68407-05-6

Basic information

• Product Name: (S)-4'-Hydroxy Warfarin
• Synonyms: (S)-4'-Hydroxy Warfarin
• CAS NO: 68407-05-6
• Molecular Formula: C19H16O5
• Molecular Weight: 324.32734
• Product Categories: Aromatics;Heterocycles;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals;Aromatics, Heterocycles, Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals
• Mol File: 68407-05-6.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Storage Temp.: -20°C Freezer, Under inert atmosphere
• Solubility: Acetone (Slightly), DMSO (Slightly), Ethanol (Slightly), Methanol (Slightly)
• CAS DataBase Reference: (S)-4'-Hydroxy Warfarin(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-4'-Hydroxy Warfarin(68407-05-6)
• EPA Substance Registry System: (S)-4'-Hydroxy Warfarin(68407-05-6)

Safety Data

• Hazardous Substances Data: 68407-05-6(Hazardous Substances Data)

Usage

Description

(S)-4'-Hydroxy Warfarin, also known as the S-enantiomer of the 4'-hydroxyl metabolite of Warfarin, is a significant compound derived from the metabolism of Warfarin. It plays a crucial role in the pharmacological effects and metabolism of Warfarin, a widely used anticoagulant medication.

Uses

Used in Pharmaceutical Industry:
(S)-4'-Hydroxy Warfarin is used as a metabolite in the development and understanding of Warfarin's pharmacological properties and its metabolism. The formation of (S)-4'-Hydroxy Warfarin is increased by quinidine during Warfarin metabolism, which can help in studying the interactions between Warfarin and other drugs, as well as optimizing Warfarin therapy for patients.
Additionally, the study of (S)-4'-Hydroxy Warfarin can contribute to the development of new anticoagulant drugs with improved safety and efficacy profiles, as understanding the metabolites and their effects can lead to the design of more targeted and effective medications.
Used in Research and Development:
(S)-4'-Hydroxy Warfarin is used as a research tool for investigating the mechanisms of action, drug interactions, and potential side effects of Warfarin. This can help researchers better understand the complexities of Warfarin's pharmacokinetics and pharmacodynamics, leading to improved drug design and personalized medicine approaches.
Furthermore, the study of (S)-4'-Hydroxy Warfarin can provide insights into the genetic and environmental factors that influence Warfarin metabolism, which can be valuable for predicting individual responses to the drug and tailoring treatment regimens accordingly.