(S)-2-Amino-3-(5-chloro-1H-indol-3-yl)propanoic acid
95%
- Product Code: 38268
CAS:
52448-15-4
Molecular Weight: | 238.67 g./mol | Molecular Formula: | C₁₁H₁₁ClN₂O₂ |
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EC Number: | MDL Number: | MFCD06797629 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in biochemical research as a specialized amino acid derivative. Its structure, featuring an indole ring with a chloro substitution, makes it valuable in studying enzyme interactions, particularly those involving tryptophan metabolism. It is often employed in the synthesis of peptide-based compounds for investigating receptor binding and signal transduction pathways. Additionally, it serves as a precursor in the development of potential therapeutic agents targeting neurological disorders, given its structural similarity to neurotransmitters. Its applications also extend to organic synthesis, where it acts as a building block for creating complex molecules with biological activity.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿5,022.00 |
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0.250 | 10-20 days | ฿10,035.00 |
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1.000 | 10-20 days | ฿20,079.00 |
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(S)-2-Amino-3-(5-chloro-1H-indol-3-yl)propanoic acid
This compound is primarily utilized in biochemical research as a specialized amino acid derivative. Its structure, featuring an indole ring with a chloro substitution, makes it valuable in studying enzyme interactions, particularly those involving tryptophan metabolism. It is often employed in the synthesis of peptide-based compounds for investigating receptor binding and signal transduction pathways. Additionally, it serves as a precursor in the development of potential therapeutic agents targeting neurological disorders, given its structural similarity to neurotransmitters. Its applications also extend to organic synthesis, where it acts as a building block for creating complex molecules with biological activity.
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