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Drug ReportsEpetraborole
Epetraborole
Epetraborole is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
Clinical
Drug
Target
Variants
Financial
Trends
Safety
Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
Max
Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
Primary completion date
Completion date
Results first post date
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Commercial
No data
Clinical
Clinical Trials
12 clinical trials
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Indications Phases 4
No data
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Lung diseasesD008171HP_0002088J98.4111
Mycobacterium avium-intracellulare infectionD015270EFO_0007386111
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
InfectionsD007239EFO_0000544123
Communicable diseasesD00314122
Urinary tract infectionsD014552EFO_0003103N39.011
PyelonephritisD011704EFO_1001141N10-N1611
Intraabdominal infectionsD05941311
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Community-acquired infectionsD01771444
Bacterial infectionsD001424A4922
Healthy volunteers/patients22
Gram-negative bacterial infectionsD01690511
Renal insufficiencyD051437HP_0000083N1911
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameEpetraborole
INNepetraborole
Description
Epetraborole is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
Classification
Small molecule
Drug classboroles, boron compounds
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Structure (InChI/SMILES or Protein Sequence)
NC[C@H]1OB(O)c2c(OCCCO)cccc21
Identifiers
PDB
CAS-ID1093643-37-8
RxCUI
ChEMBL IDCHEMBL3549142
ChEBI ID
PubChem CID
DrugBank
UNII ID6MC93Z2DF9 (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 154 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
0 adverse events reported
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