Weight | 172.231 g/mol |
---|---|
Formula | C11H12N2 |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 2 |
Aromatic Rings | 2 |
Rotatable Bonds | 0 |
Tryptoline (16502-01-5)
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- Sigma-Aldrich - Tryptoline50.90 - 168.00 USD
- Fisher Scientific - Search for Tryptoline
- TCI - Search for Tryptoline
- Tryptoline formation by a preparation from brain with 5-methyltetrahydrofolic acid and tryptamine (Science, 1975)
- Tryptoline inhibition of serotonin uptake in rat forebrain homogenates. (Journal of Pharmacology and Experimental Therapeutics, 1976)
- Pharmacological properties of tetrahydronorharmane (tryptoline). (Naunyn-schmiedebergs Archives of Pharmacology, 1977)
- Dopamine release within forebrain sites perfused with tetrahydroisoquinolines or tryptoline in the rat. (Brain Research Bulletin, 1978)
- Concentrations of Tryptoline and Methtryptoline in Rat Brain (Journal of Neurochemistry, 1989)
- Scaffold Tailoring by a Newly Detected PictetSpenglerase Activity of Strictosidine Synthase: From the Common Tryptoline Skeleton to the Rare Piperazino-indole Framework (Journal of the American Chemical Society, 2012)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CNCC2=C1C3=CC=CC=C3N2
-
InChIKeyCFTOTSJVQRFXOF-UHFFFAOYSA-N
- Pubchem - Tryptoline
- Wikipedia - tryptoline
Tryptoline, also known as tetrahydro--carboline and tetrahydronorharmane, is a natural organic derivative of beta-carboline. It is an alkaloid chemically related to tryptamines. Derivatives of tryptoline have a variety of pharmacological properties and are known collectively as tryptolines.
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