Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Epidermal growth factor receptor' and Ligand = 'BDBM3982'   

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))	BDBM3982 (CHEMBL314029 | Dimethyl 2,2 -dithiobis(1-methyl-1H...) Show SMILES COC(=O)CCc1c(SSc2c(CCC(=O)OC)c3ccccc3n2C)n(C)c2ccccc12 Show InChI InChI=1S/C26H28N2O4S2/c1-27-21-11-7-5-9-17(21)19(13-15-23(29)31-3)25(27)33-34-26-20(14-16-24(30)32-4)18-10-6-8-12-22(18)28(26)2/h5-12H,13-16H2,1-4H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Auckland Curated by ChEMBL					Assay Description Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cells				J Med Chem 38: 58-67 (1995) BindingDB Entry DOI: 10.7270/Q26Q1W8F
					More data for this Ligand-Target Pair
Epidermal growth factor receptor (Homo sapiens (Human))	BDBM3982 (CHEMBL314029 | Dimethyl 2,2 -dithiobis(1-methyl-1H...) Show SMILES COC(=O)CCc1c(SSc2c(CCC(=O)OC)c3ccccc3n2C)n(C)c2ccccc12 Show InChI InChI=1S/C26H28N2O4S2/c1-27-21-11-7-5-9-17(21)19(13-15-23(29)31-3)25(27)33-34-26-20(14-16-24(30)32-4)18-10-6-8-12-22(18)28(26)2/h5-12H,13-16H2,1-4H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Auckland					Assay Description IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...				J Med Chem 36: 2459-69 (1993) Article DOI: 10.1021/jm00069a003 BindingDB Entry DOI: 10.7270/Q2RJ4GNS
					More data for this Ligand-Target Pair