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Details

Stereochemistry RACEMIC
Molecular Formula C17H14O4
Molecular Weight 282.2907
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OXINDANAC

SMILES

OC(=O)C1CCC2=C1C=C(O)C(=C2)C(=O)C3=CC=CC=C3

InChI

InChIKey=XMTKXTUIUKKGIL-UHFFFAOYSA-N
InChI=1S/C17H14O4/c18-15-9-13-11(6-7-12(13)17(20)21)8-14(15)16(19)10-4-2-1-3-5-10/h1-5,8-9,12,18H,6-7H2,(H,20,21)

HIDE SMILES / InChI

Molecular Formula C17H14O4
Molecular Weight 282.2907
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Oxindanac, a non-steroidal anti-inflammatory drug, and is a weak cyclooxygenase inhibitor possessed antipyretic activity. This drug is used as a veterinary inflammatory drug. In addition, oxindanac was studied in phase III clinical trials for the treatment of rheumatic disorders. However, this study was discontinued.

Approval Year

PubMed

PubMed

TitleDatePubMed
The anti-oedematous efficacy of oxindanac equals that of paracetamol in acute postoperative inflammation; are weak cyclooxygenase inhibitors more effective than strong inhibitors?
1989
The use of intradermal carrageenan in calves to estimate the dose of oxindanac, a nonsteroidal anti-inflammatory drug.
1993 Oct
High performance liquid chromatography and pharmacokinetics of the non-steroidal anti-inflammatory drug oxindanac in calves.
1994 Jun
Patents

Patents

Sample Use Guides

Eight male volunteers receiving frusemide 40 mg b.d. were also given either oxindanac 300 mg b.d. or placebo in two consecutive periods separated by a treatment-free period, according to a randomized cross-over study design.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:55:46 GMT 2023
Edited
by admin
on Fri Dec 15 15:55:46 GMT 2023
Record UNII
ZY400R3BNT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
OXINDANAC
INN   MART.  
INN  
Official Name English
1H-INDENE-1-CARBOXYLIC ACID, 5-BENZOYL-2,3-DIHYDRO-6-HYDROXY-
Systematic Name English
CGP-6258
Code English
OXINDANAC [MART.]
Common Name English
oxindanac [INN]
Common Name English
5-BENZOYL-6-METHOXY-1-INDANCARBOXYLIC ACID
Systematic Name English
(±)-5-BENZOYL-6-HYDROXY-1-INDANCARBOXYLIC ACID
Systematic Name English
OXINDAZAC
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C257
Created by admin on Fri Dec 15 15:55:46 GMT 2023 , Edited by admin on Fri Dec 15 15:55:46 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID60867671
Created by admin on Fri Dec 15 15:55:46 GMT 2023 , Edited by admin on Fri Dec 15 15:55:46 GMT 2023
PRIMARY
ChEMBL
CHEMBL2107505
Created by admin on Fri Dec 15 15:55:46 GMT 2023 , Edited by admin on Fri Dec 15 15:55:46 GMT 2023
PRIMARY
FDA UNII
ZY400R3BNT
Created by admin on Fri Dec 15 15:55:46 GMT 2023 , Edited by admin on Fri Dec 15 15:55:46 GMT 2023
PRIMARY
EVMPD
SUB09532MIG
Created by admin on Fri Dec 15 15:55:46 GMT 2023 , Edited by admin on Fri Dec 15 15:55:46 GMT 2023
PRIMARY
MESH
C039724
Created by admin on Fri Dec 15 15:55:46 GMT 2023 , Edited by admin on Fri Dec 15 15:55:46 GMT 2023
PRIMARY
PUBCHEM
68879
Created by admin on Fri Dec 15 15:55:46 GMT 2023 , Edited by admin on Fri Dec 15 15:55:46 GMT 2023
PRIMARY
CAS
99910-69-7
Created by admin on Fri Dec 15 15:55:46 GMT 2023 , Edited by admin on Fri Dec 15 15:55:46 GMT 2023
SUPERSEDED
SMS_ID
100000083045
Created by admin on Fri Dec 15 15:55:46 GMT 2023 , Edited by admin on Fri Dec 15 15:55:46 GMT 2023
PRIMARY
NCI_THESAURUS
C66268
Created by admin on Fri Dec 15 15:55:46 GMT 2023 , Edited by admin on Fri Dec 15 15:55:46 GMT 2023
PRIMARY
INN
5804
Created by admin on Fri Dec 15 15:55:46 GMT 2023 , Edited by admin on Fri Dec 15 15:55:46 GMT 2023
PRIMARY
CAS
68548-99-2
Created by admin on Fri Dec 15 15:55:46 GMT 2023 , Edited by admin on Fri Dec 15 15:55:46 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY