Compile Data Set for Download or QSAR

Found 88 hits Enz. Inhib. hit(s) with all data for entry = 50018475   

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
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196149 (4-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]be...) Show SMILES O=C(N1CCOCC1)c1ccccc1NS(=O)(=O)c1cccc2nsnc12 Show InChI InChI=1S/C17H16N4O4S2/c22-17(21-8-10-25-11-9-21)12-4-1-2-5-13(12)20-27(23,24)15-7-3-6-14-16(15)19-26-18-14/h1-7,20H,8-11H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196150 (4-[4-fluoro-2-[(5-quinoxalinylsulfonyl)amino]benzo...) Show SMILES Fc1ccc(C(=O)N2CCOCC2)c(NS(=O)(=O)c2cccc3nccnc23)c1 Show InChI InChI=1S/C19H17FN4O4S/c20-13-4-5-14(19(25)24-8-10-28-11-9-24)16(12-13)23-29(26,27)17-3-1-2-15-18(17)22-7-6-21-15/h1-7,12,23H,8-11H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196151 ((3S,5S)-4-[4-chloro-2-[(5-quinoxalinylsulfonyl)ami...) Show SMILES C[C@H]1COC[C@H](C)N1C(=O)c1ccc(Cl)cc1NS(=O)(=O)c1cccc2nccnc12 Show InChI InChI=1S/C21H21ClN4O4S/c1-13-11-30-12-14(2)26(13)21(27)16-7-6-15(22)10-18(16)25-31(28,29)19-5-3-4-17-20(19)24-9-8-23-17/h3-10,13-14,25H,11-12H2,1-2H3/t13-,14-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196152 (1-[4-chloro-2-[(quinolin-8-ylsulfonyl)amino]-benzo...) Show SMILES Clc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3cccnc23)c1 Show InChI InChI=1S/C21H20ClN3O3S/c22-16-9-10-17(21(26)25-12-2-1-3-13-25)18(14-16)24-29(27,28)19-8-4-6-15-7-5-11-23-20(15)19/h4-11,14,24H,1-3,12-13H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (Homo sapiens (Human))	BDBM50196155 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES OC(=O)[C@@H]1CCCN1C(=O)c1ccc(Cl)cc1NS(=O)(=O)c1cccc2nsnc12 Show InChI InChI=1S/C18H15ClN4O5S2/c19-10-6-7-11(17(24)23-8-2-4-14(23)18(25)26)13(9-10)22-30(27,28)15-5-1-3-12-16(15)21-29-20-12/h1,3,5-7,9,14,22H,2,4,8H2,(H,25,26)/t14-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK2R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196154 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES O=C(N1CCCCC1)c1ccc(cc1NS(=O)(=O)c1cccc2nsnc12)-c1ccccc1 Show InChI InChI=1S/C24H22N4O3S2/c29-24(28-14-5-2-6-15-28)19-13-12-18(17-8-3-1-4-9-17)16-21(19)27-33(30,31)22-11-7-10-20-23(22)26-32-25-20/h1,3-4,7-13,16,27H,2,5-6,14-15H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (Homo sapiens (Human))	BDBM50196153 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES Clc1ccc(C(=O)N2CCC(CC2)N2CCCCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C23H26ClN5O3S2/c24-16-7-8-18(23(30)29-13-9-17(10-14-29)28-11-2-1-3-12-28)20(15-16)27-34(31,32)21-6-4-5-19-22(21)26-33-25-19/h4-8,15,17,27H,1-3,9-14H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK2R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (Homo sapiens (Human))	BDBM50185262 ((+/-)-2-(2-(1H-indole-2-carboxamido)benzamido)-3-p...) Show SMILES OC(=O)C(Cc1ccccc1)NC(=O)c1ccccc1NC(=O)c1cc2ccccc2[nH]1 Show InChI InChI=1S/C25H21N3O4/c29-23(28-22(25(31)32)14-16-8-2-1-3-9-16)18-11-5-7-13-20(18)27-24(30)21-15-17-10-4-6-12-19(17)26-21/h1-13,15,22,26H,14H2,(H,27,30)(H,28,29)(H,31,32)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK2R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196156 (4-[4-chloro-2-[(5-quinoxalinylsulfonyl)amino]benzo...) Show SMILES Clc1ccc(C(=O)N2CCOCC2)c(NS(=O)(=O)c2cccc3nccnc23)c1 Show InChI InChI=1S/C19H17ClN4O4S/c20-13-4-5-14(19(25)24-8-10-28-11-9-24)16(12-13)23-29(26,27)17-3-1-2-15-18(17)22-7-6-21-15/h1-7,12,23H,8-11H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196157 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES Clc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C18H17ClN4O3S2/c19-12-7-8-13(18(24)23-9-2-1-3-10-23)15(11-12)22-28(25,26)16-6-4-5-14-17(16)21-27-20-14/h4-8,11,22H,1-3,9-10H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196159 (4-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES Brc1ccc(C(=O)N2CCOCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C17H15BrN4O4S2/c18-11-4-5-12(17(23)22-6-8-26-9-7-22)14(10-11)21-28(24,25)15-3-1-2-13-16(15)20-27-19-13/h1-5,10,21H,6-9H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196158 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES CC1CC(C)CN(C1)C(=O)c1ccc(Cl)cc1NS(=O)(=O)c1cccc2nsnc12 Show InChI InChI=1S/C20H21ClN4O3S2/c1-12-8-13(2)11-25(10-12)20(26)15-7-6-14(21)9-17(15)24-30(27,28)18-5-3-4-16-19(18)23-29-22-16/h3-7,9,12-13,24H,8,10-11H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (Homo sapiens (Human))	BDBM50196160 (1-[4-bromo-2-[(isoquinolin-5-ylsulfonyl)amino]-ben...) Show SMILES Brc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3cnccc23)c1 Show InChI InChI=1S/C21H20BrN3O3S/c22-16-7-8-18(21(26)25-11-2-1-3-12-25)19(13-16)24-29(27,28)20-6-4-5-15-14-23-10-9-17(15)20/h4-10,13-14,24H,1-3,11-12H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK2R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196161 (1-[4-acetylamino-2-[(2,1,3-benzothiadiazol-4-ylsul...) Show SMILES CC(=O)Nc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C20H21N5O4S2/c1-13(26)21-14-8-9-15(20(27)25-10-3-2-4-11-25)17(12-14)24-31(28,29)18-7-5-6-16-19(18)23-30-22-16/h5-9,12,24H,2-4,10-11H2,1H3,(H,21,26)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196162 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES CC1CCCCN1C(=O)c1ccc(Cl)cc1NS(=O)(=O)c1cccc2nsnc12 Show InChI InChI=1S/C19H19ClN4O3S2/c1-12-5-2-3-10-24(12)19(25)14-9-8-13(20)11-16(14)23-29(26,27)17-7-4-6-15-18(17)22-28-21-15/h4,6-9,11-12,23H,2-3,5,10H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196163 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES Ic1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C18H17IN4O3S2/c19-12-7-8-13(18(24)23-9-2-1-3-10-23)15(11-12)22-28(25,26)16-6-4-5-14-17(16)21-27-20-14/h4-8,11,22H,1-3,9-10H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196160 (1-[4-bromo-2-[(isoquinolin-5-ylsulfonyl)amino]-ben...) Show SMILES Brc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3cnccc23)c1 Show InChI InChI=1S/C21H20BrN3O3S/c22-16-7-8-18(21(26)25-11-2-1-3-12-25)19(13-16)24-29(27,28)20-6-4-5-15-14-23-10-9-17(15)20/h4-10,13-14,24H,1-3,11-12H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196155 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES OC(=O)[C@@H]1CCCN1C(=O)c1ccc(Cl)cc1NS(=O)(=O)c1cccc2nsnc12 Show InChI InChI=1S/C18H15ClN4O5S2/c19-10-6-7-11(17(24)23-8-2-4-14(23)18(25)26)13(9-10)22-30(27,28)15-5-1-3-12-16(15)21-29-20-12/h1,3,5-7,9,14,22H,2,4,8H2,(H,25,26)/t14-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (Homo sapiens (Human))	BDBM50196164 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-3...) Show SMILES Clc1cccc(C(=O)N2CCCCC2)c1NS(=O)(=O)c1cccc2nsnc12 Show InChI InChI=1S/C18H17ClN4O3S2/c19-13-7-4-6-12(18(24)23-10-2-1-3-11-23)16(13)22-28(25,26)15-9-5-8-14-17(15)21-27-20-14/h4-9,22H,1-3,10-11H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK2R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (Homo sapiens (Human))	BDBM50196166 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-3...) Show SMILES Cc1cccc(C(=O)N2CCCCC2)c1NS(=O)(=O)c1cccc2nsnc12 Show InChI InChI=1S/C19H20N4O3S2/c1-13-7-5-8-14(19(24)23-11-3-2-4-12-23)17(13)22-28(25,26)16-10-6-9-15-18(16)21-27-20-15/h5-10,22H,2-4,11-12H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK2R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196165 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES CC(C)c1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C21H24N4O3S2/c1-14(2)15-9-10-16(21(26)25-11-4-3-5-12-25)18(13-15)24-30(27,28)19-8-6-7-17-20(19)23-29-22-17/h6-10,13-14,24H,3-5,11-12H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (Homo sapiens (Human))	BDBM50196173 ((S)-1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amin...) Show SMILES Clc1ccc(C(=O)N2CCC[C@H]2CN2CCCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C22H24ClN5O3S2/c23-15-8-9-17(22(29)28-12-4-5-16(28)14-27-10-1-2-11-27)19(13-15)26-33(30,31)20-7-3-6-18-21(20)25-32-24-18/h3,6-9,13,16,26H,1-2,4-5,10-12,14H2/t16-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK2R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196167 (2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4-ch...) Show SMILES CN(Cc1ccccc1)C(=O)c1ccc(Cl)cc1NS(=O)(=O)c1cccc2nsnc12 Show InChI InChI=1S/C21H17ClN4O3S2/c1-26(13-14-6-3-2-4-7-14)21(27)16-11-10-15(22)12-18(16)25-31(28,29)19-9-5-8-17-20(19)24-30-23-17/h2-12,25H,13H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196168 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES Clc1ccc(C(=O)N2CCc3ccccc3C2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C22H17ClN4O3S2/c23-16-8-9-17(22(28)27-11-10-14-4-1-2-5-15(14)13-27)19(12-16)26-32(29,30)20-7-3-6-18-21(20)25-31-24-18/h1-9,12,26H,10-11,13H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196174 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES FC(F)(F)c1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C19H17F3N4O3S2/c20-19(21,22)12-7-8-13(18(27)26-9-2-1-3-10-26)15(11-12)25-31(28,29)16-6-4-5-14-17(16)24-30-23-14/h4-8,11,25H,1-3,9-10H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196172 (1-[4-bromo-2-[[naphthalen-1-ylsulfonyl]amino]benzo...) Show SMILES Brc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3ccccc23)c1 Show InChI InChI=1S/C22H21BrN2O3S/c23-17-11-12-19(22(26)25-13-4-1-5-14-25)20(15-17)24-29(27,28)21-10-6-8-16-7-2-3-9-18(16)21/h2-3,6-12,15,24H,1,4-5,13-14H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196169 (1-[4-amino-2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)...) Show SMILES Nc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C18H19N5O3S2/c19-12-7-8-13(18(24)23-9-2-1-3-10-23)15(11-12)22-28(25,26)16-6-4-5-14-17(16)21-27-20-14/h4-8,11,22H,1-3,9-10,19H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196170 ((S)-4-[4-chloro-2-[(5-quinoxalinylsulfonyl)amino]b...) Show SMILES C[C@H]1COCCN1C(=O)c1ccc(Cl)cc1NS(=O)(=O)c1cccc2nccnc12 Show InChI InChI=1S/C20H19ClN4O4S/c1-13-12-29-10-9-25(13)20(26)15-6-5-14(21)11-17(15)24-30(27,28)18-4-2-3-16-19(18)23-8-7-22-16/h2-8,11,13,24H,9-10,12H2,1H3/t13-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196171 (1-[2-[(2,1,3-benzooxadiazol-4-ylsulfonyl)amino]-4-...) Show SMILES Clc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3nonc23)c1 Show InChI InChI=1S/C18H17ClN4O4S/c19-12-7-8-13(18(24)23-9-2-1-3-10-23)15(11-12)22-28(25,26)16-6-4-5-14-17(16)21-27-20-14/h4-8,11,22H,1-3,9-10H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196176 (3-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES Clc1ccc(C(=O)N2CCSC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C16H13ClN4O3S3/c17-10-4-5-11(16(22)21-6-7-25-9-21)13(8-10)20-27(23,24)14-3-1-2-12-15(14)19-26-18-12/h1-5,8,20H,6-7,9H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196175 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES SCc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C19H20N4O3S3/c24-19(23-9-2-1-3-10-23)14-8-7-13(12-27)11-16(14)22-29(25,26)17-6-4-5-15-18(17)21-28-20-15/h4-8,11,22,27H,1-3,9-10,12H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196177 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES COc1cc(NS(=O)(=O)c2cccc3nsnc23)c(cc1OC)C(=O)N1CCCCC1 Show InChI InChI=1S/C20H22N4O5S2/c1-28-16-11-13(20(25)24-9-4-3-5-10-24)15(12-17(16)29-2)23-31(26,27)18-8-6-7-14-19(18)22-30-21-14/h6-8,11-12,23H,3-5,9-10H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196180 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES COc1cc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3nsnc23)cc1Cl Show InChI InChI=1S/C19H19ClN4O4S2/c1-28-16-10-12(19(25)24-8-3-2-4-9-24)15(11-13(16)20)23-30(26,27)17-7-5-6-14-18(17)22-29-21-14/h5-7,10-11,23H,2-4,8-9H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196178 (4-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES Fc1ccc(C(=O)N2CCOCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C17H15FN4O4S2/c18-11-4-5-12(17(23)22-6-8-26-9-7-22)14(10-11)21-28(24,25)15-3-1-2-13-16(15)20-27-19-13/h1-5,10,21H,6-9H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196179 (4-[4-bromo-2-[(5-quinoxalinylsulfonyl)amino]benzoy...) Show SMILES Brc1ccc(C(=O)N2CCOCC2)c(NS(=O)(=O)c2cccc3nccnc23)c1 Show InChI InChI=1S/C19H17BrN4O4S/c20-13-4-5-14(19(25)24-8-10-28-11-9-24)16(12-13)23-29(26,27)17-3-1-2-15-18(17)22-7-6-21-15/h1-7,12,23H,8-11H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196186 (4-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES Clc1ccc(C(=O)N2CCOCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C17H15ClN4O4S2/c18-11-4-5-12(17(23)22-6-8-26-9-7-22)14(10-11)21-28(24,25)15-3-1-2-13-16(15)20-27-19-13/h1-5,10,21H,6-9H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196185 (1-[2-[(2,1,3-benzothiadiazol-4-ylcarbonyl)amino]-4...) Show SMILES Brc1ccc(C(=O)N2CCCCC2)c(NC(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C19H17BrN4O2S/c20-12-7-8-13(19(26)24-9-2-1-3-10-24)16(11-12)21-18(25)14-5-4-6-15-17(14)23-27-22-15/h4-8,11H,1-3,9-10H2,(H,21,25)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196188 (1-[4-bromo-2-[7-methyl(2,1,3-benzothiadiazol-4-yls...) Show SMILES Cc1ccc(c2nsnc12)S(=O)(=O)Nc1cc(Br)ccc1C(=O)N1CCCCC1 Show InChI InChI=1S/C19H19BrN4O3S2/c1-12-5-8-16(18-17(12)21-28-22-18)29(26,27)23-15-11-13(20)6-7-14(15)19(25)24-9-3-2-4-10-24/h5-8,11,23H,2-4,9-10H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196187 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES Clc1ccc(C(=O)N2CCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C16H13ClN4O3S2/c17-10-5-6-11(16(22)21-7-2-8-21)13(9-10)20-26(23,24)14-4-1-3-12-15(14)19-25-18-12/h1,3-6,9,20H,2,7-8H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196173 ((S)-1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amin...) Show SMILES Clc1ccc(C(=O)N2CCC[C@H]2CN2CCCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C22H24ClN5O3S2/c23-15-8-9-17(22(29)28-12-4-5-16(28)14-27-10-1-2-11-27)19(13-15)26-33(30,31)20-7-3-6-18-21(20)25-32-24-18/h3,6-9,13,16,26H,1-2,4-5,10-12,14H2/t16-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196190 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES Brc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C18H17BrN4O3S2/c19-12-7-8-13(18(24)23-9-2-1-3-10-23)15(11-12)22-28(25,26)16-6-4-5-14-17(16)21-27-20-14/h4-8,11,22H,1-3,9-10H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196184 (1-[3-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES Clc1ccc(cc1NS(=O)(=O)c1cccc2nsnc12)C(=O)N1CCCCC1 Show InChI InChI=1S/C18H17ClN4O3S2/c19-13-8-7-12(18(24)23-9-2-1-3-10-23)11-15(13)22-28(25,26)16-6-4-5-14-17(16)21-27-20-14/h4-8,11,22H,1-3,9-10H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196166 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-3...) Show SMILES Cc1cccc(C(=O)N2CCCCC2)c1NS(=O)(=O)c1cccc2nsnc12 Show InChI InChI=1S/C19H20N4O3S2/c1-13-7-5-8-14(19(24)23-11-3-2-4-12-23)17(13)22-28(25,26)16-10-6-9-15-18(16)21-27-20-15/h5-10,22H,2-4,11-12H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196181 (4-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES Ic1ccc(C(=O)N2CCOCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C17H15IN4O4S2/c18-11-4-5-12(17(23)22-6-8-26-9-7-22)14(10-11)21-28(24,25)15-3-1-2-13-16(15)20-27-19-13/h1-5,10,21H,6-9H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196182 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES CC1CN(CCN1)C(=O)c1ccc(Cl)cc1NS(=O)(=O)c1cccc2nsnc12 Show InChI InChI=1S/C18H18ClN5O3S2/c1-11-10-24(8-7-20-11)18(25)13-6-5-12(19)9-15(13)23-29(26,27)16-4-2-3-14-17(16)22-28-21-14/h2-6,9,11,20,23H,7-8,10H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196183 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES O=C(N1CCCCC1)c1ccc(OC2CCCC2)cc1NS(=O)(=O)c1cccc2nsnc12 Show InChI InChI=1S/C23H26N4O4S2/c28-23(27-13-4-1-5-14-27)18-12-11-17(31-16-7-2-3-8-16)15-20(18)26-33(29,30)21-10-6-9-19-22(21)25-32-24-19/h6,9-12,15-16,26H,1-5,7-8,13-14H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196189 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES CN1CCN(CC1)C(=O)c1ccc(Cl)cc1NS(=O)(=O)c1cccc2nsnc12 Show InChI InChI=1S/C18H18ClN5O3S2/c1-23-7-9-24(10-8-23)18(25)13-6-5-12(19)11-15(13)22-29(26,27)16-4-2-3-14-17(16)21-28-20-14/h2-6,11,22H,7-10H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (Homo sapiens (Human))	BDBM50196182 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES CC1CN(CCN1)C(=O)c1ccc(Cl)cc1NS(=O)(=O)c1cccc2nsnc12 Show InChI InChI=1S/C18H18ClN5O3S2/c1-11-10-24(8-7-20-11)18(25)13-6-5-12(19)9-15(13)23-29(26,27)16-4-2-3-14-17(16)22-28-21-14/h2-6,9,11,20,23H,7-8,10H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK2R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196193 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES COc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C19H20N4O4S2/c1-27-13-8-9-14(19(24)23-10-3-2-4-11-23)16(12-13)22-29(25,26)17-7-5-6-15-18(17)21-28-20-15/h5-9,12,22H,2-4,10-11H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196194 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)methylam...) Show SMILES CN(c1cc(Br)ccc1C(=O)N1CCCCC1)S(=O)(=O)c1cccc2nsnc12 Show InChI InChI=1S/C19H19BrN4O3S2/c1-23(29(26,27)17-7-5-6-15-18(17)22-28-21-15)16-12-13(20)8-9-14(16)19(25)24-10-3-2-4-11-24/h5-9,12H,2-4,10-11H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK-8S from human CCK1R				J Med Chem 49: 6371-90 (2006) Article DOI: 10.1021/jm060590x BindingDB Entry DOI: 10.7270/Q2MK6CHM
					More data for this Ligand-Target Pair

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