BDBM50456152 CHEMBL4216003

SMILES: CC(C)c1cn2cccc(C(=O)NCC3CCN(CC(C)(C)O)CC3)c2n1

InChI Key: InChIKey=MWTXQNNOUIKDEF-UHFFFAOYSA-N

Data: 1 EC50

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 1 hit for monomerid = 50456152   

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
Serotonin (5-HT) receptor (Homo sapiens (Human))	BDBM50456152 (CHEMBL4216003) Show SMILES CC(C)c1cn2cccc(C(=O)NCC3CCN(CC(C)(C)O)CC3)c2n1 Show InChI InChI=1S/C21H32N4O2/c1-15(2)18-13-25-9-5-6-17(19(25)23-18)20(26)22-12-16-7-10-24(11-8-16)14-21(3,4)27/h5-6,9,13,15-16,27H,7-8,10-12,14H2,1-4H3,(H,22,26)	UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	0.700	n/a	n/a	n/a	n/a
Suven Life Sciences Limited Curated by ChEMBL					Assay Description Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase re...				J Med Chem 61: 4993-5008 (2018) Article DOI: 10.1021/acs.jmedchem.8b00457 BindingDB Entry DOI: 10.7270/Q21R6T32
					More data for this Ligand-Target Pair