BDBM50216870 CHEMBL65122

SMILES: [H][C@@]12CN(Cc3ccc(F)cc3)C[C@@]1([H])c1cc(ccc1OC2)C#N

InChI Key: InChIKey=UVDIFPYXVNSROD-MAUKXSAKSA-N

Data: 2 KI

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50216870   

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))	BDBM50216870 (CHEMBL65122) Show SMILES [H][C@@]12CN(Cc3ccc(F)cc3)C[C@@]1([H])c1cc(ccc1OC2)C#N Show InChI InChI=1S/C19H17FN2O/c20-16-4-1-13(2-5-16)9-22-10-15-12-23-19-6-3-14(8-21)7-17(19)18(15)11-22/h1-7,15,18H,9-12H2/t15-,18+/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	16	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Centre de Recherches de Croissy Curated by ChEMBL					Assay Description Ability to displace [125I]iodosulpiride from human dopamine D3 (hD3) receptor transfected into CHO cells.				Bioorg Med Chem Lett 9: 2059-64 (1999) BindingDB Entry DOI: 10.7270/Q2WD42R1
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Homo sapiens (Human))	BDBM50216870 (CHEMBL65122) Show SMILES [H][C@@]12CN(Cc3ccc(F)cc3)C[C@@]1([H])c1cc(ccc1OC2)C#N Show InChI InChI=1S/C19H17FN2O/c20-16-4-1-13(2-5-16)9-22-10-15-12-23-19-6-3-14(8-21)7-17(19)18(15)11-22/h1-7,15,18H,9-12H2/t15-,18+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Centre de Recherches de Croissy Curated by ChEMBL					Assay Description Ability to displace [125I]iodosulpiride from human dopamine D2 (hD2) receptor transfected into CHO cells.				Bioorg Med Chem Lett 9: 2059-64 (1999) BindingDB Entry DOI: 10.7270/Q2WD42R1
					More data for this Ligand-Target Pair