D-Tryptophan, 5-methoxy- is an amino acid derivative that is a modified form of the essential amino acid tryptophan. It features a methoxy group (-OCH3) at the 5-position of the indole ring, which distinguishes it from standard tryptophan. This compound is known for its potential roles in biological processes, including its involvement in the synthesis of serotonin, a neurotransmitter that regulates mood, sleep, and appetite. D-Tryptophan, 5-methoxy- may exhibit various pharmacological properties, including antioxidant and anti-inflammatory effects, although specific biological activities can vary. The compound is typically characterized by its molecular structure, which includes an indole ring and an amino group, contributing to its solubility and reactivity. As with many amino acids and their derivatives, it is important to consider factors such as pH, temperature, and solvent when studying its properties and behavior in different environments. Further research may be necessary to fully elucidate its potential applications in health and medicine.

D-Tryptophan, 5-methoxy-

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(R)-2-Amino-3-(5-methoxy-1H-indol-3-yl)propanoic acid

5-Methoxy-D-tryptophan is a biaryl amino acid derivative that belongs to the class of alkaloids. It is a chiral monomeric building block derived from D-tryptophan. 5-Methoxy-D-tryptophan is commonly used in research chemicals and has been found in natural products such as lochnerine and indole. This compound exhibits unique properties and can be utilized for various applications in the field of chemistry and biochemistry. Its versatility makes it an essential component for researchers and scientists looking to explore new avenues in their studies.

CAS 89496-02-6: D-Tryptophan, 5-methoxy-

(R)-2-Amino-3-(5-methoxy-1H-indol-3-yl)propanoic acid

Ref: 10-F233032

(R)-2-Amino-3-(5-methoxy-1H-indol-3-yl)propanoic acid

Ref: IN-DA0041WE

5-Methoxy-D-tryptophan

Ref: 3D-PDA49602