VEGFR

VEGFR(血管内皮生长因子受体)

VEGFR are receptors for vascular endothelial growth factor and belong to receptor tyrosine kinases.

VEGFR 相关产品(193)

  • GC37773 structure
    GC37773TG 100801 Hydrochloride
    CAS: 1018069-81-2

    TG 100801 Hydrochloride 是TG 100572的前药,通过去酯化产生TG 100572,开发用来治疗年龄相关的黄斑变性。TG 100572是多靶点激酶抑制剂,抑制受体酪氨酸激酶 (receptor tyrosine kinases) 和Src激酶 (Src kinases); 对VEGFR1,VEGFR2,FGFR1,FGFR2,PDGFRβ,Fgr,Fyn,Hck,Lck,Lyn,Src,Yes 的 IC50 值分别为2,7,2,16,13,5,0.5,6,0.1,0.4,1,0.2。

  • GC37808 structure
    GC37808Toceranib phosphate
    CAS: 874819-74-6
    纯度: >98.00%

    A multi-targeted receptor tyrosine kinase inhibitor

  • GC37886 structure
    GC37886Vandetanib trifluoroacetate
    CAS: 338992-53-3

    A multi-kinase inhibitor

  • GC37933 structure
    GC37933WHI-P180 hydrochloride
    CAS: 153437-55-9

    A multi-kinase inhibitor

  • GC38380 structure
    GC38380Vorolanib
    CAS: 1013920-15-4
    纯度: >99.50% / >98.00%

    Vorolanib(X-82;CM082)是一种具口服活性的血管内皮生长因子受体(VEGFR)和血小板衍生生长因子受体(PDGFR)的多激酶双重抑制剂,IC 50 值分别为0.052μM、0.26 μM。

  • GC38519 structure
    GC38519Ilorasertib hydrochloride
    CAS: 1847485-91-9
    纯度: >98.50%

    A multi-kinase inhibitor

  • GC38575 structure
    GC38575CP-547632 hydrochloride
    CAS: 252003-71-7
    纯度: >98.00%

    A potent inhibitor of VEGFR2 and bFGF

  • GC39314 structure
    GC39314Tyrphostin AG1433
    CAS: 168835-90-3
    纯度: >99.00%

    Tyrphostin AG1433 (AG1433, SU1433) is a selective platelet-derived growth factor receptor β (PDGFRβ) and vascular endothelial growth factor receptor 2 (VEGFR-2, Flk-1/KDR) inhibitor with IC50s of 5.0 μM and 9.3 μM, respectively.

  • GC40755 structure
    GC40755SU 5214
    CAS: 186611-04-1
    纯度: >98.00%

    A 3-heteroaryl-2-indoline

  • GC43885 structure
    GC43885Hypothemycin
    CAS: 76958-67-3
    纯度: >95.00%

    A resorcylic acid lactone polyketide with diverse biological activities

  • GC44474 structure
    GC44474NVP-AEW541 (hydrochloride)
    CAS: 2320261-63-8
    纯度: >98.00%

    An IGF-1R inhibitor

  • GC44958 structure
    GC44958SU 5205
    CAS: 3476-86-6
    纯度: >98.00%

    An inhibitor of VEGFR2

  • GC45677 structure
    GC45677Anlotinib (hydrochloride)
    CAS: 1058157-76-8
    纯度: >95.00%

    A neuropeptide with diverse biological activities

  • GC45754 structure
    GC45754Lenvatinib-d4
    CAS: 2264050-65-7
    纯度: >99.00%

    Lenvatinib-d4 (E7080-d4) 是氘标记的 Lenvatinib。 Lenvatinib (E7080) 是一种口服的多靶点酪氨酸激酶抑制剂,可抑制 VEGFR1-3、FGFR1-4、PDGFR、KIT 和 RET,显示出有效的抗肿瘤活性。

  • GC45828 structure
    GC45828Ponatinib-d8
    CAS: 1562993-37-6
    纯度: >99.00%

    An internal standard for the quantification of ponatinib

  • GC46924 structure
    GC46924BIBF 1120-13C-d3
    纯度: >99.00%

    A neuropeptide with diverse biological activities

  • GC48118 structure
    GC48118Sunitinib-d10
    CAS: 1126721-82-1
    纯度: >99.00%

    An internal standard for the quantification of sunitinib

  • GC49686 structure
    GC49686N-desmethyl Regorafenib N-oxide
    CAS: 835621-12-0
    纯度: >90.00%

    An active metabolite of regorafenib

  • GC49700 structure
    GC49700Takeda-6d
    CAS: 1125632-93-0
    纯度: >95.00%

    A dual inhibitor of RAF kinases and VEGFR2

  • GC50028 structure
    GC50028ZM 306416 hydrochloride
    CAS: 196603-47-1

    A VEGF receptor kinase inhibitor

  • GC50233 structure
    GC50233Vatalanib succinate
    CAS: 212142-18-2

    Potent VEGFR inhibitor; also aromatase inhibitor

  • GC50330 structure
    GC50330BMS 605541
    CAS: 639858-32-5

    Potent VEGFR-2 inhibitor

  • GC60283 structure
    GC60283Pentagamavunon-1
    CAS: 27060-70-4
    纯度: >99.50%

    Pentagamavunon-1 (PGV-1) 是Curcumin 的类似物,具有口服活性,通过多个机制诱导凋亡信号,如抑制COX-2 和 VEGF。Pentagamavunon-1 (PGV-1) 可抑制 NF-κB 的激活。

  • GC60365 structure
    GC60365TIE-2/VEGFR-2 kinase-IN-1
    CAS: 453590-24-4
    纯度: >99.50%

    TIE-2/VEGFR-2 kinase-IN-1 用于合成 TIE-2 或者 VEGFR-2 抑制剂,从专利 WO2003022852 中获得,例 14。TIE-2/VEGFR-2 kinase-IN-1 用于研究不适当的血管生成相关疾病。