BDBM50236356 CHEMBL4095588

SMILES: Cl.COc1ccccc1N1CCN(CCCNC(=O)Oc2ccc(cc2)-c2ccccc2)CC1

InChI Key: InChIKey=JLAYLFLQSFRXPP-UHFFFAOYSA-N

Data: 1 IC50  1 EC50

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 = 50236356   

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))	BDBM50236356 (CHEMBL4095588) Show SMILES Cl.COc1ccccc1N1CCN(CCCNC(=O)Oc2ccc(cc2)-c2ccccc2)CC1 Show InChI InChI=1S/C27H31N3O3/c1-32-26-11-6-5-10-25(26)30-20-18-29(19-21-30)17-7-16-28-27(31)33-24-14-12-23(13-15-24)22-8-3-2-4-9-22/h2-6,8-15H,7,16-21H2,1H3,(H,28,31)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	14	n/a	n/a	n/a	n/a
Universit£ di Bologna Curated by ChEMBL					Assay Description Agonist activity at recombinant human dopamine D3 receptor expressed in CHO-K1 cells assessed as increase in cAMP accumulation after 30 mins by HTRF ...				J Med Chem 60: 2287-2304 (2017) Article DOI: 10.1021/acs.jmedchem.6b01578 BindingDB Entry DOI: 10.7270/Q29S1T9P
					More data for this Ligand-Target Pair
Fatty-acid amide hydrolase 1 (Homo sapiens (Human))	BDBM50236356 (CHEMBL4095588) Show SMILES Cl.COc1ccccc1N1CCN(CCCNC(=O)Oc2ccc(cc2)-c2ccccc2)CC1 Show InChI InChI=1S/C27H31N3O3/c1-32-26-11-6-5-10-25(26)30-20-18-29(19-21-30)17-7-16-28-27(31)33-24-14-12-23(13-15-24)22-8-3-2-4-9-22/h2-6,8-15H,7,16-21H2,1H3,(H,28,31)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.60	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ di Bologna Curated by ChEMBL					Assay Description Inhibition of human FAAH1 expressed in HEK293 cell membrane-enriched lysate using AMC arachidonyl amide as substrate preincubated for 50 mins followe...				J Med Chem 60: 2287-2304 (2017) Article DOI: 10.1021/acs.jmedchem.6b01578 BindingDB Entry DOI: 10.7270/Q29S1T9P
					More data for this Ligand-Target Pair