Paritaprevir
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Systematic (IUPAC) name | |
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(2R,6S,12Z,13aS,14aR,16aS)-N-(Cyclopropylsulfonyl)-6-{[(5-methyl-2-pyrazinyl)carbonyl]amino}-5,16-dioxo-2-(6-phenanthridinyloxy)-1,2,3,6,7,8,9,10,11,13a,14,15,16,16a-tetradecahydrocyclopropa[e]pyrrolo [1,2-a][1,4]diazacyclopentadecine-14a(5H)-carboxamide
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Clinical data | |
Trade names | Viekira Pak (in combination with ombitasvir, ritonavir and dasabuvir), Technivie/Viekirax (in combination with ombitasvir and ritonavir) |
Pregnancy category |
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Legal status |
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Routes of administration |
Oral |
Pharmacokinetic data | |
Bioavailability | was not evaluated |
Protein binding | 97–98.6% |
Metabolism | hepatic, CYP3A4 and CYP3A5 |
Onset of action | 4 to 5 hours |
Biological half-life | 5.5 hours |
Excretion | feces (88%), urine (8,8%) |
Identifiers | |
CAS Number | 1216941-48-8 |
ATC code | J05AX66 (WHO) |
PubChem | CID: 45110509 |
ChemSpider | 32700634 |
KEGG | D10580 |
ChEBI | CHEBI:85188 |
ChEMBL | CHEMBL3391662 |
Synonyms | Veruprevir; ABT-450 |
Chemical data | |
Formula | C40H43N7O7S |
Molecular mass | 765.88 g/mol |
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Paritaprevir (previously known as ABT-450) is an acylsulfonamide[1] inhibitor of the NS3-4A serine protease[2] manufactured by Abbott Laboratories[3] that shows promising results as a treatment of hepatitis C. When given in combination with ritonavir and ribavirin for 12 weeks, the rate of sustained virologic response at 24 weeks after treatment has been estimated to be 95% for those with hepatitis C virus genotype 1.[4] Resistance to treatment with paritaprevir is uncommon, because it targets the binding site, but has been seen to arise due to mutations at positions 155 and 168 in NS3.[5]p. 248
Paritaprevir is a component of Viekira Pak and Technivie.[6]
References
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