Tryptamine is a monoamine alkaloid. It contains an indole ring structure, which is similar in structure to tryptophan, and tryptophan is the source of the name. Tryptamine exists in the brain of mammals and acts as a neuromodulator or neurotransmitter . Similar to other trace amines, tryptamine binds to human trace amine-related receptor 1 (TAAR1) as an agonist.
Tryptamine is a common functional group in a group of compounds called collectively substituted tryptamine. This set includes many biologically active compounds, including neurotransmitters and psychedelics.
Tryptamine, an amine formed by the decarboxylation of tryptophan. It is formed by amine oxidase oxidation. It is the precursor formed by Harman (→ Harman alkaloid). 5-hydroxyl derivatives (5-hydroxytryptamine, 5-HT) exist in the plasma of mammals and the skin of amphibians, and have a vasoconstrictor effect.

Application of tryptamine product 
  Organic intermediates, biochemical reagents. Biological and pharmaceutical intermediates, biological reagents
It is vasoactive; may have neuromodulatory function; it is a biogenic amine formed by the decarboxylation of tryptophan by the action of L-aromatic amino acid decarboxylase.

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