Telaprevir
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


Telaprevir
Description:
Telaprevir (VX-950) is a highly selective, reversible, and potent peptidomimetic inhibitor of the HCV NS3-4A protease, the steady-state inhibitory constant (Ki) of Telaprevir is 7 nM against a genotype 1 (H strain) NS3 protease domain plus a NS4A cofactor peptide[1][2][3]. Telaprevir inhibits SARS-CoV-2 3CLpro activity[4].Product Name Alternative:
VX-950UNSPSC:
12352005Hazard Statement:
H302Target:
HCV; HCV Protease; SARS-CoVType:
Reference compoundRelated Pathways:
Anti-infection; Metabolic Enzyme/ProteaseApplications:
COVID-19-anti-virusField of Research:
InfectionAssay Protocol:
https://www.medchemexpress.com/Telaprevir.htmlPurity:
99.77Solubility:
DMSO : ≥ 50 mg/mLSmiles:
O=C (N ([C@@H]1C (N[C@H] (C (C (NC2CC2) =O) =O) CCC) =O) C[C@@]3 (CCC[C@@]31[H]) [H]) [C@@H] (NC ([C@@H] (NC (C4=NC=CN=C4) =O) C5CCCCC5) =O) C (C) (C) CMolecular Formula:
C36H53N7O6Molecular Weight:
679.85Precautions:
H302References & Citations:
[1]Lin K, et al. VX-950, a novel hepatitis C virus (HCV) NS3-4A protease inhibitor, exhibits potent antiviral activities in HCv replicon cells. Antimicrob Agents Chemother. 2006 May;50 (5) :1813-22.|[2]Perni RB, et al. Preclinical profile of VX-950, a potent, selective, and orally bioavailable inhibitor of hepatitis C virus NS3-4A serine protease. Antimicrob Agents Chemother. 2006 Mar;50 (3) :899-909.|[3]Zhang X, et al. Discovery and evolution of aloperine derivatives as a new family of HCV inhibitors with novel mechanism. Eur J Med Chem. 2018 Jan 1;143:1053-1065.|[4]Qi Sun, et al. Bardoxolone and bardoxolone methyl, two Nrf2 activators in clinical trials, inhibit SARS-CoV-2 replication and its 3C-like protease. Signal Transduct Target Ther. 2021 May 29;6 (1) :212.Shipping Conditions:
Room TemperatureStorage Conditions:
-20°C, 3 years; 4°C, 2 years (Powder)Scientific Category:
Reference compound1Clinical Information:
LaunchedCAS Number:
402957-28-2
