VEGFR


VEGF receptors are receptors for vascular endothelial growth factor (VEGF).  There are three main subtypes of VEGFR, numbered 1, 2 and 3. Also, they may be membrane-bound (mbVEGFR) or soluble (sVEGFR), depending on alternative splicing.Vascular endothelial growth factor (VEGF) is an important signaling protein involved in both vasculogenesis (the formation of the circulatory system) and angiogenesis (the growth of blood vessels from pre-existing vasculature). In vitro, VEGF has been shown to stimulate endothelial cell mitogenesis and cell migration. VEGF also enhances microvascular permeability and is sometimes referred to as vascular permeability factor.
  • SU 4312 EI2644

    SU 4312是VEGFR酪氨酸激酶的活性抑制剂。

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  • Sunitinib Malate EY0865

    Sunitinib Malate是一种多靶点受体酪氨酸激酶(RTK)抑制剂,作用于VEGFR1, VEGFR2, VEGFR3, PDGFRβ, FLT3,和CSF-1R时,IC50分别为15 nM, 38 nM, 30 nM, 55 nM, 21 nM,和35 nM。

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  • Sorafenib Tosylate EY1396

    Sorafenib Tosylate是酪氨酸激酶(VEGFR和PDGFR)和RAF/MEK/ERK级联抑制剂,同时作用于Raf-1,wtBRAF和V599EBRAF,IC50分别为6 nM, 22 nM和38 nM。

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  • Vatalanib 2HCl EY1849

    Vatalanib (PTK787; ZK-222584; CGP-79787)是VEGFR2/KDR抑制剂,IC50为37 nM,对VEGFR1/Flt-1和VEGFR3/Flt-4抑制性较弱。

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  • Regorafenib EY1782

    Regorafenib (瑞格非尼; BAY 73-4506) 是多靶点抑制剂,对VEGFR1,VEGFR2,VEGFR3,PDGFRβ,Kit,RET和Raf-1的IC50分别为13 nM,4.2 nM,46 nM,22 nM,7 nM,1.5 nM和2.5 nM。

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  • SU 4312 EI2644

    SU 4312是VEGFR酪氨酸激酶的活性抑制剂。

    More
  • Sunitinib Malate EY0865

    Sunitinib Malate是一种多靶点受体酪氨酸激酶(RTK)抑制剂,作用于VEGFR1, VEGFR2, VEGFR3, PDGFRβ, FLT3,和CSF-1R时,IC50分别为15 nM, 38 nM, 30 nM, 55 nM, 21 nM,和35 nM。

    More
  • Sorafenib Tosylate EY1396

    Sorafenib Tosylate是酪氨酸激酶(VEGFR和PDGFR)和RAF/MEK/ERK级联抑制剂,同时作用于Raf-1,wtBRAF和V599EBRAF,IC50分别为6 nM, 22 nM和38 nM。

    More
  • Vatalanib 2HCl EY1849

    Vatalanib (PTK787; ZK-222584; CGP-79787)是VEGFR2/KDR抑制剂,IC50为37 nM,对VEGFR1/Flt-1和VEGFR3/Flt-4抑制性较弱。

    More
  • Regorafenib EY1782

    Regorafenib (瑞格非尼; BAY 73-4506) 是多靶点抑制剂,对VEGFR1,VEGFR2,VEGFR3,PDGFRβ,Kit,RET和Raf-1的IC50分别为13 nM,4.2 nM,46 nM,22 nM,7 nM,1.5 nM和2.5 nM。

    More
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