Compile Data Set for Download or QSAR

Found 2 hits of ki for monomerid = 50157333   

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))	BDBM50157333 (CHEMBL3781433) Show SMILES CN1CCN(CC1)c1ccc(NC(=O)c2c(NC[C@@H](O)c3cccc(Cl)c3)cc[nH]c2=O)cc1 |r| Show InChI InChI=1S/C25H28ClN5O3/c1-30-11-13-31(14-12-30)20-7-5-19(6-8-20)29-25(34)23-21(9-10-27-24(23)33)28-16-22(32)17-3-2-4-18(26)15-17/h2-10,15,22,32H,11-14,16H2,1H3,(H,29,34)(H2,27,28,33)/t22-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	18	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Genentech Curated by ChEMBL					Assay Description Inhibition of human N-terminal GST-tagged EGFR catalytic domain (669 to 1210 residues) expressed in baculovirus expression system using Fl-EEPLYWSFPA...				ACS Med Chem Lett 7: 100-4 (2016) Article DOI: 10.1021/acsmedchemlett.5b00428 BindingDB Entry DOI: 10.7270/Q25T3NCC
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Epidermal growth factor receptor (Homo sapiens (Human))	BDBM50157333 (CHEMBL3781433) Show SMILES CN1CCN(CC1)c1ccc(NC(=O)c2c(NC[C@@H](O)c3cccc(Cl)c3)cc[nH]c2=O)cc1 |r| Show InChI InChI=1S/C25H28ClN5O3/c1-30-11-13-31(14-12-30)20-7-5-19(6-8-20)29-25(34)23-21(9-10-27-24(23)33)28-16-22(32)17-3-2-4-18(26)15-17/h2-10,15,22,32H,11-14,16H2,1H3,(H,29,34)(H2,27,28,33)/t22-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	65	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Genentech Curated by ChEMBL					Assay Description Inhibition of human EGFR catalytic domain (668 to 1210 residues) T790M/L858R double mutant using Fl-EEPLYWSFPAKKK-CONH2 peptide substrate preincubate...				ACS Med Chem Lett 7: 100-4 (2016) Article DOI: 10.1021/acsmedchemlett.5b00428 BindingDB Entry DOI: 10.7270/Q25T3NCC
					More data for this Ligand-Target Pair