Tryptamine
Template:Chembox new Tryptamine is a monoamine alkaloid found in plants and animals. It is based around the indole ring structure, and is chemically related to the amino acid tryptophan, from which its name is derived. Tryptamine is found in trace amounts in the brains of mammals and is believed to play a role as a neuromodulator or neurotransmitter.[1]
Tryptamine is also the backbone for a group of compounds known collectively as tryptamines. This group includes many biologically active compounds, including neurotransmitters and hallucinogens.
The concentration of tryptamine in rat brains is about 3.5 pmol/g.[2]
Plants containing tryptamine
Many if not most plants contain small amounts of tryptamine which is an intermediate in one biosynthetic pathway to the plant hormone indole-3-acetic acid (heteroauxin).[3] Higher concentrations can be found in many Acacia species.
Tryptamine acts as a natural pesticide in plants.[4]
Tryptamine derivatives
The most well-known tryptamines are serotonin, an important neurotransmitter, and melatonin, a hormone involved in regulating the sleep-wake cycle. Tryptamine alkaloids found in fungi, plants and animals are commonly used by humans for their psychotropic effects. Prominent examples include psilocybin (from "magic mushrooms") and DMT (from numerous plant sources, e.g. chacruna, often used in ayahuasca brews). Many synthetic tryptamines have also been made, including the migraine drug sumatriptan and its relatives. The tables below list some commonly encountered substituted tryptamines.
The tryptamine backbone can also be identified as part of the structure of some more complex compounds, for example: LSD, ibogaine and yohimbine.
A thorough investigation of dozens of tryptamine compounds was published by Ann and Alexander Shulgin under the title TiHKAL.
Short Name | Rα | R4 | R5 | R6 | RN1 | RN2 | Full Name |
---|---|---|---|---|---|---|---|
Bufotenin | H | H | OH | H | CH3 | CH3 | 5-hydroxy-N,N-dimethyltryptamine |
DMT | H | H | H | H | CH3 | CH3 | N,N-dimethyltryptamine |
Melatonin | H | H | OCH3 | H | O=CH-CH3 | H | 5-methoxy-N-acetyltryptamine |
5-MeO-DMT | H | H | OCH3 | H | CH3 | CH3 | 5-methoxy-N,N-dimethyltryptamine |
NMT | H | H | H | H | H | CH3 | N-methyltryptamine |
Psilocybin | H | PO4 | H | H | CH3 | CH3 | 4-phosphoryloxy-N,N-dimethyltryptamine |
Psilocin | H | OH | H | H | CH3 | CH3 | 4-hydroxy-N,N-dimethyltryptamine |
Serotonin | H | H | OH | H | H | H | 5-hydroxytryptamine |
Tryptophan | COOH | H | H | H | H | H | α-carboxyltryptamine |
Short Name | Rα | R4 | R5 | RN1 | RN2 | Full Name |
---|---|---|---|---|---|---|
AET | CH2CH3 | H | H | H | H | α-ethyltryptamine |
AMT | CH3 | H | H | H | H | α-methyltryptamine |
DET | H | H | H | CH2CH3 | CH2CH3 | N,N-diethyltryptamine |
DiPT | H | H | H | CH(CH3)2 | CH(CH3)2 | N,N-diisopropyltryptamine |
DPT | H | H | H | CH2CH2CH3 | CH2CH2CH3 | N,N-dipropyltryptamine |
5-MeO-AMT | CH3 | H | OCH3 | H | H | 5-methoxy-α-methyltryptamine |
4-HO-DET | H | OH | H | CH2CH3 | CH2CH3 | 4-hydroxy-N,N-diethyltryptamine |
4-HO-DIPT | H | OH | H | CH(CH3)2 | CH(CH3)2 | 4-hydroxy-N,N-diisopropyltryptamine |
5-MeO-DIPT | H | H | OCH3 | CH(CH3)2 | CH(CH3)2 | 5-methoxy-N,N-diisopropyltryptamine |
4-HO-MiPT | H | OH | H | CH(CH3)2 | CH3 | 4-hydroxy-N-isopropyl-N-methyltryptamine |
Sumatriptan | H | H | SO2NHCH3 | CH3 | CH3 | 5-methylaminosulfonyl-N,N-dimethyltryptamine |
5-DAT | H | OCH3 | H | O=CH-CH3 | O=CH-CH3 | 5-methoxy-N,N-diacetyltryptamine |
HPT | H | H | OCH3 | H | C9H13NO2 | 5-methyloxy-N-demethylhydroxyephedryltryptamine |
The Abramovitch-Shapiro tryptamine synthesis is an organic reaction for the synthesis of tryptamines starting from a beta-Carboline [5]
References
- ↑ Jones R.S. (1982). "Tryptamine: a neuromodulator or neurotransmitter in mammalian brain?". Progress in neurobiology. 19 (1&ndash, 2): 117&ndash, 139.
- ↑ Effects of tryptamine mediated through 2 states of the 5-HT ...
- ↑ Takahashi, Dean Nobutaka, Chemistry of Plant Hormones, CRC Press
- ↑ Dr. Duke's Phytochemical and Ethnobotanical Databases -- Biological Activities of TRYPTAMINE
- ↑ 880. Tryptamines, carbolines, and related compounds. Part II. A convenient synthesis of tryptamines and -carbolines R. A. Abramovitch and D. Shapiro J. Chem. Soc., 1956, 4589 - 4592, doi:10.1039/JR9560004589
See also
External links
- Tryptamine FAQ
- Tryptamine Hallucinogens and Consciousness
- Lysergic book, describes several tryptamine journeys.
- User-friendly info on Tryptamines, provided by the TRIP! Project, Toronto Canada.
- Tryptamind Psychoactives, reference site on tryptamine and other psychoactives.
Template:Hallucinogenic tryptamines Template:Triptans Template:Tryptamines