Details
Stereochemistry | RACEMIC |
Molecular Formula | C15H23N.ClH |
Molecular Weight | 253.811 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CCCC(CC1=CC=CC=C1)N2CCCC2
InChI
InChIKey=FKOFBBOQSMUYHD-UHFFFAOYSA-N
InChI=1S/C15H23N.ClH/c1-2-8-15(16-11-6-7-12-16)13-14-9-4-3-5-10-14;/h3-5,9-10,15H,2,6-8,11-13H2,1H3;1H
Prolintane is an amphetamine-related CNS stimulant and norepinephrine-dopamine reuptake inhibitor that has been used for the treatment of narcolepsy and attention deficit hyperactivity disorder in Africa, Australia, and Europe. Under the trade-name "Katovit", prolintane was commercialized by the Spanish pharmaceutical company, FHER. Katovit was sold until 2001 and was most often used by students and workers as a stimulant to provide energy, promote alertness and concentration. The use of prolintane as a doping agent in athletics has been noted worldwide. Prolintane, like many amphetamine derivatives, increases the concentration of dopamine in the synaptic cleft. Adverse effects of the drug include insomnia, nervousness, irritability, and dizziness. Overdoses of prolintane may cause hallucinations, psychosis, and death. Individuals who abuse prolintane risk becoming dependent as tolerance may develop.
Approval Year
PubMed
Title | Date | PubMed |
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[New drugs at "rave parties": ketamine and prolintane]. | 2002 |
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Application of comprehensive two-dimensional gas chromatography to drugs analysis in doping control. | 2003 Jun 6 |
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[Sleeplessness. Helping with paradoxical medication]. | 2005 Dec 8 |
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Domestic abuse of the European rave drug prolintane. | 2007 Sep |
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Simultaneous analysis of fourteen tertiary amine stimulants in human urine for doping control purposes by liquid chromatography-tandem mass spectrometry and gas chromatography-mass spectrometry. | 2010 Jan 4 |
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235831
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169914
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SUB04064MIG
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1211-28-5
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14591
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C005598
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YEG124534B
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100000085104
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CHEMBL2111047
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C170357
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214-917-0
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m9166
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141996-82-9
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SUPERSEDED |
ACTIVE MOIETY
SUBSTANCE RECORD