Ephrin Receptor

Ephrin Receptor(Ephrin受体)

Ephrin receptors (Ephs) are a group of receptors that are activated in response to binding ephrin. Ephs form the largest known subfamily of receptor tyrosine kinases (RTKs). Both Ephs and their corresponding ephrin ligands are membrane-bound proteins that require direct cell-cell interactions for Eph receptor activation. Eph/ephrin signaling has been implicated in the regulation of a host of processes critical to embryonic development including axon guidance, formation of tissue boundaries, cell migration, and segmentation. Additionally, Eph/epherin signaling has recently been identified to play a critical role in the maintenance of several processes during adulthood including long-term potentiation, angiogenesis, and stem cell differentiation and cancer. The ability of Ephs and ephrins to mediate a variety of cell-cell interactions places the Eph/ephrin system in an ideal position to regulate a variety of different biological processes during embryonic development.

Ephrin Receptor 相关产品(13)

  • GC11134 structure
    GC11134ALW-II-41-27
    CAS: 1186206-79-0
    纯度: >99.50% / >98.00%

    ALW-II-41-27 是一种 Eph 家族酪氨酸激酶抑制剂,抑制 Eph2 的 IC50 为 11 nM。

  • GC14332 structure
    GC14332NVP-BHG712
    CAS: 940310-85-0
    纯度: >99.50%

    A selective EphB4 kinase inhibitor

  • GC18168 structure
    GC18168JI-101
    CAS: 900573-88-8
    纯度: >99.00%

    An inhibitor of VEGFR2, PDGFRβ, and EphB4

  • GC25367 structure
    GC25367Ehp-inhibitor-1
    CAS: 861249-59-4

    Ehp-inhibitor-1 (Ehp inhibitor 2) is an Eph family tyrosine kinase inhibitor that targets Eph receptors.

  • GC31752 structure
    GC31752Tesevatinib (XL-647)
    CAS: 781613-23-8
    纯度: >98.00%

    A multi-kinase inhibitor

  • GC35053 structure
    GC35053123C4
    CAS: 2034159-30-1

    123C4 是一种有效、选择性的,竞争性受体酪氨酸激酶 EPHA4 激动剂,Ki 值为 0.65 μM.

  • GC36782 structure
    GC36782NVP-BHG712 isomer
    CAS: 2245892-85-5
    纯度: >99.00%

    NVP-BHG712 isomer,是NVP-BHG712 的位置异构体,与EPHA2和EPHB4显示保守非键结合。

  • GC50137 structure
    GC50137KYL
    CAS: 676657-00-4

    An EphA4 inhibitor

  • GC64856 structure
    GC64856UniPR129
    CAS: 1639159-47-9
    纯度: >99.00%

    UniPR129 是一种有效 Eph/ephrin 拮抗剂。UniPR129 具有研究癌症疾病的潜力。

  • GC68647 structure
    GC68647ALW-II-49-7
    CAS: 1135219-23-6
    纯度: >98.00%

    ALW-II-49-7是一种选择性的EphB2激酶抑制剂,其IC 50 值为40nM。

  • GC69258 structure
    GC69258Ifabotuzumab
    CAS: 2147698-66-4
    纯度: >95.00%

    Ifabotuzumab (KB004) 是靶向 EphA3 的 IgG1κ 抗体 (KD=610 pM)。Ifabotuzumab 能够导致肿瘤细胞凋亡,并激活抗体依赖性细胞介导的细胞毒作用 (ADCC),破坏肿瘤脉管系统。Ifabotuzumab 能够减少人特发性肺纤维化 (IPF) CCR10+ 细胞,改善肺纤维化。

  • GC70097 structure
    GC70097Urolithin D
    CAS: 131086-98-1
    纯度: >98.00%

    Urolithin D 是 EphA 受体 的竞争性可逆拮抗剂。Urolithin D 表现出类内选择性。

  • GC74367 structure
    GC74367Targefrin
    CAS: 3031514-44-7
    纯度: >99.00%

    Targefrin是一种有效的epha2靶向剂,作为拮抗剂。