Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C15H23N |
| Molecular Weight | 217.3498 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCC(CC1=CC=CC=C1)N2CCCC2
InChI
InChIKey=OJCPSBCUMRIPFL-UHFFFAOYSA-N
InChI=1S/C15H23N/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
| Molecular Formula | C15H23N |
| Molecular Weight | 217.3498 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
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 |
|---|---|---|
| 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. | 2010-01-04 |
|
| Domestic abuse of the European rave drug prolintane. | 2007-09 |
|
| [Sleeplessness. Helping with paradoxical medication]. | 2005-12-08 |
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| Application of comprehensive two-dimensional gas chromatography to drugs analysis in doping control. | 2003-06-06 |
|
| Visual hallucinations induced by the combination of prolintane and diphenhydramine. | 2002-01 |
|
| [New drugs at "rave parties": ketamine and prolintane]. | 2002 |
| Substance Class |
Chemical
Created
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admin
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Edited
Mon Mar 31 19:38:27 GMT 2025
by
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Mon Mar 31 19:38:27 GMT 2025
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EM4YZW677H
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Validated (UNII)
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WHO-ATC |
N06BX14
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WHO-VATC |
QN06BX14
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| Code System | Code | Type | Description | ||
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PROLINTANE
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SUB10083MIG
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493-92-5
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100000081144
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m9166
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1171
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140145-74-0
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EM4YZW677H
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DB13438
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DTXSID70862031
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34604
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C005598
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C170358
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14592
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CHEMBL2111047
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2283
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207-784-5
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SALT/SOLVATE -> PARENT |
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METABOLITE -> PARENT |
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ACTIVE MOIETY |