BDBM50088109 CHEMBL55521::N-Hydroxy-2-[(4-nitro-benzyl)-(4-(N-(2-methyl-benzene)-sulfonyl)ureido-benzenesulfonyl)-amino]-acetamide

SMILES Cc1ccccc1S(=O)(=O)NC(=O)Nc1ccc(cc1)S(=O)(=O)N(CC(=O)NO)Cc1ccc(cc1)[N+]([O-])=O

InChI Key InChIKey=MOHDKNTXJIGORP-UHFFFAOYSA-N

Data  5 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50088109   

TargetMatrix metalloproteinase-9(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50088109(CHEMBL55521 | N-Hydroxy-2-[(4-nitro-benzyl)-(4-(N-...)
Affinity DataKi:  0.700nMAssay Description:Inhibitory activity against the Matrix metalloprotease-9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeutrophil collagenase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50088109(CHEMBL55521 | N-Hydroxy-2-[(4-nitro-benzyl)-(4-(N-...)
Affinity DataKi:  1.5nMAssay Description:Inhibitory activity against the Matrix Metalloprotease-8More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target72 kDa type IV collagenase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50088109(CHEMBL55521 | N-Hydroxy-2-[(4-nitro-benzyl)-(4-(N-...)
Affinity DataKi:  1.60nMAssay Description:Inhibitory activity against the Matrix Metalloprotease 2 (MMP-2)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50088109(CHEMBL55521 | N-Hydroxy-2-[(4-nitro-benzyl)-(4-(N-...)
Affinity DataKi:  20nMAssay Description:Inhibitory activity against the Clostridium histolyticum collagenase (ChC)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetInterstitial collagenase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50088109(CHEMBL55521 | N-Hydroxy-2-[(4-nitro-benzyl)-(4-(N-...)
Affinity DataKi:  72nMAssay Description:Inhibitory activity against the Matrix Metalloprotease 1 (MMP-1)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed