Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Stromelysin-1' and Ligand = 'BDBM50097262'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Stromelysin-1 (Homo sapiens (Human))	BDBM50097262 ((R)-N*1*-[(S)-2,2-Dimethyl-1-((R)-1-phenyl-ethylca...) Show SMILES CCCCCCCCC[C@H](CC(=O)NO)C(=O)N[C@H](C(=O)N[C@H](C)c1ccccc1)C(C)(C)C Show InChI InChI=1S/C27H45N3O4/c1-6-7-8-9-10-11-13-18-22(19-23(31)30-34)25(32)29-24(27(3,4)5)26(33)28-20(2)21-16-14-12-15-17-21/h12,14-17,20,22,24,34H,6-11,13,18-19H2,1-5H3,(H,28,33)(H,29,32)(H,30,31)/t20-,22-,24-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	25	n/a	n/a	n/a	n/a	n/a	n/a
Pomona College Curated by ChEMBL					Assay Description Inhibition of MMP3				Bioorg Med Chem 15: 2223-68 (2007) Article DOI: 10.1016/j.bmc.2007.01.011 BindingDB Entry DOI: 10.7270/Q2571DBD
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50097262 ((R)-N*1*-[(S)-2,2-Dimethyl-1-((R)-1-phenyl-ethylca...) Show SMILES CCCCCCCCC[C@H](CC(=O)NO)C(=O)N[C@H](C(=O)N[C@H](C)c1ccccc1)C(C)(C)C Show InChI InChI=1S/C27H45N3O4/c1-6-7-8-9-10-11-13-18-22(19-23(31)30-34)25(32)29-24(27(3,4)5)26(33)28-20(2)21-16-14-12-15-17-21/h12,14-17,20,22,24,34H,6-11,13,18-19H2,1-5H3,(H,28,33)(H,29,32)(H,30,31)/t20-,22-,24-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	25	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Concentration required to inhibit the catalytic domain Matrix metalloprotease-3 using Nagase fluorogenic as a substrate.				Bioorg Med Chem Lett 11: 571-4 (2001) BindingDB Entry DOI: 10.7270/Q22B8X9X
					More data for this Ligand-Target Pair