BDBM50367601 CHEMBL293828

SMILES: CCCN1CCc2cc(Cl)c(O)cc2[C@@H]1c1ccccc1

InChI Key: InChIKey=UCVFZVSEYSSSHP-SFHVURJKSA-N

Data: 4 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 4 hits for monomerid = 50367601   

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 (Homo sapiens (Human))	BDBM50367601 (CHEMBL293828) Show SMILES CCCN1CCc2cc(Cl)c(O)cc2[C@@H]1c1ccccc1 Show InChI InChI=1S/C18H20ClNO/c1-2-9-20-10-8-14-11-16(19)17(21)12-15(14)18(20)13-6-4-3-5-7-13/h3-7,11-12,18,21H,2,8-10H2,1H3/t18-/m0/s1	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	178	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Antibacterial activity against Escherichia coli				J Med Chem 32: 2050-8 (1989) BindingDB Entry DOI: 10.7270/Q2RV0QXV
					More data for this Ligand-Target Pair
D(1A) dopamine receptor (RAT)	BDBM50367601 (CHEMBL293828) Show SMILES CCCN1CCc2cc(Cl)c(O)cc2[C@@H]1c1ccccc1 Show InChI InChI=1S/C18H20ClNO/c1-2-9-20-10-8-14-11-16(19)17(21)12-15(14)18(20)13-6-4-3-5-7-13/h3-7,11-12,18,21H,2,8-10H2,1H3/t18-/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	179	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of [3H]SCH-23,390 binding to Dopamine receptor D1 at 0.25 nM				J Med Chem 31: 1941-6 (1988) BindingDB Entry DOI: 10.7270/Q20002PD
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Rattus norvegicus (rat))	BDBM50367601 (CHEMBL293828) Show SMILES CCCN1CCc2cc(Cl)c(O)cc2[C@@H]1c1ccccc1 Show InChI InChI=1S/C18H20ClNO/c1-2-9-20-10-8-14-11-16(19)17(21)12-15(14)18(20)13-6-4-3-5-7-13/h3-7,11-12,18,21H,2,8-10H2,1H3/t18-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.90E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description Inhibition of [3H]spiperone binding to Dopamine receptor D2 at 0.02 nM				J Med Chem 31: 1941-6 (1988) BindingDB Entry DOI: 10.7270/Q20002PD
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Homo sapiens (Human))	BDBM50367601 (CHEMBL293828) Show SMILES CCCN1CCc2cc(Cl)c(O)cc2[C@@H]1c1ccccc1 Show InChI InChI=1S/C18H20ClNO/c1-2-9-20-10-8-14-11-16(19)17(21)12-15(14)18(20)13-6-4-3-5-7-13/h3-7,11-12,18,21H,2,8-10H2,1H3/t18-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.91E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of North Carolina Curated by ChEMBL					Assay Description In vitro inhibition of dihydrofolate reductase of Escherichia coli				J Med Chem 32: 2050-8 (1989) BindingDB Entry DOI: 10.7270/Q2RV0QXV
					More data for this Ligand-Target Pair