5-Hydroxytryptophan: Difference between revisions

>David Hedlund
*[https://isomerdesign.com/PiHKAL/explore.php?id=5149 5-Hydroxytryptophan (Isomer Design)]
>Cannabis Entity
Grammatics
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5-HTP is also popularly consumed by users of [[MDMA]] and other serotonin-releasing agents to try to reduce the negative [[MDMA#After_effects|after effects]] that begin during the substance's [[duration|come down]] period, including [[anxiety]], [[depression]], and [[cognitive fatigue]].<ref>http://www.sciencedirect.com/science/article/pii/S0306452207006732 | Wang, X.; Baumann, M. H.; Dersch, C. M.; Rothman, R. B. (2007-08-10). "Restoration of 3,4-methylenedioxymethamphetamine-induced 5-HT depletion by the administration of l-5-hydroxytryptophan". Neuroscience. 148 (1): 212–220. doi:10.1016/j.neuroscience.2007.05.024. PMID 17629409.</ref> Since 5-HTP is a precursor for the neurotransmitter [[serotonin]] and MDMA administration both depletes serotonin levels in the brain as well as inhibit the enzyme needed to produce it (i.e. tryptophan hydroxylase) for a short period after,<ref>Acute inactivation of tryptophan hydroxylase by amphetamine analogs involves the oxidation of sulfhydryl sites | http://www.maps.org/images/pdf/1989_stone_1.pdf</ref> it is believed that taking 5-HTP in the days after coming down will speed up the production of serotonin and decrease the time needed to recover (though there are many popular misconceptions and controversies as to just how effective it is for this purpose).{{Citation needed}}
5-HTP is also popularly consumed by users of [[MDMA]] and other serotonin-releasing agents to try to reduce the negative [[MDMA#After_effects|after effects]] that begin during the substance's [[duration|come down]] period, including [[anxiety]], [[depression]], and [[cognitive fatigue]].<ref>http://www.sciencedirect.com/science/article/pii/S0306452207006732 | Wang, X.; Baumann, M. H.; Dersch, C. M.; Rothman, R. B. (2007-08-10). "Restoration of 3,4-methylenedioxymethamphetamine-induced 5-HT depletion by the administration of l-5-hydroxytryptophan". Neuroscience. 148 (1): 212–220. doi:10.1016/j.neuroscience.2007.05.024. PMID 17629409.</ref> Since 5-HTP is a precursor for the neurotransmitter [[serotonin]] and MDMA administration both depletes serotonin levels in the brain as well as inhibit the enzyme needed to produce it (i.e. tryptophan hydroxylase) for a short period after,<ref>Acute inactivation of tryptophan hydroxylase by amphetamine analogs involves the oxidation of sulfhydryl sites | http://www.maps.org/images/pdf/1989_stone_1.pdf</ref> it is believed that taking 5-HTP in the days after coming down will speed up the production of serotonin and decrease the time needed to recover (though there are many popular misconceptions and controversies as to just how effective it is for this purpose).{{Citation needed}}


5-HTP should not be taken until 12 hours after one's last dose of MDMA because combining the two substance could synergistically increase brain's serotonin levels to dangerous levels -- resulting in a potentially life-threatening condition called [[serotonin syndrome]].
5-HTP should not be taken until 12 hours after one's last dose of MDMA because combining the two substances could synergistically increase brain's serotonin levels to dangerous levels -- resulting in a potentially life-threatening condition called [[serotonin syndrome]].
==Chemistry==
==Chemistry==
5-HTP or 5-Hydroxytryptophan is a synthetic indole alkaloid molecule of the [[tryptamine]] class. Tryptamines share a core structure comprised of a bicyclic indole heterocycle attached at R<sub>3</sub> to an amino group via an ethyl side chain. 5-HTP is substituted at R<sub>5</sub> of its indole heterocycle with a hydroxy (OH) functional group. It also contains propanoic acid group bound to the terminal amine R<sub>N</sub> of its tryptamine backbone. 5-HTP is the 5-hydroxy analog of [[tryptophan]], and is sold in its levorotary isomer form. 5-HTP contains the core structure of [[serotonin]] with the addition of a propanoic acid at R<sub>N</sub>, and is converted by the body into serotonin by metabolic reactions.
5-HTP or 5-Hydroxytryptophan is a synthetic indole alkaloid molecule of the [[tryptamine]] class. Tryptamines share a core structure comprised of a bicyclic indole heterocycle attached at R<sub>3</sub> to an amino group via an ethyl side chain. 5-HTP is substituted at R<sub>5</sub> of its indole heterocycle with a hydroxy (OH) functional group. It also contains propanoic acid group bound to the terminal amine R<sub>N</sub> of its tryptamine backbone. 5-HTP is the 5-hydroxy analog of [[tryptophan]], and is sold in its levorotary isomer form. 5-HTP contains the core structure of [[serotonin]] with the addition of a propanoic acid at R<sub>N</sub>, and is converted by the body into serotonin by metabolic reactions.