GlpBio

Tyrosine Kinase

Tyrosine Kinase(酪氨酸激酶)

研究方向

Tyrosine Kinase 相关产品(1402)

  • GN10737 structure
    GN10737Tanshinone IIA
    CAS: 568-72-9
    纯度: >99.50%

    Tanshinone IIA 是一种从丹参中分离出来的主要丹参酮，常用于心血管疾病和癌症的研究。

  • GN10784 structure
    GN10784Rhoifolin
    CAS: 17306-46-6
    纯度: >98.00%

    A flavonoid glycoside with diverse biological activities

  • GP26187 structure
    GP26187ErbB4 Human

    ErbB4 Human Recombinant produced in HEK293 Cells is a single, glycosylated polypeptide chain containing 863 amino acids (26-649 a

  • GP26200 structure
    GP26200TYRO3 Mouse

    TYRO3 Mouse produced in Sf9 Baculovirus cells is a single, glycosylated polypeptide chain containing 628 amino acids (31-419 aa) and having a molecular mass of 68

  • GC10627 structure
    GC10627Erlotinib
    CAS: 183321-74-6
    纯度: >99.50% / >98.00%

    Erlotinib是一种有效且口服生物可利用的表皮生长因子受体（EGFR）酪氨酸激酶抑制剂，IC 50 值为2 nM。

  • GC10944 structure
    GC10944Butein
    CAS: 487-52-5
    纯度: >98.00%

    A plant polyphenol

  • GC11126 structure
    GC11126Mutant EGFR inhibitor
    CAS: 1421373-62-7
    纯度: >99.00%

    Mutant EGFR inhibitor 是从专利WO 2013014448 A1中提取的一种有效的选择性突变EGFR抑制剂；抑制 EGFRL858R、EGFRExon 19 缺失和 EGFRT790M。

  • GC11691 structure
    GC11691AST-1306
    CAS: 897383-62-9

    An irreversible inhibitor of EGFR, HER2, and HER4

  • GC11696 structure
    GC116961-NM-PP1
    CAS: 221244-14-0
    纯度: >99.50%

    Inhibitor of modified 'analog-sensitive' kinases

  • GC12478 structure
    GC12478ARRY-380
    CAS: 937265-83-3

    An inhibitor of EGFR

  • GC13738 structure
    GC13738SKLB1002
    CAS: 1225451-84-2

    A VEGFR2 inhibitor

  • GC13854 structure
    GC13854AG-490 (Tyrphostin B42)
    CAS: 133550-30-8
    纯度: >98.00%

    AG-490 (Tyrphostin B42)是EGFR抑制剂,IC50为0.1 µM, AG-490对JAK2也有抑制作用。

  • GC13868 structure
    GC13868GNE-9605
    CAS: 1536200-31-3
    纯度: >99.50%

    A potent LRRK2 inhibitor

  • GC14288 structure
    GC14288KX2-391
    CAS: 897016-82-9
    纯度: >99.00%

    A Src kinase inhibitor

  • GC14310 structure
    GC14310NVP-ADW742
    CAS: 475488-23-4
    纯度: >99.00%

    An IGF-1R inhibitor

  • GC14695 structure
    GC14695CO-1686 (AVL-301)
    CAS: 1374640-70-6
    纯度: >99.50%

    A selective inhibitor of mutant EGFR

  • GC15669 structure
    GC15669AST-1306 TsOH
    CAS: 1050500-29-2
    纯度: >99.50%

    An irreversible inhibitor of EGFR, HER2, and HER4

  • GC16698 structure
    GC16698AZD-9291 mesylate
    CAS: 1421373-66-1
    纯度: >99.50%

    An inhibitor of mutant EGFR

  • GC17530 structure
    GC17530OSI-420
    CAS: 183320-51-6
    纯度: >98.50%

    OSI-420 (OSI-420) 是厄洛替尼的活性代谢物。厄洛替尼是一种有效的 EGFR 酪氨酸激酶抑制剂。

  • GC17647 structure
    GC17647AG-18
    CAS: 118409-57-7
    纯度: >98.50%

    An inhibitor of EGF receptor kinase

  • GC17982 structure
    GC17982Icotinib
    CAS: 610798-31-7
    纯度: >99.00% / >99.50%

    Icotinib表皮生长因子受体（EGFR；IC 50 =5nM）抑制剂，可抑制EGFR（L858R，T790M，L861Q）等突变体。

  • GC11044 structure
    GC11044Fostamatinib (R788)
    CAS: 901119-35-5
    纯度: >98.50% / >98.00%

    Fostamatinib (R788) 是活性化合物 R406 的口服前药，R406 是一种相对选择性的 Syk 小分子抑制剂。

  • GC14464 structure
    GC14464Vatalanib
    CAS: 212141-54-3

    A potent and selective VEGF receptor inhibitor

  • GC17789 structure
    GC17789A 419259 trihydrochloride
    CAS: 1435934-25-0
    纯度: >99.00%

    An inhibitor of Src family kinases