(R)-2,4-dihydroxy-N-[3-[(2-mercaptoethyl)amino]-3-oxopropyl]-3,3-dimethylbutyramide

≥95.0% (HPLC)

Reagent Code: #94812
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CAS Number 496-65-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.37 g/mol
Formula C₁₁H₂₂N₂O₄S
badge Registry Numbers
MDL Number MFCD00056757
inventory_2 Storage & Handling
Storage -20 °C, sealed, dry, inflated

description Product Description

This compound is primarily utilized in the development of pharmaceutical agents, particularly in the design of enzyme inhibitors. Its structure, featuring both hydroxyl and mercapto groups, makes it a versatile candidate for targeting enzymes involved in various metabolic pathways. It is often explored in the synthesis of drugs aimed at treating conditions related to oxidative stress or inflammation, as the thiol group can act as a reactive site for binding to specific enzyme targets. Additionally, its chiral center allows for selective interaction with biological molecules, enhancing its potential in creating enantiomerically pure therapeutics. Research also focuses on its use in prodrug formulations, where its functional groups can be modified to improve bioavailability and targeted delivery.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White Solid
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿9,100.00
(R)-2,4-dihydroxy-N-[3-[(2-mercaptoethyl)amino]-3-oxopropyl]-3,3-dimethylbutyramide
This compound is primarily utilized in the development of pharmaceutical agents, particularly in the design of enzyme inhibitors. Its structure, featuring both hydroxyl and mercapto groups, makes it a versatile candidate for targeting enzymes involved in various metabolic pathways. It is often explored in the synthesis of drugs aimed at treating conditions related to oxidative stress or inflammation, as the thiol group can act as a reactive site for binding to specific enzyme targets. Additionally, its chiral center allows for selective interaction with biological molecules, enhancing its potential in creating enantiomerically pure therapeutics. Research also focuses on its use in prodrug formulations, where its functional groups can be modified to improve bioavailability and targeted delivery.
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