Compile Data Set for Download or QSAR

Found 311 hits with Last Name = 'freedman' and Initial = 'j'   

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
Transient receptor potential cation channel subfamily V member 1 (Homo sapiens (Human))	BDBM20461 ((6E)-N-[(4-hydroxy-3-methoxyphenyl)methyl]-8-methy...) Show SMILES COc1cc(CNC(=O)CCCC\C=C\C(C)C)ccc1O Show InChI InChI=1S/C18H27NO3/c1-14(2)8-6-4-5-7-9-18(21)19-13-15-10-11-16(20)17(12-15)22-3/h6,8,10-12,14,20H,4-5,7,9,13H2,1-3H3,(H,19,21)/b8-6+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development LLC Curated by ChEMBL					Assay Description Binding affinity to human recombinant TRPV1				Bioorg Med Chem Lett 20: 7137-41 (2010) Article DOI: 10.1016/j.bmcl.2010.09.023 BindingDB Entry DOI: 10.7270/Q29W0FQ5
					More data for this Ligand-Target Pair				3D Structure (crystal)
Transient receptor potential cation channel subfamily V member 1 (Homo sapiens (Human))	BDBM50052442 ((4-Hydroxy-3-methoxy-phenyl)-acetic acid (2R,3S,3a...) Show SMILES COc1cc(CC(=O)OCC2=C[C@H]3[C@H]4O[C@]5(Cc6ccccc6)O[C@]4(C[C@@H](C)[C@]3(O5)[C@@H]3C=C(C)C(=O)[C@@]3(O)C2)C(C)=C)ccc1O |r,t:10,35,THB:23:15:26.25.24:12| Show InChI InChI=1S/C37H40O9/c1-21(2)35-17-23(4)37-27(33(35)44-36(45-35,46-37)19-24-9-7-6-8-10-24)14-26(18-34(41)30(37)13-22(3)32(34)40)20-43-31(39)16-25-11-12-28(38)29(15-25)42-5/h6-15,23,27,30,33,38,41H,1,16-20H2,2-5H3/t23-,27+,30-,33-,34-,35-,36-,37-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid PDB UniChem Similars	PDB Article PubMed	14	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development LLC Curated by ChEMBL					Assay Description Binding affinity to human recombinant TRPV1				Bioorg Med Chem Lett 20: 7137-41 (2010) Article DOI: 10.1016/j.bmcl.2010.09.023 BindingDB Entry DOI: 10.7270/Q29W0FQ5
					More data for this Ligand-Target Pair				3D Structure (crystal)
Gastrin/cholecystokinin type B receptor (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	25	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK2R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (Homo sapiens (Human))	BDBM50196191 (4-[4-iodo-2-[(5-quinoxalinylsulfonyl)amino]benzoyl...) Show SMILES Ic1ccc(C(=O)N2CCOCC2)c(NS(=O)(=O)c2cccc3nccnc23)c1 Show InChI InChI=1S/C19H17IN4O4S/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	32	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK2R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (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	40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK2R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (Homo sapiens (Human))	BDBM50478086 (CHEMBL261682) Show SMILES Brc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3nccnc23)c1 Show InChI InChI=1S/C20H19BrN4O3S/c21-14-7-8-15(20(26)25-11-2-1-3-12-25)17(13-14)24-29(27,28)18-6-4-5-16-19(18)23-10-9-22-16/h4-10,13,24H,1-3,11-12H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	63	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK2R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (Homo sapiens (Human))	BDBM50478090 (CHEMBL259762) Show SMILES Brc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3scnc23)c1 Show InChI InChI=1S/C19H18BrN3O3S2/c20-13-7-8-14(19(24)23-9-2-1-3-10-23)15(11-13)22-28(25,26)17-6-4-5-16-18(17)21-12-27-16/h4-8,11-12,22H,1-3,9-10H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	79	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK2R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (Homo sapiens (Human))	BDBM50478094 (CHEMBL408452) Show SMILES Clc1ccc(CNC(=O)c2ccc(Br)cc2NS(=O)(=O)c2cccc3nsnc23)cc1 Show InChI InChI=1S/C20H14BrClN4O3S2/c21-13-6-9-15(20(27)23-11-12-4-7-14(22)8-5-12)17(10-13)26-31(28,29)18-3-1-2-16-19(18)25-30-24-16/h1-10,26H,11H2,(H,23,27)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	501	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK2R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (Homo sapiens (Human))	BDBM50478089 (CHEMBL261636) Show SMILES Cn1nc2cccc(c2n1)S(=O)(=O)Nc1cc(Br)ccc1C(=O)N1CCCCC1 Show InChI InChI=1S/C19H20BrN5O3S/c1-24-21-15-6-5-7-17(18(15)22-24)29(27,28)23-16-12-13(20)8-9-14(16)19(26)25-10-3-2-4-11-25/h5-9,12,23H,2-4,10-11H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	794	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK2R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (Homo sapiens (Human))	BDBM50478092 (CHEMBL410708) Show SMILES Brc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3ncsc23)c1 Show InChI InChI=1S/C19H18BrN3O3S2/c20-13-7-8-14(19(24)23-9-2-1-3-10-23)16(11-13)22-28(25,26)17-6-4-5-15-18(17)27-12-21-15/h4-8,11-12,22H,1-3,9-10H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	794	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK2R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (Homo sapiens (Human))	BDBM50196192 (1-[4-bromo-2-[(quinolin-5-ylsulfonyl)amino]-benzoy...) Show SMILES Brc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3ncccc23)c1 Show InChI InChI=1S/C21H20BrN3O3S/c22-15-9-10-17(21(26)25-12-2-1-3-13-25)19(14-15)24-29(27,28)20-8-4-7-18-16(20)6-5-11-23-18/h4-11,14,24H,1-3,12-13H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	794	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK2R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid lipoxygenase ALOX15 (Homo sapiens (Human))	BDBM56150 ((6E)-4-methyl-6-[5-(2-methylphenyl)-1,2-dihydropyr...) Show SMILES Cc1ccc(O)c(c1)-c1cc([nH]n1)-c1ccccc1C Show InChI InChI=1S/C17H16N2O/c1-11-7-8-17(20)14(9-11)16-10-15(18-19-16)13-6-4-3-5-12(13)2/h3-10,20H,1-2H3,(H,18,19)	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Patents Similars	Article PubMed	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Competitive inhibition of N-terminal His6-tagged human 12/15-LOX using arachidonic acid as substrate by Dixon plot analysis				Bioorg Med Chem 24: 1183-90 (2016) Article DOI: 10.1016/j.bmc.2016.01.042 BindingDB Entry DOI: 10.7270/Q2QJ7K44
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (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	1.59E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK2R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (Homo sapiens (Human))	BDBM50478085 (CHEMBL259224) Show SMILES Brc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3[nH]cnc23)c1 Show InChI InChI=1S/C19H19BrN4O3S/c20-13-7-8-14(19(25)24-9-2-1-3-10-24)16(11-13)23-28(26,27)17-6-4-5-15-18(17)22-12-21-15/h4-8,11-12,23H,1-3,9-10H2,(H,21,22)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.59E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK2R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (Homo sapiens (Human))	BDBM50478091 (CHEMBL259751) Show SMILES Cn1nnc2c(cccc12)S(=O)(=O)Nc1cc(Br)ccc1C(=O)N1CCCCC1 Show InChI InChI=1S/C19H20BrN5O3S/c1-24-16-6-5-7-17(18(16)21-23-24)29(27,28)22-15-12-13(20)8-9-14(15)19(26)25-10-3-2-4-11-25/h5-9,12,22H,2-4,10-11H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK2R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (Homo sapiens (Human))	BDBM50478087 (CHEMBL409479) Show SMILES Brc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2ccc3ncsc3c2)c1 Show InChI InChI=1S/C19H18BrN3O3S2/c20-13-4-6-15(19(24)23-8-2-1-3-9-23)17(10-13)22-28(25,26)14-5-7-16-18(11-14)27-12-21-16/h4-7,10-12,22H,1-3,8-9H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	3.16E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK2R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair
Gastrin/cholecystokinin type B receptor (Homo sapiens (Human))	BDBM50478093 (CHEMBL410905) Show SMILES Cc1nc2cccc(c2s1)S(=O)(=O)Nc1cc(Br)ccc1C(=O)N1CCCCC1 Show InChI InChI=1S/C20H20BrN3O3S2/c1-13-22-16-6-5-7-18(19(16)28-13)29(26,27)23-17-12-14(21)8-9-15(17)20(25)24-10-3-2-4-11-24/h5-9,12,23H,2-4,10-11H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	5.01E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK2R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196195 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES O=C(N1CCCCC1)c1ccc(cc1NS(=O)(=O)c1cccc2nsnc12)-c1ccco1 Show InChI InChI=1S/C22H20N4O4S2/c27-22(26-11-2-1-3-12-26)16-10-9-15(19-7-5-13-30-19)14-18(16)25-32(28,29)20-8-4-6-17-21(20)24-31-23-17/h4-10,13-14,25H,1-3,11-12H2	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))	BDBM50196205 (2-(benzo[c][1,2,5]thiadiazole-4-sulfonamido)-N-ben...) Show SMILES Clc1ccc(C(=O)NCc2ccccc2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C20H15ClN4O3S2/c21-14-9-10-15(20(26)22-12-13-5-2-1-3-6-13)17(11-14)25-30(27,28)18-8-4-7-16-19(18)24-29-23-16/h1-11,25H,12H2,(H,22,26)	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))	BDBM50196208 (1-[2-[(2,1,3-benzothiadiazol-5-ylsulfonyl)amino]-4...) Show SMILES Brc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2ccc3nsnc3c2)c1 Show InChI InChI=1S/C18H17BrN4O3S2/c19-12-4-6-14(18(24)23-8-2-1-3-9-23)16(10-12)22-28(25,26)13-5-7-15-17(11-13)21-27-20-15/h4-7,10-11,22H,1-3,8-9H2	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))	BDBM50196209 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES Clc1cc(NS(=O)(=O)c2cccc3nsnc23)c(cc1Cl)C(=O)N1CCCCC1 Show InChI InChI=1S/C18H16Cl2N4O3S2/c19-12-9-11(18(25)24-7-2-1-3-8-24)15(10-13(12)20)23-29(26,27)16-6-4-5-14-17(16)22-28-21-14/h4-6,9-10,23H,1-3,7-8H2	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))	BDBM50196210 (1-[4-bromo-2-[(5-quinoxalinylsulfonyl)amino]benzoy...) Show SMILES Brc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3nccnc23)n1 Show InChI InChI=1S/C19H18BrN5O3S/c20-16-8-7-13(19(26)25-11-2-1-3-12-25)18(23-16)24-29(27,28)15-6-4-5-14-17(15)22-10-9-21-14/h4-10H,1-3,11-12H2,(H,23,24)	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))	BDBM50196200 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES O=C(N1CCCCC1)c1ccc(cc1NS(=O)(=O)c1cccc2nsnc12)-n1cccc1 Show InChI InChI=1S/C22H21N5O3S2/c28-22(27-13-2-1-3-14-27)17-10-9-16(26-11-4-5-12-26)15-19(17)25-32(29,30)20-8-6-7-18-21(20)24-31-23-18/h4-12,15,25H,1-3,13-14H2	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))	BDBM50196201 (1-[2-[7-bromo(2,1,3-benzothiadiazol-4-ylsulfonyl)a...) Show SMILES Brc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2ccc(Br)c3nsnc23)c1 Show InChI InChI=1S/C18H16Br2N4O3S2/c19-11-4-5-12(18(25)24-8-2-1-3-9-24)14(10-11)23-29(26,27)15-7-6-13(20)16-17(15)22-28-21-16/h4-7,10,23H,1-3,8-9H2	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
Gastrin/cholecystokinin type B receptor (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 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))	BDBM50196202 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES [O-][N+](=O)c1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C18H17N5O5S2/c24-18(22-9-2-1-3-10-22)13-8-7-12(23(25)26)11-15(13)21-30(27,28)16-6-4-5-14-17(16)20-29-19-14/h4-8,11,21H,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
Gastrin/cholecystokinin type B receptor (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 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))	BDBM50196216 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-b...) Show SMILES O=C(N1CCCCC1)c1ccccc1NS(=O)(=O)c1cccc2nsnc12 Show InChI InChI=1S/C18H18N4O3S2/c23-18(22-11-4-1-5-12-22)13-7-2-3-8-14(13)21-27(24,25)16-10-6-9-15-17(16)20-26-19-15/h2-3,6-10,21H,1,4-5,11-12H2	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))	BDBM50196212 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES O=C(N1CCCCC1)C1=C(CC(NCc2ccccc2)C=C1)NS(=O)(=O)c1cccc2nsnc12 |c:22,t:9| Show InChI InChI=1S/C25H27N5O3S2/c31-25(30-14-5-2-6-15-30)20-13-12-19(26-17-18-8-3-1-4-9-18)16-22(20)29-35(32,33)23-11-7-10-21-24(23)28-34-27-21/h1,3-4,7-13,19,26,29H,2,5-6,14-17H2	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))	BDBM50196207 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES Clc1ccc(C(=O)N2CCCCCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C19H19ClN4O3S2/c20-13-8-9-14(19(25)24-10-3-1-2-4-11-24)16(12-13)23-29(26,27)17-7-5-6-15-18(17)22-28-21-15/h5-9,12,23H,1-4,10-11H2	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))	BDBM50196213 (1-[4-bromo-2-[5-fluoro(2,1,3-benzothiadiazol-4-yls...) Show SMILES Fc1ccc2nsnc2c1S(=O)(=O)Nc1cc(Br)ccc1C(=O)N1CCCCC1 Show InChI InChI=1S/C18H16BrFN4O3S2/c19-11-4-5-12(18(25)24-8-2-1-3-9-24)15(10-11)23-29(26,27)17-13(20)6-7-14-16(17)22-28-21-14/h4-7,10,23H,1-3,8-9H2	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))	BDBM50196206 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES Clc1ccc(C(=O)N2CCCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C17H15ClN4O3S2/c18-11-6-7-12(17(23)22-8-1-2-9-22)14(10-11)21-27(24,25)15-5-3-4-13-16(15)20-26-19-13/h3-7,10,21H,1-2,8-9H2	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))	BDBM50196219 ((R)-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-/m1/s1	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))	BDBM50196211 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-6...) Show SMILES Clc1cccc(NS(=O)(=O)c2cccc3nsnc23)c1C(=O)N1CCCCC1 Show InChI InChI=1S/C18H17ClN4O3S2/c19-12-6-4-7-13(16(12)18(24)23-10-2-1-3-11-23)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 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))	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 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))	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 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))	BDBM50196215 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES Brc1cc(NS(=O)(=O)c2cccc3nsnc23)c(cc1Br)C(=O)N1CCCCC1 Show InChI InChI=1S/C18H16Br2N4O3S2/c19-12-9-11(18(25)24-7-2-1-3-8-24)15(10-13(12)20)23-29(26,27)16-6-4-5-14-17(16)22-28-21-14/h4-6,9-10,23H,1-3,7-8H2	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))	BDBM50196214 ((3R,5S)-rel-4-[4-chloro-2-[(5-quinoxalinylsulfonyl...) 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+	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))	BDBM50196220 (1-[4-bromo-2-[5-methyl(2,1,3-benzothiadiazol-4-yls...) Show SMILES Cc1ccc2nsnc2c1S(=O)(=O)Nc1cc(Br)ccc1C(=O)N1CCCCC1 Show InChI InChI=1S/C19H19BrN4O3S2/c1-12-5-8-15-17(22-28-21-15)18(12)29(26,27)23-16-11-13(20)6-7-14(16)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))	BDBM50196217 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES CCc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C20H22N4O3S2/c1-2-14-9-10-15(20(25)24-11-4-3-5-12-24)17(13-14)23-29(26,27)18-8-6-7-16-19(18)22-28-21-16/h6-10,13,23H,2-5,11-12H2,1H3	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))	BDBM50196218 (1-[2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4...) Show SMILES CN(C)c1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3nsnc23)c1 Show InChI InChI=1S/C20H23N5O3S2/c1-24(2)14-9-10-15(20(26)25-11-4-3-5-12-25)17(13-14)23-30(27,28)18-8-6-7-16-19(18)22-29-21-16/h6-10,13,23H,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
Cholecystokinin receptor type A (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 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))	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 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))	BDBM50478085 (CHEMBL259224) Show SMILES Brc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3[nH]cnc23)c1 Show InChI InChI=1S/C19H19BrN4O3S/c20-13-7-8-14(19(25)24-9-2-1-3-10-24)16(11-13)23-28(26,27)17-6-4-5-15-18(17)22-12-21-15/h4-8,11-12,23H,1-3,9-10H2,(H,21,22)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	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 & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK1R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					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 & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK1R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50196192 (1-[4-bromo-2-[(quinolin-5-ylsulfonyl)amino]-benzoy...) Show SMILES Brc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3ncccc23)c1 Show InChI InChI=1S/C21H20BrN3O3S/c22-15-9-10-17(21(26)25-12-2-1-3-13-25)19(14-15)24-29(27,28)20-8-4-7-18-16(20)6-5-11-23-18/h4-11,14,24H,1-3,12-13H2	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 & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK1R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50478086 (CHEMBL261682) Show SMILES Brc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2cccc3nccnc23)c1 Show InChI InChI=1S/C20H19BrN4O3S/c21-14-7-8-15(20(26)25-11-2-1-3-12-25)17(13-14)24-29(27,28)18-6-4-5-16-19(18)23-10-9-22-16/h4-10,13,24H,1-3,11-12H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	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 & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK1R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50478087 (CHEMBL409479) Show SMILES Brc1ccc(C(=O)N2CCCCC2)c(NS(=O)(=O)c2ccc3ncsc3c2)c1 Show InChI InChI=1S/C19H18BrN3O3S2/c20-13-4-6-15(19(24)23-8-2-1-3-9-23)17(10-13)22-28(25,26)14-5-7-16-18(11-14)27-12-21-16/h4-7,10-12,22H,1-3,8-9H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	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 & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK1R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50478088 (CHEMBL412282) Show SMILES Cn1nc2ccc(cc2n1)S(=O)(=O)Nc1cc(Br)ccc1C(=O)N1CCCCC1 Show InChI InChI=1S/C19H20BrN5O3S/c1-24-21-16-8-6-14(12-18(16)22-24)29(27,28)23-17-11-13(20)5-7-15(17)19(26)25-9-3-2-4-10-25/h5-8,11-12,23H,2-4,9-10H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	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 & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK1R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50478089 (CHEMBL261636) Show SMILES Cn1nc2cccc(c2n1)S(=O)(=O)Nc1cc(Br)ccc1C(=O)N1CCCCC1 Show InChI InChI=1S/C19H20BrN5O3S/c1-24-21-15-6-5-7-17(18(15)22-24)29(27,28)23-16-12-13(20)8-9-14(16)19(26)25-10-3-2-4-11-25/h5-9,12,23H,2-4,10-11H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	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 & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [125I]CCK8S from human CCK1R				Bioorg Med Chem 16: 3917-25 (2008) Article DOI: 10.1016/j.bmc.2008.01.059 BindingDB Entry DOI: 10.7270/Q2D79F5S
					More data for this Ligand-Target Pair

Displayed 1 to 50 (of 311 total )  |  Next  |  Last  >>

Jump to: