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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
Structure of PROLINTANE HYDROCHLORIDE

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

HIDE SMILES / InChI

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 ( + / - )

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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

PubMed

TitleDatePubMed
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
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
by admin
on Mon Mar 31 17:46:12 GMT 2025
Edited
by admin
on Mon Mar 31 17:46:12 GMT 2025
Record UNII
YEG124534B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PROLINTANE HYDROCHLORIDE
MART.   MI   USAN   WHO-DD  
USAN  
Official Name English
CATOVITAN
Preferred Name English
PROLINTANE HYDROCHLORIDE [USAN]
Common Name English
PYRROLIDINE, 1-(1-(PHENYLMETHYL)BUTYL)-, HYDROCHLORIDE
Systematic Name English
VILESCON
Brand Name English
KATOVIT
Brand Name English
Prolintane hydrochloride [WHO-DD]
Common Name English
KATOVIT N
Brand Name English
PROMOTIL
Brand Name English
PROLINTANE HYDROCHLORIDE [MART.]
Common Name English
PROLINTANE HYDROCHLORIDE [MI]
Common Name English
1-(?-Propylphenethyl)pyrrolidine hydrochloride
Systematic Name English
SP-732
Code English
VILLESCON
Brand Name English
NSC-169914
Code English
PYRROLIDINE, 1-(1-BENZYLBUTYL)-, HYDROCHLORIDE
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID201350200
Created by admin on Mon Mar 31 17:46:12 GMT 2025 , Edited by admin on Mon Mar 31 17:46:12 GMT 2025
PRIMARY
RXCUI
235831
Created by admin on Mon Mar 31 17:46:12 GMT 2025 , Edited by admin on Mon Mar 31 17:46:12 GMT 2025
PRIMARY RxNorm
NSC
169914
Created by admin on Mon Mar 31 17:46:12 GMT 2025 , Edited by admin on Mon Mar 31 17:46:12 GMT 2025
PRIMARY
EVMPD
SUB04064MIG
Created by admin on Mon Mar 31 17:46:12 GMT 2025 , Edited by admin on Mon Mar 31 17:46:12 GMT 2025
PRIMARY
CAS
1211-28-5
Created by admin on Mon Mar 31 17:46:12 GMT 2025 , Edited by admin on Mon Mar 31 17:46:12 GMT 2025
PRIMARY
PUBCHEM
14591
Created by admin on Mon Mar 31 17:46:12 GMT 2025 , Edited by admin on Mon Mar 31 17:46:12 GMT 2025
PRIMARY
MESH
C005598
Created by admin on Mon Mar 31 17:46:12 GMT 2025 , Edited by admin on Mon Mar 31 17:46:12 GMT 2025
PRIMARY
FDA UNII
YEG124534B
Created by admin on Mon Mar 31 17:46:12 GMT 2025 , Edited by admin on Mon Mar 31 17:46:12 GMT 2025
PRIMARY
SMS_ID
100000085104
Created by admin on Mon Mar 31 17:46:12 GMT 2025 , Edited by admin on Mon Mar 31 17:46:12 GMT 2025
PRIMARY
ChEMBL
CHEMBL2111047
Created by admin on Mon Mar 31 17:46:12 GMT 2025 , Edited by admin on Mon Mar 31 17:46:12 GMT 2025
PRIMARY
NCI_THESAURUS
C170357
Created by admin on Mon Mar 31 17:46:12 GMT 2025 , Edited by admin on Mon Mar 31 17:46:12 GMT 2025
PRIMARY
ECHA (EC/EINECS)
214-917-0
Created by admin on Mon Mar 31 17:46:12 GMT 2025 , Edited by admin on Mon Mar 31 17:46:12 GMT 2025
PRIMARY
MERCK INDEX
m9166
Created by admin on Mon Mar 31 17:46:12 GMT 2025 , Edited by admin on Mon Mar 31 17:46:12 GMT 2025
PRIMARY Merck Index
CAS
141996-82-9
Created by admin on Mon Mar 31 17:46:12 GMT 2025 , Edited by admin on Mon Mar 31 17:46:12 GMT 2025
SUPERSEDED
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