CAS 608-07-1

5-Methoxytryptamine

Description:

5-Methoxytryptamine, also known as 5-MT, is an indoleamine compound that is structurally related to serotonin and melatonin. It is characterized by the presence of a methoxy group (-OCH3) at the 5-position of the tryptamine backbone. This compound is a naturally occurring neurotransmitter and is found in various biological systems, where it plays a role in modulating physiological processes. 5-Methoxytryptamine exhibits properties similar to those of serotonin, influencing mood, sleep, and circadian rhythms. It is soluble in water and organic solvents, making it versatile for various applications in biochemical research. The compound has garnered interest for its potential therapeutic effects, particularly in the context of mood disorders and sleep regulation. However, its pharmacological profile and mechanisms of action are still under investigation. As with many tryptamines, caution is advised regarding its use, as it may interact with serotonin receptors and other neurotransmitter systems.

Formula: C₁₁H₁₄N₂O

InChI: InChI=1S/C11H14N2O/c1-14-9-2-3-11-10(6-9)8(4-5-12)7-13-11/h2-3,6-7,13H,4-5,12H2,1H3

InChI key: InChIKey=JTEJPPKMYBDEMY-UHFFFAOYSA-N

SMILES: C(CN)C=1C=2C(NC1)=CC=C(OC)C2

Synonyms:

• (5-methoxy-1H-indol-3-yl)acetic acid
• 1H-Indole-3-ethanamine, 5-methoxy-
• 2-(5-Methoxy-1H-indol-3-yl)ethan-1-amine
• 2-(5-Methoxyindol-3-yl)ethylamin
• 2-(5-Methoxyindol-3-yl)ethylamine
• 2-(5-Methoxyindole-3-Yl)Ethylamine
• 2-(5-Metoxiindol-3-Il)Etilamina
• 2-(5-methoxy-1H-indol-3-yl)ethanamine
• 2-[5-(Methyloxy)-1H-indol-3-yl]ethanamine
• 3-(2-Aminoethyl)-5-methoxyindole
• 5-22-12-00018
• 5-MeOT
• 5-Methoxy-1H-indole-3-ethanamine
• 5-Mot
• 5Mot
• Brn 0145587
• Deacetylmelatonin
• Indole, 3-(2-aminoethyl)-5-methoxy-
• Meksamin (free base)
• Methoxytryptamine
• Mexamine
• Mexamine base
• Nsc 56422

5-Methoxytryptamine

CAS: 608-07-1

Formula: C₁₁H₁₄N₂O

Purity: min. 98.0 %

Color and Shape: White to Light yellow to Light orange powder to crystal

Molecular weight: 190.25

Ref: 3B-M0131

Melatonin Related Compound A (2-(5-methoxy-1H-indol-3-yl)ethanamine)

CAS: 608-07-1

Aromatic or modified aromatic heterocyclic compounds withnitrogen hetero-atom(s) only nesoi

Formula: C₁₁H₁₄N₂O

Color and Shape: Light Brown Powder

Molecular weight: 190.11061

Ref: 45-1380116

5-Methoxytryptamine

CAS: 608-07-1

Formula: C₁₁H₁₄N₂O

Purity: 98%

Color and Shape: Solid

Molecular weight: 190.2417

Ref: IN-DA003I03

Melatonin EP Impurity C (Melatonin USP Related Compound A)

CAS: 608-07-1

Formula: C₁₁H₁₄N₂O

Molecular weight: 190.25

Ref: 4Z-M-769

2-(5-Methoxy-1H-indol-3-yl)ethanamine (5-Methoxytryptamine)

Controlled Product

CAS: 608-07-1

Formula: C₁₁H₁₄N₂O

Color and Shape: Neat

Molecular weight: 190.24

Ref: 86-MM1373.01

Melatonin EP Impurity C

CAS: 608-07-1

Formula: C₁₁H₁₄N₂O

Molecular weight: 190.25

Ref: ST-EA-CP-M166003

5-Methoxytryptamine

Controlled Product

CAS: 608-07-1

Impurity Melatonin USP Related Compound A
Applications A tryptamine derivative that is closely related to the neurotransmitter Melatonin (M215000) and Serotonin (S274980). It acts as a full agonist at the 5-HT1, 5-HT2, 5-HT4, 5-HT6, and 5-HT7 receptors but has no affinity for the 5-HT3 receptor (1,2,3,4). Melatonin USP Related Compound A.
References (1) Yamada, J. et al.: Eur. J. Pharmacol., 323, 235 (1997)(2) Craig, D.A. et al.: NAun. Schmied. Arch. Pharmacol., 342, 9 (1990) (3) Hemedah, M. et al.: Br. J. Pharmacol., 126, 179 (1999)(4) Millan-Plano, S. et al.: Int. J. Mol. Sci., 11, 312 (2010)

Formula: C₁₁H₁₄N₂O

Color and Shape: Neat

Molecular weight: 190.24

Ref: TR-M271695

5-Methoxytryptamine, free base

Controlled Product

CAS: 608-07-1

5-Methoxytryptamine is a competitive inhibitor of serotonin receptors.

Formula: C₁₁H₁₄N₂O

Purity: Min. 99.0 Area-%

Molecular weight: 190.25 g/mol

Ref: 3D-M-3550

5-methoxytryptamine

Controlled Product

CAS: 608-07-1

5-methoxytryptamine

Color and Shape: Light Brown

Ref: 47-1078