Radalbuvir
Chemical compound
- US: Investigational New Drug
- 5-(3,3-Dimethylbut-1-yn-1-yl)-3-{(1R)-N-[(1s,4s)-4-hydroxy-4-({[(3S)-oxolan-3-yl]oxy}methyl)cyclohexyl]-4-methylcyclohex-3-ene-1-carboxamido}thiophene-2-carboxylic acid
- 1314795-11-3
- 53259022
- 31140180
- 273K4V0SPC
- Interactive image
- CC1=CC[C@@H](CC1)C(=O)N([C@H]2CC[C@](CC2)(O)CO[C@@H]3COCC3)c4c(sc(c4)C#CC(C)(C)C)C(=O)O
InChI
- InChI=1S/C30H41NO6S/c1-20-5-7-21(8-6-20)27(32)31(25-17-24(11-13-29(2,3)4)38-26(25)28(33)34)22-9-14-30(35,15-10-22)19-37-23-12-16-36-18-23/h5,17,21-23,35H,6-10,12,14-16,18-19H2,1-4H3,(H,33,34)/t21-,22-,23-,30+/m0/s1
- Key:MUICUPWICXUNRS-GDCCIXDYSA-N
Radalbuvir (INN,[1] also known as GS-9669) is an experimental antiviral drug for the treatment of hepatitis C virus (HCV) infection developed by Gilead Sciences. Radalbuvir acts as an NS5B inhibitor. It is currently in clinical trials.[2] It targets NS5B polymerase.[3]
References
- ^ "International Nonproprietary Names for Pharmaceutical Substances" (PDF). WHO Drug Information. Vol. 28, no. 4. 2014. Archived from the original (PDF) on 2015-04-02.
- ^ "Search of: GS-9669 — List Results". ClinicalTrials.gov.
- ^ Borgia G, Maraolo AE, Nappa S, Gentile I, Buonomo AR (March 2018). "NS5B polymerase inhibitors in phase II clinical trials for HCV infection". Expert Opinion on Investigational Drugs. 27 (3): 243–250. doi:10.1080/13543784.2018.1420780. PMID 29271672. S2CID 3672885.
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NS3/4A protease inhibitors (–previr) | |
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NS5A inhibitors (–asvir) | |
NS5B RNA polymerase inhibitors (–buvir) |
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Combination drugs |
Interferon | |
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3CL protease inhibitors (–trelvir) | |
RNA pol inhibitors | |
Multiple/Unknown/Other |
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- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
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