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Details

Stereochemistry ACHIRAL
Molecular Formula C17H11Cl3NO4S.Na.H2O
Molecular Weight 472.703
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ENOLICAM SODIUM

SMILES

O.[Na+].[O-]C1=C(CCS(=O)(=O)C2=C1C=C(Cl)C=C2)C(=O)NC3=CC=C(Cl)C(Cl)=C3

InChI

InChIKey=AVERBMQHYOZACV-UHFFFAOYSA-M
InChI=1S/C17H12Cl3NO4S.Na.H2O/c18-9-1-4-15-12(7-9)16(22)11(5-6-26(15,24)25)17(23)21-10-2-3-13(19)14(20)8-10;;/h1-4,7-8,22H,5-6H2,(H,21,23);;1H2/q;+1;/p-1

HIDE SMILES / InChI

Molecular Formula C17H12Cl3NO4S
Molecular Weight 432.705
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula HO
Molecular Weight 17.0073
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Enolicam (CGS 5391B) is a non-steroidal anti-inflammatory drug with combined cyclooxygenase and lipoxygenase inhibitory activity. It is able to trap oxygen radicals. Enolicam was effective in animal models of traumatic shock and osteoarthritis.

Approval Year

PubMed

PubMed

TitleDatePubMed
A new model of osteoarthritis in rabbits. II. Evaluation of anti-osteoarthritic effects of selected antirheumatic drugs administered systemically.
1983 Sep
Inhibitors of lipoxygenase products improve survival in traumatic shock.
1984 Oct
Diclofenac and enolicam as ocular anti-inflammatory drugs in rabbit corneal wound model.
1986 Spring
The amplified chemiluminescence test to characterize antirheumatic drugs as oxygen radical scavengers.
1987 Apr 1
Amiodarone causes acute oxidant lung injury in ventilated and perfused rabbit lungs.
1988 Jul
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:25:33 GMT 2023
Edited
by admin
on Fri Dec 15 15:25:33 GMT 2023
Record UNII
C3QYZ005LS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ENOLICAM SODIUM
USAN   WHO-DD  
USAN  
Official Name English
1-BENZOTHIEPIN-4-CARBOXAMIDE, 7-CHLORO-N-(3,4-DICHLOROPHENYL)-2,3-DIHYDRO-5-HYDROXY-, 1,1-DIOXIDE, MONOSODIUM SALT, MONOHYDRATE
Systematic Name English
3',4',7-TRICHLORO-2,3-DIHYDRO-5-HYDROXY-1-BENZOTHIEPIN-4-CARBOXANILIDE 1,1-DIOXIDE, MONOSODIUM SALT, MONOHYDRATE
Systematic Name English
Enolicam sodium [WHO-DD]
Common Name English
ENOLICAM SODIUM [USAN]
Common Name English
1-BENZOTHIEPIN-4-CARBOXAMIDE, 7-CHLORO-N-(3,4-DICHLOROPHENYL)-2,3-DIHYDRO-5-HYDROXY-, 1,1-DIOXIDE, SODIUM SALT, HYDRATE (1:1:1)
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C257
Created by admin on Fri Dec 15 15:25:33 GMT 2023 , Edited by admin on Fri Dec 15 15:25:33 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C73086
Created by admin on Fri Dec 15 15:25:33 GMT 2023 , Edited by admin on Fri Dec 15 15:25:33 GMT 2023
PRIMARY
EPA CompTox
DTXSID30994367
Created by admin on Fri Dec 15 15:25:33 GMT 2023 , Edited by admin on Fri Dec 15 15:25:33 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110813
Created by admin on Fri Dec 15 15:25:33 GMT 2023 , Edited by admin on Fri Dec 15 15:25:33 GMT 2023
PRIMARY
CAS
73574-69-3
Created by admin on Fri Dec 15 15:25:33 GMT 2023 , Edited by admin on Fri Dec 15 15:25:33 GMT 2023
PRIMARY
FDA UNII
C3QYZ005LS
Created by admin on Fri Dec 15 15:25:33 GMT 2023 , Edited by admin on Fri Dec 15 15:25:33 GMT 2023
PRIMARY
PUBCHEM
23663945
Created by admin on Fri Dec 15 15:25:33 GMT 2023 , Edited by admin on Fri Dec 15 15:25:33 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
ANHYDROUS->SOLVATE
Related Record Type Details
ACTIVE MOIETY