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Cyasterone

CAS No. 17086-76-9

Cyasterone ( Cyasterone | AI3-44890 | AI3 44890 )

产品货号. M18117 CAS No. 17086-76-9

Cyasterone是一种天然EGFR抑制剂,可通过调节EGFR信号通路抑制A549和MGC823细胞的生长,可能是一种有前途的抗癌化合物。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥518 有现货
10MG ¥915 有现货
25MG ¥1725 有现货
50MG ¥2584 有现货
100MG ¥3848 有现货
200MG 获取报价 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
    Cyasterone
  • 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
    Cyasterone是一种天然EGFR抑制剂,可通过调节EGFR信号通路抑制A549和MGC823细胞的生长,可能是一种有前途的抗癌化合物。
  • 产品描述
    Cyasterone was demonstrated potential inhibition effect in skin carcinoma cells.
  • 体外实验
    Cyasterone exerts cytotoxicity on multiple cell lines: HeLa (IC50=77.24 μg/ml);HepG-2 (IC50=52.03 μg/ml);MCF-7 (IC50=82.07μg/ml) andMCF-7 (IC50=82.07 μg/ml). And It has none cytotoxicity (IC50>400 μg/ml) on 3 types of carcinoma (HT-29, Caco-2, T47D) and 1 type of normal (NIH 3T3) cell lines.Cyasterone (0-60 μg/ml; 48 hours) causes a significantly decreasing of the cell proliferation. It inhibits cell growth as a dose-dependent manner, exhibits IC50 values of 38.50 μg/ml and 32.96 μg/ml, respectively.Cyasterone (0-60 μg/ml; 24 hours) decreases p-EGFR, p-MEK, and p-mTOR as a dose-dependent manner in A549 cells, it affects the MAPK signaling pathway activities. Cell Viability Assay Cell Line:A549 cells and MGC823 cells Concentration:0 μg/ml, 20 μg/ml, 40 μg/ml, 60 μg/mlIncubation Time:24 hours Result:Inhibited cellproliferation as a dose-dependent manner. Western Blot Analysis Cell Line:A549 cellsConcentration:0 μg/ml, 20 μg/ml, 40 μg/ml, 60 μg/ml Incubation Time:24 hours Result:Surpressed p-EGFR, p-MEK, and p-mTOR expression.
  • 体内实验
    Cyasterone (intraperitoneal injection; 5 mg/kg, 10 mg/kg and 15 mg/kg; 21 days) has anti-proliferation effect in vivo and inhibits MGC823 cells xenografted tumor growth in vivo with few changes in body weights. Animal Model:MGC823 xenograft tumor in BALB/C-nu mice Dosage:5 mg/kg, 10 mg/kg and 15 mg/kg Administration:Intraperitoneal injection Result:Inhibited MGC823 xenograft tumor growth in vivo.
  • 同义词
    Cyasterone | AI3-44890 | AI3 44890
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    EGFR
  • 研究领域
    Cancer
  • 适应症
    ——

化学信息

  • CAS Number
    17086-76-9
  • 分子量
    520.66
  • 分子式
    C29H44O8
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 100 mg/mL (192.07 mM)
  • SMILES
    O1C(=O)[C@H]([C@@H]([C@H]1C)C[C@H]([C@@](C)([C@H]1CC[C@]2(C3=CC(=O)[C@@H]4C[C@H]([C@H](C[C@@]4([C@H]3CC[C@]12C)C)O)O)O)O)O)C
  • 化学全称
    5-beta-Stigmast-7-en-26-oic acid, 2-beta,3-beta,14,20,22,28-hexahydroxy-6-oxo-, gamma-lactone, (22R,24S,25S,28R)-

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. Hirayama Y,et al. Stereochemical assignment of C-24 and C-25 of amarasterone A, a putative biosynthetic intermediate of cyasterone. J Org Chem. 2014 Jun 20;79(12):5471-7.
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