BDBM13096 CGS 27023A Analog 24::N-hydroxy-2-[(4-methoxybenzene)(3-phenylpropyl)sulfonamido]acetamide

SMILES: COc1ccc(cc1)S(=O)(=O)N(CCCc1ccccc1)CC(=O)NO

InChI Key: InChIKey=HQBHGTOYWBOXIB-UHFFFAOYSA-N

Data: 1 KI

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 13096   

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
Stromelysin-1 (Homo sapiens (Human))	BDBM13096 (CGS 27023A Analog 24 | N-hydroxy-2-[(4-methoxybenz...) Show SMILES COc1ccc(cc1)S(=O)(=O)N(CCCc1ccccc1)CC(=O)NO Show InChI InChI=1S/C18H22N2O5S/c1-25-16-9-11-17(12-10-16)26(23,24)20(14-18(21)19-22)13-5-8-15-6-3-2-4-7-15/h2-4,6-7,9-12,22H,5,8,13-14H2,1H3,(H,19,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	125	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Pharmaceuticals					Assay Description Stromelysin inhibitory activity is based on the hydrolysis of substance P by recombinant human stromelysin to generate a fragment, substance P 7-11, ...				J Med Chem 40: 2525-32 (1997) Article DOI: 10.1021/jm960871c BindingDB Entry DOI: 10.7270/Q2MW2FC7
					More data for this Ligand-Target Pair