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
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)
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 | ( + / - ) |
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: O19183 Gene ID: 791253.0 Gene Symbol: PTGS2 Target Organism: Equus caballus (Horse) |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | QUADRISOL Approved UseReduction of inflammation and relief of pain associated with musculo-skeletal disorders and soft tissue lesions (traumatic injuries and surgical trauma). Launch Date1997 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:37:59 GMT 2023
by
admin
on
Fri Dec 15 16:37:59 GMT 2023
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Record UNII |
OKX88EO7OI
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Record Status |
Validated (UNII)
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Record Version |
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WHO-VATC |
QM01AE90
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EMA VETERINARY ASSESSMENT REPORTS |
QUADRISOL [AUTHORIZED]
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NCI_THESAURUS |
C257
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7298
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m11403
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32292
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C66652
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100000079096
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DTXSID5049077
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71109-09-6
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VEDAPROFEN
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2812
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72158
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CHEMBL2104464
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GG-7
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SUB00031MIG
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275-196-6
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Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE |
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SALT/SOLVATE -> PARENT |
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ENANTIOMER -> RACEMATE |
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Related Record | Type | Details | ||
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ACTIVE MOIETY |
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