BDBM50088112 2-[3-(4-Fluoro-phenyl)-1-(4-nitro-benzyl)-ureido]-N-hydroxy-acetamide::CHEMBL56065

SMILES ONC(=O)CN(Cc1ccc(cc1)[N+]([O-])=O)C(=O)Nc1ccc(F)cc1

InChI Key InChIKey=NEUXHEKNAOUEQU-UHFFFAOYSA-N

Data  5 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50088112   

Target72 kDa type IV collagenase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50088112(2-[3-(4-Fluoro-phenyl)-1-(4-nitro-benzyl)-ureido]-...)
Affinity DataKi:  9nMAssay Description:Inhibitory activity against the Matrix Metalloprotease 2 (MMP-2)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMatrix metalloproteinase-9(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50088112(2-[3-(4-Fluoro-phenyl)-1-(4-nitro-benzyl)-ureido]-...)
Affinity DataKi:  11nMAssay 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
LigandPNGBDBM50088112(2-[3-(4-Fluoro-phenyl)-1-(4-nitro-benzyl)-ureido]-...)
Affinity DataKi:  12nMAssay Description:Inhibitory activity against the Matrix Metalloprotease-8More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50088112(2-[3-(4-Fluoro-phenyl)-1-(4-nitro-benzyl)-ureido]-...)
Affinity DataKi:  21nMAssay 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
LigandPNGBDBM50088112(2-[3-(4-Fluoro-phenyl)-1-(4-nitro-benzyl)-ureido]-...)
Affinity DataKi:  30nMAssay Description:Inhibitory activity against the Matrix Metalloprotease 1 (MMP-1)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed