High affinity VEGF-receptor antagonists
    1.
    发明授权
    High affinity VEGF-receptor antagonists 有权
    高亲和力VEGF受体拮抗剂

    公开(公告)号:US08334239B2

    公开(公告)日:2012-12-18

    申请号:US12166042

    申请日:2008-07-01

    IPC分类号: C40B30/04

    摘要: A cell-based screen is reported can be used to identify specific receptor-binding compounds in a combinatorial library of peptoids (N-alkylglycine oligomers) displayed on beads. This strategy was applied to the isolation of Vascular Endothelial Growth Factor Receptor 2 (VEGFR2)-binding peptoids, which were optimized to create lead compounds with high affinity for VEGFR2. One of these peptoids was shown to be an antagonist of VEGF-VEGFR2 interaction and receptor function.

    摘要翻译: 据报道,基于细胞的筛选可以鉴定出显示在珠粒上的拟肽(N-烷基甘氨酸寡聚物)的组合文库中的特异性受体结合化合物。 该策略被应用于分离血管内皮生长因子受体2(VEGFR2)结合的拟肽,其被优化以产生对VEGFR2具有高亲和力的铅化合物。 这些拟肽中的一种被证明是VEGF-VEGFR2相互作用和受体功能的拮抗剂。

    HIGH AFFINITY VEGF-RECEPTOR ANTAGONISTS
    3.
    发明申请
    HIGH AFFINITY VEGF-RECEPTOR ANTAGONISTS 有权
    高亲和力VEGF受体拮抗剂

    公开(公告)号:US20110077201A1

    公开(公告)日:2011-03-31

    申请号:US12950425

    申请日:2010-11-19

    摘要: A cell-based screen is reported can be used to identify specific receptor-binding compounds in a combinatorial library of peptoids (N-alkylglycine oligomers) displayed on beads. This strategy was applied to the isolation of Vascular Endothelial Growth Factor Receptor 2 (VEGFR2)-binding peptoids, which were optimized to create lead compounds with high affinity for VEGFR2. One of these peptoids was shown to be an antagonist of VEGF-VEGFR2 interaction and receptor function.

    摘要翻译: 据报道,基于细胞的筛选可以鉴定出显示在珠粒上的拟肽(N-烷基甘氨酸寡聚物)的组合文库中的特异性受体结合化合物。 该策略被应用于分离血管内皮生长因子受体2(VEGFR2)结合的拟肽,其被优化以产生对VEGFR2具有高亲和力的铅化合物。 这些拟肽中的一种被证明是VEGF-VEGFR2相互作用和受体功能的拮抗剂。

    HIGH AFFINITY VEGF-RECEPTOR ANTAGONISTS
    5.
    发明申请
    HIGH AFFINITY VEGF-RECEPTOR ANTAGONISTS 有权
    高亲和力VEGF受体拮抗剂

    公开(公告)号:US20090246124A1

    公开(公告)日:2009-10-01

    申请号:US12166042

    申请日:2008-07-01

    摘要: A cell-based screen is reported can be used to identify specific receptor-binding compounds in a combinatorial library of peptoids (N-alkylglycine oligomers) displayed on beads. This strategy was applied to the isolation of Vascular Endothelial Growth Factor Receptor 2 (VEGFR2)-binding peptoids, which were optimized to create lead compounds with high affinity for VEGFR2. One of these peptoids was shown to be an antagonist of VEGF-VEGFR2 interaction and receptor function.

    摘要翻译: 据报道,基于细胞的筛选可以鉴定出显示在珠粒上的拟肽(N-烷基甘氨酸寡聚物)的组合文库中的特异性受体结合化合物。 该策略被应用于分离血管内皮生长因子受体2(VEGFR2)结合的拟肽,其被优化以产生对VEGFR2具有高亲和力的铅化合物。 这些拟肽中的一种被证明是VEGF-VEGFR2相互作用和受体功能的拮抗剂。