Doripenem

drug
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Also known as DoribaxS-4661SID50112763SID144206061SID170465085DORIPENEM (MONOHYDRATE)DoripenemÊDoripenemÂ

Summary

Doripenem (CHEMBL491571) is an approved small molecule (ATC J01DH04); indicated across 11 conditions including urinary tract infection and pyelonephritis.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: J01DH04
  • Indications: 11 conditions
  • Clinical trials: 24
  • Chemistry: 420.5 Da · C15H24N4O6S2

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL491571
NameDoripenem
TypeSmall molecule
Max phase4
FDA approvedno
PubChem CID73303
ATCJ01DH04
Molecular formulaC15H24N4O6S2
Molecular weight420.5
InChIKeyAVAACINZEOAHHE-VFZPANTDSA-N

SMILES: C[C@@H]1[C@@H]2[C@H](C(=O)N2C(=C1S[C@H]3C[C@H](NC3)CNS(=O)(=O)N)C(=O)O)[C@@H](C)O

IUPAC name: (4R,5S,6S)-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-3-[(3S,5S)-5-[(sulfamoylamino)methyl]pyrrolidin-3-yl]sulfanyl-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid

Also known as: Doribax, Doripenem, S-4661, doripenem, DORIPENEM, SID50112763, SID144206061, SID170465085, DORIPENEM (MONOHYDRATE), DoripenemÊ, Doripenem (monohydrate), DoripenemÂ

Parent form; salt/anhydrous children: CHEMBL1276416, CHEMBL4303454

Patent coverage: 3,321 distinct patent families (13,372 SureChEMBL compound mentions), from 1 matched compound structure(s). 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: 2 (assay-derived). Sample: Voltage-dependent L-type calcium channel subunit alpha-1C, Prostaglandin G/H synthase 1.

Bioactivity

ChEMBL activities: 1 potent at pChembl ≥ 5 of 2 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
CACNA1C5.7IC501995nMCHEMBL_ACT_15258113

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

11 indications (4 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).

IndicationTrial phaseMONDOEFO
urinary tract infection4MONDO:0100338EFO:0003103
pyelonephritis4MONDO:0006939EFO:1001141
bacterial infectious disease4MONDO:0005113EFO:0000771
pneumonia3MONDO:0005249EFO:0003106
pancreatitis3MONDO:0004982EFO:0000278
appendicitis3MONDO:0005649EFO:0007149
infectious peritonitis3MONDO:0004522EFO:0008588
cholecystitis3MONDO:0002155HP:0001082
meningitis1MONDO:0021108MONDO:0021108

2 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 24.

Phase distribution

PhaseTrials
PHASE311
PHASE46
PHASE23
PHASE13
PHASE2/PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00965848PHASE4COMPLETEDA Safety and Efficacy Study of Doripenem in Participants With Nosocomial Pneumonia, Complicated Intra-Abdominal Infections and Urinary Tract Infections
NCT00986102PHASE4COMPLETEDPROUD Study: A Prospective Study on the Usage Patterns of Doripenem in the Asia Pacific Region
NCT01027897PHASE4COMPLETEDPharmacokinetic and Pharmacodynamic Evaluation of Doripenem in Critically Ill Trauma Patients
NCT01311141PHASE4COMPLETEDTarget Site Pharmacokinetics of Doripenem After a Single Dose of 500mg in Healthy Volunteers Dori_MD_1
NCT01401010PHASE4COMPLETEDPharmacokinetic/Pharmacodynamic Study of Doripenem in Febrile Neutropenic Patients
NCT01467648PHASE4COMPLETEDThe Pharmacodynamics of Doripenem Between 4-hour and 1-hour Infusion in Patients With Ventilator-associated Pneumonia
NCT00210938PHASE3COMPLETEDDoripenem in the Treatment of Complicated Intra-Abdominal Infections
NCT00210990PHASE3COMPLETEDDoripenem in the Treatment of Complicated Lower Urinary Tract Infection or Pyelonephritis
NCT00211003PHASE3COMPLETEDDoripenem in the Treatment of Hospital-Acquired Pneumonia
NCT00211016PHASE3COMPLETEDDoripenem in the Treatment of Ventilator-Associated Pneumonia
NCT00229060PHASE3COMPLETEDDoripenem in the Treatment of Complicated Intra-Abdominal Infections
NCT00589693PHASE3TERMINATEDTo Compare Safety and Efficacy of Doripenem Versus Imipenem-Cilastatin in Patients With Ventilator-Associated Pneumonia
NCT01110382PHASE3TERMINATEDA Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
NCT01110408PHASE3TERMINATEDA Safety and Tolerability Study of Doripenem Compared With Cefepime in Children Hospitalized With Complicated Urinary Tract Infections
NCT01110421PHASE3TERMINATEDA Safety and Tolerability Study of Doripenem Compared With Cefepime in Hospitalized Children With Bacterial Pneumonia
NCT01595438PHASE3COMPLETEDCeftazidime-Avibactam Compared With Doripenem Followed by Oral Therapy for Hospitalized Adults With Complicated UTIs (Urinary Tract Infections)
NCT01599806PHASE3COMPLETEDCeftazidime-Avibactam Compared With Doripenem Followed by Oral Therapy for Hospitalized Adults With Complicated UTIs (Urinary Tract Infections)
NCT02134106PHASE2/PHASE3WITHDRAWNRandomized-controlled Trial (RCT) on Combination Antibiotic for Infections Caused by Gram-negative Bacteria
NCT00502801PHASE2COMPLETEDAn Effectiveness, Safety, and Microbiology Study of Doripenem in Patients With Nosocomial (Hospital-acquired) Pneumonia
NCT00515034PHASE2COMPLETEDA Safety and Tolerability Study of Doripenem in Patients With Abdominal Infections or Pneumonia
NCT01281462PHASE2COMPLETEDComparative Study of Coadministered Ceftaroline Fosamil and NXL104 vs. Intravenous Doripenem in Adult Subjects With Complicated Urinary Tract Infections
NCT00925392PHASE1COMPLETEDDoripenem Intrapulmonary Pharmacokinetics in Healthy Adult Subjects
NCT01366651PHASE1TERMINATEDA Study of Doripenem in CerebrospinalFluid After Doripenem Administration in Pediatric Patients Less Than 1 Year of Age
NCT01381848PHASE1COMPLETEDA Study of Doripenem in Infants Less Than 12 Weeks of Age

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).