Compile Data Set for Download or QSAR

Found 70 hits with Last Name = 'sznaidman' and Initial = 'ml'   

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
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50033666 (2-[(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methox...) Show SMILES Nc1nc2n(COCCOP(O)(=O)OP(O)(O)=O)cnc2c(=O)[nH]1 Show InChI InChI=1S/C8H13N5O9P2/c9-8-11-6-5(7(14)12-8)10-3-13(6)4-20-1-2-21-24(18,19)22-23(15,16)17/h3H,1-2,4H2,(H,18,19)(H2,15,16,17)(H3,9,11,12,14)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049967 (CHEMBL174603 | [4-(5-Amino-7-oxo-6,7-dihydro-[1,2,...) Show SMILES Nc1nc2n(COCCCCP(O)(O)=O)nnc2c(=O)[nH]1 Show InChI InChI=1S/C9H15N6O5P/c10-9-11-7-6(8(16)12-9)13-14-15(7)5-20-3-1-2-4-21(17,18)19/h1-5H2,(H2,17,18,19)(H3,10,11,12,16)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	48	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049963 (CHEMBL368924 | [7-(6-Amino-4-oxo-4,5-dihydro-pyraz...) Show SMILES Nc1nc2n(CCCCCCC(F)(F)P(O)(O)=O)ncc2c(=O)[nH]1 Show InChI InChI=1S/C12H18F2N5O4P/c13-12(14,24(21,22)23)5-3-1-2-4-6-19-9-8(7-16-19)10(20)18-11(15)17-9/h7H,1-6H2,(H2,21,22,23)(H3,15,17,18,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	49	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049969 (CHEMBL172316 | Phosphoric acid mono-[4-(2-amino-6-...) Show SMILES Nc1nc2n(COCCCCOP(O)(O)=O)cnc2c(=O)[nH]1 Show InChI InChI=1S/C10H16N5O6P/c11-10-13-8-7(9(16)14-10)12-5-15(8)6-20-3-1-2-4-21-22(17,18)19/h5H,1-4,6H2,(H2,17,18,19)(H3,11,13,14,16)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	51	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049966 (CHEMBL177948 | [4-(2-Amino-6-oxo-1,6-dihydro-purin...) Show SMILES Nc1nc2n(COCCCCP(O)(O)=O)cnc2c(=O)[nH]1 Show InChI InChI=1S/C10H16N5O5P/c11-10-13-8-7(9(16)14-10)12-5-15(8)6-20-3-1-2-4-21(17,18)19/h5H,1-4,6H2,(H2,17,18,19)(H3,11,13,14,16)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	56	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049971 (CHEMBL177190 | [7-(2-Amino-6-oxo-1,6-dihydro-purin...) Show SMILES Nc1nc2n(CCCCCCC(F)(F)P(O)(O)=O)cnc2c(=O)[nH]1 Show InChI InChI=1S/C12H18F2N5O4P/c13-12(14,24(21,22)23)5-3-1-2-4-6-19-7-16-8-9(19)17-11(15)18-10(8)20/h7H,1-6H2,(H2,21,22,23)(H3,15,17,18,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	57	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049954 (CHEMBL369052 | [5-(5-Amino-7-oxo-6,7-dihydro-[1,2,...) Show SMILES Nc1nc2n(CCCCCP(O)(O)=O)nnc2c(=O)[nH]1 Show InChI InChI=1S/C9H15N6O4P/c10-9-11-7-6(8(16)12-9)13-14-15(7)4-2-1-3-5-20(17,18)19/h1-5H2,(H2,17,18,19)(H3,10,11,12,16)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049959 (CHEMBL173142 | [5-(5-Amino-7-oxo-6,7-dihydro-[1,2,...) Show SMILES Nc1nc2n(COCCCCCP(O)(O)=O)nnc2c(=O)[nH]1 Show InChI InChI=1S/C10H17N6O5P/c11-10-12-8-7(9(17)13-10)14-15-16(8)6-21-4-2-1-3-5-22(18,19)20/h1-6H2,(H2,18,19,20)(H3,11,12,13,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	96	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049972 (CHEMBL176448 | [5-(2-Amino-6-oxo-1,6-dihydro-purin...) Show SMILES Nc1nc2n(COCCCCCP(O)(O)=O)cnc2c(=O)[nH]1 Show InChI InChI=1S/C11H18N5O5P/c12-11-14-9-8(10(17)15-11)13-6-16(9)7-21-4-2-1-3-5-22(18,19)20/h6H,1-5,7H2,(H2,18,19,20)(H3,12,14,15,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	160	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049957 (CHEMBL366963 | [6-(5-Amino-7-oxo-6,7-dihydro-[1,2,...) Show SMILES Nc1nc2n(COCCCCCCP(O)(O)=O)nnc2c(=O)[nH]1 Show InChI InChI=1S/C11H19N6O5P/c12-11-13-9-8(10(18)14-11)15-16-17(9)7-22-5-3-1-2-4-6-23(19,20)21/h1-7H2,(H2,19,20,21)(H3,12,13,14,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	190	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049968 (CHEMBL177945 | [6-(2-Amino-6-oxo-1,6-dihydro-purin...) Show SMILES Nc1nc2n(COCCCCCCP(O)(O)=O)cnc2c(=O)[nH]1 Show InChI InChI=1S/C12H20N5O5P/c13-12-15-10-9(11(18)16-12)14-7-17(10)8-22-5-3-1-2-4-6-23(19,20)21/h7H,1-6,8H2,(H2,19,20,21)(H3,13,15,16,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	220	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049955 (CHEMBL175362 | [5-(6-Amino-4-oxo-4,5-dihydro-pyraz...) Show SMILES Nc1nc2n(COCCCCCP(O)(O)=O)ncc2c(=O)[nH]1 Show InChI InChI=1S/C11H18N5O5P/c12-11-14-9-8(10(17)15-11)6-13-16(9)7-21-4-2-1-3-5-22(18,19)20/h6H,1-5,7H2,(H2,18,19,20)(H3,12,14,15,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	230	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049960 (CHEMBL368064 | [6-(5-Amino-7-oxo-6,7-dihydro-[1,2,...) Show SMILES Nc1nc2n(CCCCCCP(O)(O)=O)nnc2c(=O)[nH]1 Show InChI InChI=1S/C10H17N6O4P/c11-10-12-8-7(9(17)13-10)14-15-16(8)5-3-1-2-4-6-21(18,19)20/h1-6H2,(H2,18,19,20)(H3,11,12,13,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	360	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049961 (CHEMBL354409 | [8-(2-Amino-6-oxo-1,6-dihydro-purin...) Show SMILES Nc1nc2n(CCCCCCCCP(O)(O)=O)cnc2c(=O)[nH]1 Show InChI InChI=1S/C13H22N5O4P/c14-13-16-11-10(12(19)17-13)15-9-18(11)7-5-3-1-2-4-6-8-23(20,21)22/h9H,1-8H2,(H2,20,21,22)(H3,14,16,17,19)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	390	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049962 (CHEMBL172844 | [7-(2-Amino-6-oxo-1,6-dihydro-purin...) Show SMILES Nc1nc2n(CCCCCCCP(O)(O)=O)cnc2c(=O)[nH]1 Show InChI InChI=1S/C12H20N5O4P/c13-12-15-10-9(11(18)16-12)14-8-17(10)6-4-2-1-3-5-7-22(19,20)21/h8H,1-7H2,(H2,19,20,21)(H3,13,15,16,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	530	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049958 (CHEMBL172306 | [5-(5-Amino-7-oxo-6,7-dihydro-[1,2,...) Show SMILES Nc1nc2nn(COCCCCCP(O)(O)=O)nc2c(=O)[nH]1 Show InChI InChI=1S/C10H17N6O5P/c11-10-12-8-7(9(17)13-10)14-16(15-8)6-21-4-2-1-3-5-22(18,19)20/h1-6H2,(H2,18,19,20)(H3,11,12,13,15,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	550	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049970 (CHEMBL176480 | TCMDC-137339 | [7-(6-Amino-4-oxo-4,...) Show SMILES Nc1nc2n(CCCCCCCP(O)(O)=O)ncc2c(=O)[nH]1 Show InChI InChI=1S/C12H20N5O4P/c13-12-15-10-9(11(18)16-12)8-14-17(10)6-4-2-1-3-5-7-22(19,20)21/h8H,1-7H2,(H2,19,20,21)(H3,13,15,16,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	580	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049964 (CHEMBL173083 | [6-(6-Amino-4-oxo-4,5-dihydro-pyraz...) Show SMILES Nc1nc2n(COCCCCCCP(O)(O)=O)ncc2c(=O)[nH]1 Show InChI InChI=1S/C12H20N5O5P/c13-12-15-10-9(11(18)16-12)7-14-17(10)8-22-5-3-1-2-4-6-23(19,20)21/h7H,1-6,8H2,(H2,19,20,21)(H3,13,15,16,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	630	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049956 (CHEMBL176649 | [8-(6-Amino-4-oxo-4,5-dihydro-pyraz...) Show SMILES Nc1nc2n(CCCCCCCCP(O)(O)=O)ncc2c(=O)[nH]1 Show InChI InChI=1S/C13H22N5O4P/c14-13-16-11-10(12(19)17-13)9-15-18(11)7-5-3-1-2-4-6-8-23(20,21)22/h9H,1-8H2,(H2,20,21,22)(H3,14,16,17,19)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049965 (CHEMBL176447 | [10-(2-Amino-6-oxo-1,6-dihydro-puri...) Show SMILES Nc1nc2n(CCCCCCCCCCP(O)(O)=O)cnc2c(=O)[nH]1 Show InChI InChI=1S/C15H26N5O4P/c16-15-18-13-12(14(21)19-15)17-11-20(13)9-7-5-3-1-2-4-6-8-10-25(22,23)24/h11H,1-10H2,(H2,22,23,24)(H3,16,18,19,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Purine nucleoside phosphorylase (Homo sapiens (Human))	BDBM50049973 (CHEMBL175305 | [4-(5-Amino-7-oxo-6,7-dihydro-[1,2,...) Show SMILES Nc1nc2n(CCCCP(O)(O)=O)nnc2c(=O)[nH]1 Show InChI InChI=1S/C8H13N6O4P/c9-8-10-6-5(7(15)11-8)12-13-14(6)3-1-2-4-19(16,17)18/h1-4H2,(H2,16,17,18)(H3,9,10,11,15)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	7.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Co. Curated by ChEMBL					Assay Description In vitro inhibition of purine nucleoside phosphorylase isolated from human erythrocytes.				J Med Chem 39: 949-56 (1996) Article DOI: 10.1021/jm950736k BindingDB Entry DOI: 10.7270/Q2SN082H
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM28661 (2-{2-methyl-4-[({4-methyl-2-[4-(trifluoromethyl)ph...) Show SMILES Cc1nc(sc1CSc1ccc(OCC(O)=O)c(C)c1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C21H18F3NO3S2/c1-12-9-16(7-8-17(12)28-10-19(26)27)29-11-18-13(2)25-20(30-18)14-3-5-15(6-4-14)21(22,23)24/h3-9H,10-11H2,1-2H3,(H,26,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE PC cid PC sid PDB UniChem Patents Similars	PDB PubMed	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Binding affinity for human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair				3D Structure (crystal)
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127222 (CHEMBL38508 | GW-0742 | {4-[2-(3-Fluoro-4-trifluor...) Show SMILES Cc1nc(sc1CSc1ccc(OCC(O)=O)c(C)c1)-c1ccc(c(F)c1)C(F)(F)F Show InChI InChI=1S/C21H17F4NO3S2/c1-11-7-14(4-6-17(11)29-9-19(27)28)30-10-18-12(2)26-20(31-18)13-3-5-15(16(22)8-13)21(23,24)25/h3-8H,9-10H2,1-2H3,(H,27,28)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PDB PubMed	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Binding affinity for human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair				3D Structure (crystal)
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127221 (CHEMBL289887 | {2-Methyl-4-[4-methyl-2-(4-trifluor...) Show SMILES Cc1nc(oc1CSc1ccc(OCC(O)=O)c(C)c1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C21H18F3NO4S/c1-12-9-16(7-8-17(12)28-10-19(26)27)30-11-18-13(2)25-20(29-18)14-3-5-15(6-4-14)21(22,23)24/h3-9H,10-11H2,1-2H3,(H,26,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Maximum transcriptional activation of human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127223 (CHEMBL37013 | {2-Methyl-4-[4-methyl-2-(4-trifluoro...) Show SMILES Cc1nc(oc1COc1ccc(OCC(O)=O)c(C)c1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C21H18F3NO5/c1-12-9-16(7-8-17(12)29-11-19(26)27)28-10-18-13(2)25-20(30-18)14-3-5-15(6-4-14)21(22,23)24/h3-9H,10-11H2,1-2H3,(H,26,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	30	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Binding affinity for human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127215 (3-{4-[4-Methyl-2-(4-trifluoromethyl-phenyl)-thiazo...) Show SMILES Cc1nc(sc1COc1ccc(CCC(O)=O)cc1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C21H18F3NO3S/c1-13-18(12-28-17-9-2-14(3-10-17)4-11-19(26)27)29-20(25-13)15-5-7-16(8-6-15)21(22,23)24/h2-3,5-10H,4,11-12H2,1H3,(H,26,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	30	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Binding affinity for human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127218 (3-{2-Methyl-4-[4-methyl-2-(4-trifluoromethyl-pheny...) Show SMILES Cc1nc(sc1COc1ccc(CCC(O)=O)c(C)c1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C22H20F3NO3S/c1-13-11-18(9-5-15(13)6-10-20(27)28)29-12-19-14(2)26-21(30-19)16-3-7-17(8-4-16)22(23,24)25/h3-5,7-9,11H,6,10,12H2,1-2H3,(H,27,28)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Binding affinity for human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127220 (CHEMBL37495 | {4-[4-Methyl-2-(4-trifluoromethyl-ph...) Show SMILES Cc1nc(oc1CSc1ccc(OCC(O)=O)cc1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C20H16F3NO4S/c1-12-17(11-29-16-8-6-15(7-9-16)27-10-18(25)26)28-19(24-12)13-2-4-14(5-3-13)20(21,22)23/h2-9H,10-11H2,1H3,(H,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	90	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Binding affinity for human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127224 (3-{4-[4-Methyl-2-(4-trifluoromethyl-phenyl)-oxazol...) Show SMILES Cc1nc(oc1COc1ccc(CCC(O)=O)cc1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C21H18F3NO4/c1-13-18(12-28-17-9-2-14(3-10-17)4-11-19(26)27)29-20(25-13)15-5-7-16(8-6-15)21(22,23)24/h2-3,5-10H,4,11-12H2,1H3,(H,26,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	90	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Binding affinity for human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127216 (CHEMBL416794 | {4-[4-Methyl-2-(4-trifluoromethyl-p...) Show SMILES Cc1nc(oc1COc1ccc(OCC(O)=O)cc1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C20H16F3NO5/c1-12-17(10-27-15-6-8-16(9-7-15)28-11-18(25)26)29-19(24-12)13-2-4-14(5-3-13)20(21,22)23/h2-9H,10-11H2,1H3,(H,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	340	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Binding affinity for human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127217 ((E)-3-{2-Methyl-4-[4-methyl-2-(4-trifluoromethyl-p...) Show SMILES Cc1nc(sc1COc1ccc(\C=C\C(O)=O)c(C)c1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C22H18F3NO3S/c1-13-11-18(9-5-15(13)6-10-20(27)28)29-12-19-14(2)26-21(30-19)16-3-7-17(8-4-16)22(23,24)25/h3-11H,12H2,1-2H3,(H,27,28)/b10-6+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Binding affinity for human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127219 (CHEMBL39129 | {4-[4-Methyl-2-(4-trifluoromethyl-ph...) Show SMILES Cc1nc(sc1COc1ccc(CC(O)=O)cc1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C20H16F3NO3S/c1-12-17(11-27-16-8-2-13(3-9-16)10-18(25)26)28-19(24-12)14-4-6-15(7-5-14)20(21,22)23/h2-9H,10-11H2,1H3,(H,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Binding affinity for human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127225 (4-[4-Methyl-2-(4-trifluoromethyl-phenyl)-oxazol-5-...) Show SMILES Cc1nc(oc1COc1ccc(cc1)C(O)=O)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C19H14F3NO4/c1-11-16(10-26-15-8-4-13(5-9-15)18(24)25)27-17(23-11)12-2-6-14(7-3-12)19(20,21)22/h2-9H,10H2,1H3,(H,24,25)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Binding affinity for human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127223 (CHEMBL37013 | {2-Methyl-4-[4-methyl-2-(4-trifluoro...) Show SMILES Cc1nc(oc1COc1ccc(OCC(O)=O)c(C)c1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C21H18F3NO5/c1-12-9-16(7-8-17(12)29-11-19(26)27)28-10-18-13(2)25-20(30-18)14-3-5-15(6-4-14)21(22,23)24/h3-9H,10-11H2,1-2H3,(H,26,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	30	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Binding affinity for human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127225 (4-[4-Methyl-2-(4-trifluoromethyl-phenyl)-oxazol-5-...) Show SMILES Cc1nc(oc1COc1ccc(cc1)C(O)=O)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C19H14F3NO4/c1-11-16(10-26-15-8-4-13(5-9-15)18(24)25)27-17(23-11)12-2-6-14(7-3-12)19(20,21)22/h2-9H,10H2,1H3,(H,24,25)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	5.90E+3	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Maximum transcriptional activation of human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127216 (CHEMBL416794 | {4-[4-Methyl-2-(4-trifluoromethyl-p...) Show SMILES Cc1nc(oc1COc1ccc(OCC(O)=O)cc1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C20H16F3NO5/c1-12-17(10-27-15-6-8-16(9-7-15)28-11-18(25)26)29-19(24-12)13-2-4-14(5-3-13)20(21,22)23/h2-9H,10-11H2,1H3,(H,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	470	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Maximum transcriptional activation of human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127217 ((E)-3-{2-Methyl-4-[4-methyl-2-(4-trifluoromethyl-p...) Show SMILES Cc1nc(sc1COc1ccc(\C=C\C(O)=O)c(C)c1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C22H18F3NO3S/c1-13-11-18(9-5-15(13)6-10-20(27)28)29-12-19-14(2)26-21(30-19)16-3-7-17(8-4-16)22(23,24)25/h3-11H,12H2,1-2H3,(H,27,28)/b10-6+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	n/a	n/a	n/a	n/a	20	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Maximum transcriptional activation of human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127222 (CHEMBL38508 | GW-0742 | {4-[2-(3-Fluoro-4-trifluor...) Show SMILES Cc1nc(sc1CSc1ccc(OCC(O)=O)c(C)c1)-c1ccc(c(F)c1)C(F)(F)F Show InChI InChI=1S/C21H17F4NO3S2/c1-11-7-14(4-6-17(11)29-9-19(27)28)30-10-18-12(2)26-20(31-18)13-3-5-15(16(22)8-13)21(23,24)25/h3-8H,9-10H2,1-2H3,(H,27,28)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PDB PubMed	n/a	n/a	n/a	n/a	1	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Maximum transcriptional activation of human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair				3D Structure (crystal)
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127219 (CHEMBL39129 | {4-[4-Methyl-2-(4-trifluoromethyl-ph...) Show SMILES Cc1nc(sc1COc1ccc(CC(O)=O)cc1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C20H16F3NO3S/c1-12-17(11-27-16-8-2-13(3-9-16)10-18(25)26)28-19(24-12)14-4-6-15(7-5-14)20(21,22)23/h2-9H,10-11H2,1H3,(H,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	1.90E+3	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Maximum transcriptional activation of human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127215 (3-{4-[4-Methyl-2-(4-trifluoromethyl-phenyl)-thiazo...) Show SMILES Cc1nc(sc1COc1ccc(CCC(O)=O)cc1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C21H18F3NO3S/c1-13-18(12-28-17-9-2-14(3-10-17)4-11-19(26)27)29-20(25-13)15-5-7-16(8-6-15)21(22,23)24/h2-3,5-10H,4,11-12H2,1H3,(H,26,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	90	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Maximum transcriptional activation of human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM28661 (2-{2-methyl-4-[({4-methyl-2-[4-(trifluoromethyl)ph...) Show SMILES Cc1nc(sc1CSc1ccc(OCC(O)=O)c(C)c1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C21H18F3NO3S2/c1-12-9-16(7-8-17(12)28-10-19(26)27)29-11-18-13(2)25-20(30-18)14-3-5-15(6-4-14)21(22,23)24/h3-9H,10-11H2,1-2H3,(H,26,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE PC cid PC sid PDB UniChem Patents Similars	PDB PubMed	n/a	n/a	n/a	n/a	1	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Maximum transcriptional activation of human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair				3D Structure (crystal)
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127224 (3-{4-[4-Methyl-2-(4-trifluoromethyl-phenyl)-oxazol...) Show SMILES Cc1nc(oc1COc1ccc(CCC(O)=O)cc1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C21H18F3NO4/c1-13-18(12-28-17-9-2-14(3-10-17)4-11-19(26)27)29-20(25-13)15-5-7-16(8-6-15)21(22,23)24/h2-3,5-10H,4,11-12H2,1H3,(H,26,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	60	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Maximum transcriptional activation of human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127220 (CHEMBL37495 | {4-[4-Methyl-2-(4-trifluoromethyl-ph...) Show SMILES Cc1nc(oc1CSc1ccc(OCC(O)=O)cc1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C20H16F3NO4S/c1-12-17(11-29-16-8-6-15(7-9-16)27-10-18(25)26)28-19(24-12)13-2-4-14(5-3-13)20(21,22)23/h2-9H,10-11H2,1H3,(H,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	420	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Maximum transcriptional activation of human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50127221 (CHEMBL289887 | {2-Methyl-4-[4-methyl-2-(4-trifluor...) Show SMILES Cc1nc(oc1CSc1ccc(OCC(O)=O)c(C)c1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C21H18F3NO4S/c1-12-9-16(7-8-17(12)28-10-19(26)27)30-11-18-13(2)25-20(29-18)14-3-5-15(6-4-14)21(22,23)24/h3-9H,10-11H2,1-2H3,(H,26,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	10	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Maximum transcriptional activation of human PPAR delta receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50127216 (CHEMBL416794 | {4-[4-Methyl-2-(4-trifluoromethyl-p...) Show SMILES Cc1nc(oc1COc1ccc(OCC(O)=O)cc1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C20H16F3NO5/c1-12-17(10-27-15-6-8-16(9-7-15)28-11-18(25)26)29-19(24-12)13-2-4-14(5-3-13)20(21,22)23/h2-9H,10-11H2,1H3,(H,25,26)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	9.80E+3	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Maximum transcriptional activation of human PPAR gamma receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Mus musculus)	BDBM28661 (2-{2-methyl-4-[({4-methyl-2-[4-(trifluoromethyl)ph...) Show SMILES Cc1nc(sc1CSc1ccc(OCC(O)=O)c(C)c1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C21H18F3NO3S2/c1-12-9-16(7-8-17(12)28-10-19(26)27)29-11-18-13(2)25-20(30-18)14-3-5-15(6-4-14)21(22,23)24/h3-9H,10-11H2,1-2H3,(H,26,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Activity against murine PPAR gamma receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor alpha (Homo sapiens (Human))	BDBM50127218 (3-{2-Methyl-4-[4-methyl-2-(4-trifluoromethyl-pheny...) Show SMILES Cc1nc(sc1COc1ccc(CCC(O)=O)c(C)c1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C22H20F3NO3S/c1-13-11-18(9-5-15(13)6-10-20(27)28)29-12-19-14(2)26-21(30-19)16-3-7-17(8-4-16)22(23,24)25/h3-5,7-9,11H,6,10,12H2,1-2H3,(H,27,28)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	1.70E+3	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Maximum transcriptional activation of human PPAR alpha receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50127218 (3-{2-Methyl-4-[4-methyl-2-(4-trifluoromethyl-pheny...) Show SMILES Cc1nc(sc1COc1ccc(CCC(O)=O)c(C)c1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C22H20F3NO3S/c1-13-11-18(9-5-15(13)6-10-20(27)28)29-12-19-14(2)26-21(30-19)16-3-7-17(8-4-16)22(23,24)25/h3-5,7-9,11H,6,10,12H2,1-2H3,(H,27,28)	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	n/a	n/a	4.20E+3	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Maximum transcriptional activation of human PPAR gamma receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50127219 (CHEMBL39129 | {4-[4-Methyl-2-(4-trifluoromethyl-ph...) Show SMILES Cc1nc(sc1COc1ccc(CC(O)=O)cc1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C20H16F3NO3S/c1-12-17(11-27-16-8-2-13(3-9-16)10-18(25)26)28-19(24-12)14-4-6-15(7-5-14)20(21,22)23/h2-9H,10-11H2,1H3,(H,25,26)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	7.90E+3	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Maximum transcriptional activation of human PPAR gamma receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM28661 (2-{2-methyl-4-[({4-methyl-2-[4-(trifluoromethyl)ph...) Show SMILES Cc1nc(sc1CSc1ccc(OCC(O)=O)c(C)c1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C21H18F3NO3S2/c1-12-9-16(7-8-17(12)28-10-19(26)27)29-11-18-13(2)25-20(30-18)14-3-5-15(6-4-14)21(22,23)24/h3-9H,10-11H2,1-2H3,(H,26,27)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	850	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Maximum transcriptional activation of human PPAR gamma receptor				Bioorg Med Chem Lett 13: 1517-21 (2003) BindingDB Entry DOI: 10.7270/Q2VQ322G
					More data for this Ligand-Target Pair

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