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Buclizine dihydrochloride

Buclizine dihydrochloride

产品编号 T6426   CAS 129-74-8
别名: 盐酸安其敏, Longifene, Buclina, Buclizine HCl, UCB-4445

Buclizine dihydrochloride (Buclina) 是可口服的一种哌嗪组胺 H1 受体拮抗剂,主要具有止吐和抗眩晕活性。

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Buclizine dihydrochloride Chemical Structure
Buclizine dihydrochloride, CAS 129-74-8
规格 价格/CNY 货期 数量
100 mg ¥ 415 现货
1 mL * 10 mM (in DMSO) ¥ 195 现货
其他形式的 Buclizine dihydrochloride:
千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
重组蛋白限时优惠
产品目录号及名称: Buclizine dihydrochloride (T6426)
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纯度: 99.56%
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参考文献
产品描述 Buclizine dihydrochloride (Buclina) is the hydrochloride salt form of buclizine, a piperazine histamine H1 receptor antagonist with primarily antiemetic and antivertigo activities. Buclizine dihydrochloride binds to and blocks the histamine H1 receptor, thereby preventing the symptoms that are caused by histamine activity. Buclizine dihydrochloride exerts its anti-emetic effect by binding to and blocking the muscarinic and histamine receptors in the vomiting center of the central nervous system (CNS). This may prevent activation of the chemoreceptor trigger zone (CTZ) and may reduce nausea and vomiting.
体外活性 Buclizine hydrochloride, a piperazine derivative, is a sedating antihistamine with antimuscarinic and moderate sedative action. Buclizine is used in the prevention and treatment of nausea, vomiting, and dizziness associated with motion sickness. Additionally, it has been used in the management of vertigo in diseases affecting the vestibular apparatus. Although the mechanism by which buclizine exerts its antiemetic and antivertigo effects has not been fully elucidated, its central anticholinergic properties are partially responsible. The drug depresses labyrinth excitability and vestibular stimulation, and it may affect the medullary chemoreceptor trigger zone. It also possesses anticholinergic, antihistaminic, central nervous system depressant, and local anesthetic effects. [1]
激酶实验 Topoisomerase I Catalytic Actioity Assay [1]: Topoisomerase I Catalytic Actioity Assay: The enzymatic activity is analyzed by the DNA unwinding assay. DNA topoisomerase I, from TopoGEN (1 unit, which is defined as the amount of enzyme that converts 0.5 μg of superhelical DNA to the relaxed state in 30 minutes at 37 °C), is incubated with 0.5 μg of 6x174 RF DNA, in the presence or absence of Beta-Lapachone, in 20 μL of relaxation buffer (50 mM Tris (pH 7.5). 50 mM KCI, 10 mM MgCl2, 0.5 mM dithiothreitol, 0.5 mM EDTA, 30 μg/mL bovine serum albumin) for 30 minutes at 37 °C. Reactions are stopped by adding 1% SDS and proteinase K (50 μg/mL). After an additional 1-hour incubation at 37 °C, the products are separated by electrophoresis in 1% agarose gel in TAE buffer (0.04 M tris acetate, 0.001 M EDTA). The gel is stained with ethidium bromide after electrophoresis. The photographic negative is scanned with an NIH image analysis system.
别名 盐酸安其敏, Longifene, Buclina, Buclizine HCl, UCB-4445
分子量 505.95
分子式 C28H33ClN2·2HCl
CAS No. 129-74-8

存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度

DMSO: 11 mg/mL (21.74 mM), Sonication is recommended.

溶液配制表

可选溶剂 浓度 体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 1.9765 mL 9.8824 mL 19.7648 mL 49.412 mL
5 mM 0.3953 mL 1.9765 mL 3.953 mL 9.8824 mL
10 mM 0.1976 mL 0.9882 mL 1.9765 mL 4.9412 mL
20 mM 0.0988 mL 0.4941 mL 0.9882 mL 2.4706 mL

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TargetMol Library Books参考文献

1. Mostafa GA, et al. Profiles Drug Subst Excip Relat Methodol, 2011, 36:1-33.
SB-616234-A Elemicin Ziprasidone (R)-Mirtazapine (Rac)-WAY-161503 GR 113808 Doxepin hydrochloride Vortioxetine

相关化合物库

该产品包含在如下化合物库中:
神经退行性疾病化合物库 抑制剂库 抗癌上市药物库 GPCR靶点分子库 药物功能重定位化合物库 膜蛋白靶向化合物库 抗癌药物库 已知活性化合物库 神经信号分子库 表型筛选靶点鉴定库

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体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。

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Keywords

Buclizine dihydrochloride 129-74-8 GPCR/G Protein Immunology/Inflammation Neuroscience 5-HT Receptor AChR Histamine Receptor teratogen Inhibitor MCF-7 anti-tumor activity antiallergic 盐酸安其敏 Longifene antihistamine inhibit Buclizine Dihydrochloride UCB 4445 Buclina Buclizine HCl UCB4445 UCB-4445 Buclizine inhibitor

 

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