t
tryptamine
Chemical compound
Also known as 1H-indole-3-ethanamine · 2-(3-indolyl)ethylamine · 2-(1H-indol-3-yl)ethanamine · Tryptamin · 2-Indol-3-yl-ethylamine · 3-Indoleethylamine
- Formula
- C₁₀H₁₂N₂
1
- C₁₀H₁₂N₂
- Mass
- 160.1 Da
1
- 160.1 Da
- Melting point
- 114°C
1
- 114°C
Overview
Chemistry
All data
160 statements · 59% with external sources · numbers in brackets are citations
- Canonical SMILES
- C1=CC=C2C(=C1)C(=CN2)CCN
1
- C1=CC=C2C(=C1)C(=CN2)CCN
- Physically interacts with
- 5-hydroxytryptamine receptor 1B subject has role: agonist
1
- 5-hydroxytryptamine receptor 1D subject has role: agonist
1
- 5-hydroxytryptamine receptor 1E subject has role: agonist
1
- 5-hydroxytryptamine receptor 1F subject has role: agonist
1
- 5-hydroxytryptamine receptor 2A subject has role: agonist
1
- 5-hydroxytryptamine receptor 2B subject has role: agonist
1
- 5-hydroxytryptamine receptor 2C subject has role: agonist
1
- 5-hydroxytryptamine receptor 7 subject has role: agonist
1
- 5-hydroxytryptamine receptor 1B subject has role: agonist
- Found in taxon
- Dicorynia guianensis
- Lens culinaris
- Panaeolus goossensiae
- Panaeolus semiovatus
- Panaeolus antillarum
- Mimosa somnians
- Prosopis nigra
1
- Tachigali paniculata
1
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- Actinidia chinensis
- Amphimedon
- Catharanthus roseus
7
Sources- 1.Stated in Continuous Production of Indole Alkaloids by Gel-Entrapped Cells of Catharanthus Roseus
- 2.Stated in Secondary metabolite biosynthesis in cultured cells of Catharanthus roseus (L.) G. Don immobilized by adhesion to glass fibres
- 3.Stated in Tryptophan decarboxylase activity in transformed roots fromCatharanthus roseus and its relationship to tryptamine, ajmalicine, and catharanthine accumulation during the culture cycle
- 4.Stated in The effect of the aggregate size on the production of ajmalicine and tryptamine in Catharanthus roseus suspension culture
- 5.Stated in Stimulation of Indole Alkaloid Content in Vanadium-Treated Catharanthus roseus Suspension Cultures
- 6.Stated in Influence of Sucrose on Levels of Ajmalicine, Serpentine, and Tryptamine in Catharanthus roseus Cells in vitro
- Cinchona robusta
- Tabernaemontana divaricata
4
Sources- 1.Stated in Comparison of terpenoid indole alkaloid production and degradation in two cell lines of Tabernaemontana divaricata
- 2.Stated in Terpenoid indole alkaloid biotransformation capacity of suspension cultures of Tabernaemontana divaricata
- 3.Stated in Analysis of several iridoid and indole precursors of terpenoid indole alkaloids with a single HPLC run
- 4.Stated in Search for Factors Related to the Indole Alkaloid Production in Cell Suspension Cultures of Tabernaemontana divaricata
- Hordeum vulgare
- tomato
- Nitraria komarovii
- Nitraria schoberi
- Pereskia aculeata
- Peucedanum palustre
- Prosopis alpataco
- Prosopis chilensis
- Prosopis pugionata
- Prunus domestica
- Rauvolfia serpentina
2
Sources- 1.Stated in Development of an efficient system for the separation of indole alkaloids by high performance liquid chromatography and its applications.
- 2.Stated in Divergence of the indole alkaloid pattern in two somatic hybrid plant cell subcultures of Rauvolfia serpentina x Rhazya stricta
- Solanum melongena
- Stichodactyla gigantea
- Tabernaemontana elegans
- Tecoma stans
1
- Theobroma cacao
- Virola calophylla
- Centaurea montana
- Chimonanthus praecox
- Desmodium triflorum
- Isis minorbrachyblasta
- Homo sapiens
- Ototropis elegans
- Polygala tenuifolia
1
- Prosopis alba
1
- Sophora flavescens
- Acacia baileyana
- Mimosa scabrella
- pomegranate
- Desmodium styracifolium
- house mouse
- Sunhangia elegans
- Grona triflora
- Anthozoa
1
- Neltuma glandulosa
- Pisum sativum
- Capsicum annuum
- Lactuca sativa
- Brassica
- Aspergillus fumigatus
- Vachellia rigidula
1
- Cinchona calisaya
- Solanum
On other databases
38 identifiers linking tryptamine across the web's reference databases
- Cannabis Database ID004844
- CAS Registry Number61-54-1
- ChEBI ID16765
- ChEMBL IDCHEMBL6640
- ChemSpider ID1118
- DrugBank IDDB08653
- DSSTOX compound identifierDTXCID3042922
- DSSTox substance IDDTXSID2075340
- EC number200-510-5
- ECHA Substance Infocard ID100.000.464
- Freebase ID/m/02kcb94
- Gmelin number603448
- Gran Enciclopèdia Catalana IDtriptamina
- Gran Enciclopèdia Catalana ID (former scheme)0148354
- Guide to Pharmacology Ligand ID125
- Human Metabolome Database IDHMDB0000303
- InChIInChI=1S/C10H12N2/c11-6-5-8-7-12-10-4-2-1-3-9(8)10/h1-4,7,12H,5-6,11H2
- InChIKeyAPJYDQYYACXCRM-UHFFFAOYSA-N
- J9U entity ID987007553512905171
- KEGG IDC00398
- KNApSAcK IDC00001434
- Library of Congress Authorities IDsh85138304
- MassBank accession IDMSBNK-Fac_Eng_Univ_Tokyo-JP002028
- Microsoft Academic ID (discontinued)2777135210
- NALT ID17373
- NMRShiftDB structure ID20143557
- OpenAlex IDC2777135210
- PDB ligand IDTSS
- PDB structure ID2IUQ
- Probes And Drugs IDPD000807
- PubChem CID1150
- Reaxys registry number125513
- SPLASHsplash10-00di-1900000000-ac580ff9d9d90ed4712f
- SureChEMBL ID26725
- UniChem compound ID228432
- UNII422ZU9N5TV
- Yale LUX IDconcept/2da4d9b2-09d2-4dd2-b232-f0fdd347f664
- ZVG number35780