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− | {{Chembox/SectGeneral}} |
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+ | |ImageFile2=Tryptamine-3d-sticks.png |
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− | {{Chembox/IUPACName|3-(2-Aminoethyl)indole}} |
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+ | |IUPACName=2-(1H-indol-3-yl)ethanamine |
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+ | |OtherNames= |
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− | {{Chembox/SMILES|<nowiki>NCCC1=CNC2=C1C=CC=C2</nowiki>}} |
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− | {{Chembox |
+ | |Section1= {{Chembox Identifiers |
+ | | CASNo=61-54-1 |
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− | {{Chembox/Bottom}} |
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+ | | PubChem=1150 |
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+ | | SMILES=C1=CC=C2C(=C1)C(=CN2)CCN |
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+ | }} |
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+ | |Section2= {{Chembox Properties |
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⚫ | |||
+ | | MolarMass=160.216 |
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+ | | Appearance= |
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+ | | Density= |
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+ | | MeltingPt= |
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+ | | BoilingPt= |
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+ | | Solubility= |
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+ | }} |
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+ | |Section3= {{Chembox Hazards |
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+ | | MainHazards= |
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+ | | FlashPt= |
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+ | | Autoignition= |
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+ | }} |
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+ | }} |
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+ | '''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 amine|trace]] amounts in the [[brain]]s of [[mammal]]s and is believed to play a role as a [[neuromodulator]] or [[neurotransmitter]].<ref>{{cite journal |
||
+ | | author = Jones R.S. |
||
+ | | year = 1982 |
||
+ | | title = Tryptamine: a neuromodulator or neurotransmitter in mammalian brain? |
||
+ | | journal = Progress in neurobiology |
||
+ | | volume = 19 |
||
+ | | number = 1–2 |
||
+ | | pages = 117–139 |
||
+ | }}</ref> |
||
+ | Tryptamine is also the backbone for a group of compounds known collectively as '''tryptamines'''. This group includes many [[Biological activity|biologically active]] [[Chemical compound|compound]]s, including [[neurotransmitter]]s and [[hallucinogen]]s. |
||
+ | The concentration of tryptamine in rat brains is about 3.5 [[picomole|pmol]]/g.<ref>[http://linkinghub.elsevier.com/retrieve/pii/S0300483X06004100 Effects of tryptamine mediated through 2 states of the 5-HT ...]</ref> |
||
⚫ | |||
+ | |||
+ | ==Plants containing tryptamine== |
||
+ | |||
+ | Many if not most plants contain small amounts of tryptamine which is an intermediate in one [[metabolism|biosynthetic pathway]] to the plant hormone [[indole-3-acetic acid]] (heteroauxin).<ref name="plant">[http://books.google.com/books?id=PQ2nWAPzPcIC&pg=RA3-PA43&lpg=RA3-PA43&dq=acacia+tryptamine+-gum&source=web&ots=zFe1pKHsLM&sig=b8edsYiycL4nsy8sd9rvQti_6CA#PRA3-PA43,M1 Takahashi, Dean Nobutaka, Chemistry of Plant Hormones, [[CRC Press]] ]</ref> Higher concentrations can be found in many [[Acacia]] species. |
||
+ | |||
+ | Tryptamine acts as a natural pesticide in plants.<ref>[http://www.ars-grin.gov/cgi-bin/duke/chem-activities.pl Dr. Duke's Phytochemical and Ethnobotanical Databases -- Biological Activities of TRYPTAMINE]</ref> |
||
+ | |||
+ | ==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 [[animal]]s are commonly used by [[humans]] for their [[psychotropic]] effects. Prominent examples include [[psilocybin]] (from "[[Psychedelic mushroom|magic mushroom]]s") and [[dimethyltryptamine|DMT]] (from numerous plant sources, e.g. [[chacruna]], often used in [[ayahuasca]] brews). Many [[chemical synthesis|synthetic]] tryptamines have also been made, including the [[migraine]] [[medication|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 |
The tryptamine backbone can also be identified as part of the structure of some |
||
− | more complex compounds, for example: |
+ | more complex compounds, for example: [[LSD]], [[ibogaine]] and [[yohimbine]]. |
A thorough investigation of dozens of tryptamine compounds was published by [[Ann Shulgin|Ann]] and [[Alexander Shulgin]] under the title [[TiHKAL]]. |
A thorough investigation of dozens of tryptamine compounds was published by [[Ann Shulgin|Ann]] and [[Alexander Shulgin]] under the title [[TiHKAL]]. |
||
+ | {{-}} |
||
+ | {| class="wikitable" |
||
⚫ | |||
+ | |+ '''Naturally occurring tryptamines''' |
||
+ | |+ (''see also'' [[Table of naturally occurring tryptamines]]) |
||
⚫ | |||
+ | ! Short Name |
||
+ | ! R<sup>α</sup> |
||
+ | ! R<sup>4</sup> |
||
+ | ! R<sup>5</sup> |
||
+ | ! R<sup>6</sup> |
||
+ | ! R<sup>N1</sup> |
||
+ | ! R<sup>N2</sup> |
||
+ | ! Full Name |
||
⚫ | |||
+ | | [[Bufotenin]] || H || H || OH ||H || CH<sub>3</sub> || CH<sub>3</sub> || 5-hydroxy-''N,N''-dimethyltryptamine |
||
⚫ | |||
+ | | [[Dimethyltryptamine|DMT]] || H || H || H || H || [[Methyl|CH<sub>3</sub>]] ||CH<sub>3</sub> || ''N,N''-dimethyltryptamine |
||
⚫ | |||
+ | | [[Melatonin]] || H || H || [[Methoxy|OCH<sub>3</sub>]] || H|| [[acetyl|O=CH-CH<sub>3</sub>]] ||H || 5-methoxy-''N''-acetyltryptamine |
||
⚫ | |||
+ | | [[5-MeO-DMT]] || H || H || OCH<sub>3</sub> ||H || CH<sub>3</sub> || CH<sub>3</sub> || 5-methoxy-''N,N''-dimethyltryptamine |
||
⚫ | |||
+ | | [[N-methyltryptamine|NMT]] || H || H || H || H || H ||CH<sub>3</sub> || ''N''-methyltryptamine |
||
⚫ | |||
+ | | [[Psilocybin]] || H || PO<sub>4</sub> || H || H || CH<sub>3</sub> || CH<sub>3</sub> || 4-phosphoryloxy-''N,N''-dimethyltryptamine |
||
⚫ | |||
+ | | [[Psilocin]] || H || [[Hydroxy|OH]] || H || H || CH<sub>3</sub> || CH<sub>3</sub> || 4-hydroxy-''N,N''-dimethyltryptamine |
||
⚫ | |||
+ | | [[Serotonin]] || H || H || OH ||H ||H ||H || 5-hydroxytryptamine |
||
⚫ | |||
+ | | [[Tryptophan]] || [[Carboxyl|COOH]] || H || H || H || H || H || α-carboxyltryptamine |
||
⚫ | |||
⚫ | |||
+ | {| class="wikitable" |
||
⚫ | |||
− | <br style="clear: both"> |
||
− | |||
− | {| border="1" cellspacing="0" |
||
|- |
|- |
||
− | |+ ''' |
+ | |+ '''Synthetic tryptamines''' |
|- |
|- |
||
! Short Name |
! Short Name |
||
− | ! R< |
+ | ! R<sup>α</sup> |
− | ! R< |
+ | ! R<sup>4</sup> |
− | ! R< |
+ | ! R<sup>5</sup> |
− | ! R< |
+ | ! R<sup>N1</sup> |
− | ! R< |
+ | ! R<sup>N2</sup> |
! Full Name |
! Full Name |
||
|- |
|- |
||
| [[Alpha-ethyltryptamine|AET]] |
| [[Alpha-ethyltryptamine|AET]] |
||
| [[Ethyl|CH<sub>2</sub>CH<sub>3</sub>]] |
| [[Ethyl|CH<sub>2</sub>CH<sub>3</sub>]] |
||
− | | |
+ | | H |
− | | |
+ | | H |
− | | |
+ | | H |
− | | |
+ | | H |
+ | | α-ethyltryptamine |
||
− | | α-[[ethyl]]<nowiki>tryptamine</nowiki> |
||
|- |
|- |
||
| [[Alphamethyltryptamine|AMT]] |
| [[Alphamethyltryptamine|AMT]] |
||
| [[Methyl|CH<sub>3</sub>]] |
| [[Methyl|CH<sub>3</sub>]] |
||
− | | |
+ | | H |
− | | |
+ | | H |
− | | |
+ | | H |
− | | |
+ | | H |
+ | | α-methyltryptamine |
||
− | | α-[[methyl]]<nowiki>tryptamine</nowiki> |
||
⚫ | |||
− | | [[serotonin]] |
||
⚫ | |||
⚫ | |||
− | | [[Hydroxy|OH]] |
||
⚫ | |||
⚫ | |||
− | | 5-[[hydroxy]]<nowiki>tryptamine</nowiki> |
||
|- |
|- |
||
| [[diethyltryptamine|DET]] |
| [[diethyltryptamine|DET]] |
||
− | | |
+ | | H |
− | | |
+ | | H |
− | | |
+ | | H |
− | | |
+ | | CH<sub>2</sub>CH<sub>3</sub> |
− | | |
+ | | CH<sub>2</sub>CH<sub>3</sub> |
+ | | ''N,N''-diethyltryptamine |
||
− | | N,N-di[[ethyl]]<nowiki>tryptamine</nowiki> |
||
|- |
|- |
||
| [[diisopropyltryptamine|DiPT]] |
| [[diisopropyltryptamine|DiPT]] |
||
− | | |
+ | | H |
− | | |
+ | | H |
− | | |
+ | | H |
| [[Isopropyl|CH(CH<sub>3</sub>)<sub>2</sub>]] |
| [[Isopropyl|CH(CH<sub>3</sub>)<sub>2</sub>]] |
||
− | | |
+ | | CH(CH<sub>3</sub>)<sub>2</sub> |
+ | | ''N,N''-diisopropyltryptamine |
||
− | | N,N-di[[isopropyl]]<nowiki>tryptamine</nowiki> |
||
⚫ | |||
− | | [[dimethyltryptamine|DMT]] |
||
⚫ | |||
⚫ | |||
⚫ | |||
⚫ | |||
− | | [[Methyl|CH<sub>3</sub>]] |
||
− | | N,N-di[[methyl]]<nowiki>tryptamine</nowiki> |
||
|- |
|- |
||
| [[dipropyltryptamine|DPT]] |
| [[dipropyltryptamine|DPT]] |
||
− | | |
+ | | H |
− | | |
+ | | H |
− | | |
+ | | H |
⚫ | |||
| [[Propyl|CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub>]] |
| [[Propyl|CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub>]] |
||
⚫ | |||
− | | N,N-di[[propyl]]<nowiki>tryptamine</nowiki> |
||
+ | | ''N,N''-dipropyltryptamine |
||
⚫ | |||
− | | [[melatonin]] |
||
− | | |
||
− | | |
||
− | | [[Methoxy|OCH<sub>3</sub>]] |
||
− | | [[acetyl|O=CH-CH<sub>3</sub>]] |
||
− | | |
||
− | | 5-[[methoxy]]-N-[[acetyl]]<nowiki>tryptamine</nowiki> |
||
|- |
|- |
||
| [[5-MeO-AMT]] |
| [[5-MeO-AMT]] |
||
− | | |
+ | | CH<sub>3</sub> |
− | | |
+ | | H |
| [[Methoxy|OCH<sub>3</sub>]] |
| [[Methoxy|OCH<sub>3</sub>]] |
||
− | | |
+ | | H |
− | | |
+ | | H |
− | | 5- |
+ | | 5-methoxy-α-methyltryptamine |
|- |
|- |
||
− | | [[ |
+ | | [[4-HO-DET]] |
− | | |
+ | | H |
− | | |
+ | | OH |
+ | | H |
||
− | | [[Hydroxy|OH]] |
||
− | | |
+ | | CH<sub>2</sub>CH<sub>3</sub> |
− | | |
+ | | CH<sub>2</sub>CH<sub>3</sub> |
− | | |
+ | | 4-hydroxy-''N,N''-diethyltryptamine |
|- |
|- |
||
− | | [[4-HO- |
+ | | [[4-HO-DIPT]] |
− | | |
+ | | H |
− | | |
+ | | OH |
− | | |
+ | | H |
− | | |
+ | | CH(CH<sub>3</sub>)<sub>2</sub> |
− | | |
+ | | CH(CH<sub>3</sub>)<sub>2</sub> |
− | | 4- |
+ | | 4-hydroxy-''N,N''-diisopropyltryptamine |
⚫ | |||
− | | [[4-HO-DIPT|iprocin]] |
||
− | | |
||
− | | [[hydroxy|OH]] |
||
− | | |
||
− | | [[Isopropyl|CH(CH<sub>3</sub>)<sub>2</sub>]] |
||
− | | [[Isopropyl|CH(CH<sub>3</sub>)<sub>2</sub>]] |
||
− | | 4-[[hydroxy]]-N,N-di[[isopropyl]]<nowiki>tryptamine</nowiki> |
||
|- |
|- |
||
| [[5-MeO-DIPT]] |
| [[5-MeO-DIPT]] |
||
− | | |
+ | | H |
− | | |
+ | | H |
− | | |
+ | | OCH<sub>3</sub> |
− | | |
+ | | CH(CH<sub>3</sub>)<sub>2</sub> |
− | | |
+ | | CH(CH<sub>3</sub>)<sub>2</sub> |
− | | 5- |
+ | | 5-methoxy-''N,N''-diisopropyltryptamine |
|- |
|- |
||
− | | [[ |
+ | | [[4-HO-MiPT]] |
− | | |
+ | | H |
− | | |
+ | | OH |
+ | | H |
||
− | | [[Methoxy|OCH<sub>3</sub>]] |
||
− | | |
+ | | CH(CH<sub>3</sub>)<sub>2</sub> |
− | | |
+ | | CH<sub>3</sub> |
+ | | 4-hydroxy-''N''-isopropyl-''N''-methyltryptamine |
||
− | | 5-[[methoxy]]-N,N-di[[methyl]]<nowiki>tryptamine</nowiki> |
||
|- |
|- |
||
− | | [[ |
+ | | [[Sumatriptan]] |
− | | |
+ | | H |
+ | | H |
||
− | | [[hydroxy|OH]] |
||
⚫ | |||
− | | |
||
− | | |
+ | | CH<sub>3</sub> |
− | | |
+ | | CH<sub>3</sub> |
+ | | 5-methylaminosulfonyl-''N,N''-dimethyltryptamine |
||
− | | 4-[[hydroxy]]-N-[[isopropyl]]-N-[[methyl]]<nowiki>tryptamine</nowiki> |
||
|- |
|- |
||
+ | | [[5-DAT]] || H || [[Methoxy|OCH<sub>3</sub>]] || H|| [[acetyl|O=CH-CH<sub>3</sub>]] || [[acetyl|O=CH-CH<sub>3</sub>]] || 5-methoxy-''N,N''-diacetyltryptamine |
||
− | | [[psilocin]] |
||
− | | |
||
− | | [[hydroxy|OH]] |
||
− | | |
||
− | | [[Methyl|CH<sub>3</sub>]] |
||
− | | [[Methyl|CH<sub>3</sub>]] |
||
− | | 4-[[hydroxy]]-N,N-di[[methyl]]<nowiki>tryptamine</nowiki> |
||
⚫ | |||
− | | [[psilocybin]] |
||
− | | |
||
− | | OPO<sub>3</sub>H<sub>2</sub> |
||
− | | |
||
− | | [[Methyl|CH<sub>3</sub>]] |
||
− | | [[Methyl|CH<sub>3</sub>]] |
||
− | | 4-phosphoryloxy-N,N-di[[methyl]]<nowiki>tryptamine</nowiki> |
||
⚫ | |||
− | | [[sumatriptan]] |
||
− | | |
||
− | | |
||
− | | SO<sub>2</sub>NHCH<sub>3</sub> |
||
− | | [[Methyl|CH<sub>3</sub>]] |
||
− | | [[Methyl|CH<sub>3</sub>]] |
||
− | | 5-methylaminosulfonyl-N,N-di[[methyl]]<nowiki>tryptamine</nowiki> |
||
|- |
|- |
||
+ | | [[HPT]] || H || H || OCH<sub>3</sub> || H || C<sub>9</sub>H<sub>13</sub>NO<sub>2</sub> || 5-methyloxy-''N''-demethylhydroxyephedryltryptamine |
||
|} |
|} |
||
+ | |||
+ | The '''Abramovitch-Shapiro tryptamine synthesis''' is an [[organic reaction]] for the synthesis of tryptamines starting from a [[beta-Carboline]] <ref>''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}}</ref> |
||
+ | |||
+ | ==References== |
||
+ | {{reflist}} |
||
== See also == |
== See also == |
||
+ | * [[Trace amine]] |
||
* [[beta-Carboline]] |
* [[beta-Carboline]] |
||
* [[Ergoline]] |
* [[Ergoline]] |
||
Line 189: | Line 213: | ||
* [http://www.erowid.org/psychoactives/faqs/faqs_tryptamine.shtml Tryptamine FAQ] |
* [http://www.erowid.org/psychoactives/faqs/faqs_tryptamine.shtml Tryptamine FAQ] |
||
* [http://www.tryptamind.com/tryptamine.html Tryptamine Hallucinogens and Consciousness] |
* [http://www.tryptamind.com/tryptamine.html Tryptamine Hallucinogens and Consciousness] |
||
− | * [http://www.lysergicbook.com Lysergic book], describes several tryptamine journeys. |
||
* [http://www.tripproject.ca/march/drugContent.php?info=researchchemicals User-friendly info on Tryptamines], provided by the TRIP! Project, Toronto Canada. |
* [http://www.tripproject.ca/march/drugContent.php?info=researchchemicals User-friendly info on Tryptamines], provided by the TRIP! Project, Toronto Canada. |
||
* [http://www.tryptamind.com/ Tryptamind Psychoactives], reference site on tryptamine and other psychoactives. |
* [http://www.tryptamind.com/ Tryptamind Psychoactives], reference site on tryptamine and other psychoactives. |
||
− | {{ChemicalSources}} |
||
{{Hallucinogenic tryptamines}} |
{{Hallucinogenic tryptamines}} |
||
Line 200: | Line 222: | ||
{{Tryptamines}} |
{{Tryptamines}} |
||
+ | [[Category:Amines]] |
||
+ | [[Category:Neurotransmitters]] |
||
[[Category:Tryptamines|*]] |
[[Category:Tryptamines|*]] |
||
+ | [[Category:Vasocinstrictor drugs]] |
||
+ | <!-- |
||
− | :de:Tryptamin |
||
+ | [[de:Tryptamine]] |
||
⚫ | |||
+ | [[fr:Tryptamine]] |
||
⚫ | |||
+ | [[hr:Triptamin]] |
||
⚫ | |||
+ | [[lt:Triptaminas]] |
||
⚫ | |||
⚫ | |||
⚫ | |||
+ | [[fi:Tryptamiini]] |
||
+ | --> |
||
{{enWP|Tryptamine}} |
{{enWP|Tryptamine}} |
Revision as of 08:04, 13 January 2008
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style="background: #F8EABA; text-align: center;" colspan="2" | Tryptamine |
---|---|
File:Tryptamine.png | |
File:Tryptamine-3d-sticks.png | |
2-(1H-indol-3-yl)ethanamine | |
Identifiers | |
CAS number | 61-54-1 |
PubChem | 1150 |
SMILES | C1=CC=C2C(=C1)C(=CN2)CCN |
Properties | |
Molecular formula | C10H12N2 |
Molar mass | 160.216 |
Hazards | |
style="background: #F8EABA; text-align: center;" colspan="2" | Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
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: 117–139.
- ↑ 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,
- REDIRECT Template:Doi
See also
- Trace amine
- beta-Carboline
- Ergoline
- TiHKAL
- PiHKAL
External links
- Tryptamine FAQ
- Tryptamine Hallucinogens and Consciousness
- User-friendly info on Tryptamines, provided by the TRIP! Project, Toronto Canada.
- Tryptamind Psychoactives, reference site on tryptamine and other psychoactives.
Tryptamines edit |
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