Tyrosine Kinase

Tyrosine Kinase(酪氨酸激酶)

研究方向

Tyrosine Kinase 相关产品(1402)

  • 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。

  • GC13697 structure
    GC13697AG-1024
    CAS: 65678-07-1
    纯度: >98.50%

    AG-1024是一种可逆的,竞争性和选择性的胰岛素样生长因子-1受体(IGF-1R)抑制剂,IC 50 值为7μM。AG-1024能够抑制胰岛素受体(IR)的磷酸化,IC 50 值为57μM。

  • GC13761 structure
    GC13761AZD8931 (Sapitinib)
    CAS: 848942-61-0
    纯度: >99.50%

    A reversible inhibitor of ErbB1/EGFR, ErbB2/HER2, and ErbB3/HER3

  • GC13914 structure
    GC13914Flumatinib mesylate
    CAS: 895519-91-2
    纯度: >99.50%

    A Bcr-Abl inhibitor

  • GC14189 structure
    GC14189AZD-3463
    CAS: 1356962-20-3
    纯度: >99.50%

    An ALK and IGF-1R inhibitor

  • GC14214 structure
    GC14214BMS-777607
    CAS: 1025720-94-8
    纯度: >99.00%

    BMS-777607 是一种泛 TAM 抑制剂,对不同类型的癌症显示出抗肿瘤活性。

  • GC14238 structure
    GC14238Brivanib Alaninate (BMS-582664)
    CAS: 649735-63-7
    纯度: >99.00%

    A prodrug form of brivanib

  • GC14256 structure
    GC14256Tivantinib (ARQ 197)
    CAS: 905854-02-6
    纯度: >99.50%

    An inhibitor of c-Met

  • GC14315 structure
    GC14315SU14813 maleate
    CAS: 849643-15-8
    纯度: >99.50%

    A dual VEGFR and PDGFR family kinase inhibitor

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

    A selective EphB4 kinase inhibitor

  • GC14396 structure
    GC14396Ponatinib (AP24534)
    CAS: 943319-70-8
    纯度: >99.00%

    Ponatinib (AP24534)是一种多靶点酪氨酸激酶抑制剂,可抑制Abl(IC 50 =0.37nM),PDGFRα(IC 50 =1.1nM),VEGFR2(IC 50 =1.5nM),FGFR1(IC 50 =2.2nM)和Src(IC 50 =5.4nM)的活性。

  • GC14407 structure
    GC14407PF-431396
    CAS: 717906-29-1
    纯度: >98.50%

    A FAK/PYK2 dual inhibitor

  • GC14489 structure
    GC14489Y 11
    CAS: 1086639-59-9
    纯度: >95.00%

    An inhibitor of FAK1

  • GC14534 structure
    GC14534Regorafenib monohydrate
    CAS: 1019206-88-2
    纯度: >99.50%

    A multi-kinase inhibitor

  • GC14552 structure
    GC14552LDK378
    CAS: 1032900-25-6
    纯度: >99.50%

    An ALK inhibitor

  • GC14592 structure
    GC14592KW 2449
    CAS: 1000669-72-6
    纯度: >99.50%

    A multi-kinase inhibitor

  • GC14606 structure
    GC14606Regorafenib hydrochloride
    CAS: 835621-07-3
    纯度: >99.50%

    A multi-kinase inhibitor

  • GC14660 structure
    GC14660SU 5402
    CAS: 215543-92-3
    纯度: >98.00%

    SU 5402是一种多靶点受体酪氨酸激酶抑制剂,对血管内皮生长因子受体2(VEGF-R2)和成纤维细胞生长因子受体1(FGF-R1)酪氨酸激酶活性的IC 50 分别为20nM和30nM。

  • GC14683 structure
    GC14683Sunitinib malate
    CAS: 341031-54-7
    纯度: >99.00%

    A multi-kinase inhibitor

  • GC14729 structure
    GC14729(R)-Crizotinib
    CAS: 877399-52-5
    纯度: >99.50%

    A c-MET and ALK receptor tyrosine kinase inhibitor

  • GC14733 structure
    GC14733SU14813
    CAS: 627908-92-3
    纯度: >98.50%

    A dual VEGFR and PDGFR family kinase inhibitor

  • GC14807 structure
    GC14807Fingolimod (FTY720) HCl
    CAS: 162359-56-0
    纯度: >99.50% / >99.00%

    芬戈莫德(FTY720)是一种免疫抑制剂,通常用于治疗多发性硬化症,也有抗癌作用,可以作为HDACi(组蛋白脱乙酰酶抑制剂)。

  • GC14898 structure
    GC14898Tie2 kinase inhibitor
    CAS: 948557-43-5
    纯度: >99.00%

    Tie2 kinase inhibitor是一种可逆的选择性Tie2抑制剂,IC50为250 nM。

  • GC15022 structure
    GC15022Vandetanib (ZD6474)
    CAS: 443913-73-3
    纯度: >99.50%

    A multi-kinase inhibitor