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Details

Stereochemistry RACEMIC
Molecular Formula C7H10N3O6S.Na
Molecular Weight 287.226
Optical Activity ( + / - )
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AVE-1330A

SMILES

[Na+].NC(=O)[C@@H]1CC[C@@H]2C[N@]1C(=O)N2OS([O-])(=O)=O

InChI

InChIKey=RTCIKUMODPANKX-JBUOLDKXSA-M
InChI=1S/C7H11N3O6S.Na/c8-6(11)5-2-1-4-3-9(5)7(12)10(4)16-17(13,14)15;/h4-5H,1-3H2,(H2,8,11)(H,13,14,15);/q;+1/p-1/t4-,5+;/m1./s1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C7H10N3O6S
Molecular Weight 264.236
Charge -1
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
In vitro activity of the {beta}-lactamase inhibitor NXL104 against KPC-2 carbapenemase and Enterobacteriaceae expressing KPC carbapenemases.
2009 Aug
In vitro activity of avibactam (NXL104) in combination with β-lactams against Gram-negative bacteria, including OXA-48 β-lactamase-producing Klebsiella pneumoniae.
2012 Jan
Avibactam is a covalent, reversible, non-β-lactam β-lactamase inhibitor.
2012 Jul 17
Kinetics of avibactam inhibition against Class A, C, and D β-lactamases.
2013 Sep 27
In vivo efficacy of humanized exposures of Ceftazidime-Avibactam in comparison with Ceftazidime against contemporary Enterobacteriaceae isolates.
2014 Nov
Role of the Outer Membrane and Porins in Susceptibility of β-Lactamase-Producing Enterobacteriaceae to Ceftazidime-Avibactam.
2015 Dec 14
Randomized pharmacokinetic and drug-drug interaction studies of ceftazidime, avibactam, and metronidazole in healthy subjects.
2015 Oct
Substance Class Chemical
Created
by admin
on Sat Dec 16 07:57:40 GMT 2023
Edited
by admin
on Sat Dec 16 07:57:40 GMT 2023
Record UNII
C8SM6IRW7G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AVE-1330A
Common Name English
SULFURIC ACID, MONO((1R,2S,5R)-2-(AMINOCARBONYL)-7-OXO-1,6-DIAZABICYCLO(3.2.1)OCT-6-YL) ESTER, SODIUM SALT (1:1), REL-
Systematic Name English
AVIBACTAM SODIUM, (±)-
Common Name English
1,6-DIAZABICYCLO(3.2.1)OCTANE-2-CARBOXAMIDE, 7-OXO-6-(SULFOOXY)-, MONOSODIUM SALT, (1R,2S,5R)-REL-
Systematic Name English
Code System Code Type Description
CAS
790235-32-4
Created by admin on Sat Dec 16 07:57:40 GMT 2023 , Edited by admin on Sat Dec 16 07:57:40 GMT 2023
SUPERSEDED
CAS
396731-20-7
Created by admin on Sat Dec 16 07:57:40 GMT 2023 , Edited by admin on Sat Dec 16 07:57:40 GMT 2023
PRIMARY
FDA UNII
C8SM6IRW7G
Created by admin on Sat Dec 16 07:57:40 GMT 2023 , Edited by admin on Sat Dec 16 07:57:40 GMT 2023
PRIMARY
PUBCHEM
24944097
Created by admin on Sat Dec 16 07:57:40 GMT 2023 , Edited by admin on Sat Dec 16 07:57:40 GMT 2023
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER
Related Record Type Details
ACTIVE MOIETY