Name | zidebactam |
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Synonyms |
zidebactam
1,6-Diazabicyclo[3.2.1]octane-2-carboxylic acid, 7-oxo-6-(sulfooxy)-, 2-[2-[(3R)-3-piperidinylcarbonyl]hydrazide], (2S,5R)- YPM97423DB (2S,5R)-7-Oxo-N'-[(3R)-3-piperidinylcarbonyl]-6-(sulfooxy)-1,6-diazabicyclo[3.2.1]octane-2-carbohydrazide |
Description | Zidebactam (WCK-5107) is a potent β-lactamase inhibitor[1]. Zidebactam also is a penicillin-binding protein2 (PBP2) inhibitor with an IC50 of 0.26 μg/mL[2]. |
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Related Catalog | |
Target |
IC50: 0.26 μg/mL (P. aeruginosa PAO1 PBP2)[2] |
In Vitro | Zidebactam (WCK-5107) inhibits WT Enterobacteriaceae with a MIC50 of 0.25 mg/L. Zidebactam alone exhibits variable activity when tested against E. coli (MIC50/90 0.12/0.12 mg/L) and Enterobacter spp. (MIC50/90 0.12/0.25 mg/L)[1]. |
References |
Density | 1.6±0.1 g/cm3 |
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Molecular Formula | C13H21N5O7S |
Molecular Weight | 391.40 |
Exact Mass | 391.116180 |
LogP | -3.01 |
Index of Refraction | 1.653 |
Storage condition | 2-8℃ |