5-Methoxytryptamine (5-MT), also known as mexamine, is a tryptamine derivative closely related to the neurotransmitters serotonin and melatonin. 5-MT has been shown to occur naturally in the body in low levels. It is biosynthesized via the deacetylation of melatonin in the pineal gland. The protective effect of 5-methoxytryptamine (a metabolite of melatonin) in human keratinocytes against ultraviolet B (UVB) radiation was studied. Melatonin and its metabolites ameliorate ultraviolet B-induced damage in human epidermal keratinocytes.
In terms of application, 5-Methoxytryptamine exhibits several significant properties. One of its primary areas of interest is its role in neuroscience and psychiatry. It is known to interact with serotonin receptors in the brain, particularly the 5-HT2A receptor, which is associated with mood regulation and perception. In addition to its neuropharmacological effects, 5-Methoxytryptamine has been investigated for its role in psychotropic research. It is often used as a research tool to understand the mechanisms of psychoactive substances and their interactions with neurotransmitter systems. Moreover, 5-Methoxytryptamine has been explored in the context of entheogenic research, which examines the use of psychoactive substances in spiritual or religious practices. Its psychoactive effects and interactions with serotonin receptors contribute to its interest in studies on altered states of consciousness and their therapeutic applications. The chemical synthesis of 5-Methoxytryptamine typically involves the introduction of a methoxy group into the tryptamine structure. This process is often achieved through a series of chemical reactions that modify the indole ring of tryptamine. Characterization of the synthesized compound is performed using analytical techniques such as high-performance liquid chromatography (HPLC) and mass spectrometry (MS), which ensure the purity and identity of the final product. In summary, 5-Methoxytryptamine is a chemically intriguing compound with applications spanning neuropharmacology, psychiatry, and psychotropic research. Its interaction with serotonin receptors and potential therapeutic effects make it a subject of ongoing interest in the study of neurotransmitter systems and psychoactive substances.
Brand: Soarwin
CAS No.: 608-07-1
EC Number: 210-153-7
Molecular Formula: C11H14N2O
Density: 1.0815 (rough estimate)
Melting point: 121-123°C(lit.)
Boiling point: 325.75°C(Predicted)
