N-[3-(2-Furyl)acryloyl]-Phe-Gly-Gly

≥95%

Reagent Code: #99145
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CAS Number 64967-39-1

science Other reagents with same CAS 64967-39-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 399.40 g/mol
Formula C₂₀H₂₁N₃O₆
inventory_2 Storage & Handling
Storage -20℃, inert gas atmosphere

description Product Description

This compound, N-[3-(2-Furyl)acryloyl]-Phe-Gly-Gly (FAPGG), is a chromogenic peptide substrate primarily used in biochemical research for spectrophotometric assays of enzyme activity, particularly proteases and peptidases such as angiotensin-converting enzyme (ACE). The furylacryloyl group allows monitoring of hydrolysis through changes in absorbance at 330 nm, aiding in the study of enzyme kinetics and mechanisms. It supports the development of enzyme inhibitors for therapeutic applications, including those targeting inflammation and cancer-related processes. Additionally, it is employed in peptide synthesis, as a model compound in structural studies to investigate peptide interactions and conformational dynamics, and in drug discovery to identify and optimize bioactive peptides.

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Test Parameter Specification
Appearance Solid
Purity 95-100
Melting Point 240-250

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿42,980.00
inventory 25mg
10-20 days ฿3,360.00
inventory 100mg
10-20 days ฿8,980.00

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N-[3-(2-Furyl)acryloyl]-Phe-Gly-Gly
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This compound, N-[3-(2-Furyl)acryloyl]-Phe-Gly-Gly (FAPGG), is a chromogenic peptide substrate primarily used in biochemical research for spectrophotometric assays of enzyme activity, particularly proteases and peptidases such as angiotensin-converting enzyme (ACE). The furylacryloyl group allows monitoring of hydrolysis through changes in absorbance at 330 nm, aiding in the study of enzyme kinetics and mechanisms. It supports the development of enzyme inhibitors for therapeutic applications, including t

This compound, N-[3-(2-Furyl)acryloyl]-Phe-Gly-Gly (FAPGG), is a chromogenic peptide substrate primarily used in biochemical research for spectrophotometric assays of enzyme activity, particularly proteases and peptidases such as angiotensin-converting enzyme (ACE). The furylacryloyl group allows monitoring of hydrolysis through changes in absorbance at 330 nm, aiding in the study of enzyme kinetics and mechanisms. It supports the development of enzyme inhibitors for therapeutic applications, including those targeting inflammation and cancer-related processes. Additionally, it is employed in peptide synthesis, as a model compound in structural studies to investigate peptide interactions and conformational dynamics, and in drug discovery to identify and optimize bioactive peptides.

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