Compile Data Set for Download or QSAR

Found 44 hits Enz. Inhib. hit(s) with all data for entry = 50046957   

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
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50095155 ((S)-1-[(S)-2-Amino-3-(4-hydroxy-phenyl)-propionyl]...) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1ccccc1)C(N)=O |r| Show InChI InChI=1S/C34H38N6O5/c35-26(17-22-12-14-24(41)15-13-22)34(45)40-16-6-11-30(40)33(44)39-29(19-23-20-37-27-10-5-4-9-25(23)27)32(43)38-28(31(36)42)18-21-7-2-1-3-8-21/h1-5,7-10,12-15,20,26,28-30,37,41H,6,11,16-19,35H2,(H2,36,42)(H,38,43)(H,39,44)/t26-,28-,29-,30-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	0.700	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from rat cortical MOR by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50140041 (CHEMBL3765059) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2ccccc2)NC1=O |r| Show InChI InChI=1S/C35H42N6O7/c36-27(18-23-9-13-25(42)14-10-23)32(45)39-28-8-4-5-17-37-31(44)21-38-33(46)29(20-24-11-15-26(43)16-12-24)40-35(48)30(41-34(28)47)19-22-6-2-1-3-7-22/h1-3,6-7,9-16,27-30,42-43H,4-5,8,17-21,36H2,(H,37,44)(H,38,46)(H,39,45)(H,40,48)(H,41,47)/t27-,28+,29-,30-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	0.990	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from rat cortical MOR by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50140039 (CHEMBL3764556) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC1=O |r| Show InChI InChI=1S/C37H43N7O7/c38-28(17-22-8-12-25(45)13-9-22)34(48)42-30-7-3-4-16-39-33(47)21-41-35(49)31(18-23-10-14-26(46)15-11-23)43-37(51)32(44-36(30)50)19-24-20-40-29-6-2-1-5-27(24)29/h1-2,5-6,8-15,20,28,30-32,40,45-46H,3-4,7,16-19,21,38H2,(H,39,47)(H,41,49)(H,42,48)(H,43,51)(H,44,50)/t28-,30+,31-,32-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from rat cortical MOR by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50139929 (CHEMBL3763920) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2cccnc2)NC1=O |r| Show InChI InChI=1S/C34H41N7O7/c35-26(16-21-6-10-24(42)11-7-21)31(45)39-27-5-1-2-15-37-30(44)20-38-32(46)28(17-22-8-12-25(43)13-9-22)40-34(48)29(41-33(27)47)18-23-4-3-14-36-19-23/h3-4,6-14,19,26-29,42-43H,1-2,5,15-18,20,35H2,(H,37,44)(H,38,46)(H,39,45)(H,40,48)(H,41,47)/t26-,27+,28-,29-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from rat cortical MOR by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50139926 (CHEMBL3764157) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCNC(N)=O)NC1=O |r| Show InChI InChI=1S/C32H44N8O8/c33-23(16-19-6-10-21(41)11-7-19)28(44)38-24-4-1-2-14-35-27(43)18-37-29(45)26(17-20-8-12-22(42)13-9-20)40-31(47)25(39-30(24)46)5-3-15-36-32(34)48/h6-13,23-26,41-42H,1-5,14-18,33H2,(H,35,43)(H,37,45)(H,38,44)(H,39,46)(H,40,47)(H3,34,36,48)/t23-,24+,25-,26-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	9	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from rat cortical MOR by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50139928 (CHEMBL3763985) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2ccncc2)NC1=O |r| Show InChI InChI=1S/C34H41N7O7/c35-26(17-21-4-8-24(42)9-5-21)31(45)39-27-3-1-2-14-37-30(44)20-38-32(46)28(18-22-6-10-25(43)11-7-22)40-34(48)29(41-33(27)47)19-23-12-15-36-16-13-23/h4-13,15-16,26-29,42-43H,1-3,14,17-20,35H2,(H,37,44)(H,38,46)(H,39,45)(H,40,48)(H,41,47)/t26-,27+,28-,29-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	9.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from rat cortical MOR by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50140042 (CHEMBL3763495) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CNC(=O)c2ccccc2N)NC1=O |r| Show InChI InChI=1S/C36H44N8O8/c37-26-6-2-1-5-25(26)32(48)40-19-30-36(52)43-29(18-22-10-14-24(46)15-11-22)34(50)41-20-31(47)39-16-4-3-7-28(35(51)44-30)42-33(49)27(38)17-21-8-12-23(45)13-9-21/h1-2,5-6,8-15,27-30,45-46H,3-4,7,16-20,37-38H2,(H,39,47)(H,40,48)(H,41,50)(H,42,49)(H,43,52)(H,44,51)/t27-,28+,29-,30-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	14	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from rat cortical MOR by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50139927 (CHEMBL3765741) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCNC(N)=N)NC1=O |r| Show InChI InChI=1S/C32H45N9O7/c33-23(16-19-6-10-21(42)11-7-19)28(45)39-24-4-1-2-14-36-27(44)18-38-29(46)26(17-20-8-12-22(43)13-9-20)41-31(48)25(40-30(24)47)5-3-15-37-32(34)35/h6-13,23-26,42-43H,1-5,14-18,33H2,(H,36,44)(H,38,46)(H,39,45)(H,40,47)(H,41,48)(H4,34,35,37)/t23-,24+,25-,26-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	17	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from rat cortical MOR by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM50140041 (CHEMBL3765059) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2ccccc2)NC1=O |r| Show InChI InChI=1S/C35H42N6O7/c36-27(18-23-9-13-25(42)14-10-23)32(45)39-28-8-4-5-17-37-31(44)21-38-33(46)29(20-24-11-15-26(43)16-12-24)40-35(48)30(41-34(28)47)19-22-6-2-1-3-7-22/h1-3,6-7,9-16,27-30,42-43H,4-5,8,17-21,36H2,(H,37,44)(H,38,46)(H,39,45)(H,40,48)(H,41,47)/t27-,28+,29-,30-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	39	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from rat cortical DOR after 2.5 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM50140039 (CHEMBL3764556) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC1=O |r| Show InChI InChI=1S/C37H43N7O7/c38-28(17-22-8-12-25(45)13-9-22)34(48)42-30-7-3-4-16-39-33(47)21-41-35(49)31(18-23-10-14-26(46)15-11-23)43-37(51)32(44-36(30)50)19-24-20-40-29-6-2-1-5-27(24)29/h1-2,5-6,8-15,20,28,30-32,40,45-46H,3-4,7,16-19,21,38H2,(H,39,47)(H,41,49)(H,42,48)(H,43,51)(H,44,50)/t28-,30+,31-,32-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	99	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from rat cortical DOR after 2.5 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50140040 (CHEMBL3763905) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2ccc(O)cc2)NC1=O |r| Show InChI InChI=1S/C35H42N6O8/c36-27(17-21-4-10-24(42)11-5-21)32(46)39-28-3-1-2-16-37-31(45)20-38-33(47)29(18-22-6-12-25(43)13-7-22)40-35(49)30(41-34(28)48)19-23-8-14-26(44)15-9-23/h4-15,27-30,42-44H,1-3,16-20,36H2,(H,37,45)(H,38,47)(H,39,46)(H,40,49)(H,41,48)/t27-,28+,29-,30-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	114	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from rat cortical MOR by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM50140040 (CHEMBL3763905) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2ccc(O)cc2)NC1=O |r| Show InChI InChI=1S/C35H42N6O8/c36-27(17-21-4-10-24(42)11-5-21)32(46)39-28-3-1-2-16-37-31(45)20-38-33(47)29(18-22-6-12-25(43)13-7-22)40-35(49)30(41-34(28)48)19-23-8-14-26(44)15-9-23/h4-15,27-30,42-44H,1-3,16-20,36H2,(H,37,45)(H,38,47)(H,39,46)(H,40,49)(H,41,48)/t27-,28+,29-,30-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	171	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from rat cortical DOR after 2.5 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM50095155 ((S)-1-[(S)-2-Amino-3-(4-hydroxy-phenyl)-propionyl]...) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1ccccc1)C(N)=O |r| Show InChI InChI=1S/C34H38N6O5/c35-26(17-22-12-14-24(41)15-13-22)34(45)40-16-6-11-30(40)33(44)39-29(19-23-20-37-27-10-5-4-9-25(23)27)32(43)38-28(31(36)42)18-21-7-2-1-3-8-21/h1-5,7-10,12-15,20,26,28-30,37,41H,6,11,16-19,35H2,(H2,36,42)(H,38,43)(H,39,44)/t26-,28-,29-,30-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	575	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from rat cortical DOR after 2.5 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM50140038 (CHEMBL3764234) Show SMILES [H][C@@]12Cc3ccccc3CN1[C@@H](Cc1ccc(O)cc1)C(=O)NCC(=O)NCCCC[C@@H](NC2=O)C(=O)[C@@H](N)Cc1ccc(O)cc1 |r| Show InChI InChI=1S/C35H41N5O6/c36-28(17-22-8-12-26(41)13-9-22)33(44)29-7-3-4-16-37-32(43)20-38-34(45)30(18-23-10-14-27(42)15-11-23)40-21-25-6-2-1-5-24(25)19-31(40)35(46)39-29/h1-2,5-6,8-15,28-31,41-42H,3-4,7,16-21,36H2,(H,37,43)(H,38,45)(H,39,46)/t28-,29+,30-,31-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	600	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from rat cortical DOR after 2.5 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM50140037 (CHEMBL3763452) Show SMILES [H][C@@]12Cc3ccc(O)cc3CN1[C@@H](Cc1ccc(O)cc1)C(=O)NCC(=O)NCCCC[C@@H](NC2=O)C(=O)[C@@H](N)Cc1ccc(O)cc1 |r| Show InChI InChI=1S/C35H41N5O7/c36-28(15-21-4-9-25(41)10-5-21)33(45)29-3-1-2-14-37-32(44)19-38-34(46)30(16-22-6-11-26(42)12-7-22)40-20-24-17-27(43)13-8-23(24)18-31(40)35(47)39-29/h4-13,17,28-31,41-43H,1-3,14-16,18-20,36H2,(H,37,44)(H,38,46)(H,39,47)/t28-,29+,30-,31-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	631	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from rat cortical DOR after 2.5 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM50140042 (CHEMBL3763495) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CNC(=O)c2ccccc2N)NC1=O |r| Show InChI InChI=1S/C36H44N8O8/c37-26-6-2-1-5-25(26)32(48)40-19-30-36(52)43-29(18-22-10-14-24(46)15-11-22)34(50)41-20-31(47)39-16-4-3-7-28(35(51)44-30)42-33(49)27(38)17-21-8-12-23(45)13-9-21/h1-2,5-6,8-15,27-30,45-46H,3-4,7,16-20,37-38H2,(H,39,47)(H,40,48)(H,41,50)(H,42,49)(H,43,52)(H,44,51)/t27-,28+,29-,30-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	865	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from rat cortical DOR after 2.5 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50140038 (CHEMBL3764234) Show SMILES [H][C@@]12Cc3ccccc3CN1[C@@H](Cc1ccc(O)cc1)C(=O)NCC(=O)NCCCC[C@@H](NC2=O)C(=O)[C@@H](N)Cc1ccc(O)cc1 |r| Show InChI InChI=1S/C35H41N5O6/c36-28(17-22-8-12-26(41)13-9-22)33(44)29-7-3-4-16-37-32(43)20-38-34(45)30(18-23-10-14-27(42)15-11-23)40-21-25-6-2-1-5-24(25)19-31(40)35(46)39-29/h1-2,5-6,8-15,28-31,41-42H,3-4,7,16-21,36H2,(H,37,43)(H,38,45)(H,39,46)/t28-,29+,30-,31-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	991	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from rat cortical MOR by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50140037 (CHEMBL3763452) Show SMILES [H][C@@]12Cc3ccc(O)cc3CN1[C@@H](Cc1ccc(O)cc1)C(=O)NCC(=O)NCCCC[C@@H](NC2=O)C(=O)[C@@H](N)Cc1ccc(O)cc1 |r| Show InChI InChI=1S/C35H41N5O7/c36-28(15-21-4-9-25(41)10-5-21)33(45)29-3-1-2-14-37-32(44)19-38-34(46)30(16-22-6-11-26(42)12-7-22)40-20-24-17-27(43)13-8-23(24)18-31(40)35(47)39-29/h4-13,17,28-31,41-43H,1-3,14-16,18-20,36H2,(H,37,44)(H,38,46)(H,39,47)/t28-,29+,30-,31-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	1.13E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from rat cortical MOR by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM50139929 (CHEMBL3763920) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2cccnc2)NC1=O |r| Show InChI InChI=1S/C34H41N7O7/c35-26(16-21-6-10-24(42)11-7-21)31(45)39-27-5-1-2-15-37-30(44)20-38-32(46)28(17-22-8-12-25(43)13-9-22)40-34(48)29(41-33(27)47)18-23-4-3-14-36-19-23/h3-4,6-14,19,26-29,42-43H,1-2,5,15-18,20,35H2,(H,37,44)(H,38,46)(H,39,45)(H,40,48)(H,41,47)/t26-,27+,28-,29-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.28E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from rat cortical DOR after 2.5 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM50139928 (CHEMBL3763985) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2ccncc2)NC1=O |r| Show InChI InChI=1S/C34H41N7O7/c35-26(17-21-4-8-24(42)9-5-21)31(45)39-27-3-1-2-14-37-30(44)20-38-32(46)28(18-22-6-10-25(43)11-7-22)40-34(48)29(41-33(27)47)19-23-12-15-36-16-13-23/h4-13,15-16,26-29,42-43H,1-3,14,17-20,35H2,(H,37,44)(H,38,46)(H,39,45)(H,40,48)(H,41,47)/t26-,27+,28-,29-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	2.27E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from rat cortical DOR after 2.5 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM50140042 (CHEMBL3763495) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CNC(=O)c2ccccc2N)NC1=O |r| Show InChI InChI=1S/C36H44N8O8/c37-26-6-2-1-5-25(26)32(48)40-19-30-36(52)43-29(18-22-10-14-24(46)15-11-22)34(50)41-20-31(47)39-16-4-3-7-28(35(51)44-30)42-33(49)27(38)17-21-8-12-23(45)13-9-21/h1-2,5-6,8-15,27-30,45-46H,3-4,7,16-20,37-38H2,(H,39,47)(H,40,48)(H,41,50)(H,42,49)(H,43,52)(H,44,51)/t27-,28+,29-,30-/m0/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.23E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]U69,593 from guinea pig KOR after 2 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM50139926 (CHEMBL3764157) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCNC(N)=O)NC1=O |r| Show InChI InChI=1S/C32H44N8O8/c33-23(16-19-6-10-21(41)11-7-19)28(44)38-24-4-1-2-14-35-27(43)18-37-29(45)26(17-20-8-12-22(42)13-9-20)40-31(47)25(39-30(24)46)5-3-15-36-32(34)48/h6-13,23-26,41-42H,1-5,14-18,33H2,(H,35,43)(H,37,45)(H,38,44)(H,39,46)(H,40,47)(H3,34,36,48)/t23-,24+,25-,26-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.32E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from rat cortical DOR after 2.5 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM50140041 (CHEMBL3765059) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2ccccc2)NC1=O |r| Show InChI InChI=1S/C35H42N6O7/c36-27(18-23-9-13-25(42)14-10-23)32(45)39-28-8-4-5-17-37-31(44)21-38-33(46)29(20-24-11-15-26(43)16-12-24)40-35(48)30(41-34(28)47)19-22-6-2-1-3-7-22/h1-3,6-7,9-16,27-30,42-43H,4-5,8,17-21,36H2,(H,37,44)(H,38,46)(H,39,45)(H,40,48)(H,41,47)/t27-,28+,29-,30-/m0/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	4.45E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]U69,593 from guinea pig KOR after 2 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM50095155 ((S)-1-[(S)-2-Amino-3-(4-hydroxy-phenyl)-propionyl]...) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1ccccc1)C(N)=O |r| Show InChI InChI=1S/C34H38N6O5/c35-26(17-22-12-14-24(41)15-13-22)34(45)40-16-6-11-30(40)33(44)39-29(19-23-20-37-27-10-5-4-9-25(23)27)32(43)38-28(31(36)42)18-21-7-2-1-3-8-21/h1-5,7-10,12-15,20,26,28-30,37,41H,6,11,16-19,35H2,(H2,36,42)(H,38,43)(H,39,44)/t26-,28-,29-,30-/m0/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	5.07E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]U69,593 from guinea pig KOR after 2 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM50139929 (CHEMBL3763920) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2cccnc2)NC1=O |r| Show InChI InChI=1S/C34H41N7O7/c35-26(16-21-6-10-24(42)11-7-21)31(45)39-27-5-1-2-15-37-30(44)20-38-32(46)28(17-22-8-12-25(43)13-9-22)40-34(48)29(41-33(27)47)18-23-4-3-14-36-19-23/h3-4,6-14,19,26-29,42-43H,1-2,5,15-18,20,35H2,(H,37,44)(H,38,46)(H,39,45)(H,40,48)(H,41,47)/t26-,27+,28-,29-/m0/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.33E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]U69,593 from guinea pig KOR after 2 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM50140039 (CHEMBL3764556) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC1=O |r| Show InChI InChI=1S/C37H43N7O7/c38-28(17-22-8-12-25(45)13-9-22)34(48)42-30-7-3-4-16-39-33(47)21-41-35(49)31(18-23-10-14-26(46)15-11-23)43-37(51)32(44-36(30)50)19-24-20-40-29-6-2-1-5-27(24)29/h1-2,5-6,8-15,20,28,30-32,40,45-46H,3-4,7,16-19,21,38H2,(H,39,47)(H,41,49)(H,42,48)(H,43,51)(H,44,50)/t28-,30+,31-,32-/m0/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	8.16E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]U69,593 from guinea pig KOR after 2 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM50139926 (CHEMBL3764157) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCNC(N)=O)NC1=O |r| Show InChI InChI=1S/C32H44N8O8/c33-23(16-19-6-10-21(41)11-7-19)28(44)38-24-4-1-2-14-35-27(43)18-37-29(45)26(17-20-8-12-22(42)13-9-20)40-31(47)25(39-30(24)46)5-3-15-36-32(34)48/h6-13,23-26,41-42H,1-5,14-18,33H2,(H,35,43)(H,37,45)(H,38,44)(H,39,46)(H,40,47)(H3,34,36,48)/t23-,24+,25-,26-/m0/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	8.43E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]U69,593 from guinea pig KOR after 2 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM50139927 (CHEMBL3765741) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCNC(N)=N)NC1=O |r| Show InChI InChI=1S/C32H45N9O7/c33-23(16-19-6-10-21(42)11-7-19)28(45)39-24-4-1-2-14-36-27(44)18-38-29(46)26(17-20-8-12-22(43)13-9-20)41-31(48)25(40-30(24)47)5-3-15-37-32(34)35/h6-13,23-26,42-43H,1-5,14-18,33H2,(H,36,44)(H,38,46)(H,39,45)(H,40,47)(H,41,48)(H4,34,35,37)/t23-,24+,25-,26-/m0/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	8.53E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]U69,593 from guinea pig KOR after 2 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM50139927 (CHEMBL3765741) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCNC(N)=N)NC1=O |r| Show InChI InChI=1S/C32H45N9O7/c33-23(16-19-6-10-21(42)11-7-19)28(45)39-24-4-1-2-14-36-27(44)18-38-29(46)26(17-20-8-12-22(43)13-9-20)41-31(48)25(40-30(24)47)5-3-15-37-32(34)35/h6-13,23-26,42-43H,1-5,14-18,33H2,(H,36,44)(H,38,46)(H,39,45)(H,40,47)(H,41,48)(H4,34,35,37)/t23-,24+,25-,26-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD 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
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DPDPE from rat cortical DOR after 2.5 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM50140040 (CHEMBL3763905) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2ccc(O)cc2)NC1=O |r| Show InChI InChI=1S/C35H42N6O8/c36-27(17-21-4-10-24(42)11-5-21)32(46)39-28-3-1-2-16-37-31(45)20-38-33(47)29(18-22-6-12-25(43)13-7-22)40-35(49)30(41-34(28)48)19-23-8-14-26(44)15-9-23/h4-15,27-30,42-44H,1-3,16-20,36H2,(H,37,45)(H,38,47)(H,39,46)(H,40,49)(H,41,48)/t27-,28+,29-,30-/m0/s1	PDB UniProtKB/SwissProt B.MOAD 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
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]U69,593 from guinea pig KOR after 2 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM50140037 (CHEMBL3763452) Show SMILES [H][C@@]12Cc3ccc(O)cc3CN1[C@@H](Cc1ccc(O)cc1)C(=O)NCC(=O)NCCCC[C@@H](NC2=O)C(=O)[C@@H](N)Cc1ccc(O)cc1 |r| Show InChI InChI=1S/C35H41N5O7/c36-28(15-21-4-9-25(41)10-5-21)33(45)29-3-1-2-14-37-32(44)19-38-34(46)30(16-22-6-11-26(42)12-7-22)40-20-24-17-27(43)13-8-23(24)18-31(40)35(47)39-29/h4-13,17,28-31,41-43H,1-3,14-16,18-20,36H2,(H,37,44)(H,38,46)(H,39,47)/t28-,29+,30-,31-/m0/s1	PDB UniProtKB/SwissProt B.MOAD 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
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]U69,593 from guinea pig KOR after 2 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM50139928 (CHEMBL3763985) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2ccncc2)NC1=O |r| Show InChI InChI=1S/C34H41N7O7/c35-26(17-21-4-8-24(42)9-5-21)31(45)39-27-3-1-2-14-37-30(44)20-38-32(46)28(18-22-6-10-25(43)11-7-22)40-34(48)29(41-33(27)47)19-23-12-15-36-16-13-23/h4-13,15-16,26-29,42-43H,1-3,14,17-20,35H2,(H,37,44)(H,38,46)(H,39,45)(H,40,48)(H,41,47)/t26-,27+,28-,29-/m0/s1	PDB UniProtKB/SwissProt B.MOAD 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
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]U69,593 from guinea pig KOR after 2 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM50140038 (CHEMBL3764234) Show SMILES [H][C@@]12Cc3ccccc3CN1[C@@H](Cc1ccc(O)cc1)C(=O)NCC(=O)NCCCC[C@@H](NC2=O)C(=O)[C@@H](N)Cc1ccc(O)cc1 |r| Show InChI InChI=1S/C35H41N5O6/c36-28(17-22-8-12-26(41)13-9-22)33(44)29-7-3-4-16-37-32(43)20-38-34(45)30(18-23-10-14-27(42)15-11-23)40-21-25-6-2-1-5-24(25)19-31(40)35(46)39-29/h1-2,5-6,8-15,28-31,41-42H,3-4,7,16-21,36H2,(H,37,43)(H,38,45)(H,39,46)/t28-,29+,30-,31-/m0/s1	PDB UniProtKB/SwissProt B.MOAD 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
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]U69,593 from guinea pig KOR after 2 hrs by liquid scintillation counting method				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50140041 (CHEMBL3765059) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2ccccc2)NC1=O |r| Show InChI InChI=1S/C35H42N6O7/c36-27(18-23-9-13-25(42)14-10-23)32(45)39-28-8-4-5-17-37-31(44)21-38-33(46)29(20-24-11-15-26(43)16-12-24)40-35(48)30(41-34(28)47)19-22-6-2-1-3-7-22/h1-3,6-7,9-16,27-30,42-43H,4-5,8,17-21,36H2,(H,37,44)(H,38,46)(H,39,45)(H,40,48)(H,41,47)/t27-,28+,29-,30-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.30	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Agonist activity at human MOR expressed in CHO cells assessed as induction of membrane potential change measured every 3 secs for 30 secs by fluoresc...				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM21015 ((2S)-2-{2-[(2R)-2-[(2S)-2-amino-3-(4-hydroxyphenyl...) Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCC(=O)N(C)[C@@H](Cc1ccccc1)C(=O)NCCO Show InChI InChI=1S/C26H35N5O6/c1-17(30-25(36)21(27)14-19-8-10-20(33)11-9-19)24(35)29-16-23(34)31(2)22(26(37)28-12-13-32)15-18-6-4-3-5-7-18/h3-11,17,21-22,32-33H,12-16,27H2,1-2H3,(H,28,37)(H,29,35)(H,30,36)/t17-,21+,22+/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.5	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Agonist activity at human MOR expressed in CHO cells assessed as induction of membrane potential change measured every 3 secs for 30 secs by fluoresc...				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50000092 ((-)-(etorphine) | (-)-morphine | (1S,5R,13R,14S)-1...) Show SMILES CN1CC[C@@]23[C@H]4Oc5c2c(C[C@@H]1[C@@H]3C=C[C@@H]4O)ccc5O |r,c:16,TLB:13:12:8.9.10:3.2.1| Show InChI InChI=1S/C17H19NO3/c1-18-7-6-17-10-3-5-13(20)16(17)21-15-12(19)4-2-9(14(15)17)8-11(10)18/h2-5,10-11,13,16,19-20H,6-8H2,1H3/t10-,11+,13-,16-,17-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	DrugBank PDB Article PubMed	n/a	n/a	6.30	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Agonist activity at human MOR expressed in CHO cells assessed as induction of membrane potential change measured every 3 secs for 30 secs by fluoresc...				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair				3D Structure (crystal)
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50139929 (CHEMBL3763920) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2cccnc2)NC1=O |r| Show InChI InChI=1S/C34H41N7O7/c35-26(16-21-6-10-24(42)11-7-21)31(45)39-27-5-1-2-15-37-30(44)20-38-32(46)28(17-22-8-12-25(43)13-9-22)40-34(48)29(41-33(27)47)18-23-4-3-14-36-19-23/h3-4,6-14,19,26-29,42-43H,1-2,5,15-18,20,35H2,(H,37,44)(H,38,46)(H,39,45)(H,40,48)(H,41,47)/t26-,27+,28-,29-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	11	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Agonist activity at human MOR expressed in CHO cells assessed as induction of membrane potential change measured every 3 secs for 30 secs by fluoresc...				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50140039 (CHEMBL3764556) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC1=O |r| Show InChI InChI=1S/C37H43N7O7/c38-28(17-22-8-12-25(45)13-9-22)34(48)42-30-7-3-4-16-39-33(47)21-41-35(49)31(18-23-10-14-26(46)15-11-23)43-37(51)32(44-36(30)50)19-24-20-40-29-6-2-1-5-27(24)29/h1-2,5-6,8-15,20,28,30-32,40,45-46H,3-4,7,16-19,21,38H2,(H,39,47)(H,41,49)(H,42,48)(H,43,51)(H,44,50)/t28-,30+,31-,32-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	24	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Agonist activity at human MOR expressed in CHO cells assessed as induction of membrane potential change measured every 3 secs for 30 secs by fluoresc...				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50139928 (CHEMBL3763985) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2ccncc2)NC1=O |r| Show InChI InChI=1S/C34H41N7O7/c35-26(17-21-4-8-24(42)9-5-21)31(45)39-27-3-1-2-14-37-30(44)20-38-32(46)28(18-22-6-10-25(43)11-7-22)40-34(48)29(41-33(27)47)19-23-12-15-36-16-13-23/h4-13,15-16,26-29,42-43H,1-3,14,17-20,35H2,(H,37,44)(H,38,46)(H,39,45)(H,40,48)(H,41,47)/t26-,27+,28-,29-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	32	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Agonist activity at human MOR expressed in CHO cells assessed as induction of membrane potential change measured every 3 secs for 30 secs by fluoresc...				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50139926 (CHEMBL3764157) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCNC(N)=O)NC1=O |r| Show InChI InChI=1S/C32H44N8O8/c33-23(16-19-6-10-21(41)11-7-19)28(44)38-24-4-1-2-14-35-27(43)18-37-29(45)26(17-20-8-12-22(42)13-9-20)40-31(47)25(39-30(24)46)5-3-15-36-32(34)48/h6-13,23-26,41-42H,1-5,14-18,33H2,(H,35,43)(H,37,45)(H,38,44)(H,39,46)(H,40,47)(H3,34,36,48)/t23-,24+,25-,26-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	67	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Agonist activity at human MOR expressed in CHO cells assessed as induction of membrane potential change measured every 3 secs for 30 secs by fluoresc...				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50140040 (CHEMBL3763905) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2ccc(O)cc2)NC1=O |r| Show InChI InChI=1S/C35H42N6O8/c36-27(17-21-4-10-24(42)11-5-21)32(46)39-28-3-1-2-16-37-31(45)20-38-33(47)29(18-22-6-12-25(43)13-7-22)40-35(49)30(41-34(28)48)19-23-8-14-26(44)15-9-23/h4-15,27-30,42-44H,1-3,16-20,36H2,(H,37,45)(H,38,47)(H,39,46)(H,40,49)(H,41,48)/t27-,28+,29-,30-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	70	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Agonist activity at human MOR expressed in CHO cells assessed as induction of membrane potential change measured every 3 secs for 30 secs by fluoresc...				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50139927 (CHEMBL3765741) Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCCNC(=O)CNC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCNC(N)=N)NC1=O |r| Show InChI InChI=1S/C32H45N9O7/c33-23(16-19-6-10-21(42)11-7-19)28(45)39-24-4-1-2-14-36-27(44)18-38-29(46)26(17-20-8-12-22(43)13-9-20)41-31(48)25(40-30(24)47)5-3-15-37-32(34)35/h6-13,23-26,42-43H,1-5,14-18,33H2,(H,36,44)(H,38,46)(H,39,45)(H,40,47)(H,41,48)(H4,34,35,37)/t23-,24+,25-,26-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	131	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Agonist activity at human MOR expressed in CHO cells assessed as induction of membrane potential change measured every 3 secs for 30 secs by fluoresc...				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50140038 (CHEMBL3764234) Show SMILES [H][C@@]12Cc3ccccc3CN1[C@@H](Cc1ccc(O)cc1)C(=O)NCC(=O)NCCCC[C@@H](NC2=O)C(=O)[C@@H](N)Cc1ccc(O)cc1 |r| Show InChI InChI=1S/C35H41N5O6/c36-28(17-22-8-12-26(41)13-9-22)33(44)29-7-3-4-16-37-32(43)20-38-34(45)30(18-23-10-14-27(42)15-11-23)40-21-25-6-2-1-5-24(25)19-31(40)35(46)39-29/h1-2,5-6,8-15,28-31,41-42H,3-4,7,16-21,36H2,(H,37,43)(H,38,45)(H,39,46)/t28-,29+,30-,31-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	678	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Agonist activity at human MOR expressed in CHO cells assessed as induction of membrane potential change measured every 3 secs for 30 secs by fluoresc...				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50140037 (CHEMBL3763452) Show SMILES [H][C@@]12Cc3ccc(O)cc3CN1[C@@H](Cc1ccc(O)cc1)C(=O)NCC(=O)NCCCC[C@@H](NC2=O)C(=O)[C@@H](N)Cc1ccc(O)cc1 |r| Show InChI InChI=1S/C35H41N5O7/c36-28(15-21-4-9-25(41)10-5-21)33(45)29-3-1-2-14-37-32(44)19-38-34(46)30(16-22-6-11-26(42)12-7-22)40-20-24-17-27(43)13-8-23(24)18-31(40)35(47)39-29/h4-13,17,28-31,41-43H,1-3,14-16,18-20,36H2,(H,37,44)(H,38,46)(H,39,47)/t28-,29+,30-,31-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.25E+3	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Agonist activity at human MOR expressed in CHO cells assessed as induction of membrane potential change measured every 3 secs for 30 secs by fluoresc...				J Med Chem 59: 1239-45 (2016) Article DOI: 10.1021/acs.jmedchem.5b01899 BindingDB Entry DOI: 10.7270/Q2CV4KKT
					More data for this Ligand-Target Pair