Avibactam
A beta-lactamase inhibitor that inactivates enzymes produced by resistant bacteria that would otherwise destroy cephalosporin and other beta-lactam antibiotics. It is always used in combination with a partner antibiotic to restore activity against carbapenem-resistant organisms.
Berat Molekul
265,2500 g/mol
LogP
-1,80
TPSA
139,00 Ų
Lipinski RO5
Lulus
Area Terapeutik
Mekanisme Kerja
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 …
Struktur 2D
Cite this structure
Embed this structure
SMILES
NC(=O)[C@@H]1CC[C@@H]2CN1C(=O)N2OS(=O)(=O)O
InChI
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
Molecular Formula
C7H11N3O6S
HBD / HBA
2 / 6
Ikatan yang Dapat Dirotasi
3
Atom Berat
17
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.
Pertanyaan yang Sering Diajukan
A beta-lactamase inhibitor that inactivates enzymes produced by resistant bacteria that would otherwise destroy cephalosporin and other beta-lactam antibiotics. It is always used in combination with a partner antibiotic to restore activity against carbapenem-resistant organisms.
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 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). CHEMBL1689063. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 9835049. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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