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 language | English |
|---|---|
| Title of host publication | Journal of Pharmaceutical Sciences |
| Pages | 1785-1789 |
| Number of pages | 5 |
| Volume | 62 |
| Edition | 11 |
| DOIs | |
| State | Published - 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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