Ombitasvir
From Infogalactic: the planetary knowledge core
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Systematic (IUPAC) name | |
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Methyl ((R)-1-((S)-2-((4-((2S,5S)-1-(4-(tert-butyl)phenyl)-5-(4-((R)-1-((methoxycarbonyl)-L-valyl)pyrrolidine-2-carboxamido)phenyl)pyrrolidin-2-yl)phenyl)carbamoyl)pyrrolidin-1-yl)-3-methyl-1-oxobutan-2-yl)carbamate
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Clinical data | |
Trade names | Viekira Pak (with ombitasvir, paritaprevir, ritonavir and dasabuvir), Technivie (with ombitasvir, paritaprevir, and ritonavir) |
Legal status |
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Routes of administration |
Oral |
Pharmacokinetic data | |
Bioavailability | not determined |
Protein binding | ~99.9% |
Metabolism | amide hydrolysis followed by oxidation |
Onset of action | ~4 to 5 hours |
Biological half-life | 21 to 25 hours |
Excretion | mostly with feces (90.2%) |
Identifiers | |
CAS Number | 1258226-87-7 |
PubChem | CID: 54767916 |
ChemSpider | 31136214 |
ChEBI | CHEBI:85183 |
Synonyms | ABT-267 |
Chemical data | |
Formula | C50H67N7O8 |
Molecular mass | 894.11 g/mol |
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Ombitasvir is an antiviral drug for the treatment of hepatitis C virus (HCV) infection. In the United States, it is approved by the Food and Drug Administration for use in combination with paritaprevir, ritonavir and dasabuvir in the product Viekira Pak for the treatment of HCV genotype 1,[1][2] and with paritaprevir and ritonavir in the product Technivie for the treatment of HCV genotype 4.[3][4]
Ombitasvir acts by inhibiting the HCV protein NS5A.[5]
References
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- Antivirals
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