Avibactam
drugOn this page
Also known as Avibactam component of zaviceftaNxl-104Nxl-104 free acidAvibactam (sodium)
Summary
Avibactam (CHEMBL1689063) is an approved small-molecule antibacterial drug; indicated across 8 conditions including pneumonia and bacterial infectious disease.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- Indications: 8 conditions
- Clinical trials: 8
- Chemistry: 265.25 Da · C7H11N3O6S
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1689063 |
| Name | Avibactam |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | no |
| PubChem CID | 9835049 |
| ChEBI | CHEBI:85984 |
| Molecular formula | C7H11N3O6S |
| Molecular weight | 265.25 |
| InChIKey | NDCUAPJVLWFHHB-UHNVWZDZSA-N |
SMILES: C1C[C@H](N2C[C@@H]1N(C2=O)OS(=O)(=O)O)C(=O)N
IUPAC name: [(2S,5R)-2-carbamoyl-7-oxo-1,6-diazabicyclo[3.2.1]octan-6-yl] hydrogen sulfate
ChEBI definition: A member of the class of azabicycloalkanes that is (2S,5R)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxamide in which the amino hydrogen at position 6 is replaced by a sulfooxy group. Used (in the form of its sodium salt) in combination with ceftazidime pentahydrate for the treatment of complicated urinary tract infections including pyelonephritis.
Pharmacological roles (ChEBI): antibacterial drug, antimicrobial agent, EC 3.5.2.6 (β-lactamase) inhibitor.
Also known as: Avibactam, Avibactam component of zavicefta, Nxl-104, Nxl-104 free acid, AVIBACTAM, Avibactam (sodium), avibactam
Parent form; salt/anhydrous children: CHEMBL2107817
Patent coverage: 581 distinct patent families (1,178 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 1,176 (100%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.
Targets
Targets
Broader ChEMBL bioactivity targets: 7 (assay-derived). Sample: Metallo-beta-lactamase type 2, Beta-lactamase TEM, Beta-lactamase, Beta-lactamase OXA-23, Beta-lactamase OXA-1, Beta-lactamase, Carbapenem-hydrolyzing beta-lactamase KPC.
Bioactivity
ChEMBL activities: 10 potent at pChembl ≥ 5 of 10 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| P62593 | 8.72 | IC50 | 1.9 | nM | CHEMBL_ACT_23183621 |
| P05364 | 7 | IC50 | 100 | nM | CHEMBL_ACT_5298798 |
| P13661 | 6.89 | IC50 | 130 | nM | CHEMBL_ACT_25498504 |
| P24735 | 6.89 | IC50 | 128 | nM | CHEMBL_ACT_5298799 |
| P14488 | 6.85 | IC50 | 141.1 | nM | CHEMBL_ACT_25095745 |
| Q9F663 | 6.73 | IC50 | 186 | nM | CHEMBL_ACT_25498500 |
| P05364 | 6.04 | IC50 | 923 | nM | CHEMBL_ACT_25498502 |
| Q9L4P2 | 5.77 | Ki | 1700 | nM | CHEMBL_ACT_20658851 |
| Q9L4P2 | 5.63 | IC50 | 2320 | nM | CHEMBL_ACT_25498508 |
| P05364 | 5.11 | Ki | 7700 | nM | CHEMBL_ACT_5298805 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
8 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| pneumonia | 3 | MONDO:0005249 | EFO:0003106 |
| bacterial infectious disease | 3 | MONDO:0005113 | EFO:0000771 |
| pyelonephritis | 3 | MONDO:0006939 | EFO:1001141 |
| urinary tract infection | 2 | MONDO:0100338 | EFO:0003103 |
| gram-negative bacterial infections | 2 | MONDO:0021678 | MONDO:0021678 |
| kidney failure | 1 | MONDO:0001106 | HP:0000083 |
2 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 8.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE1 | 5 |
| PHASE4 | 1 |
| PHASE2 | 1 |
| Not specified | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT02504827 | PHASE4 | COMPLETED | Steady-state Pharmacokinetics of Ceftazidime/Avibactam in Cystic Fibrosis |
| NCT07431307 | PHASE2 | NOT_YET_RECRUITING | Safety, Pharmacokinetics and Efficacy of BV100 Plus Low Dose Polymyxin B Plus Ceftazidime/Avibactam, or Plus Cefiderocol in Patients With Pulmonary and Extrapulmonary Infections Due to Carbapenem-resistant Acinetobacter Baumannii-calcoaceticus Complex |
| NCT01430910 | PHASE1 | COMPLETED | A Study to Assess the Levels of Two Antibiotics in the Blood When Given Together and Separately |
| NCT01689207 | PHASE1 | COMPLETED | To Investigate the Safety and Tolerability of Aztreonam-Avibactam (ATM-AVI) |
| NCT02822950 | PHASE1 | COMPLETED | A Study of Avycaz (Ceftazidime/Avibactam) Pharmacokinetics/Pharmacodynamics (PK/PD) in Critically Ill Patients |
| NCT05588531 | PHASE1 | COMPLETED | Study on Tolerance, Pharmacokinetics and Drug Interaction of YK-1169 in Healthy Volunteers |
| NCT06593054 | PHASE1 | COMPLETED | To Learn How Different Forms of Study Medicine Are Taken up Into the Blood and the Effect of Food on Study Medicine in Healthy Adults |
| NCT06210542 | Not specified | NOT_YET_RECRUITING | Precise Treatment of Ceftazidime-Avibactam in Patients With CRO Infections Under the Guidance of TDM and PPK Model |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
- Diseases: pneumonia, bacterial infectious disease, pyelonephritis