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Vaniprevir CAS NO 923590-37-8


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CAS No.:923590-37-8

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Vaniprevir is a potent and selective protease inhibitor specifically designed to target the hepatitis C virus (HCV). This high-purity active pharmaceutical ingredient (API) is critical for antiviral research and the development of next-generation therapeutic formulations. It is primarily utilized by pharmaceutical R&D teams, contract research organizations (CROs), and manufacturers engaged in antiviral drug discovery and production.

Application

  • Pharmaceutical API: Core active ingredient in the formulation of antiviral medications targeting Hepatitis C Virus (HCV) genotypes.
  • Clinical Research: Used in preclinical and clinical studies to evaluate efficacy, pharmacokinetics, and safety profiles of new HCV treatments.
  • Reference Standard: Serves as a high-purity analytical standard for quality control and method validation in pharmaceutical laboratories.
  • Drug Discovery & Development: A key compound for medicinal chemistry research, supporting the development of novel protease inhibitor-based therapies.
  • Combinatorial Therapy Research: Investigated for use in combination with other direct-acting antiviral agents (DAAs) to enhance treatment efficacy and overcome resistance.

Basic Information

Product Name Vaniprevir
CAS No. 923590-37-8
Molecular Formula C₄₀H₅₀N₆O₉S
Molecular Weight 766.93 g/mol
Synonyms MK-7009; Vanihep; (1R,3aS,6aR)-N-[(2S)-2-Cyclohexyl-2-[(pyrazinylcarbonyl)amino]acetyl]-3-[(2S)-2-[[(cyclopropylsulfonyl)amino]carbonylamino]-3,3-dimethylbutanoyl]-6,6a-dihydro-3aH-cyclopenta[b]pyrrol-4(1H)-carboxamide; HCV NS3/4A Protease Inhibitor MK-7009
EINECS Contact for details

Quality Control

Our Vaniprevir is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, residual solvent analysis, and identification by spectroscopic methods, to ensure it meets stringent specifications for pharmaceutical use. Certificates of Analysis (COA) with detailed batch data are provided to guarantee traceability and compliance with relevant guidelines.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). The product is light-sensitive and should be handled under appropriate conditions to maintain stability.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to structure
Identification (HPLC) Retention time matches reference standard
Assay (HPLC) ≥98.0%
Related Substances (HPLC) Total impurities ≤2.0% Any single unknown impurity ≤0.5%
Residual Solvents (GC) Complies with ICH Q3C guidelines
Loss on Drying ≤0.5%
Heavy Metals ≤20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.

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