[CAS NO. 1365970-03-1]  Glecaprevir

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PRODUCTS SPECIFICATIONS [1365970-03-1]

Distributor
Catalog
HY-17634
Brand
MCE
CAS
1365970-03-1

DESCRIPTION [1365970-03-1]

Overview

MDLMFCD30533436
Molecular Weight838.87
Molecular FormulaC38H46F4N6O9S
SMILESO=C([C@H]1N(C([C@@H](NC(O[C@@]2([H])[C@@]3([H])CCC2)=O)C(C)(C)C)=O)C[C@@](OC4=NC5=CC=CC=C5N=C4C(F)(/C=C/CO3)F)([H])C1)N[C@]6([C@H](C(F)F)C6)C(NS(=O)(C7(CC7)C)=O)=O

For research use only. We do not sell to patients.


Summary

Glecaprevir is a novel HCV NS3/4A protease inhibitor, with IC 50 values ranging from 3.5 to 11.3 nM. Glecaprevir is also a SARS-CoV 3CL pro inhibitor with an IC 50 of 4.09 μM [2] .


IC50 & Target

IC50: 3.5~11.3 nM (HCV NS3/4A protease) [1]


In Vitro

Glecaprevir inhibits the enzymatic activity of HCV genotype 1-6 NS3/4A proteases with half maximal inhibitory concentration (IC 50 ) values ranging from 3.5 to 11.3 nM in a biochemical assay. Glecaprevir inhibites HCV subgenomic stable replicons containing proteases from HCV genotypes 1a, 1b, 2a, 2b, 3a, 4a, 5a, 6a and 6e in Huh-7 cells with 50% effective concentration (EC 50 ) values ranging from 0.21 to 4.6 nM. Glecaprevir is active against a replicon containing protease from genotype 3, the most difficult-to-treat HCV genotype, with an EC 50 value of 1.9 nM, which is 10- and 44-fold lower than those for paritaprevir and grazoprevir, respectively. The median Glecaprevir EC 50 values against replicons containing these genotype 1a, 1b, 2a, 2b, 3a, 4a, 4d, and 5a clinical samples are 0.08, 0.29, 1.6, 2.2, 2.3, 0.41, 0.17, and 0.12 nM, respectively, with an overall median EC 50 value of 0.30 nM (range=0.05~3.8 nM) [1] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.


Clinical Trial

NCT Number Sponsor Condition Start Date Phase
NCT03117569 Kirby Institute
Hepatitis C, Chronic
August 21, 2017 Phase 3
NCT04017338 Jordan Feld|University Health Network, Toronto
Lung Transplant Infection|Heart Transplant Infection|Kidney Transplant Infection|Kidney Pancreas Infection|Hepatitis C
August 6, 2018 Phase 3
NCT02738138 AbbVie
Hepatitis C Virus Infection|Human Immunodeficiency Virus Infection|Chronic Hepatitis C|Compensated Cirrhosis and Non-cirrhotics
May 17, 2016 Phase 3

Appearance

Solid


Shipping

Room temperature in continental US; may vary elsewhere.


Storage

Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month

Solvent & Solubility

In Vitro:

DMSO : ≥ 83.3 mg/mL ( 99.30 mM )

* "≥" means soluble, but saturation unknown.

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 1.1921 mL 5.9604 mL 11.9208 mL
5 mM 0.2384 mL 1.1921 mL 2.3842 mL
10 mM 0.1192 mL 0.5960 mL 1.1921 mL
* Please refer to the solubility information to select the appropriate solvent.
In Vivo:
  • 1.

    Add each solvent one by one: 10% DMSO >> 40% PEG300 >> 5% Tween-80 >> 45% saline

    Solubility: ≥ 2.08 mg/mL (2.48 mM); Clear solution

  • 2.

    Add each solvent one by one: 10% DMSO >> 90% corn oil

    Solubility: ≥ 2.08 mg/mL (2.48 mM); Clear solution

* All of the co-solvents are available by MCE.