About 11 results found for searched term "EGFR-IN-3" (0.054 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M9642 | EGFR inhibitor 324674 | EGFR/HER2 |
| EGFR-IN-12 | ||
| EGFR inhibitor 324674 is a cell permeable, potent and selective EGFR inhibitor with IC50 of 21 nM. | ||
| M22265 | EGFR-IN-3 | Others |
| EGFR-IN-3 | ||
| M31301 | Recombinant Human VEGFR1 Protein (HEK293, C-Fc) | Cytokines and Growth Factors |
| Vascular endothelial growth factor receptor 1; FLT-1 | ||
| Human Vascular endothelial growth factor receptor 1(VEGFR-1, FLT-1) is a member of the the class III subfamily of receptor tyrosine kinases (RTKs) and Tyr protein kinase family and CSF-1/PDGF receptor subfamily. VEGFR-1 plays an essential role as a negative regulator of embryonic angiogenesis by inhibiting excessive proliferation of endothelial cells and promote endothelial cell proliferation, survival and angiogenesis in adulthood. | ||
| M42082 | EGFR/BRAFV600E-IN-3 | EGFR/HER2 |
| EGFR/BRAFV600E-IN-3 is a EGFR, BRAFV600E and EGFRT790M inhibitor with IC50 value of 57 nM, 68 nM and 9.70 nM. | ||
| M42092 | EGFR-IN-83 | EGFR/HER2 |
| EGFR-IN-83 is an EGFR inhibitor (IC50: 2.53 nM). | ||
| M43536 | TIE-2/VEGFR-2 kinase-IN-3 | VEGFR/PDGFR |
| TIE-2/VEGFR-2 kinase-IN-3, benzimidazole, is a potent TIE-2 and VEGFR-2 tyrosine kinase receptors inhibitors with IC50 values of 6.9 nM and 3.5 nM, respectively. | ||
| M43543 | hCA/VEGFR-2-IN-3 | VEGFR/PDGFR |
| hCA/VEGFR-2-IN-3 is an indolinonylbenzenesulfonamide and a potential dual inhibitor of cancer-associated hCA IX/XII and VEGFR-2. | ||
| M43547 | VEGFR-2-IN-31 | VEGFR/PDGFR |
| VEGFR-2-IN-31 is a potent VEGFR-2 inhibitor (IC50=8.93 nM), and an anti-prostate cancer agent. | ||
| M43549 | VEGFR-2-IN-32 | VEGFR/PDGFR |
| VEGFR-2-IN-32 is an inhibitor of VEGFR-2 with an IC50 of 8.93 nM. | ||
| M43551 | VEGFR-2-IN-33 | VEGFR/PDGFR |
| VEGFR-2-IN-33 is a VEGFR inhibitor (IC50: 61.04 nM). | ||
| M43553 | VEGFR2-IN-3 | VEGFR/PDGFR |
| VEGFR2-IN-3 is a potent VEGFR2 inhibitor. | ||
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