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S88112

Clemizole

源叶(MedMol) 98%
  • 英文名:
  • Clemizole
  • 别名:
  • CAS号:
  • 442-52-4
  • 分子式:
  • C19H20ClN3
  • 分子量:
  • 325.84
  • 核磁/质谱:
品牌货号产品规格价格(RMB) 库存(上海) 北京 武汉 南京 数量计量单位 加入购物车...
源叶(MedMol) S88112-5mg 98% ¥352.00元 9 - - - EA 加入购物车
源叶(MedMol) S88112-10mg 98% ¥640.00元 3 - - - EA 加入购物车
源叶(MedMol) S88112-50mg 98% ¥2400.00元 5 - - - EA 加入购物车
源叶(MedMol) S88112-100mg 98% ¥3360.00元 4 - - - EA 加入购物车
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参考文献

质检证书(COA)

摩尔浓度计算器

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  • 产品描述: Clemizole is an H1 histamine receptor antagonist, can inhibit NS4B's RNA binding and hepatitis C virus (HCV) replication.
  • 靶点: HCV Protease;Histamine Receptor;HCVProtease; HistamineReceptor
  • 体内研究:
    Clemizole hydrochloride has an unexpectedly short plasma half-life (measured at 0.15 hours) which is very rapidly biotransformed into a glucuronide (M14) and a dealkylated metabolite (M12) and into a variety of lesser metabolites in C57BL/6J mice
  • 细胞实验: Clemizole hydrochloride is dissolved in DMSO and stored, and then diluted with appropriate media before use. Huh7.5 cells are maintained in DMEM supplemented with 1% L-glutamine, 1% penicillin, 1% streptomycin, 1× nonessential amino acids and 10% FBS. Cell lines are passaged twice weekly after treatment with 0.05% trypsin-0.02% EDTA and seeding at a dilution of 1:5. Subconfluent Huh7.5 cells are trypsinized and collected by centrifugation at 700 g for 5 min. The cells are then washed three times in ice-cold RNase-free PBS and resuspended at 1.5×107 cells/mL in PBS. Wild-type or mutant FL-J6/JFH-5′C19Rluc2AUbi RNA for electroporation is generated by transcription of XbaI linearized DNA templates using the T7 MEGAscript kit, followed by purification (RNA transcription and fluorescent labeling). We mixed 5 μg of RNA with 400 μL of washed Huh7.5 cells in a 2-mm-gap cuvette (BTX) and immediately pulsed (0.82 kV, five 99 μs pulses) with a BTX-830 electroporator. After a 10 min recovery at 25°C, pulsed cells are dil
  • 参考文献:
    1. Richter JM, et al. Clemizole hydrochloride is a novel and potent inhibitor of transient receptor potential channel TRPC5. Mol Pharmacol. 2014 Nov;86(5):514-21. 2. Nishimura T, et al. Using chimeric mice with humanized livers to predict human drug metabolism and a drug-drug interaction. J Pharmacol Exp Ther. 2013 Feb;344(2):388-96. 3. Einav S, et al. Discovery of a hepatitis C target and its pharmacological inhibitors by microfluidic affinity analysis. Nat Biotechnol. 2008 Sep;26(9):1019-27.
  • 溶解性: Soluble  in  DMSO
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 3.069 ml 15.345 ml 30.69 ml
    5 mM 0.614 ml 3.069 ml 6.138 ml
    10 mM 0.307 ml 1.534 ml 3.069 ml
    50 mM 0.061 ml 0.307 ml 0.614 ml
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