Chemical Structure : Grazoprevir
CAS No.: 1350514-68-9
Catalog No.: PC-25228Not For Human Use, Lab Use Only.
Grazoprevir (MK-5172) is a potent, selective inhibitor of HCV NS3/4A protease with broad activity across genotypes and resistant variants, with Ki values of 0.01 nM (gt1b), 0.01 nM (gt1a), 0.08 nM (gt2a), 0.15 nM (gt2b), 0.90 nM (gt3a), respectively, also inhibits SARS-CoV-2 3CLpro activity.
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2 mg | $78 | In stock | |
5 mg | $128 | In stock | |
10 mg | $198 | In stock | |
25 mg | $328 | In stock | |
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Grazoprevir (MK-5172) is a potent, selective inhibitor of HCV NS3/4A protease with broad activity across genotypes and resistant variants, with Ki values of 0.01 nM (gt1b), 0.01 nM (gt1a), 0.08 nM (gt2a), 0.15 nM (gt2b), 0.90 nM (gt3a), respectively, also inhibits SARS-CoV-2 3CLpro activity.
M.Wt | 766.91 | |
Formula | C38H50N6O9S | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
(33R,35S,91R,92R,5S)-5-(tert-Butyl)-N-((1R,2S)-1-((cyclopropylsulfonyl)carbamoyl)-2-vinylcyclopropyl)-17-methoxy-4,7-dioxo-2,8-dioxa-6-aza-1(2,3)-quinoxalina-3(3,1)-pyrrolidina-9(1,2)-cyclopropanacyclotetradecaphane-35-carboxamide |
1. Summa V, et al. Antimicrob Agents Chemother. 2012 Aug;56(8):4161-7.
2. Harper S, et al. ACS Med Chem Lett. 2012 Mar 2;3(4):332-6.
3. Qi Sun, et al. Signal Transduct Target Ther. 2021 May 29;6(1):212.
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