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125602-71-3

中文名稱 貝托斯汀
英文名稱 BEPOTASTINE
CAS 125602-71-3
分子式 C21H25ClN2O3
分子量 388.89
MOL 文件 125602-71-3.mol
更新日期 2026/05/26 14:26:10
125602-71-3 結(jié)構(gòu)式 125602-71-3 結(jié)構(gòu)式

基本信息

中文別名
貝托司汀
貝托斯汀
(+)-BEPOTASTINE
BEPOTASTINE >
90%
4-[4-[(4-氯苯基)吡啶-2-基甲氧基]哌啶-1-基]丁酸
英文別名
BEPOTASTINE
Bepotastine >
Bepotastine >90%
betotastine besilate
Bepotastine free base
-4-(4-((4-Chlorophenyl)
(190786-43-7) bepotastine
4-[(S)-(4-chlorophenyl)-2-pyridinylMethoxy]-
4-(4-[(1S)(4-CHLOROPHENYL)-2-PYRIDYLMETHOXY]PIPERIDYL)BUTANOIC ACID
4-[4-[(4-Chlorophenyl)pyridin-2-ylmethoxy]piperidin-1-yl]butanoic acid
所屬類別
生物化工:激動劑抑制劑

物理化學性質(zhì)

熔點56 - 58°C
沸點546.8±50.0 °C(Predicted)
密度1.26
儲存條件-20°C Freezer, Under inert atmosphere
溶解度可溶于DMSO(少許)、甲醇(少許)
酸度系數(shù)(pKa)4.44±0.10(Predicted)
形態(tài)固體
顏色白色至淺米色
貝托斯汀價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2026/03/03S5940貝托斯汀
Bepotastine
125602-71-35mg794.66元
2025/12/22HY-I0021貝托斯汀
Bepotastine
125602-71-31 mg300元
2025/12/22HY-I0021貝托斯汀
Bepotastine
125602-71-310mM * 1mLin DMSO642元

常見問題列表

生物活性
Bepotastine是一種非鎮(zhèn)靜的、選擇性histamine 1 (H1) receptor拮抗劑。
靶點

Histamine H1 receptor

體外研究

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).

體內(nèi)研究

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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