Details
Stereochemistry | RACEMIC |
Molecular Formula | C7H11N3O6S |
Molecular Weight | 265.244 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)[C@@H]1CC[C@@H]2C[N@]1C(=O)N2OS(O)(=O)=O
InChI
InChIKey=NDCUAPJVLWFHHB-UHNVWZDZSA-N
InChI=1S/C7H11N3O6S/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)/t4-,5+/m1/s1
Approval Year
PubMed
Title | Date | PubMed |
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In vitro activity of the {beta}-lactamase inhibitor NXL104 against KPC-2 carbapenemase and Enterobacteriaceae expressing KPC carbapenemases. | 2009 Aug |
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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 |
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Avibactam is a covalent, reversible, non-β-lactam β-lactamase inhibitor. | 2012 Jul 17 |
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Kinetics of avibactam inhibition against Class A, C, and D β-lactamases. | 2013 Sep 27 |
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In vivo efficacy of humanized exposures of Ceftazidime-Avibactam in comparison with Ceftazidime against contemporary Enterobacteriaceae isolates. | 2014 Nov |
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Role of the Outer Membrane and Porins in Susceptibility of β-Lactamase-Producing Enterobacteriaceae to Ceftazidime-Avibactam. | 2015 Dec 14 |
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Randomized pharmacokinetic and drug-drug interaction studies of ceftazidime, avibactam, and metronidazole in healthy subjects. | 2015 Oct |
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396731-14-9
Created by
admin on Sat Dec 16 07:59:41 GMT 2023 , Edited by admin on Sat Dec 16 07:59:41 GMT 2023
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06MFO7817I
Created by
admin on Sat Dec 16 07:59:41 GMT 2023 , Edited by admin on Sat Dec 16 07:59:41 GMT 2023
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9835049
Created by
admin on Sat Dec 16 07:59:41 GMT 2023 , Edited by admin on Sat Dec 16 07:59:41 GMT 2023
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794508-22-8
Created by
admin on Sat Dec 16 07:59:41 GMT 2023 , Edited by admin on Sat Dec 16 07:59:41 GMT 2023
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SUPERSEDED |
ACTIVE MOIETY