Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C22H23NO3 |
| Molecular Weight | 349.4229 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC[C@@]1(CC(O)=O)OC[C@H](CC2=CC=CC=C2)C3=C1NC4=C3C=CC=C4
InChI
InChIKey=BUUODSZYUAZDIF-AOMKIAJQSA-N
InChI=1S/C22H23NO3/c1-2-22(13-19(24)25)21-20(17-10-6-7-11-18(17)23-21)16(14-26-22)12-15-8-4-3-5-9-15/h3-11,16,23H,2,12-14H2,1H3,(H,24,25)/t16-,22-/m0/s1
| Molecular Formula | C22H23NO3 |
| Molecular Weight | 349.4229 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Dexpemedolac is long-acting non-narcotic analgesic. Dexpemedolac exhibited potent analgesic effects against chemically induced pain in rats and mice and against inflammatory pain in rats. Dexpemedolac differed from standard nonsteroidal anti-inflammatory drugs (NSAIDs) in that the doses, which produced analgesia were much lower than those required for either anti-inflammatory or gastric irritant effects. The common to the NCAIDs class actions are antipyresis and inhibitory effects on platelet aggregation. In yeast-induced hyperthermic rats, dexpemedolac exhibited antipyretic actions, whereas the drug did not affect body temperature in normothermic animals. Aggregation of human platelets was inhibited by high concentrations of dexpemedolac.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:27:41 GMT 2025
by
admin
on
Mon Mar 31 18:27:41 GMT 2025
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| Record UNII |
5285077I2I
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| Record Status |
Validated (UNII)
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| Record Version |
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6918042
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114030-44-3
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DTXSID801350791
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5285077I2I
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100000083411
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7260
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CHEMBL430916
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FF-42
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SUB07043MIG
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C166805
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |
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