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YTX-465

CAS No. 2225824-53-1

YTX-465 ( —— )

产品货号. M28861 CAS No. 2225824-53-1

YTX-465 是硬脂酰辅酶 A 去饱和酶 (IC50s = 39 nM) 和 Ole1 (IC50s = 30.4 μM) 的抑制剂。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥5038 有现货
10MG ¥7962 有现货
25MG ¥11826 有现货
50MG ¥15957 有现货
100MG ¥21465 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
    YTX-465
  • 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
    YTX-465 是硬脂酰辅酶 A 去饱和酶 (IC50s = 39 nM) 和 Ole1 (IC50s = 30.4 μM) 的抑制剂。
  • 产品描述
    YTX-465 is an inhibitor of both stearoyl-CoA desaturase(IC50s = 39 nM) and Ole1 (IC50s = 30.4 μM).(In Vitro):YTX-465 rescued growth to a similar magnitude but was >100-fold more potent than YTX-528(EC50 = 0.013 μM). Kinetic growth studies demonstrated that the most effective concentration of YTX-465 (0.050 μM) restored growth rates to that of approximately 40% of the wild-type strain treated with the same concentration of YTX-465. In wild-type yeast, YTX-465 strongly reduced fatty desaturation in a concentration-dependent manner, with a 50% reduction in desaturation at 0.03 μM YTX-465.
  • 体外实验
    YTX-465 (1-10000 nM) has an EC50 value of 0.013 μM for α-synuclein (α-syn) toxicity rescue.YTX-465 (0.05 μM; 0-2 days) rescue the growth of α-Syn-expressing yeast.YTX-465 (0, 10, 40, 160, 640, 2500 nM; 4h) increases the level of Ole1 protein in wild-type yeast expressing OLE1 in a concentration-dependent manner, that indicate YTX-465 induce a negative feedback loop.YTX-465 (0, 0.03, 0.09, 0.27, 0.81 μM; 6 hours) reduces fatty desaturation in a concentration-dependent manner in wild-type yeast, with a 50% reduction in desaturation at 0.03 μM.YTX-465 (0.25 μM; 8 hours) decreases the desaturation index (DI) for all major classes of membrane phospholipids in wild-type yeast.
  • 体内实验
    ——
  • 同义词
    ——
  • 通路
    Metabolic Enzyme/Protease
  • 靶点
    SCD
  • 受体
    EML4-ALK
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    2225824-53-1
  • 分子量
    458.51
  • 分子式
    C25H26N6O3
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 100 mg/mL (218.10 mM)
  • SMILES
    Cc1nn(C)c2c1ccc(-c1noc(C(CC3)CCN3C(CNC(c3ccccc3)=O)=O)n1)c2
  • 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.Iikubo K, et al. Synthesis and structure-activity relationships of pyrazine-2-carboxamide derivatives as novel echinoderm microtubule-associated protein-like 4 (EML4)-anaplastic lymphoma kinase (ALK) inhibitors. Bioorg Med Chem. 2019 Apr 15;27(8):1683-1692.
产品手册
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