Stimulant and NDRI drug
Pharmaceutical compound
Prolintane Trade names Catovit, Katovit, Promotil, Villescon Routes of administration By mouth , intranasal , rectal Drug class Stimulant ; Norepinephrine–dopamine reuptake inhibitor (NDRI)ATC code Legal status
1-(1-phenylpentan-2-yl)pyrrolidine
CAS Number PubChem CID ChemSpider UNII ChEMBL CompTox Dashboard (EPA ) ECHA InfoCard 100.007.077 Formula C 15 H 23 N Molar mass 217.356 g·mol−1 3D model (JSmol ) Melting point 133 °C (271 °F) Boiling point 153 °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
Y Key:OJCPSBCUMRIPFL-UHFFFAOYSA-N
Y
N Y (what is this?) (verify)
Prolintane is a central nervous system (CNS) stimulant [ 2] and norepinephrine–dopamine reuptake inhibitor (NDRI) of the phenylalkylpyrrolidine family developed in the 1950s.[ 3] Being an amphetamine derivative, it is closely related in chemical structure to other drugs such as pyrovalerone , MDPV , and propylhexedrine , and has a similar mechanism of action .[ 4] Many cases of prolintane abuse have been reported.[ 5]
Under the brand name Katovit , 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
References
^ 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. Retrieved 2023-08-16 .
^ 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 .
^ GB Patent 807835
^ 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 .
^ 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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