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S82500

ELR510444

源叶(MedMol) 95%
  • 英文名:
  • ELR510444
  • 别名:
  • N-[5-(5-cyano-thiophen-2-yl)-2-methylphenyl]-4-methyl-benzenesulfonamide
  • CAS号:
  • 1233948-35-0
  • 分子式:
  • C19H16N2O2S2
  • 分子量:
  • 368.4725
  • 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) S82500-1mg 95% ¥240.00元 9 0 0 0 EA 加入购物车
源叶(MedMol) S82500-2mg 95% ¥320.00元 9 0 0 0 EA 加入购物车
源叶(MedMol) S82500-5mg 95% ¥600.00元 10 0 0 0 EA 加入购物车
源叶(MedMol) S82500-10mg 95% ¥800.00元 7 0 0 0 EA 加入购物车
源叶(MedMol) S82500-50mg 95% ¥2800.00元 7 0 0 0 EA 加入购物车
源叶(MedMol) S82500-100mg 95% ¥4400.00元 预计交期:2-3天 0 0 0 EA 加入购物车
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  • 提示:详情请下载说明书。
  • 产品描述: ELR-510444 is a novel microtubule disruptor with potential antivascular effects and in vivo antitumor efficacy, causing a loss of cellular microtubules and the formation of aberrant mitotic spindles and leading to mitotic arrest and apoptosis of cancer cells.
  • 靶点: Microtubule
  • 体外研究: ELR510444 has potent microtubule-disrupting activity, causing a loss of cellular microtubules and the formation of aberrant mitotic spindles and leading to mitotic arrest and apoptosis of cancer cells. ELR510444 potently inhibits cell proliferation with an IC(50) value of 30.9 nM in MDA-MB-231 cells, inhibits the rate and extent of purified tubulin assembly, and displaces colchicine from tubulin, indicating that the drug directly interacts with tubulin at the colchicine-binding site. ELR510444 is not a substrate for the P-glycoprotein drug transporter and retains activity in βIII-tubulin-overexpressing cell lines, suggesting that it circumvents both clinically relevant mechanisms of drug resistance to this class of agents
  • 体内研究: ELR510444 shows potent antitumor activity in the MDA-MB-231 xenograft model. A low concentration of ELR510444 (30 nM) rapidly alters endothelial cell shape
  • 细胞实验: Cell lines: 2H-11 tumor endothelial cells Concentrations: 1-100 nM Incubation Time: 1 h Method: 2H-11 cells are plated on glass coverslips and allowed to attach and grow for 24 h. Drugs are then added for 1 h, and cells are fixed with paraformaldehyde and permeabilized with Triton X-100. F-Actin and DNA are stained with tetramethylrhodamine B isothiocyanate-conjugated phalloidin and DAPI, respectively.
  • 动物实验: Animal Models: BALB/c nude mice Dosages: 3, 6, and 12.5 mg/kg Administration: s.c.
  • 参考文献:
    1. Risinger AL, et al. ELR510444, a novel microtubule disruptor with multiple mechanisms of action. J Pharmacol Exp Ther. 2011, 336(3):652-60.
  • 溶解性: Soluble  in  DMSO、Ethanol
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 2.714 ml 13.57 ml 27.139 ml
    5 mM 0.543 ml 2.714 ml 5.428 ml
    10 mM 0.271 ml 1.357 ml 2.714 ml
    50 mM 0.054 ml 0.271 ml 0.543 ml
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