Found 4 hits for monomerid = 50411665 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)) | BDBM50411665
(CHEMBL402087)Show SMILES Cc1ccc2c(cccc2n1)-c1nnc(SCCCN2CCc3cc4nc(oc4c(C)c3CC2)C(C)(C)C)n1C Show InChI InChI=1S/C32H38N6OS/c1-20-11-12-24-25(9-7-10-26(24)33-20)29-35-36-31(37(29)6)40-18-8-15-38-16-13-22-19-27-28(21(2)23(22)14-17-38)39-30(34-27)32(3,4)5/h7,9-12,19H,8,13-18H2,1-6H3 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 39.8 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
GlaxoSmithKline
Curated by ChEMBL
| Assay Description Antagonist activity at human dopamine D3 receptor by cell based GTPgammaS binding assay |
Bioorg Med Chem Lett 18: 901-7 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.066 BindingDB Entry DOI: 10.7270/Q2MK6F32 |
More data for this Ligand-Target Pair | |
D(2) dopamine receptor
(Homo sapiens (Human)) | BDBM50411665
(CHEMBL402087)Show SMILES Cc1ccc2c(cccc2n1)-c1nnc(SCCCN2CCc3cc4nc(oc4c(C)c3CC2)C(C)(C)C)n1C Show InChI InChI=1S/C32H38N6OS/c1-20-11-12-24-25(9-7-10-26(24)33-20)29-35-36-31(37(29)6)40-18-8-15-38-16-13-22-19-27-28(21(2)23(22)14-17-38)39-30(34-27)32(3,4)5/h7,9-12,19H,8,13-18H2,1-6H3 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| >1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
GlaxoSmithKline
Curated by ChEMBL
| Assay Description Antagonist activity at dopamine D2 receptor by GTPgammaS binding assay |
Bioorg Med Chem Lett 18: 901-7 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.066 BindingDB Entry DOI: 10.7270/Q2MK6F32 |
More data for this Ligand-Target Pair | |
Histamine H1 receptor
(Homo sapiens (Human)) | BDBM50411665
(CHEMBL402087)Show SMILES Cc1ccc2c(cccc2n1)-c1nnc(SCCCN2CCc3cc4nc(oc4c(C)c3CC2)C(C)(C)C)n1C Show InChI InChI=1S/C32H38N6OS/c1-20-11-12-24-25(9-7-10-26(24)33-20)29-35-36-31(37(29)6)40-18-8-15-38-16-13-22-19-27-28(21(2)23(22)14-17-38)39-30(34-27)32(3,4)5/h7,9-12,19H,8,13-18H2,1-6H3 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 1.58E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
GlaxoSmithKline
Curated by ChEMBL
| Assay Description Antagonist activity at histamine H1 receptor by FLIPR assay |
Bioorg Med Chem Lett 18: 901-7 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.066 BindingDB Entry DOI: 10.7270/Q2MK6F32 |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily H member 2
(Homo sapiens (Human)) | BDBM50411665
(CHEMBL402087)Show SMILES Cc1ccc2c(cccc2n1)-c1nnc(SCCCN2CCc3cc4nc(oc4c(C)c3CC2)C(C)(C)C)n1C Show InChI InChI=1S/C32H38N6OS/c1-20-11-12-24-25(9-7-10-26(24)33-20)29-35-36-31(37(29)6)40-18-8-15-38-16-13-22-19-27-28(21(2)23(22)14-17-38)39-30(34-27)32(3,4)5/h7,9-12,19H,8,13-18H2,1-6H3 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 251 | n/a | n/a | n/a | n/a | n/a | n/a |
GlaxoSmithKline
Curated by ChEMBL
| Assay Description Displacement of [3H]Dofetilide from human ERG |
Bioorg Med Chem Lett 18: 901-7 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.066 BindingDB Entry DOI: 10.7270/Q2MK6F32 |
More data for this Ligand-Target Pair | |