
Meclizine
CAS No. 569-65-3
Meclizine ( Meclozine )
产品货号. M29639 CAS No. 569-65-3
Meclizine (Meclozine), an antihistamine, reversibly inhibits the interaction of histamine at the H1 receptors.
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
200MG | 获取报价 | 有现货 |
![]() ![]() |
500MG | 获取报价 | 有现货 |
![]() ![]() |
生物学信息
-
产品名称Meclizine
-
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
-
产品简述Meclizine (Meclozine), an antihistamine, reversibly inhibits the interaction of histamine at the H1 receptors.
-
产品描述Meclizine (Meclozine), an antihistamine, reversibly inhibits the interaction of histamine at the H1 receptors. Meclizine is a member of the piperazine class of H1 antagonists. Meclizine is an effective anti-motion sickness agent. Meclizine crosses the blood–brain barrier. Meclizine is an agonist ligand for mouse constitutive androstane receptor (CAR) and an inverse agonist for Human CAR. Meclizine can be used for the research of polyQ toxicity disorders, such as Huntington's disease.Meclizine (Meclozine; 50 μM; 24 hours) significantly increases cell survival in STHdh cells at 24 h after the removal of serum, evidently by suppressing apoptosis, based on caspase 3 and 7 cleavage. The rescue is dose-dependent with an EC50 of 17.3 μm, and a maximum efficacy of 218% increased survival over vehicle. Meclizine protects striatal cells expressing polyglutamine (polyQ)-expanded huntingtin from serum withdrawal-induced apoptosis of mutant (STHdhQ111/111) and wild-type (STHdhQ7/7) striatal cells.
-
体外实验Meclizine (Meclozine; 50 μM; 24 hours) significantly increases cell survival in STHdh cells at 24 h after the removal of serum, evidently by suppressing apoptosis, based on caspase 3 and 7 cleavage. The rescue is dose-dependent with an EC50 of 17.3 μm, and a maximum efficacy of 218% increased survival over vehicle. Meclizine protects striatal cells expressing polyglutamine (polyQ)-expanded huntingtin from serum withdrawal-induced apoptosis of mutant (STHdhQ111/111) and wild-type (STHdhQ7/7) striatal cells. Cell Viability Assay Cell Line:The murine striatal cells expressing wild-type (STHdhQ7/7) or mutant (STHdhQ111/111) huntingtin protein Concentration:50 μM Incubation Time:24 hours Result:Significantly increased cell survival in STHdhQ111/111 cells at 24 h after the removal of serum. Western Blot Analysis Cell Line:Mutant (STHdhQ111/111) and wild-type (STHdhQ7/7) striatal cells Concentration:50 μM Incubation Time:0, 4, 10, 24 hours Result:Suppressed apoptosis, based on caspase 3 and 7 cleavage.
-
体内实验Meclizine (Meclozine; 10-100 mg/kg; ip) protects mouse against kidney ischemia. Pretreatment with 100 mg/kg of Meclizine, 17 or 24 h prior to ischemia shows kidney protection in mice. Meclizine reduces mitochondrial oxygen consumption by directly inhibiting the Kennedy pathway of phosphatidylethanolamine biosynthesis and up-regulated glycolysis. Animal Model:8-10 wk old male C57BL/6 mice Dosage:10, 30, 60 or 100 mg/kg Administration:Administered intraperitoneallyResult:Protected mice from kidney ischemia-reperfusion injury.
-
同义词Meclozine
-
通路Neuroscience
-
靶点Other Targets
-
受体——
-
研究领域——
-
适应症——
化学信息
-
CAS Number569-65-3
-
分子量390.95
-
分子式C25H27ClN2
-
纯度>98% (HPLC)
-
溶解度——
-
SMILES——
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1. Priti N. Patel, et al. Safety and Efficacy in the Treatment and Prevention of Motion Sickness.
2. Vishal M Gohil, et al. Meclizine is neuroprotective in models of Huntington's disease. Hum Mol Genet. 2011 Jan 15;20(2):294-300.
产品手册




关联产品
-
Meclizine
Meclizine (Meclozine), an antihistamine, reversibly inhibits the interaction of histamine at the H1 receptors.
-
Carazolol-d7
Carazolol-d7 is the deuterium labeled Carazolol.Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process.
-
Terazosin
Terazosin is a quinazoline derivative and a competitive and orally active α1-adrenoceptor antagonist.