| Weight | 215.34 g/mol |
|---|---|
| Formula | C15H21N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
Fencamfamin (1209-98-9)
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- Amphetamine, mazindol, and fencamfamin in narcolepsy. (BMJ, 1985)
- Interactions of oestrogenic and progestational steroids with dexamphetamine and fencamfamin in mice. (British Journal of Pharmacology, 1969)
- Das Reserpin-Parkinsonoid beim Schimpansen und seine Behandlung mit Fencamfamin (Naunyn-schmiedebergs Archives of Pharmacology, 1968)
- A Controlled Out-Patient Trial with Fencamfamin (British Journal of Psychiatry, 1964)
- Fencamfamin Versus Placebo in Depressed Patients (The Journal of new drugs, 1964)
- An EEG study of 2-phenyl-3-ethylaminobicyclo-(2,2,1)-heptane HCL (Fencamfamin hydrochloride) (Life Sciences, 1966)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCNC1C2CCC(C2)C1C3=CC=CC=C3
-
InChIKeyIKFBPFGUINLYQI-UHFFFAOYSA-N
- Pubchem - Fencamfamin
- Wikipedia - fencamfamin
Fencamfamin (INN), also known as fencamfamine or by the brand names Glucoenergan and Reactivan, is a stimulant which was developed by Merck in the 1960s.
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