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Vaniprevir
🥰Excellent
Catalog No. T8675Cas No. 923590-37-8
Alias MK-7009, MK7009
Vaniprevir is a non-covalent competitive HCV NS3/4A protease inhibitor, an antiviral drug that acts directly on the hepatitis C virus. Vaniprevir blocks the viral replication process by inhibiting the activity of HCV NS3/4A protease.
Vaniprevir
🥰Excellent
Purity: 97.41%
Catalog No. T8675Alias MK-7009, MK7009Cas No. 923590-37-8
Vaniprevir is a non-covalent competitive HCV NS3/4A protease inhibitor, an antiviral drug that acts directly on the hepatitis C virus. Vaniprevir blocks the viral replication process by inhibiting the activity of HCV NS3/4A protease.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $879 | In Stock | |
| 5 mg | $1,790 | In Stock | |
| 10 mg | $2,420 | In Stock | |
| 25 mg | $3,600 | In Stock | |
| 50 mg | $4,850 | In Stock |
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Purity:97.41%
ee:100%
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All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.Product Introduction
Bioactivity
Chemical Properties
| Description | Vaniprevir is a non-covalent competitive HCV NS3/4A protease inhibitor, an antiviral drug that acts directly on the hepatitis C virus. Vaniprevir blocks the viral replication process by inhibiting the activity of HCV NS3/4A protease. |
| In vitro | Sensitivity of 39 HCV-treated clinical isolates to VX-950 (telaprevir), SCH-503034 (boceprevir), ITMN-191, Vaniprevir, and TMC-435350 were evaluated using a replicon-based NS3 protease phenotype assay. Some natural changes in susceptibility between these isolates were observed when testing all five HCV PIs (VX-950, SCH-503034, ITMN-191, Vaniprevir, and TMC-435350). The order of variations is from minimum to maximum Vaniprevir < VX-950 < ITMN-191 < SCH-503034 < TMC-435350. [6] |
| Alias | MK-7009, MK7009 |
| Molecular Weight | 757.94 |
| Formula | C38H55N5O9S |
| Cas No. | 923590-37-8 |
| Smiles | N(C(=O)[C@H]1N2C[C@@](C1)(OC(=O)N3CC=4C(C3)=CC=CC4CCCCC(C)(C)COC(=O)N[C@@H]([C@](C)(C)C)C2=O)[H])[C@@]5(C(NS(=O)(=O)C6CC6)=O)[C@H](CC)C5 |
| Relative Density. | 1.33g/cm3 |
Storage & Solubility Information
| Storage | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||||||||||||
| Solubility Information | DMSO: 8 mg/mL (10.55 mM), Sonication is recommended. | ||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||
DMSO
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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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