Grundinformationen
- Standard-SMILES
COc1ccc2[nH]cc(CCN)c2c1- InChIKey
JTEJPPKMYBDEMY-UHFFFAOYSA-N- Summenformel
- C11H14N2O
- Durchschnittliche Molmasse
- 190,24 g/mol
- Monoisotopische Masse
- 190,11061307
Überblick
5-methoxytryptamine is a member of the class of tryptamines that is the methyl ether derivative of serotonin. It has a role as a 5-hydroxytryptamine 2B receptor agonist, a 5-hydroxytryptamine 2C receptor agonist, a 5-hydroxytryptamine 2A receptor agonist, an antioxidant, a serotonergic agonist, a neuroprotective agent, a radiation protective agent, a mouse metabolite, a cardioprotective agent and a human metabolite. It is a member of tryptamines, an aromatic ether and a primary amino compound. It is functionally related to a serotonin. It is a conjugate base of a 5-methoxytryptamine(1+).
Namen und Bezeichner
- Bevorzugter Name
- 5-Methoxytryptamine
- IUPAC
- 2-(5-methoxy-1H-indol-3-yl)ethanamine
- Lokaler Name
- 2-(5-Methoxyindol-3-yl)ethylamin
- Englischer Name
- 5-Methoxytryptamine
- Summenformel
- C11H14N2O
- Molmasse
- 190.24
Namen und Synonyme
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Datenbank-Bezeichner
- CAS
608-07-1- PubChem CID
- 1833
- DTXSID
DTXSID60209638- ChEMBL
CHEMBL8165- ChEBI
CHEBI:2089- UNII
- 3VMW6141KC
- EC Number
- 210-153-7
- Nikkaji
- J7.009B
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 0,5
- Polarare Oberfläche (TPSA)
- 51 Ų
- H-Brücken-Donoren
- 2
- H-Brücken-Akzeptoren
- 2
- Frei drehbare Bindungen
- 3
- Schwere Atome
- 14
- Formalladung
- 0
- Komplexität
- 186
Experimentelle und physikochemische Eigenschaften
Collision Cross Section
143.3 Ų [M+H]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]
142.7 Ų [M+Na]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]
141.18 Ų [M-H]- [CCS Type: DT; Method: single field calibrated with Agilent tune mix (Agilent)]
Physikochemische Eigenschaften
- Schmelzpunkt
- 121 · 121-123 °C (lit.)
- Siedepunkt
- 325.75 °C · 325.75°C (rough estimate)
- Dichte
- 1.0815 · 1.0815 (rough estimate)
- Brechungsindex
- 1.57 · 1.5700 (estimate)
- storage temp.
- 2 · 2-8°C
- Löslichkeit
- Chloroform (Slightly), Methanol (Slightly)
- pka
- 16.91 · 16.91±0.30(Predicted)
- Aggregatzustand
- crystalline
- Farbe
- white
- Merck
- 13 · 13,6032
- BRN
- 145587 · 145587
- InChI
- InChI=1S/C11H14N2O/c1-14-9-2-3-11-10(6-9)8(4-5-12)7-13-11/h2-3,6-7,13H,4-5,12H2,1H3
- InChIKey
- JTEJPPKMYBDEMY-UHFFFAOYSA-N
- SMILES
- N1C2=C(C=C(OC)C=C2)C(CCN)=C1
- CAS Datenbank
- 608 · 608-07-1(CAS DataBase Reference)
- NIST chemische Informationen
- 5 · 5-Methoxytryptamine(608-07-1)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
This chemical does not meet GHS hazard criteria for 2% (1 of 49) of reports.
Warning
H302 (95.9%): Harmful if swallowed [Warning Acute toxicity, oral]
P264, P270, P301+P317, P330, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 49 reports by companies from 5 notifications to the ECHA C&L Inventory.
Gefahrenhinweise
Sicherheitsdaten
- F
- 8
- wgk
- 3
- hs_code
- 29339900
- RTECS-Nr.
- NL4110000
- risk_code
- 22-36/37/38-20/21/22
- Toxizität
- LD50 intraperitoneal in mouse: 176mg/kg
- hazard_code
- Xn
- safety_code
- 36-26
- Speicherklasse
- 11 - Combustible Solids
- Hazard Classifications
- Acute Tox. 4 Oral
Chemie und Industrie
Pharmakologische Informationen
Anwendungen
Beschreibung5-Methoxytryptamine (5-MT), also known as mexamine, is a tryptamine derivative closely related to the neurotransmitters serotonin and melatonin. 5-MT has been shown to occur naturally in the body in low levels.It is biosynthesized via the deacetylation of melatonin in the pineal gland.The protective effect of 5-methoxytryptamine (a metabolite of melatonin) in human keratinocytes against ultraviolet B (UVB) radiation was studied.Melatonin and its metabolites ameliorate ultraviolet B-induced damage in human epidermal keratinocytes.
Verwenden5-Methoxytryptamine (Mexamine, Methoxytryptamine) is a tryptamine derivative that is closely related to the neurotransmitter Melatonin (M215000) and Serotonin (S274980). It acts as a full agonist at the 5-HT1, 5-HT2, 5-HT4, 5-HT6, and 5-HT7 receptors but has no affinity for the 5-HT3 receptor.
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Ergänzende Hinweise
DefinitionChEBI: 5-methoxytryptamine is a member of the class of tryptamines that is the methyl ether derivative of serotonin. It has a role as a serotonergic agonist, a human metabolite, a mouse metabolite, a 5-hydroxytryptamine 2A receptor agonist, a 5-hydroxytryptamine 2C receptor agonist, a 5-hydroxytryptamine 2B receptor agonist, an antioxidant, a radiation protective agent, a neuroprotective agent and a cardioprotective agent. It is a member of tryptamines, an aromatic ether and a primary amino compound. It derives from a serotonin. It is a conjugate base of a 5-methoxytryptamine(1+).
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