Methyl benzoyl-L-tryptophyl-D-phenylalaninate

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Reagent Code: #99214
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CAS Number 1435265-06-7

science Other reagents with same CAS 1435265-06-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 469.53 g/mol
Formula C₂₈H₂₇N₃O₄
badge Registry Numbers
MDL Number MFCD32197174
thermostat Physical Properties
Boiling Point 790.8±60.0℃at 760 mmHg
inventory_2 Storage & Handling
Density 1.259±0.06 g/cm3(Predicted)
Storage 2-8℃, dry, sealed,

description Product Description

This compound is primarily utilized in research settings, particularly in the study of peptide synthesis and enzyme inhibition. It serves as a substrate or inhibitor in experiments involving proteases, aiding in the understanding of enzyme mechanisms and kinetics. Additionally, it is explored in the development of peptide-based drugs, where its structure can be modified to enhance binding affinity or stability. Its application extends to the investigation of biochemical pathways, contributing to advancements in medicinal chemistry and drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿58,005.00
inventory 250mg
10-20 days ฿23,238.00
inventory 100mg
10-20 days ฿11,583.00

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Methyl benzoyl-L-tryptophyl-D-phenylalaninate
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This compound is primarily utilized in research settings, particularly in the study of peptide synthesis and enzyme inhibition. It serves as a substrate or inhibitor in experiments involving proteases, aiding in the understanding of enzyme mechanisms and kinetics. Additionally, it is explored in the development of peptide-based drugs, where its structure can be modified to enhance binding affinity or stability. Its application extends to the investigation of biochemical pathways, contributing to advancem

This compound is primarily utilized in research settings, particularly in the study of peptide synthesis and enzyme inhibition. It serves as a substrate or inhibitor in experiments involving proteases, aiding in the understanding of enzyme mechanisms and kinetics. Additionally, it is explored in the development of peptide-based drugs, where its structure can be modified to enhance binding affinity or stability. Its application extends to the investigation of biochemical pathways, contributing to advancements in medicinal chemistry and drug discovery.

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