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Details

Stereochemistry ACHIRAL
Molecular Formula C18H19ClN2
Molecular Weight 298.81
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CYCLIRAMINE

SMILES

CN1CCC(CC1)=C(C2=CC=C(Cl)C=C2)C3=NC=CC=C3

InChI

InChIKey=HZNVLDCWAVIXRK-UHFFFAOYSA-N
InChI=1S/C18H19ClN2/c1-21-12-9-15(10-13-21)18(17-4-2-3-11-20-17)14-5-7-16(19)8-6-14/h2-8,11H,9-10,12-13H2,1H3

HIDE SMILES / InChI
Cycliramine is a substituted piperidine derivative discovered by Schering Corp. The drug is claimed to have antihistamine, antispasmodic, antiacetylcholine and analgesic activity.

Approval Year

Name Type Language
CYCLIRAMINE
INN  
INN  
Official Name English
4-(P-CHLORO-.ALPHA.-2-PYRIDYLBENZYLIDENE)-1-METHYLPIPERIDINE
Preferred Name English
cycliramine [INN]
Common Name English
PYRIDINE, 2-((4-CHLOROPHENYL)(1-METHYL-4-PIPERIDINYLIDENE)METHYL)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29578
Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025
Code System Code Type Description
ChEMBL
CHEMBL1618128
Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025
PRIMARY
EVMPD
SUB06846MIG
Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025
PRIMARY
SMS_ID
100000083748
Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025
PRIMARY
PUBCHEM
22017
Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025
PRIMARY
CAS
47128-12-1
Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025
PRIMARY
NCI_THESAURUS
C87479
Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025
PRIMARY
FDA UNII
N61YTN00CK
Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025
PRIMARY
INN
1622
Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025
PRIMARY
EPA CompTox
DTXSID50963752
Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025
PRIMARY