BDBM50526023 CHEMBL4439370

SMILES: Fc1ccc2[nH]cc(C3CCCN(CCCCn4c(=O)c(-c5ccccc5F)c5ccccn5c4=O)C3)c2c1

InChI Key: InChIKey=WWJIYPPDCNQYTL-UHFFFAOYSA-N

Data: 2 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 2 hits for monomerid = 50526023   

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
Sodium-dependent serotonin transporter (Rattus norvegicus (rat))	BDBM50526023 (CHEMBL4439370) Show SMILES Fc1ccc2[nH]cc(C3CCCN(CCCCn4c(=O)c(-c5ccccc5F)c5ccccn5c4=O)C3)c2c1 |(23.53,-42.07,;22.03,-42.37,;21.54,-43.84,;20.03,-44.14,;19.01,-42.99,;17.48,-42.98,;17.01,-41.51,;18.27,-40.62,;18.28,-39.08,;19.62,-38.32,;19.64,-36.78,;18.31,-35.99,;16.98,-36.76,;15.65,-35.98,;14.31,-36.75,;12.98,-35.97,;11.64,-36.73,;10.31,-35.95,;10.32,-34.41,;11.66,-33.65,;8.99,-33.63,;8.99,-32.1,;7.67,-31.33,;7.67,-29.79,;9.01,-29.02,;10.34,-29.79,;10.33,-31.33,;11.66,-32.11,;7.66,-34.4,;6.33,-33.62,;5,-34.4,;5,-35.94,;6.33,-36.7,;7.65,-35.94,;8.98,-36.71,;8.97,-38.25,;16.96,-38.3,;19.51,-41.53,;21.01,-41.23,)| Show InChI InChI=1S/C31H30F2N4O2/c32-22-12-13-27-24(18-22)25(19-34-27)21-8-7-15-35(20-21)14-5-6-17-37-30(38)29(23-9-1-2-10-26(23)33)28-11-3-4-16-36(28)31(37)39/h1-4,9-13,16,18-19,21,34H,5-8,14-15,17,20H2	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	115	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Medical University of Warsaw Curated by ChEMBL					Assay Description Displacement of [3H]-citalopram from SERT in rat cortex tissue measured after 60 mins by microbeta scintillation counting analysis				Eur J Med Chem 166: 144-158 (2019) Article DOI: 10.1016/j.ejmech.2019.01.031
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Homo sapiens (Human))	BDBM50526023 (CHEMBL4439370) Show SMILES Fc1ccc2[nH]cc(C3CCCN(CCCCn4c(=O)c(-c5ccccc5F)c5ccccn5c4=O)C3)c2c1 |(23.53,-42.07,;22.03,-42.37,;21.54,-43.84,;20.03,-44.14,;19.01,-42.99,;17.48,-42.98,;17.01,-41.51,;18.27,-40.62,;18.28,-39.08,;19.62,-38.32,;19.64,-36.78,;18.31,-35.99,;16.98,-36.76,;15.65,-35.98,;14.31,-36.75,;12.98,-35.97,;11.64,-36.73,;10.31,-35.95,;10.32,-34.41,;11.66,-33.65,;8.99,-33.63,;8.99,-32.1,;7.67,-31.33,;7.67,-29.79,;9.01,-29.02,;10.34,-29.79,;10.33,-31.33,;11.66,-32.11,;7.66,-34.4,;6.33,-33.62,;5,-34.4,;5,-35.94,;6.33,-36.7,;7.65,-35.94,;8.98,-36.71,;8.97,-38.25,;16.96,-38.3,;19.51,-41.53,;21.01,-41.23,)| Show InChI InChI=1S/C31H30F2N4O2/c32-22-12-13-27-24(18-22)25(19-34-27)21-8-7-15-35(20-21)14-5-6-17-37-30(38)29(23-9-1-2-10-26(23)33)28-11-3-4-16-36(28)31(37)39/h1-4,9-13,16,18-19,21,34H,5-8,14-15,17,20H2	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	218	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Medical University of Warsaw Curated by ChEMBL					Assay Description Displacement of [3H]-8-OH-DPAT from recombinant human 5HT1A receptor expressed in CHO cell membranes measured after 60 mins by microbeta scintillatio...				Eur J Med Chem 166: 144-158 (2019) Article DOI: 10.1016/j.ejmech.2019.01.031
					More data for this Ligand-Target Pair