H-β-HoPhe(4-NO2)-OH

98%

Reagent Code: #38457
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CAS Number 270062-87-8

science Other reagents with same CAS 270062-87-8

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scatter_plot Molecular Information
Weight 224.2133 g/mol
Formula C₁₀H₁₂N₂O₄
badge Registry Numbers
MDL Number MFCD08461688
inventory_2 Storage & Handling
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description Product Description

This chemical is primarily utilized in peptide synthesis and pharmaceutical research. It serves as a building block for creating modified peptides, particularly in studies focusing on enzyme inhibitors and receptor ligands. Its nitro group enhances its reactivity, making it valuable for designing compounds with specific biological activities. Additionally, it is used in the development of fluorescent probes and biochemical tools for studying protein interactions and cellular processes. Its unique structure allows for precise modifications in peptide chains, aiding in the exploration of structure-activity relationships in drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,078.00

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H-β-HoPhe(4-NO2)-OH
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This chemical is primarily utilized in peptide synthesis and pharmaceutical research. It serves as a building block for creating modified peptides, particularly in studies focusing on enzyme inhibitors and receptor ligands. Its nitro group enhances its reactivity, making it valuable for designing compounds with specific biological activities. Additionally, it is used in the development of fluorescent probes and biochemical tools for studying protein interactions and cellular processes. Its unique structu

This chemical is primarily utilized in peptide synthesis and pharmaceutical research. It serves as a building block for creating modified peptides, particularly in studies focusing on enzyme inhibitors and receptor ligands. Its nitro group enhances its reactivity, making it valuable for designing compounds with specific biological activities. Additionally, it is used in the development of fluorescent probes and biochemical tools for studying protein interactions and cellular processes. Its unique structure allows for precise modifications in peptide chains, aiding in the exploration of structure-activity relationships in drug discovery.

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