Aurora Kinase

Aurora Kinase(极光激酶)

Aurora kinases are a family of serine-threonine kinases of three highly homologous members, including aurora A kinase, aurora B kinase and aurora C kinase, which are responsible for chromosome assembly and segregation during mitosis. Aurora kinases are characterized by two domains: a regulatory domain in the NH2 terminus and a catalytic domain in the COOH terminus, in which an A-Box and a D-Box found correspondingly in each domain are responsible for protein degradation. Aurora A kinase plays an important role in centrosome function and duplication, mitotic entry and bipolar spindle assembly; while Aurora B kinase is the catalytic component of the chromosomal passenger complex regulating the accurate segregation of the chromatids at mitosis, histone modification and cytokinesis. Aurora C kinase is less studied and expressed restrictedly in the testes.

Aurora Kinase 相关产品(57)

  • GC68147 structure
    GC68147dAURK-4 hydrochloride

    dAURK-4 hydrochloride 是 Alisertib 的一种衍生物,是一种有效的选择性 AURKA (Aurora A) 降解剂。dAURK-4 hydrochloride 具有抗癌作用。

  • GC69068 structure
    GC69068ENMD-2076 Tartrate
    CAS: 1453868-32-0
    纯度: >99.00%

    ENMD-2076 Tartrate 是多靶点激酶抑制剂,抑制 Aurora A,Flt3,KDR/VEGFR2,Flt4/VEGFR3,FGFR1,FGFR2,Src,PDGFRα 的IC50 值分别为1.86,14,58.2,15.9,92.7,70.8,20.2 and 56.4 nM。

  • GC70030 structure
    GC70030Tinengotinib
    CAS: 2230490-29-4

    Tinengotinib 是一种或多种蛋白激酶的调节剂,例如 Aurora 激酶和 VEGFR 激酶。Tinengotinib 具有研究这些激酶异常介导的疾病的潜力,尤其是癌症相关疾病 (摘自专利 WO2018108079A1)。

  • GC72964 structure
    GC72964Aurkin A
    CAS: 1534060-58-6
    纯度: >98.00%

    Aurkin A是极光A激酶(Aurora A Kinase,也称Aurka)与TPX2相互作用的变抗抑制剂,通过靶向TPX2结合位点,Kd为3.77 μM。

  • GC73375 structure
    GC73375Aurora Kinases-IN-3
    CAS: 2840558-83-8
    纯度: >98.00%

    Aurora Kinases-IN-3(化合物15a)是一种口服活性AURKB抑制剂,通过破坏AURKB的有丝分裂定位来引发AURKB抑制活性。

  • GC73744 structure
    GC73744JAB-2485
    CAS: 2899209-55-1
    纯度: >98.00%

    JAB-2485是一种有效的选择性极光激酶a (AURKA)抑制剂,IC50为0.33 nM。

  • GC73753 structure
    GC73753EGFR/AURKB-IN-1
    CAS: 3008543-34-5
    纯度: 不显示

    EGFR/AURKB-IN-1(化合物7)是双靶向EGFR/AURKB抑制剂,抑制L858R EGFR和AURKB的磷酸化,ic50值分别为0.07和1.1。

  • GC74000 structure
    GC74000DBPR728
    CAS: 2702965-64-6
    纯度: >98.00%

    DBPR728是6K465的酰基前药,携带较少的氢键供体。

  • GC10442 structure
    GC10442MK-8745
    CAS: 885325-71-3
    纯度: >99.00%

    An Aurora A kinase inhibitor