CAS 33468-33-6

4-Methyl-L-tryptophan

Description:

4-Methyl-L-tryptophan is an amino acid derivative and a structural analog of the essential amino acid L-tryptophan. It is characterized by the presence of a methyl group attached to the fourth carbon of the indole ring, which alters its biochemical properties compared to L-tryptophan. This compound is known for its role in various biological processes, including protein synthesis and neurotransmitter production. It can influence serotonin levels in the brain, potentially affecting mood and behavior. 4-Methyl-L-tryptophan is also studied for its potential applications in pharmacology and biochemistry, particularly in the context of cancer research and immunology, as it may modulate immune responses. The substance is typically found in a crystalline form and is soluble in polar solvents. Its molecular structure includes a carboxyl group, an amino group, and an indole side chain, which contribute to its reactivity and interactions in biological systems. As with many amino acids, it plays a crucial role in metabolic pathways and can serve as a building block for proteins.

Formula: C₁₂H₁₄N₂O₂

InChI: InChI=1S/C12H14N2O2/c1-7-3-2-4-10-11(7)8(6-14-10)5-9(13)12(15)16/h2-4,6,9,14H,5,13H2,1H3,(H,15,16)/t9-/m0/s1

InChI key: InChIKey=FPJGLSZLQLNZIW-VIFPVBQESA-N

SMILES: C([C@@H](C(O)=O)N)C=1C=2C(NC1)=CC=CC2C

Synonyms:

• (2S)-2-Amino-3-(4-methyl-1H-indol-3-yl)propanoic acid
• L-4-Methyltryptophan
• Tryptophan, 4-methyl-, L-
• 4-Methyl-L-tryptophan
• L-Tryptophan, 4-methyl-

4-Methyl-L-tryptophan

CAS: 33468-33-6

4-Methyl-L-tryptophan

Purity: 97%

Molecular weight: 218.25g/mol

Ref: 54-OR452025

4-Methyl-L-tryptophan

CAS: 33468-33-6

4-Methyl-L-tryptophan is a tryptophan analog that can be used as a chemical tool to study biochemical properties. It has been shown to be an effective substrate for the synthesis of anthranilate and dimethylallyltryptophan, which are important intermediates in the biosynthesis of biologically active compounds. 4-Methyl-L-tryptophan also has a hydroxyl group that reacts with 3-hydroxyanthranilic acid, which is involved in the synthesis of indole alkaloids such as tryptamine and serotonin. The reaction mechanism of this compound is not well understood at this time.

Formula: C₁₂H₁₄N₂O₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 218.25 g/mol

Ref: 3D-IBA46833