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SMILES: CCOC1CN(C)CCc2cc(Cl)c(O)cc12

InChI Key: InChIKey=UWJZELKDZCMKAN-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50280432   

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(1A) dopamine receptor (RAT)	BDBM50280432 (8-Chloro-5-ethoxy-3-methyl-2,3,4,5-tetrahydro-1H-b...) Show SMILES CCOC1CN(C)CCc2cc(Cl)c(O)cc12 Show InChI InChI=1S/C13H18ClNO2/c1-3-17-13-8-15(2)5-4-9-6-11(14)12(16)7-10(9)13/h6-7,13,16H,3-5,8H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article	24	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Binding affinity towards Dopamine receptor D1 in rat striatal tissue by [3H]-SCH- 23390 displacement.				Bioorg Med Chem Lett 2: 399-402 (1992) Article DOI: 10.1016/S0960-894X(00)80155-9 BindingDB Entry DOI: 10.7270/Q2C53KRS
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Rattus norvegicus (rat))	BDBM50280432 (8-Chloro-5-ethoxy-3-methyl-2,3,4,5-tetrahydro-1H-b...) Show SMILES CCOC1CN(C)CCc2cc(Cl)c(O)cc12 Show InChI InChI=1S/C13H18ClNO2/c1-3-17-13-8-15(2)5-4-9-6-11(14)12(16)7-10(9)13/h6-7,13,16H,3-5,8H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Binding affinity towards Dopamine receptor D2 in rat striatal tissue by [3H]-spiperone displacement.				Bioorg Med Chem Lett 2: 399-402 (1992) Article DOI: 10.1016/S0960-894X(00)80155-9 BindingDB Entry DOI: 10.7270/Q2C53KRS
					More data for this Ligand-Target Pair