BDBM50193430 CHEMBL3985152

SMILES: COCOc1ccc(CNC(=O)CCCCCN2CCN(CC2)c2ccccc2-c2ccccc2)cc1

InChI Key: InChIKey=HUFSUMIWNMPJOE-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 = 50193430   

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))	BDBM50193430 (CHEMBL3985152) Show SMILES COCOc1ccc(CNC(=O)CCCCCN2CCN(CC2)c2ccccc2-c2ccccc2)cc1 Show InChI InChI=1S/C31H39N3O3/c1-36-25-37-28-17-15-26(16-18-28)24-32-31(35)14-6-3-9-19-33-20-22-34(23-21-33)30-13-8-7-12-29(30)27-10-4-2-5-11-27/h2,4-5,7-8,10-13,15-18H,3,6,9,14,19-25H2,1H3,(H,32,35)	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Bari"A. Moro" Curated by ChEMBL					Assay Description Displacement of [3H]-5-CT from human 5-HT7b receptor expressed in HEK293 cell membranes after 1 hr by microbeta counting analysis				Eur J Med Chem 120: 363-79 (2016) Article DOI: 10.1016/j.ejmech.2016.05.005 BindingDB Entry DOI: 10.7270/Q25T3NF8
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Homo sapiens (Human))	BDBM50193430 (CHEMBL3985152) Show SMILES COCOc1ccc(CNC(=O)CCCCCN2CCN(CC2)c2ccccc2-c2ccccc2)cc1 Show InChI InChI=1S/C31H39N3O3/c1-36-25-37-28-17-15-26(16-18-28)24-32-31(35)14-6-3-9-19-33-20-22-34(23-21-33)30-13-8-7-12-29(30)27-10-4-2-5-11-27/h2,4-5,7-8,10-13,15-18H,3,6,9,14,19-25H2,1H3,(H,32,35)	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	36	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Bari"A. Moro" Curated by ChEMBL					Assay Description Displacement of [3H]raclopride from human dopamine D2L receptor expressed in HEK293 cell membranes after 1 hr by microbeta counting analysis				Eur J Med Chem 120: 363-79 (2016) Article DOI: 10.1016/j.ejmech.2016.05.005 BindingDB Entry DOI: 10.7270/Q25T3NF8
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Homo sapiens (Human))	BDBM50193430 (CHEMBL3985152) Show SMILES COCOc1ccc(CNC(=O)CCCCCN2CCN(CC2)c2ccccc2-c2ccccc2)cc1 Show InChI InChI=1S/C31H39N3O3/c1-36-25-37-28-17-15-26(16-18-28)24-32-31(35)14-6-3-9-19-33-20-22-34(23-21-33)30-13-8-7-12-29(30)27-10-4-2-5-11-27/h2,4-5,7-8,10-13,15-18H,3,6,9,14,19-25H2,1H3,(H,32,35)	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	86	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Bari"A. Moro" Curated by ChEMBL					Assay Description Displacement of [3H]-8-OH-DPAT from human 5-HT1A receptor expressed in HEK293 cell membranes after 1 hr by microbeta counting analysis				Eur J Med Chem 120: 363-79 (2016) Article DOI: 10.1016/j.ejmech.2016.05.005 BindingDB Entry DOI: 10.7270/Q25T3NF8
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 6 (Homo sapiens (Human))	BDBM50193430 (CHEMBL3985152) Show SMILES COCOc1ccc(CNC(=O)CCCCCN2CCN(CC2)c2ccccc2-c2ccccc2)cc1 Show InChI InChI=1S/C31H39N3O3/c1-36-25-37-28-17-15-26(16-18-28)24-32-31(35)14-6-3-9-19-33-20-22-34(23-21-33)30-13-8-7-12-29(30)27-10-4-2-5-11-27/h2,4-5,7-8,10-13,15-18H,3,6,9,14,19-25H2,1H3,(H,32,35)	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	413	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Bari"A. Moro" Curated by ChEMBL					Assay Description Displacement of [3H]-LSD from human 5-HT6 receptor expressed in HEK293 cell membranes after 1 hr by microbeta counting analysis				Eur J Med Chem 120: 363-79 (2016) Article DOI: 10.1016/j.ejmech.2016.05.005 BindingDB Entry DOI: 10.7270/Q25T3NF8
					More data for this Ligand-Target Pair