| Name | zidebactam |
|---|---|
| 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]. |
|---|---|
| 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 |
|---|---|
| Molecular Formula | C13H21N5O7S |
| Molecular Weight | 391.40 |
| Exact Mass | 391.116180 |
| LogP | -3.01 |
| Index of Refraction | 1.653 |
| Storage condition | 2-8℃ |