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Novel lβ-Methylcarbapenems Having Cyclic Sulfonamide Moieties: Synthesis and Evaluation ofin-vitroBiological Activity - Part II
- Source :
- Archiv der Pharmazie. 342:528-532
- Publication Year :
- 2009
- Publisher :
- Wiley, 2009.
-
Abstract
- The synthesis of a new series of 1beta-methylcarbapenems having cyclic sulfonamide moieties is described. Their in-vitro antibacterial activities against both Gram-positive and Gram-negative bacteria were tested and the effect of a substituent on the pyrrolidine ring was investigated. One particular compound IIIe having a [1,2,5]thiadiazolidin 1,1-dioxide moiety showed the most potent antibacterial activity.
- Subjects :
- chemistry.chemical_classification
Sulfonamides
Microbial Viability
Molecular Structure
Stereochemistry
Drug Evaluation, Preclinical
Substituent
Pharmaceutical Science
Biological activity
Meropenem
Ring (chemistry)
Combinatorial chemistry
Pyrrolidine
In vitro
Anti-Bacterial Agents
Sulfonamide
Imipenem
Structure-Activity Relationship
chemistry.chemical_compound
Carbapenems
chemistry
Drug Discovery
Moiety
Thienamycins
Antibacterial activity
Subjects
Details
- ISSN :
- 15214184 and 03656233
- Volume :
- 342
- Database :
- OpenAIRE
- Journal :
- Archiv der Pharmazie
- Accession number :
- edsair.doi.dedup.....f758d4ab8f3a9a03b91b9e8f13c3e878