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Grazoprevir

Chemical Structure : Grazoprevir

CAS No.: 1350514-68-9

Grazoprevir (MK-5172, MK5172)

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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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

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.

Physicochemical Properties

M.Wt 766.91
Formula C38H50N6O9S
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

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

References

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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