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Prolintane

From Wikipedia, the free encyclopedia
Stimulant and NDRI drug
Pharmaceutical compound
Prolintane
Clinical data
Trade namesCatovit, Katovit, Promotil, Villescon
Routes of
administration
By mouth,intranasal,rectal
Drug classStimulant;Norepinephrine–dopamine reuptake inhibitor (NDRI)
ATC code
Legal status
Legal status
Identifiers
  • 1-(1-phenylpentan-2-yl)pyrrolidine
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.007.077Edit this at Wikidata
Chemical and physical data
FormulaC15H23N
Molar mass217.356 g·mol−1
3D model (JSmol)
Melting point133 °C (271 °F)
Boiling point153 °C (307 °F)
  • CCCC(N1CCCC1)CC2=CC=CC=C2
  • 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 checkY
  • Key:OJCPSBCUMRIPFL-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Prolintane is acentral nervous system (CNS)stimulant[2] andnorepinephrine–dopamine reuptake inhibitor (NDRI) of thephenylalkylpyrrolidine family developed in the 1950s.[3] Being anamphetamine derivative, it is closely related inchemical structure to other drugs such aspyrovalerone,MDPV, andpropylhexedrine, and has a similarmechanism of action.[4] Many cases of prolintaneabuse have been reported.[5]

Under the brand nameKatovit, prolintane was commercialized by the Spanish pharmaceutical company FHER until 2001. It was most often used by students and workers as a stimulant to provide energy and increase alertness and concentration.[medical citation needed]

See also

[edit]

References

[edit]
  1. ^Anvisa (2023-03-31)."RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 784 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese).Diário Oficial da União (published 2023-04-04).Archived from the original on 2023-08-03. Retrieved2023-08-16.
  2. ^Hollister LE, Gillespie HK (March–April 1970). "A new stimulant, prolintane hydrochloride, compared with dextroamphetamine in fatigued volunteers".The Journal of Clinical Pharmacology and the Journal of New Drugs.10 (2):103–9.doi:10.1177/009127007001000205.PMID 4392006.
  3. ^GB Patent 807835
  4. ^Nicholson AN, Stone BM, Jones MM (November 1980)."Wakefullness and reduced rapid eye movement sleep: studies with prolintane and pemoline".British Journal of Clinical Pharmacology.10 (5):465–72.doi:10.1111/j.1365-2125.1980.tb01790.x.PMC 1430138.PMID 7437258.
  5. ^Kyle PB, Daley WP (September 2007)."Domestic abuse of the European rave drug prolintane".Journal of Analytical Toxicology.31 (7):415–8.doi:10.1093/jat/31.7.415.PMID 17725890.
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