Avibactam Sodium
The sodium salt of avibactam, formulated for intravenous use in combination with ceftazidime to treat serious infections caused by drug-resistant Gram-negative bacteria. By protecting the partner antibiotic from enzymatic destruction, it restores its bactericidal activity.
الوزن الجزيئي
287,2300 g/mol
TPSA
141,00 Ų
المجالات العلاجية
آلية العمل
Inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), preventing transpeptidation and cross-linking of peptidoglycan chains. This weakens the bacterial cell wall, leading to osmotic lysis and cell death.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), preventing transpeptidation and cross-linking of peptidoglycan chains. This weakens the bacterial cell wall, leading to osmotic lysis and cell …
البنية ثنائية الأبعاد
Cite this structure
Embed this structure
SMILES
NC(=O)[C@@H]1CC[C@@H]2CN1C(=O)N2OS(=O)(=O)[O-].[Na+]
InChI
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
Molecular Formula
C7H10N3NaO6S
HBD / HBA
1 / 6
الروابط القابلة للدوران
3
الذرات الثقيلة
18
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
الأسئلة الشائعة
The sodium salt of avibactam, formulated for intravenous use in combination with ceftazidime to treat serious infections caused by drug-resistant Gram-negative bacteria. By protecting the partner antibiotic from enzymatic destruction, it restores its bactericidal activity.
Inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), preventing transpeptidation and cross-linking of peptidoglycan chains. This weakens the bacterial cell wall, leading to osmotic lysis and cell death.
Yes, Avibactam Sodium is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL2107817. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 24944097. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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