BDBM50201706 (3R,4R)-4-(2,3-dimethylphenoxy)piperidin-3-ol::CHEMBL230479

SMILES Cc1cccc(O[C@@H]2CCNC[C@H]2O)c1C

InChI Key InChIKey=ZHFIAFNZGWCLHU-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:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 50201706   

TargetDipeptidyl peptidase 1(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201706((3R,4R)-4-(2,3-dimethylphenoxy)piperidin-3-ol | CH...)
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 K(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201706((3R,4R)-4-(2,3-dimethylphenoxy)piperidin-3-ol | CH...)
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 F(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201706((3R,4R)-4-(2,3-dimethylphenoxy)piperidin-3-ol | CH...)
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 K(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201706((3R,4R)-4-(2,3-dimethylphenoxy)piperidin-3-ol | CH...)
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 B(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201706((3R,4R)-4-(2,3-dimethylphenoxy)piperidin-3-ol | CH...)
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
TargetCathepsin S(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201706((3R,4R)-4-(2,3-dimethylphenoxy)piperidin-3-ol | CH...)
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
TargetCathepsin L2(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201706((3R,4R)-4-(2,3-dimethylphenoxy)piperidin-3-ol | CH...)
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
TargetProcathepsin L(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201706((3R,4R)-4-(2,3-dimethylphenoxy)piperidin-3-ol | CH...)
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
TargetPro-cathepsin H(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201706((3R,4R)-4-(2,3-dimethylphenoxy)piperidin-3-ol | CH...)
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