null

SMILES: CN(C1CCCCC1)S(=O)(=O)c1ccc(Cn2c(C)nc3ccccc23)cc1

InChI Key: InChIKey=MUXHEFBAOKARLM-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50280482   

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
Platelet-activating factor receptor (Homo sapiens (Human))	BDBM50280482 (BB-182 | CHEMBL418608 | N-Cyclohexyl-N-methyl-4-(2...) Show SMILES CN(C1CCCCC1)S(=O)(=O)c1ccc(Cn2c(C)nc3ccccc23)cc1 Show InChI InChI=1S/C22H27N3O2S/c1-17-23-21-10-6-7-11-22(21)25(17)16-18-12-14-20(15-13-18)28(26,27)24(2)19-8-4-3-5-9-19/h6-7,10-15,19H,3-5,8-9,16H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article	n/a	n/a	300	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of [3H]PAF receptor binding to washed human platelet membranes determined in vitro				Bioorg Med Chem Lett 3: 1499-1504 (1993) Article DOI: 10.1016/S0960-894X(00)80006-2 BindingDB Entry DOI: 10.7270/Q2CC115V
					More data for this Ligand-Target Pair
Platelet-activating factor receptor (Homo sapiens (Human))	BDBM50280482 (BB-182 | CHEMBL418608 | N-Cyclohexyl-N-methyl-4-(2...) Show SMILES CN(C1CCCCC1)S(=O)(=O)c1ccc(Cn2c(C)nc3ccccc23)cc1 Show InChI InChI=1S/C22H27N3O2S/c1-17-23-21-10-6-7-11-22(21)25(17)16-18-12-14-20(15-13-18)28(26,27)24(2)19-8-4-3-5-9-19/h6-7,10-15,19H,3-5,8-9,16H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article	n/a	n/a	300	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Antagonistic activity for inhibition of [3H]PAF receptor binding to washed human platelet membranes.				Bioorg Med Chem Lett 2: 597-602 (1992) Article DOI: 10.1016/S0960-894X(01)81205-1 BindingDB Entry DOI: 10.7270/Q2CF9QK7
					More data for this Ligand-Target Pair