Compile Data Set for Download or QSAR

Found 49 hits with Last Name = 'lee' and Initial = 'ki'   

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
Genome polyprotein (Coxsackievirus B3 (strain Nancy))	BDBM50462020 (CHEMBL515513) Show SMILES ClC1=C(Nc2cccc(Cl)c2)C(=O)c2[nH]c(nc2C1=O)-c1ccncc1 |c:1| Show InChI InChI=1S/C18H10Cl2N4O2/c19-10-2-1-3-11(8-10)22-13-12(20)16(25)14-15(17(13)26)24-18(23-14)9-4-6-21-7-5-9/h1-8,22H,(H,23,24)	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	550	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...				Bioorg Med Chem Lett 28: 2533-2538 (2018) Article DOI: 10.1016/j.bmcl.2018.05.046 BindingDB Entry DOI: 10.7270/Q2HT2S0T
					More data for this Ligand-Target Pair
Genome polyprotein (Coxsackievirus B3 (strain Nancy))	BDBM50462028 (CHEMBL4226173) Show SMILES Clc1ccc(SC2=C(Sc3ccc(Cl)cc3)C(=O)c3[nH]c(nc3C2=O)-c2ccncc2)cc1 |c:6| Show InChI InChI=1S/C24H13Cl2N3O2S2/c25-14-1-5-16(6-2-14)32-22-20(30)18-19(29-24(28-18)13-9-11-27-12-10-13)21(31)23(22)33-17-7-3-15(26)4-8-17/h1-12H,(H,28,29)	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	570	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...				Bioorg Med Chem Lett 28: 2533-2538 (2018) Article DOI: 10.1016/j.bmcl.2018.05.046 BindingDB Entry DOI: 10.7270/Q2HT2S0T
					More data for this Ligand-Target Pair
Genome polyprotein (Coxsackievirus B3 (strain Nancy))	BDBM50106501 (6,7-Dichloro-5,8-quinolinequinone | 6,7-Dichloro-q...) Show SMILES ClC1=C(Cl)C(=O)c2ncccc2C1=O |c:1| Show InChI InChI=1S/C9H3Cl2NO2/c10-5-6(11)9(14)7-4(8(5)13)2-1-3-12-7/h1-3H	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	630	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...				Bioorg Med Chem Lett 28: 2533-2538 (2018) Article DOI: 10.1016/j.bmcl.2018.05.046 BindingDB Entry DOI: 10.7270/Q2HT2S0T
					More data for this Ligand-Target Pair
Genome polyprotein (Coxsackievirus B3 (strain Nancy))	BDBM50462022 (CHEMBL4227412) Show SMILES Cc1[nH]c2ccccc2c1C1=C(Cl)C(=O)c2ncccc2C1=O |c:12| Show InChI InChI=1S/C18H11ClN2O2/c1-9-13(10-5-2-3-7-12(10)21-9)14-15(19)18(23)16-11(17(14)22)6-4-8-20-16/h2-8,21H,1H3	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	730	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...				Bioorg Med Chem Lett 28: 2533-2538 (2018) Article DOI: 10.1016/j.bmcl.2018.05.046 BindingDB Entry DOI: 10.7270/Q2HT2S0T
					More data for this Ligand-Target Pair
Genome polyprotein (Coxsackievirus B3 (strain Nancy))	BDBM50462021 (CHEMBL4227020) Show SMILES O=C1c2nc([nH]c2C(=O)C(Sc2ccccc2)=C1Sc1ccccc1)-c1ccncc1 |c:18| Show InChI InChI=1S/C24H15N3O2S2/c28-20-18-19(27-24(26-18)15-11-13-25-14-12-15)21(29)23(31-17-9-5-2-6-10-17)22(20)30-16-7-3-1-4-8-16/h1-14H,(H,26,27)	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	790	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...				Bioorg Med Chem Lett 28: 2533-2538 (2018) Article DOI: 10.1016/j.bmcl.2018.05.046 BindingDB Entry DOI: 10.7270/Q2HT2S0T
					More data for this Ligand-Target Pair
Genome polyprotein (Coxsackievirus B3 (strain Nancy))	BDBM50462025 (CHEMBL331941) Show SMILES Cc1nc2c([nH]1)C(=O)C(Nc1ccc(C)cc1)=C(Cl)C2=O |t:18| Show InChI InChI=1S/C15H12ClN3O2/c1-7-3-5-9(6-4-7)19-11-10(16)14(20)12-13(15(11)21)18-8(2)17-12/h3-6,19H,1-2H3,(H,17,18)	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	830	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...				Bioorg Med Chem Lett 28: 2533-2538 (2018) Article DOI: 10.1016/j.bmcl.2018.05.046 BindingDB Entry DOI: 10.7270/Q2HT2S0T
					More data for this Ligand-Target Pair
Genome polyprotein (Coxsackievirus B3 (strain Nancy))	BDBM50462019 (CHEMBL259499) Show SMILES Cc1nc2c([nH]1)C(=O)C(Nc1ccc(cc1)C(F)(F)F)=C(Cl)C2=O |t:21| Show InChI InChI=1S/C15H9ClF3N3O2/c1-6-20-11-12(21-6)14(24)10(9(16)13(11)23)22-8-4-2-7(3-5-8)15(17,18)19/h2-5,22H,1H3,(H,20,21)	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	840	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...				Bioorg Med Chem Lett 28: 2533-2538 (2018) Article DOI: 10.1016/j.bmcl.2018.05.046 BindingDB Entry DOI: 10.7270/Q2HT2S0T
					More data for this Ligand-Target Pair
Genome polyprotein (Human rhinovirus 14)	BDBM50462014 (CHEMBL4224853) Show SMILES COc1ccc(OC2=C(Cl)C(=O)c3ccccc3C2=O)c(c1)[N+]([O-])=O |c:7| Show InChI InChI=1S/C17H10ClNO6/c1-24-9-6-7-13(12(8-9)19(22)23)25-17-14(18)15(20)10-4-2-3-5-11(10)16(17)21/h2-8H,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	850	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of recombinant human rhinovirus protease 3C using fluorogenic-Dabcyl-KTSAVLQSGFRKME-Edan as substrate after 5 mins by FRET assay				Bioorg Med Chem Lett 28: 2533-2538 (2018) Article DOI: 10.1016/j.bmcl.2018.05.046 BindingDB Entry DOI: 10.7270/Q2HT2S0T
					More data for this Ligand-Target Pair
Genome polyprotein (Coxsackievirus B3 (strain Nancy))	BDBM50462026 (CHEMBL4229177) Show SMILES Cc1nc2c([nH]1)C(=O)C(Cl)=C(Nc1cc(F)cc(F)c1)C2=O |t:10| Show InChI InChI=1S/C14H8ClF2N3O2/c1-5-18-11-12(19-5)14(22)10(9(15)13(11)21)20-8-3-6(16)2-7(17)4-8/h2-4,20H,1H3,(H,18,19)	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	900	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...				Bioorg Med Chem Lett 28: 2533-2538 (2018) Article DOI: 10.1016/j.bmcl.2018.05.046 BindingDB Entry DOI: 10.7270/Q2HT2S0T
					More data for this Ligand-Target Pair
Genome polyprotein (Coxsackievirus B3 (strain Nancy))	BDBM50462023 (CHEMBL4226298) Show SMILES Cc1[nH]c2ccccc2c1C1=C(O)C(=O)c2ncccc2C1=O |c:12| Show InChI InChI=1S/C18H12N2O3/c1-9-13(10-5-2-3-7-12(10)20-9)14-16(21)11-6-4-8-19-15(11)18(23)17(14)22/h2-8,20,22H,1H3	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...				Bioorg Med Chem Lett 28: 2533-2538 (2018) Article DOI: 10.1016/j.bmcl.2018.05.046 BindingDB Entry DOI: 10.7270/Q2HT2S0T
					More data for this Ligand-Target Pair
Genome polyprotein (Coxsackievirus B3 (strain Nancy))	BDBM50462018 (CHEMBL4225972) Show SMILES FC(F)C(F)(F)Oc1ccc(cc1N1C(=O)C=CC1=O)N1C(=O)C=CC1=O |c:17,25| Show InChI InChI=1S/C16H8F4N2O5/c17-15(18)16(19,20)27-10-2-1-8(21-11(23)3-4-12(21)24)7-9(10)22-13(25)5-6-14(22)26/h1-7,15H	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...				Bioorg Med Chem Lett 28: 2533-2538 (2018) Article DOI: 10.1016/j.bmcl.2018.05.046 BindingDB Entry DOI: 10.7270/Q2HT2S0T
					More data for this Ligand-Target Pair
Genome polyprotein (Coxsackievirus B3 (strain Nancy))	BDBM50462015 (CHEMBL4227149) Show SMILES Oc1ccc(OC2=C(Oc3ccc(O)cc3)C(=O)c3ncccc3C2=O)cc1 |c:6| Show InChI InChI=1S/C21H13NO6/c23-12-3-7-14(8-4-12)27-20-18(25)16-2-1-11-22-17(16)19(26)21(20)28-15-9-5-13(24)6-10-15/h1-11,23-24H	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...				Bioorg Med Chem Lett 28: 2533-2538 (2018) Article DOI: 10.1016/j.bmcl.2018.05.046 BindingDB Entry DOI: 10.7270/Q2HT2S0T
					More data for this Ligand-Target Pair
Genome polyprotein (Coxsackievirus B3 (strain Nancy))	BDBM50462014 (CHEMBL4224853) Show SMILES COc1ccc(OC2=C(Cl)C(=O)c3ccccc3C2=O)c(c1)[N+]([O-])=O |c:7| Show InChI InChI=1S/C17H10ClNO6/c1-24-9-6-7-13(12(8-9)19(22)23)25-17-14(18)15(20)10-4-2-3-5-11(10)16(17)21/h2-8H,1H3	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...				Bioorg Med Chem Lett 28: 2533-2538 (2018) Article DOI: 10.1016/j.bmcl.2018.05.046 BindingDB Entry DOI: 10.7270/Q2HT2S0T
					More data for this Ligand-Target Pair
Genome polyprotein (Coxsackievirus B3 (strain Nancy))	BDBM50462017 (CHEMBL4229199) Show SMILES COC(=O)\C=C\C(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)C |r,@@:17| Show InChI InChI=1S/C14H23NO5/c1-9(2)12(10(16)7-8-11(17)19-6)15-13(18)20-14(3,4)5/h7-9,12H,1-6H3,(H,15,18)/b8-7+/t12-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...				Bioorg Med Chem Lett 28: 2533-2538 (2018) Article DOI: 10.1016/j.bmcl.2018.05.046 BindingDB Entry DOI: 10.7270/Q2HT2S0T
					More data for this Ligand-Target Pair
Epidermal growth factor receptor (Homo sapiens (Human))	BDBM50178490 (7,12-dioxo-5-(2-piperidin-1-yl-ethoxy)-7,12-dihydr...) Show SMILES COC(=O)c1c(OCCN2CCCCC2)c2ccccc2c2oc3c(C(=O)c4ccccc4C3=O)c12 Show InChI InChI=1S/C29H25NO6/c1-34-29(33)23-21-22-24(31)17-9-3-4-10-18(17)25(32)28(22)36-27(21)20-12-6-5-11-19(20)26(23)35-16-15-30-13-7-2-8-14-30/h3-6,9-12H,2,7-8,13-16H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against EGFR kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Platelet-derived growth factor receptor beta (Homo sapiens (Human))	BDBM4367 ((3Z)-2-amino-3-[(3,4,5-trihydroxyphenyl)methyliden...) Show SMILES Oc1cc(C=C(C#N)C(=N)C(C#N)C#N)cc(O)c1O |w:4.3| Show InChI InChI=1S/C13H8N4O3/c14-4-8(12(17)9(5-15)6-16)1-7-2-10(18)13(20)11(19)3-7/h1-3,9,17-20H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against PDGFRbeta kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Epidermal growth factor receptor (Homo sapiens (Human))	BDBM4367 ((3Z)-2-amino-3-[(3,4,5-trihydroxyphenyl)methyliden...) Show SMILES Oc1cc(C=C(C#N)C(=N)C(C#N)C#N)cc(O)c1O |w:4.3| Show InChI InChI=1S/C13H8N4O3/c14-4-8(12(17)9(5-15)6-16)1-7-2-10(18)13(20)11(19)3-7/h1-3,9,17-20H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against EGFR kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM4367 ((3Z)-2-amino-3-[(3,4,5-trihydroxyphenyl)methyliden...) Show SMILES Oc1cc(C=C(C#N)C(=N)C(C#N)C#N)cc(O)c1O |w:4.3| Show InChI InChI=1S/C13H8N4O3/c14-4-8(12(17)9(5-15)6-16)1-7-2-10(18)13(20)11(19)3-7/h1-3,9,17-20H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against VEGFR2 kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50178490 (7,12-dioxo-5-(2-piperidin-1-yl-ethoxy)-7,12-dihydr...) Show SMILES COC(=O)c1c(OCCN2CCCCC2)c2ccccc2c2oc3c(C(=O)c4ccccc4C3=O)c12 Show InChI InChI=1S/C29H25NO6/c1-34-29(33)23-21-22-24(31)17-9-3-4-10-18(17)25(32)28(22)36-27(21)20-12-6-5-11-19(20)26(23)35-16-15-30-13-7-2-8-14-30/h3-6,9-12H,2,7-8,13-16H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against VEGFR2 kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Fibroblast growth factor receptor 1 (Homo sapiens (Human))	BDBM4367 ((3Z)-2-amino-3-[(3,4,5-trihydroxyphenyl)methyliden...) Show SMILES Oc1cc(C=C(C#N)C(=N)C(C#N)C#N)cc(O)c1O |w:4.3| Show InChI InChI=1S/C13H8N4O3/c14-4-8(12(17)9(5-15)6-16)1-7-2-10(18)13(20)11(19)3-7/h1-3,9,17-20H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against FGFR1 kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Epidermal growth factor receptor (Homo sapiens (Human))	BDBM50178494 (5-(2-diethylamino-ethoxy)-7,12-dioxo-7,12-dihydro-...) Show SMILES CCN(CC)CCOc1c(C(=O)OC)c2c3c(oc2c2ccccc12)C(=O)c1ccccc1C3=O Show InChI InChI=1S/C28H25NO6/c1-4-29(5-2)14-15-34-25-18-12-8-9-13-19(18)26-20(22(25)28(32)33-3)21-23(30)16-10-6-7-11-17(16)24(31)27(21)35-26/h6-13H,4-5,14-15H2,1-3H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against EGFR kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Genome polyprotein (Coxsackievirus B3 (strain Nancy))	BDBM50462016 (CHEMBL3213811) Show SMILES Cc1ccc(N\N=C\c2c(O)cc(C)oc2=O)cc1 Show InChI InChI=1S/C14H14N2O3/c1-9-3-5-11(6-4-9)16-15-8-12-13(17)7-10(2)19-14(12)18/h3-8,16-17H,1-2H3/b15-8+	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...				Bioorg Med Chem Lett 28: 2533-2538 (2018) Article DOI: 10.1016/j.bmcl.2018.05.046 BindingDB Entry DOI: 10.7270/Q2HT2S0T
					More data for this Ligand-Target Pair
Platelet-derived growth factor receptor beta (Homo sapiens (Human))	BDBM50178490 (7,12-dioxo-5-(2-piperidin-1-yl-ethoxy)-7,12-dihydr...) Show SMILES COC(=O)c1c(OCCN2CCCCC2)c2ccccc2c2oc3c(C(=O)c4ccccc4C3=O)c12 Show InChI InChI=1S/C29H25NO6/c1-34-29(33)23-21-22-24(31)17-9-3-4-10-18(17)25(32)28(22)36-27(21)20-12-6-5-11-19(20)26(23)35-16-15-30-13-7-2-8-14-30/h3-6,9-12H,2,7-8,13-16H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against PDGFRbeta kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50178492 (7,12-dioxo-5-(2-pyrrolidin-1-yl-ethoxy)-7,12-dihyd...) Show SMILES COC(=O)c1c(OCCN2CCCC2)c2ccccc2c2oc3c(C(=O)c4ccccc4C3=O)c12 Show InChI InChI=1S/C28H23NO6/c1-33-28(32)22-20-21-23(30)16-8-2-3-9-17(16)24(31)27(21)35-26(20)19-11-5-4-10-18(19)25(22)34-15-14-29-12-6-7-13-29/h2-5,8-11H,6-7,12-15H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against VEGFR2 kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Genome polyprotein (Coxsackievirus B3 (strain Nancy))	BDBM50462024 (CHEMBL4225121) Show SMILES CN(CC(C(=O)c1ccc(Cl)cc1)n1cnc2ccccc2c1=O)Cc1ccccc1 Show InChI InChI=1S/C25H22ClN3O2/c1-28(15-18-7-3-2-4-8-18)16-23(24(30)19-11-13-20(26)14-12-19)29-17-27-22-10-6-5-9-21(22)25(29)31/h2-14,17,23H,15-16H2,1H3	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...				Bioorg Med Chem Lett 28: 2533-2538 (2018) Article DOI: 10.1016/j.bmcl.2018.05.046 BindingDB Entry DOI: 10.7270/Q2HT2S0T
					More data for this Ligand-Target Pair
Fibroblast growth factor receptor 1 (Homo sapiens (Human))	BDBM50178490 (7,12-dioxo-5-(2-piperidin-1-yl-ethoxy)-7,12-dihydr...) Show SMILES COC(=O)c1c(OCCN2CCCCC2)c2ccccc2c2oc3c(C(=O)c4ccccc4C3=O)c12 Show InChI InChI=1S/C29H25NO6/c1-34-29(33)23-21-22-24(31)17-9-3-4-10-18(17)25(32)28(22)36-27(21)20-12-6-5-11-19(20)26(23)35-16-15-30-13-7-2-8-14-30/h3-6,9-12H,2,7-8,13-16H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against FGFR1 kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Platelet-derived growth factor receptor beta (Homo sapiens (Human))	BDBM50178495 (5-(2-dimethylamino-ethoxy)-7,12-dioxo-7,12-dihydro...) Show SMILES COC(=O)c1c(OCCN(C)C)c2ccccc2c2oc3c(C(=O)c4ccccc4C3=O)c12 Show InChI InChI=1S/C26H21NO6/c1-27(2)12-13-32-23-16-10-6-7-11-17(16)24-18(20(23)26(30)31-3)19-21(28)14-8-4-5-9-15(14)22(29)25(19)33-24/h4-11H,12-13H2,1-3H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against PDGFRbeta kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Genome polyprotein (Coxsackievirus B3 (strain Nancy))	BDBM50462027 (CHEMBL4227809) Show SMILES CC1(C)CC2=C(C(=O)C1)C(Nc1ccccc1)(C(=O)O2)C(F)(F)F |c:4| Show InChI InChI=1S/C17H16F3NO3/c1-15(2)8-11(22)13-12(9-15)24-14(23)16(13,17(18,19)20)21-10-6-4-3-5-7-10/h3-7,21H,8-9H2,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	Article PubMed	n/a	n/a	8.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...				Bioorg Med Chem Lett 28: 2533-2538 (2018) Article DOI: 10.1016/j.bmcl.2018.05.046 BindingDB Entry DOI: 10.7270/Q2HT2S0T
					More data for this Ligand-Target Pair
Genome polyprotein (Human rhinovirus 14)	BDBM50462026 (CHEMBL4229177) Show SMILES Cc1nc2c([nH]1)C(=O)C(Cl)=C(Nc1cc(F)cc(F)c1)C2=O |t:10| Show InChI InChI=1S/C14H8ClF2N3O2/c1-5-18-11-12(19-5)14(22)10(9(15)13(11)21)20-8-3-6(16)2-7(17)4-8/h2-4,20H,1H3,(H,18,19)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	8.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of recombinant human rhinovirus protease 3C using fluorogenic-Dabcyl-KTSAVLQSGFRKME-Edan as substrate after 5 mins by FRET assay				Bioorg Med Chem Lett 28: 2533-2538 (2018) Article DOI: 10.1016/j.bmcl.2018.05.046 BindingDB Entry DOI: 10.7270/Q2HT2S0T
					More data for this Ligand-Target Pair
Platelet-derived growth factor receptor beta (Homo sapiens (Human))	BDBM50178492 (7,12-dioxo-5-(2-pyrrolidin-1-yl-ethoxy)-7,12-dihyd...) Show SMILES COC(=O)c1c(OCCN2CCCC2)c2ccccc2c2oc3c(C(=O)c4ccccc4C3=O)c12 Show InChI InChI=1S/C28H23NO6/c1-33-28(32)22-20-21-23(30)16-8-2-3-9-17(16)24(31)27(21)35-26(20)19-11-5-4-10-18(19)25(22)34-15-14-29-12-6-7-13-29/h2-5,8-11H,6-7,12-15H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against PDGFRbeta kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Fibroblast growth factor receptor 1 (Homo sapiens (Human))	BDBM50178494 (5-(2-diethylamino-ethoxy)-7,12-dioxo-7,12-dihydro-...) Show SMILES CCN(CC)CCOc1c(C(=O)OC)c2c3c(oc2c2ccccc12)C(=O)c1ccccc1C3=O Show InChI InChI=1S/C28H25NO6/c1-4-29(5-2)14-15-34-25-18-12-8-9-13-19(18)26-20(22(25)28(32)33-3)21-23(30)16-10-6-7-11-17(16)24(31)27(21)35-26/h6-13H,4-5,14-15H2,1-3H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against FGFR1 kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Epidermal growth factor receptor (Homo sapiens (Human))	BDBM50178492 (7,12-dioxo-5-(2-pyrrolidin-1-yl-ethoxy)-7,12-dihyd...) Show SMILES COC(=O)c1c(OCCN2CCCC2)c2ccccc2c2oc3c(C(=O)c4ccccc4C3=O)c12 Show InChI InChI=1S/C28H23NO6/c1-33-28(32)22-20-21-23(30)16-8-2-3-9-17(16)24(31)27(21)35-26(20)19-11-5-4-10-18(19)25(22)34-15-14-29-12-6-7-13-29/h2-5,8-11H,6-7,12-15H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against EGFR kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Platelet-derived growth factor receptor beta (Homo sapiens (Human))	BDBM50178491 (5-(3-dimethylamino-propoxy)-7,12-dioxo-7,12-dihydr...) Show SMILES COC(=O)c1c(OCCCN(C)C)c2ccccc2c2oc3c(C(=O)c4ccccc4C3=O)c12 Show InChI InChI=1S/C27H23NO6/c1-28(2)13-8-14-33-24-17-11-6-7-12-18(17)25-19(21(24)27(31)32-3)20-22(29)15-9-4-5-10-16(15)23(30)26(20)34-25/h4-7,9-12H,8,13-14H2,1-3H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.02E+4	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against PDGFRbeta kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Genome polyprotein (Coxsackievirus B3 (strain Nancy))	BDBM36895 (1-(2,3-dihydro-1,4-benzodioxin-6-yl)-3-(1,2,4,5-te...) Show SMILES O=C(CCN1CCc2ccccc2CC1)c1ccc2OCCOc2c1 Show InChI InChI=1S/C21H23NO3/c23-19(18-5-6-20-21(15-18)25-14-13-24-20)9-12-22-10-7-16-3-1-2-4-17(16)8-11-22/h1-6,15H,7-14H2	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.11E+4	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...				Bioorg Med Chem Lett 28: 2533-2538 (2018) Article DOI: 10.1016/j.bmcl.2018.05.046 BindingDB Entry DOI: 10.7270/Q2HT2S0T
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50178494 (5-(2-diethylamino-ethoxy)-7,12-dioxo-7,12-dihydro-...) Show SMILES CCN(CC)CCOc1c(C(=O)OC)c2c3c(oc2c2ccccc12)C(=O)c1ccccc1C3=O Show InChI InChI=1S/C28H25NO6/c1-4-29(5-2)14-15-34-25-18-12-8-9-13-19(18)26-20(22(25)28(32)33-3)21-23(30)16-10-6-7-11-17(16)24(31)27(21)35-26/h6-13H,4-5,14-15H2,1-3H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.26E+4	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against VEGFR2 kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Epidermal growth factor receptor (Homo sapiens (Human))	BDBM50178493 (5-methoxy-7,12-dioxo-7,12-dihydro-dinaphtho[1,2-b;...) Show SMILES COC(=O)c1c(OC)c2ccccc2c2oc3c(C(=O)c4ccccc4C3=O)c12 Show InChI InChI=1S/C23H14O6/c1-27-20-13-9-5-6-10-14(13)21-15(17(20)23(26)28-2)16-18(24)11-7-3-4-8-12(11)19(25)22(16)29-21/h3-10H,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.26E+4	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against EGFR kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50178495 (5-(2-dimethylamino-ethoxy)-7,12-dioxo-7,12-dihydro...) Show SMILES COC(=O)c1c(OCCN(C)C)c2ccccc2c2oc3c(C(=O)c4ccccc4C3=O)c12 Show InChI InChI=1S/C26H21NO6/c1-27(2)12-13-32-23-16-10-6-7-11-17(16)24-18(20(23)26(30)31-3)19-21(28)14-8-4-5-9-15(14)22(29)25(19)33-24/h4-11H,12-13H2,1-3H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against VEGFR2 kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Epidermal growth factor receptor (Homo sapiens (Human))	BDBM50178491 (5-(3-dimethylamino-propoxy)-7,12-dioxo-7,12-dihydr...) Show SMILES COC(=O)c1c(OCCCN(C)C)c2ccccc2c2oc3c(C(=O)c4ccccc4C3=O)c12 Show InChI InChI=1S/C27H23NO6/c1-28(2)13-8-14-33-24-17-11-6-7-12-18(17)25-19(21(24)27(31)32-3)20-22(29)15-9-4-5-10-16(15)23(30)26(20)34-25/h4-7,9-12H,8,13-14H2,1-3H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.36E+4	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against EGFR kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50178491 (5-(3-dimethylamino-propoxy)-7,12-dioxo-7,12-dihydr...) Show SMILES COC(=O)c1c(OCCCN(C)C)c2ccccc2c2oc3c(C(=O)c4ccccc4C3=O)c12 Show InChI InChI=1S/C27H23NO6/c1-28(2)13-8-14-33-24-17-11-6-7-12-18(17)25-19(21(24)27(31)32-3)20-22(29)15-9-4-5-10-16(15)23(30)26(20)34-25/h4-7,9-12H,8,13-14H2,1-3H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.55E+4	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against VEGFR2 kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Platelet-derived growth factor receptor beta (Homo sapiens (Human))	BDBM50178494 (5-(2-diethylamino-ethoxy)-7,12-dioxo-7,12-dihydro-...) Show SMILES CCN(CC)CCOc1c(C(=O)OC)c2c3c(oc2c2ccccc12)C(=O)c1ccccc1C3=O Show InChI InChI=1S/C28H25NO6/c1-4-29(5-2)14-15-34-25-18-12-8-9-13-19(18)26-20(22(25)28(32)33-3)21-23(30)16-10-6-7-11-17(16)24(31)27(21)35-26/h6-13H,4-5,14-15H2,1-3H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.59E+4	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against PDGFRbeta kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Fibroblast growth factor receptor 1 (Homo sapiens (Human))	BDBM50178495 (5-(2-dimethylamino-ethoxy)-7,12-dioxo-7,12-dihydro...) Show SMILES COC(=O)c1c(OCCN(C)C)c2ccccc2c2oc3c(C(=O)c4ccccc4C3=O)c12 Show InChI InChI=1S/C26H21NO6/c1-27(2)12-13-32-23-16-10-6-7-11-17(16)24-18(20(23)26(30)31-3)19-21(28)14-8-4-5-9-15(14)22(29)25(19)33-24/h4-11H,12-13H2,1-3H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.36E+4	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against FGFR1 kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Fibroblast growth factor receptor 1 (Homo sapiens (Human))	BDBM50178492 (7,12-dioxo-5-(2-pyrrolidin-1-yl-ethoxy)-7,12-dihyd...) Show SMILES COC(=O)c1c(OCCN2CCCC2)c2ccccc2c2oc3c(C(=O)c4ccccc4C3=O)c12 Show InChI InChI=1S/C28H23NO6/c1-33-28(32)22-20-21-23(30)16-8-2-3-9-17(16)24(31)27(21)35-26(20)19-11-5-4-10-18(19)25(22)34-15-14-29-12-6-7-13-29/h2-5,8-11H,6-7,12-15H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.38E+4	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against FGFR1 kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Epidermal growth factor receptor (Homo sapiens (Human))	BDBM50178495 (5-(2-dimethylamino-ethoxy)-7,12-dioxo-7,12-dihydro...) Show SMILES COC(=O)c1c(OCCN(C)C)c2ccccc2c2oc3c(C(=O)c4ccccc4C3=O)c12 Show InChI InChI=1S/C26H21NO6/c1-27(2)12-13-32-23-16-10-6-7-11-17(16)24-18(20(23)26(30)31-3)19-21(28)14-8-4-5-9-15(14)22(29)25(19)33-24/h4-11H,12-13H2,1-3H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against EGFR kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Fibroblast growth factor receptor 1 (Homo sapiens (Human))	BDBM50178491 (5-(3-dimethylamino-propoxy)-7,12-dioxo-7,12-dihydr...) Show SMILES COC(=O)c1c(OCCCN(C)C)c2ccccc2c2oc3c(C(=O)c4ccccc4C3=O)c12 Show InChI InChI=1S/C27H23NO6/c1-28(2)13-8-14-33-24-17-11-6-7-12-18(17)25-19(21(24)27(31)32-3)20-22(29)15-9-4-5-10-16(15)23(30)26(20)34-25/h4-7,9-12H,8,13-14H2,1-3H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.84E+4	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against FGFR1 kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Fibroblast growth factor receptor 1 (Homo sapiens (Human))	BDBM50178493 (5-methoxy-7,12-dioxo-7,12-dihydro-dinaphtho[1,2-b;...) Show SMILES COC(=O)c1c(OC)c2ccccc2c2oc3c(C(=O)c4ccccc4C3=O)c12 Show InChI InChI=1S/C23H14O6/c1-27-20-13-9-5-6-10-14(13)21-15(17(20)23(26)28-2)16-18(24)11-7-3-4-8-12(11)19(25)22(16)29-21/h3-10H,1-2H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against FGFR1 kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Platelet-derived growth factor receptor beta (Homo sapiens (Human))	BDBM50178496 (7,12-dioxo-5-propoxy-7,12-dihydro-dinaphtho[1,2-b;...) Show SMILES CCCOc1c(C(=O)OC)c2c3c(oc2c2ccccc12)C(=O)c1ccccc1C3=O Show InChI InChI=1S/C25H18O6/c1-3-12-30-22-15-10-6-7-11-16(15)23-17(19(22)25(28)29-2)18-20(26)13-8-4-5-9-14(13)21(27)24(18)31-23/h4-11H,3,12H2,1-2H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against PDGFRbeta kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Epidermal growth factor receptor (Homo sapiens (Human))	BDBM50178496 (7,12-dioxo-5-propoxy-7,12-dihydro-dinaphtho[1,2-b;...) Show SMILES CCCOc1c(C(=O)OC)c2c3c(oc2c2ccccc12)C(=O)c1ccccc1C3=O Show InChI InChI=1S/C25H18O6/c1-3-12-30-22-15-10-6-7-11-16(15)23-17(19(22)25(28)29-2)18-20(26)13-8-4-5-9-14(13)21(27)24(18)31-23/h4-11H,3,12H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against EGFR kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Platelet-derived growth factor receptor beta (Homo sapiens (Human))	BDBM50178493 (5-methoxy-7,12-dioxo-7,12-dihydro-dinaphtho[1,2-b;...) Show SMILES COC(=O)c1c(OC)c2ccccc2c2oc3c(C(=O)c4ccccc4C3=O)c12 Show InChI InChI=1S/C23H14O6/c1-27-20-13-9-5-6-10-14(13)21-15(17(20)23(26)28-2)16-18(24)11-7-3-4-8-12(11)19(25)22(16)29-21/h3-10H,1-2H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against PDGFRbeta kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair
Fibroblast growth factor receptor 1 (Homo sapiens (Human))	BDBM50178496 (7,12-dioxo-5-propoxy-7,12-dihydro-dinaphtho[1,2-b;...) Show SMILES CCCOc1c(C(=O)OC)c2c3c(oc2c2ccccc12)C(=O)c1ccccc1C3=O Show InChI InChI=1S/C25H18O6/c1-3-12-30-22-15-10-6-7-11-16(15)23-17(19(22)25(28)29-2)18-20(26)13-8-4-5-9-14(13)21(27)24(18)31-23/h4-11H,3,12H2,1-2H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibitory activity against FGFR1 kinase				Bioorg Med Chem Lett 16: 737-42 (2005) Article DOI: 10.1016/j.bmcl.2005.08.115 BindingDB Entry DOI: 10.7270/Q2SF2VQR
					More data for this Ligand-Target Pair