BDBM50105456 2-Benzylamino-N-hydroxy-2-methyl-3-(4-phenoxy-benzenesulfonyl)-propionamide::CHEMBL91124

SMILES CC(CS(=O)(=O)c1ccc(Oc2ccccc2)cc1)(NCc1ccccc1)C(=O)NO

InChI Key InChIKey=UDYKJHQVNSKFHV-UHFFFAOYSA-N

Data  5 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50105456   

Target72 kDa type IV collagenase(Homo sapiens (Human))
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM50105456(2-Benzylamino-N-hydroxy-2-methyl-3-(4-phenoxy-benz...)
Affinity DataIC50:  0.200nMAssay Description:Inhibition of human recombinant MMP2 by colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target72 kDa type IV collagenase(Homo sapiens (Human))
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM50105456(2-Benzylamino-N-hydroxy-2-methyl-3-(4-phenoxy-benz...)
Affinity DataIC50:  0.200nMAssay Description:Inhibition of human recombinant MMP2 by colorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetInterstitial collagenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50105456(2-Benzylamino-N-hydroxy-2-methyl-3-(4-phenoxy-benz...)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibitory activity against human Matrix metalloprotease-1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCollagenase 3(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50105456(2-Benzylamino-N-hydroxy-2-methyl-3-(4-phenoxy-benz...)
Affinity DataIC50:  0.300nMAssay Description:Inhibitory activity against human Matrix metalloprotease-13More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target72 kDa type IV collagenase(Homo sapiens (Human))
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM50105456(2-Benzylamino-N-hydroxy-2-methyl-3-(4-phenoxy-benz...)
Affinity DataIC50:  0.200nMAssay Description:Inhibitory activity against human Matrix metalloprotease-2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed