null

SMILES: O=C(N(CC1CCC1)[C@H]1CCNC1)c1ccccc1Oc1ccccc1

InChI Key: InChIKey=WQAXZHUMPQMMEW-SFHVURJKSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50297081   

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
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50297081 ((S)-N-(cyclobutylmethyl)-2-phenoxy-N-(pyrrolidin-3...) Show SMILES O=C(N(CC1CCC1)[C@H]1CCNC1)c1ccccc1Oc1ccccc1 |r| Show InChI InChI=1S/C22H26N2O2/c25-22(24(16-17-7-6-8-17)18-13-14-23-15-18)20-11-4-5-12-21(20)26-19-9-2-1-3-10-19/h1-5,9-12,17-18,23H,6-8,13-16H2/t18-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	7	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Displacement of [3H]nisoxetine from human recombinant NET expressed in HEK293 cells by scintillation proximity assay				Bioorg Med Chem Lett 19: 4579-83 (2009) Article DOI: 10.1016/j.bmcl.2009.06.096 BindingDB Entry DOI: 10.7270/Q2NV9J96
					More data for this Ligand-Target Pair
Sodium-dependent serotonin transporter (Homo sapiens (Human))	BDBM50297081 ((S)-N-(cyclobutylmethyl)-2-phenoxy-N-(pyrrolidin-3...) Show SMILES O=C(N(CC1CCC1)[C@H]1CCNC1)c1ccccc1Oc1ccccc1 |r| Show InChI InChI=1S/C22H26N2O2/c25-22(24(16-17-7-6-8-17)18-13-14-23-15-18)20-11-4-5-12-21(20)26-19-9-2-1-3-10-19/h1-5,9-12,17-18,23H,6-8,13-16H2/t18-/m0/s1	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	151	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Displacement of [3H]citalopram from human recombinant SERT expressed in HEK293 cells by scintillation proximity assay				Bioorg Med Chem Lett 19: 4579-83 (2009) Article DOI: 10.1016/j.bmcl.2009.06.096 BindingDB Entry DOI: 10.7270/Q2NV9J96
					More data for this Ligand-Target Pair
Sodium-dependent dopamine transporter (Homo sapiens (Human))	BDBM50297081 ((S)-N-(cyclobutylmethyl)-2-phenoxy-N-(pyrrolidin-3...) Show SMILES O=C(N(CC1CCC1)[C@H]1CCNC1)c1ccccc1Oc1ccccc1 |r| Show InChI InChI=1S/C22H26N2O2/c25-22(24(16-17-7-6-8-17)18-13-14-23-15-18)20-11-4-5-12-21(20)26-19-9-2-1-3-10-19/h1-5,9-12,17-18,23H,6-8,13-16H2/t18-/m0/s1	NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Displacement of radioligand from human recombinant DAT expressed in HEK293 cells by scintillation proximity assay				Bioorg Med Chem Lett 19: 4579-83 (2009) Article DOI: 10.1016/j.bmcl.2009.06.096 BindingDB Entry DOI: 10.7270/Q2NV9J96
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50297081 ((S)-N-(cyclobutylmethyl)-2-phenoxy-N-(pyrrolidin-3...) Show SMILES O=C(N(CC1CCC1)[C@H]1CCNC1)c1ccccc1Oc1ccccc1 |r| Show InChI InChI=1S/C22H26N2O2/c25-22(24(16-17-7-6-8-17)18-13-14-23-15-18)20-11-4-5-12-21(20)26-19-9-2-1-3-10-19/h1-5,9-12,17-18,23H,6-8,13-16H2/t18-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	760	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Displacement of [3H]dofetilide from human ERG				Bioorg Med Chem Lett 19: 4579-83 (2009) Article DOI: 10.1016/j.bmcl.2009.06.096 BindingDB Entry DOI: 10.7270/Q2NV9J96
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50297081 ((S)-N-(cyclobutylmethyl)-2-phenoxy-N-(pyrrolidin-3...) Show SMILES O=C(N(CC1CCC1)[C@H]1CCNC1)c1ccccc1Oc1ccccc1 |r| Show InChI InChI=1S/C22H26N2O2/c25-22(24(16-17-7-6-8-17)18-13-14-23-15-18)20-11-4-5-12-21(20)26-19-9-2-1-3-10-19/h1-5,9-12,17-18,23H,6-8,13-16H2/t18-/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	65	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Inhibition of CYP2D6				Bioorg Med Chem Lett 19: 4579-83 (2009) Article DOI: 10.1016/j.bmcl.2009.06.096 BindingDB Entry DOI: 10.7270/Q2NV9J96
					More data for this Ligand-Target Pair