Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C19H19Cl2N3O3 |
| Molecular Weight | 408.278 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ClCCCCC(=O)NNC(=O)N1CC2=CC=CC=C2OC3=CC=C(Cl)C=C13
InChI
InChIKey=OUNSOXPSCMCFHX-UHFFFAOYSA-N
InChI=1S/C19H19Cl2N3O3/c20-10-4-3-7-18(25)22-23-19(26)24-12-13-5-1-2-6-16(13)27-17-9-8-14(21)11-15(17)24/h1-2,5-6,8-9,11H,3-4,7,10,12H2,(H,22,25)(H,23,26)
| Molecular Formula | C19H19Cl2N3O3 |
| Molecular Weight | 408.278 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Pinadoline is a competitive PGE2 antagonist. It is an analgesic agent. Pinadoline demonstrated the antinociceptive activity in the rat using the writhing and the formalin tests. In the writhing test, pinadoline was significantly more potent than inhibitors of PG synthesis, but less potent than opiate analgesics. In the formalin test, pinadoline appeared less active than aspirin and ibuprofen and more active than acetaminophen. Pinadoline does not possess the antiinflammatory activity of aspirin and ibuprofen and may be more like acetaminophen, which had diminished antiinflammatory activity. At high concentrations, pinadoline is a non-competitive antagonist of serotonin in guinea-pig ileum.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2881791
Curator's Comment: Rat data
150 and 300 mg/kg in a volume of 2 ml/kg
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 09:16:51 GMT 2025
by
admin
on
Wed Apr 02 09:16:51 GMT 2025
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| Record UNII |
KUO32K2TRD
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| Record Status |
Validated (UNII)
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NCI_THESAURUS |
C241
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ACTIVE MOIETY |