Fepradinol
Fepradinol is an orally active nonsteroidal anti-inflammatory agent. Fepradinol inhibits the increase in vascular permeability induced by histamine, 5-hydroxytryptamine, and bradykinin, reduces exudate volume, prevents leukocyte migration, and suppresses acute inflammation models. Fepradinol also induces thrombotic vasculopathy with epidermal necrosis, without leukocytoclastic vasculitis; triggers occlusive contact dermatitis presenting as purpuric papulonecrotic lesions, and causes strongly positive patch test reactions. Fepradinol can be used in research related to occlusive contact dermatitis and acute inflammation.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- CAS 番号: 36981-91-6
- 分子式: C12H19NO2
- 分子量:209.28
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性
製品説明
体内実験
Fepradinol (25 mg/kg; oral; single administration; 30 minutes before zymosan injection) inhibited dye exudation by 67.2% in the early phase (30 min) of zymosan-induced rat peritonitis, and reduced exudate volume by 27% and dye exudation by 50% in the late phase (3 h)[2].
Fepradinol (100 mg/kg; oral; single administration; administered immediately after carrageenan injection) reduced exudate volume by 67.2% and leukocyte migration by 76.4% in a carrageenan-induced rat pleurisy model[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Wistar (male, 5-7 weeks old, 150-200 g)[2]
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Dosage:25 mg/kg
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Administration:p.o.; single dose; 30 min prior to mediator injection
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Result:Inhibited histamine-induced vascular permeability by 81.1%.
Inhibited serotonin-induced vascular permeability by 82.0%.
Inhibited bradykinin-induced vascular permeability by 64.1%.
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Animal Model:Wistar (male, 150-200 g)[2]
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Dosage:100 mg/kg
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Administration:p.o.; single dose; immediately after carrageenin injection
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Result:Reduced pleural exudate volume by 67.2%.
Inhibited leucocyte mobilization by 76.4%.
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Animal Model:Wistar (male, 150-200 g)[2]
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Dosage:25 mg/kg
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Administration:p.o.; single dose; 30 min prior to zymosan injection
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Result:Inhibited dye extravasation by 67.2% at 30 min after zymosan challenge with no effect on exudate volume.
Reduced exudate volume by 27% at 3 h after zymosan challenge.
Inhibited dye extravasation by 50% at 3 h after zymosan challenge.
化学情報
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CAS 番号 36981-91-6
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分子量 209.28
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分子式 C12H19NO2
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SMILES
OC(CNC(C)(C)CO)C1=CC=CC=C1
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)