Compile Data Set for Download or QSAR

Found 20 hits with Last Name = 'metcalf' and Initial = 'md'   

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 (Homo sapiens (Human))	BDBM50221416 (22-methyl-(2S,13R)-14-oxa-11,22-diazaheptacyclo[13...) Show SMILES CN1CC[C@@]23[C@H]4Oc5c2c(C[C@@H]1[C@]3(O)Cc1c4[nH]c2ccccc12)ccc5O |r| Show InChI InChI=1S/C23H22N2O3/c1-25-9-8-22-18-12-6-7-16(26)20(18)28-21(22)19-14(11-23(22,27)17(25)10-12)13-4-2-3-5-15(13)24-19/h2-7,17,21,24,26-27H,8-11H2,1H3/t17-,21+,22+,23-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	0.900	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Displacement of [3H]p-Cl-DPDPE from delta opioid receptor				Bioorg Med Chem Lett 17: 5916-7 (2007) Article DOI: 10.1016/j.bmcl.2007.07.098 BindingDB Entry DOI: 10.7270/Q2RV0NFR
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50221413 ((1S,2S,13R,21R)-7-fluoro-22-methyl-14-oxa-11,22-di...) Show SMILES CN1CC[C@@]23[C@H]4Oc5c2c(C[C@@H]1[C@]3(O)Cc1c4[nH]c2ccc(F)cc12)ccc5O Show InChI InChI=1S/C23H21FN2O3/c1-26-7-6-22-18-11-2-5-16(27)20(18)29-21(22)19-14(10-23(22,28)17(26)8-11)13-9-12(24)3-4-15(13)25-19/h2-5,9,17,21,25,27-28H,6-8,10H2,1H3/t17-,21+,22+,23-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Displacement of [3H]p-Cl-DPDPE from delta opioid receptor				Bioorg Med Chem Lett 17: 5916-7 (2007) Article DOI: 10.1016/j.bmcl.2007.07.098 BindingDB Entry DOI: 10.7270/Q2RV0NFR
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50221417 ((1S,2S,13R,21R)-7-iodo-22-methyl-14-oxa-11,22-diaz...) Show SMILES CN1CC[C@@]23[C@H]4Oc5c2c(C[C@@H]1[C@]3(O)Cc1c4[nH]c2ccc(I)cc12)ccc5O Show InChI InChI=1S/C23H21IN2O3/c1-26-7-6-22-18-11-2-5-16(27)20(18)29-21(22)19-14(10-23(22,28)17(26)8-11)13-9-12(24)3-4-15(13)25-19/h2-5,9,17,21,25,27-28H,6-8,10H2,1H3/t17-,21+,22+,23-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Displacement of [3H]p-Cl-DPDPE from delta opioid receptor				Bioorg Med Chem Lett 17: 5916-7 (2007) Article DOI: 10.1016/j.bmcl.2007.07.098 BindingDB Entry DOI: 10.7270/Q2RV0NFR
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50221414 ((1S,2S,13R,21R)-7-chloro-22-methyl-14-oxa-11,22-di...) Show SMILES CN1CC[C@@]23[C@H]4Oc5c2c(C[C@@H]1[C@]3(O)Cc1c4[nH]c2ccc(Cl)cc12)ccc5O Show InChI InChI=1S/C23H21ClN2O3/c1-26-7-6-22-18-11-2-5-16(27)20(18)29-21(22)19-14(10-23(22,28)17(26)8-11)13-9-12(24)3-4-15(13)25-19/h2-5,9,17,21,25,27-28H,6-8,10H2,1H3/t17-,21+,22+,23-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Displacement of [3H]p-Cl-DPDPE from delta opioid receptor				Bioorg Med Chem Lett 17: 5916-7 (2007) Article DOI: 10.1016/j.bmcl.2007.07.098 BindingDB Entry DOI: 10.7270/Q2RV0NFR
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50221415 ((1S,2S,13R,21R)-7-bromo-22-methyl-14-oxa-11,22-dia...) Show SMILES CN1CC[C@@]23[C@H]4Oc5c2c(C[C@@H]1[C@]3(O)Cc1c4[nH]c2ccc(Br)cc12)ccc5O Show InChI InChI=1S/C23H21BrN2O3/c1-26-7-6-22-18-11-2-5-16(27)20(18)29-21(22)19-14(10-23(22,28)17(26)8-11)13-9-12(24)3-4-15(13)25-19/h2-5,9,17,21,25,27-28H,6-8,10H2,1H3/t17-,21+,22+,23-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	8.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Displacement of [3H]p-Cl-DPDPE from delta opioid receptor				Bioorg Med Chem Lett 17: 5916-7 (2007) Article DOI: 10.1016/j.bmcl.2007.07.098 BindingDB Entry DOI: 10.7270/Q2RV0NFR
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50221413 ((1S,2S,13R,21R)-7-fluoro-22-methyl-14-oxa-11,22-di...) Show SMILES CN1CC[C@@]23[C@H]4Oc5c2c(C[C@@H]1[C@]3(O)Cc1c4[nH]c2ccc(F)cc12)ccc5O Show InChI InChI=1S/C23H21FN2O3/c1-26-7-6-22-18-11-2-5-16(27)20(18)29-21(22)19-14(10-23(22,28)17(26)8-11)13-9-12(24)3-4-15(13)25-19/h2-5,9,17,21,25,27-28H,6-8,10H2,1H3/t17-,21+,22+,23-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	21	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Activity at mu opioid receptor assessed as stimulation of [35S]GTP-gamma-S binding				Bioorg Med Chem Lett 17: 5916-7 (2007) Article DOI: 10.1016/j.bmcl.2007.07.098 BindingDB Entry DOI: 10.7270/Q2RV0NFR
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50221414 ((1S,2S,13R,21R)-7-chloro-22-methyl-14-oxa-11,22-di...) Show SMILES CN1CC[C@@]23[C@H]4Oc5c2c(C[C@@H]1[C@]3(O)Cc1c4[nH]c2ccc(Cl)cc12)ccc5O Show InChI InChI=1S/C23H21ClN2O3/c1-26-7-6-22-18-11-2-5-16(27)20(18)29-21(22)19-14(10-23(22,28)17(26)8-11)13-9-12(24)3-4-15(13)25-19/h2-5,9,17,21,25,27-28H,6-8,10H2,1H3/t17-,21+,22+,23-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	47	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Activity at mu opioid receptor assessed as stimulation of [35S]GTP-gamma-S binding				Bioorg Med Chem Lett 17: 5916-7 (2007) Article DOI: 10.1016/j.bmcl.2007.07.098 BindingDB Entry DOI: 10.7270/Q2RV0NFR
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50221417 ((1S,2S,13R,21R)-7-iodo-22-methyl-14-oxa-11,22-diaz...) Show SMILES CN1CC[C@@]23[C@H]4Oc5c2c(C[C@@H]1[C@]3(O)Cc1c4[nH]c2ccc(I)cc12)ccc5O Show InChI InChI=1S/C23H21IN2O3/c1-26-7-6-22-18-11-2-5-16(27)20(18)29-21(22)19-14(10-23(22,28)17(26)8-11)13-9-12(24)3-4-15(13)25-19/h2-5,9,17,21,25,27-28H,6-8,10H2,1H3/t17-,21+,22+,23-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	66	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Activity at mu opioid receptor assessed as stimulation of [35S]GTP-gamma-S binding				Bioorg Med Chem Lett 17: 5916-7 (2007) Article DOI: 10.1016/j.bmcl.2007.07.098 BindingDB Entry DOI: 10.7270/Q2RV0NFR
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50221415 ((1S,2S,13R,21R)-7-bromo-22-methyl-14-oxa-11,22-dia...) Show SMILES CN1CC[C@@]23[C@H]4Oc5c2c(C[C@@H]1[C@]3(O)Cc1c4[nH]c2ccc(Br)cc12)ccc5O Show InChI InChI=1S/C23H21BrN2O3/c1-26-7-6-22-18-11-2-5-16(27)20(18)29-21(22)19-14(10-23(22,28)17(26)8-11)13-9-12(24)3-4-15(13)25-19/h2-5,9,17,21,25,27-28H,6-8,10H2,1H3/t17-,21+,22+,23-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	71	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Activity at mu opioid receptor assessed as stimulation of [35S]GTP-gamma-S binding				Bioorg Med Chem Lett 17: 5916-7 (2007) Article DOI: 10.1016/j.bmcl.2007.07.098 BindingDB Entry DOI: 10.7270/Q2RV0NFR
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50221416 (22-methyl-(2S,13R)-14-oxa-11,22-diazaheptacyclo[13...) Show SMILES CN1CC[C@@]23[C@H]4Oc5c2c(C[C@@H]1[C@]3(O)Cc1c4[nH]c2ccccc12)ccc5O |r| Show InChI InChI=1S/C23H22N2O3/c1-25-9-8-22-18-12-6-7-16(26)20(18)28-21(22)19-14(11-23(22,27)17(25)10-12)13-4-2-3-5-15(13)24-19/h2-7,17,21,24,26-27H,8-11H2,1H3/t17-,21+,22+,23-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	105	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Activity at mu opioid receptor assessed as stimulation of [35S]GTP-gamma-S binding				Bioorg Med Chem Lett 17: 5916-7 (2007) Article DOI: 10.1016/j.bmcl.2007.07.098 BindingDB Entry DOI: 10.7270/Q2RV0NFR
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50221417 ((1S,2S,13R,21R)-7-iodo-22-methyl-14-oxa-11,22-diaz...) Show SMILES CN1CC[C@@]23[C@H]4Oc5c2c(C[C@@H]1[C@]3(O)Cc1c4[nH]c2ccc(I)cc12)ccc5O Show InChI InChI=1S/C23H21IN2O3/c1-26-7-6-22-18-11-2-5-16(27)20(18)29-21(22)19-14(10-23(22,28)17(26)8-11)13-9-12(24)3-4-15(13)25-19/h2-5,9,17,21,25,27-28H,6-8,10H2,1H3/t17-,21+,22+,23-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	160	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Displacement of [3H]U-69593 from cloned kappa opioid receptor				Bioorg Med Chem Lett 17: 5916-7 (2007) Article DOI: 10.1016/j.bmcl.2007.07.098 BindingDB Entry DOI: 10.7270/Q2RV0NFR
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50221415 ((1S,2S,13R,21R)-7-bromo-22-methyl-14-oxa-11,22-dia...) Show SMILES CN1CC[C@@]23[C@H]4Oc5c2c(C[C@@H]1[C@]3(O)Cc1c4[nH]c2ccc(Br)cc12)ccc5O Show InChI InChI=1S/C23H21BrN2O3/c1-26-7-6-22-18-11-2-5-16(27)20(18)29-21(22)19-14(10-23(22,28)17(26)8-11)13-9-12(24)3-4-15(13)25-19/h2-5,9,17,21,25,27-28H,6-8,10H2,1H3/t17-,21+,22+,23-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	250	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Displacement of [3H]U-69593 from cloned kappa opioid receptor				Bioorg Med Chem Lett 17: 5916-7 (2007) Article DOI: 10.1016/j.bmcl.2007.07.098 BindingDB Entry DOI: 10.7270/Q2RV0NFR
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50221413 ((1S,2S,13R,21R)-7-fluoro-22-methyl-14-oxa-11,22-di...) Show SMILES CN1CC[C@@]23[C@H]4Oc5c2c(C[C@@H]1[C@]3(O)Cc1c4[nH]c2ccc(F)cc12)ccc5O Show InChI InChI=1S/C23H21FN2O3/c1-26-7-6-22-18-11-2-5-16(27)20(18)29-21(22)19-14(10-23(22,28)17(26)8-11)13-9-12(24)3-4-15(13)25-19/h2-5,9,17,21,25,27-28H,6-8,10H2,1H3/t17-,21+,22+,23-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	310	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Displacement of [3H]U-69593 from cloned kappa opioid receptor				Bioorg Med Chem Lett 17: 5916-7 (2007) Article DOI: 10.1016/j.bmcl.2007.07.098 BindingDB Entry DOI: 10.7270/Q2RV0NFR
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50221414 ((1S,2S,13R,21R)-7-chloro-22-methyl-14-oxa-11,22-di...) Show SMILES CN1CC[C@@]23[C@H]4Oc5c2c(C[C@@H]1[C@]3(O)Cc1c4[nH]c2ccc(Cl)cc12)ccc5O Show InChI InChI=1S/C23H21ClN2O3/c1-26-7-6-22-18-11-2-5-16(27)20(18)29-21(22)19-14(10-23(22,28)17(26)8-11)13-9-12(24)3-4-15(13)25-19/h2-5,9,17,21,25,27-28H,6-8,10H2,1H3/t17-,21+,22+,23-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	360	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Displacement of [3H]U-69593 from cloned kappa opioid receptor				Bioorg Med Chem Lett 17: 5916-7 (2007) Article DOI: 10.1016/j.bmcl.2007.07.098 BindingDB Entry DOI: 10.7270/Q2RV0NFR
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50221416 (22-methyl-(2S,13R)-14-oxa-11,22-diazaheptacyclo[13...) Show SMILES CN1CC[C@@]23[C@H]4Oc5c2c(C[C@@H]1[C@]3(O)Cc1c4[nH]c2ccccc12)ccc5O |r| Show InChI InChI=1S/C23H22N2O3/c1-25-9-8-22-18-12-6-7-16(26)20(18)28-21(22)19-14(11-23(22,27)17(25)10-12)13-4-2-3-5-15(13)24-19/h2-7,17,21,24,26-27H,8-11H2,1H3/t17-,21+,22+,23-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	515	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Displacement of [3H]U-69593 from cloned kappa opioid receptor				Bioorg Med Chem Lett 17: 5916-7 (2007) Article DOI: 10.1016/j.bmcl.2007.07.098 BindingDB Entry DOI: 10.7270/Q2RV0NFR
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50221413 ((1S,2S,13R,21R)-7-fluoro-22-methyl-14-oxa-11,22-di...) Show SMILES CN1CC[C@@]23[C@H]4Oc5c2c(C[C@@H]1[C@]3(O)Cc1c4[nH]c2ccc(F)cc12)ccc5O Show InChI InChI=1S/C23H21FN2O3/c1-26-7-6-22-18-11-2-5-16(27)20(18)29-21(22)19-14(10-23(22,28)17(26)8-11)13-9-12(24)3-4-15(13)25-19/h2-5,9,17,21,25,27-28H,6-8,10H2,1H3/t17-,21+,22+,23-/m1/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	n/a	n/a	1.08E+3	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Activity at mu opioid receptor assessed as stimulation of [35S]GTPgammaS binding				Bioorg Med Chem Lett 17: 5916-7 (2007) Article DOI: 10.1016/j.bmcl.2007.07.098 BindingDB Entry DOI: 10.7270/Q2RV0NFR
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50221413 ((1S,2S,13R,21R)-7-fluoro-22-methyl-14-oxa-11,22-di...) Show SMILES CN1CC[C@@]23[C@H]4Oc5c2c(C[C@@H]1[C@]3(O)Cc1c4[nH]c2ccc(F)cc12)ccc5O Show InChI InChI=1S/C23H21FN2O3/c1-26-7-6-22-18-11-2-5-16(27)20(18)29-21(22)19-14(10-23(22,28)17(26)8-11)13-9-12(24)3-4-15(13)25-19/h2-5,9,17,21,25,27-28H,6-8,10H2,1H3/t17-,21+,22+,23-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	16	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Activity at delta opioid receptor assessed as stimulation of [35S]GTPgammaS binding				Bioorg Med Chem Lett 17: 5916-7 (2007) Article DOI: 10.1016/j.bmcl.2007.07.098 BindingDB Entry DOI: 10.7270/Q2RV0NFR
					More data for this Ligand-Target Pair
Mu-type opioid receptor (MOUSE)	BDBM50373764 (CHEMBL401590) Show SMILES CCOC(=O)CCCN1CC[C@@]2(C)[C@@H](C)C1Cc1ccc(O)cc21 |w:15.16,TLB:7:8:13:17.23.16,THB:22:23:13:10.8.9| Show InChI InChI=1S/C20H29NO3/c1-4-24-19(23)6-5-10-21-11-9-20(3)14(2)18(21)12-15-7-8-16(22)13-17(15)20/h7-8,13-14,18,22H,4-6,9-12H2,1-3H3/t14-,18?,20-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	1.79E+4	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Agonist activity at mu opioid receptor in Swiss mouse vas deferens assessed as inhibition of electrically-stimulated twitch				Bioorg Med Chem 16: 869-73 (2008) Article DOI: 10.1016/j.bmc.2007.10.030 BindingDB Entry DOI: 10.7270/Q2XW4KN1
					More data for this Ligand-Target Pair
Mu-type opioid receptor (MOUSE)	BDBM50373765 (CHEMBL271026) Show SMILES C[C@H]1C2Cc3ccc(O)cc3[C@@]1(C)CCN2CC(O)=O |w:2.2,TLB:9:10:1:13.15.14,16:15:1:4.10.3| Show InChI InChI=1S/C16H21NO3/c1-10-14-7-11-3-4-12(18)8-13(11)16(10,2)5-6-17(14)9-15(19)20/h3-4,8,10,14,18H,5-7,9H2,1-2H3,(H,19,20)/t10-,14?,16-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	9.79E+3	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Agonist activity at mu opioid receptor in Swiss mouse vas deferens assessed as inhibition of electrically-stimulated twitch				Bioorg Med Chem 16: 869-73 (2008) Article DOI: 10.1016/j.bmc.2007.10.030 BindingDB Entry DOI: 10.7270/Q2XW4KN1
					More data for this Ligand-Target Pair
Mu-type opioid receptor (MOUSE)	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 Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL DrugBank KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	n/a	n/a	n/a	n/a	395	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Agonist activity at mu opioid receptor in Swiss mouse vas deferens assessed as inhibition of electrically-stimulated twitch				Bioorg Med Chem 16: 869-73 (2008) Article DOI: 10.1016/j.bmc.2007.10.030 BindingDB Entry DOI: 10.7270/Q2XW4KN1
					More data for this Ligand-Target Pair				3D Structure (crystal)