Buclizine HCl
CAS No. 129-74-8
Buclizine HCl ( —— )
产品货号. M17929 CAS No. 129-74-8
Buclizine HCl 是 Buclizine 的盐酸盐形式,Buclizine 是一种哌嗪组胺 H1 受体拮抗剂,主要具有止吐和抗眩晕活性。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
规格 | 价格/人民币 | 库存 | 数量 |
50MG | ¥243 | 有现货 |
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100MG | ¥340 | 有现货 |
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200MG | ¥446 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Buclizine HCl
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Buclizine HCl 是 Buclizine 的盐酸盐形式,Buclizine 是一种哌嗪组胺 H1 受体拮抗剂,主要具有止吐和抗眩晕活性。
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产品描述Buclizine HCl is the hydrochloride salt form of buclizine, a piperazine histamine H1 receptor antagonist with primarily antiemetic and antivertigo activities. Buclizine binds to and blocks the histamine H1 receptor, thereby preventing the symptoms that are caused by histamine activity. Buclizine 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.
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体外实验Buclizine (0.1-100 μM; 72 h) inhibits growth of MCF-7 cells.Buclizine (9.625-77 μM; 72 h) arrests the cell cycle in the G1 phase in a dose-dependent manner.Buclizine (0-75 μM; 72 h) decreases TCTP (translationally controlled tumor protein) and cell cycle regulatory proteins expression in MCF-7 cells, increases pro-apoptotic MCL-1S expression. Cell Proliferation Assay.Cell Line:MCF-7 cells.Concentration:0-100 μM.Incubation Time:72 hours Result: Showed considerable growth inhibition (IC50=19.18 μM).Cell Cycle Analysis.Cell Line:MCF-7 cells Concentration:9.625, 19.25, 38.5, and 77 μM Incubation Time:72 hours Result:Increased the percentages of cells in the G1 phase to 73% at 77 μM.Western Blot Analysis Cell Line:MCF-7 cells Concentration:0-75 μM Incubation Time:72 hours Result:Decreased TCTP expression by 40% at 75 μM.Decreased cyclin D1, cyclin D3, CDK2 and CDK4 expression after 72 h.
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体内实验Buclizine dihydrochloride (30-200 mg/kg; tenth to fifteenth and twelfth to fifteenth days of gestation) shows potent teratogens in the rat. Animal Model:Eighty-seven mature female rats weighing 240±20 grams.Dosage:30, 40, 60, 100, and 200 mg/kg Administration:30-200 mg/kg; tenth to fifteenth and twelfth to fifteenth days of gestation Result:Resulted in malformations in 100% of the young at a dose level of 60-100 mg/kg.
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同义词——
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通路Others
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靶点Other Targets
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受体HT| Cholinergic
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研究领域Others-Field
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适应症——
化学信息
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CAS Number129-74-8
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分子量505.95
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分子式C28H33ClN2·2HCl
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 2.5 mg/mL (4.94 mM)
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SMILESCC(C)(C)c1ccc(cc1)CN1CCN(CC1)C(c1ccccc1)c1ccc(cc1)Cl.Cl.Cl
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Mostafa GA, et al. Profiles Drug Subst Excip Relat Methodol, 2011, 36:1-33.
产品手册
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