Zidebactam
CAS No. 1436861-97-0
Zidebactam( WCK-5107 )
Catalog No. M23601 CAS No. 1436861-97-0
Zidebactam is an effective β-lactamase inhibitor.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 180 | In Stock |
|
| 10MG | 297 | In Stock |
|
| 25MG | 506 | In Stock |
|
| 50MG | 714 | In Stock |
|
| 100MG | 1004 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameZidebactam
-
NoteResearch use only, not for human use.
-
Brief DescriptionZidebactam is an effective β-lactamase inhibitor.
-
DescriptionZidebactam is an effective β-lactamase inhibitor. Zidebactam also is a penicillin-binding protein2 inhibitor (IC50: 0.26 μg/mL).
-
In VitroZidebactam (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 0.12/0.12mg/L) and Enterobacter spp. (MIC50/90 0.12/0.25mg/L).
-
In Vivo——
-
SynonymsWCK-5107
-
PathwayGPCR/G Protein
-
TargetAntibacterial
-
RecptorPBP2|β-Lactamase
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1436861-97-0
-
Formula Weight391.4
-
Molecular FormulaC13H21N5O7S
-
Purity>98% (HPLC)
-
SolubilityH2O:50 mg/mL (127.75 mM; Need ultrasonic)
-
SMILESOS(ON([C@@H]1CC[C@@H](C(NNC([C@H]2CNCCC2)=O)=O)N2C1)C2=O)(=O)=O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Sader HS, et al. WCK 5222 (cefepime/zidebactam) antimicrobial activity tested against Gram-negative organisms producing clinically relevant β-lactamases. J Antimicrob Chemother. 2017 Jun 1;72(6):1696-1703.
molnova catalog
related products
-
Ornidazole (Levo-)
Ornidazole Levo- is the levo-isomer of Ornidazole.
-
CCG 2979
CCG 2979 is a small molecule inhibitor of gene expression of streptokinase (SK), a critical group A streptococcal (GAS) virulence factor.
-
Amorolfine HCL
Amorolfine HCL is an antifungal reagent. It exerts the antifungal activity by selectively interrupting two steps in the pathway of ergosterol synthesis and eventually disrupting the function and structure of fungal cell membrane. Amorolfine, a morpholine antifungal drug, can inhibit D14 reductase and D7-D8 isomerase.
Cart
sales@molnova.com