Synthesis and elastase inhibitory activity of 6α-chloro-2,2-dimethyl-3α-(pivaloyloxy)methylpenam sulfone, 6α-chloro-2,2-dimethyl-3-exo-methylenepenam sulfone, benzyl and methyl 6α-substituted penicillanate sulfones
✍ Scribed by Carlos E. Boschetti; Oreste A. Mascaretti; Julia A. Cricco; Oscar A. Roveri
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 587 KB
- Volume
- 3
- Category
- Article
- ISSN
- 0968-0896
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✦ Synopsis
The triflates and pivalates of 3 alpha-hydroxymethyl-6-substituted-2,2-dimethylpenam sulfones 3, 5; methyl and benzyl 6-substituted penicillanates 6-9 and 3-exo-methylene-6-substituted-2,2-dimethylpenam sulfone 4 were synthesized. These novel compounds were evaluated as elastase inhibitors using porcine pancreatic elastase. The effects that structural modifications of substituents on C-3 and C-6 in the penam nucleus have on elastase activity were examined and several similarities and distinctions were identified when compared to the reported penicillin esters and amides elastase inhibitors.
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The synthesis and in vitro synergies of (6R)-6-(~-hydroxybenzyl)-2[~-methoxyiminomethyl-2~methylpenam-30~-carboxylate 1,1-dioxide (4) and 2~-acyl-2~-methylpenam-3ct-carboxylate l,l-dioxide (15) are described. Compound 15 showed good in vitro synergy in combination with piperacillin and ceftazidime a