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OTS-964

CAS No. 1338545-07-5

OTS-964 ( OTS964 )

产品货号. M11360 CAS No. 1338545-07-5

OTS-964 是 OTS514 的二甲基化衍生物,是有效的选择性 TOPK 抑制剂,IC50 为 28 nM。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥437 有现货
5MG ¥689 有现货
10MG ¥1021 有现货
25MG ¥1677 有现货
50MG ¥2989 有现货
100MG ¥4447 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
    OTS-964
  • 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
    OTS-964 是 OTS514 的二甲基化衍生物,是有效的选择性 TOPK 抑制剂,IC50 为 28 nM。
  • 产品描述
    OTS-964 is a dimethylated derivative of OTS514 and potent, selective TOPK inhibitor with IC50 of 28 nM, exhibits excellent in vivo efficacy with liposomal formulation; inhibits the growth of TOPK-positive cells with low IC50 values (A549 IC50=31 nM), decreases autophosphorylation of TOPK (Thr9), as well as phosphorylation of histone H3 (Ser10), in both T47D and LU-99 cells; the liposomal OTS964 causes complete regression of tumors without any detectable toxicity in the xenograft models.
  • 体外实验
    OTS964 hydrochloride (10 nM; 48 hours) suppresses cancer cell proliferation. OTS964 hydrochloride (10 nM; 48 hours) increases cancer cell death. OTS964 (0.1-2 μM; 24 and 48 hours) increases the expression of LC3-II and decreases the expression of P62, both in a dose-dependent manner. Cell Proliferation Assay Cell Line:LU-99 cells.Concentration:10 nM Incubation Time:48 hours Result:Suppressed cancer cell proliferation.Apoptosis Analysis Cell Line:LU-99 cells Concentration:10 nM Incubation Time:48 hoursResult:Increased cancer cell death.Western Blot AnalysisCell Line:Hs683 cells, H4 cells Concentration:0.1, 1, 2 μM Incubation Time:24 and 48 hours Result:Increased the expression of LC3-II and decreased the expression of P62, both in a dose-dependent manner.
  • 体内实验
    OTS964 hydrochloride (intravenously; 40 mg/kg on days 1, 4, 8, 11, 15, and 18) makes tumors shrinking even after the treatment and finally revealing complete regression. OTS964 hydrochloride (oral administration; 50 or 100 mg/kg/day for 2 weeks) ultimately achieves complete tumor regression. Animal Model:Nude mice bearing LU-99 lung cancer cells Dosage:40 mg/kg Administration:Intravenously; on days 1, 4, 8, 11, 15, and 18 Result:The tumors continued shrinking even after the treatment and finally revealed complete regression. Animal Model:Nude mice bearing LU-99 lung cancer cellsDosage:50 or 100 mg/kg Administration:Oral administration; once every day for 2 weeks Result:Achieved complete tumor regression.
  • 同义词
    OTS964
  • 通路
    MAPK/ERK Signaling
  • 靶点
    MEK
  • 受体
    TOPK
  • 研究领域
    Cancer
  • 适应症
    ——

化学信息

  • CAS Number
    1338545-07-5
  • 分子量
    428.9748
  • 分子式
    C23H25ClN2O2S
  • 纯度
    >98% (HPLC)
  • 溶解度
    10 mM in DMSO
  • SMILES
    CC1=CC(=C(C2=C1NC(=O)C3=C2C=CS3)C4=CC=C(C=C4)C(C)CN(C)C)O.Cl
  • 化学全称
    Thieno[2,3-c]quinolin-4(5H)-one, 9-[4-[(1R)-2-(dimethylamino)-1-methylethyl]phenyl]-8-hydroxy-6-methyl-, hydrochloride (1:1)

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. Matsuo Y, et al. Sci Transl Med. 2014 Oct 22;6(259):259ra145. 2. Ikeda Y, et al. Clin Cancer Res. 2016 Dec 15;22(24):6110-6117. 3. Pirovano G, et al. Br J Cancer. 2017 Aug 8;117(4):503-512. 4. Sugimori M, et al. Oncotarget. 2017 Dec 9;9(3):3043-3059.
产品手册
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