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BDBM50316938 1-(4-fluorobenzyl)-2-(1-methylpiperidin-3-yl)-1H-benzo[d]imidazole::CHEMBL1087089

SMILES: CN1CCCC(C1)c1nc2ccccc2n1Cc1ccc(F)cc1

InChI Key: InChIKey=AXIFLPLKZRNVDP-UHFFFAOYSA-N

Data: 4 KI 2 IC50

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 50316938
Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50 nM	k_off s^-1	k_on M^-1s^-1	pH	Temp °C
Cytochrome P450 3A4 (Human)	BDBM50316938 (1-(4-fluorobenzyl)-2-(1-methylpiperidin-3-yl)-1H-b...) Show SMILES Show InChI	GoogleScholar	UniChem		n/a	n/a	>5.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
TBA					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Human)	BDBM50316938 (1-(4-fluorobenzyl)-2-(1-methylpiperidin-3-yl)-1H-b...) Show SMILES Show InChI	GoogleScholar	UniChem		n/a	n/a	2.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
TBA					More data for this Ligand-Target Pair
Histamine H1 receptor (Human)	BDBM50316938 (1-(4-fluorobenzyl)-2-(1-methylpiperidin-3-yl)-1H-b...) Show SMILES Show InChI	GoogleScholar	UniChem		0.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
TBA					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M1 (Human)	BDBM50316938 (1-(4-fluorobenzyl)-2-(1-methylpiperidin-3-yl)-1H-b...) Show SMILES Show InChI	GoogleScholar	UniChem		2.90E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
TBA					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Human)	BDBM50316938 (1-(4-fluorobenzyl)-2-(1-methylpiperidin-3-yl)-1H-b...) Show SMILES Show InChI	GoogleScholar	UniChem		>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
TBA					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Human)	BDBM50316938 (1-(4-fluorobenzyl)-2-(1-methylpiperidin-3-yl)-1H-b...) Show SMILES Show InChI	GoogleScholar	UniChem		>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
TBA					More data for this Ligand-Target Pair