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Uprifosbuvir
Uprifosbuvir is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
Therapeutic Areas
No data
Trade Name
FDA
EMA
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Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Labels
FDA
EMA
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Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
No data
HCPCS
No data
Clinical
Clinical Trials
8 clinical trials
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Indications Phases 4
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Indications Phases 3
No data
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Hepatitis cD006526B19.2145
Chronic hepatitis cD019698EFO_0004220B18.2223
Liver diseasesD008107EFO_0001421K70-K7711
Virus diseasesD014777B3411
Rna virus infectionsD01232711
Digestive system diseasesD004066EFO_0000405K92.911
HepatitisD006505HP_0012115K75.911
Viral hepatitis humanD006525EFO_000419611
Flaviviridae infectionsD018178EFO_000727411
Indications Phases 1
No data
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameUPRIFOSBUVIR
INNuprifosbuvir
Description
Uprifosbuvir (MK-3682) is an antiviral drug developed for the treatment of hepatitis C. It is a nucleotide analogue which acts as an NS5B RNA polymerase inhibitor. As of 2019 it was in Phase III human clinical trials.
Classification
Small molecule
Drug classphosphoro-derivatives; antivirals: RNA polymerase (NS5B) inhibitors
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
CC(C)OC(=O)[C@@H](C)N[P@@](=O)(OC[C@H]1O[C@@H](n2ccc(=O)[nH]c2=O)[C@](C)(Cl)[C@@H]1O)Oc1ccccc1
Identifiers
PDB
CAS-ID1496551-77-9
RxCUI
ChEMBL IDCHEMBL3833371
ChEBI ID
PubChem CID90055716
DrugBankDB15206
UNII IDJW31KPS26S (ChemIDplus, GSRS)
Target
Agency Approved
No data
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 49 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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125 adverse events reported
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