null

SMILES: O=C1Cc2ccccc2N1CCCCCN1CCN(CC1)c1cccc2[nH]cnc12

InChI Key: InChIKey=XNSRYAXPXINABJ-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50267738   

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 1A (Homo sapiens (Human))	BDBM50267738 (1-{5-[4-(1H)-benzimidazol-4-yl)piperazin-1-yl]pent...) Show SMILES O=C1Cc2ccccc2N1CCCCCN1CCN(CC1)c1cccc2[nH]cnc12 Show InChI InChI=1S/C24H29N5O/c30-23-17-19-7-2-3-9-21(19)29(23)12-5-1-4-11-27-13-15-28(16-14-27)22-10-6-8-20-24(22)26-18-25-20/h2-3,6-10,18H,1,4-5,11-17H2,(H,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	18.1	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Complutense de Madrid Curated by ChEMBL					Assay Description Displacement of [3H]8-OH-DPAT from human recombinant 5HT1A receptor expressed in HEK293 cells				J Med Chem 52: 2384-92 (2009) Article DOI: 10.1021/jm8014553 BindingDB Entry DOI: 10.7270/Q2B8580P
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 7 (Homo sapiens (Human))	BDBM50267738 (1-{5-[4-(1H)-benzimidazol-4-yl)piperazin-1-yl]pent...) Show SMILES O=C1Cc2ccccc2N1CCCCCN1CCN(CC1)c1cccc2[nH]cnc12 Show InChI InChI=1S/C24H29N5O/c30-23-17-19-7-2-3-9-21(19)29(23)12-5-1-4-11-27-13-15-28(16-14-27)22-10-6-8-20-24(22)26-18-25-20/h2-3,6-10,18H,1,4-5,11-17H2,(H,25,26)	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	68	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Complutense de Madrid Curated by ChEMBL					Assay Description Displacement of [3H]LSD from human recombinant 5HT7 receptor expressed in CHOK1 cells				J Med Chem 52: 2384-92 (2009) Article DOI: 10.1021/jm8014553 BindingDB Entry DOI: 10.7270/Q2B8580P
					More data for this Ligand-Target Pair