null

SMILES: C(C[C@H]1CC[C@@H](CC1)Nc1ncccn1)CN1CCN(CC1)c1ccccc1

InChI Key: InChIKey=GXOXNWXNCBKFTM-MEMLXQNLSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50063289   

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(2) dopamine receptor (Homo sapiens (Human))	BDBM50063289 (CHEMBL165140 | {4-[3-(4-Phenyl-piperazin-1-yl)-pro...) Show SMILES C(C[C@H]1CC[C@@H](CC1)Nc1ncccn1)CN1CCN(CC1)c1ccccc1 |wU:5.8,wD:2.1,(7.79,-8.8,;6.25,-8.89,;5.4,-7.59,;6.11,-6.22,;5.26,-4.94,;3.72,-5.01,;3.03,-6.39,;3.87,-7.7,;2.88,-3.72,;3.56,-2.34,;2.72,-1.06,;3.42,.32,;4.97,.4,;5.81,-.89,;5.11,-2.27,;8.63,-10.11,;10.18,-10.01,;11.02,-11.32,;12.56,-11.24,;13.25,-9.86,;12.41,-8.56,;10.88,-8.64,;14.79,-9.78,;15.63,-11.07,;17.16,-10.97,;17.86,-9.61,;16.99,-8.31,;15.47,-8.41,)| Show InChI InChI=1S/C23H33N5/c1-2-7-22(8-3-1)28-18-16-27(17-19-28)15-4-6-20-9-11-21(12-10-20)26-23-24-13-5-14-25-23/h1-3,5,7-8,13-14,20-21H,4,6,9-12,15-19H2,(H,24,25,26)/t20-,21-	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description Binding affinity determined by measuring its ability to displace [3H]-N-0437 radioligand in CHO-K1 cells on Cloned Human Dopamine receptor D2				J Med Chem 41: 760-71 (1998) Article DOI: 10.1021/jm9707378 BindingDB Entry DOI: 10.7270/Q20G3J97
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50063289 (CHEMBL165140 | {4-[3-(4-Phenyl-piperazin-1-yl)-pro...) Show SMILES C(C[C@H]1CC[C@@H](CC1)Nc1ncccn1)CN1CCN(CC1)c1ccccc1 |wU:5.8,wD:2.1,(7.79,-8.8,;6.25,-8.89,;5.4,-7.59,;6.11,-6.22,;5.26,-4.94,;3.72,-5.01,;3.03,-6.39,;3.87,-7.7,;2.88,-3.72,;3.56,-2.34,;2.72,-1.06,;3.42,.32,;4.97,.4,;5.81,-.89,;5.11,-2.27,;8.63,-10.11,;10.18,-10.01,;11.02,-11.32,;12.56,-11.24,;13.25,-9.86,;12.41,-8.56,;10.88,-8.64,;14.79,-9.78,;15.63,-11.07,;17.16,-10.97,;17.86,-9.61,;16.99,-8.31,;15.47,-8.41,)| Show InChI InChI=1S/C23H33N5/c1-2-7-22(8-3-1)28-18-16-27(17-19-28)15-4-6-20-9-11-21(12-10-20)26-23-24-13-5-14-25-23/h1-3,5,7-8,13-14,20-21H,4,6,9-12,15-19H2,(H,24,25,26)/t20-,21-	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	16	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description The binding affinity of the compound was determined by measuring its ability to displace [3H]-8-OH-DPAT radioligand in 5-hydroxytryptamine 1A recepto...				J Med Chem 41: 760-71 (1998) Article DOI: 10.1021/jm9707378 BindingDB Entry DOI: 10.7270/Q20G3J97
					More data for this Ligand-Target Pair
D(3) dopamine receptor (Homo sapiens (Human))	BDBM50063289 (CHEMBL165140 | {4-[3-(4-Phenyl-piperazin-1-yl)-pro...) Show SMILES C(C[C@H]1CC[C@@H](CC1)Nc1ncccn1)CN1CCN(CC1)c1ccccc1 |wU:5.8,wD:2.1,(7.79,-8.8,;6.25,-8.89,;5.4,-7.59,;6.11,-6.22,;5.26,-4.94,;3.72,-5.01,;3.03,-6.39,;3.87,-7.7,;2.88,-3.72,;3.56,-2.34,;2.72,-1.06,;3.42,.32,;4.97,.4,;5.81,-.89,;5.11,-2.27,;8.63,-10.11,;10.18,-10.01,;11.02,-11.32,;12.56,-11.24,;13.25,-9.86,;12.41,-8.56,;10.88,-8.64,;14.79,-9.78,;15.63,-11.07,;17.16,-10.97,;17.86,-9.61,;16.99,-8.31,;15.47,-8.41,)| Show InChI InChI=1S/C23H33N5/c1-2-7-22(8-3-1)28-18-16-27(17-19-28)15-4-6-20-9-11-21(12-10-20)26-23-24-13-5-14-25-23/h1-3,5,7-8,13-14,20-21H,4,6,9-12,15-19H2,(H,24,25,26)/t20-,21-	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	54	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Warner-Lambert Company Curated by ChEMBL					Assay Description Binding affinity determined by measuring displacement of [3H]-spiperone from cloned Human Dopamine receptor D3 in CHO-K1 cells				J Med Chem 41: 760-71 (1998) Article DOI: 10.1021/jm9707378 BindingDB Entry DOI: 10.7270/Q20G3J97
					More data for this Ligand-Target Pair