| Weight | 217.356 g/mol |
|---|---|
| Formula | C15H23N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 5 |
Prolintane (493-92-5)
1-(alpha-propylphenethyl)pyrrolidine · Promotil · phenylpyrrolidinylpentan
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- Wakefullness and reduced rapid eye movement sleep: studies with prolintane and pemoline. (British Journal of Clinical Pharmacology, 1980)
- Metabolism of a pharmacologically active pyrrolidine derivative (prolintane) by lactam formation. (Cellular and Molecular Life Sciences, 1972)
- A new stimulant, prolintane hydrochloride, compared with dextroamphetamine in fatigued volunteers. (The Journal of clinical pharmacology and the journal of new drugs, 1970)
- The effect of methylphenidate and prolintane on the metabolism of ethyl biscoumacetate (Clinical Pharmacology & Therapeutics, 1971)
- Metabolism of Drugs. LXXVI. The Metabolic Fate of Prolintane in Rabbits (Chemical & Pharmaceutical Bulletin, 1972)
- Comparison of the acute physical and mental effects of ephedrine, fenfluramine, phentermine and prolintane. (Methods and Findings in Experimental and Clinical Pharmacology, 1984)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1-(alpha-propylphenethyl)pyrrolidine
- Promotil
- phenylpyrrolidinylpentan
- prolintane hydrochloride
- Katovit
-
SMILESCCCC(CC1=CC=CC=C1)N2CCCC2
-
InChIKeyOJCPSBCUMRIPFL-UHFFFAOYSA-N
- Pubchem - Prolintane
- Wikipedia - prolintane
Prolintane (Catovit, Katovit, Promotil, Villescon) is a stimulant and norepinephrine-dopamine reuptake inhibitor developed in the 1950s. It is closely related in chemical structure to other drugs such as pyrovalerone, MDPV, and propylhexedrine and it has a similar mechanism of action. Many cases of prolintane abuse have been reported.
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