Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kJ/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Epidermal growth factor receptor (Homo sapiens (Human)) | BDBM195873![]() (US9670213, Compound 018 N-(3-(2-(4-morpholinopheny...) | PDB KEGG UniProtKB/SwissProt antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet ![]() | PC cid PC sid UniChem | Article PubMed | n/a | n/a | 2.90 | n/a | n/a | n/a | n/a | n/a | n/a |
East China University of Science & Technology Curated by ChEMBL | Assay Description Inhibition of EGFR T790M/L858R double mutant (unknown origin) using Tyr 4 peptide as substrate after 1.5 hrs by FRET-based Z'-LYTE assay | J Med Chem 56: 7821-37 (2013) Article DOI: 10.1021/jm401045n BindingDB Entry DOI: 10.7270/Q21V5HW9 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Epidermal growth factor receptor [T790M,L858R] (Homo sapiens (Human)) | BDBM195873![]() (US9670213, Compound 018 N-(3-(2-(4-morpholinopheny...) | PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet ![]() | PC cid PC sid UniChem | US Patent | n/a | n/a | 3.02 | n/a | n/a | n/a | n/a | n/a | 25 |
East China University of Science and Technology US Patent | Assay Description In vitro enzyme activity assay: wild-type and various mutants (T790M, L858R, L861Q, L858 R/T790M) EGFR, Z′-Lyte Kinase Assay Kit were purchased... | US Patent US9670213 (2017) BindingDB Entry DOI: 10.7270/Q23R0R1P | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Epidermal growth factor receptor [L858R] (Homo sapiens (Human)) | BDBM195873![]() (US9670213, Compound 018 N-(3-(2-(4-morpholinopheny...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet ![]() | PC cid PC sid UniChem | US Patent | n/a | n/a | 5.83 | n/a | n/a | n/a | n/a | n/a | 25 |
East China University of Science and Technology US Patent | Assay Description In vitro enzyme activity assay: wild-type and various mutants (T790M, L858R, L861Q, L858 R/T790M) EGFR, Z′-Lyte Kinase Assay Kit were purchased... | US Patent US9670213 (2017) BindingDB Entry DOI: 10.7270/Q23R0R1P | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Epidermal growth factor receptor (Homo sapiens (Human)) | BDBM195873![]() (US9670213, Compound 018 N-(3-(2-(4-morpholinopheny...) | PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![]() | PC cid PC sid UniChem | Article PubMed | n/a | n/a | 7 | n/a | n/a | n/a | n/a | n/a | n/a |
East China University of Science & Technology Curated by ChEMBL | Assay Description Inhibition of wild type EGFR (unknown origin) using Tyr 4 peptide as substrate after 1.5 hrs by FRET-based Z'-LYTE assay | J Med Chem 56: 7821-37 (2013) Article DOI: 10.1021/jm401045n BindingDB Entry DOI: 10.7270/Q21V5HW9 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Epidermal growth factor receptor (Homo sapiens (Human)) | BDBM195873![]() (US9670213, Compound 018 N-(3-(2-(4-morpholinopheny...) | PDB KEGG UniProtKB/SwissProt antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet ![]() | PC cid PC sid UniChem | Article PubMed | n/a | n/a | 7.30 | n/a | n/a | n/a | n/a | n/a | n/a |
East China University of Science & Technology Curated by ChEMBL | Assay Description Inhibition of EGFR L858R mutant (unknown origin) using Tyr 4 peptide as substrate after 1.5 hrs by FRET-based Z'-LYTE assay | J Med Chem 56: 7821-37 (2013) Article DOI: 10.1021/jm401045n BindingDB Entry DOI: 10.7270/Q21V5HW9 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Epidermal growth factor receptor (Homo sapiens (Human)) | BDBM195873![]() (US9670213, Compound 018 N-(3-(2-(4-morpholinopheny...) | PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![]() | PC cid PC sid UniChem | US Patent | n/a | n/a | 7.94 | n/a | n/a | n/a | n/a | n/a | 25 |
East China University of Science and Technology US Patent | Assay Description In vitro enzyme activity assay: wild-type and various mutants (T790M, L858R, L861Q, L858 R/T790M) EGFR, Z′-Lyte Kinase Assay Kit were purchased... | US Patent US9670213 (2017) BindingDB Entry DOI: 10.7270/Q23R0R1P | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Tyrosine-protein kinase Blk (Homo sapiens (Human)) | BDBM195873![]() (US9670213, Compound 018 N-(3-(2-(4-morpholinopheny...) | Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet ![]() | PC cid PC sid UniChem | US Patent | n/a | n/a | 41 | n/a | n/a | n/a | n/a | n/a | 25 |
East China University of Science and Technology US Patent | Assay Description In vitro enzyme activity assay: wild-type and various mutants (T790M, L858R, L861Q, L858 R/T790M) EGFR, Z′-Lyte Kinase Assay Kit were purchased... | US Patent US9670213 (2017) BindingDB Entry DOI: 10.7270/Q23R0R1P | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM195873![]() (US9670213, Compound 018 N-(3-(2-(4-morpholinopheny...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![]() | PC cid PC sid UniChem | US Patent | n/a | n/a | 798 | n/a | n/a | n/a | n/a | n/a | 25 |
East China University of Science and Technology US Patent | Assay Description In vitro enzyme activity assay: wild-type and various mutants (T790M, L858R, L861Q, L858 R/T790M) EGFR, Z′-Lyte Kinase Assay Kit were purchased... | US Patent US9670213 (2017) BindingDB Entry DOI: 10.7270/Q23R0R1P | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM195873![]() (US9670213, Compound 018 N-(3-(2-(4-morpholinopheny...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![]() | PC cid PC sid UniChem | Article PubMed | n/a | n/a | 1.14E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
East China University of Science & Technology Curated by ChEMBL | Assay Description Inhibition of human N-terminal GST-tagged FLT3 (564 to 993 residues) expressed in baculovirus expression system using peptide FAM-P2 as substrate inc... | J Med Chem 59: 6187-200 (2016) Article DOI: 10.1021/acs.jmedchem.6b00374 BindingDB Entry DOI: 10.7270/Q2J38X35 | |||||||||||
More data for this Ligand-Target Pair |