| Weight | 310.441 g/mol |
|---|---|
| Formula | C20H26N2O |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
Endabuse (83-74-9)
Ibogaine · NIH-10567 · 12 Methoxyibogamine
Score:
#333 in Neuroscience
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#1509 in Biology
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#1772 in Chemistry
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- Noncompetitive Functional Inhibition at Diverse, Human Nicotinic Acetylcholine Receptor Subtypes by Bupropion, Phencyclidine, and Ibogaine (Journal of Pharmacology and Experimental Therapeutics, 1999)
- Degeneration of purkinje cells in parasagittal zones of the cerebellar vermis after treatment with ibogaine or harmaline (Neuroscience, 1993)
- Effects and aftereffects of ibogaine on morphine self-administration in rats (European Journal of Pharmacology, 1991)
- Inhibitory effects of ibogaine on cocaine self-administration in rats (European Journal of Pharmacology, 1993)
- 100 years of ibogaine: neurochemical and pharmacological actions of a putative anti-addictive drug. (Pharmacological Reviews, 1995)
- Glial Cell Line-Derived Neurotrophic Factor Mediates the Desirable Actions of the Anti-Addiction Drug Ibogaine against Alcohol Consumption (The Journal of Neuroscience, 2005)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Ibogaine
- NIH-10567
- 12 Methoxyibogamine
- NIH10567
- 12-Methoxyibogamine
- NIH 10567
-
SMILESCCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC
-
InChIKeyHSIBGVUMFOSJPD-UHFFFAOYSA-N
- Pubchem - Endabuse
- Wikipedia - ibogaine
Ibogaine is a naturally occurring psychoactive substance found in plants in the Apocynaceae family such as Tabernanthe iboga, Voacanga africana and Tabernaemontana undulata. It is a psychedelic with dissociative properties. Ibogaine is not currently approved for any medical uses in the United States.
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