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CPS-11

CAS No. 145945-21-7

CPS-11 ( —— )

产品货号. M33976 CAS No. 145945-21-7

CPS-11 (N-(Hydroxymethyl)thalidomide) 是 Thalidomide (HY-14658) 类似物,是一种有效的抗癌剂 (anti-cancer agent)。CPS-11 可抑制 NF-κB,激活 NFAT,通过升高 ROS 抑制细胞因子表达。CPS-11 对 MM (多发性骨髓瘤)细胞系表现出更广泛的活性谱和更高的效力。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥5129 有现货
5MG ¥7203 有现货
10MG ¥9529 有现货
25MG ¥12356 有现货
50MG ¥15484 有现货
100MG ¥19125 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    CPS-11
  • 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
    CPS-11 (N-(Hydroxymethyl)thalidomide) 是 Thalidomide (HY-14658) 类似物,是一种有效的抗癌剂 (anti-cancer agent)。CPS-11 可抑制 NF-κB,激活 NFAT,通过升高 ROS 抑制细胞因子表达。CPS-11 对 MM (多发性骨髓瘤)细胞系表现出更广泛的活性谱和更高的效力。
  • 产品描述
    CPS-11 (N-(Hydroxymethyl)thalidomide) a Thalidomide (HY-14658) analogue, is a potent anti-cancer agent. CPS-11 inhibits NF-κB, activates NFAT, and repress cytokine expression through elevated ROS. CPS-11 exhibits a wider activity spectrum and higher potency against MM (multiple myeloma) cell lines.
  • 体外实验
    CPS-11 abrogates ability of bone marrow stromal cells (BMSCs) to induce proliferation of MM cells, confirming its ability to target tumor cells in the bone marrow microenvironment.CPS-11 (0-200 μM, 0 or 4 h) shows virtually no effect on activation of p38 and only slight, transient activation of ATF2 and HSP27.CPS-11 (0-100 μM, 24 or 48 h) was no toxic to H157 cells, WT MEFs or the p38α-/- MEFs at doses as high as 100 μM.CPS-11 (50 μM, 24 or 48 h) does not induce apoptosis in H157 cells.Western Blot Analysis Cell Line:H157 cells, PC3 cells, HUVEC cells Concentration:0, 1, 5, 10, 20, 50, 100 and 200 μM Incubation Time:0, 15 min, 30 min, 1 h, 2 h, and 4 h Result:Showed virtually no effect on activation of p38 and only slight, transient activation of ATF2 and HSP27. Increased Akt phosphorylation within 15 minutes, and decreased Akt phosphorylation from 15 minutes to 4 hours.Cell Cytotoxicity Assay Cell Line:H157 cells, wild-type (WT) mouse embryonic fibroblasts (MEF) and p38α-/- MEF Concentration:0, 20, 50, and 100 μM Incubation Time:24 or 48 hours Result:Showed no toxic to H157 cells at doses as high as 100 μM and an incubation time of 48 hours. had no toxic effect on either the WT MEFs or the p38α-/- MEFs at doses as high as 100 μM.Apoptosis Analysis Cell Line:H157 cells Concentration:50 μM Incubation Time:24 or 48 hours Result:Did not induce apoptosis in H157 cells at either time point.
  • 体内实验
    ——
  • 同义词
    ——
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    Reactive Oxygen Species | NF-κB | Dehydrogenase
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    145945-21-7
  • 分子量
    288.26
  • 分子式
    C14H12N2O5
  • 纯度
    >98% (HPLC)
  • 溶解度
    ——
  • SMILES
    O=C1N(C(=O)C=2C1=CC=CC2)C3C(=O)N(CO)C(=O)CC3
  • 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. Aragon-Ching JB, et al. Thalidomide analogues as anticancer drugs. Recent Pat Anticancer Drug Discov. 2007 Jun;2(2):167-74. ?
产品手册
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