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Search Results for " epidermal growth factor "

20

Compounds

Cat No. Product Name Synonyms Targets
T8679 Epidermal Growth Factor EGFR
Epidermal Growth Factor binds to epidermal growth factor receptor (EGFR) and stimulates cell growth and proliferation. It is approved for the treatment of diabetic foot ulcers.
T21723L Epidermal Growth Factor Receptor Peptide Acetate Epidermal Growth Factor Receptor Peptide Acetate(96249-43-3 Free base) Others
Epidermal Growth Factor Receptor Peptide Acetate (Epidermal Growth Factor Receptor Peptide Acetate(96249-43-3 Free base)) exists on the cell surface and is activated by the binding of its specific ligands.EGFR belongs t...
TP2229 Epidermal growth factor receptor (994-1002) acetyl/amide Others
The epidermal growth factor receptor is the cell-surface receptor for members of the epidermal growth factor family of extracellular protein ligands.
T3466 FIIN-3 EGFR , FGFR
FIIN-3 is an irreversible inhibitor of FGFR.
T5475 ZD-4190 EGFR , VEGFR
ZD-4190 is a compound that inhibits both the vascular endothelial growth factor receptor 2 (VEGFR2) and the epidermal growth factor receptor (EGFR) signaling pathways, utilized in cancer treatment.
T2705 Mutant EGFR inhibitor EGFR
Mutant EGFR inhibitor is a selective and potent Mutated EGFR inhibitor, inhibits L858R activating mutant, the Exonl9 deletion activating mutant and the T790M resistance mutant.
T11160 EGFR-IN-5 EGFR
EGFR-IN-5 is a selective inhibitor of EGFR. The IC50s for EGFR, EGFR(L858R), EGFR(L858R/T790M), and EGFR(L858R/T790M/C797S) are 10.4, 1.1, 34, 7.2 nM, respectively.
TL0016 Sulforaphene Apoptosis , ERK , EGFR , NF-κB
Sulforaphene is a natural product isolated from radish seeds, exhibits an ED50 against velvetleaf seedlings approximately 2 x 10 -4 M. Sulforaphene promotes cancer cells apoptosis and inhibits migration via inhibiting EG...
T8976 PD-089828 EGFR , FGFR , PDGFR , Src
PD 089828 is a competitive inhibitor of the receptor tyrosine kinases FGFR1, PDGFRβ, and EGFR (IC50s = 0.15, 1.76, and 5.47 µM, respectively) and a noncompetitive inhibitor of the nonreceptor tyrosine kinase c-Src (IC50 ...
T16343 NRC-2694 EGFR
NRC-2694 is an antagonist of the epidermal growth factor receptor (EGFR). It has anti-cancer and anti-proliferative properties.
T5410 PD158780 EGFR
PD 158780 reversibly inhibits auto and transphosphorylation of all four members of the ErbB receptor superfamily: EGFR, ErbB2, ErbB3, and ErbB4 (IC50s: 8μM, 49 nM, 52 nM, and 52 nM in cell assay).
T6733 WZ-3146 EGFR
WZ3146 is a mutant-selective irreversible inhibitor of EGFR(L858R) and EGFR(E746_A750) with IC50 of 2 nM and 2 nM; does not inhibit ERBB2 phosphorylation (T798I).
T23176 PP 3 Src
PP 3 is a Negative control for the Src kinase inhibitor PP 2
T2491 AZ-5104 EGFR
AZ5104 is a potent EGFR inhibitor.
T11162 EGFR-IN-8 EGFR , c-Met/HGFR
EGFR-IN-8, a dual inhibitor targeting both EGFR and c-Met, shows potential as a promising candidate for further development in treating EGFR TKI-resistant NSCLC.
T10534 BI-4020 EGFR
BI-4020 is a fourth-generation, orally active, and non-covalent inhibitor of EGFR tyrosine kinase. BI-4020 exhibits activity agains the triple mutant EGFR del19 T790M C797S variant (IC50=0.2 nM in BaF3 cell lines), the d...
T7819 TAS0728 EGFR , HER
TAS0728 is a HER2 inhibitor, with antitumor activity
T23127 PD-161570 PD 161570 EGFR , FGFR , PDGFR , Src
PD-161570 is a potent and ATP-competitive human FGF-1 receptor inhibitor with an IC50 of 39.9 nM and a Ki of 42 nM. PD-161570 also inhibits the PDGFR, EGFR and c-Src tyrosine kinases with IC50 values of 310 nM, 240 nM, a...
T4296 MTX-211 MTX 211 EGFR , PI3K
MTX-211, an inhibitor of EGFR and PI3K, is used for the therapy of cancer and other diseases.
T6824 EAI045 EGFR
EAI045, an allosteric inhibitor, targets towards drug-resistant EGFR mutants but avoids the wild-type receptor.
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