U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C18H28ClNO.ClH
Molecular Weight 346.335
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLOFENCICLAN HYDROCHLORIDE

SMILES

Cl.CCN(CC)CCOC1(CCCCC1)C2=CC=C(Cl)C=C2

InChI

InChIKey=GHTNEJJXVUMOPX-UHFFFAOYSA-N
InChI=1S/C18H28ClNO.ClH/c1-3-20(4-2)14-15-21-18(12-6-5-7-13-18)16-8-10-17(19)11-9-16;/h8-11H,3-7,12-15H2,1-2H3;1H

HIDE SMILES / InChI

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

Molecular Formula C18H28ClNO
Molecular Weight 309.874
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Clofenciclan is a dopamine-releasing agent, developed by Boehringer & Soehne in the 1950s for the treatment of Parkinson's disease. Compared to other anti-parkinsonian drugs of the time, clofenciclan lacked peripheral anticholinergic properties and caused pronounced stimulation of the central nervous system.

Approval Year

Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:48:52 GMT 2025
Edited
by admin
on Mon Mar 31 18:48:52 GMT 2025
Record UNII
8FR9OY53P6
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLOFENCICLAN HYDROCHLORIDE
WHO-DD  
Common Name English
2-((1-(P-CHLOROPHENYL)CYCLOHEXYL)OXY)TRIETHYLAMINE HYDROCHLORIDE
Preferred Name English
Clofenciclan hydrochloride [WHO-DD]
Common Name English
ETHANAMINE, 2-((1-(4-CHLOROPHENYL)CYCLOHEXYL)OXY)-N,N-DIETHYL-, HYDROCHLORIDE (1:1)
Systematic Name English
CLOFENCICLAN HCL
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID80928172
Created by admin on Mon Mar 31 18:48:52 GMT 2025 , Edited by admin on Mon Mar 31 18:48:52 GMT 2025
PRIMARY
PUBCHEM
25903
Created by admin on Mon Mar 31 18:48:52 GMT 2025 , Edited by admin on Mon Mar 31 18:48:52 GMT 2025
PRIMARY
EVMPD
SUB01355MIG
Created by admin on Mon Mar 31 18:48:52 GMT 2025 , Edited by admin on Mon Mar 31 18:48:52 GMT 2025
PRIMARY
FDA UNII
8FR9OY53P6
Created by admin on Mon Mar 31 18:48:52 GMT 2025 , Edited by admin on Mon Mar 31 18:48:52 GMT 2025
PRIMARY
ECHA (EC/EINECS)
236-403-5
Created by admin on Mon Mar 31 18:48:52 GMT 2025 , Edited by admin on Mon Mar 31 18:48:52 GMT 2025
PRIMARY
SMS_ID
100000087951
Created by admin on Mon Mar 31 18:48:52 GMT 2025 , Edited by admin on Mon Mar 31 18:48:52 GMT 2025
PRIMARY
CAS
13352-70-0
Created by admin on Mon Mar 31 18:48:52 GMT 2025 , Edited by admin on Mon Mar 31 18:48:52 GMT 2025
PRIMARY
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ACTIVE MOIETY