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贝托斯汀
产品纠错
CAS号:125602-71-3 | 英文名称:(S)-Bepotastine
分子式
分子量
EINECS号
MDL
Smiles
InChIKey
乙二醇化学百科
基本信息
中文名称 贝托斯汀
英文名称 BEPOTASTINE
CAS号 125602-71-3
分子式 C21H25ClN2O3
分子量 388.89
EINECS号 200-258-5
物化性质
熔点 56 - 58°C
沸点 546.8±50.0 °C(Predicted)
密度 1.26
溶解度 可溶于DMSO(少许)、甲醇(少许)
形态 固体
酸度系数(pKa) 4.44±0.10(Predicted)
颜色 白色至浅棕色
安全信息
生产及用途
Bepotastine是一种非镇静的、选择性histamine 1 (H1) receptor拮抗剂。

Histamine H1 receptor

Bepotastine possesses additional anti-allergic activity including stabilization of mast cell function, inhibition of eosinophilic infiltration, inhibition of IL-5 production, and inhibition of leukotriene B4 (LTB4) and LTD4 activity.
Bepotastine significantly inhibits antigen-induced stimulation of IL-5 production in human peripheral blood mononuclear cells (PBMCs) at concentrations of 10-100 μM and the effect is enhanced when the PBMCs are pre-incubated with Bepotastine.
Leukotriene B4 increased Ca2+ concentration in cultured neutrophils, which is suppressed by Bepotastine besilate (1-100 μM). Leukotriene B4 increased Ca2+ concentration in cultured dorsal root ganglion neurons, which is also suppressed by Bepotastine besilate (100 μM).

Bepotastine besilate (10 mg/kg) inhibits scratching induced by an intradermal injection of histamine (100 nmol/site), but not serotonin (100 nmol/site).
Bepotastine besilate (1-10 mg/kg, oral) dose-dependently suppresses scratching induced by substance P (100 nmol/site) and leukotriene B4 (0.03 nmol/site). Bepotastine in vivo dose-dependently inhibits the acceleration of histamine-induced vascular permeability and inhibits homologous passive cutaneous anaphylaxis in guinea pig studies.
In mouse models of itching, oral Bepotastine inhibits the frequency and duration of scratching behavior.

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