[1,2‐b]‐pyridazines and pyridazino[2,3‐a]‐s‐triazines series synthesized, antimicrobial activity screened
  • Pyridazino[2,3‐a]‐s‐triazine‐2,4‐diones—synthesized, in vitro antimicrobial activity screened
  • Pyrimido[1,2‐b]pyridazine‐2,4‐diones—synthesized, in vitro antimicrobial activity screened
  • Structure‐activity relationships—substituted pyrimido[1,2‐b]pyridazines and pyridazino[2,3‐a]‐s‐triazines synthesized, antimicrobial activity screened

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