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￥ 0.00 Protein Tyrosine Kinases
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MGCD-265 (Glesatinib)
Catalog No. A10587 c-Met 抑制剂MGCD-265 (Glesatinib)是一种多靶酪氨酸激酶抑制剂，可与多种RTK（包括c-Met受体（HGFR）结合并抑制其磷酸化。Tek/Tie-2受体；VEGFR类型1、2和3；和MST1R。 了解更多 -
BMS-794833
Catalog No. A10154 -
Vatalanib (PTK787) 2HCl
Catalog No. A10967 VEGFR 抑制剂Vatalanib (PTK787) 2HCl是一种小分子蛋白激酶抑制剂，可抑制抑制所有已知VEGF受体以及血小板衍生的生长因子受体β和c-kit的血管生成，但对VEGFR-2的选择性最高。 了解更多 -
Raf265 derivative
Catalog No. A10774 RAF/VEGFR 抑制剂Raf265 derivative是Raf265的衍生物，Raf265是一种口服，高度选择性的RAF和VEGFR激酶抑制剂，IC50为5至10μM。 了解更多 -
CYC116 (CYC-116)
Catalog No. A10248 Aurora Kinase 抑制剂CYC116 (CYC-116)是一种有效的Aurora A/B抑制剂，Ki为8.0 nM/9.2 nM，对VEGFR2(Ki为44 nM)作用稍弱。 了解更多 -
Buflomedil HCl
Catalog No. A11737 -
ZM 323881 hydrochloride
Catalog No. A11954 -
E-7050 (Golvatinib)
Catalog No. A11396 E-7050 (Golvatinib)是具有潜在抗肿瘤活性的c-Met(肝细胞生长因子受体)和VEGFR-2(血管内皮生长因子受体-2)酪氨酸激酶的口服生物可利用双重激酶抑制剂。 了解更多 -
SKLB1002
Catalog No. A13234 -
TG 100801
Catalog No. A13819 -
SAR131675
Catalog No. A13377 -
SKLB610
Catalog No. A13465 -
Fruquintinib
Catalog No. A14393 -
BMS-817378
Catalog No. A15792 -
Altiratinib (DCC2701)
Catalog No. A14387 c-Met/VEGFR 抑制剂Altiratinib (DCC2701)是一种新型的c-MET/TIE-2/VEGFR抑制剂；与体外HGF拮抗剂相比，可有效降低体内的肿瘤负荷并阻断c-MET pTyr（1349）介导的信号传导，细胞生长和迁移。 了解更多 -
NVP-BAW2881
Catalog No. A12693 VEGFR 抑制剂NVP-BAW2881是有效的选择性VEGFR抑制剂（血管内皮生长因子受体酪氨酸激酶抑制剂），IC50 为值9 nM，具有抑制慢性和急性皮肤炎症的作用。 了解更多 -
BFH772
Catalog No. A16342 -
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SU-5408
Catalog No. A17154 -
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Cediranib maleate
Catalog No. A21857 VEGFR inhibitorCediranib maleate (AZD-2171 maleate) is a highly potent, orally available VEGFR inhibitor with IC50s of <1, <3, 5, 5, 36, 2 nM for Flt1, KDR, Flt4, PDGFRα, PDGFRβ, c-Kit, respectively. 了解更多 -
NVP-ADW742
Catalog No. A10658 -
NVP-AEW541
Catalog No. A11021 IGF-1R 抑制剂NVP-AEW541是一种选择性的IGF-1R激酶抑制剂，可抑制IGF-1R的自磷酸化活性（IC50 = 0.086 uM）并阻止IGF-1介导的MCF-7细胞存活和增殖（IC50分别为0.16和1.64 uM）。 了解更多 -
AG-1024 (Tyrphostin)
Catalog No. A11400 IGF-1R 抑制剂AG-1024 (Tyrphostin)是胰岛素样生长因子-1 (IGF-1) 和胰岛素受体酪氨酸激酶活性的特异性抑制剂。与胰岛素受体相比，IGF-1的IC50值更低。还抑制胰岛素刺激的细胞增殖。 了解更多 -
GSK1838705A
Catalog No. A11175 IGF-1R 抑制剂GSK1838705A是一种小分子激酶抑制剂，其抑制IGF-IR和胰岛素受体的IC50分别为2.0和1.6 nmol/L。 了解更多 -
Indirubin Derivative E804
Catalog No. A21052 IGF1R inhibitorE 804 is a potent inhibitor of Insulin-like Growth Factor 1 Receptor (IGF1R), with an IC50 of 0.65 μM for IGF1R. 了解更多 -
BMS-536924
Catalog No. A11054 -
GSK1904529A
Catalog No. A10440 -
PQ 401
Catalog No. A11951 -
AC220 (Quizartinib)
Catalog No. A10027 FLT3 抑制剂AC220 (Quizartinib)是一种有效的选择性FLT3抑制剂，对于MC4-11和A375，IC50分别为0.56±0.3 nM和> 10 mM。 了解更多 -
Pacritinib (SB1518)
Catalog No. A12694 JAK2/FLT3 抑制剂Pacritinib (SB1518)是Janus激酶2（JAK2）和JAK2突变体JAK2V617F的口服生物利用抑制剂，无细胞试验中IC50分别为23和22 nM，具有潜在的抗肿瘤活性。Pacritinib与JAK2竞争ATP结合，这可能导致抑制JAK2活化，抑制JAK-STAT信号传导途径以及半胱天冬酶依赖性凋亡。 了解更多 -
Pexidartinib (PLX3397)
Catalog No. A15520 CSF1/Kit/FLT3 抑制剂Pexidartinib (PLX3397)是KIT，CSF1R和FLT3的小分子酪氨酸激酶（RTK）抑制剂，具有潜在的抗肿瘤活性。 了解更多 -
TG-02 (SB1317)
Catalog No. A11962 -
G-749
Catalog No. A14214 -
Gilteritinib (ASP2215)
Catalog No. A14411 FLT3/Axl 抑制剂Gilteritinib (ASP2215)是一种有效的FLT3/AXL抑制剂，对具有AML突变或FLT3-ITD和FLT3-D835的AML具有有效的抗白血病活性。 了解更多
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