Found 3 hits of ki for monomerid = 50128089 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 |
Kappa-type opioid receptor
(Homo sapiens (Human)) | BDBM50128089
(CHEMBL2369370 | Tyr-Gly-Pro-Phe-Leu-Arg-NH2)Show SMILES [#6]-[#6](-[#6])-[#6]-[#6@H](-[#7]-[#6](=O)-[#6@H](-[#6]-c1ccccc1)-[#7]-[#6](=O)-[#6@@H]-1-[#6]-[#6]-[#6]-[#7]-1-[#6](=O)-[#6]-[#7]-[#6](=O)-[#6@@H](-[#7])-[#6]-c1ccc(-[#8])cc1)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#6](-[#7])=O Show InChI InChI=1S/C37H54N10O7/c1-22(2)18-28(34(52)44-27(32(39)50)10-6-16-42-37(40)41)45-35(53)29(20-23-8-4-3-5-9-23)46-36(54)30-11-7-17-47(30)31(49)21-43-33(51)26(38)19-24-12-14-25(48)15-13-24/h3-5,8-9,12-15,22,26-30,48H,6-7,10-11,16-21,38H2,1-2H3,(H2,39,50)(H,43,51)(H,44,52)(H,45,53)(H,46,54)(H4,40,41,42)/t26-,27-,28-,29-,30?/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 3.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of California
Curated by ChEMBL
| Assay Description In vitro binding affinity towards human Opioid receptor kappa 1 on CHO cell membranes using [3H]diprenorphine displacement. |
J Med Chem 46: 2104-9 (2003)
Article DOI: 10.1021/jm020125+ BindingDB Entry DOI: 10.7270/Q2NZ88CF |
More data for this Ligand-Target Pair | |
Mu-type opioid receptor
(Homo sapiens (Human)) | BDBM50128089
(CHEMBL2369370 | Tyr-Gly-Pro-Phe-Leu-Arg-NH2)Show SMILES [#6]-[#6](-[#6])-[#6]-[#6@H](-[#7]-[#6](=O)-[#6@H](-[#6]-c1ccccc1)-[#7]-[#6](=O)-[#6@@H]-1-[#6]-[#6]-[#6]-[#7]-1-[#6](=O)-[#6]-[#7]-[#6](=O)-[#6@@H](-[#7])-[#6]-c1ccc(-[#8])cc1)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#6](-[#7])=O Show InChI InChI=1S/C37H54N10O7/c1-22(2)18-28(34(52)44-27(32(39)50)10-6-16-42-37(40)41)45-35(53)29(20-23-8-4-3-5-9-23)46-36(54)30-11-7-17-47(30)31(49)21-43-33(51)26(38)19-24-12-14-25(48)15-13-24/h3-5,8-9,12-15,22,26-30,48H,6-7,10-11,16-21,38H2,1-2H3,(H2,39,50)(H,43,51)(H,44,52)(H,45,53)(H,46,54)(H4,40,41,42)/t26-,27-,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
| 3.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of California
Curated by ChEMBL
| Assay Description In vitro binding affinity to human Opioid receptor mu 1 on CHO cell membranes using [3H]diprenorphine displacement. |
J Med Chem 46: 2104-9 (2003)
Article DOI: 10.1021/jm020125+ BindingDB Entry DOI: 10.7270/Q2NZ88CF |
More data for this Ligand-Target Pair | |
Delta-type opioid receptor
(Homo sapiens (Human)) | BDBM50128089
(CHEMBL2369370 | Tyr-Gly-Pro-Phe-Leu-Arg-NH2)Show SMILES [#6]-[#6](-[#6])-[#6]-[#6@H](-[#7]-[#6](=O)-[#6@H](-[#6]-c1ccccc1)-[#7]-[#6](=O)-[#6@@H]-1-[#6]-[#6]-[#6]-[#7]-1-[#6](=O)-[#6]-[#7]-[#6](=O)-[#6@@H](-[#7])-[#6]-c1ccc(-[#8])cc1)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#6](-[#7])=O Show InChI InChI=1S/C37H54N10O7/c1-22(2)18-28(34(52)44-27(32(39)50)10-6-16-42-37(40)41)45-35(53)29(20-23-8-4-3-5-9-23)46-36(54)30-11-7-17-47(30)31(49)21-43-33(51)26(38)19-24-12-14-25(48)15-13-24/h3-5,8-9,12-15,22,26-30,48H,6-7,10-11,16-21,38H2,1-2H3,(H2,39,50)(H,43,51)(H,44,52)(H,45,53)(H,46,54)(H4,40,41,42)/t26-,27-,28-,29-,30?/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of California
Curated by ChEMBL
| Assay Description In vitro binding affinity to human Opioid receptor delta 1 on CHO cell membranes using [3H]diprenorphine displacement. |
J Med Chem 46: 2104-9 (2003)
Article DOI: 10.1021/jm020125+ BindingDB Entry DOI: 10.7270/Q2NZ88CF |
More data for this Ligand-Target Pair | |