BDBM50134685 CHEMBL3745853

SMILES: Fc1ccc(cc1)S(=O)(=O)N(CC1CC1)C1CCN(CCOc2ccccc2-c2ccccc2)CC1

InChI Key: InChIKey=XIPPMBYEJXCYMK-UHFFFAOYSA-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 = 50134685   

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
5-hydroxytryptamine receptor 7 (Homo sapiens (Human))	BDBM50134685 (CHEMBL3745853) Show SMILES Fc1ccc(cc1)S(=O)(=O)N(CC1CC1)C1CCN(CCOc2ccccc2-c2ccccc2)CC1 Show InChI InChI=1S/C29H33FN2O3S/c30-25-12-14-27(15-13-25)36(33,34)32(22-23-10-11-23)26-16-18-31(19-17-26)20-21-35-29-9-5-4-8-28(29)24-6-2-1-3-7-24/h1-9,12-15,23,26H,10-11,16-22H2	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	18	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Medical College Curated by ChEMBL					Assay Description Displacement of [3H]-5-CT from human 5-HT7B receptor expressed in HEK293 cells incubated for 1 hr				Bioorg Med Chem 24: 130-9 (2016) BindingDB Entry DOI: 10.7270/Q2W95C1P
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Homo sapiens (Human))	BDBM50134685 (CHEMBL3745853) Show SMILES Fc1ccc(cc1)S(=O)(=O)N(CC1CC1)C1CCN(CCOc2ccccc2-c2ccccc2)CC1 Show InChI InChI=1S/C29H33FN2O3S/c30-25-12-14-27(15-13-25)36(33,34)32(22-23-10-11-23)26-16-18-31(19-17-26)20-21-35-29-9-5-4-8-28(29)24-6-2-1-3-7-24/h1-9,12-15,23,26H,10-11,16-22H2	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	37	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Medical College Curated by ChEMBL					Assay Description Displacement of [3H]-Raclopride from human dopamine D2L receptor expressed in HEK293 cells incubated for 1 hr				Bioorg Med Chem 24: 130-9 (2016) BindingDB Entry DOI: 10.7270/Q2W95C1P
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2A (Homo sapiens (Human))	BDBM50134685 (CHEMBL3745853) Show SMILES Fc1ccc(cc1)S(=O)(=O)N(CC1CC1)C1CCN(CCOc2ccccc2-c2ccccc2)CC1 Show InChI InChI=1S/C29H33FN2O3S/c30-25-12-14-27(15-13-25)36(33,34)32(22-23-10-11-23)26-16-18-31(19-17-26)20-21-35-29-9-5-4-8-28(29)24-6-2-1-3-7-24/h1-9,12-15,23,26H,10-11,16-22H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Medical College Curated by ChEMBL					Assay Description Displacement of [3H]-ketanserin from human 5-HT2A receptor expressed in HEK293 cells incubated for 1 hr				Bioorg Med Chem 24: 130-9 (2016) BindingDB Entry DOI: 10.7270/Q2W95C1P
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Homo sapiens (Human))	BDBM50134685 (CHEMBL3745853) Show SMILES Fc1ccc(cc1)S(=O)(=O)N(CC1CC1)C1CCN(CCOc2ccccc2-c2ccccc2)CC1 Show InChI InChI=1S/C29H33FN2O3S/c30-25-12-14-27(15-13-25)36(33,34)32(22-23-10-11-23)26-16-18-31(19-17-26)20-21-35-29-9-5-4-8-28(29)24-6-2-1-3-7-24/h1-9,12-15,23,26H,10-11,16-22H2	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	342	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Medical College Curated by ChEMBL					Assay Description Displacement of [3H]-8-OH-DPAT from human 5-HT1A receptor expressed in HEK293 cells incubated for 1 hr				Bioorg Med Chem 24: 130-9 (2016) BindingDB Entry DOI: 10.7270/Q2W95C1P
					More data for this Ligand-Target Pair