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Catalog: | HY-17634 |
Brand: | MCE |
CAS: | 1365970-03-1 |
MDL | MFCD30533436 |
---|---|
Molecular Weight | 838.87 |
Molecular Formula | C38H46F4N6O9S |
SMILES | O=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 |
IC50: 3.5~11.3 nM (HCV NS3/4A protease) [1]
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.
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 |
NCT02296905 | AbbVie |
Hepatic Impairment
|
October 2014 | Phase 1 |
NCT02441283 | AbbVie |
Hepatitis C
|
June 22, 2015 | Phase 2|Phase 3 |
NCT05446857 | White River Junction Veterans Affairs Medical Center |
Ptsd
|
January 1, 2023 | Phase 2|Phase 3 |
NCT05582681 | Weill Medical College of Cornell University|AbbVie |
Hepatitis C
|
October 2022 | Phase 4 |
NCT03123965 | AbbVie |
Hepatitis C Virus Infection
|
||
NCT04515797 | Massachusetts General Hospital |
Kidney Failure|Hepatitis C|Kidney Disease, Chronic
|
May 1, 2021 | Phase 4 |
NCT01995071 | AbbVie |
Chronic Hepatitis C|Hepatitis C Virus|Compensated Cirrhosis
|
November 2013 | Phase 2 |
NCT04047680 | National Taiwan University Hospital |
Hepatitis C|Renal Disease|Viral Hepatitis C
|
February 2015 | |
NCT04614142 | Massachusetts General Hospital |
End Stage Renal Disease|Chronic Hepatitis c
|
November 13, 2020 | Phase 4 |
NCT02243280 | AbbVie |
Chronic Hepatitis C|Hepatitis C Virus|HCV
|
August 2014 | Phase 2 |
NCT02442258 | AbbVie |
Renal Impairment
|
March 2015 | Phase 1 |
NCT02243293 | AbbVie |
Chronic Hepatitis C|Hepatitis C Virus
|
September 19, 2014 | Phase 2|Phase 3 |
Solid
Room temperature in continental US; may vary elsewhere.
Powder | -20°C | 3 years |
---|---|---|
4°C | 2 years | |
In solvent | -80°C | 6 months |
-20°C | 1 month |
DMSO : ≥ 83.3 mg/mL ( 99.30 mM )
* "≥" means soluble, but saturation unknown.
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 |
Add each solvent one by one: 10% DMSO >> 90% corn oil
Solubility: ≥ 2.08 mg/mL (2.48 mM); Clear solution
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