Found 3 hits for monomerid = 50108962 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
(Homo sapiens (Human)) | BDBM50108962
(CHEMBL3597151)Show SMILES CC(C)C[C@H](NC(=O)[C@H](CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(O)=O)NC(=O)C(C)(C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(N)=O)NC(=O)CCCNC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)[C@@H](C)O)C(N)=O |r| Show InChI InChI=1S/C89H146N20O27/c1-45(2)35-58(74(94)121)102-84(131)64(44-135-87-73(120)72(119)71(118)65(43-110)136-87)106-79(126)56(24-17-19-33-91)101-81(128)60(37-47(5)6)103-75(122)49(9)97-78(125)55(23-16-18-32-90)100-80(127)57(30-31-69(116)117)107-88(134)89(11,12)109-85(132)61(38-48(7)8)105-83(130)63(41-66(93)113)98-67(114)25-20-34-95-77(124)59(36-46(3)4)104-82(129)62(40-51-21-14-13-15-22-51)99-68(115)42-96-86(133)70(50(10)111)108-76(123)54(92)39-52-26-28-53(112)29-27-52/h13-15,21-22,26-29,45-50,54-65,70-73,87,110-112,118-120H,16-20,23-25,30-44,90-92H2,1-12H3,(H2,93,113)(H2,94,121)(H,95,124)(H,96,133)(H,97,125)(H,98,114)(H,99,115)(H,100,127)(H,101,128)(H,102,131)(H,103,122)(H,104,129)(H,105,130)(H,106,126)(H,107,134)(H,108,123)(H,109,132)(H,116,117)/t49-,50+,54-,55-,56-,57-,58-,59-,60-,61-,62-,63-,64-,65+,70-,71+,72-,73+,87+/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL KEGG PC cid PC sid UniChem
Similars
| PubMed
| 4.20 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
The University of Arizona
Curated by ChEMBL
| Assay Description Displacement of [3H]-naltrindole from human delta opioid receptor expressed in CHO cells after 3 hrs by scintillation counting analysis |
J Med Chem 58: 5728-41 (2015)
BindingDB Entry DOI: 10.7270/Q2KH0Q33 |
More data for this Ligand-Target Pair | |
Mu-type opioid receptor
(Homo sapiens (Human)) | BDBM50108962
(CHEMBL3597151)Show SMILES CC(C)C[C@H](NC(=O)[C@H](CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(O)=O)NC(=O)C(C)(C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(N)=O)NC(=O)CCCNC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)[C@@H](C)O)C(N)=O |r| Show InChI InChI=1S/C89H146N20O27/c1-45(2)35-58(74(94)121)102-84(131)64(44-135-87-73(120)72(119)71(118)65(43-110)136-87)106-79(126)56(24-17-19-33-91)101-81(128)60(37-47(5)6)103-75(122)49(9)97-78(125)55(23-16-18-32-90)100-80(127)57(30-31-69(116)117)107-88(134)89(11,12)109-85(132)61(38-48(7)8)105-83(130)63(41-66(93)113)98-67(114)25-20-34-95-77(124)59(36-46(3)4)104-82(129)62(40-51-21-14-13-15-22-51)99-68(115)42-96-86(133)70(50(10)111)108-76(123)54(92)39-52-26-28-53(112)29-27-52/h13-15,21-22,26-29,45-50,54-65,70-73,87,110-112,118-120H,16-20,23-25,30-44,90-92H2,1-12H3,(H2,93,113)(H2,94,121)(H,95,124)(H,96,133)(H,97,125)(H,98,114)(H,99,115)(H,100,127)(H,101,128)(H,102,131)(H,103,122)(H,104,129)(H,105,130)(H,106,126)(H,107,134)(H,108,123)(H,109,132)(H,116,117)/t49-,50+,54-,55-,56-,57-,58-,59-,60-,61-,62-,63-,64-,65+,70-,71+,72-,73+,87+/m0/s1 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL KEGG PC cid PC sid UniChem
Similars
| PubMed
| 4.30 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
The University of Arizona
Curated by ChEMBL
| Assay Description Displacement of [3H]-DAMGO from human mu opioid receptor expressed in CHO cells after 60 mins by scintillation counting analysis |
J Med Chem 58: 5728-41 (2015)
BindingDB Entry DOI: 10.7270/Q2KH0Q33 |
More data for this Ligand-Target Pair | |
Kappa-type opioid receptor
(Homo sapiens (Human)) | BDBM50108962
(CHEMBL3597151)Show SMILES CC(C)C[C@H](NC(=O)[C@H](CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(O)=O)NC(=O)C(C)(C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(N)=O)NC(=O)CCCNC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)[C@@H](C)O)C(N)=O |r| Show InChI InChI=1S/C89H146N20O27/c1-45(2)35-58(74(94)121)102-84(131)64(44-135-87-73(120)72(119)71(118)65(43-110)136-87)106-79(126)56(24-17-19-33-91)101-81(128)60(37-47(5)6)103-75(122)49(9)97-78(125)55(23-16-18-32-90)100-80(127)57(30-31-69(116)117)107-88(134)89(11,12)109-85(132)61(38-48(7)8)105-83(130)63(41-66(93)113)98-67(114)25-20-34-95-77(124)59(36-46(3)4)104-82(129)62(40-51-21-14-13-15-22-51)99-68(115)42-96-86(133)70(50(10)111)108-76(123)54(92)39-52-26-28-53(112)29-27-52/h13-15,21-22,26-29,45-50,54-65,70-73,87,110-112,118-120H,16-20,23-25,30-44,90-92H2,1-12H3,(H2,93,113)(H2,94,121)(H,95,124)(H,96,133)(H,97,125)(H,98,114)(H,99,115)(H,100,127)(H,101,128)(H,102,131)(H,103,122)(H,104,129)(H,105,130)(H,106,126)(H,107,134)(H,108,123)(H,109,132)(H,116,117)/t49-,50+,54-,55-,56-,57-,58-,59-,60-,61-,62-,63-,64-,65+,70-,71+,72-,73+,87+/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL KEGG PC cid PC sid UniChem
Similars
| PubMed
| 11 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
The University of Arizona
Curated by ChEMBL
| Assay Description Displacement of [3H]-U69593 from human kappa opioid receptor expressed in CHO cells after 60 mins by scintillation counting analysis |
J Med Chem 58: 5728-41 (2015)
BindingDB Entry DOI: 10.7270/Q2KH0Q33 |
More data for this Ligand-Target Pair | |