| Weight | 174.247 g/mol |
|---|---|
| Formula | C11H14N2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
3-(2-Methylaminoethyl)indole (61-49-4, 942-27-8)
N-methyltryptamine hydrochloride · N-methyltryptamine · N-methyltryptamine oxalate
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- Sigma-Aldrich - Search for 3-(2-Methylaminoethyl)indole
- Fisher Scientific - Search for 3-(2-Methylaminoethyl)indole
- TCI - Search for 3-(2-Methylaminoethyl)indole
- The Chemistry of Indoles. CIII. 1) Simple Syntheses of Serotonin, N-Methylserotonin, Bufotenine, 5-Methoxy-N-methyltryptamine, Bufobutanoic Acid, N-(Indol-3-yl)methyl-5-methoxy-N-methyltryptamine, and Lespedamine Based on 1-Hydroxyindole Chemistry (Chemical & Pharmaceutical Bulletin, 2001)
- Sensitive determination of alpha-methyltryptamine (AMT) and 5-methoxy-N,N-diisopropyltryptamine (5MeO-DIPT) in whole blood and urine using gas chromatography-mass spectrometry (Journal of Chromatography B, 2005)
- 428. 5-Methoxy-N-methyltryptamine: a new indole alkaloid from Phalaris arundinacea L. (Journal of The Chemical Society (resumed), 1958)
- The relationship between the metabolic fate and pharmacological action of 5-methoxy-N-methyltryptamine (Biochemical Pharmacology, 1964)
- Further characterization and quantitative determination of 5-methoxy-N-methyltryptamine in Phalaris arundinacea (Phytochemistry, 1977)
- CALYCANTHINE II. THE DEGRADATION OF CALYCANTHINE TO N-METHYLTRYPTAMINE (Canadian journal of research, 1931)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - N-methyltryptamine hydrochloride
- N-methyltryptamine
- N-methyltryptamine oxalate
-
SMILESCNCCC1=CNC2=CC=CC=C21
-
InChIKeyNCIKQJBVUNUXLW-UHFFFAOYSA-N
- Pubchem - 3-(2-Methylaminoethyl)indole
- Wikipedia - N-methyltryptamine
N-Methyltryptamine (NMT) is a member of the substituted tryptamine chemical class and a natural product which is biosynthesized in the human body from tryptamine by certain N-methyltransferase enzymes, such as indolethylamine N-methyltransferase. It is a common component in human urine. NMT is an alkaloid derived from L-tryptophan that has been found in the bark, shoots and leaves of several plant genera, including Virola, Acacia, Mimosa, and Desmanthusoften together with the related compounds N,N-dimethyltryptamine (DMT) and 5-methoxy-N,N-dimethyltryptamine (5-MeO-DMT).
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