CAS NO: | 153439-40-8 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
500mg | 电议 |
1 g | 电议 |
5 g | 电议 |
生物活性 |
Fexofenadine (MDL-16455) hydrochloride is an orally active and nonsedativeH1receptorantagonist. Fexofenadine hydrochloride can be used in allergic rhinitis and chronic idiopathic urticarial research[1][2][3]. |
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IC50& Target[1] |
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体外研究 (In Vitro) |
Fexofenadine (1-100 μM; 1 h) inhibits the expression of IL-6 protein in nasal fibroblasts in a dose-dependent manner[2].
Western Blot Analysis[2]
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体内研究 (In Vivo) |
Fexofenadine hydrochloride (oral administration; 5-20 mg/kg; once daily; 3 w) suppresses both eosinophilia and systemic anaphylaxis in C57BL/6 mice infected withT. spiralis[1].
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Clinical Trial |
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分子量 |
538.12 |
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性状 |
Solid |
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Formula |
C32H40ClNO4 |
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CAS 号 |
153439-40-8 |
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中文名称 |
盐酸非索非那定 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
4°C, sealed storage, away from moisture *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) |
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溶解性数据 |
In Vitro:
DMSO : ≥ 100 mg/mL(185.83 mM) H2O :< 0.1 mg/mL (ultrasonic;warming;heat to 60℃)(insoluble) *"≥" means soluble, but saturation unknown.
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In Vivo:
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