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Names

5-Hydroxytryptophan
α-Carboxy-5-hydroxytryptamine
5-HTP

IUPAC names

5-Hydroxy-L-tryptophan
(2S)-2-Amino-3-(5-hydroxy-1H-indol-3-yl)propanoic acid

ID 5149 · Formula C₁₁H₁₂N₂O₃ · Molecular weight 220.225

InChI InChI=1S/C11H12N2O3/c12-9(11(15)16)3-6-5-13-10-2-1-7(14)4-8(6)10/h1-2,4-5,9,13-14H,3,12H2,(H,15,16)/t9-/m0/s1

InChI Key LDCYZAJDBXYCGN-VIFPVBQESA-N This stereoisomer Any stereoisomer

SMILES OC(=O)[C@H](Cc1c[nH]c2c1cc(O)cc2)N

ChemSpider 388413
PubChem 439280
Wikidata Q238544
Wikipedia 5-Hydroxytryptophan
PsychonautWiki 5-HTP

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EMCDDA. New drugs in Europe, 2011, European Monitoring Centre for Drugs and Drug Addiction, Lisbon, 1 Apr 2012. 401 kB.

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Helm, K. Synthese und funktionelle In-vitro-Pharmakologie neuer Liganden des 5-HT_2A-Rezeptors aus der Klasse. Ph. D. Thesis, Universität Regensburg, Dresden, 1 Jan 2014. 3.2 MB. #3

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Dean, JG. Indolethylamine-N-methyltransferase polymorphisms: Genetic and biochemical approaches for study of endogenous N,N-dimethyltryptamine. Front. Neurosci., 23 Apr 2018, 12 n/a. 2.1 MB. https://doi.org/10.3389/fnins.2018.00232 #5-hydroxytryptophan

Takahashi, M; Nagashima, M; Suzuki, J; Seto, T; Yasuda, I; Yoshida, T. Creation and application of psychoactive designer drugs data library using liquid chromatography with photodiode array spectrophotometry detector and gas chromatography–mass spectrometry. Talanta, 15 Feb 2009, 77 (4), 1245–1272. 1.2 MB. https://doi.org/10.1016/j.talanta.2008.07.062 #5-HO-TP

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Blei, F; Baldeweg, F; Fricke, J; Hoffmeister, D. Biocatalytic production of psilocybin and derivatives in tryptophan synthase-enhanced reactions. Chem. Eur. J., 17 Jul 2018, 24 (40), 10028–10031. 969 kB. https://doi.org/10.1002/chem.201801047 #15 LC,MS,NMR

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7-Hydroxytryptophan

7 Dec 2019 · · Isomer Design