Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Fibroblast growth factor receptor 1' and Ligand = 'BDBM50504106'   

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
Fibroblast growth factor receptor 1 (Homo sapiens (Human))	BDBM50504106 (CHEMBL4462946) Show SMILES CN(C)C\C=C\C(=O)Nc1ccc(cc1)-n1nc2c(c1-c1oc3ccc(Cl)cc3c1C)c(N)n[nH]c2=O |(69.7,-43.56,;68.16,-43.57,;67.4,-44.91,;67.38,-42.24,;65.84,-42.25,;65.06,-40.92,;63.52,-40.93,;62.76,-42.27,;62.75,-39.6,;61.21,-39.62,;60.44,-40.95,;58.9,-40.96,;58.13,-39.63,;58.88,-38.3,;60.42,-38.28,;56.59,-39.64,;55.7,-40.89,;54.23,-40.42,;54.23,-38.89,;55.68,-38.41,;56.15,-36.95,;55.24,-35.7,;56.14,-34.45,;55.81,-32.96,;56.94,-31.93,;58.41,-32.39,;59.55,-31.36,;58.74,-33.9,;57.6,-34.93,;57.61,-36.46,;58.86,-37.36,;52.9,-38.11,;52.9,-36.57,;51.57,-38.89,;51.57,-40.43,;52.9,-41.19,;52.9,-42.73,)| Show InChI InChI=1S/C26H24ClN7O3/c1-14-18-13-15(27)6-11-19(18)37-24(14)23-21-22(26(36)31-30-25(21)28)32-34(23)17-9-7-16(8-10-17)29-20(35)5-4-12-33(2)3/h4-11,13H,12H2,1-3H3,(H2,28,30)(H,29,35)(H,31,36)/b5-4+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Shanghai University Curated by ChEMBL					Assay Description Irreversible inhibition of human FGFR1 using poly (Glu, Tyr)4:1 as substrate measured after 60 mins				J Med Chem 62: 7473-7488 (2019) Article DOI: 10.1021/acs.jmedchem.9b00510 BindingDB Entry DOI: 10.7270/Q2KP85D8
					More data for this Ligand-Target Pair
Fibroblast growth factor receptor 1 (Homo sapiens (Human))	BDBM50504106 (CHEMBL4462946) Show SMILES CN(C)C\C=C\C(=O)Nc1ccc(cc1)-n1nc2c(c1-c1oc3ccc(Cl)cc3c1C)c(N)n[nH]c2=O |(69.7,-43.56,;68.16,-43.57,;67.4,-44.91,;67.38,-42.24,;65.84,-42.25,;65.06,-40.92,;63.52,-40.93,;62.76,-42.27,;62.75,-39.6,;61.21,-39.62,;60.44,-40.95,;58.9,-40.96,;58.13,-39.63,;58.88,-38.3,;60.42,-38.28,;56.59,-39.64,;55.7,-40.89,;54.23,-40.42,;54.23,-38.89,;55.68,-38.41,;56.15,-36.95,;55.24,-35.7,;56.14,-34.45,;55.81,-32.96,;56.94,-31.93,;58.41,-32.39,;59.55,-31.36,;58.74,-33.9,;57.6,-34.93,;57.61,-36.46,;58.86,-37.36,;52.9,-38.11,;52.9,-36.57,;51.57,-38.89,;51.57,-40.43,;52.9,-41.19,;52.9,-42.73,)| Show InChI InChI=1S/C26H24ClN7O3/c1-14-18-13-15(27)6-11-19(18)37-24(14)23-21-22(26(36)31-30-25(21)28)32-34(23)17-9-7-16(8-10-17)29-20(35)5-4-12-33(2)3/h4-11,13H,12H2,1-3H3,(H2,28,30)(H,29,35)(H,31,36)/b5-4+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
Shanghai University Curated by ChEMBL					Assay Description Inhibition of human FGFR1 using poly (Glu, Tyr)4:1 as substrate measured after 60 mins by ELISA				J Med Chem 62: 7473-7488 (2019) Article DOI: 10.1021/acs.jmedchem.9b00510 BindingDB Entry DOI: 10.7270/Q2KP85D8
					More data for this Ligand-Target Pair