[CAS NO. 850876-88-9]  Danoprevir (ITMN-191)

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PRODUCTS SPECIFICATIONS [850876-88-9]

Store
Catalog
SLK-S1183
Brand
Selleck
CAS
850876-88-9

DESCRIPTION [850876-88-9]

Overview

MDLMFCD16038038
Molecular Weight731.83
Molecular FormulaC35H46FN5O9S
SMILESC(NS(=O)(=O)C1CC1)(=O)[C@]23[C@@](C2)(/C=C\CCCCC[C@H](NC(OC(C)(C)C)=O)C(=O)N4[C@](C(=O)N3)(C[C@@H](OC(=O)N5CC=6C(C5)=C(F)C=CC6)C4)[H])[H]

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM1.3664 mL6.8322 mL13.6644 mL
5 mM0.2733 mL1.3664 mL2.7329 mL
10 mM0.1366 mL0.6832 mL1.3664 mL
50 mM0.0273 mL0.1366 mL0.2733 mL

Description

Danoprevir (ITMN-191, RG7227) is a peptidomimetic inhibitor of the of hepatitis C virus (HCV) with of 0.2-3.5 nM, inhibition effect for HCV genotypes 1A/1B/4/5/6 is ~10-fold higher than 2B/3A. Phase 2.

Features

A peptidomimetic inhibitor of the NS3/4A protease of hepatitis C virus (HCV).

Targets

HCV NS3/4A protease [1]
0.2 nM-3.5 nM

In vitro

Danoprevir (0.29 nM) inhibits the reference genotype 1 NS3/4A protease half-maximally, but a high dose of Danoprevir (10 μM) shows no appreciably inhibition in a panel of 79 proteases, ion channels, transporters, and cell surface receptors. Danoprevir remains bound to and inhibits NS3/4A for more than 5 hours after its initial association. Danoprevir (45 nM) eliminates a patient-derived HCV genotype 1b replicon from hepatocyte-derived Huh7 cells with an EC50 of 1.8 nM. In HCV subgenomic replicon cell lines containing the individual mutations, V36M, R109K, and V170A substitutions confer little or no resistance to Danoprevir, but the R155K substitution confers a high level (62-fold increase) of resistance to Danoprevir. In Huh7.5 cells transfected with chimeric recombinant virus, Danoprevir shows antiviral inhibition effects against HCV genotypes 1, 4 and 6 with IC50 of 2-3 nM, which are >100-fold lower than genotypes 2/3/5 (280-750 nM).

In vivo

Danoprevir (30 mg/kg) administered to rats or monkeys shows that its concentrations in liver 12 hours after dosing exceed the Danoprevir concentration required to eliminate replicon RNA from cells.


Synonyms

2H-Isoindole-2-carboxylic acid, 4-fluoro-1,3-dihydro-, (2R,6S,13aS,14aR,16aS)-14a-[[(cyclopropylsulfonyl)amino]carbonyl]-6-[[(1,1-dimethylethoxy)carbonyl]amino]-1,2,3,5,6,7,8,9,10,11,13a,14,14a,15,16,16a-hexadecahydro-5,16-dioxocyclopropa[e]pyrrolo[1,2-a][1,4]diazacyclopentadecin-2-yl ester
ITMN 191
Intermune ITMN-191
Danoprevir
R 7227
ITMN B
R 05190591
EBP 521