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Details

Stereochemistry RACEMIC
Molecular Formula C16H16ClNO3
Molecular Weight 305.756
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLOFEVERINE

SMILES

OC1=CC2=C(C=C1O)C(COC3=CC=C(Cl)C=C3)NCC2

InChI

InChIKey=GVALVWDQPXGPCE-UHFFFAOYSA-N
InChI=1S/C16H16ClNO3/c17-11-1-3-12(4-2-11)21-9-14-13-8-16(20)15(19)7-10(13)5-6-18-14/h1-4,7-8,14,18-20H,5-6,9H2

HIDE SMILES / InChI

Molecular Formula C16H16ClNO3
Molecular Weight 305.756
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Clofeverine is a compound synthesized by the Japanese company Fujisawa Pharmaceutical. Clofeverine is a highly selective relaxant for gastrointestinal smooth muscles with a beta-receptor stimulative nature. On isolated ileum, the inhibitory effect of clofeverine for spontaneous motility was comparable to that of isoproterenol and 100 times higher than that of papaverine.

Approval Year

Substance Class Chemical
Created
by admin
on Wed Apr 02 06:52:42 GMT 2025
Edited
by admin
on Wed Apr 02 06:52:42 GMT 2025
Record UNII
584A0O55XM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
6,7-ISOQUINOLINEDIOL, 1-((4-CHLOROPHENOXY)METHYL)-1,2,3,4-TETRAHYDRO-
Preferred Name English
CLOFEVERINE
INN  
INN  
Official Name English
1-((P-CHLOROPHENOXY)METHYL)-1,2,3,4-TETRAHYDRO-6,7-ISOQUINOLINEDIOL
Common Name English
clofeverine [INN]
Common Name English
CLOFEVERINE [JAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C66880
Created by admin on Wed Apr 02 06:52:42 GMT 2025 , Edited by admin on Wed Apr 02 06:52:42 GMT 2025
Code System Code Type Description
FDA UNII
584A0O55XM
Created by admin on Wed Apr 02 06:52:42 GMT 2025 , Edited by admin on Wed Apr 02 06:52:42 GMT 2025
PRIMARY
NCI_THESAURUS
C77986
Created by admin on Wed Apr 02 06:52:42 GMT 2025 , Edited by admin on Wed Apr 02 06:52:42 GMT 2025
PRIMARY
SMS_ID
100000084313
Created by admin on Wed Apr 02 06:52:42 GMT 2025 , Edited by admin on Wed Apr 02 06:52:42 GMT 2025
PRIMARY
INN
3531
Created by admin on Wed Apr 02 06:52:42 GMT 2025 , Edited by admin on Wed Apr 02 06:52:42 GMT 2025
PRIMARY
ChEMBL
CHEMBL2106010
Created by admin on Wed Apr 02 06:52:42 GMT 2025 , Edited by admin on Wed Apr 02 06:52:42 GMT 2025
PRIMARY
PUBCHEM
194700
Created by admin on Wed Apr 02 06:52:42 GMT 2025 , Edited by admin on Wed Apr 02 06:52:42 GMT 2025
PRIMARY
EPA CompTox
DTXSID70969433
Created by admin on Wed Apr 02 06:52:42 GMT 2025 , Edited by admin on Wed Apr 02 06:52:42 GMT 2025
PRIMARY
CAS
54340-63-5
Created by admin on Wed Apr 02 06:52:42 GMT 2025 , Edited by admin on Wed Apr 02 06:52:42 GMT 2025
PRIMARY
EVMPD
SUB06703MIG
Created by admin on Wed Apr 02 06:52:42 GMT 2025 , Edited by admin on Wed Apr 02 06:52:42 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY