| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V128813 | Andamertinib | 2254145-43-0 | Andamertinib is an EGFR inhibitor with anti-tumor activity. |
|
V130105 | Bevasiranib sodium scrambled negative control | The Bevasiranib sodium scrambled negative control is a negative control with the sequence of bevasiranib sodium scrambled. | |
|
V88961 | Biotin HER-2 substrate peptide | Biotin HER-2 substrate peptide is a substrate for HER4 and HER2/NEU tyrosine kinases, with a Km value of 60 μM for the HER2/NEU kinase domain. | |
|
V118559 | CHNQD-01281 | 2762488-97-9 | CHNQD-01281 is a brevidin A derivative and an EGFR regulator. |
|
V133208 | Darlifarnib | 3065226-39-0 | Darlifarnib is an orally effective farnesyltransferase inhibitor. |
|
V134515 | DSPE-PEG2000-Mal-Cys-ATWLPPR | DSPE-PEG2000-Mal-Cys-ATWLPPR is a polyethylene glycol (PEG) compound composed of DSPE and a tumor angiogenesis-targeting peptide (A7R). | |
|
V118907 | EGFR d746-750 Recombinant Human Active Protein Kinase | EGFR is a driver of tumorigenesis. | |
|
V119618 | EGFR ligand-14-PEG3-Boc | 2230825-46-2 | EGFR ligand-14-PEG3-Boc contains an EGFR ligand and a linker group. |
|
V114934 | EGFR ligand-18 | EGFR ligand-18 is a PROTAC target protein ligand that can be used to synthesize PROTACs, such as PROTAC EGFR degrader 16. | |
|
V84605 | EGFR ligand-2 | 2737283-20-2 | |
|
V85416 | EGFR T790M/L858R-IN-3 | ||
|
V134930 | EGFR T790M/L858R-IN-9 | EGFR T790M/L858R-IN-9 is an EGFR-L858R/T790M inhibitor that exhibits potent phosphorylation inhibition of EGFR-L858R/T790M mutant kinase, with an IC50 value of 0.0064µM. | |
|
V134932 | EGFR WT/T790M-IN-4 | EGFR WT/T790M-IN-4 is an anticancer drug. | |
|
V103782 | EGFR-IN-104 | 2758904-45-7 | EGFR-IN-104 (Compound A23) is a potent EGFR inhibitor with IC50 values of 0.33 μM and 0.133 μM for EGFRL858R/T790M and EGFRDel19/T790M/C797S, respectively. |
|
V99889 | EGFR-IN-121 | 418799-16-3 | EGFR-IN-121 (Compound 15) is a dual inhibitor of EGFR and VEGFR-2 with IC50 of 84 nM and 3.5 nM, respectively. |
|
V94977 | EGFR-IN-127 | EGFR-IN-127 is an ATP-competitive EGFR inhibitor with IC50 of 136.3 nM and 161.2 nM for EGFRdel19 and EGFRdel19/T790M/C797S, respectively. | |
|
V93031 | EGFR-IN-133 | 2809982-26-9 | EGFR-IN-133 (Compound 24) is an inhibitor of EGFR, inhibiting EGFR wild-type, L858R/T790M, d19/T790M, L858R/T790M/C797S and d19/T790M/C797S mutants with IC50 of 0.1, 0.044, 0.036, 0.04 and 0.054 nM, respectively. |
|
V118795 | EGFR-IN-171 | EGFR-IN-171 is an epidermal growth factor receptor (EGFR) inhibitor with an IC50 value of 0.19 μM. | |
|
V115928 | EGFR-IN-183 | EGFR-IN-183 (compound 5q) is an EGFR inhibitor. | |
|
V111346 | EGFR-IN-186 | EGFR-IN-186 is a potent EGFR inhibitor with an IC50 value of 0.065 µM. |