Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C16H14N2O2.ClH |
| Molecular Weight | 302.756 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC(C(O)=O)C1=CC=C(C=C1)C2=CN3C=CC=CC3=N2
InChI
InChIKey=ZAZZTGZTOKMUAK-UHFFFAOYSA-N
InChI=1S/C16H14N2O2.ClH/c1-11(16(19)20)12-5-7-13(8-6-12)14-10-18-9-3-2-4-15(18)17-14;/h2-11H,1H3,(H,19,20);1H
Miroprofen, an imidazopyridine derivative, possesses anti-inflammatory properties. It was shown that this compound could be effective in suppressing pain responses and acute inflammation accompanied by increased vascular permeability. Analgesic effect of this compound was studied in post-extraction pain. However, information about the current study of this agent is not available.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| [Analgesic effects of miroprofen in post-extraction pain]. | 1983-05 |
|
| [Double blind controlled study of miroprofen in acute upper respiratory tract infections--comparison with ibuprofen]. | 1982-05 |
|
| Anti-inflammatory activity of an imidazopyridine derivative (miroprofen). | 1981 |
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68139034
Created by
admin on Tue Apr 01 17:15:47 GMT 2025 , Edited by admin on Tue Apr 01 17:15:47 GMT 2025
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D9K358LMF8
Created by
admin on Tue Apr 01 17:15:47 GMT 2025 , Edited by admin on Tue Apr 01 17:15:47 GMT 2025
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55843-87-3
Created by
admin on Tue Apr 01 17:15:47 GMT 2025 , Edited by admin on Tue Apr 01 17:15:47 GMT 2025
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PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD
