Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C12H16BNO5S |
| Molecular Weight | 297.135 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OB1O[C@H](CC(O)=O)CC[C@@H]1NC(=O)CC2=CC=CS2
InChI
InChIKey=IOOWNWLVCOUUEX-WPRPVWTQSA-N
InChI=1S/C12H16BNO5S/c15-11(7-9-2-1-5-20-9)14-10-4-3-8(6-12(16)17)19-13(10)18/h1-2,5,8,10,18H,3-4,6-7H2,(H,14,15)(H,16,17)/t8-,10-/m0/s1
| Molecular Formula | C12H16BNO5S |
| Molecular Weight | 297.135 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Vaborbactam (formerly RPX7009) is a new beta-lactamase inhibitor based on a cyclic boronic acid pharmacophore. Vaborbactam is a highly active beta-lactamase inhibitor that restores activity of meropenem and other beta-lactam antibiotics in beta-lactamase-producing bacteria, particularly KPC-producing CRE. Meropenem in combination with vaborbactam (VABOMERE) is indicated for the treatment of patients 18 years and older with
complicated urinary tract infections including pyelonephritis caused by designated susceptible bacteria. The vaborbactam component of VABOMERE is a non-suicidal beta-lactamase inhibitor that protects meropenem from degradation by certain serine beta-lactamases such as Klebsiella pneumoniae carbapenemase (KPC). Vaborbactam does not have any antibacterial activity. Vaborbactam does not decrease the activity of meropenem against meropenem-susceptible organisms.
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: GO:0008800 Sources: https://www.ncbi.nlm.nih.gov/pubmed/28848018 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Curative | VABOMERE Approved UseVABOMERE (meropenem and vaborbactam) is a combination of meropenem, a penem antibacterial, and vaborbactam, a beta-lactamase inhibitor, indicated for the treatment of patients 18 years and older with complicated urinary tract infections (cUTI) including pyelonephritis caused by designated susceptible bacteria. Launch Date2017 |
|||
| Curative | Unknown Approved UseUnknown |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
5.03 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
250 mg single, intravenous dose: 250 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
9.97 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
500 mg single, intravenous dose: 500 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
15.3 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
750 mg single, intravenous dose: 750 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
21.8 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
1000 mg single, intravenous dose: 1000 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
27.8 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
1250 mg single, intravenous dose: 1250 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
32.9 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
1500 mg single, intravenous dose: 1500 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
41.6 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
2000 mg single, intravenous dose: 2000 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
4.81 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
250 mg 3 times / day multiple, intravenous dose: 250 mg route of administration: Intravenous experiment type: MULTIPLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
21.3 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
1000 mg 3 times / day multiple, intravenous dose: 1000 mg route of administration: Intravenous experiment type: MULTIPLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
33.4 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
1500 mg 3 times / day multiple, intravenous dose: 1500 mg route of administration: Intravenous experiment type: MULTIPLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
40.9 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
2000 mg 3 times / day multiple, intravenous dose: 2000 mg route of administration: Intravenous experiment type: MULTIPLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
16.6 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
250 mg single, intravenous dose: 250 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
35.6 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
500 mg single, intravenous dose: 500 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
51.8 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
750 mg single, intravenous dose: 750 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
79.3 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
1000 mg single, intravenous dose: 1000 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
100 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
1250 mg single, intravenous dose: 1250 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
114 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
1500 mg single, intravenous dose: 1500 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
144 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
2000 mg single, intravenous dose: 2000 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
16.3 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
250 mg 3 times / day multiple, intravenous dose: 250 mg route of administration: Intravenous experiment type: MULTIPLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
74.6 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
1000 mg 3 times / day multiple, intravenous dose: 1000 mg route of administration: Intravenous experiment type: MULTIPLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
118 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
1500 mg 3 times / day multiple, intravenous dose: 1500 mg route of administration: Intravenous experiment type: MULTIPLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
145 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
2000 mg 3 times / day multiple, intravenous dose: 2000 mg route of administration: Intravenous experiment type: MULTIPLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
1.17 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
250 mg single, intravenous dose: 250 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
1.35 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
500 mg single, intravenous dose: 500 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
1.24 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
750 mg single, intravenous dose: 750 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
1.41 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
1000 mg single, intravenous dose: 1000 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
1.32 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
1250 mg single, intravenous dose: 1250 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
1.4 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
1500 mg single, intravenous dose: 1500 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
1.51 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
2000 mg single, intravenous dose: 2000 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
1.17 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
250 mg 3 times / day multiple, intravenous dose: 250 mg route of administration: Intravenous experiment type: MULTIPLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
1.43 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
1000 mg 3 times / day multiple, intravenous dose: 1000 mg route of administration: Intravenous experiment type: MULTIPLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
1.65 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
1500 mg 3 times / day multiple, intravenous dose: 1500 mg route of administration: Intravenous experiment type: MULTIPLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
1.66 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
2000 mg 3 times / day multiple, intravenous dose: 2000 mg route of administration: Intravenous experiment type: MULTIPLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
Funbound
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
67% EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27527080 |
250 mg single, intravenous dose: 250 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
VABORBACTAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
Doses
| Dose | Population | Adverse events |
|---|---|---|
2 g 3 times / day multiple, intravenous Recommended Dose: 2 g, 3 times / day Route: intravenous Route: multiple Dose: 2 g, 3 times / day Sources: |
healthy, adult Health Status: healthy Age Group: adult Sources: |
Disc. AE: Chest discomfort... AEs leading to discontinuation/dose reduction: Chest discomfort (3.8%) Sources: |
2 g 3 times / day multiple, intravenous Recommended Dose: 2 g, 3 times / day Route: intravenous Route: multiple Dose: 2 g, 3 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: M+F Sources: |
Disc. AE: Pyrexia, Drug hypersensitivity... AEs leading to discontinuation/dose reduction: Pyrexia (0.3%) Sources: Drug hypersensitivity (0.3%) Hypersensitivity (0.3%) Septic shock (0.3%) Infusion related reaction (0.7%) |
2 g 3 times / day multiple, intravenous Highest studied dose|Recommended Dose: 2 g, 3 times / day Route: intravenous Route: multiple Dose: 2 g, 3 times / day Sources: |
unhealthy Health Status: unhealthy Sources: |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Chest discomfort | 3.8% Disc. AE |
2 g 3 times / day multiple, intravenous Recommended Dose: 2 g, 3 times / day Route: intravenous Route: multiple Dose: 2 g, 3 times / day Sources: |
healthy, adult Health Status: healthy Age Group: adult Sources: |
| Drug hypersensitivity | 0.3% Disc. AE |
2 g 3 times / day multiple, intravenous Recommended Dose: 2 g, 3 times / day Route: intravenous Route: multiple Dose: 2 g, 3 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: M+F Sources: |
| Hypersensitivity | 0.3% Disc. AE |
2 g 3 times / day multiple, intravenous Recommended Dose: 2 g, 3 times / day Route: intravenous Route: multiple Dose: 2 g, 3 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: M+F Sources: |
| Pyrexia | 0.3% Disc. AE |
2 g 3 times / day multiple, intravenous Recommended Dose: 2 g, 3 times / day Route: intravenous Route: multiple Dose: 2 g, 3 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: M+F Sources: |
| Septic shock | 0.3% Disc. AE |
2 g 3 times / day multiple, intravenous Recommended Dose: 2 g, 3 times / day Route: intravenous Route: multiple Dose: 2 g, 3 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: M+F Sources: |
| Infusion related reaction | 0.7% Disc. AE |
2 g 3 times / day multiple, intravenous Recommended Dose: 2 g, 3 times / day Route: intravenous Route: multiple Dose: 2 g, 3 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: M+F Sources: |
Overview
| CYP3A4 | CYP2C9 | CYP2D6 | hERG |
|---|---|---|---|
OverviewOther
| Other Inhibitor | Other Substrate | Other Inducer |
|---|---|---|
Drug as perpetrator
Drug as victim
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2017/209776Orig1s000ClinPharmR.pdf#page=26 Page: 26.0 |
no | |||
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2017/209776Orig1s000ClinPharmR.pdf#page=26 Page: 26.0 |
no | |||
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2017/209776Orig1s000ClinPharmR.pdf#page=26 Page: 26.0 |
no | |||
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2017/209776Orig1s000ClinPharmR.pdf#page=26 Page: 26.0 |
no |
Tox targets
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2017/209776Orig1s000PharmR.pdf#page=31 Page: 31.0 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Vaborbactam: Spectrum of Beta-Lactamase Inhibition and Impact of Resistance Mechanisms on Activity in Enterobacteriaceae. | 2017-11 |
|
| Effect of the β-Lactamase Inhibitor Vaborbactam Combined with Meropenem against Serine Carbapenemase-Producing Enterobacteriaceae. | 2016-09 |
Patents
Sample Use Guides
Administer VABOMERE 4 grams (meropenem 2 grams and vaborbactam 2 grams) every 8 hours by intravenous infusion over 3 hours for up to 14 days, in patients 18 years of age and older with an estimated glomerular filtration rate (eGFR) ≥50 mL/min/1.73m2
Dosage adjustment is recommended in patients with renal impairment who have an eGFR less than 50 mL/min/ 1.73m2
Route of Administration:
Intravenous
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/27381386
The activity of meropenem combined with the serine β-lactamase inhibitor vaborbactam (formerly RPX7009) was studied against 315 serine carbapenemase-producing Enterobacteriaceae (CPE) isolates by use of checkerboard-designed panels to assess the optimal inhibitor concentration (range tested, 0.5 to 32 μg/ml). Overall, meropenem alone (MIC50 and MIC90, 16 and >64 μg/ml, respectively) inhibited only 2.2% of the isolates at ≤1 μg/ml (the CLSI susceptibility breakpoint) and 7.3% of the isolates at ≤2 μg/ml (the EUCAST breakpoint). Vaborbactam restored meropenem activity for 72.7 to 98.1% of CPE isolates at ≤2 μg/ml, and maximum potentiation was achieved with fixed concentrations of ≥8 μg/ml of the inhibitor (≥96.5% of isolates were inhibited at ≤2 μg/ml of meropenem-vaborbactam). Meropenem-vaborbactam with a fixed concentration of 8 μg/ml of the inhibitor (MIC50, ≤0.06 μg/ml for all organisms) inhibited 93.7% of the CPE isolates displaying elevated meropenem MICs at ≤1 μg/ml. Meropenem-vaborbactam MICs were elevated for isolates producing metallo-β-lactamases (MIC, 16 to >64 μg/ml) or displaying decreased expression of OmpK37 and/or elevated expression of the AcrAB-TolC efflux system (MIC, 16 μg/ml). Vaborbactam showed no antibacterial activity alone (all MICs, >64 μg/ml).
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:53:24 GMT 2025
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admin
on
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| Record UNII |
1C75676F8V
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Validated (UNII)
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NCI_THESAURUS |
C471
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WHO-ATC |
J01DH52
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NDF-RT |
N0000175930
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Vaborbactam
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1575712-03-6
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1C75676F8V
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BINDER->LIGAND |
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AMOUNT EXCRETED
URINE
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TARGET -> INHIBITOR |
KOFF=0.000017 (1/S), RESIDENCE TIME=992 (MIN), STOICHIOMETRY=1
REVERSIBLE
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ACTIVE MOIETY |
| Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
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| Volume of Distribution | PHARMACOKINETIC |
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