Acetyl-L-phenylalanine methyl amide

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Reagent Code: #59277
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CAS Number 17186-60-6

science Other reagents with same CAS 17186-60-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.27 g/mol
Formula C₁₂H₁₆N₂O₂
badge Registry Numbers
MDL Number MFCD00237509
thermostat Physical Properties
Melting Point 185.32 °C(Predicted)
Boiling Point ~518.2 °Cat 760 mmHg (Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Acetyl-L-phenylalanine methyl amide is a protected dipeptide analog primarily used as a model substrate in biochemical assays for proteolytic enzymes, such as carboxypeptidases and endopeptidases. It enables studies of enzyme kinetics, substrate specificity, hydrolysis mechanisms, and inhibitor screening. Valuable in pharmaceutical research for developing protease inhibitors targeting neurological and metabolic disorders. Its chiral structure also supports applications in asymmetric synthesis and stereochemical studies in organic chemistry.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿41,751.00
inventory 1g
10-20 days ฿10,431.00
inventory 250mg
10-20 days ฿5,850.00

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Acetyl-L-phenylalanine methyl amide
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Acetyl-L-phenylalanine methyl amide is a protected dipeptide analog primarily used as a model substrate in biochemical assays for proteolytic enzymes, such as carboxypeptidases and endopeptidases. It enables studies of enzyme kinetics, substrate specificity, hydrolysis mechanisms, and inhibitor screening. Valuable in pharmaceutical research for developing protease inhibitors targeting neurological and metabolic disorders. Its chiral structure also supports applications in asymmetric synthesis and stereoc

Acetyl-L-phenylalanine methyl amide is a protected dipeptide analog primarily used as a model substrate in biochemical assays for proteolytic enzymes, such as carboxypeptidases and endopeptidases. It enables studies of enzyme kinetics, substrate specificity, hydrolysis mechanisms, and inhibitor screening. Valuable in pharmaceutical research for developing protease inhibitors targeting neurological and metabolic disorders. Its chiral structure also supports applications in asymmetric synthesis and stereochemical studies in organic chemistry.

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