null

SMILES: NC(=O)c1sccc1NC(=O)CCCCN1CCN(CC1)c1ccccc1

InChI Key: InChIKey=CKWRIKJZKDOTMM-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50504208   

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))	BDBM50504208 (CHEMBL4590226) Show SMILES NC(=O)c1sccc1NC(=O)CCCCN1CCN(CC1)c1ccccc1 Show InChI InChI=1S/C20H26N4O2S/c21-20(26)19-17(9-15-27-19)22-18(25)8-4-5-10-23-11-13-24(14-12-23)16-6-2-1-3-7-16/h1-3,6-7,9,15H,4-5,8,10-14H2,(H2,21,26)(H,22,25)	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.90	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ di Catania Curated by ChEMBL					Assay Description Displacement of [3H]-5-HT from human 5HT7 receptor expressed in CHO-K1 cells incubated for 40 mins in presence of serotonin by liquid scintillation c...				Eur J Med Chem 183: (2019) Article DOI: 10.1016/j.ejmech.2019.111690
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Homo sapiens (Human))	BDBM50504208 (CHEMBL4590226) Show SMILES NC(=O)c1sccc1NC(=O)CCCCN1CCN(CC1)c1ccccc1 Show InChI InChI=1S/C20H26N4O2S/c21-20(26)19-17(9-15-27-19)22-18(25)8-4-5-10-23-11-13-24(14-12-23)16-6-2-1-3-7-16/h1-3,6-7,9,15H,4-5,8,10-14H2,(H2,21,26)(H,22,25)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	39	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ di Catania Curated by ChEMBL					Assay Description Displacement of [3H]-8-OH-DPAT from human 5-HT1A receptor expressed in CHO-K1 cells incubated for 60 mins by liquid scintillation counting method				Eur J Med Chem 183: (2019) Article DOI: 10.1016/j.ejmech.2019.111690
					More data for this Ligand-Target Pair