Tryptamine (compound): Difference between revisions
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{{For|the chemical class based on the tryptamine structure|Substituted tryptamine}} | {{For|the chemical class based on the tryptamine structure|Substituted tryptamine}} | ||
'''Tryptamine''' is a monoamine alkaloid found in animals, plants and fungi.{{citation needed}} It contains an indole ring structure, and is structurally similar to the amino acid tryptophan, from which the name derives. Tryptamine is found in trace amounts in the brains of mammals and is hypothesized to play a role as a neuromodulator or neurotransmitter.<ref name="Jones1982">Jones R.S. | '''Tryptamine''' is a [[monoamine]] [[alkaloid]] found in animals, plants and fungi.{{citation needed}} It contains an indole ring structure, and is structurally similar to the amino acid tryptophan, from which the name derives. Tryptamine is found in trace amounts in the brains of mammals and is hypothesized to play a role as a neuromodulator or [[neurotransmitter]].<ref name="Jones1982">{{cite journal | vauthors=((Jones, R. S. G.)) | journal=Progress in Neurobiology | title=Tryptamine: a neuromodulator or neurotransmitter in mammalian brain? | volume=19 | issue=1–2 | pages=117–139 | date= January 1982 | url=https://linkinghub.elsevier.com/retrieve/pii/0301008282900235 | issn=03010082 | doi=10.1016/0301-0082(82)90023-5}}</ref> | ||
==Chemistry== | ==Chemistry== | ||
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==Pharmacology== | ==Pharmacology== | ||
Tryptamine is hypothesized to play a role as a neuromodulator or neurotransmitter.<ref name="Jones1982"/> Similar to other trace amines, tryptamine binds to human trace amine-associated receptor 1 (TAAR1) as an agonist.<ref>Khan | Tryptamine is hypothesized to play a role as a neuromodulator or [[neurotransmitter]].<ref name="Jones1982"/> Similar to other trace amines, tryptamine binds to human trace amine-associated [[receptor]] 1 (TAAR1) as an [[agonist]].<ref>{{cite journal | vauthors=((Khan, M. Z.)), ((Nawaz, W.)) | journal=Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie | title=The emerging roles of human trace amines and human trace amine-associated receptors (hTAARs) in central nervous system | volume=83 | pages=439–449 | date= October 2016 | issn=1950-6007 | doi=10.1016/j.biopha.2016.07.002}}</ref> | ||
==See also== | ==See also== | ||
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==References== | ==References== | ||
<references /> | <references /> | ||
[[Category:Alkaloid]] | |||
[[Category:Neurotransmitter]] | [[Category:Neurotransmitter]] | ||
[[Category:Tryptamine]] | [[Category:Tryptamine]] | ||
Latest revision as of 18:21, 31 January 2025
| Tryptamine (compound) | |||||
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| Chemical Nomenclature | |||||
| Common names | Indolylethylamine | ||||
| Systematic name | 2-(1H-indol-3-yl)ethanamine | ||||
| Class Membership | |||||
| Chemical class | Arylethylamine / Indole | ||||
| Routes of Administration | |||||
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| Interactions | |||||
Tryptamine is a monoamine alkaloid found in animals, plants and fungi.[citation needed] It contains an indole ring structure, and is structurally similar to the amino acid tryptophan, from which the name derives. Tryptamine is found in trace amounts in the brains of mammals and is hypothesized to play a role as a neuromodulator or neurotransmitter.[1]
Chemistry
The tryptamine molecule is an indole alkaloid comprised of an indole ring attached to a monoamine (single nitrogen group-containing) chain. It is a derivative of the amino acid tryptophan.
Pharmacology
Tryptamine is hypothesized to play a role as a neuromodulator or neurotransmitter.[1] Similar to other trace amines, tryptamine binds to human trace amine-associated receptor 1 (TAAR1) as an agonist.[2]
See also
External links
References
- ↑ 1.0 1.1 Jones, R. S. G. (January 1982). "Tryptamine: a neuromodulator or neurotransmitter in mammalian brain?". Progress in Neurobiology. 19 (1–2): 117–139. doi:10.1016/0301-0082(82)90023-5. ISSN 0301-0082.
- ↑ Khan, M. Z., Nawaz, W. (October 2016). "The emerging roles of human trace amines and human trace amine-associated receptors (hTAARs) in central nervous system". Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie. 83: 439–449. doi:10.1016/j.biopha.2016.07.002. ISSN 1950-6007.