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ODM-203

CAS No. 1430723-35-5

ODM-203 ( —— )

产品货号. M20920 CAS No. 1430723-35-5

ODM-203 是 FGFR 和 VEGFR 的选择性抑制剂,具有很强的抗肿瘤活性,并诱导抗肿瘤免疫。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥292 有现货
5MG ¥478 有现货
10MG ¥786 有现货
25MG ¥1725 有现货
50MG ¥2973 有现货
100MG ¥4423 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
    ODM-203
  • 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
    ODM-203 是 FGFR 和 VEGFR 的选择性抑制剂,具有很强的抗肿瘤活性,并诱导抗肿瘤免疫。
  • 产品描述
    ODM-203 a Selective Inhibitor of FGFR and VEGFR Shows Strong Antitumor Activity and Induces Antitumor Immunity.(In Vitro):ODM-203 (eight-dose concentration series up to 3 μM; 96 h) potently inhibits FGFR signaling and proliferation in several FGFR-dependent cell lines.ODM-203 (eight-dose concentration series up to 3 μM; 10 days) inhibits endothelial tubule formation.ODM-203 (1, 10, 100, 1000 nM; 1 h) inhibiting FGFR and VEGFR cellular signaling in HUVEC cells.(In Vivo):ODM-203 (20, 40 mg/kg; p.o.; single daily for 21 days) inhibits FGFR phosphorylation and tumor growth in several FGFR-dependent xenografts by suppressing FGFR signaling in tumors.ODM-203 (7, 20, 40 mg/kg; p.o.; single daily for 21 days) shows strong anti-tumor activity in a VEGFR-dependent angiogenic orthotopic syngenic model (Renca) and suppresses angiogenesis.ODM-203 (20, 40 mg/kg; p.o.; single daily for 5 days) activates immune response in the tumor microenvironment.
  • 体外实验
    ODM-203 (eight-dose concentration series up to 3 μM; 96 h) potently inhibits FGFR signaling and proliferation in several FGFR-dependent cell lines.ODM-203 (eight-dose concentration series up to 3 μM; 10 days) inhibits endothelial tubule formation.ODM-203 (1, 10, 100, 1000 nM; 1 h) inhibiting FGFR and VEGFR cellular signaling in HUVEC cells. Cell Viability AssayCell Line:H1581 (ATCC-CRL-5878), SNU16 (ATCC-CRL-5974) and RT4 (HTB2) cells Concentration:Eight-dose concentration series up to 3 μM Incubation Time:96 h Result:Suppressed cell proliferation in a dose-dependent manner in H1581 (IC50=104 nM), SNU16 (IC50=132 nM) and RT4 cells (IC50=192 nM).Cell Viability Assay Cell Line:HUVECs and human umbilical vein endothelial cells (co-culture)Concentration:Eight-dose concentration series up to 3 μM Incubation Time:10 days (media and test agents were replaced every 2-3 days )Result:Inhibited endothelial tubule formation in a dose-dependent manner at non-toxic concentrations with an IC50 value of 33 nM.Western Blot Analysis Cell Line:HUVEC cells Concentration:1, 10, 100, 1000 nM Incubation Time:1 h Result:Suppressed both FGFR and VEGFR signaling.
  • 体内实验
    ODM-203 (20, 40 mg/kg; p.o.; single daily for 21 days) inhibits FGFR phosphorylation and tumor growth in several FGFR-dependent xenografts by suppressing FGFR signaling in tumors.ODM-203 (7, 20, 40 mg/kg; p.o.; single daily for 21 days) shows strong anti-tumor activity in a VEGFR-dependent angiogenic orthotopic syngenic model (Renca) and suppresses angiogenesis.ODM-203 (20, 40 mg/kg; p.o.; single daily for 5 days) activates immune response in the tumor microenvironment. Animal Model:Athymic Nude-Foxn1nu female mice (9-week-old; subcutaneous xenograft models).Dosage:20, 40 mg/kg Administration:Oral administration; single daily for 21 days.Result:Significantly inhibited tumour growth for 21 consecutive days.Showed tumor growth inhibition (TGI) in RT4 xenografts was 37% and 92% with dosage of 20 and 40 mg/kg, respectively.Animal Model:Male balb/c mice (8-week-old; orthotopic renca syngenic model).Dosage:7, 20, 40 mg/kg Administration:Oral administration; single daily for 21 days.Result:Showed tumor growth inhibition were 39%, 58% and 75% for dosage of 7, 20 and 40 mg/kg, respectively.Inhibited formation of lung metastasis, and suppressed angiogenesis.Animal Model:Male balb/c male mice (5 to 7-week-old; renca subcutaneous tumor model).Dosage:20, 40 mg/kg Administration:Oral administration; single daily for 5 days.Result:Resulted in an increase in the percentage of total and CD4 T cells.Decreased the expression of immune check points PD-1 and PD-L1 and increased IFN-γ expression on both CD8 T cells and NK cells.
  • 同义词
    ——
  • 通路
    Angiogenesis
  • 靶点
    FGFR
  • 受体
    FGFR|VEGFR
  • 研究领域
    Cancer
  • 适应症
    Solid tumours

化学信息

  • CAS Number
    1430723-35-5
  • 分子量
    505.54
  • 分子式
    C26H21F2N5O2S
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 66.67 mg/mL (131.88 mM)
  • SMILES
    Cn1cc(-c2ccc3c(c2)ncn3-c2cc(NS(=O)(=O)C3CC3)cc(-c3ccc(F)cc3F)c2)cn1
  • 化学全称
    N-(2'4'-Difluoro-5-(5-(1-methyl-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)-[11'-biphenyl]-3-yl)cyclopropanesulfonamide

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.Tim H Holmstr?m Anu-Maarit Moilanen Tarja Ikonenet al.ODM-203 a Selective Inhibitor of FGFR and VEGFR Shows Strong Antitumor Activity and Induces Antitumor Immunity[J].Mol Cancer Ther 18 (1) 28-38 Jan 2019
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