生物活性 | |||
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描述 | The COX‐2 isoform is constitutively expressed in a range of tissues and organs, and it is primarily induced by damage or tissue injury as a proinflammatory inducible enzyme and is responsible for the production of inducible enzymes which are converted into various eicosanoids[3]. Firocoxib is a COX-2 selective NSAID. Cats receiving 3 mg/kg firocoxib had lower postoperative pain scores (both Colorado pain scale scores and composite pain scores) than those in the control group[4]. Treatment with firocoxib orally at a dose rate of 5.7 to 8.5 mg/kg prior to induction of acute arthritis in dogs resulted in a high level of analgesia from the first post-treatment assessment at 3.5 h through 24 h post-treatment[5]. |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.97mL 0.59mL 0.30mL |
14.86mL 2.97mL 1.49mL |
29.73mL 5.95mL 2.97mL |
参考文献 |
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