Compile Data Set for Download or QSAR

Found 5185 hits with Last Name = 'hayashi' and Initial = 'k'   

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
Delta-type opioid receptor (MOUSE)	BDBM50253136 (CHEMBL4075409) Show SMILES [H][C@]12CN(C3CCC4(O1)C1Cc5ccc(O)cc5C4(CCN1CC=C)C23)C(=O)c1ccccc1 |r,TLB:3:4:18:8.1,2:1:18:5.6.4,6:7:21.20.19:10.17.11,17:18:8.1:5.6.4,16:17:21.20.19:7,THB:19:18:8.1:5.6.4| Show InChI InChI=1S/C28H30N2O3/c1-2-13-29-14-12-27-21-16-20(31)9-8-19(21)15-24(29)28(27)11-10-22-25(27)23(33-28)17-30(22)26(32)18-6-4-3-5-7-18/h2-9,16,22-25,31H,1,10-15,17H2/t22?,23-,24?,25?,27?,28?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	0.109	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Laboratory of Medicinal Chemistry, School of Pharmacy, Kitasato University, 5-9-1, Shirokane, Minato-ku, Tokyo 108-8641, Japan; Discovery Research Laboratories, Nippon Chemiphar Co., Ltd., 1-22, Hiko Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from delta opioid receptor in mouse whole brain without cerebellum membrane				Bioorg Med Chem Lett 27: 2742-2745 (2017) Article DOI: 10.1016/j.bmcl.2017.04.059 BindingDB Entry DOI: 10.7270/Q2H134GP
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50253129 (CHEMBL4066752) Show SMILES [H][C@]12CN(C3CCC4(O1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)C(=O)c1ccccc1 |r,TLB:3:4:18:8.1,2:1:18:5.6.4,6:7:21.20.19:10.17.11,17:18:8.1:5.6.4,22:21:7:10.17.11,16:17:21.20.19:7,THB:19:18:8.1:5.6.4| Show InChI InChI=1S/C29H32N2O3/c32-21-9-8-20-14-25-29-11-10-23-26(24(34-29)17-31(23)27(33)19-4-2-1-3-5-19)28(29,22(20)15-21)12-13-30(25)16-18-6-7-18/h1-5,8-9,15,18,23-26,32H,6-7,10-14,16-17H2/t23?,24-,25?,26?,28?,29?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	0.154	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Laboratory of Medicinal Chemistry, School of Pharmacy, Kitasato University, 5-9-1, Shirokane, Minato-ku, Tokyo 108-8641, Japan; Discovery Research Laboratories, Nippon Chemiphar Co., Ltd., 1-22, Hiko Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from human delta opioid receptor expressed in CHO cells				Bioorg Med Chem Lett 27: 2742-2745 (2017) Article DOI: 10.1016/j.bmcl.2017.04.059 BindingDB Entry DOI: 10.7270/Q2H134GP
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50254132 (CHEMBL4083940) Show SMILES [H][C@]12CN(C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)C(=O)c1ccccc1 |r,TLB:17:18:4.6.5:8.1,16:17:7:21.20.19,6:7:21.20.19:10.11.17,8:7:21.20.19:10.11.17,2:1:18:4.6.5,3:4:18:8.1,22:21:7:10.11.17,THB:12:11:7:21.20.19,19:18:4.6.5:8.1| Show InChI InChI=1S/C30H34N2O2/c33-23-9-8-21-14-26-29-11-10-25-27(22(16-29)18-32(25)28(34)20-4-2-1-3-5-20)30(29,24(21)15-23)12-13-31(26)17-19-6-7-19/h1-5,8-9,15,19,22,25-27,33H,6-7,10-14,16-18H2/t22-,25?,26?,27?,29?,30?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.211	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from human recombinant DOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50253140 (CHEMBL4081856) Show SMILES [H][C@]12CN(C3CCC4(O1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)S(=O)(=O)c1ccccc1 |r,TLB:16:17:21.20.19:7,3:4:18:8.1,2:1:18:5.6.4,6:7:21.20.19:10.17.11,17:18:8.1:5.6.4,THB:19:18:8.1:5.6.4| Show InChI InChI=1S/C28H32N2O4S/c31-20-9-8-19-14-25-28-11-10-23-26(27(28,22(19)15-20)12-13-29(25)16-18-6-7-18)24(34-28)17-30(23)35(32,33)21-4-2-1-3-5-21/h1-5,8-9,15,18,23-26,31H,6-7,10-14,16-17H2/t23?,24-,25?,26?,27?,28?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.221	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Laboratory of Medicinal Chemistry, School of Pharmacy, Kitasato University, 5-9-1, Shirokane, Minato-ku, Tokyo 108-8641, Japan; Discovery Research Laboratories, Nippon Chemiphar Co., Ltd., 1-22, Hiko Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from human delta opioid receptor expressed in CHO cells				Bioorg Med Chem Lett 27: 2742-2745 (2017) Article DOI: 10.1016/j.bmcl.2017.04.059 BindingDB Entry DOI: 10.7270/Q2H134GP
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50254124 (CHEMBL4103044) Show SMILES [H][C@]12CN(C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)C(=O)c1ccoc1 |r,TLB:17:18:4.6.5:8.1,16:17:7:21.20.19,6:7:21.20.19:10.11.17,8:7:21.20.19:10.11.17,2:1:18:4.6.5,3:4:18:8.1,22:21:7:10.11.17,THB:12:11:7:21.20.19,19:18:4.6.5:8.1| Show InChI InChI=1S/C28H32N2O3/c31-21-4-3-18-11-24-27-7-5-23-25(20(13-27)15-30(23)26(32)19-6-10-33-16-19)28(27,22(18)12-21)8-9-29(24)14-17-1-2-17/h3-4,6,10,12,16-17,20,23-25,31H,1-2,5,7-9,11,13-15H2/t20-,23?,24?,25?,27?,28?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.221	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]U-69,593 from human recombinant KOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM50274257 ((2E)-N-[(1S,5R,13R,14R,17S)-4-(cyclopropylmethyl)-...) Show SMILES CN([C@@H]1CC[C@@]2(O)[C@H]3Cc4ccc(O)c5O[C@@H]1[C@]2(CCN3CC1CC1)c45)C(=O)\C=C\c1ccco1 |r,TLB:4:5:9.25.8:18.20.19,THB:6:5:9.25.8:18.20.19| Show InChI InChI=1S/C28H32N2O5/c1-29(23(32)9-7-19-3-2-14-34-19)20-10-11-28(33)22-15-18-6-8-21(31)25-24(18)27(28,26(20)35-25)12-13-30(22)16-17-4-5-17/h2-3,6-9,14,17,20,22,26,31,33H,4-5,10-13,15-16H2,1H3/b9-7+/t20-,22-,26+,27+,28-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	0.225	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Kitasato University Curated by ChEMBL					Assay Description Displacement of [3H]U69593 from guinea pig cerebellum kappa opioid receptor				Bioorg Med Chem Lett 20: 121-4 (2010) Article DOI: 10.1016/j.bmcl.2009.11.027 BindingDB Entry DOI: 10.7270/Q2GX4CJH
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50254133 (CHEMBL4076632) Show SMILES [H][C@]12CN(C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)C(=O)Nc1ccccc1 |r,TLB:17:18:4.6.5:8.1,16:17:7:21.20.19,6:7:21.20.19:10.11.17,8:7:21.20.19:10.11.17,2:1:18:4.6.5,3:4:18:8.1,22:21:7:10.11.17,THB:12:11:7:21.20.19,19:18:4.6.5:8.1| Show InChI InChI=1S/C30H35N3O2/c34-23-9-8-20-14-26-29-11-10-25-27(30(29,24(20)15-23)12-13-32(26)17-19-6-7-19)21(16-29)18-33(25)28(35)31-22-4-2-1-3-5-22/h1-5,8-9,15,19,21,25-27,34H,6-7,10-14,16-18H2,(H,31,35)/t21-,25?,26?,27?,29?,30?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.265	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from human recombinant DOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Delta-type opioid receptor (MOUSE)	BDBM50253129 (CHEMBL4066752) Show SMILES [H][C@]12CN(C3CCC4(O1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)C(=O)c1ccccc1 |r,TLB:3:4:18:8.1,2:1:18:5.6.4,6:7:21.20.19:10.17.11,17:18:8.1:5.6.4,22:21:7:10.17.11,16:17:21.20.19:7,THB:19:18:8.1:5.6.4| Show InChI InChI=1S/C29H32N2O3/c32-21-9-8-20-14-25-29-11-10-23-26(24(34-29)17-31(23)27(33)19-4-2-1-3-5-19)28(29,22(20)15-21)12-13-30(25)16-18-6-7-18/h1-5,8-9,15,18,23-26,32H,6-7,10-14,16-17H2/t23?,24-,25?,26?,28?,29?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	0.274	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Laboratory of Medicinal Chemistry, School of Pharmacy, Kitasato University, 5-9-1, Shirokane, Minato-ku, Tokyo 108-8641, Japan; Discovery Research Laboratories, Nippon Chemiphar Co., Ltd., 1-22, Hiko Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from delta opioid receptor in mouse whole brain without cerebellum membrane				Bioorg Med Chem Lett 27: 2742-2745 (2017) Article DOI: 10.1016/j.bmcl.2017.04.059 BindingDB Entry DOI: 10.7270/Q2H134GP
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Homo sapiens (Human))	BDBM50031962 (3-(5,7-Dimethyl-2-propyl-imidazo[4,5-b]pyridin-3-y...) Show SMILES CCCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(cc3ccccc3c(=O)c2c1)-c1nnn[nH]1 Show InChI InChI=1S/C28H25N7O/c1-4-7-24-30-25-16(2)12-17(3)29-28(25)35(24)15-18-10-11-21-22(13-18)26(36)20-9-6-5-8-19(20)14-23(21)27-31-33-34-32-27/h5-6,8-14H,4,7,15H2,1-3H3,(H,31,32,33,34)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.290	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Shionogi & Co., Ltd. Curated by ChEMBL					Assay Description Ability to displace [125I]-AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1				J Med Chem 38: 2728-41 (1995) BindingDB Entry DOI: 10.7270/Q23B5Z5Q
					More data for this Ligand-Target Pair
Delta-type opioid receptor (MOUSE)	BDBM50253138 (CHEMBL4076303) Show SMILES [H][C@]12CN(C3CCC4(O1)C1Cc5ccc(O)cc5C4(CCN1C)C23)C(=O)c1ccccc1 |r,TLB:3:4:18:8.1,2:1:18:5.6.4,6:7:21.20.19:10.17.11,17:18:8.1:5.6.4,16:17:21.20.19:7,THB:19:18:8.1:5.6.4| Show InChI InChI=1S/C26H28N2O3/c1-27-12-11-25-19-14-18(29)8-7-17(19)13-22(27)26(25)10-9-20-23(25)21(31-26)15-28(20)24(30)16-5-3-2-4-6-16/h2-8,14,20-23,29H,9-13,15H2,1H3/t20?,21-,22?,23?,25?,26?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.301	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Laboratory of Medicinal Chemistry, School of Pharmacy, Kitasato University, 5-9-1, Shirokane, Minato-ku, Tokyo 108-8641, Japan; Discovery Research Laboratories, Nippon Chemiphar Co., Ltd., 1-22, Hiko Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from delta opioid receptor in mouse whole brain without cerebellum membrane				Bioorg Med Chem Lett 27: 2742-2745 (2017) Article DOI: 10.1016/j.bmcl.2017.04.059 BindingDB Entry DOI: 10.7270/Q2H134GP
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50253140 (CHEMBL4081856) Show SMILES [H][C@]12CN(C3CCC4(O1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)S(=O)(=O)c1ccccc1 |r,TLB:16:17:21.20.19:7,3:4:18:8.1,2:1:18:5.6.4,6:7:21.20.19:10.17.11,17:18:8.1:5.6.4,THB:19:18:8.1:5.6.4| Show InChI InChI=1S/C28H32N2O4S/c31-20-9-8-19-14-25-28-11-10-23-26(27(28,22(19)15-20)12-13-29(25)16-18-6-7-18)24(34-28)17-30(23)35(32,33)21-4-2-1-3-5-21/h1-5,8-9,15,18,23-26,31H,6-7,10-14,16-17H2/t23?,24-,25?,26?,27?,28?/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.308	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Laboratory of Medicinal Chemistry, School of Pharmacy, Kitasato University, 5-9-1, Shirokane, Minato-ku, Tokyo 108-8641, Japan; Discovery Research Laboratories, Nippon Chemiphar Co., Ltd., 1-22, Hiko Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from human mu opioid receptor expressed in CHO cells				Bioorg Med Chem Lett 27: 2742-2745 (2017) Article DOI: 10.1016/j.bmcl.2017.04.059 BindingDB Entry DOI: 10.7270/Q2H134GP
					More data for this Ligand-Target Pair
Delta-type opioid receptor (MOUSE)	BDBM50010652 (CHEMBL3264742) Show SMILES [H][C@]12O[C@]34CC[C@@]5(OCOc6c(O)ccc7C[C@@]3([H])N(CC3CC3)CC[C@]4(c67)[C@]15[H])N(Cc1ccccc1)C2=O |r,TLB:20:19:3:27.15.16,THB:7:6:26:1.2| Show InChI InChI=1S/C30H32N2O5/c33-21-9-8-20-14-22-29-10-11-30-26(25(37-29)27(34)32(30)16-18-4-2-1-3-5-18)28(29,23(20)24(21)35-17-36-30)12-13-31(22)15-19-6-7-19/h1-5,8-9,19,22,25-26,33H,6-7,10-17H2/t22-,25+,26+,28+,29-,30+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	0.313	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Kitasato University Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from delta opioid receptor in mouse whole brain cerebellum membrane				ACS Med Chem Lett 5: 368-72 (2014) Article DOI: 10.1021/ml400491k BindingDB Entry DOI: 10.7270/Q2GF0W23
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50254124 (CHEMBL4103044) Show SMILES [H][C@]12CN(C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)C(=O)c1ccoc1 |r,TLB:17:18:4.6.5:8.1,16:17:7:21.20.19,6:7:21.20.19:10.11.17,8:7:21.20.19:10.11.17,2:1:18:4.6.5,3:4:18:8.1,22:21:7:10.11.17,THB:12:11:7:21.20.19,19:18:4.6.5:8.1| Show InChI InChI=1S/C28H32N2O3/c31-21-4-3-18-11-24-27-7-5-23-25(20(13-27)15-30(23)26(32)19-6-10-33-16-19)28(27,22(18)12-21)8-9-29(24)14-17-1-2-17/h3-4,6,10,12,16-17,20,23-25,31H,1-2,5,7-9,11,13-15H2/t20-,23?,24?,25?,27?,28?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.313	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from human recombinant DOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Mu-type opioid receptor (MOUSE)	BDBM50253129 (CHEMBL4066752) Show SMILES [H][C@]12CN(C3CCC4(O1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)C(=O)c1ccccc1 |r,TLB:3:4:18:8.1,2:1:18:5.6.4,6:7:21.20.19:10.17.11,17:18:8.1:5.6.4,22:21:7:10.17.11,16:17:21.20.19:7,THB:19:18:8.1:5.6.4| Show InChI InChI=1S/C29H32N2O3/c32-21-9-8-20-14-25-29-11-10-23-26(24(34-29)17-31(23)27(33)19-4-2-1-3-5-19)28(29,22(20)15-21)12-13-30(25)16-18-6-7-18/h1-5,8-9,15,18,23-26,32H,6-7,10-14,16-17H2/t23?,24-,25?,26?,28?,29?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	0.325	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Laboratory of Medicinal Chemistry, School of Pharmacy, Kitasato University, 5-9-1, Shirokane, Minato-ku, Tokyo 108-8641, Japan; Discovery Research Laboratories, Nippon Chemiphar Co., Ltd., 1-22, Hiko Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from mu opioid receptor in mouse whole brain without cerebellum membrane				Bioorg Med Chem Lett 27: 2742-2745 (2017) Article DOI: 10.1016/j.bmcl.2017.04.059 BindingDB Entry DOI: 10.7270/Q2H134GP
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50254133 (CHEMBL4076632) Show SMILES [H][C@]12CN(C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)C(=O)Nc1ccccc1 |r,TLB:17:18:4.6.5:8.1,16:17:7:21.20.19,6:7:21.20.19:10.11.17,8:7:21.20.19:10.11.17,2:1:18:4.6.5,3:4:18:8.1,22:21:7:10.11.17,THB:12:11:7:21.20.19,19:18:4.6.5:8.1| Show InChI InChI=1S/C30H35N3O2/c34-23-9-8-20-14-26-29-11-10-25-27(30(29,24(20)15-23)12-13-32(26)17-19-6-7-19)21(16-29)18-33(25)28(35)31-22-4-2-1-3-5-22/h1-5,8-9,15,19,21,25-27,34H,6-7,10-14,16-18H2,(H,31,35)/t21-,25?,26?,27?,29?,30?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.336	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]U-69,593 from human recombinant KOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50254131 (CHEMBL4094845) Show SMILES [H][C@]12CN(C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)c1cnccn1 |r,TLB:17:18:4.6.5:8.1,16:17:7:21.20.19,6:7:21.20.19:10.11.17,8:7:21.20.19:10.11.17,2:1:18:4.6.5,3:4:18:8.1,22:21:7:10.11.17,THB:12:11:7:21.20.19,19:18:4.6.5:8.1| Show InChI InChI=1S/C27H32N4O/c32-20-4-3-18-11-23-26-6-5-22-25(19(13-26)16-31(22)24-14-28-8-9-29-24)27(26,21(18)12-20)7-10-30(23)15-17-1-2-17/h3-4,8-9,12,14,17,19,22-23,25,32H,1-2,5-7,10-11,13,15-16H2/t19-,22?,23?,25?,26?,27?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.356	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from human recombinant DOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50254132 (CHEMBL4083940) Show SMILES [H][C@]12CN(C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)C(=O)c1ccccc1 |r,TLB:17:18:4.6.5:8.1,16:17:7:21.20.19,6:7:21.20.19:10.11.17,8:7:21.20.19:10.11.17,2:1:18:4.6.5,3:4:18:8.1,22:21:7:10.11.17,THB:12:11:7:21.20.19,19:18:4.6.5:8.1| Show InChI InChI=1S/C30H34N2O2/c33-23-9-8-21-14-26-29-11-10-25-27(22(16-29)18-32(25)28(34)20-4-2-1-3-5-20)30(29,24(21)15-23)12-13-31(26)17-19-6-7-19/h1-5,8-9,15,19,22,25-27,33H,6-7,10-14,16-18H2/t22-,25?,26?,27?,29?,30?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.362	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]U-69,593 from human recombinant KOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Delta-type opioid receptor (MOUSE)	BDBM50253137 (CHEMBL4076673) Show SMILES [H][C@]12CN(C3CCC4(O1)C1Cc5ccc(O)cc5C4(CCN1CCCOC)C23)C(=O)c1ccccc1 |r,TLB:3:4:18:8.1,2:1:18:5.6.4,6:7:21.20.19:10.17.11,17:18:8.1:5.6.4,16:17:21.20.19:7,THB:19:18:8.1:5.6.4| Show InChI InChI=1S/C29H34N2O4/c1-34-15-5-13-30-14-12-28-22-17-21(32)9-8-20(22)16-25(30)29(28)11-10-23-26(28)24(35-29)18-31(23)27(33)19-6-3-2-4-7-19/h2-4,6-9,17,23-26,32H,5,10-16,18H2,1H3/t23?,24-,25?,26?,28?,29?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Patents	Article PubMed	0.368	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Laboratory of Medicinal Chemistry, School of Pharmacy, Kitasato University, 5-9-1, Shirokane, Minato-ku, Tokyo 108-8641, Japan; Discovery Research Laboratories, Nippon Chemiphar Co., Ltd., 1-22, Hiko Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from delta opioid receptor in mouse whole brain without cerebellum membrane				Bioorg Med Chem Lett 27: 2742-2745 (2017) Article DOI: 10.1016/j.bmcl.2017.04.059 BindingDB Entry DOI: 10.7270/Q2H134GP
					More data for this Ligand-Target Pair
Mu-type opioid receptor (MOUSE)	BDBM50253138 (CHEMBL4076303) Show SMILES [H][C@]12CN(C3CCC4(O1)C1Cc5ccc(O)cc5C4(CCN1C)C23)C(=O)c1ccccc1 |r,TLB:3:4:18:8.1,2:1:18:5.6.4,6:7:21.20.19:10.17.11,17:18:8.1:5.6.4,16:17:21.20.19:7,THB:19:18:8.1:5.6.4| Show InChI InChI=1S/C26H28N2O3/c1-27-12-11-25-19-14-18(29)8-7-17(19)13-22(27)26(25)10-9-20-23(25)21(31-26)15-28(20)24(30)16-5-3-2-4-6-16/h2-8,14,20-23,29H,9-13,15H2,1H3/t20?,21-,22?,23?,25?,26?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.383	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Laboratory of Medicinal Chemistry, School of Pharmacy, Kitasato University, 5-9-1, Shirokane, Minato-ku, Tokyo 108-8641, Japan; Discovery Research Laboratories, Nippon Chemiphar Co., Ltd., 1-22, Hiko Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from mu opioid receptor in mouse whole brain without cerebellum membrane				Bioorg Med Chem Lett 27: 2742-2745 (2017) Article DOI: 10.1016/j.bmcl.2017.04.059 BindingDB Entry DOI: 10.7270/Q2H134GP
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Homo sapiens (Human))	BDBM50031954 (3-(2-Cyclopropyl-5,7-dimethyl-imidazo[4,5-b]pyridi...) Show SMILES Cc1cc(C)c2nc(C3CC3)n(Cc3ccc4c(cc5ccccc5c(=O)c4c3)-c3nnn[nH]3)c2n1 Show InChI InChI=1S/C28H23N7O/c1-15-11-16(2)29-28-24(15)30-27(18-8-9-18)35(28)14-17-7-10-21-22(12-17)25(36)20-6-4-3-5-19(20)13-23(21)26-31-33-34-32-26/h3-7,10-13,18H,8-9,14H2,1-2H3,(H,31,32,33,34)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.450	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Shionogi & Co., Ltd. Curated by ChEMBL					Assay Description Ability to displace [125I]-AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1				J Med Chem 38: 2728-41 (1995) BindingDB Entry DOI: 10.7270/Q23B5Z5Q
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50254124 (CHEMBL4103044) Show SMILES [H][C@]12CN(C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)C(=O)c1ccoc1 |r,TLB:17:18:4.6.5:8.1,16:17:7:21.20.19,6:7:21.20.19:10.11.17,8:7:21.20.19:10.11.17,2:1:18:4.6.5,3:4:18:8.1,22:21:7:10.11.17,THB:12:11:7:21.20.19,19:18:4.6.5:8.1| Show InChI InChI=1S/C28H32N2O3/c31-21-4-3-18-11-24-27-7-5-23-25(20(13-27)15-30(23)26(32)19-6-10-33-16-19)28(27,22(18)12-21)8-9-29(24)14-17-1-2-17/h3-4,6,10,12,16-17,20,23-25,31H,1-2,5,7-9,11,13-15H2/t20-,23?,24?,25?,27?,28?/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.455	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from human recombinant MOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50254123 (CHEMBL4068691) Show SMILES [H][C@]12CN(C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)C(=O)c1ccccn1 |r,TLB:17:18:4.6.5:8.1,16:17:7:21.20.19,6:7:21.20.19:10.11.17,8:7:21.20.19:10.11.17,2:1:18:4.6.5,3:4:18:8.1,22:21:7:10.11.17,THB:12:11:7:21.20.19,19:18:4.6.5:8.1| Show InChI InChI=1S/C29H33N3O2/c33-21-7-6-19-13-25-28-9-8-24-26(20(15-28)17-32(24)27(34)23-3-1-2-11-30-23)29(28,22(19)14-21)10-12-31(25)16-18-4-5-18/h1-3,6-7,11,14,18,20,24-26,33H,4-5,8-10,12-13,15-17H2/t20-,24?,25?,26?,28?,29?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	0.458	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from human recombinant DOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Delta-type opioid receptor (MOUSE)	BDBM50253139 (CHEMBL4096314) Show SMILES [H][C@]12CN(C3CCC4(O1)C1Cc5ccc(O)cc5C4(CCN1CCc1ccccc1)C23)C(=O)c1ccccc1 |r,TLB:3:4:18:8.1,2:1:18:5.6.4,6:7:21.20.19:10.17.11,17:18:8.1:5.6.4,16:17:21.20.19:7,THB:19:18:8.1:5.6.4| Show InChI InChI=1S/C33H34N2O3/c36-25-12-11-24-19-29-33-15-13-27-30(28(38-33)21-35(27)31(37)23-9-5-2-6-10-23)32(33,26(24)20-25)16-18-34(29)17-14-22-7-3-1-4-8-22/h1-12,20,27-30,36H,13-19,21H2/t27?,28-,29?,30?,32?,33?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	MMDB PC cid PC sid UniChem Patents	Article PubMed	0.458	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Laboratory of Medicinal Chemistry, School of Pharmacy, Kitasato University, 5-9-1, Shirokane, Minato-ku, Tokyo 108-8641, Japan; Discovery Research Laboratories, Nippon Chemiphar Co., Ltd., 1-22, Hiko Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from delta opioid receptor in mouse whole brain without cerebellum membrane				Bioorg Med Chem Lett 27: 2742-2745 (2017) Article DOI: 10.1016/j.bmcl.2017.04.059 BindingDB Entry DOI: 10.7270/Q2H134GP
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50254131 (CHEMBL4094845) Show SMILES [H][C@]12CN(C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)c1cnccn1 |r,TLB:17:18:4.6.5:8.1,16:17:7:21.20.19,6:7:21.20.19:10.11.17,8:7:21.20.19:10.11.17,2:1:18:4.6.5,3:4:18:8.1,22:21:7:10.11.17,THB:12:11:7:21.20.19,19:18:4.6.5:8.1| Show InChI InChI=1S/C27H32N4O/c32-20-4-3-18-11-23-26-6-5-22-25(19(13-26)16-31(22)24-14-28-8-9-29-24)27(26,21(18)12-20)7-10-30(23)15-17-1-2-17/h3-4,8-9,12,14,17,19,22-23,25,32H,1-2,5-7,10-11,13,15-16H2/t19-,22?,23?,25?,26?,27?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.479	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]U-69,593 from human recombinant KOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Homo sapiens (Human))	BDBM50031953 (3-(2-Ethyl-6-methoxy-[1,5]naphthyridin-4-yloxymeth...) Show SMILES CCc1cc(OCc2ccc3c(cc4ccccc4c(=O)c3c2)-c2nnn[nH]2)c2nc(OC)ccc2n1 Show InChI InChI=1S/C28H22N6O3/c1-3-18-14-24(26-23(29-18)10-11-25(30-26)36-2)37-15-16-8-9-20-21(12-16)27(35)19-7-5-4-6-17(19)13-22(20)28-31-33-34-32-28/h4-14H,3,15H2,1-2H3,(H,31,32,33,34)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	0.480	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Shionogi & Co., Ltd. Curated by ChEMBL					Assay Description Ability to displace [125I]-AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1				J Med Chem 38: 2728-41 (1995) BindingDB Entry DOI: 10.7270/Q23B5Z5Q
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Homo sapiens (Human))	BDBM50031957 (5,7-Dimethyl-2-propyl-3-[11-(1H-tetrazol-5-yl)-5H-...) Show SMILES CCCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(Cc3ccccc3C=C2c2nnn[nH]2)c1 |c:30| Show InChI InChI=1S/C28H27N7/c1-4-7-25-30-26-17(2)12-18(3)29-28(26)35(25)16-19-10-11-23-22(13-19)14-20-8-5-6-9-21(20)15-24(23)27-31-33-34-32-27/h5-6,8-13,15H,4,7,14,16H2,1-3H3,(H,31,32,33,34)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	0.490	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Shionogi & Co., Ltd. Curated by ChEMBL					Assay Description Ability to displace [125I]-AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1				J Med Chem 38: 2728-41 (1995) BindingDB Entry DOI: 10.7270/Q23B5Z5Q
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50253158 (CHEMBL4100943) Show SMILES [H][C@]12CN(Cc3ccccc3)C3CCC4(O1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23 |r,TLB:3:11:25:15.1,2:1:25:12.13.11,13:14:28.27.26:17.24.18,24:25:15.1:12.13.11,29:28:14:17.24.18,23:24:28.27.26:14,THB:26:25:15.1:12.13.11| Show InChI InChI=1S/C29H34N2O2/c32-22-9-8-21-14-26-29-11-10-24-27(25(33-29)18-31(24)17-19-4-2-1-3-5-19)28(29,23(21)15-22)12-13-30(26)16-20-6-7-20/h1-5,8-9,15,20,24-27,32H,6-7,10-14,16-18H2/t24?,25-,26?,27?,28?,29?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.501	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Laboratory of Medicinal Chemistry, School of Pharmacy, Kitasato University, 5-9-1, Shirokane, Minato-ku, Tokyo 108-8641, Japan; Discovery Research Laboratories, Nippon Chemiphar Co., Ltd., 1-22, Hiko Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from human delta opioid receptor expressed in CHO cells				Bioorg Med Chem Lett 27: 2742-2745 (2017) Article DOI: 10.1016/j.bmcl.2017.04.059 BindingDB Entry DOI: 10.7270/Q2H134GP
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50254120 (CHEMBL4076681) Show SMILES [H][C@]12CN(C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)C(=O)Oc1ccccc1 |r,TLB:17:18:4.6.5:8.1,16:17:7:21.20.19,6:7:21.20.19:10.11.17,8:7:21.20.19:10.11.17,2:1:18:4.6.5,3:4:18:8.1,22:21:7:10.11.17,THB:12:11:7:21.20.19,19:18:4.6.5:8.1| Show InChI InChI=1S/C30H34N2O3/c33-22-9-8-20-14-26-29-11-10-25-27(30(29,24(20)15-22)12-13-31(26)17-19-6-7-19)21(16-29)18-32(25)28(34)35-23-4-2-1-3-5-23/h1-5,8-9,15,19,21,25-27,33H,6-7,10-14,16-18H2/t21-,25?,26?,27?,29?,30?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.522	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]U-69,593 from human recombinant KOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Delta-type opioid receptor (MOUSE)	BDBM50010658 (CHEMBL3264747) Show SMILES [H][C@]12O[C@]34CC[C@@]5(OCOc6c(O)ccc7C[C@@]3([H])N(CC3CC3)CC[C@]4(c67)[C@]15[H])N(C2=O)c1ccccc1 |r,TLB:20:19:3:27.15.16,THB:7:6:26:1.2| Show InChI InChI=1S/C29H30N2O5/c32-20-9-8-18-14-21-28-10-11-29-25(24(36-28)26(33)31(29)19-4-2-1-3-5-19)27(28,22(18)23(20)34-16-35-29)12-13-30(21)15-17-6-7-17/h1-5,8-9,17,21,24-25,32H,6-7,10-16H2/t21-,24+,25+,27+,28-,29+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	0.534	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Kitasato University Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from delta opioid receptor in mouse whole brain cerebellum membrane				ACS Med Chem Lett 5: 368-72 (2014) Article DOI: 10.1021/ml400491k BindingDB Entry DOI: 10.7270/Q2GF0W23
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50254133 (CHEMBL4076632) Show SMILES [H][C@]12CN(C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)C(=O)Nc1ccccc1 |r,TLB:17:18:4.6.5:8.1,16:17:7:21.20.19,6:7:21.20.19:10.11.17,8:7:21.20.19:10.11.17,2:1:18:4.6.5,3:4:18:8.1,22:21:7:10.11.17,THB:12:11:7:21.20.19,19:18:4.6.5:8.1| Show InChI InChI=1S/C30H35N3O2/c34-23-9-8-20-14-26-29-11-10-25-27(30(29,24(20)15-23)12-13-32(26)17-19-6-7-19)21(16-29)18-33(25)28(35)31-22-4-2-1-3-5-22/h1-5,8-9,15,19,21,25-27,34H,6-7,10-14,16-18H2,(H,31,35)/t21-,25?,26?,27?,29?,30?/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.545	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from human recombinant MOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Mu-type opioid receptor (MOUSE)	BDBM50253139 (CHEMBL4096314) Show SMILES [H][C@]12CN(C3CCC4(O1)C1Cc5ccc(O)cc5C4(CCN1CCc1ccccc1)C23)C(=O)c1ccccc1 |r,TLB:3:4:18:8.1,2:1:18:5.6.4,6:7:21.20.19:10.17.11,17:18:8.1:5.6.4,16:17:21.20.19:7,THB:19:18:8.1:5.6.4| Show InChI InChI=1S/C33H34N2O3/c36-25-12-11-24-19-29-33-15-13-27-30(28(38-33)21-35(27)31(37)23-9-5-2-6-10-23)32(33,26(24)20-25)16-18-34(29)17-14-22-7-3-1-4-8-22/h1-12,20,27-30,36H,13-19,21H2/t27?,28-,29?,30?,32?,33?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	MMDB PC cid PC sid UniChem Patents	Article PubMed	0.548	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Laboratory of Medicinal Chemistry, School of Pharmacy, Kitasato University, 5-9-1, Shirokane, Minato-ku, Tokyo 108-8641, Japan; Discovery Research Laboratories, Nippon Chemiphar Co., Ltd., 1-22, Hiko Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from mu opioid receptor in mouse whole brain without cerebellum membrane				Bioorg Med Chem Lett 27: 2742-2745 (2017) Article DOI: 10.1016/j.bmcl.2017.04.059 BindingDB Entry DOI: 10.7270/Q2H134GP
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50254123 (CHEMBL4068691) Show SMILES [H][C@]12CN(C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)C(=O)c1ccccn1 |r,TLB:17:18:4.6.5:8.1,16:17:7:21.20.19,6:7:21.20.19:10.11.17,8:7:21.20.19:10.11.17,2:1:18:4.6.5,3:4:18:8.1,22:21:7:10.11.17,THB:12:11:7:21.20.19,19:18:4.6.5:8.1| Show InChI InChI=1S/C29H33N3O2/c33-21-7-6-19-13-25-28-9-8-24-26(20(15-28)17-32(24)27(34)23-3-1-2-11-30-23)29(28,22(19)14-21)10-12-31(25)16-18-4-5-18/h1-3,6-7,11,14,18,20,24-26,33H,4-5,8-10,12-13,15-17H2/t20-,24?,25?,26?,28?,29?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	0.564	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]U-69,593 from human recombinant KOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50254132 (CHEMBL4083940) Show SMILES [H][C@]12CN(C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)C(=O)c1ccccc1 |r,TLB:17:18:4.6.5:8.1,16:17:7:21.20.19,6:7:21.20.19:10.11.17,8:7:21.20.19:10.11.17,2:1:18:4.6.5,3:4:18:8.1,22:21:7:10.11.17,THB:12:11:7:21.20.19,19:18:4.6.5:8.1| Show InChI InChI=1S/C30H34N2O2/c33-23-9-8-21-14-26-29-11-10-25-27(22(16-29)18-32(25)28(34)20-4-2-1-3-5-20)30(29,24(21)15-23)12-13-31(26)17-19-6-7-19/h1-5,8-9,15,19,22,25-27,33H,6-7,10-14,16-18H2/t22-,25?,26?,27?,29?,30?/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.578	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from human recombinant MOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Mu-type opioid receptor (GUINEA PIG)	BDBM50274257 ((2E)-N-[(1S,5R,13R,14R,17S)-4-(cyclopropylmethyl)-...) Show SMILES CN([C@@H]1CC[C@@]2(O)[C@H]3Cc4ccc(O)c5O[C@@H]1[C@]2(CCN3CC1CC1)c45)C(=O)\C=C\c1ccco1 |r,TLB:4:5:9.25.8:18.20.19,THB:6:5:9.25.8:18.20.19| Show InChI InChI=1S/C28H32N2O5/c1-29(23(32)9-7-19-3-2-14-34-19)20-10-11-28(33)22-15-18-6-8-21(31)25-24(18)27(28,26(20)35-25)12-13-30(22)16-17-4-5-17/h2-3,6-9,14,17,20,22,26,31,33H,4-5,10-13,15-16H2,1H3/b9-7+/t20-,22-,26+,27+,28-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	0.582	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Kitasato University Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from guinea pig forebrain mu opioid receptor				Bioorg Med Chem Lett 20: 121-4 (2010) Article DOI: 10.1016/j.bmcl.2009.11.027 BindingDB Entry DOI: 10.7270/Q2GX4CJH
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50254130 (CHEMBL4061334) Show SMILES [H][C@]12CN(Cc3ccccc3)C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23 |r,TLB:24:25:11.13.12:15.1,23:24:14:28.27.26,13:14:28.27.26:17.18.24,15:14:28.27.26:17.18.24,2:1:25:11.13.12,3:11:25:15.1,29:28:14:17.18.24,THB:19:18:14:28.27.26,26:25:11.13.12:15.1| Show InChI InChI=1S/C30H36N2O/c33-24-9-8-22-14-27-29-11-10-26-28(23(16-29)19-32(26)18-20-4-2-1-3-5-20)30(29,25(22)15-24)12-13-31(27)17-21-6-7-21/h1-5,8-9,15,21,23,26-28,33H,6-7,10-14,16-19H2/t23-,26?,27?,28?,29?,30?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	MMDB PC cid PC sid UniChem Patents Similars	Article PubMed	0.585	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from human recombinant DOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50253129 (CHEMBL4066752) Show SMILES [H][C@]12CN(C3CCC4(O1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)C(=O)c1ccccc1 |r,TLB:3:4:18:8.1,2:1:18:5.6.4,6:7:21.20.19:10.17.11,17:18:8.1:5.6.4,22:21:7:10.17.11,16:17:21.20.19:7,THB:19:18:8.1:5.6.4| Show InChI InChI=1S/C29H32N2O3/c32-21-9-8-20-14-25-29-11-10-23-26(24(34-29)17-31(23)27(33)19-4-2-1-3-5-19)28(29,22(20)15-21)12-13-30(25)16-18-6-7-18/h1-5,8-9,15,18,23-26,32H,6-7,10-14,16-17H2/t23?,24-,25?,26?,28?,29?/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	0.627	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Laboratory of Medicinal Chemistry, School of Pharmacy, Kitasato University, 5-9-1, Shirokane, Minato-ku, Tokyo 108-8641, Japan; Discovery Research Laboratories, Nippon Chemiphar Co., Ltd., 1-22, Hiko Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from human mu opioid receptor expressed in CHO cells				Bioorg Med Chem Lett 27: 2742-2745 (2017) Article DOI: 10.1016/j.bmcl.2017.04.059 BindingDB Entry DOI: 10.7270/Q2H134GP
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Homo sapiens (Human))	BDBM50031960 (3-(2-Ethyl-quinolin-4-yloxymethyl)-11-(1H-tetrazol...) Show SMILES CCc1cc(OCc2ccc3c(cc4ccccc4c(=O)c3c2)-c2nnn[nH]2)c2ccccc2n1 Show InChI InChI=1S/C28H21N5O2/c1-2-19-15-26(22-9-5-6-10-25(22)29-19)35-16-17-11-12-21-23(13-17)27(34)20-8-4-3-7-18(20)14-24(21)28-30-32-33-31-28/h3-15H,2,16H2,1H3,(H,30,31,32,33)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.650	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Shionogi & Co., Ltd. Curated by ChEMBL					Assay Description Ability to displace [125I]-AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1				J Med Chem 38: 2728-41 (1995) BindingDB Entry DOI: 10.7270/Q23B5Z5Q
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50253140 (CHEMBL4081856) Show SMILES [H][C@]12CN(C3CCC4(O1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)S(=O)(=O)c1ccccc1 |r,TLB:16:17:21.20.19:7,3:4:18:8.1,2:1:18:5.6.4,6:7:21.20.19:10.17.11,17:18:8.1:5.6.4,THB:19:18:8.1:5.6.4| Show InChI InChI=1S/C28H32N2O4S/c31-20-9-8-19-14-25-28-11-10-23-26(27(28,22(19)15-20)12-13-29(25)16-18-6-7-18)24(34-28)17-30(23)35(32,33)21-4-2-1-3-5-21/h1-5,8-9,15,18,23-26,31H,6-7,10-14,16-17H2/t23?,24-,25?,26?,27?,28?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.658	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Laboratory of Medicinal Chemistry, School of Pharmacy, Kitasato University, 5-9-1, Shirokane, Minato-ku, Tokyo 108-8641, Japan; Discovery Research Laboratories, Nippon Chemiphar Co., Ltd., 1-22, Hiko Curated by ChEMBL					Assay Description Displacement of [3H]U-69,593 from human kappa opioid receptor expressed in CHO cells				Bioorg Med Chem Lett 27: 2742-2745 (2017) Article DOI: 10.1016/j.bmcl.2017.04.059 BindingDB Entry DOI: 10.7270/Q2H134GP
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Homo sapiens (Human))	BDBM50031961 (3-(2-Ethyl-5,7-dimethyl-imidazo[4,5-b]pyridin-3-yl...) Show SMILES CCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(cc3ccccc3c(=O)c2c1)-c1nnn[nH]1 Show InChI InChI=1S/C27H23N7O/c1-4-23-29-24-15(2)11-16(3)28-27(24)34(23)14-17-9-10-20-21(12-17)25(35)19-8-6-5-7-18(19)13-22(20)26-30-32-33-31-26/h5-13H,4,14H2,1-3H3,(H,30,31,32,33)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.660	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Shionogi & Co., Ltd. Curated by ChEMBL					Assay Description Ability to displace [125I]-AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1				J Med Chem 38: 2728-41 (1995) BindingDB Entry DOI: 10.7270/Q23B5Z5Q
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Homo sapiens (Human))	BDBM50031955 (5,7-Dimethyl-2-propyl-3-[11-(1H-tetrazol-5-yl)-dib...) Show SMILES CCCc1nc2c(C)cc(C)nc2n1Cc1ccc2c(Oc3ccccc3C=C2c2nnn[nH]2)c1 |c:30| Show InChI InChI=1S/C27H25N7O/c1-4-7-24-29-25-16(2)12-17(3)28-27(25)34(24)15-18-10-11-20-21(26-30-32-33-31-26)14-19-8-5-6-9-22(19)35-23(20)13-18/h5-6,8-14H,4,7,15H2,1-3H3,(H,30,31,32,33)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	0.700	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Shionogi & Co., Ltd. Curated by ChEMBL					Assay Description Ability to displace [125I]-AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1				J Med Chem 38: 2728-41 (1995) BindingDB Entry DOI: 10.7270/Q23B5Z5Q
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50254123 (CHEMBL4068691) Show SMILES [H][C@]12CN(C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)C(=O)c1ccccn1 |r,TLB:17:18:4.6.5:8.1,16:17:7:21.20.19,6:7:21.20.19:10.11.17,8:7:21.20.19:10.11.17,2:1:18:4.6.5,3:4:18:8.1,22:21:7:10.11.17,THB:12:11:7:21.20.19,19:18:4.6.5:8.1| Show InChI InChI=1S/C29H33N3O2/c33-21-7-6-19-13-25-28-9-8-24-26(20(15-28)17-32(24)27(34)23-3-1-2-11-30-23)29(28,22(19)14-21)10-12-31(25)16-18-4-5-18/h1-3,6-7,11,14,18,20,24-26,33H,4-5,8-10,12-13,15-17H2/t20-,24?,25?,26?,28?,29?/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	0.726	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from human recombinant MOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Delta-type opioid receptor (MOUSE)	BDBM50253135 (CHEMBL4060073) Show SMILES [H][C@]12CN(C3CCC4(O1)C1Cc5ccc(O)cc5C4(CCN1CC(C)C)C23)C(=O)c1ccccc1 |r,TLB:3:4:18:8.1,2:1:18:5.6.4,6:7:21.20.19:10.17.11,17:18:8.1:5.6.4,16:17:21.20.19:7,THB:19:18:8.1:5.6.4| Show InChI InChI=1S/C29H34N2O3/c1-18(2)16-30-13-12-28-22-15-21(32)9-8-20(22)14-25(30)29(28)11-10-23-26(28)24(34-29)17-31(23)27(33)19-6-4-3-5-7-19/h3-9,15,18,23-26,32H,10-14,16-17H2,1-2H3/t23?,24-,25?,26?,28?,29?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	0.760	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Laboratory of Medicinal Chemistry, School of Pharmacy, Kitasato University, 5-9-1, Shirokane, Minato-ku, Tokyo 108-8641, Japan; Discovery Research Laboratories, Nippon Chemiphar Co., Ltd., 1-22, Hiko Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from delta opioid receptor in mouse whole brain without cerebellum membrane				Bioorg Med Chem Lett 27: 2742-2745 (2017) Article DOI: 10.1016/j.bmcl.2017.04.059 BindingDB Entry DOI: 10.7270/Q2H134GP
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50254122 (CHEMBL4098662) Show SMILES [H][C@]12CN(CC3CCCCC3)C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23 |r,TLB:24:25:11.13.12:15.1,23:24:14:28.27.26,13:14:28.27.26:17.18.24,15:14:28.27.26:17.18.24,2:1:25:11.13.12,3:11:25:15.1,29:28:14:17.18.24,THB:19:18:14:28.27.26,26:25:11.13.12:15.1| Show InChI InChI=1S/C30H42N2O/c33-24-9-8-22-14-27-29-11-10-26-28(23(16-29)19-32(26)18-20-4-2-1-3-5-20)30(29,25(22)15-24)12-13-31(27)17-21-6-7-21/h8-9,15,20-21,23,26-28,33H,1-7,10-14,16-19H2/t23-,26?,27?,28?,29?,30?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.781	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]U-69,593 from human recombinant KOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50254131 (CHEMBL4094845) Show SMILES [H][C@]12CN(C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)c1cnccn1 |r,TLB:17:18:4.6.5:8.1,16:17:7:21.20.19,6:7:21.20.19:10.11.17,8:7:21.20.19:10.11.17,2:1:18:4.6.5,3:4:18:8.1,22:21:7:10.11.17,THB:12:11:7:21.20.19,19:18:4.6.5:8.1| Show InChI InChI=1S/C27H32N4O/c32-20-4-3-18-11-23-26-6-5-22-25(19(13-26)16-31(22)24-14-28-8-9-29-24)27(26,21(18)12-20)7-10-30(23)15-17-1-2-17/h3-4,8-9,12,14,17,19,22-23,25,32H,1-2,5-7,10-11,13,15-16H2/t19-,22?,23?,25?,26?,27?/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.813	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from human recombinant MOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50254120 (CHEMBL4076681) Show SMILES [H][C@]12CN(C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)C(=O)Oc1ccccc1 |r,TLB:17:18:4.6.5:8.1,16:17:7:21.20.19,6:7:21.20.19:10.11.17,8:7:21.20.19:10.11.17,2:1:18:4.6.5,3:4:18:8.1,22:21:7:10.11.17,THB:12:11:7:21.20.19,19:18:4.6.5:8.1| Show InChI InChI=1S/C30H34N2O3/c33-22-9-8-20-14-26-29-11-10-25-27(30(29,24(20)15-22)12-13-31(26)17-19-6-7-19)21(16-29)18-32(25)28(34)35-23-4-2-1-3-5-23/h1-5,8-9,15,19,21,25-27,33H,6-7,10-14,16-18H2/t21-,25?,26?,27?,29?,30?/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.826	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from human recombinant MOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50254120 (CHEMBL4076681) Show SMILES [H][C@]12CN(C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)C(=O)Oc1ccccc1 |r,TLB:17:18:4.6.5:8.1,16:17:7:21.20.19,6:7:21.20.19:10.11.17,8:7:21.20.19:10.11.17,2:1:18:4.6.5,3:4:18:8.1,22:21:7:10.11.17,THB:12:11:7:21.20.19,19:18:4.6.5:8.1| Show InChI InChI=1S/C30H34N2O3/c33-22-9-8-20-14-26-29-11-10-25-27(30(29,24(20)15-22)12-13-31(26)17-19-6-7-19)21(16-29)18-32(25)28(34)35-23-4-2-1-3-5-23/h1-5,8-9,15,19,21,25-27,33H,6-7,10-14,16-18H2/t21-,25?,26?,27?,29?,30?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.833	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from human recombinant DOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Mu-type opioid receptor (MOUSE)	BDBM50253136 (CHEMBL4075409) Show SMILES [H][C@]12CN(C3CCC4(O1)C1Cc5ccc(O)cc5C4(CCN1CC=C)C23)C(=O)c1ccccc1 |r,TLB:3:4:18:8.1,2:1:18:5.6.4,6:7:21.20.19:10.17.11,17:18:8.1:5.6.4,16:17:21.20.19:7,THB:19:18:8.1:5.6.4| Show InChI InChI=1S/C28H30N2O3/c1-2-13-29-14-12-27-21-16-20(31)9-8-19(21)15-24(29)28(27)11-10-22-25(27)23(33-28)17-30(22)26(32)18-6-4-3-5-7-18/h2-9,16,22-25,31H,1,10-15,17H2/t22?,23-,24?,25?,27?,28?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	0.833	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Laboratory of Medicinal Chemistry, School of Pharmacy, Kitasato University, 5-9-1, Shirokane, Minato-ku, Tokyo 108-8641, Japan; Discovery Research Laboratories, Nippon Chemiphar Co., Ltd., 1-22, Hiko Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from mu opioid receptor in mouse whole brain without cerebellum membrane				Bioorg Med Chem Lett 27: 2742-2745 (2017) Article DOI: 10.1016/j.bmcl.2017.04.059 BindingDB Entry DOI: 10.7270/Q2H134GP
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50254121 (CHEMBL4067629) Show SMILES [H][C@]12CN(C3CCC4(C1)C1Cc5ccc(O)cc5C4(CCN1CC1CC1)C23)c1ccccc1 |r,TLB:17:18:4.6.5:8.1,16:17:7:21.20.19,6:7:21.20.19:10.11.17,8:7:21.20.19:10.11.17,2:1:18:4.6.5,3:4:18:8.1,22:21:7:10.11.17,THB:12:11:7:21.20.19,19:18:4.6.5:8.1| Show InChI InChI=1S/C29H34N2O/c32-23-9-8-20-14-26-28-11-10-25-27(21(16-28)18-31(25)22-4-2-1-3-5-22)29(28,24(20)15-23)12-13-30(26)17-19-6-7-19/h1-5,8-9,15,19,21,25-27,32H,6-7,10-14,16-18H2/t21-,25?,26?,27?,28?,29?/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.953	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Chemiphar Co., Ltd Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from human recombinant MOR expressed in CHO cell membranes				Bioorg Med Chem Lett 27: 3495-3498 (2017) Article DOI: 10.1016/j.bmcl.2017.05.072 BindingDB Entry DOI: 10.7270/Q25H7JPK
					More data for this Ligand-Target Pair
Delta-type opioid receptor (MOUSE)	BDBM50039029 ((+)-4-((alpha R)-((2S,5R)-4-allyl-2,5-dimethylpipe...) Show SMILES CCN(CC)C(=O)c1ccc(cc1)[C@@H](N1C[C@@H](C)N(CC=C)C[C@@H]1C)c1cccc(OC)c1 |r| Show InChI InChI=1S/C28H39N3O2/c1-7-17-30-19-22(5)31(20-21(30)4)27(25-11-10-12-26(18-25)33-6)23-13-15-24(16-14-23)28(32)29(8-2)9-3/h7,10-16,18,21-22,27H,1,8-9,17,19-20H2,2-6H3/t21-,22+,27-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	1	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Kitasato University Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from delta opioid receptor in mouse whole brain cerebellum membrane				ACS Med Chem Lett 5: 368-72 (2014) Article DOI: 10.1021/ml400491k BindingDB Entry DOI: 10.7270/Q2GF0W23
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Homo sapiens (Human))	BDBM50031964 (3-[(5-Ethyl-pyrazolo[1,5-a]pyrimidin-7-ylamino)-me...) Show SMILES CCc1cc(NCc2ccc3c(cc4ccccc4c(=O)c3c2)-c2nnn[nH]2)n2nccc2n1 Show InChI InChI=1S/C25H20N8O/c1-2-17-13-23(33-22(28-17)9-10-27-33)26-14-15-7-8-19-20(11-15)24(34)18-6-4-3-5-16(18)12-21(19)25-29-31-32-30-25/h3-13,26H,2,14H2,1H3,(H,29,30,31,32)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	1.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Shionogi & Co., Ltd. Curated by ChEMBL					Assay Description Ability to displace [125I]-AII binding to COS cells transfected with a cDNA encoding human Angiotensin II receptor, type 1				J Med Chem 38: 2728-41 (1995) BindingDB Entry DOI: 10.7270/Q23B5Z5Q
					More data for this Ligand-Target Pair

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