Compile Data Set for Download or QSAR

Found 4 hits Enz. Inhib. hit(s) with Target = 'Stromelysin-1' and Ligand = 'BDBM50031771'   

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))	BDBM50031771 ((R)-3-((S)-1-Methylcarbamoyl-2-phenyl-ethylcarbamo...) Show SMILES CNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CCCC(=O)NCCc1ccccc1)CC(=O)NO Show InChI InChI=1S/C26H34N4O5/c1-27-26(34)22(17-20-11-6-3-7-12-20)29-25(33)21(18-24(32)30-35)13-8-14-23(31)28-16-15-19-9-4-2-5-10-19/h2-7,9-12,21-22,35H,8,13-18H2,1H3,(H,27,34)(H,28,31)(H,29,33)(H,30,32)/t21-,22+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sterling Winthrop Pharmaceuticals Research Division Curated by ChEMBL					Assay Description Inhibitory potency against human stromelysin, MMP-3				J Med Chem 38: 2570-81 (1995) BindingDB Entry DOI: 10.7270/Q2GM86B5
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50031771 ((R)-3-((S)-1-Methylcarbamoyl-2-phenyl-ethylcarbamo...) Show SMILES CNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CCCC(=O)NCCc1ccccc1)CC(=O)NO Show InChI InChI=1S/C26H34N4O5/c1-27-26(34)22(17-20-11-6-3-7-12-20)29-25(33)21(18-24(32)30-35)13-8-14-23(31)28-16-15-19-9-4-2-5-10-19/h2-7,9-12,21-22,35H,8,13-18H2,1H3,(H,27,34)(H,28,31)(H,29,33)(H,30,32)/t21-,22+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human fibroblast stromelysin, matrix metalloproteinase-3				Bioorg Med Chem Lett 5: 343-348 (1995) Article DOI: 10.1016/0960-894X(95)00032-O BindingDB Entry DOI: 10.7270/Q2JH3M44
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50031771 ((R)-3-((S)-1-Methylcarbamoyl-2-phenyl-ethylcarbamo...) Show SMILES CNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CCCC(=O)NCCc1ccccc1)CC(=O)NO Show InChI InChI=1S/C26H34N4O5/c1-27-26(34)22(17-20-11-6-3-7-12-20)29-25(33)21(18-24(32)30-35)13-8-14-23(31)28-16-15-19-9-4-2-5-10-19/h2-7,9-12,21-22,35H,8,13-18H2,1H3,(H,27,34)(H,28,31)(H,29,33)(H,30,32)/t21-,22+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6	n/a	n/a	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))	BDBM50031771 ((R)-3-((S)-1-Methylcarbamoyl-2-phenyl-ethylcarbamo...) Show SMILES CNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CCCC(=O)NCCc1ccccc1)CC(=O)NO Show InChI InChI=1S/C26H34N4O5/c1-27-26(34)22(17-20-11-6-3-7-12-20)29-25(33)21(18-24(32)30-35)13-8-14-23(31)28-16-15-19-9-4-2-5-10-19/h2-7,9-12,21-22,35H,8,13-18H2,1H3,(H,27,34)(H,28,31)(H,29,33)(H,30,32)/t21-,22+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	<100	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human fibroblast stromelysin, matrix metalloprotease-3 (potent inhibitor)				Bioorg Med Chem Lett 5: 343-348 (1995) Article DOI: 10.1016/0960-894X(95)00032-O BindingDB Entry DOI: 10.7270/Q2JH3M44
					More data for this Ligand-Target Pair