null

SMILES: Fc1ccc(NC(=O)c2ccc(SCc3ccc(cc3)-n3cncn3)nc2)cc1

InChI Key: InChIKey=DIBKFYNBWFTSRL-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 150844   

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))	BDBM150844 (US8981106, 33) Show SMILES Fc1ccc(NC(=O)c2ccc(SCc3ccc(cc3)-n3cncn3)nc2)cc1 Show InChI InChI=1S/C21H16FN5OS/c22-17-4-6-18(7-5-17)26-21(28)16-3-10-20(24-11-16)29-12-15-1-8-19(9-2-15)27-14-23-13-25-27/h1-11,13-14H,12H2,(H,26,28)	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Syntrix Biosystems Curated by ChEMBL					Assay Description Antagonist activity at CXCR2 in human PMNs assessed as inhibition of CXCL1-induced intracellular Ca2+ release by fluorescence based calcium flux assa...				J Med Chem 57: 8378-97 (2014) Article DOI: 10.1021/jm500827t BindingDB Entry DOI: 10.7270/Q2FX7C22
					More data for this Ligand-Target Pair
C-X-C chemokine receptor type 2 (Homo sapiens (Human))	BDBM150844 (US8981106, 33) Show SMILES Fc1ccc(NC(=O)c2ccc(SCc3ccc(cc3)-n3cncn3)nc2)cc1 Show InChI InChI=1S/C21H16FN5OS/c22-17-4-6-18(7-5-17)26-21(28)16-3-10-20(24-11-16)29-12-15-1-8-19(9-2-15)27-14-23-13-25-27/h1-11,13-14H,12H2,(H,26,28)	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	37
Syntrix Biosystems, Inc. US Patent					Assay Description An in vitro assay showed inhibition of CXCR2-mediated intracellular calcium release. Briefly, human neutrophils were suspended in HBSS- (without Ca2+...				US Patent US8981106 (2015) BindingDB Entry DOI: 10.7270/Q2WW7GC1
					More data for this Ligand-Target Pair