(S)-2-Amino-3-(4-methoxy-1H-indol-3-yl)propanoic acid

98%

Reagent Code: #47712
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CAS Number 406938-53-2

science Other reagents with same CAS 406938-53-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.25 g/mol
Formula C₁₂H₁₄N₂O₃
badge Registry Numbers
MDL Number MFCD17214440
thermostat Physical Properties
Boiling Point 478.3±45.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound, also known as 4-methoxy-L-tryptophan, is a specialty chemical utilized primarily in biochemical and pharmacological research. Structurally similar to L-tryptophan—the natural precursor in serotonin biosynthesis—it is employed as a substrate analog or probe in studies of neurotransmitter synthesis, enzymatic mechanisms (e.g., tryptophan hydroxylase), and metabolic pathways involving indoles and amino acids. Researchers use it to investigate serotonin function and its roles in neurological disorders such as depression and anxiety. It also supports pharmaceutical development for serotonin modulation and synthesis of related compounds.

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Test Parameter Specification
Appearance Yellow 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 ฿28,630.00
inventory 100mg
10-20 days ฿14,310.00

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(S)-2-Amino-3-(4-methoxy-1H-indol-3-yl)propanoic acid
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This compound, also known as 4-methoxy-L-tryptophan, is a specialty chemical utilized primarily in biochemical and pharmacological research. Structurally similar to L-tryptophan—the natural precursor in serotonin biosynthesis—it is employed as a substrate analog or probe in studies of neurotransmitter synthesis, enzymatic mechanisms (e.g., tryptophan hydroxylase), and metabolic pathways involving indoles and amino acids. Researchers use it to investigate serotonin function and its roles in neurological d

This compound, also known as 4-methoxy-L-tryptophan, is a specialty chemical utilized primarily in biochemical and pharmacological research. Structurally similar to L-tryptophan—the natural precursor in serotonin biosynthesis—it is employed as a substrate analog or probe in studies of neurotransmitter synthesis, enzymatic mechanisms (e.g., tryptophan hydroxylase), and metabolic pathways involving indoles and amino acids. Researchers use it to investigate serotonin function and its roles in neurological disorders such as depression and anxiety. It also supports pharmaceutical development for serotonin modulation and synthesis of related compounds.

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