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Details

Stereochemistry RACEMIC
Molecular Formula C19H22O2
Molecular Weight 282.3768
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VEDAPROFEN

SMILES

CC(C(O)=O)C1=CC=C(C2CCCCC2)C3=C1C=CC=C3

InChI

InChIKey=VZUGVMQFWFVFBX-UHFFFAOYSA-N
InChI=1S/C19H22O2/c1-13(19(20)21)15-11-12-16(14-7-3-2-4-8-14)18-10-6-5-9-17(15)18/h5-6,9-14H,2-4,7-8H2,1H3,(H,20,21)

HIDE SMILES / InChI

Molecular Formula C19H22O2
Molecular Weight 282.3768
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: O19183
Gene ID: 791253.0
Gene Symbol: PTGS2
Target Organism: Equus caballus (Horse)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
QUADRISOL

Approved Use

Reduction of inflammation and relief of pain associated with musculo-skeletal disorders and soft tissue lesions (traumatic injuries and surgical trauma).

Launch Date

1997
PubMed

PubMed

TitleDatePubMed
Influence of vedaprofen (Quadrisol) on quality and freezability of stallion semen.
2005 Nov
Vedaprofen therapy in cats with upper respiratory tract infection or following ovariohysterectomy.
2007 Feb

Sample Use Guides

Twice daily administration. An initial dose of 2 mg/kg (2.0 ml/100 kg) is followed by a maintenance dose of 1 mg/kg (1.0 ml/100 kg) given every 12 hours. Treatment can be continued for a maximum of 14 consecutive days.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:37:59 GMT 2023
Edited
by admin
on Fri Dec 15 16:37:59 GMT 2023
Record UNII
OKX88EO7OI
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VEDAPROFEN
INN   JAN   MART.   MI   USAN  
INN   USAN  
Official Name English
CERM10202
Code English
VEDAPROFEN FOR VETERINARY USE
EP  
Common Name English
1-NAPHTHALENEACETIC ACID, 4-CYCLOHEXYL-.ALPHA.-METHYL-, (±)-
Common Name English
VEDAPROFEN [MI]
Common Name English
CERM-10202
Code English
VEDAPROFEN [JAN]
Common Name English
1-NAPHTHALENEACETIC ACID, 4-CYCLOHEXYL-.ALPHA.-METHYL-
Common Name English
VEDAPROFEN [EMA EPAR VETERINARY]
Common Name English
vedaprofen [INN]
Common Name English
VEDAPROFEN [USAN]
Common Name English
VEDAPROFEN FOR VETERINARY USE [EP MONOGRAPH]
Common Name English
PM-150
Code English
QUADRISOL
Brand Name English
PM150
Code English
VEDAPROFEN [MART.]
Common Name English
Classification Tree Code System Code
WHO-VATC QM01AE90
Created by admin on Fri Dec 15 16:37:59 GMT 2023 , Edited by admin on Fri Dec 15 16:37:59 GMT 2023
EMA VETERINARY ASSESSMENT REPORTS QUADRISOL [AUTHORIZED]
Created by admin on Fri Dec 15 16:37:59 GMT 2023 , Edited by admin on Fri Dec 15 16:37:59 GMT 2023
NCI_THESAURUS C257
Created by admin on Fri Dec 15 16:37:59 GMT 2023 , Edited by admin on Fri Dec 15 16:37:59 GMT 2023
Code System Code Type Description
INN
7298
Created by admin on Fri Dec 15 16:37:59 GMT 2023 , Edited by admin on Fri Dec 15 16:37:59 GMT 2023
PRIMARY
MERCK INDEX
m11403
Created by admin on Fri Dec 15 16:37:59 GMT 2023 , Edited by admin on Fri Dec 15 16:37:59 GMT 2023
PRIMARY Merck Index
CHEBI
32292
Created by admin on Fri Dec 15 16:37:59 GMT 2023 , Edited by admin on Fri Dec 15 16:37:59 GMT 2023
PRIMARY
NCI_THESAURUS
C66652
Created by admin on Fri Dec 15 16:37:59 GMT 2023 , Edited by admin on Fri Dec 15 16:37:59 GMT 2023
PRIMARY
SMS_ID
100000079096
Created by admin on Fri Dec 15 16:37:59 GMT 2023 , Edited by admin on Fri Dec 15 16:37:59 GMT 2023
PRIMARY
EPA CompTox
DTXSID5049077
Created by admin on Fri Dec 15 16:37:59 GMT 2023 , Edited by admin on Fri Dec 15 16:37:59 GMT 2023
PRIMARY
CAS
71109-09-6
Created by admin on Fri Dec 15 16:37:59 GMT 2023 , Edited by admin on Fri Dec 15 16:37:59 GMT 2023
PRIMARY
WIKIPEDIA
VEDAPROFEN
Created by admin on Fri Dec 15 16:37:59 GMT 2023 , Edited by admin on Fri Dec 15 16:37:59 GMT 2023
PRIMARY
DRUG CENTRAL
2812
Created by admin on Fri Dec 15 16:37:59 GMT 2023 , Edited by admin on Fri Dec 15 16:37:59 GMT 2023
PRIMARY
PUBCHEM
72158
Created by admin on Fri Dec 15 16:37:59 GMT 2023 , Edited by admin on Fri Dec 15 16:37:59 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104464
Created by admin on Fri Dec 15 16:37:59 GMT 2023 , Edited by admin on Fri Dec 15 16:37:59 GMT 2023
PRIMARY
USAN
GG-7
Created by admin on Fri Dec 15 16:37:59 GMT 2023 , Edited by admin on Fri Dec 15 16:37:59 GMT 2023
PRIMARY
FDA UNII
OKX88EO7OI
Created by admin on Fri Dec 15 16:37:59 GMT 2023 , Edited by admin on Fri Dec 15 16:37:59 GMT 2023
PRIMARY
EVMPD
SUB00031MIG
Created by admin on Fri Dec 15 16:37:59 GMT 2023 , Edited by admin on Fri Dec 15 16:37:59 GMT 2023
PRIMARY
ECHA (EC/EINECS)
275-196-6
Created by admin on Fri Dec 15 16:37:59 GMT 2023 , Edited by admin on Fri Dec 15 16:37:59 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY