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

Details

Stereochemistry RACEMIC
Molecular Formula C20H26ClNO
Molecular Weight 331.88
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLOFENETAMINE

SMILES

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

InChI

InChIKey=IKFQEQVEOQNTRJ-UHFFFAOYSA-N
InChI=1S/C20H26ClNO/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

HIDE SMILES / InChI

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 17:37:27 GMT 2023
Edited
by admin
on Fri Dec 15 17:37:27 GMT 2023
Record UNII
5YH9CQF0FP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLOFENETAMINE
INN   WHO-DD  
INN  
Official Name English
Clofenetamine [WHO-DD]
Common Name English
ETHANAMINE, 2-(1-(4-CHLOROPHENYL)-1-PHENYLETHOXY)-N,N-DIETHYL-
Systematic Name English
clofenetamine [INN]
Common Name English
2-(P-CHLORO-.ALPHA.-METHYL-.ALPHA.-PHENYLBENZYLOXY)TRIETHYLAMINE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C66880
Created by admin on Fri Dec 15 17:37:27 GMT 2023 , Edited by admin on Fri Dec 15 17:37:27 GMT 2023
Code System Code Type Description
INN
1183
Created by admin on Fri Dec 15 17:37:27 GMT 2023 , Edited by admin on Fri Dec 15 17:37:27 GMT 2023
PRIMARY
FDA UNII
5YH9CQF0FP
Created by admin on Fri Dec 15 17:37:27 GMT 2023 , Edited by admin on Fri Dec 15 17:37:27 GMT 2023
PRIMARY
EVMPD
SUB06699MIG
Created by admin on Fri Dec 15 17:37:27 GMT 2023 , Edited by admin on Fri Dec 15 17:37:27 GMT 2023
PRIMARY
EPA CompTox
DTXSID20862081
Created by admin on Fri Dec 15 17:37:27 GMT 2023 , Edited by admin on Fri Dec 15 17:37:27 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110777
Created by admin on Fri Dec 15 17:37:27 GMT 2023 , Edited by admin on Fri Dec 15 17:37:27 GMT 2023
PRIMARY
CAS
511-46-6
Created by admin on Fri Dec 15 17:37:27 GMT 2023 , Edited by admin on Fri Dec 15 17:37:27 GMT 2023
PRIMARY
SMS_ID
100000084291
Created by admin on Fri Dec 15 17:37:27 GMT 2023 , Edited by admin on Fri Dec 15 17:37:27 GMT 2023
PRIMARY
NCI_THESAURUS
C77984
Created by admin on Fri Dec 15 17:37:27 GMT 2023 , Edited by admin on Fri Dec 15 17:37:27 GMT 2023
PRIMARY
PUBCHEM
71812
Created by admin on Fri Dec 15 17:37:27 GMT 2023 , Edited by admin on Fri Dec 15 17:37:27 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY