Compile Data Set for Download or QSAR

Found 21 hits Enz. Inhib. hit(s) with all data for entry = 50035031   

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 (Rattus norvegicus (rat))	BDBM21864 ((21R)-22-(cyclopropylmethyl)-14-oxa-11,22-diazahep...) Show SMILES [H][C@@]12Cc3ccc(O)c4OC5c6[nH]c7ccccc7c6CC1(O)C5(CCN2CC1CC1)c34 |THB:27:26:21:31.2.3| Show InChI InChI=1S/C26H26N2O3/c29-19-8-7-15-11-20-26(30)12-17-16-3-1-2-4-18(16)27-22(17)24-25(26,21(15)23(19)31-24)9-10-28(20)13-14-5-6-14/h1-4,7-8,14,20,24,27,29-30H,5-6,9-13H2/t20-,24?,25?,26?/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	PubMed	0.0620	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to inhibit binding of SNC80 to delta opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM21864 ((21R)-22-(cyclopropylmethyl)-14-oxa-11,22-diazahep...) Show SMILES [H][C@@]12Cc3ccc(O)c4OC5c6[nH]c7ccccc7c6CC1(O)C5(CCN2CC1CC1)c34 |THB:27:26:21:31.2.3| Show InChI InChI=1S/C26H26N2O3/c29-19-8-7-15-11-20-26(30)12-17-16-3-1-2-4-18(16)27-22(17)24-25(26,21(15)23(19)31-24)9-10-28(20)13-14-5-6-14/h1-4,7-8,14,20,24,27,29-30H,5-6,9-13H2/t20-,24?,25?,26?/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	PubMed	0.220	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]U-69593 from kappa opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM21864 ((21R)-22-(cyclopropylmethyl)-14-oxa-11,22-diazahep...) Show SMILES [H][C@@]12Cc3ccc(O)c4OC5c6[nH]c7ccccc7c6CC1(O)C5(CCN2CC1CC1)c34 |THB:27:26:21:31.2.3| Show InChI InChI=1S/C26H26N2O3/c29-19-8-7-15-11-20-26(30)12-17-16-3-1-2-4-18(16)27-22(17)24-25(26,21(15)23(19)31-24)9-10-28(20)13-14-5-6-14/h1-4,7-8,14,20,24,27,29-30H,5-6,9-13H2/t20-,24?,25?,26?/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	PubMed	3.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]DADL from delta opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM50366623 (CHEMBL1744389) Show SMILES COc1ccc2C[C@H]3N(CC4CC4)CC[C@@]45C(Oc1c24)c1[nH]c2ccccc2c1C[C@@]35O |r| Show InChI InChI=1S/C27H28N2O3/c1-31-20-9-8-16-12-21-27(30)13-18-17-4-2-3-5-19(17)28-23(18)25-26(27,22(16)24(20)32-25)10-11-29(21)14-15-6-7-15/h2-5,8-9,15,21,25,28,30H,6-7,10-14H2,1H3/t21-,25?,26+,27-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	6.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]DAMGO from mu opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM21864 ((21R)-22-(cyclopropylmethyl)-14-oxa-11,22-diazahep...) Show SMILES [H][C@@]12Cc3ccc(O)c4OC5c6[nH]c7ccccc7c6CC1(O)C5(CCN2CC1CC1)c34 |THB:27:26:21:31.2.3| Show InChI InChI=1S/C26H26N2O3/c29-19-8-7-15-11-20-26(30)12-17-16-3-1-2-4-18(16)27-22(17)24-25(26,21(15)23(19)31-24)9-10-28(20)13-14-5-6-14/h1-4,7-8,14,20,24,27,29-30H,5-6,9-13H2/t20-,24?,25?,26?/m0/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	PubMed	8.85	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to inhibit binding of U-69,593 to kappa opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM21864 ((21R)-22-(cyclopropylmethyl)-14-oxa-11,22-diazahep...) Show SMILES [H][C@@]12Cc3ccc(O)c4OC5c6[nH]c7ccccc7c6CC1(O)C5(CCN2CC1CC1)c34 |THB:27:26:21:31.2.3| Show InChI InChI=1S/C26H26N2O3/c29-19-8-7-15-11-20-26(30)12-17-16-3-1-2-4-18(16)27-22(17)24-25(26,21(15)23(19)31-24)9-10-28(20)13-14-5-6-14/h1-4,7-8,14,20,24,27,29-30H,5-6,9-13H2/t20-,24?,25?,26?/m0/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	PubMed	8.90	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]DADL from delta opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM50366623 (CHEMBL1744389) Show SMILES COc1ccc2C[C@H]3N(CC4CC4)CC[C@@]45C(Oc1c24)c1[nH]c2ccccc2c1C[C@@]35O |r| Show InChI InChI=1S/C27H28N2O3/c1-31-20-9-8-16-12-21-27(30)13-18-17-4-2-3-5-19(17)28-23(18)25-26(27,22(16)24(20)32-25)10-11-29(21)14-15-6-7-15/h2-5,8-9,15,21,25,28,30H,6-7,10-14H2,1H3/t21-,25?,26+,27-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	9	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to inhibit binding of SNC80 to delta opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM21864 ((21R)-22-(cyclopropylmethyl)-14-oxa-11,22-diazahep...) Show SMILES [H][C@@]12Cc3ccc(O)c4OC5c6[nH]c7ccccc7c6CC1(O)C5(CCN2CC1CC1)c34 |THB:27:26:21:31.2.3| Show InChI InChI=1S/C26H26N2O3/c29-19-8-7-15-11-20-26(30)12-17-16-3-1-2-4-18(16)27-22(17)24-25(26,21(15)23(19)31-24)9-10-28(20)13-14-5-6-14/h1-4,7-8,14,20,24,27,29-30H,5-6,9-13H2/t20-,24?,25?,26?/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	PubMed	27	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]DAMGO from mu opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM50366621 (CHEMBL1743886) Show SMILES O[C@]12Cc3c([nH]c4ccccc34)C3Oc4c5c(C[C@H]1N(CC1CC1)CC[C@@]235)ccc4OCCCc1ccccc1 |r| Show InChI InChI=1S/C35H36N2O3/c38-35-20-26-25-10-4-5-11-27(25)36-31(26)33-34(35)16-17-37(21-23-12-13-23)29(35)19-24-14-15-28(32(40-33)30(24)34)39-18-6-9-22-7-2-1-3-8-22/h1-5,7-8,10-11,14-15,23,29,33,36,38H,6,9,12-13,16-21H2/t29-,33?,34+,35-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	99	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]DADL from delta opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM50083727 (16-benzyloxy-22-cyclopropylmethyl-14-oxa-11,22-dia...) Show SMILES O[C@]12Cc3c([nH]c4ccccc34)C3Oc4c5c(CC1N(CC1CC1)CC[C@@]235)ccc4OCc1ccccc1 |THB:27:16:1:19.25.24,14:15:1:19.25.24| Show InChI InChI=1S/C33H32N2O3/c36-33-17-24-23-8-4-5-9-25(23)34-29(24)31-32(33)14-15-35(18-20-10-11-20)27(33)16-22-12-13-26(30(38-31)28(22)32)37-19-21-6-2-1-3-7-21/h1-9,12-13,20,27,31,34,36H,10-11,14-19H2/t27?,31?,32-,33+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	103	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]DADL from delta opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50083727 (16-benzyloxy-22-cyclopropylmethyl-14-oxa-11,22-dia...) Show SMILES O[C@]12Cc3c([nH]c4ccccc34)C3Oc4c5c(CC1N(CC1CC1)CC[C@@]235)ccc4OCc1ccccc1 |THB:27:16:1:19.25.24,14:15:1:19.25.24| Show InChI InChI=1S/C33H32N2O3/c36-33-17-24-23-8-4-5-9-25(23)34-29(24)31-32(33)14-15-35(18-20-10-11-20)27(33)16-22-12-13-26(30(38-31)28(22)32)37-19-21-6-2-1-3-7-21/h1-9,12-13,20,27,31,34,36H,10-11,14-19H2/t27?,31?,32-,33+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	396	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]DAMGO from mu opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50366623 (CHEMBL1744389) Show SMILES COc1ccc2C[C@H]3N(CC4CC4)CC[C@@]45C(Oc1c24)c1[nH]c2ccccc2c1C[C@@]35O |r| Show InChI InChI=1S/C27H28N2O3/c1-31-20-9-8-16-12-21-27(30)13-18-17-4-2-3-5-19(17)28-23(18)25-26(27,22(16)24(20)32-25)10-11-29(21)14-15-6-7-15/h2-5,8-9,15,21,25,28,30H,6-7,10-14H2,1H3/t21-,25?,26+,27-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	411	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to inhibit binding of [3H]DAMGO to mu opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM50083727 (16-benzyloxy-22-cyclopropylmethyl-14-oxa-11,22-dia...) Show SMILES O[C@]12Cc3c([nH]c4ccccc34)C3Oc4c5c(CC1N(CC1CC1)CC[C@@]235)ccc4OCc1ccccc1 |THB:27:16:1:19.25.24,14:15:1:19.25.24| Show InChI InChI=1S/C33H32N2O3/c36-33-17-24-23-8-4-5-9-25(23)34-29(24)31-32(33)14-15-35(18-20-10-11-20)27(33)16-22-12-13-26(30(38-31)28(22)32)37-19-21-6-2-1-3-7-21/h1-9,12-13,20,27,31,34,36H,10-11,14-19H2/t27?,31?,32-,33+/m0/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	728	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]U-69593 from kappa opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM50366622 (CHEMBL1202098) Show SMILES OC12Cc3c([nH]c4ccccc34)C3Oc4c5c(CC1N(CC1CC1)CCC235)ccc4OCCc1ccccc1 |TLB:0:1:19.24.25:16.17.15,2:1:19.24.25:16.17.15,THB:27:16:1:19.24.25,14:15:1:19.24.25,20:19:1:16.17.15| Show InChI InChI=1S/C34H34N2O3/c37-34-19-25-24-8-4-5-9-26(24)35-30(25)32-33(34)15-16-36(20-22-10-11-22)28(34)18-23-12-13-27(31(39-32)29(23)33)38-17-14-21-6-2-1-3-7-21/h1-9,12-13,22,28,32,35,37H,10-11,14-20H2	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.04E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]DADL from delta opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM50366623 (CHEMBL1744389) Show SMILES COc1ccc2C[C@H]3N(CC4CC4)CC[C@@]45C(Oc1c24)c1[nH]c2ccccc2c1C[C@@]35O |r| Show InChI InChI=1S/C27H28N2O3/c1-31-20-9-8-16-12-21-27(30)13-18-17-4-2-3-5-19(17)28-23(18)25-26(27,22(16)24(20)32-25)10-11-29(21)14-15-6-7-15/h2-5,8-9,15,21,25,28,30H,6-7,10-14H2,1H3/t21-,25?,26+,27-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.76E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to inhibit binding of U-69,593 to kappa opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50366623 (CHEMBL1744389) Show SMILES COc1ccc2C[C@H]3N(CC4CC4)CC[C@@]45C(Oc1c24)c1[nH]c2ccccc2c1C[C@@]35O |r| Show InChI InChI=1S/C27H28N2O3/c1-31-20-9-8-16-12-21-27(30)13-18-17-4-2-3-5-19(17)28-23(18)25-26(27,22(16)24(20)32-25)10-11-29(21)14-15-6-7-15/h2-5,8-9,15,21,25,28,30H,6-7,10-14H2,1H3/t21-,25?,26+,27-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.51E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to inhibit binding of [3H]DAMGO to mu opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM50366623 (CHEMBL1744389) Show SMILES COc1ccc2C[C@H]3N(CC4CC4)CC[C@@]45C(Oc1c24)c1[nH]c2ccccc2c1C[C@@]35O |r| Show InChI InChI=1S/C27H28N2O3/c1-31-20-9-8-16-12-21-27(30)13-18-17-4-2-3-5-19(17)28-23(18)25-26(27,22(16)24(20)32-25)10-11-29(21)14-15-6-7-15/h2-5,8-9,15,21,25,28,30H,6-7,10-14H2,1H3/t21-,25?,26+,27-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	3.91E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]U-69593 from kappa opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM50366621 (CHEMBL1743886) Show SMILES O[C@]12Cc3c([nH]c4ccccc34)C3Oc4c5c(C[C@H]1N(CC1CC1)CC[C@@]235)ccc4OCCCc1ccccc1 |r| Show InChI InChI=1S/C35H36N2O3/c38-35-20-26-25-10-4-5-11-27(25)36-31(26)33-34(35)16-17-37(21-23-12-13-23)29(35)19-24-14-15-28(32(40-33)30(24)34)39-18-6-9-22-7-2-1-3-8-22/h1-5,7-8,10-11,14-15,23,29,33,36,38H,6,9,12-13,16-21H2/t29-,33?,34+,35-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	>5.32E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]U-69593 from kappa opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50366622 (CHEMBL1202098) Show SMILES OC12Cc3c([nH]c4ccccc34)C3Oc4c5c(CC1N(CC1CC1)CCC235)ccc4OCCc1ccccc1 |TLB:0:1:19.24.25:16.17.15,2:1:19.24.25:16.17.15,THB:27:16:1:19.24.25,14:15:1:19.24.25,20:19:1:16.17.15| Show InChI InChI=1S/C34H34N2O3/c37-34-19-25-24-8-4-5-9-26(24)35-30(25)32-33(34)15-16-36(20-22-10-11-22)28(34)18-23-12-13-27(31(39-32)29(23)33)38-17-14-21-6-2-1-3-7-21/h1-9,12-13,22,28,32,35,37H,10-11,14-20H2	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	>6.25E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]DAMGO from mu opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50366621 (CHEMBL1743886) Show SMILES O[C@]12Cc3c([nH]c4ccccc34)C3Oc4c5c(C[C@H]1N(CC1CC1)CC[C@@]235)ccc4OCCCc1ccccc1 |r| Show InChI InChI=1S/C35H36N2O3/c38-35-20-26-25-10-4-5-11-27(25)36-31(26)33-34(35)16-17-37(21-23-12-13-23)29(35)19-24-14-15-28(32(40-33)30(24)34)39-18-6-9-22-7-2-1-3-8-22/h1-5,7-8,10-11,14-15,23,29,33,36,38H,6,9,12-13,16-21H2/t29-,33?,34+,35-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	>6.25E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]DAMGO from mu opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM50366622 (CHEMBL1202098) Show SMILES OC12Cc3c([nH]c4ccccc34)C3Oc4c5c(CC1N(CC1CC1)CCC235)ccc4OCCc1ccccc1 |TLB:0:1:19.24.25:16.17.15,2:1:19.24.25:16.17.15,THB:27:16:1:19.24.25,14:15:1:19.24.25,20:19:1:16.17.15| Show InChI InChI=1S/C34H34N2O3/c37-34-19-25-24-8-4-5-9-26(24)35-30(25)32-33(34)15-16-36(20-22-10-11-22)28(34)18-23-12-13-27(31(39-32)29(23)33)38-17-14-21-6-2-1-3-7-21/h1-9,12-13,22,28,32,35,37H,10-11,14-20H2	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	>7.04E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]U-69593 from kappa opioid receptor				Bioorg Med Chem Lett 9: 3435-8 (2000) BindingDB Entry DOI: 10.7270/Q2GT5NPZ
					More data for this Ligand-Target Pair