59040-30-1
Chemical Structure
Nafazatrom
Synonym(s): Bay g 6575
- CAS No.: 59040-30-1
- Formula:C16H16N2O2
- Molecular Weight:268.31
IUPAC Name: 5-methyl-2-(2-(naphthalen-2-yloxy)ethyl)-2,4-dihydro-3H-pyrazol-3-one
InChIKey: ISBUYSPRIJRBKX-UHFFFAOYSA-N
SMILES: O=C1N(N=C(C1)C)CCOC2=CC=C3C=CC=CC3=C2
Biological Activity: Nafazatrom (Bay g 6575) is an orally active cardioprotective agent that protects against ischemic damage. Nafazatrom dose-dependently inhibits neutrophil aggregation, superoxide anion generation, arachidonic acid metabolism, and to a lesser extent the release of β-glucosidase, platelet aggregation or arachidonic acid in vitro. Acid metabolism has no significant effect. In a dog ischemia-reperfusion model, Nafazatrom (10 mg/kg; po) reduced infarct size and the occurrence of arrhythmias and rescued ischemic myocardial function without affecting any hemodynamic changes. The basis of Nafazatrom's cardioprotection may be inhibition of neutrophil function and cellular infiltration in vitro[1].
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Nafazatrom | Nafazatrom (Bay g 6575) is an orally active cardioprotective agent that protects against ischemic damage. Nafazatrom dose-dependently inhibits neutrophil aggregation, superoxide anion generation, arachidonic acid metabolism, and to a lesser extent the release of β-glucosidase, platelet aggregation or arachidonic acid in vitro. Acid metabolism has no significant effect. In a dog ischemia-reperfusion model, Nafazatrom (10 mg/kg; po) reduced infarct size and the occurrence of arrhythmias and rescued ischemic myocardial function without affecting any hemodynamic changes. The basis of Nafazatrom's cardioprotection may be inhibition of neutrophil function and cellular infiltration in vitro. | |||||||||||||||||||||
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Keywords
