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

Details

Stereochemistry RACEMIC
Molecular Formula C20H26ClNO.ClH
Molecular Weight 368.34
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLOFENETAMINE HYDROCHLORIDE

SMILES

Cl.CCN(CC)CCOC(C)(C1=CC=CC=C1)C2=CC=C(Cl)C=C2

InChI

InChIKey=YYLMTOXXJALHSQ-UHFFFAOYSA-N
InChI=1S/C20H26ClNO.ClH/c1-4-22(5-2)15-16-23-20(3,17-9-7-6-8-10-17)18-11-13-19(21)14-12-18;/h6-14H,4-5,15-16H2,1-3H3;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 C20H26ClNO
Molecular Weight 331.88
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Clofenetamine is a haloxanthine antihistamine compound discovered by Searle & Co in the 1940s.

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 17:26:46 GMT 2023
Edited
by admin
on Fri Dec 15 17:26:46 GMT 2023
Record UNII
HV7XNV10CB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLOFENETAMINE HYDROCHLORIDE
WHO-DD  
Common Name English
ETHANAMINE, 2-(1-(4-CHLOROPHENYL)-1-PHENYLETHOXY)-N,N-DIETHYL-,HYDROCHLORIDE
Common Name English
2-(P-CHLORO-.ALPHA.-METHYL-.ALPHA.-PHENYLBENZYLOXY)TRIETHYLAMINE HYDROCHLORIDE
Common Name English
CLOFENETAMINE HCL
Common Name English
Clofenetamine hydrochloride [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C66880
Created by admin on Fri Dec 15 17:26:46 GMT 2023 , Edited by admin on Fri Dec 15 17:26:46 GMT 2023
Code System Code Type Description
FDA UNII
HV7XNV10CB
Created by admin on Fri Dec 15 17:26:46 GMT 2023 , Edited by admin on Fri Dec 15 17:26:46 GMT 2023
PRIMARY
CAS
2019-16-1
Created by admin on Fri Dec 15 17:26:46 GMT 2023 , Edited by admin on Fri Dec 15 17:26:46 GMT 2023
PRIMARY
PUBCHEM
71811
Created by admin on Fri Dec 15 17:26:46 GMT 2023 , Edited by admin on Fri Dec 15 17:26:46 GMT 2023
PRIMARY
EVMPD
SUB01356MIG
Created by admin on Fri Dec 15 17:26:46 GMT 2023 , Edited by admin on Fri Dec 15 17:26:46 GMT 2023
PRIMARY
SMS_ID
100000087954
Created by admin on Fri Dec 15 17:26:46 GMT 2023 , Edited by admin on Fri Dec 15 17:26:46 GMT 2023
PRIMARY
EPA CompTox
DTXSID40942253
Created by admin on Fri Dec 15 17:26:46 GMT 2023 , Edited by admin on Fri Dec 15 17:26:46 GMT 2023
PRIMARY
NCI_THESAURUS
C77985
Created by admin on Fri Dec 15 17:26:46 GMT 2023 , Edited by admin on Fri Dec 15 17:26:46 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY