Found 9 hits for monomerid = 50010652 Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
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 UniProtKB/TrEMBL
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 | |
Mu-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
| 3.10 | 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 mu 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 | |
Kappa-type opioid receptor
(Cavia porcellus (domestic guinea pig)) | 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
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| 5.10 | 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 kappa opioid receptor in guinea pig 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)) | 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
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 | n/a | n/a | 1.80 | n/a | n/a | n/a | n/a |
Kitasato University
Curated by ChEMBL
| Assay Description Agonist activity at human mu opioid receptor expressed in HEK293 cells by CellKey method |
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)) | 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 DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 1.5 | n/a | n/a | n/a | n/a |
Kitasato University
Curated by ChEMBL
| Assay Description Agonist activity at human delta opioid receptor expressed in HEK293 cells by CellKey method |
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 | |
Kappa-type opioid receptor
(Homo sapiens (Human)) | 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 DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 81 | n/a | n/a | n/a | n/a |
Kitasato University
Curated by ChEMBL
| Assay Description Agonist activity at human kappa opioid receptor expressed in CHO cells assessed as [35S]-GTP[gammaS] binding |
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 | |
Kappa-type opioid receptor
(Homo sapiens (Human)) | 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 DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 40 | n/a | n/a | n/a | n/a |
Kitasato University
Curated by ChEMBL
| Assay Description Agonist activity at human kappa opioid receptor expressed in HEK293 cells by CellKey method |
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)) | 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
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 | n/a | n/a | 2.80 | n/a | n/a | n/a | n/a |
Kitasato University
Curated by ChEMBL
| Assay Description Agonist activity at human mu opioid receptor expressed in CHO cells assessed as [35S]-GTP[gammaS] binding |
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)) | 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 DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 1.10 | n/a | n/a | n/a | n/a |
Kitasato University
Curated by ChEMBL
| Assay Description Agonist activity at human delta opioid receptor expressed in CHO cells assessed as [35S]-GTP[gammaS] binding |
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 | |