BDBM50201707 5-((2,3-dimethylphenoxy)methyl)-3-methyloxazolidin-2-one::CHEMBL397973

SMILES CN1CC(COc2cccc(C)c2C)OC1=O

InChI Key InChIKey=UWNKJJCNLMBGKB-UHFFFAOYSA-N

Data  9 IC50

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 50201707   

TargetCathepsin B(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201707(5-((2,3-dimethylphenoxy)methyl)-3-methyloxazolidin...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human recombinant cathepsin BMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPro-cathepsin H(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201707(5-((2,3-dimethylphenoxy)methyl)-3-methyloxazolidin...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human recombinant cathepsin HMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetDipeptidyl peptidase 1(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201707(5-((2,3-dimethylphenoxy)methyl)-3-methyloxazolidin...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human recombinant cathepsin CMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCathepsin F(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201707(5-((2,3-dimethylphenoxy)methyl)-3-methyloxazolidin...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human recombinant cathepsin FMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCathepsin S(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201707(5-((2,3-dimethylphenoxy)methyl)-3-methyloxazolidin...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human recombinant cathepsin SMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProcathepsin L(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201707(5-((2,3-dimethylphenoxy)methyl)-3-methyloxazolidin...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human recombinant cathepsin LMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCathepsin K(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201707(5-((2,3-dimethylphenoxy)methyl)-3-methyloxazolidin...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human recombinant cathepsin KMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCathepsin K(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201707(5-((2,3-dimethylphenoxy)methyl)-3-methyloxazolidin...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human recombinant cathepsin XMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCathepsin L2(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201707(5-((2,3-dimethylphenoxy)methyl)-3-methyloxazolidin...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human recombinant cathepsin VMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed