HER2

HER2 is a member of the epidermal growth factor. It initiates the EGF downstream cascade by forming a heterodimer with other ligand-bound EGF receptor. It is associated with breast and ovarian cancers.

HER2 相关产品(15)

  • GC10250 structure
    GC10250Mubritinib (TAK 165)
    CAS: 366017-09-6
    纯度: >99.50%

    Mubritinib (TAK 165)是一种有效的选择性 HER2/ErbB2 抑制剂,其IC 50 为6nM。

  • GC10606 structure
    GC10606BMS-599626 Hydrochloride
    CAS: 873837-23-1
    纯度: >99.50%

    BMS-599626 Hydrochloride (AC480 Hydrochloride) 是一种选择性的口服生物可利用的 HER1 和 HER2 抑制剂,IC50 分别为 20 和 30 nM。 BMS-599626 Hydrochloride 对 HER4 (IC50=190 nM) 的效力降低约 8 倍,对 VEGFR2、c-Kit、Lck、MEK 的效力超过 100 倍。 BMS-599626 Hydrochloride 抑制肿瘤细胞增殖,并有可能增加肿瘤对放疗的反应。

  • GC10707 structure
    GC10707Afatinib dimaleate
    CAS: 850140-73-7
    纯度: >99.50%

    An inhibitor of EGFR and ErbB2

  • GC11172 structure
    GC11172TAK-285
    CAS: 871026-44-7
    纯度: >98.00%

    A dual inhibitor of EGFR and HER2

  • GC12087 structure
    GC12087Canertinib dihydrochloride
    CAS: 289499-45-2
    纯度: >99.00%

    A pan-ErbB tyrosine kinase inhibitor

  • GC13091 structure
    GC13091CP-724714
    CAS: 383432-38-0
    纯度: >99.00%

    A selective HER2/ErbB2 tyrosine kinase inhibitor

  • GC13257 structure
    GC13257AC480 (BMS-599626)
    CAS: 714971-09-2

    A dual inhibitor of EGFR and HER2

  • GC13608 structure
    GC13608Lapatinib
    CAS: 231277-92-2
    纯度: >99.50%

    Lapatinib是一种口服的双重EGFR和HER2酪氨酸激酶抑制剂,对HER2阳性乳腺癌具有显著疗效。Lapatinib对纯化的EGFR和HER2的半数抑制浓度(IC₅₀)值分别为10.2nM和9.8nM。

  • GC15271 structure
    GC15271Tyrphostin AG 879
    CAS: 148741-30-4
    纯度: >99.50%

    A non-specific tyrphostin ErbB2 inhibitor

  • GC16008 structure
    GC16008CUDC-101
    CAS: 1012054-59-9
    纯度: >99.00%

    A multi-target inhibitor of HDACs, EGFR, and HER2

  • GC16593 structure
    GC16593Lapatinib Ditosylate
    CAS: 388082-78-8
    纯度: >99.50%

    Lapatinib Ditosylate (GW572016 ditosylate monohydrate) 是有效的 ErbB-2 和 EGFR 酪氨酸激酶结构域抑制剂,对纯化的 EGFR 和 ErbB-2 的 IC50 值分别为 10.2 和 9.8 nM。

  • GC17473 structure
    GC17473Pelitinib (EKB-569)
    CAS: 257933-82-7
    纯度: >98.00%

    An EGFR receptor tyrosine kinase inhibitor

  • GC10362 structure
    GC10362Neratinib (HKI-272)
    CAS: 698387-09-6
    纯度: >99.50%

    A dual inhibitor of EGFR and HER2

  • GC13296 structure
    GC13296Afatinib(BIBW2992)
    CAS: 439081-18-2

    Afatinib(BIBW2992)是一种口服、选择性ErbB家族受体酪氨酸激酶(RTK)抑制剂,其对EGFR激酶的IC 50 值为0.05nM,对HER2激酶为14nM,对HER4激酶为1nM。

  • GC17916 structure
    GC17916Poziotinib
    CAS: 1092364-38-9

    An inhibitor of EGFRs