Found 4 hits for monomerid = 50411696 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)) | BDBM50411696
(CHEMBL256473)Show SMILES Cc1ccc2c(cccc2n1)-c1nnc(SCCCN2CCc3cc4nc(oc4cc3CC2)C(C)(F)F)n1C Show InChI InChI=1S/C29H30F2N6OS/c1-18-8-9-21-22(6-4-7-23(21)32-18)26-34-35-28(36(26)3)39-15-5-12-37-13-10-19-16-24-25(17-20(19)11-14-37)38-27(33-24)29(2,30)31/h4,6-9,16-17H,5,10-15H2,1-3H3 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 6.31 | 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)) | BDBM50411696
(CHEMBL256473)Show SMILES Cc1ccc2c(cccc2n1)-c1nnc(SCCCN2CCc3cc4nc(oc4cc3CC2)C(C)(F)F)n1C Show InChI InChI=1S/C29H30F2N6OS/c1-18-8-9-21-22(6-4-7-23(21)32-18)26-34-35-28(36(26)3)39-15-5-12-37-13-10-19-16-24-25(17-20(19)11-14-37)38-27(33-24)29(2,30)31/h4,6-9,16-17H,5,10-15H2,1-3H3 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| >794 | 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)) | BDBM50411696
(CHEMBL256473)Show SMILES Cc1ccc2c(cccc2n1)-c1nnc(SCCCN2CCc3cc4nc(oc4cc3CC2)C(C)(F)F)n1C Show InChI InChI=1S/C29H30F2N6OS/c1-18-8-9-21-22(6-4-7-23(21)32-18)26-34-35-28(36(26)3)39-15-5-12-37-13-10-19-16-24-25(17-20(19)11-14-37)38-27(33-24)29(2,30)31/h4,6-9,16-17H,5,10-15H2,1-3H3 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| >2.00E+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 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)) | BDBM50411696
(CHEMBL256473)Show SMILES Cc1ccc2c(cccc2n1)-c1nnc(SCCCN2CCc3cc4nc(oc4cc3CC2)C(C)(F)F)n1C Show InChI InChI=1S/C29H30F2N6OS/c1-18-8-9-21-22(6-4-7-23(21)32-18)26-34-35-28(36(26)3)39-15-5-12-37-13-10-19-16-24-25(17-20(19)11-14-37)38-27(33-24)29(2,30)31/h4,6-9,16-17H,5,10-15H2,1-3H3 | 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 | 1.26E+3 | 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 | |