tryptamine (Q409439)

tryptamine (English)

19 October 2016

C₁₀H₁₂N₂

1 reference

tryptamine (English)

19 October 2016

C1=CC=C2C(=C1)C(=CN2)CCN

1 reference

tryptamine (English)

19 October 2016

114.0 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Dicorynia guianensis

1 reference

Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968

Lens culinaris

1 reference

Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968

Panaeolus goossensiae

1 reference

Species identification and chemical analysis of psychoactive fungi in the Hawaiian islands

Panaeolus semiovatus

1 reference

Species identification and chemical analysis of psychoactive fungi in the Hawaiian islands

Panaeolus antillarum

1 reference

Species identification and chemical analysis of psychoactive fungi in the Hawaiian islands

Mimosa somnians

1 reference

The Occurrence of Tryptamine and N-Methyltryptamine in Mimosa somnians

Prosopis nigra

1 reference

Alkaloids of Prosopis nigra

Tachigali paniculata

1 reference

Indole Alkylamines from Tachigalia paniculata

Actinidia chinensis

1 reference

High-performance liquid chromatographic analysis of tetrahydro-β-carbolines in food plants

Amphimedon

1 reference

Keramaphidin C and keramamine C plausible biogenetic precursors of manzamine C from an Okinawan marine sponge

Catharanthus roseus

7 references

Continuous Production of Indole Alkaloids by Gel-Entrapped Cells of Catharanthus Roseus

Secondary metabolite biosynthesis in cultured cells of Catharanthus roseus (L.) G. Don immobilized by adhesion to glass fibres

Tryptophan decarboxylase activity in transformed roots fromCatharanthus roseus and its relationship to tryptamine, ajmalicine, and catharanthine accumulation during the culture cycle

The effect of the aggregate size on the production of ajmalicine and tryptamine in Catharanthus roseus suspension culture

Stimulation of Indole Alkaloid Content in Vanadium-Treated Catharanthus roseus Suspension Cultures

Influence of Sucrose on Levels of Ajmalicine, Serpentine, and Tryptamine in Catharanthus roseus Cells in vitro

Geraniol-10-hydroxylase Activity and Its Relation to Monoterpene Indole Alkaloid Accumulation in Cell Suspension Cultures of Catharanthus roseus

Cinchona robusta

1 reference

Thermospray Liquid Chromatography/Mass Spectrometry (TSP LC/MS) Analysis of the Alkaloids from Cinchona in vitro Cultures

Tabernaemontana divaricata

4 references

Comparison of terpenoid indole alkaloid production and degradation in two cell lines of Tabernaemontana divaricata

Terpenoid indole alkaloid biotransformation capacity of suspension cultures of Tabernaemontana divaricata

Analysis of several iridoid and indole precursors of terpenoid indole alkaloids with a single HPLC run

Search for Factors Related to the Indole Alkaloid Production in Cell Suspension Cultures of Tabernaemontana divaricata

Hordeum vulgare

1 reference

Accumulation of Tryptamine in Barley Leaves Irradiated with UV Light

tomato

1 reference

High-performance liquid chromatographic analysis of tetrahydro-β-carbolines in food plants

Nitraria komarovii

1 reference

Alkaloids of Nitraria komarovii. XIII. Nitramine N-oxide and the structure of dehydroschoberine

Nitraria schoberi

2 references

Alkaloids from Nitraria schoberi. O-acetylnitraraine

Chemical Characterization and Pharmacological Activity of Nazlinin, a Novel Indole Alkaloid from Nitraria schoberi

Pereskia aculeata

1 reference

Pereskia aculeata: A plant food with antinociceptive activity.

Peucedanum palustre

1 reference

Optimization of the HPLC analysis of biogenic amines in Peucedanum palustre plants and cell culture lines

Prosopis alpataco

1 reference

Biologically active alkaloids and a free radical scavenger from Prosopis species

Prosopis chilensis

1 reference

Biologically active alkaloids and a free radical scavenger from Prosopis species

Prosopis pugionata

1 reference

Biologically active alkaloids and a free radical scavenger from Prosopis species

Prunus domestica

1 reference

High-performance liquid chromatographic analysis of tetrahydro-β-carbolines in food plants

Rauvolfia serpentina

2 references

Development of an efficient system for the separation of indole alkaloids by high performance liquid chromatography and its applications.

Divergence of the indole alkaloid pattern in two somatic hybrid plant cell subcultures of Rauvolfia serpentina x Rhazya stricta

Solanum melongena

1 reference

High-performance liquid chromatographic analysis of tetrahydro-β-carbolines in food plants

Stichodactyla gigantea

1 reference

Characterization of compounds that induce symbiosis between sea anemone and anemone fish

Tabernaemontana elegans

1 reference

Characterization of a Suspension Culture of Tabernaemontana elegans on Growth, Nutrient Uptake, and Accumulation of Indole Alkaloids*

Tecoma stans

1 reference

Indolic compounds in the leaves of Tecoma stans

cacao

1 reference

Tetrahydro-beta-carbolines, potential neuroactive alkaloids, in chocolate and cocoa.

Virola calophylla

1 reference

Monoamine oxidase inhibitors in South American hallucinogenic plants Part 2: Constituents of orally-active Myristicaceous hallucinogens

Centaurea montana

1 reference

Montamine, a unique dimeric indole alkaloid, from the seeds of Centaurea montana (Asteraceae), and its in vitro cytotoxic activity against the CaCo2 colon cancer cells

Chimonanthus praecox

1 reference

Two new tryptamine-derived alkaloids from Chimonanthus praecox f. concolor

Desmodium triflorum

1 reference

Chemical and pharmacological evaluation of Desmodium pulchellum

Isis minorbrachyblasta

1 reference

New Steroids and a New Alkaloid from the GorgonianIsis minorbrachyblasta:Structures, Cytotoxicity, and Antilarval Activity

Homo sapiens

2 references

Recon 2.2: from reconstruction to model of human metabolism

A community-driven global reconstruction of human metabolism.

Ototropis elegans

1 reference

β-Phenethylamine, tetrahydroisoquinoline and indole Alkaloids of Desmodium tiliaefolium

Polygala tenuifolia

1 reference

Lactonic lignans of Polygala chinensis

Prosopis alba

1 reference

Alkaloids of Prosopis nigra

Sophora flavescens

1 reference

Correction: Chae, H.S., et al. Anti-Inflammatory Effects of 6,8-Diprenyl-7,4'-dihydroxyflavanone from Sophora tonkinensis on Lipopolysaccharide-Stimulated RAW 264.7 Cells. Molecules. 2016, 21, 1049.

Acacia baileyana

1 reference

Alkaloids of the Australian Leguminosae. VII. Nb-Methyltetrahydroharman from Acacia complanata A. Cunn. ex Benth

Mimosa scabrella

1 reference

The Occurrence of Tryptamine and N-Methyltryptamine in Mimosa somnians

Punica granatum

1 reference

Punica granatum (pomegranate) and its potential for prevention and treatment of inflammation and cancer

Desmodium styracifolium

1 reference

β-Phenethylamine, tetrahydroisoquinoline and indole Alkaloids of Desmodium tiliaefolium

house mouse

2 references

Keine GEMA-Gebühren für Hintergrundmusik

1H-Nuclear magnetic resonance-based metabolomic analysis of brain in mice with nicotine treatment

Sunhangia elegans

1 reference

β-Phenethylamine, tetrahydroisoquinoline and indole Alkaloids of Desmodium tiliaefolium

Grona triflora

1 reference

Chemical and pharmacological evaluation of Desmodium pulchellum

1 reference

1 reference

Indolizidine, antiinfective and antiparasitic compounds from Prosopis glandulosa var. glandulosa

Pisum sativum

1 reference

Auxin biosynthesis in pea: characterization of the tryptamine pathway.

Capsicum annuum

2 references

Metabolomics of capsicum ripening reveals modification of the ethylene related-pathway and carbon metabolism

HPLC analysis of serotonin, tryptamine, tyramine, and the hydroxycinnamic acid amides of serotonin and tyramine in food vegetables

lettuce

1 reference

HPLC analysis of serotonin, tryptamine, tyramine, and the hydroxycinnamic acid amides of serotonin and tyramine in food vegetables

Brassica

1 reference

HPLC analysis of serotonin, tryptamine, tyramine, and the hydroxycinnamic acid amides of serotonin and tyramine in food vegetables

Aspergillus fumigatus

1 reference

Substrate promiscuity of the cyclic dipeptide prenyltransferases from Aspergillus fumigatus ( section sign).

Vachellia rigidula

1 reference

Toxic amines and alkaloids from acacia rigidula

Cinchona calisaya

1 reference

Thermospray Liquid Chromatography/Mass Spectrometry (TSP LC/MS) Analysis of the Alkaloids from Cinchona in vitro Cultures

Solanum

1 reference

HPLC analysis of serotonin, tryptamine, tyramine, and the hydroxycinnamic acid amides of serotonin and tyramine in food vegetables

physically interacts with

5-hydroxytryptamine receptor 1B

1 reference

5-hydroxytryptamine receptor 1D

17 August 2016

1 reference

5-hydroxytryptamine receptor 1E

17 August 2016

1 reference

5-hydroxytryptamine receptor 1F

17 August 2016

1 reference

5-hydroxytryptamine receptor 2A

17 August 2016

1 reference

5-hydroxytryptamine receptor 2B

17 August 2016

1 reference

5-hydroxytryptamine receptor 2C

17 August 2016

1 reference

5-hydroxytryptamine receptor 7

17 August 2016

1 reference

https://plantreactome.gramene.org/PathwayBrowser/#/R-OSA-2744345&DTAB=MT

17 August 2016

1 reference

0 references

0 references

0 references

Tryptamine

0 references

Identifiers

InChI

InChI=1S/C10H12N2/c11-6-5-8-7-12-10-4-2-1-3-9(8)10/h1-4,7,12H,5-6,11H2

1 reference

tryptamine (English)

19 October 2016

2 references

tryptamine (English)

19 October 2016

ChEBI release 2020-09-01

2 references

tryptamine (English)

19 October 2016

https://commonchemistry.cas.org/detail?cas_rn=61-54-1

10 April 2021

1 reference

Tryptamine (English)

19 October 2016

2 references

tryptamine (English)

19 October 2016

Reaxys registry number

125513

1 reference

tryptamine (English)

19 October 2016

603448

0 references

ChEBI ID

16765

mapping relation type

2 references

tryptamine (English)

19 October 2016

International Chemical Identifier

InChI

InChI=1S/C10H12N2/c11-6-5-8-7-12-10-4-2-1-3-9(8)10/h1-4,7,12H,5-6,11H2

1 reference

TRYPTAMINE (English)

19 October 2016

2 references

inferred from InChIKey

MSBNK-Fac_Eng_Univ_Tokyo-JP002028

1 reference

MassBank accession ID

0 references

MSBNK-Keio_Univ-KO004142

0 references

MSBNK-Keio_Univ-KO004143

0 references

MSBNK-Keio_Univ-KO004144

0 references

MSBNK-Keio_Univ-KO004145

0 references

MSBNK-Keio_Univ-KO004146

0 references

MSBNK-Osaka_Univ-OUF00478

0 references

MSBNK-RIKEN-PR010102

0 references

MSBNK-RIKEN-PR010103

0 references

MSBNK-GL_Sciences_Inc-GLS00090

0 references

MSBNK-Kazusa-KZ000271

0 references

MSBNK-Kazusa-KZ000272

0 references

MSBNK-Waters-WA002432

0 references

MSBNK-Waters-WA002433

0 references

MSBNK-Waters-WA002434

0 references

MSBNK-Waters-WA002435

0 references

MSBNK-Waters-WA002436

0 references

SPLASH

splash10-00di-1900000000-ac580ff9d9d90ed4712f

0 references

splash10-00dr-2900000000-037af42e76613b924496

0 references

splash10-00di-1900000000-0f82cbf608e15678c41e

0 references

splash10-0006-0900000000-0572e0c6753816d29646

0 references

splash10-0006-0900000000-a3617243f16ac1d19ca3

0 references

splash10-0006-0900000000-5198dc18989eb021ff2b

0 references

splash10-014l-2900000000-3b3b79050401c23f0c22

0 references

splash10-014l-7900000000-b62047ba50e6464b146c

0 references

splash10-00di-2900000000-a7c4e80f196945c43f38

0 references

splash10-00di-7900000000-3900b703ce7b512e882b

0 references

splash10-00di-8900000000-f45a71db0a2ef37bb21e

0 references

splash10-0002-9500000000-d3eecf05360806329213

0 references

splash10-0006-0900000000-0fbbcff854f5a41fb318

0 references

splash10-0006-0900000000-7ad809b36e3dedf35e7c

0 references

splash10-0006-0900000000-bb699b23c5872ac8e0fd

0 references

splash10-0006-0900000000-8884114564e97033c718

0 references

splash10-0006-0900000000-d113e6c4030c76229b27

0 references

splash10-0006-0900000000-a69907c9797dfe0b761d

0 references

splash10-0006-1900000000-7239ee0f8829a50e886e

0 references

splash10-00di-2900000000-830c8a076e1bd787d36b

0 references

splash10-014l-7900000000-630a258032b083d5d676

0 references

splash10-001i-2900000000-6a48efe719d0f7482467

0 references

splash10-00kf-0900000000-24ae4f71c6de13d45134

0 references

splash10-03di-0900000000-b73564ce7b9f5f38af40

0 references

splash10-00di-2900000000-bd00339c48e04ebcf419

0 references

NMRShiftDB structure ID

20143557

1 reference

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

0 references

2 references

DSSTOX compound identifier

0 references

1 reference

Global Substance Registration System

UNII

422ZU9N5TV

tryptamine (English)

ECHA Substance Infocard ID

19 October 2016

100.000.464

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.000.464

27 December 2018

2-(indol-3-yl)ethylamine (English)

quotation

CAS no.: 61-54-1 (English)

1 reference

1 reference

tryptamine (English)

19 October 2016

1 reference

Human Metabolome Database ID

HMDB0000303

2 references

based on heuristic

inferred from InChIKey

3 references

tryptamine (English)

19 October 2016

inferred from InChIKey

UNII

422ZU9N5TV

2 references

Global Substance Registration System

UNII

422ZU9N5TV

tryptamine (English)

19 October 2016

Gran Enciclopèdia Catalana ID

0 references

0 references

0 references

1 reference

28 October 2013

0 references

triptamina

0 references

Gran Enciclopèdia Catalana ID (former scheme)

0148354

0 references

Microsoft Academic ID

0 references

0 references

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

1 reference

2IUQ (English)

19 October 2016

1 reference

2PQL (English)

19 October 2016

1 reference

3RXI (English)

19 October 2016

1 reference

3ATM (English)

19 October 2016

1 reference

2AGW (English)

19 October 2016

1 reference

4GE1 (English)

19 October 2016

1 reference

2FPB (English)