null

SMILES: NCc1c(Cl)ccc(NC(=O)Nc2ccccc2Br)c1O

InChI Key: InChIKey=PUIOJSBMQYTVBS-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50152763   

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
C-X-C chemokine receptor type 2 (Homo sapiens (Human))	BDBM50152763 (1-(3-Aminomethyl-4-chloro-2-hydroxy-phenyl)-3-(2-b...) Show SMILES NCc1c(Cl)ccc(NC(=O)Nc2ccccc2Br)c1O Show InChI InChI=1S/C14H13BrClN3O2/c15-9-3-1-2-4-11(9)18-14(21)19-12-6-5-10(16)8(7-17)13(12)20/h1-6,20H,7,17H2,(H2,18,19,21)	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	114	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Concentration required to inhibit [125I]IL-8 binding towards C-X-C chemokine receptor type 2 of human expressed in CHO cells				Bioorg Med Chem Lett 14: 4375-8 (2004) Article DOI: 10.1016/j.bmcl.2004.06.097 BindingDB Entry DOI: 10.7270/Q2SQ914M
					More data for this Ligand-Target Pair
C-X-C chemokine receptor type 1 (Homo sapiens (Human))	BDBM50152763 (1-(3-Aminomethyl-4-chloro-2-hydroxy-phenyl)-3-(2-b...) Show SMILES NCc1c(Cl)ccc(NC(=O)Nc2ccccc2Br)c1O Show InChI InChI=1S/C14H13BrClN3O2/c15-9-3-1-2-4-11(9)18-14(21)19-12-6-5-10(16)8(7-17)13(12)20/h1-6,20H,7,17H2,(H2,18,19,21)	PDB UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Concentration required to inhibit [125I]-IL-8 binding towards C-X-C chemokine receptor type 1 of human expressed in CHO cells				Bioorg Med Chem Lett 14: 4375-8 (2004) Article DOI: 10.1016/j.bmcl.2004.06.097 BindingDB Entry DOI: 10.7270/Q2SQ914M
					More data for this Ligand-Target Pair