Compile Data Set for Download or QSAR

Found 94 hits with Last Name = 'baek' and Initial = 'jy'   

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
M-phase inducer phosphatase 2 (Homo sapiens (Human))	BDBM50177318 (2-(4-(7-(4-tetradecylbenzoyl)cyclopenta[d][1,2]oxa...) Show SMILES CCCCCCCCCCCCCCc1ccc(cc1)C(=O)c1ccc2c(nocc12)-c1ccc(OCC(O)=O)cc1 Show InChI InChI=1S/C36H43NO5/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-27-15-17-29(18-16-27)36(40)32-24-23-31-33(32)25-42-37-35(31)28-19-21-30(22-20-28)41-26-34(38)39/h15-25H,2-14,26H2,1H3,(H,38,39)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	120	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 cdc25B phosphatase				Bioorg Med Chem Lett 16: 499-502 (2005) Article DOI: 10.1016/j.bmcl.2005.10.062 BindingDB Entry DOI: 10.7270/Q2319VFG
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50177318 (2-(4-(7-(4-tetradecylbenzoyl)cyclopenta[d][1,2]oxa...) Show SMILES CCCCCCCCCCCCCCc1ccc(cc1)C(=O)c1ccc2c(nocc12)-c1ccc(OCC(O)=O)cc1 Show InChI InChI=1S/C36H43NO5/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-27-15-17-29(18-16-27)36(40)32-24-23-31-33(32)25-42-37-35(31)28-19-21-30(22-20-28)41-26-34(38)39/h15-25H,2-14,26H2,1H3,(H,38,39)	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	140	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 recombinant human PTP1B				Bioorg Med Chem Lett 16: 499-502 (2005) Article DOI: 10.1016/j.bmcl.2005.10.062 BindingDB Entry DOI: 10.7270/Q2319VFG
					More data for this Ligand-Target Pair
Receptor-type tyrosine-protein phosphatase C (Homo sapiens (Human))	BDBM50177318 (2-(4-(7-(4-tetradecylbenzoyl)cyclopenta[d][1,2]oxa...) Show SMILES CCCCCCCCCCCCCCc1ccc(cc1)C(=O)c1ccc2c(nocc12)-c1ccc(OCC(O)=O)cc1 Show InChI InChI=1S/C36H43NO5/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-27-15-17-29(18-16-27)36(40)32-24-23-31-33(32)25-42-37-35(31)28-19-21-30(22-20-28)41-26-34(38)39/h15-25H,2-14,26H2,1H3,(H,38,39)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	150	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 CD45 phosphatase				Bioorg Med Chem Lett 16: 499-502 (2005) Article DOI: 10.1016/j.bmcl.2005.10.062 BindingDB Entry DOI: 10.7270/Q2319VFG
					More data for this Ligand-Target Pair
Serine/threonine-protein phosphatase PP1-gamma catalytic subunit (Homo sapiens (Human))	BDBM50177318 (2-(4-(7-(4-tetradecylbenzoyl)cyclopenta[d][1,2]oxa...) Show SMILES CCCCCCCCCCCCCCc1ccc(cc1)C(=O)c1ccc2c(nocc12)-c1ccc(OCC(O)=O)cc1 Show InChI InChI=1S/C36H43NO5/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-27-15-17-29(18-16-27)36(40)32-24-23-31-33(32)25-42-37-35(31)28-19-21-30(22-20-28)41-26-34(38)39/h15-25H,2-14,26H2,1H3,(H,38,39)	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	220	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 Protein phosphatase 1				Bioorg Med Chem Lett 16: 499-502 (2005) Article DOI: 10.1016/j.bmcl.2005.10.062 BindingDB Entry DOI: 10.7270/Q2319VFG
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115725 (3-(1-Indol-1-yl-3,4-dioxo-3,4-dihydro-naphthalen-2...) Show SMILES CCOC(=O)CCC1=C(c2ccccc2C(=O)C1=O)n1ccc2ccccc12 |t:7| Show InChI InChI=1S/C23H19NO4/c1-2-28-20(25)12-11-18-21(24-14-13-15-7-3-6-10-19(15)24)16-8-4-5-9-17(16)22(26)23(18)27/h3-10,13-14H,2,11-12H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	270	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 Protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP)				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50177324 (2-(4-(7-pentadecanoylcyclopenta[d][1,2]oxazin-4-yl...) Show SMILES CCCCCCCCCCCCCCC(=O)c1ccc2c(nocc12)-c1ccc(OCC(O)=O)cc1 Show InChI InChI=1S/C30H39NO5/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-28(32)25-19-20-26-27(25)21-36-31-30(26)23-15-17-24(18-16-23)35-22-29(33)34/h15-21H,2-14,22H2,1H3,(H,33,34)	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	270	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 recombinant human PTP1B				Bioorg Med Chem Lett 16: 499-502 (2005) Article DOI: 10.1016/j.bmcl.2005.10.062 BindingDB Entry DOI: 10.7270/Q2319VFG
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115722 (4-Cyclohexyl-[1,2]naphthoquinone | CHEMBL58737) Show SMILES O=C1C=C(C2CCCCC2)c2ccccc2C1=O |t:2| Show InChI InChI=1S/C16H16O2/c17-15-10-14(11-6-2-1-3-7-11)12-8-4-5-9-13(12)16(15)18/h4-5,8-11H,1-3,6-7H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	320	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115756 (3-(5,6-Dioxo-8-phenyl-5,6-dihydro-naphthalen-2-yl)...) Show SMILES COC(=O)CCc1ccc2C(=O)C(=O)C=C(c3ccccc3)c2c1 |t:14| Show InChI InChI=1S/C20H16O4/c1-24-19(22)10-8-13-7-9-15-17(11-13)16(12-18(21)20(15)23)14-5-3-2-4-6-14/h2-7,9,11-12H,8,10H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	330	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 Protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP)				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115733 (3-(3,4-Dioxo-1-phenyl-3,4-dihydro-naphthalen-2-yl)...) Show SMILES CCOC(=O)CCC1=C(c2ccccc2)c2ccccc2C(=O)C1=O |c:7| Show InChI InChI=1S/C21H18O4/c1-2-25-18(22)13-12-17-19(14-8-4-3-5-9-14)15-10-6-7-11-16(15)20(23)21(17)24/h3-11H,2,12-13H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	430	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 Protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP)				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115766 (4-(4-Hydroxy-phenyl)-[1,2]naphthoquinone | CHEMBL5...) Show SMILES Oc1ccc(cc1)C1=CC(=O)C(=O)c2ccccc12 |t:8| Show InChI InChI=1S/C16H10O3/c17-11-7-5-10(6-8-11)14-9-15(18)16(19)13-4-2-1-3-12(13)14/h1-9,17H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	440	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115760 (4-(2,5-Difluoro-phenyl)-[1,2]naphthoquinone | CHEM...) Show SMILES Fc1ccc(F)c(c1)C1=CC(=O)C(=O)c2ccccc12 |t:9| Show InChI InChI=1S/C16H8F2O2/c17-9-5-6-14(18)13(7-9)12-8-15(19)16(20)11-4-2-1-3-10(11)12/h1-8H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	500	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase YopH (Yersinia enterocolitica)	BDBM50177318 (2-(4-(7-(4-tetradecylbenzoyl)cyclopenta[d][1,2]oxa...) Show SMILES CCCCCCCCCCCCCCc1ccc(cc1)C(=O)c1ccc2c(nocc12)-c1ccc(OCC(O)=O)cc1 Show InChI InChI=1S/C36H43NO5/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-27-15-17-29(18-16-27)36(40)32-24-23-31-33(32)25-42-37-35(31)28-19-21-30(22-20-28)41-26-34(38)39/h15-25H,2-14,26H2,1H3,(H,38,39)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	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 Inhibitory activity against YOP protein tyrosine phosphatase				Bioorg Med Chem Lett 16: 499-502 (2005) Article DOI: 10.1016/j.bmcl.2005.10.062 BindingDB Entry DOI: 10.7270/Q2319VFG
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115721 (3-(3,4-Dioxo-1-phenyl-3,4-dihydro-naphthalen-2-yl)...) Show SMILES CCN(CC)C(=O)CCC1=C(c2ccccc2)c2ccccc2C(=O)C1=O |c:9| Show InChI InChI=1S/C23H23NO3/c1-3-24(4-2)20(25)15-14-19-21(16-10-6-5-7-11-16)17-12-8-9-13-18(17)22(26)23(19)27/h5-13H,3-4,14-15H2,1-2H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	610	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 Protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP)				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115739 (CHEMBL56948 | [4-(1-Indol-1-yl-3,4-dioxo-3,4-dihyd...) Show SMILES CC(C)(C)OC(=O)COc1ccc(CC2=C(c3ccccc3C(=O)C2=O)n2ccc3ccccc23)cc1 |t:14| Show InChI InChI=1S/C31H27NO5/c1-31(2,3)37-27(33)19-36-22-14-12-20(13-15-22)18-25-28(32-17-16-21-8-4-7-11-26(21)32)23-9-5-6-10-24(23)29(34)30(25)35/h4-17H,18-19H2,1-3H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	650	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 Protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP)				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115740 ((7,8-Dioxo-5-phenyl-7,8-dihydro-naphthalen-1-yl)-c...) Show SMILES CCOC(=O)Nc1cccc2C(=CC(=O)C(=O)c12)c1ccccc1 |c:11| Show InChI InChI=1S/C19H15NO4/c1-2-24-19(23)20-15-10-6-9-13-14(12-7-4-3-5-8-12)11-16(21)18(22)17(13)15/h3-11H,2H2,1H3,(H,20,23)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	650	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115746 (3-[7-(2-Methoxycarbonyl-ethyl)-3,4-dioxo-1-phenyl-...) Show SMILES COC(=O)CCC1=C(c2ccccc2)c2cc(CCC(=O)OC)ccc2C(=O)C1=O |c:6| Show InChI InChI=1S/C24H22O6/c1-29-20(25)12-9-15-8-10-17-19(14-15)22(16-6-4-3-5-7-16)18(24(28)23(17)27)11-13-21(26)30-2/h3-8,10,14H,9,11-13H2,1-2H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	680	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 Protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP)				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Receptor-type tyrosine-protein phosphatase F (Homo sapiens (Human))	BDBM50177318 (2-(4-(7-(4-tetradecylbenzoyl)cyclopenta[d][1,2]oxa...) Show SMILES CCCCCCCCCCCCCCc1ccc(cc1)C(=O)c1ccc2c(nocc12)-c1ccc(OCC(O)=O)cc1 Show InChI InChI=1S/C36H43NO5/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-27-15-17-29(18-16-27)36(40)32-24-23-31-33(32)25-42-37-35(31)28-19-21-30(22-20-28)41-26-34(38)39/h15-25H,2-14,26H2,1H3,(H,38,39)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	690	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 LAR protein tyrosine phosphatase				Bioorg Med Chem Lett 16: 499-502 (2005) Article DOI: 10.1016/j.bmcl.2005.10.062 BindingDB Entry DOI: 10.7270/Q2319VFG
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50177317 (2-(4-(7-(4-methoxybenzoyl)cyclopenta[d][1,2]oxazin...) Show SMILES COc1ccc(cc1)C(=O)c1ccc2c(nocc12)-c1ccc(OCC(O)=O)cc1 Show InChI InChI=1S/C23H17NO6/c1-28-16-6-4-15(5-7-16)23(27)19-11-10-18-20(19)12-30-24-22(18)14-2-8-17(9-3-14)29-13-21(25)26/h2-12H,13H2,1H3,(H,25,26)	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	800	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 recombinant human PTP1B				Bioorg Med Chem Lett 16: 499-502 (2005) Article DOI: 10.1016/j.bmcl.2005.10.062 BindingDB Entry DOI: 10.7270/Q2319VFG
					More data for this Ligand-Target Pair
Receptor-type tyrosine-protein phosphatase C (Homo sapiens (Human))	BDBM50099778 (4-Phenyl-[1,2]naphthoquinone | CHEMBL51447) Show SMILES O=C1C=C(c2ccccc2)c2ccccc2C1=O |t:2| Show InChI InChI=1S/C16H10O2/c17-15-10-14(11-6-2-1-3-7-11)12-8-4-5-9-13(12)16(15)18/h1-10H	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	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 In vitro inhibitory activity of the compound against recombinant human CD45 using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50099778 (4-Phenyl-[1,2]naphthoquinone | CHEMBL51447) Show SMILES O=C1C=C(c2ccccc2)c2ccccc2C1=O |t:2| Show InChI InChI=1S/C16H10O2/c17-15-10-14(11-6-2-1-3-7-11)12-8-4-5-9-13(12)16(15)18/h1-10H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	860	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115755 (3-(8-Indol-1-yl-5,6-dioxo-5,6-dihydro-naphthalen-2...) Show SMILES COC(=O)CCc1ccc2C(=O)C(=O)C=C(c2c1)n1ccc2ccccc12 |c:14| Show InChI InChI=1S/C22H17NO4/c1-27-21(25)9-7-14-6-8-16-17(12-14)19(13-20(24)22(16)26)23-11-10-15-4-2-3-5-18(15)23/h2-6,8,10-13H,7,9H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	920	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 Protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP)				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115763 (7-Pentyloxy-4-phenyl-[1,2]naphthoquinone | CHEMBL5...) Show SMILES CCCCCOc1ccc2C(=CC(=O)C(=O)c2c1)c1ccccc1 |c:10| Show InChI InChI=1S/C21H20O3/c1-2-3-7-12-24-16-10-11-17-18(15-8-5-4-6-9-15)14-20(22)21(23)19(17)13-16/h4-6,8-11,13-14H,2-3,7,12H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	920	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115751 (3-[1-Indol-1-yl-6-(2-methoxycarbonyl-ethyl)-3,4-di...) Show SMILES COC(=O)CCC1=C(c2ccc(CCC(=O)OC)cc2C(=O)C1=O)n1ccc2ccccc12 |t:6| Show InChI InChI=1S/C26H23NO6/c1-32-22(28)11-8-16-7-9-18-20(15-16)26(31)25(30)19(10-12-23(29)33-2)24(18)27-14-13-17-5-3-4-6-21(17)27/h3-7,9,13-15H,8,10-12H2,1-2H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	940	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 Protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP)				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115761 (4-[2-(3,4-Dioxo-1-phenyl-3,4-dihydro-naphthalen-2-...) Show SMILES CCOC(=O)c1ccc(CCC2=C(c3ccccc3)c3ccccc3C(=O)C2=O)cc1 |c:11| Show InChI InChI=1S/C27H22O4/c1-2-31-27(30)20-15-12-18(13-16-20)14-17-23-24(19-8-4-3-5-9-19)21-10-6-7-11-22(21)25(28)26(23)29/h3-13,15-16H,2,14,17H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.01E+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 Protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP)				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115728 (CHEMBL57841 | [4-(1-Indol-1-yl-3,4-dioxo-3,4-dihyd...) Show SMILES OC(=O)COc1ccc(CC2=C(c3ccccc3C(=O)C2=O)n2ccc3ccccc23)cc1 |t:10| Show InChI InChI=1S/C27H19NO5/c29-24(30)16-33-19-11-9-17(10-12-19)15-22-25(28-14-13-18-5-1-4-8-23(18)28)20-6-2-3-7-21(20)26(31)27(22)32/h1-14H,15-16H2,(H,29,30)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.01E+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 Protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP)				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115729 (CHEMBL292843 | [4-(3,4-Dioxo-3,4-dihydro-naphthale...) Show SMILES CCOC(=O)COc1ccc(cc1)C1=CC(=O)C(=O)c2ccccc12 |t:14| Show InChI InChI=1S/C20H16O5/c1-2-24-19(22)12-25-14-9-7-13(8-10-14)17-11-18(21)20(23)16-6-4-3-5-15(16)17/h3-11H,2,12H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.07E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115737 (4-(1H-Indol-3-yl)-[1,2]naphthoquinone | CHEMBL6070...) Show SMILES O=C1C=C(c2c[nH]c3ccccc23)c2ccccc2C1=O |t:2| Show InChI InChI=1S/C18H11NO2/c20-17-9-14(11-5-1-2-7-13(11)18(17)21)15-10-19-16-8-4-3-6-12(15)16/h1-10,19H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.13E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115727 (4-(2-Nitro-phenyl)-[1,2]naphthoquinone | CHEMBL592...) Show SMILES [O-][N+](=O)c1ccccc1C1=CC(=O)C(=O)c2ccccc12 |t:10| Show InChI InChI=1S/C16H9NO4/c18-15-9-13(10-5-1-2-7-12(10)16(15)19)11-6-3-4-8-14(11)17(20)21/h1-9H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	1.17E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase YopH (Yersinia enterocolitica)	BDBM50177316 (2-(4-(7-(4-(aminomethyl)benzoyl)cyclopenta[d][1,2]...) Show SMILES NCc1ccc(cc1)C(=O)c1ccc2c(nocc12)-c1ccc(OCC(O)=O)cc1 Show InChI InChI=1S/C23H18N2O5/c24-11-14-1-3-16(4-2-14)23(28)19-10-9-18-20(19)12-30-25-22(18)15-5-7-17(8-6-15)29-13-21(26)27/h1-10,12H,11,13,24H2,(H,26,27)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.19E+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 YOP protein tyrosine phosphatase				Bioorg Med Chem Lett 16: 499-502 (2005) Article DOI: 10.1016/j.bmcl.2005.10.062 BindingDB Entry DOI: 10.7270/Q2319VFG
					More data for this Ligand-Target Pair
Receptor-type tyrosine-protein phosphatase C (Homo sapiens (Human))	BDBM50177316 (2-(4-(7-(4-(aminomethyl)benzoyl)cyclopenta[d][1,2]...) Show SMILES NCc1ccc(cc1)C(=O)c1ccc2c(nocc12)-c1ccc(OCC(O)=O)cc1 Show InChI InChI=1S/C23H18N2O5/c24-11-14-1-3-16(4-2-14)23(28)19-10-9-18-20(19)12-30-25-22(18)15-5-7-17(8-6-15)29-13-21(26)27/h1-10,12H,11,13,24H2,(H,26,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.23E+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 CD45 phosphatase				Bioorg Med Chem Lett 16: 499-502 (2005) Article DOI: 10.1016/j.bmcl.2005.10.062 BindingDB Entry DOI: 10.7270/Q2319VFG
					More data for this Ligand-Target Pair
Serine/threonine-protein phosphatase PP1-gamma catalytic subunit (Homo sapiens (Human))	BDBM50177316 (2-(4-(7-(4-(aminomethyl)benzoyl)cyclopenta[d][1,2]...) Show SMILES NCc1ccc(cc1)C(=O)c1ccc2c(nocc12)-c1ccc(OCC(O)=O)cc1 Show InChI InChI=1S/C23H18N2O5/c24-11-14-1-3-16(4-2-14)23(28)19-10-9-18-20(19)12-30-25-22(18)15-5-7-17(8-6-15)29-13-21(26)27/h1-10,12H,11,13,24H2,(H,26,27)	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+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 Protein phosphatase 1				Bioorg Med Chem Lett 16: 499-502 (2005) Article DOI: 10.1016/j.bmcl.2005.10.062 BindingDB Entry DOI: 10.7270/Q2319VFG
					More data for this Ligand-Target Pair
M-phase inducer phosphatase 1 (Homo sapiens (Human))	BDBM50177318 (2-(4-(7-(4-tetradecylbenzoyl)cyclopenta[d][1,2]oxa...) Show SMILES CCCCCCCCCCCCCCc1ccc(cc1)C(=O)c1ccc2c(nocc12)-c1ccc(OCC(O)=O)cc1 Show InChI InChI=1S/C36H43NO5/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-27-15-17-29(18-16-27)36(40)32-24-23-31-33(32)25-42-37-35(31)28-19-21-30(22-20-28)41-26-34(38)39/h15-25H,2-14,26H2,1H3,(H,38,39)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.33E+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 cdc25A phosphatase				Bioorg Med Chem Lett 16: 499-502 (2005) Article DOI: 10.1016/j.bmcl.2005.10.062 BindingDB Entry DOI: 10.7270/Q2319VFG
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115744 ((7,8-Dioxo-5-phenyl-7,8-dihydro-naphthalen-1-yl)-c...) Show SMILES O=C(Nc1cccc2C(=CC(=O)C(=O)c12)c1ccccc1)OCc1ccccc1 |c:8| Show InChI InChI=1S/C24H17NO4/c26-21-14-19(17-10-5-2-6-11-17)18-12-7-13-20(22(18)23(21)27)25-24(28)29-15-16-8-3-1-4-9-16/h1-14H,15H2,(H,25,28)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.34E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115765 (4-Benzyl-[1,2]naphthoquinone | CHEMBL292386) Show SMILES O=C1C=C(Cc2ccccc2)c2ccccc2C1=O |t:2| Show InChI InChI=1S/C17H12O2/c18-16-11-13(10-12-6-2-1-3-7-12)14-8-4-5-9-15(14)17(16)19/h1-9,11H,10H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.42E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115735 (CHEMBL58354 | [4-(3,4-Dioxo-1-phenyl-3,4-dihydro-n...) Show SMILES CC(C)(C)OC(=O)COc1ccc(CC2=C(c3ccccc3)c3ccccc3C(=O)C2=O)cc1 |c:14| Show InChI InChI=1S/C29H26O5/c1-29(2,3)34-25(30)18-33-21-15-13-19(14-16-21)17-24-26(20-9-5-4-6-10-20)22-11-7-8-12-23(22)27(31)28(24)32/h4-16H,17-18H2,1-3H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.48E+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 Protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP)				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115748 (CHEMBL301436 | [4-(3,4-Dioxo-1-phenyl-3,4-dihydro-...) Show SMILES OC(=O)COc1ccc(CC2=C(c3ccccc3)c3ccccc3C(=O)C2=O)cc1 |c:10| Show InChI InChI=1S/C25H18O5/c26-22(27)15-30-18-12-10-16(11-13-18)14-21-23(17-6-2-1-3-7-17)19-8-4-5-9-20(19)24(28)25(21)29/h1-13H,14-15H2,(H,26,27)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.54E+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 Protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP)				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115731 (4-(3,4-Dioxo-3,4-dihydro-naphthalen-1-yl)-benzoic ...) Show SMILES COC(=O)c1ccc(cc1)C1=CC(=O)C(=O)c2ccccc12 |t:11| Show InChI InChI=1S/C18H12O4/c1-22-18(21)12-8-6-11(7-9-12)15-10-16(19)17(20)14-5-3-2-4-13(14)15/h2-10H,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.54E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115738 (4-(2-Hydroxy-phenyl)-[1,2]naphthoquinone | CHEMBL6...) Show SMILES Oc1ccccc1C1=CC(=O)C(=O)c2ccccc12 |t:8| Show InChI InChI=1S/C16H10O3/c17-14-8-4-3-6-11(14)13-9-15(18)16(19)12-7-2-1-5-10(12)13/h1-9,17H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM22851 (1,2-Dione-Based Compound, 8 | 1,2-dihydronaphthale...) Show SMILES O=C1C=Cc2ccccc2C1=O |c:2| Show InChI InChI=1S/C10H6O2/c11-9-6-5-7-3-1-2-4-8(7)10(9)12/h1-6H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.64E+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 Protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP)				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50177322 (2-(2,6-dibromo-4-(7-(4-methoxybenzoyl)cyclopenta[d...) Show SMILES COc1ccc(cc1)C(=O)c1ccc2c(nocc12)-c1cc(Br)c(OCC(O)=O)c(Br)c1 Show InChI InChI=1S/C23H15Br2NO6/c1-30-14-4-2-12(3-5-14)22(29)16-7-6-15-17(16)10-32-26-21(15)13-8-18(24)23(19(25)9-13)31-11-20(27)28/h2-10H,11H2,1H3,(H,27,28)	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	1.64E+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 recombinant human PTP1B				Bioorg Med Chem Lett 16: 499-502 (2005) Article DOI: 10.1016/j.bmcl.2005.10.062 BindingDB Entry DOI: 10.7270/Q2319VFG
					More data for this Ligand-Target Pair
Receptor-type tyrosine-protein phosphatase C (Homo sapiens (Human))	BDBM50115731 (4-(3,4-Dioxo-3,4-dihydro-naphthalen-1-yl)-benzoic ...) Show SMILES COC(=O)c1ccc(cc1)C1=CC(=O)C(=O)c2ccccc12 |t:11| Show InChI InChI=1S/C18H12O4/c1-22-18(21)12-8-6-11(7-9-12)15-10-16(19)17(20)14-5-3-2-4-13(14)15/h2-10H,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.65E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity of the compound against recombinant human CD45 using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
M-phase inducer phosphatase 2 (Homo sapiens (Human))	BDBM50115737 (4-(1H-Indol-3-yl)-[1,2]naphthoquinone | CHEMBL6070...) Show SMILES O=C1C=C(c2c[nH]c3ccccc23)c2ccccc2C1=O |t:2| Show InChI InChI=1S/C18H11NO2/c20-17-9-14(11-5-1-2-7-13(11)18(17)21)15-10-19-16-8-4-3-6-12(15)16/h1-10,19H	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.95E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity of the compound against recombinant human Cdc25B using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50177320 (2-(4-(7-(3-methoxybenzoyl)cyclopenta[d][1,2]oxazin...) Show SMILES COc1cccc(c1)C(=O)c1ccc2c(nocc12)-c1ccc(OCC(O)=O)cc1 Show InChI InChI=1S/C23H17NO6/c1-28-17-4-2-3-15(11-17)23(27)19-10-9-18-20(19)12-30-24-22(18)14-5-7-16(8-6-14)29-13-21(25)26/h2-12H,13H2,1H3,(H,25,26)	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	1.96E+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 recombinant human PTP1B				Bioorg Med Chem Lett 16: 499-502 (2005) Article DOI: 10.1016/j.bmcl.2005.10.062 BindingDB Entry DOI: 10.7270/Q2319VFG
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115743 (7-Methoxy-4-phenyl-[1,2]naphthoquinone | CHEMBL587...) Show SMILES COc1ccc2C(=CC(=O)C(=O)c2c1)c1ccccc1 |c:6| Show InChI InChI=1S/C17H12O3/c1-20-12-7-8-13-14(11-5-3-2-4-6-11)10-16(18)17(19)15(13)9-12/h2-10H,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.04E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115764 (2-(5-Indol-1-yl-7,8-dioxo-7,8-dihydro-naphthalen-2...) Show SMILES OC(=O)C(Cc1ccccc1)Oc1ccc2C(=CC(=O)C(=O)c2c1)n1ccc2ccccc12 |c:17| Show InChI InChI=1S/C27H19NO5/c29-24-16-23(28-13-12-18-8-4-5-9-22(18)28)20-11-10-19(15-21(20)26(24)30)33-25(27(31)32)14-17-6-2-1-3-7-17/h1-13,15-16,25H,14H2,(H,31,32)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	2.07E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
M-phase inducer phosphatase 2 (Homo sapiens (Human))	BDBM50115731 (4-(3,4-Dioxo-3,4-dihydro-naphthalen-1-yl)-benzoic ...) Show SMILES COC(=O)c1ccc(cc1)C1=CC(=O)C(=O)c2ccccc12 |t:11| Show InChI InChI=1S/C18H12O4/c1-22-18(21)12-8-6-11(7-9-12)15-10-16(19)17(20)14-5-3-2-4-13(14)15/h2-10H,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.13E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity of the compound against recombinant human Cdc25B using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115749 (CHEMBL57036 | [2-(3,4-Dioxo-3,4-dihydro-naphthalen...) Show SMILES CCOC(=O)COc1ccccc1C1=CC(=O)C(=O)c2ccccc12 |t:14| Show InChI InChI=1S/C20H16O5/c1-2-24-19(22)12-25-18-10-6-5-8-14(18)16-11-17(21)20(23)15-9-4-3-7-13(15)16/h3-11H,2,12H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.15E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115758 (CHEMBL59240 | [1,1']Binaphthalenyl-3,4-dione) Show SMILES O=C1C=C(c2ccccc2C1=O)c1cccc2ccccc12 |c:2| Show InChI InChI=1S/C20H12O2/c21-19-12-18(16-9-3-4-10-17(16)20(19)22)15-11-5-7-13-6-1-2-8-14(13)15/h1-12H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.15E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50177316 (2-(4-(7-(4-(aminomethyl)benzoyl)cyclopenta[d][1,2]...) Show SMILES NCc1ccc(cc1)C(=O)c1ccc2c(nocc12)-c1ccc(OCC(O)=O)cc1 Show InChI InChI=1S/C23H18N2O5/c24-11-14-1-3-16(4-2-14)23(28)19-10-9-18-20(19)12-30-25-22(18)15-5-7-17(8-6-15)29-13-21(26)27/h1-10,12H,11,13,24H2,(H,26,27)	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	2.16E+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 recombinant human PTP1B				Bioorg Med Chem Lett 16: 499-502 (2005) Article DOI: 10.1016/j.bmcl.2005.10.062 BindingDB Entry DOI: 10.7270/Q2319VFG
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50115757 ((7,8-Dioxo-5-phenyl-7,8-dihydro-naphthalen-2-yl)-c...) Show SMILES O=C(Nc1ccc2C(=CC(=O)C(=O)c2c1)c1ccccc1)OCc1ccccc1 |c:7| Show InChI InChI=1S/C24H17NO4/c26-22-14-20(17-9-5-2-6-10-17)19-12-11-18(13-21(19)23(22)27)25-24(28)29-15-16-7-3-1-4-8-16/h1-14H,15H2,(H,25,28)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.25E+3	n/a	n/a	n/a	n/a	n/a	n/a
Korea Research Institute of Chemical Technology Curated by ChEMBL					Assay Description In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP) as a substrate				Bioorg Med Chem Lett 12: 1941-6 (2002) BindingDB Entry DOI: 10.7270/Q2QZ2999
					More data for this Ligand-Target Pair

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