CAS 21438-63-1

L-Methionine, L-tryptophyl-

Description:

L-Methionine, L-tryptophyl- is a dipeptide composed of the amino acids L-methionine and L-tryptophan. It is characterized by its structure, which includes a methionine residue linked to a tryptophan residue through a peptide bond. This compound is notable for its role in protein synthesis and its potential biological activities, including antioxidant properties and involvement in metabolic processes. L-methionine is an essential amino acid, meaning it must be obtained through diet, while L-tryptophan is a precursor for serotonin, a neurotransmitter that regulates mood. The dipeptide may exhibit unique properties compared to its constituent amino acids, such as enhanced solubility or altered bioavailability. In terms of applications, it may be utilized in nutritional supplements, pharmaceuticals, or research settings to study peptide behavior and interactions. As with many peptides, stability and solubility can vary based on environmental conditions, such as pH and temperature. Overall, L-Methionine, L-tryptophyl- represents a significant area of interest in biochemistry and nutrition.

Formula: C₁₆H₂₁N₃O₃S

InChI: InChI=1S/C16H21N3O3S/c1-23-7-6-14(16(21)22)19-15(20)12(17)8-10-9-18-13-5-3-2-4-11(10)13/h2-5,9,12,14,18H,6-8,17H2,1H3,(H,19,20)(H,21,22)/t12-,14-/m0/s1

InChI key: InChIKey=BVZABQIRMYTKCF-JSGCOSHPSA-N

SMILES: C([C@@H](C(N[C@@H](CCSC)C(O)=O)=O)N)C=1C=2C(NC1)=CC=CC2

Synonyms:

• L-Methionine, N-L-tryptophyl-
• L-Methionine, L-tryptophyl-
• Methionine, N-L-tryptophyl-, L-
• L-Tryptophanyl-L-methionine
• L-Tryptophyl-L-methionine

H-Trp-Met-OH

CAS: 21438-63-1

Bachem ID: 4009571.

Formula: C₁₆H₂₁N₃O₃S

Purity: > 98%

Color and Shape: White Powder

Molecular weight: 335.43

Ref: 01-4009571

H-Trp-Met-OH

CAS: 21438-63-1

The molecular formula for H-Trp-Met-OH is CHNOS. It is a neutral, solubilized, imino amide residue of L-phenylalanine. The compound has not been identified but it is presumed to be an azide or sulfate ester of tyrosine. This compound was isolated from the membranes of bacteria and peptidases break it down into other amino acids with the exception of lysine. The yield from this reaction is unknown.

Formula: C₁₆H₂₁N₃O₃S

Purity: Min. 95%

Molecular weight: 335.42 g/mol

Ref: 3D-FT108198