BDBM50216817 (3R)-6-cyclohexyl-N-hydroxy-3-(3-{[(phenylsulfonyl)amino]carbonyl}-1,2,4-oxadiazol-5-yl)hexanamide::CHEMBL439012

SMILES: ONC(=O)C[C@@H](CCCC1CCCCC1)c1nc(no1)C(=O)NS(=O)(=O)c1ccccc1

InChI Key: InChIKey=JBPHFUSOSQRLMX-MRXNPFEDSA-N

Data: 7 IC50

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 7 hits for monomerid = 50216817   

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
Matrix metalloproteinase-9 (Homo sapiens (Human))	BDBM50216817 ((3R)-6-cyclohexyl-N-hydroxy-3-(3-{[(phenylsulfonyl...) Show SMILES ONC(=O)C[C@@H](CCCC1CCCCC1)c1nc(no1)C(=O)NS(=O)(=O)c1ccccc1 Show InChI InChI=1S/C21H28N4O6S/c26-18(23-28)14-16(11-7-10-15-8-3-1-4-9-15)21-22-19(24-31-21)20(27)25-32(29,30)17-12-5-2-6-13-17/h2,5-6,12-13,15-16,28H,1,3-4,7-11,14H2,(H,23,26)(H,25,27)/t16-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	6.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Inhibition of MMP9				J Med Chem 50: 3442-56 (2007) Article DOI: 10.1021/jm061010z BindingDB Entry DOI: 10.7270/Q2W66KGB
					More data for this Ligand-Target Pair
Matrix metalloproteinase-14 (MMP14) (Homo sapiens (Human))	BDBM50216817 ((3R)-6-cyclohexyl-N-hydroxy-3-(3-{[(phenylsulfonyl...) Show SMILES ONC(=O)C[C@@H](CCCC1CCCCC1)c1nc(no1)C(=O)NS(=O)(=O)c1ccccc1 Show InChI InChI=1S/C21H28N4O6S/c26-18(23-28)14-16(11-7-10-15-8-3-1-4-9-15)21-22-19(24-31-21)20(27)25-32(29,30)17-12-5-2-6-13-17/h2,5-6,12-13,15-16,28H,1,3-4,7-11,14H2,(H,23,26)(H,25,27)/t16-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Inhibition of MMP14				J Med Chem 50: 3442-56 (2007) Article DOI: 10.1021/jm061010z BindingDB Entry DOI: 10.7270/Q2W66KGB
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50216817 ((3R)-6-cyclohexyl-N-hydroxy-3-(3-{[(phenylsulfonyl...) Show SMILES ONC(=O)C[C@@H](CCCC1CCCCC1)c1nc(no1)C(=O)NS(=O)(=O)c1ccccc1 Show InChI InChI=1S/C21H28N4O6S/c26-18(23-28)14-16(11-7-10-15-8-3-1-4-9-15)21-22-19(24-31-21)20(27)25-32(29,30)17-12-5-2-6-13-17/h2,5-6,12-13,15-16,28H,1,3-4,7-11,14H2,(H,23,26)(H,25,27)/t16-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	9.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Inhibition of MMP2				J Med Chem 50: 3442-56 (2007) Article DOI: 10.1021/jm061010z BindingDB Entry DOI: 10.7270/Q2W66KGB
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50216817 ((3R)-6-cyclohexyl-N-hydroxy-3-(3-{[(phenylsulfonyl...) Show SMILES ONC(=O)C[C@@H](CCCC1CCCCC1)c1nc(no1)C(=O)NS(=O)(=O)c1ccccc1 Show InChI InChI=1S/C21H28N4O6S/c26-18(23-28)14-16(11-7-10-15-8-3-1-4-9-15)21-22-19(24-31-21)20(27)25-32(29,30)17-12-5-2-6-13-17/h2,5-6,12-13,15-16,28H,1,3-4,7-11,14H2,(H,23,26)(H,25,27)/t16-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	7.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Inhibition of MMP3				J Med Chem 50: 3442-56 (2007) Article DOI: 10.1021/jm061010z BindingDB Entry DOI: 10.7270/Q2W66KGB
					More data for this Ligand-Target Pair
Collagenase 3 (Homo sapiens (Human))	BDBM50216817 ((3R)-6-cyclohexyl-N-hydroxy-3-(3-{[(phenylsulfonyl...) Show SMILES ONC(=O)C[C@@H](CCCC1CCCCC1)c1nc(no1)C(=O)NS(=O)(=O)c1ccccc1 Show InChI InChI=1S/C21H28N4O6S/c26-18(23-28)14-16(11-7-10-15-8-3-1-4-9-15)21-22-19(24-31-21)20(27)25-32(29,30)17-12-5-2-6-13-17/h2,5-6,12-13,15-16,28H,1,3-4,7-11,14H2,(H,23,26)(H,25,27)/t16-/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Inhibition of MMP13				J Med Chem 50: 3442-56 (2007) Article DOI: 10.1021/jm061010z BindingDB Entry DOI: 10.7270/Q2W66KGB
					More data for this Ligand-Target Pair
Bone morphogenetic protein 1 (Homo sapiens (Human))	BDBM50216817 ((3R)-6-cyclohexyl-N-hydroxy-3-(3-{[(phenylsulfonyl...) Show SMILES ONC(=O)C[C@@H](CCCC1CCCCC1)c1nc(no1)C(=O)NS(=O)(=O)c1ccccc1 Show InChI InChI=1S/C21H28N4O6S/c26-18(23-28)14-16(11-7-10-15-8-3-1-4-9-15)21-22-19(24-31-21)20(27)25-32(29,30)17-12-5-2-6-13-17/h2,5-6,12-13,15-16,28H,1,3-4,7-11,14H2,(H,23,26)(H,25,27)/t16-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	7	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Inhibition of human procollagen C-proteinase expressed in CHO cells				J Med Chem 50: 3442-56 (2007) Article DOI: 10.1021/jm061010z BindingDB Entry DOI: 10.7270/Q2W66KGB
					More data for this Ligand-Target Pair
Interstitial collagenase (Homo sapiens (Human))	BDBM50216817 ((3R)-6-cyclohexyl-N-hydroxy-3-(3-{[(phenylsulfonyl...) Show SMILES ONC(=O)C[C@@H](CCCC1CCCCC1)c1nc(no1)C(=O)NS(=O)(=O)c1ccccc1 Show InChI InChI=1S/C21H28N4O6S/c26-18(23-28)14-16(11-7-10-15-8-3-1-4-9-15)21-22-19(24-31-21)20(27)25-32(29,30)17-12-5-2-6-13-17/h2,5-6,12-13,15-16,28H,1,3-4,7-11,14H2,(H,23,26)(H,25,27)/t16-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Inhibition of MMP1				J Med Chem 50: 3442-56 (2007) Article DOI: 10.1021/jm061010z BindingDB Entry DOI: 10.7270/Q2W66KGB
					More data for this Ligand-Target Pair