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Ozagrel
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| Systematic (IUPAC) name | |
| (E)-3-[4-(imidazol-1-ylmethyl)phenyl]prop-2-enoic acid | |
| Identifiers | |
| CAS number | |
| ATC code | ? |
| PubChem | |
| Chemical data | |
| Formula | C13H12N2O2 |
| Mol. mass | 228.24 g/mol |
| SMILES | & |
| Pharmacokinetic data | |
| Bioavailability | ? |
| Metabolism | ? |
| Half life | ? |
| Excretion | ? |
| Therapeutic considerations | |
| Pregnancy cat. |
? |
| Legal status |
℞ Prescription only |
| Routes | Oral |
Ozagrel (INN) is a thromboxane A2 synthesis inhibitor.[1]
References
- ^ Loo MH, Egan D, Vaughan ED, Marion D, Felsen D, Weisman S (March 1987). "The effect of the thromboxane A2 synthesis inhibitor OKY-046 on renal function in rabbits following release of unilateral ureteral obstruction". J. Urol. 137 (3): 571–6. PMID 3820396.
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Wikipedia content modification information:
- This page was last modified on 7 August 2008, at 18:19.
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