null

SMILES: [Na+].CCc1cc(c(O)cc1OCCCCCC(C)(C)c1nn[n-]n1)-c1cccc(F)c1

InChI Key: InChIKey=WNNCYXDUCJVGNU-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50231625   

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
Leukotriene B4 receptor 1/2 (Homo sapiens (Human))	BDBM50231625 (CHEMBL128067) Show SMILES [Na+].CCc1cc(c(O)cc1OCCCCCC(C)(C)c1nn[n-]n1)-c1cccc(F)c1 Show InChI InChI=1S/C23H28FN4O2/c1-4-16-14-19(17-9-8-10-18(24)13-17)20(29)15-21(16)30-12-7-5-6-11-23(2,3)22-25-27-28-26-22/h8-10,13-15H,4-7,11-12H2,1-3H3,(H-,25,26,27,28,29)/q-1	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description Inhibition of [3H]LTB4 receptor binding in guinea pig lung membrane				J Med Chem 36: 3978-81 (1993) Article DOI: 10.1021/jm00076a029 BindingDB Entry DOI: 10.7270/Q20V8G1H
					More data for this Ligand-Target Pair
Leukotriene B4 receptor 1/2 (Homo sapiens (Human))	BDBM50231625 (CHEMBL128067) Show SMILES [Na+].CCc1cc(c(O)cc1OCCCCCC(C)(C)c1nn[n-]n1)-c1cccc(F)c1 Show InChI InChI=1S/C23H28FN4O2/c1-4-16-14-19(17-9-8-10-18(24)13-17)20(29)15-21(16)30-12-7-5-6-11-23(2,3)22-25-27-28-26-22/h8-10,13-15H,4-7,11-12H2,1-3H3,(H-,25,26,27,28,29)/q-1	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description Inhibition of [3H]LTB4 receptor binding in human neutrophils				J Med Chem 36: 3978-81 (1993) Article DOI: 10.1021/jm00076a029 BindingDB Entry DOI: 10.7270/Q20V8G1H
					More data for this Ligand-Target Pair