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Details

Stereochemistry ABSOLUTE
Molecular Formula C13H21N5O7S.2H2O
Molecular Weight 427.431
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Zidebactam dihydrate

SMILES

O.O.OS(=O)(=O)ON1[C@H]2C[N@]([C@@H](CC2)C(=O)NNC(=O)[C@@H]3CCCNC3)C1=O

InChI

InChIKey=JMMRGZPABAFUJE-XYSAUEOZSA-N
InChI=1S/C13H21N5O7S.2H2O/c19-11(8-2-1-5-14-6-8)15-16-12(20)10-4-3-9-7-17(10)13(21)18(9)25-26(22,23)24;;/h8-10,14H,1-7H2,(H,15,19)(H,16,20)(H,22,23,24);2*1H2/t8-,9-,10+;;/m1../s1

HIDE SMILES / InChI
Zidebactam (also known as WCK 5107), a beta-lactam enhancer that belongs to the bicyclo-acyl hydrazide series. This drug inhibits the penicillin-binding protein and is participating in phase I clinical trial to treat the bacterial infection.

Approval Year

PubMed

PubMed

TitleDatePubMed
WCK 5107 (Zidebactam) and WCK 5153 Are Novel Inhibitors of PBP2 Showing Potent "β-Lactam Enhancer" Activity against Pseudomonas aeruginosa, Including Multidrug-Resistant Metallo-β-Lactamase-Producing High-Risk Clones.
2017-06
Patents

Sample Use Guides

3 g of zidebactam (1 g q8h) and 6 g of cefepime (2 g q8h) or 6 administered as IV infusions every q8h, over a period of 60 minutes.
Route of Administration: Intravenous
Name Type Language
1,6-Diazabicyclo[3.2.1]octane-2-carboxylic acid, 7-oxo-6-(sulfooxy)-, 2-[2-[(3R)-3-piperidinylcarbonyl]hydrazide], hydrate (1:2), (1R,2S,5R)-
Preferred Name English
Zidebactam dihydrate
Common Name English
Code System Code Type Description
PUBCHEM
156613482
Created by admin on Wed Apr 02 16:34:44 GMT 2025 , Edited by admin on Wed Apr 02 16:34:44 GMT 2025
PRIMARY
CAS
1996664-59-5
Created by admin on Wed Apr 02 16:34:44 GMT 2025 , Edited by admin on Wed Apr 02 16:34:44 GMT 2025
PRIMARY
FDA UNII
TE54T8WC4T
Created by admin on Wed Apr 02 16:34:44 GMT 2025 , Edited by admin on Wed Apr 02 16:34:44 GMT 2025
PRIMARY