
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)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥292 | 有现货 |
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5MG | ¥478 | 有现货 |
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10MG | ¥786 | 有现货 |
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25MG | ¥1725 | 有现货 |
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50MG | ¥2973 | 有现货 |
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100MG | ¥4423 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称ODM-203
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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
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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。
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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.
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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.
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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.
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同义词——
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通路Angiogenesis
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靶点FGFR
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受体FGFR|VEGFR
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研究领域Cancer
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适应症Solid tumours
化学信息
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CAS Number1430723-35-5
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分子量505.54
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分子式C26H21F2N5O2S
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 66.67 mg/mL (131.88 mM)
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SMILESCn1cc(-c2ccc3c(c2)ncn3-c2cc(NS(=O)(=O)C3CC3)cc(-c3ccc(F)cc3F)c2)cn1
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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
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储存条件(-20℃)
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运输条件With Ice Pack
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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