Skip to content
prolintane

Structure via PubChem · Public domain (PubChem)

EntityQ1653730· pop 11· linked from 1,661 articles

prolintane

Sign in to save

Prolintane is a central nervous system (CNS) stimulant and norepinephrine–dopamine reuptake inhibitor (NDRI) of the phenylalkylpyrrolidine family developed in the 1950s. 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. Many cases of prolintane abuse have been reported.

Chemical data

Formula
C15H23N
Molecular weight
217.35 g/mol
IUPAC name
1-(1-phenylpentan-2-yl)pyrrolidine

via PubChem

Drug data · ChEMBL

Max clinical phase
Phase 2
Molecule type
Small molecule
Indications
attention deficit hyperactivity disorder

via ChEMBL · EBI

~1 min read

Encyclopedic overview

2 sections
Contents
  • See also
  • References

Prolintane is a central nervous system (CNS) stimulant and norepinephrine–dopamine reuptake inhibitor (NDRI) of the phenylalkylpyrrolidine family developed in the 1950s. 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. Many cases of prolintane abuse have been reported.

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. Prolintane and substituted prolintane analogs (fluoro and methyl) show DAT and NET inhibition in the low nano molecular range, which is consistent with NDRI psychostimulants such a methylphenidate. In addition 4-substituted analogs have SERT inhibition which correlates with amphetamine SAR such as fenfluramine. == See also == α-PVP (β-ketone-prolintane, prolintanone) Methylenedioxypyrovalerone (MDPV) Pyrovalerone (Centroton, Thymergix) Phenylpropylaminopentane (PPAP)

Excerpted from Wikipedia’s “prolintane” article, available under the CC BY-SA 4.0 licence.