Compile Data Set for Download or QSAR

Found 89 hits with Last Name = 'pelton' and Initial = 'pd'   

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
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306617 ((S)-1-fluoro-3-((S)-3-(3-(1,1,2,2-tetrafluoroethox...) Show SMILES O[C@H](CF)CN1[C@H](COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)C(F)F)c1 |r| Show InChI InChI=1S/C26H21F8NO4/c27-12-17(36)13-35-21-9-3-8-20(15-4-1-7-19(10-15)39-26(32,33)34)23(21)37-14-22(35)16-5-2-6-18(11-16)38-25(30,31)24(28)29/h1-11,17,22,24,36H,12-14H2/t17-,22-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	14	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306605 ((S)-1,1,1-trifluoro-3-((S)-3-(3-(1,1,2,2-tetrafluo...) Show SMILES O[C@@H](CN1[C@H](COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F |r| Show InChI InChI=1S/C26H19F10NO4/c27-23(28)25(32,33)40-16-6-2-5-15(11-16)20-13-39-22-18(14-4-1-7-17(10-14)41-26(34,35)36)8-3-9-19(22)37(20)12-21(38)24(29,30)31/h1-11,20-21,23,38H,12-13H2/t20-,21+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	26	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50276347 ((+/-)-1,1,1-trifluoro-3-(2-(3-(1,1,2,2-tetrafluoro...) Show SMILES OC(CN1C(CCc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F Show InChI InChI=1S/C27H21F10NO3/c28-24(29)26(33,34)40-17-6-2-5-16(13-17)21-11-10-20-19(15-4-1-7-18(12-15)41-27(35,36)37)8-3-9-22(20)38(21)14-23(39)25(30,31)32/h1-9,12-13,21,23-24,39H,10-11,14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	33	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50276347 ((+/-)-1,1,1-trifluoro-3-(2-(3-(1,1,2,2-tetrafluoro...) Show SMILES OC(CN1C(CCc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F Show InChI InChI=1S/C27H21F10NO3/c28-24(29)26(33,34)40-17-6-2-5-16(13-17)21-11-10-20-19(15-4-1-7-18(12-15)41-27(35,36)37)8-3-9-22(20)38(21)14-23(39)25(30,31)32/h1-9,12-13,21,23-24,39H,10-11,14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	33	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50277885 (CHEMBL490868 | Tetrahydroquinline A) Show SMILES O[C@@H](CN1[C@H](CCc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)F)c1)C(F)(F)F |r| Show InChI InChI=1S/C26H20F9NO3/c27-24(28,29)23(37)14-36-21(16-5-2-7-18(13-16)39-26(33,34)35)11-10-20-19(8-3-9-22(20)36)15-4-1-6-17(12-15)38-25(30,31)32/h1-9,12-13,21,23,37H,10-11,14H2/t21-,23+/m1/s1	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	39	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306608 ((S)-1,1,1-trifluoro-3-((S)-3-(3-(1,1,2,2-tetrafluo...) Show SMILES O[C@@H](CN1[C@H](COc2c1cccc2-c1cc(F)c(F)c(F)c1)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F |r| Show InChI InChI=1S/C25H17F10NO3/c26-16-8-13(9-17(27)21(16)28)15-5-2-6-18-22(15)38-11-19(36(18)10-20(37)24(31,32)33)12-3-1-4-14(7-12)39-25(34,35)23(29)30/h1-9,19-20,23,37H,10-11H2/t19-,20+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	41	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306605 ((S)-1,1,1-trifluoro-3-((S)-3-(3-(1,1,2,2-tetrafluo...) Show SMILES O[C@@H](CN1[C@H](COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F |r| Show InChI InChI=1S/C26H19F10NO4/c27-23(28)25(32,33)40-16-6-2-5-15(11-16)20-13-39-22-18(14-4-1-7-17(10-14)41-26(34,35)36)8-3-9-19(22)37(20)12-21(38)24(29,30)31/h1-11,20-21,23,38H,12-13H2/t20-,21+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	45	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306607 ((S)-3-((S)-8-(3,5-difluorophenyl)-3-(3-(1,1,2,2-te...) Show SMILES O[C@@H](CN1[C@H](COc2c1cccc2-c1cc(F)cc(F)c1)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F |r| Show InChI InChI=1S/C25H18F9NO3/c26-15-7-14(8-16(27)10-15)18-5-2-6-19-22(18)37-12-20(35(19)11-21(36)24(30,31)32)13-3-1-4-17(9-13)38-25(33,34)23(28)29/h1-10,20-21,23,36H,11-12H2/t20-,21+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	50	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50277959 (3-(5-(3-chlorophenyl)-2-(3-(1,1,2,2-te trafluoroet...) Show SMILES OC(CN1C(CCc2c1cccc2-c1cccc(Cl)c1)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F Show InChI InChI=1S/C26H21ClF7NO2/c27-17-6-1-4-15(12-17)19-8-3-9-22-20(19)10-11-21(35(22)14-23(36)25(30,31)32)16-5-2-7-18(13-16)37-26(33,34)24(28)29/h1-9,12-13,21,23-24,36H,10-11,14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	64	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306619 ((S)-1-((S)-3-(3-(1,1,2,2-tetrafluoroethoxy)phenyl)...) Show SMILES C[C@H](O)CN1[C@H](COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)C(F)F)c1 |r| Show InChI InChI=1S/C26H22F7NO4/c1-15(35)13-34-21-10-4-9-20(16-5-2-8-19(11-16)38-26(31,32)33)23(21)36-14-22(34)17-6-3-7-18(12-17)37-25(29,30)24(27)28/h2-12,15,22,24,35H,13-14H2,1H3/t15-,22+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	88	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306611 ((S)-1,1,1-trifluoro-3-((S)-3-(3-(trifluoromethoxy)...) Show SMILES O[C@@H](CN1[C@H](COc2c1cccc2-c1cc(F)c(F)c(F)c1)c1cccc(OC(F)(F)F)c1)C(F)(F)F |r| Show InChI InChI=1S/C24H16F9NO3/c25-16-8-13(9-17(26)21(16)27)15-5-2-6-18-22(15)36-11-19(34(18)10-20(35)23(28,29)30)12-3-1-4-14(7-12)37-24(31,32)33/h1-9,19-20,35H,10-11H2/t19-,20+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	94	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50278012 (1,1,1-tri fluoro-3-(2-(3-(1,1,2,2-tetrafluoroethox...) Show SMILES OC(CN1C(CCc2c1cccc2-c1cccc(c1)C(F)(F)F)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F Show InChI InChI=1S/C27H21F10NO2/c28-24(29)27(36,37)40-18-7-2-5-16(13-18)21-11-10-20-19(15-4-1-6-17(12-15)25(30,31)32)8-3-9-22(20)38(21)14-23(39)26(33,34)35/h1-9,12-13,21,23-24,39H,10-11,14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	96	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306612 ((S)-3-((S)-3,8-bis(3-(trifluoromethoxy)phenyl)-2H-...) Show SMILES O[C@@H](CN1[C@H](COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)F)c1)C(F)(F)F |r| Show InChI InChI=1S/C25H18F9NO4/c26-23(27,28)21(36)12-35-19-9-3-8-18(14-4-1-6-16(10-14)38-24(29,30)31)22(19)37-13-20(35)15-5-2-7-17(11-15)39-25(32,33)34/h1-11,20-21,36H,12-13H2/t20-,21+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	107	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50278011 (1,1,1-trifluoro-3-(5-(3-fluorophenyl) -2-(3-(1,1,2...) Show SMILES OC(CN1C(CCc2c1cccc2-c1cccc(F)c1)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F Show InChI InChI=1S/C26H21F8NO2/c27-17-6-1-4-15(12-17)19-8-3-9-22-20(19)10-11-21(35(22)14-23(36)25(30,31)32)16-5-2-7-18(13-16)37-26(33,34)24(28)29/h1-9,12-13,21,23-24,36H,10-11,14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	117	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50277727 (3-(2,5-bis(3-(trifluoromethoxy) phenyl)-3,4-dihydr...) Show SMILES OC(CN1C(CCc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)F)c1)C(F)(F)F Show InChI InChI=1S/C26H20F9NO3/c27-24(28,29)23(37)14-36-21(16-5-2-7-18(13-16)39-26(33,34)35)11-10-20-19(8-3-9-22(20)36)15-4-1-6-17(12-15)38-25(30,31)32/h1-9,12-13,21,23,37H,10-11,14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	125	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50277884 ((R)-1-((R)-2,5-bis(3-(trifluoromethoxy)phenyl)-3,4...) Show SMILES C[C@@H](O)CN1[C@H](CCc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)F)c1 |r| Show InChI InChI=1S/C26H23F6NO3/c1-16(34)15-33-23(18-6-3-8-20(14-18)36-26(30,31)32)12-11-22-21(9-4-10-24(22)33)17-5-2-7-19(13-17)35-25(27,28)29/h2-10,13-14,16,23,34H,11-12,15H2,1H3/t16-,23-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	125	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50278055 (1,1,1-trifluoro -3-(5-(3-methoxyphenyl)-2-(3-(1,1,...) Show SMILES COc1cccc(c1)-c1cccc2N(CC(O)C(F)(F)F)C(CCc12)c1cccc(OC(F)(F)C(F)F)c1 Show InChI InChI=1S/C27H24F7NO3/c1-37-18-7-2-5-16(13-18)20-9-4-10-23-21(20)11-12-22(35(23)15-24(36)26(30,31)32)17-6-3-8-19(14-17)38-27(33,34)25(28)29/h2-10,13-14,22,24-25,36H,11-12,15H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	126	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306602 (3-methyl-1-(3-(3-(1,1,2,2-tetrafluoroethoxy)phenyl...) Show SMILES CC(C)C(O)CN1C(COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)C(F)F)c1 Show InChI InChI=1S/C28H26F7NO4/c1-16(2)24(37)14-36-22-11-5-10-21(17-6-3-9-20(12-17)40-28(33,34)35)25(22)38-15-23(36)18-7-4-8-19(13-18)39-27(31,32)26(29)30/h3-13,16,23-24,26,37H,14-15H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	129	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306612 ((S)-3-((S)-3,8-bis(3-(trifluoromethoxy)phenyl)-2H-...) Show SMILES O[C@@H](CN1[C@H](COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)F)c1)C(F)(F)F |r| Show InChI InChI=1S/C25H18F9NO4/c26-23(27,28)21(36)12-35-19-9-3-8-18(14-4-1-6-16(10-14)38-24(29,30)31)22(19)37-13-20(35)15-5-2-7-17(11-15)39-25(32,33)34/h1-11,20-21,36H,12-13H2/t20-,21+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	133	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50277688 (1,1,1-trifluoro-3-(5-(3-(trifluoromethoxy)phenyl)-...) Show SMILES OC(CN1C(CCc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(c1)C(F)(F)F)C(F)(F)F Show InChI InChI=1S/C26H20F9NO2/c27-24(28,29)17-6-1-5-16(12-17)21-11-10-20-19(15-4-2-7-18(13-15)38-26(33,34)35)8-3-9-22(20)36(21)14-23(37)25(30,31)32/h1-9,12-13,21,23,37H,10-11,14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	143	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50277688 (1,1,1-trifluoro-3-(5-(3-(trifluoromethoxy)phenyl)-...) Show SMILES OC(CN1C(CCc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(c1)C(F)(F)F)C(F)(F)F Show InChI InChI=1S/C26H20F9NO2/c27-24(28,29)17-6-1-5-16(12-17)21-11-10-20-19(15-4-2-7-18(13-15)38-26(33,34)35)8-3-9-22(20)36(21)14-23(37)25(30,31)32/h1-9,12-13,21,23,37H,10-11,14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	143	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306618 ((R)-1-fluoro-3-((S)-3-(3-(1,1,2,2-tetrafluoroethox...) Show SMILES O[C@@H](CF)CN1[C@H](COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)C(F)F)c1 |r| Show InChI InChI=1S/C26H21F8NO4/c27-12-17(36)13-35-21-9-3-8-20(15-4-1-7-19(10-15)39-26(32,33)34)23(21)37-14-22(35)16-5-2-6-18(11-16)38-25(30,31)24(28)29/h1-11,17,22,24,36H,12-14H2/t17-,22+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	147	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306604 (4-propyl-3-(3-(1,1,2,2-tetrafluoroethoxy)phenyl)-8...) Show SMILES CCCN1C(COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)C(F)F)c1 Show InChI InChI=1S/C26H22F7NO3/c1-2-12-34-21-11-5-10-20(16-6-3-9-19(13-16)37-26(31,32)33)23(21)35-15-22(34)17-7-4-8-18(14-17)36-25(29,30)24(27)28/h3-11,13-14,22,24H,2,12,15H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	190	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306610 ((S)-3-((S)-8-(3,5-difluorophenyl)-3-(3-(trifluorom...) Show SMILES O[C@@H](CN1[C@H](COc2c1cccc2-c1cc(F)cc(F)c1)c1cccc(OC(F)(F)F)c1)C(F)(F)F |r| Show InChI InChI=1S/C24H17F8NO3/c25-15-7-14(8-16(26)10-15)18-5-2-6-19-22(18)35-12-20(33(19)11-21(34)23(27,28)29)13-3-1-4-17(9-13)36-24(30,31)32/h1-10,20-21,34H,11-12H2/t20-,21+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	193	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306613 (3-(3-(3-chlorophenyl)-8-(3-(trifluoromethoxy)pheny...) Show SMILES OC(CN1C(COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(Cl)c1)C(F)(F)F Show InChI InChI=1S/C24H18ClF6NO3/c25-16-6-1-5-15(10-16)20-13-34-22-18(14-4-2-7-17(11-14)35-24(29,30)31)8-3-9-19(22)32(20)12-21(33)23(26,27)28/h1-11,20-21,33H,12-13H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	214	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50277459 (3-(2-(3-(1,1,2,2-tetrafluoroethoxy)phenyl )-1-(3,3...) Show SMILES OC(CN1C(CCc2c1cccc2-c1cccc(c1)C#N)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F Show InChI InChI=1S/C27H21F7N2O2/c28-25(29)27(33,34)38-19-7-2-6-18(13-19)22-11-10-21-20(17-5-1-4-16(12-17)14-35)8-3-9-23(21)36(22)15-24(37)26(30,31)32/h1-9,12-13,22,24-25,37H,10-11,15H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	235	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306616 (3-(3-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)-8-(3-(...) Show SMILES OC(CN1C(COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1ccc2OC(F)(F)Oc2c1)C(F)(F)F Show InChI InChI=1S/C25H17F8NO5/c26-23(27,28)21(35)11-34-17-6-2-5-16(13-3-1-4-15(9-13)37-24(29,30)31)22(17)36-12-18(34)14-7-8-19-20(10-14)39-25(32,33)38-19/h1-10,18,21,35H,11-12H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	271	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306606 (1,1,1-trifluoro-3-(8-(3-fluorophenyl)-3-(3-(1,1,2,...) Show SMILES OC(CN1C(COc2c1cccc2-c1cccc(F)c1)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F Show InChI InChI=1S/C25H19F8NO3/c26-16-6-1-4-14(10-16)18-8-3-9-19-22(18)36-13-20(34(19)12-21(35)24(29,30)31)15-5-2-7-17(11-15)37-25(32,33)23(27)28/h1-11,20-21,23,35H,12-13H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	322	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50277812 (1-(2,5-bis(3-(trifluoromethoxy) phenyl)-3,4-dihydr...) Show SMILES CC(C)C(O)CN1C(CCc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)F)c1 Show InChI InChI=1S/C28H27F6NO3/c1-17(2)26(36)16-35-24(19-7-4-9-21(15-19)38-28(32,33)34)13-12-23-22(10-5-11-25(23)35)18-6-3-8-20(14-18)37-27(29,30)31/h3-11,14-15,17,24,26,36H,12-13,16H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	326	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50277773 (1-(2,5-bis(3-(trifluoromethoxy)phenyl)-3,4-dihydro...) Show SMILES OC(CF)CN1C(CCc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)F)c1 Show InChI InChI=1S/C26H22F7NO3/c27-14-18(35)15-34-23(17-5-2-7-20(13-17)37-26(31,32)33)11-10-22-21(8-3-9-24(22)34)16-4-1-6-19(12-16)36-25(28,29)30/h1-9,12-13,18,23,35H,10-11,14-15H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	331	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306615 (1,1,1-trifluoro-3-(8-(3-(trifluoromethoxy)phenyl)-...) Show SMILES OC(CN1C(COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(SC(F)(F)F)c1)C(F)(F)F Show InChI InChI=1S/C25H18F9NO3S/c26-23(27,28)21(36)12-35-19-9-3-8-18(14-4-1-6-16(10-14)38-24(29,30)31)22(19)37-13-20(35)15-5-2-7-17(11-15)39-25(32,33)34/h1-11,20-21,36H,12-13H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	360	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50277921 (3-(5-(2,3-dichlorophenyl )-2-(3-(1,1,2,2-tetrafluo...) Show SMILES OC(CN1C(CCc2c1cccc2-c1cccc(Cl)c1Cl)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F Show InChI InChI=1S/C26H20Cl2F7NO2/c27-19-8-2-7-18(23(19)28)16-6-3-9-21-17(16)10-11-20(36(21)13-22(37)25(31,32)33)14-4-1-5-15(12-14)38-26(34,35)24(29)30/h1-9,12,20,22,24,37H,10-11,13H2	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	400	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306614 (3-(3-(3-ethoxyphenyl)-8-(3-(trifluoromethoxy)pheny...) Show SMILES CCOc1cccc(c1)C1COc2c(cccc2-c2cccc(OC(F)(F)F)c2)N1CC(O)C(F)(F)F Show InChI InChI=1S/C26H23F6NO4/c1-2-35-18-8-4-7-17(13-18)22-15-36-24-20(16-6-3-9-19(12-16)37-26(30,31)32)10-5-11-21(24)33(22)14-23(34)25(27,28)29/h3-13,22-23,34H,2,14-15H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	490	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50277460 (1,1,1-trifluoro-3-(2-(3-(1,1,2,2-tetrafluoroethoxy...) Show SMILES OC(CN1C(CCc2c1cccc2-c1ccc(OC(F)(F)F)cc1)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F Show InChI InChI=1S/C27H21F10NO3/c28-24(29)26(33,34)40-18-4-1-3-16(13-18)21-12-11-20-19(15-7-9-17(10-8-15)41-27(35,36)37)5-2-6-22(20)38(21)14-23(39)25(30,31)32/h1-10,13,21,23-24,39H,11-12,14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	500	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306603 (2-methyl-1-(3-(3-(1,1,2,2-tetrafluoroethoxy)phenyl...) Show SMILES CC(C)(O)CN1C(COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)C(F)F)c1 Show InChI InChI=1S/C27H24F7NO4/c1-25(2,36)15-35-21-11-5-10-20(16-6-3-9-19(12-16)39-27(32,33)34)23(21)37-14-22(35)17-7-4-8-18(13-17)38-26(30,31)24(28)29/h3-13,22,24,36H,14-15H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	560	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306609 ((S)-3-((S)-8-(3,5-bis(trifluoromethyl)phenyl)-3-(3...) Show SMILES O[C@@H](CN1[C@H](COc2c1cccc2-c1cc(cc(c1)C(F)(F)F)C(F)(F)F)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F |r| Show InChI InChI=1S/C27H18F13NO3/c28-23(29)27(39,40)44-17-4-1-3-13(9-17)20-12-43-22-18(5-2-6-19(22)41(20)11-21(42)26(36,37)38)14-7-15(24(30,31)32)10-16(8-14)25(33,34)35/h1-10,20-21,23,42H,11-12H2/t20-,21+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	580	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human cholesteryl ester transfer protein by scintillation proximity assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50276280 (3-(5-(4-chloro-3-ethylphenoxy)-2 -(3-(1,1,2,2-tetr...) Show SMILES CCc1cc(Oc2cccc3N(CC(O)C(F)(F)F)C(CCc23)c2cccc(OC(F)(F)C(F)F)c2)ccc1Cl Show InChI InChI=1S/C28H25ClF7NO3/c1-2-16-13-18(9-11-21(16)29)39-24-8-4-7-23-20(24)10-12-22(37(23)15-25(38)27(32,33)34)17-5-3-6-19(14-17)40-28(35,36)26(30)31/h3-9,11,13-14,22,25-26,38H,2,10,12,15H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	600	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50276280 (3-(5-(4-chloro-3-ethylphenoxy)-2 -(3-(1,1,2,2-tetr...) Show SMILES CCc1cc(Oc2cccc3N(CC(O)C(F)(F)F)C(CCc23)c2cccc(OC(F)(F)C(F)F)c2)ccc1Cl Show InChI InChI=1S/C28H25ClF7NO3/c1-2-16-13-18(9-11-21(16)29)39-24-8-4-7-23-20(24)10-12-22(37(23)15-25(38)27(32,33)34)17-5-3-6-19(14-17)40-28(35,36)26(30)31/h3-9,11,13-14,22,25-26,38H,2,10,12,15H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	600	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50277811 (1-(2,5-bis(3-(trifluoromethoxy)phenyl)-3,4-dihydro...) Show SMILES OC(CCl)CN1C(CCc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)F)c1 Show InChI InChI=1S/C26H22ClF6NO3/c27-14-18(35)15-34-23(17-5-2-7-20(13-17)37-26(31,32)33)11-10-22-21(8-3-9-24(22)34)16-4-1-6-19(12-16)36-25(28,29)30/h1-9,12-13,18,23,35H,10-11,14-15H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	744	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50306605 ((S)-1,1,1-trifluoro-3-((S)-3-(3-(1,1,2,2-tetrafluo...) Show SMILES O[C@@H](CN1[C@H](COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F |r| Show InChI InChI=1S/C26H19F10NO4/c27-23(28)25(32,33)40-16-6-2-5-15(11-16)20-13-39-22-18(14-4-1-7-17(10-14)41-26(34,35)36)8-3-9-19(22)37(20)12-21(38)24(29,30)31/h1-11,20-21,23,38H,12-13H2/t20-,21+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of cholesteryl ester transfer protein in human plasma by [3H]CE HDL assay				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50277492 (1,1,1-trifluoro-3-(5-(pyridin-3-yl)-2-(3-(1,1,2,2-...) Show SMILES OC(CN1C(CCc2c1cccc2-c1cccnc1)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F Show InChI InChI=1S/C25H21F7N2O2/c26-23(27)25(31,32)36-17-6-1-4-15(12-17)20-10-9-19-18(16-5-3-11-33-13-16)7-2-8-21(19)34(20)14-22(35)24(28,29)30/h1-8,11-13,20,22-23,35H,9-10,14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50277886 (CHEMBL491072 | Tetrahydroquinoline B) Show SMILES O[C@H](CN1[C@H](CCc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)F)c1)C(F)(F)F |r| Show InChI InChI=1S/C26H20F9NO3/c27-24(28,29)23(37)14-36-21(16-5-2-7-18(13-16)39-26(33,34)35)11-10-20-19(8-3-9-22(20)36)15-4-1-6-17(12-15)38-25(30,31)32/h1-9,12-13,21,23,37H,10-11,14H2/t21-,23-/m1/s1	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	>3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cytochrome P450 2C9 (Homo sapiens (Human))	BDBM50306605 ((S)-1,1,1-trifluoro-3-((S)-3-(3-(1,1,2,2-tetrafluo...) Show SMILES O[C@@H](CN1[C@H](COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F |r| Show InChI InChI=1S/C26H19F10NO4/c27-23(28)25(32,33)40-16-6-2-5-15(11-16)20-13-39-22-18(14-4-1-7-17(10-14)41-26(34,35)36)8-3-9-19(22)37(20)12-21(38)24(29,30)31/h1-11,20-21,23,38H,12-13H2/t20-,21+/m1/s1	PDB MMDB 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	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of CYP2C9 in human liver microsomes				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cytochrome P450 1A2 (Homo sapiens (Human))	BDBM50306605 ((S)-1,1,1-trifluoro-3-((S)-3-(3-(1,1,2,2-tetrafluo...) Show SMILES O[C@@H](CN1[C@H](COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F |r| Show InChI InChI=1S/C26H19F10NO4/c27-23(28)25(32,33)40-16-6-2-5-15(11-16)20-13-39-22-18(14-4-1-7-17(10-14)41-26(34,35)36)8-3-9-19(22)37(20)12-21(38)24(29,30)31/h1-11,20-21,23,38H,12-13H2/t20-,21+/m1/s1	PDB MMDB 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	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of CYP1A2 in human liver microsomes				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50306605 ((S)-1,1,1-trifluoro-3-((S)-3-(3-(1,1,2,2-tetrafluo...) Show SMILES O[C@@H](CN1[C@H](COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F |r| Show InChI InChI=1S/C26H19F10NO4/c27-23(28)25(32,33)40-16-6-2-5-15(11-16)20-13-39-22-18(14-4-1-7-17(10-14)41-26(34,35)36)8-3-9-19(22)37(20)12-21(38)24(29,30)31/h1-11,20-21,23,38H,12-13H2/t20-,21+/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of CYP2D6 in human liver microsomes				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cytochrome P450 2C19 (Homo sapiens (Human))	BDBM50306605 ((S)-1,1,1-trifluoro-3-((S)-3-(3-(1,1,2,2-tetrafluo...) Show SMILES O[C@@H](CN1[C@H](COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F |r| Show InChI InChI=1S/C26H19F10NO4/c27-23(28)25(32,33)40-16-6-2-5-15(11-16)20-13-39-22-18(14-4-1-7-17(10-14)41-26(34,35)36)8-3-9-19(22)37(20)12-21(38)24(29,30)31/h1-11,20-21,23,38H,12-13H2/t20-,21+/m1/s1	PDB MMDB 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	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of CYP2C19 in human liver microsomes				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50306605 ((S)-1,1,1-trifluoro-3-((S)-3-(3-(1,1,2,2-tetrafluo...) Show SMILES O[C@@H](CN1[C@H](COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F |r| Show InChI InChI=1S/C26H19F10NO4/c27-23(28)25(32,33)40-16-6-2-5-15(11-16)20-13-39-22-18(14-4-1-7-17(10-14)41-26(34,35)36)8-3-9-19(22)37(20)12-21(38)24(29,30)31/h1-11,20-21,23,38H,12-13H2/t20-,21+/m1/s1	PDB MMDB 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	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of CYP3A4 tissue isoform in human liver microsomes				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50306605 ((S)-1,1,1-trifluoro-3-((S)-3-(3-(1,1,2,2-tetrafluo...) Show SMILES O[C@@H](CN1[C@H](COc2c1cccc2-c1cccc(OC(F)(F)F)c1)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F |r| Show InChI InChI=1S/C26H19F10NO4/c27-23(28)25(32,33)40-16-6-2-5-15(11-16)20-13-39-22-18(14-4-1-7-17(10-14)41-26(34,35)36)8-3-9-19(22)37(20)12-21(38)24(29,30)31/h1-11,20-21,23,38H,12-13H2/t20-,21+/m1/s1	PDB MMDB 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	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of CYP3A4 muscle isoform in human liver microsomes				Bioorg Med Chem Lett 20: 1432-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.096 BindingDB Entry DOI: 10.7270/Q2WW7HRC
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50277557 (1,1,1-trifluoro-3-(5-(3-isopropylphenyl)-2-(3-(1,1...) Show SMILES CC(C)c1cccc(c1)-c1cccc2N(CC(O)C(F)(F)F)C(CCc12)c1cccc(OC(F)(F)C(F)F)c1 Show InChI InChI=1S/C29H28F7NO2/c1-17(2)18-6-3-7-19(14-18)22-10-5-11-25-23(22)12-13-24(37(25)16-26(38)28(32,33)34)20-8-4-9-21(15-20)39-29(35,36)27(30)31/h3-11,14-15,17,24,26-27,38H,12-13,16H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.77E+5	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair
Cholesteryl ester transfer protein (Homo sapiens (Human))	BDBM50277556 (1,1,1-trifluoro-3-(2-(3-(1,1,2,2-tetrafluoroethoxy...) Show SMILES OC(CN1C(CCc2c1cccc2-c1cccs1)c1cccc(OC(F)(F)C(F)F)c1)C(F)(F)F Show InChI InChI=1S/C24H20F7NO2S/c25-22(26)24(30,31)34-15-5-1-4-14(12-15)18-10-9-16-17(20-8-3-11-35-20)6-2-7-19(16)32(18)13-21(33)23(27,28)29/h1-8,11-12,18,21-22,33H,9-10,13H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.17E+5	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research & Development Curated by ChEMBL					Assay Description Inhibition of human plasma derived CETP				Bioorg Med Chem Lett 19: 2456-60 (2009) Article DOI: 10.1016/j.bmcl.2009.03.051 BindingDB Entry DOI: 10.7270/Q2W37W6T
					More data for this Ligand-Target Pair

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