Drug Information

Drug General Information
Drug ID
D03EMO
Former ID
DNC007030
Drug Name
(RS/SR)-2-[1-(4-chlorophenyl)hexyl]piperidine
Drug Type
Small molecular drug
Indication Discovery agent Investigative [528619]
Structure
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2D MOL

3D MOL
Formula
C17H26ClN
Canonical SMILES
CCCCCC(C1CCCCN1)C2=CC=C(C=C2)Cl
InChI
1S/C17H26ClN/c1-2-3-4-7-16(17-8-5-6-13-19-17)14-9-11-15(18)12-10-14/h9-12,16-17,19H,2-8,13H2,1H3
InChIKey
PAZWPXLTYQROKI-UHFFFAOYSA-N
PubChem Compound ID
16102754
Target and Pathway
Target(s) Sodium-dependent dopamine transporter Target Info Inhibitor [528619]
KEGG Pathway Dopaminergic synapse
Parkinson's disease
Cocaine addiction
Amphetamine addiction
Alcoholism
PANTHER Pathway Adrenaline and noradrenaline biosynthesis
Parkinson disease
Dopamine receptor mediated signaling pathway
Pathway Interaction Database Alpha-synuclein signaling
Reactome Na+/Cl- dependent neurotransmitter transporters
WikiPathways Monoamine Transport
NRF2 pathway
Dopaminergic Neurogenesis
Parkinsons Disease Pathway
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds
Neurotransmitter Clearance In The Synaptic Cleft
References
Ref 528619J Med Chem. 2007 Jan 25;50(2):219-32.Slow-onset, long-duration, alkyl analogues of methylphenidate with enhanced selectivity for the dopamine transporter.
Ref 528619J Med Chem. 2007 Jan 25;50(2):219-32.Slow-onset, long-duration, alkyl analogues of methylphenidate with enhanced selectivity for the dopamine transporter.

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