Found 3 hits for monomerid = 50416716 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 |
D(3) dopamine receptor
(Homo sapiens (Human)) | BDBM50416716
(CHEMBL1224698)Show SMILES CC(C)c1ccc(cc1)S(=O)(=O)Nc1ccc(cc1)[C@@]12C[C@@H]1CN(CC=C)C2 |r| Show InChI InChI=1S/C23H28N2O2S/c1-4-13-25-15-20-14-23(20,16-25)19-7-9-21(10-8-19)24-28(26,27)22-11-5-18(6-12-22)17(2)3/h4-12,17,20,24H,1,13-16H2,2-3H3/t20-,23+/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 2.51 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
GlaxoSmithKline Medicines Research Centre
Curated by ChEMBL
| Assay Description Antagonist activity at dopamine D3 receptor by GTPgammaS binding assay |
Bioorg Med Chem Lett 20: 5491-4 (2010)
Article DOI: 10.1016/j.bmcl.2010.07.073 BindingDB Entry DOI: 10.7270/Q2R78GFH |
More data for this Ligand-Target Pair | |
D(2) dopamine receptor
(Homo sapiens (Human)) | BDBM50416716
(CHEMBL1224698)Show SMILES CC(C)c1ccc(cc1)S(=O)(=O)Nc1ccc(cc1)[C@@]12C[C@@H]1CN(CC=C)C2 |r| Show InChI InChI=1S/C23H28N2O2S/c1-4-13-25-15-20-14-23(20,16-25)19-7-9-21(10-8-19)24-28(26,27)22-11-5-18(6-12-22)17(2)3/h4-12,17,20,24H,1,13-16H2,2-3H3/t20-,23+/m1/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 63.1 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
GlaxoSmithKline Medicines Research Centre
Curated by ChEMBL
| Assay Description Antagonist activity at dopamine D2 receptor by GTPgammaS binding assay |
Bioorg Med Chem Lett 20: 5491-4 (2010)
Article DOI: 10.1016/j.bmcl.2010.07.073 BindingDB Entry DOI: 10.7270/Q2R78GFH |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily H member 2
(Homo sapiens (Human)) | BDBM50416716
(CHEMBL1224698)Show SMILES CC(C)c1ccc(cc1)S(=O)(=O)Nc1ccc(cc1)[C@@]12C[C@@H]1CN(CC=C)C2 |r| Show InChI InChI=1S/C23H28N2O2S/c1-4-13-25-15-20-14-23(20,16-25)19-7-9-21(10-8-19)24-28(26,27)22-11-5-18(6-12-22)17(2)3/h4-12,17,20,24H,1,13-16H2,2-3H3/t20-,23+/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 100 | n/a | n/a | n/a | n/a | n/a | n/a |
GlaxoSmithKline Medicines Research Centre
Curated by ChEMBL
| Assay Description Inhibition of human ERG |
Bioorg Med Chem Lett 20: 5491-4 (2010)
Article DOI: 10.1016/j.bmcl.2010.07.073 BindingDB Entry DOI: 10.7270/Q2R78GFH |
More data for this Ligand-Target Pair | |