DL-threo-β-Methylaspartic acid

98%

Reagent Code: #57468
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CAS Number 6667-60-3

science Other reagents with same CAS 6667-60-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 147.13 g/mol
Formula C₅H₉NO₄
badge Registry Numbers
MDL Number MFCD00037770
inventory_2 Storage & Handling
Storage room temperature

description Product Description

DL-threo-β-Methylaspartic acid is primarily used in biochemical research as a substrate or inhibitor in enzymatic studies. It plays a significant role in understanding the mechanisms of enzymes involved in amino acid metabolism, particularly those that interact with aspartic acid derivatives. This compound is also utilized in the study of bacterial metabolism, as it can mimic natural substrates and help elucidate metabolic pathways. Additionally, it has applications in the development of enzyme inhibitors for potential therapeutic use, particularly in targeting specific enzymes associated with diseases. Its stereochemistry makes it valuable for exploring stereospecific enzymatic reactions and designing chiral molecules in medicinal chemistry.

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Test Parameter Specification
Appearance White to off-white powder or crystals
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,560.00
inventory 1g
10-20 days ฿9,080.00

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DL-threo-β-Methylaspartic acid
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DL-threo-β-Methylaspartic acid is primarily used in biochemical research as a substrate or inhibitor in enzymatic studies. It plays a significant role in understanding the mechanisms of enzymes involved in amino acid metabolism, particularly those that interact with aspartic acid derivatives. This compound is also utilized in the study of bacterial metabolism, as it can mimic natural substrates and help elucidate metabolic pathways. Additionally, it has applications in the development of enzyme inhibitor

DL-threo-β-Methylaspartic acid is primarily used in biochemical research as a substrate or inhibitor in enzymatic studies. It plays a significant role in understanding the mechanisms of enzymes involved in amino acid metabolism, particularly those that interact with aspartic acid derivatives. This compound is also utilized in the study of bacterial metabolism, as it can mimic natural substrates and help elucidate metabolic pathways. Additionally, it has applications in the development of enzyme inhibitors for potential therapeutic use, particularly in targeting specific enzymes associated with diseases. Its stereochemistry makes it valuable for exploring stereospecific enzymatic reactions and designing chiral molecules in medicinal chemistry.

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