Found 4 hits for monomerid = 50411693 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)) | BDBM50411693
(CHEMBL270567)Show SMILES Cc1cc(-c2nc3cc4CCN(CCCSc5nnc(-c6cccc7nc(C)ccc67)n5C)CCc4cc3o2)n(C)n1 Show InChI InChI=1S/C32H34N8OS/c1-20-9-10-24-25(7-5-8-26(24)33-20)30-35-36-32(38(30)3)42-16-6-13-40-14-11-22-18-27-29(19-23(22)12-15-40)41-31(34-27)28-17-21(2)37-39(28)4/h5,7-10,17-19H,6,11-16H2,1-4H3 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 7.94 | 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)) | BDBM50411693
(CHEMBL270567)Show SMILES Cc1cc(-c2nc3cc4CCN(CCCSc5nnc(-c6cccc7nc(C)ccc67)n5C)CCc4cc3o2)n(C)n1 Show InChI InChI=1S/C32H34N8OS/c1-20-9-10-24-25(7-5-8-26(24)33-20)30-35-36-32(38(30)3)42-16-6-13-40-14-11-22-18-27-29(19-23(22)12-15-40)41-31(34-27)28-17-21(2)37-39(28)4/h5,7-10,17-19H,6,11-16H2,1-4H3 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| >501 | 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)) | BDBM50411693
(CHEMBL270567)Show SMILES Cc1cc(-c2nc3cc4CCN(CCCSc5nnc(-c6cccc7nc(C)ccc67)n5C)CCc4cc3o2)n(C)n1 Show InChI InChI=1S/C32H34N8OS/c1-20-9-10-24-25(7-5-8-26(24)33-20)30-35-36-32(38(30)3)42-16-6-13-40-14-11-22-18-27-29(19-23(22)12-15-40)41-31(34-27)28-17-21(2)37-39(28)4/h5,7-10,17-19H,6,11-16H2,1-4H3 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| >2.51E+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)) | BDBM50411693
(CHEMBL270567)Show SMILES Cc1cc(-c2nc3cc4CCN(CCCSc5nnc(-c6cccc7nc(C)ccc67)n5C)CCc4cc3o2)n(C)n1 Show InChI InChI=1S/C32H34N8OS/c1-20-9-10-24-25(7-5-8-26(24)33-20)30-35-36-32(38(30)3)42-16-6-13-40-14-11-22-18-27-29(19-23(22)12-15-40)41-31(34-27)28-17-21(2)37-39(28)4/h5,7-10,17-19H,6,11-16H2,1-4H3 | 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 | 501 | 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 | |