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AMG-337

CAS No. 1173699-31-4

AMG-337 ( AMG337 | AMG 337 )

产品货号. M10584 CAS No. 1173699-31-4

AMG-337 是一种有效的选择性 MET 抑制剂,生化 IC50 为 1 nM;抑制 PC3 细胞中 HGF 介导的 MET 磷酸化。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥389 有现货
5MG ¥624 有现货
10MG ¥1021 有现货
25MG ¥1677 有现货
50MG ¥2989 有现货
100MG ¥4447 有现货
200MG ¥6383 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
    AMG-337
  • 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
    AMG-337 是一种有效的选择性 MET 抑制剂,生化 IC50 为 1 nM;抑制 PC3 细胞中 HGF 介导的 MET 磷酸化。
  • 产品描述
    AMG-337 is a potent and selective inhibitor of MET with biochemical IC50 of 1 nM; inhibits of HGF-mediated MET phosphorylation in PC3 cells; shows desirable preclinical pharmacokinetics, significant inhibition of MET phosphorylation in mice, and robust tumor growth inhibition in a MET-dependent mouse efficacy model.Gastric Cancer Phase 2 Clinical(In Vitro):AMG 337 (0-3 μM; 72 h) inhibits proliferation in MET-dependent cancer cell lines.AMG 337 (0-300 nM; 0-24 h; MKN-45, SNU-620, and SNU-5 cells) inhibits signaling through the PI3K and MAPK pathways in MET-amplified gastric cancer cell lines, resulting in an inhibition of MET-dependent cell proliferation and induction of apoptosis.(In Vivo):AMG 337 (0-30 mg/kg; p.o.; daily, for 28 d) inhibits MET signaling in tumor xenografts and inhibits tumor growth in MET-dependent tumor xenograft models.AMG 337 (0-3 mg/kg; p.o.; once, for 3 or 24 h) is associated with increased necrosis in the MET-dependent SNU-620 tumor xenograft model.
  • 体外实验
    AMG 337 (0-3 μM; 72 h) inhibits proliferation in MET-dependent cancer cell lines.AMG 337 (0-300 nM; 0-24 h; MKN-45, SNU-620, and SNU-5 cells) inhibits signaling through the PI3K and MAPK pathways in MET-amplified gastric cancer cell lines, resulting in an inhibition of MET-dependent cell proliferation and induction of apoptosis. Apoptosis Analysis Cell Line:MKN-45 and SNU-620 cells Concentration:0, 3, 10, 30, 100 and 300 nM Incubation Time:24 hours Result:Increased the number of cells undergoing apoptosis.Cell Cycle Analysis Cell Line:MKN-45 and SNU-620 cells Concentration:0, 3, 10, 30, 100 and 300 nM Incubation Time:24 hours Result:Increased in a dose-dependent in cells in the G1 phase and with concurrent reduction of cells in S-phase.Western Blot Analysis Cell Line:MKN-45, SNU-620, and SNU-5 cells Concentration:100 nM Incubation Time:2 hours Result:Inhibited MET phosphorylation and phosphorylation of downstream effectors.Western Blot Analysis Cell Line:MKN-45, SNU-620, and SNU-5 cells Concentration:100 nM Incubation Time:24 hours Result:Induced PARP and caspase-3 cleavage in SNU-620 and SNU-5 cells.
  • 体内实验
    AMG 337 (0-30 mg/kg; p.o.; daily, for 28 d) inhibits MET signaling in tumor xenografts and inhibits tumor growth in MET-dependent tumor xenograft models.AMG 337 (0-3 mg/kg; p.o.; once, for 3 or 24 h) is associated with increased necrosis in the MET-dependent SNU-620 tumor xenograft model. Animal Model:Female CD1 nu/nu mice bearing SNU-620, SNU-5, or U-87 MG xenografts Dosage:0, 0.3, and 1 mg/kg (SNU-620 xenograft); 0, 0.3, 1, 3, and 10 mg/kg (SNU-5 xenograft); 0, 3, 10 and 30 mg/kg (U-87 xenograft)Administration:Oral administration; daily, for 28 days Result:Inhibited tumor growth in MET-dependent tumor xenograft models.Animal Model:Female CD1 nu/nu mice bearing SNU-620, SNU-5, or U-87 MG xenograftsDosage:0.1, 0.5, 0.75, 1, 2, and 3 mg/kg Administration:Oral administration; once, for 3 hours Result:Inhibited Gab-1 phosphorylation in a dose-dependent manner.Animal Model:Female CD1 nu/nu mice with SNU-620 xenograft model (6-11 weeks of age; 20-26 g)Dosage:0, 0.3, 1, and 3 mg/kg Administration:Oral administration; once, for 3 or 24 hours Result:Increased immunohistochemical staining with anti-caspase-3 antibody and decreased immunohistochemical staining with anti-BrdU antibody.
  • 同义词
    AMG337 | AMG 337
  • 通路
    Angiogenesis
  • 靶点
    c-Met/HGFR
  • 受体
    Met|Met(H1094R)|Met(M1250T)|Met(V1092I)|Met(Y1230H)
  • 研究领域
    Cancer
  • 适应症
    Gastric Cancer

化学信息

  • CAS Number
    1173699-31-4
  • 分子量
    463.4643
  • 分子式
    C23H22FN7O3
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO: ≥ 30 mg/mL
  • SMILES
    O=C1C2=C(N=CC(OCCOC)=C2)C=CN1[C@@H](C3=NN=C4C(F)=CC(C5=CN(C)N=C5)=CN43)C
  • 化学全称
    1,6-Naphthyridin-5(6H)-one, 6-[(1R)-1-[8-fluoro-6-(1-methyl-1H-pyrazol-4-yl)-1,2,4-triazolo[4,3-a]pyridin-3-yl]ethyl]-3-(2-methoxyethoxy)-

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. Boezio AA, et al. J Med Chem. 2016 Mar 24;59(6):2328-42. 2. Hughes PE, et al. Mol Cancer Ther. 2016 Jul;15(7):1568-79. 3. Du Z, et al. Mol Cancer Ther. 2016 Jun;15(6):1227-37.
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