BDBM50201703 (1S,2S)-2-bromo-7-oxa-5-aza-bicyclo[3.2.1]octan-6-one::CHEMBL397972

SMILES Br[C@H]1CCN2C[C@@H]1OC2=O

InChI Key InChIKey=VVSXVRNUMNINTL-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 = 50201703   

TargetPro-cathepsin H(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201703((1S,2S)-2-bromo-7-oxa-5-aza-bicyclo[3.2.1]octan-6-...)
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
TargetCathepsin K(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201703((1S,2S)-2-bromo-7-oxa-5-aza-bicyclo[3.2.1]octan-6-...)
Affinity DataIC50: 1.00E+4nMAssay 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
TargetDipeptidyl peptidase 1(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201703((1S,2S)-2-bromo-7-oxa-5-aza-bicyclo[3.2.1]octan-6-...)
Affinity DataIC50: 1.00E+4nMAssay 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 L2(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201703((1S,2S)-2-bromo-7-oxa-5-aza-bicyclo[3.2.1]octan-6-...)
Affinity DataIC50: 1.00E+4nMAssay 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
TargetCathepsin K(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201703((1S,2S)-2-bromo-7-oxa-5-aza-bicyclo[3.2.1]octan-6-...)
Affinity DataIC50: 3.00E+4nMAssay 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
LigandPNGBDBM50201703((1S,2S)-2-bromo-7-oxa-5-aza-bicyclo[3.2.1]octan-6-...)
Affinity DataIC50: 1.00E+4nMAssay 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
LigandPNGBDBM50201703((1S,2S)-2-bromo-7-oxa-5-aza-bicyclo[3.2.1]octan-6-...)
Affinity DataIC50: 4.55E+3nMAssay 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
LigandPNGBDBM50201703((1S,2S)-2-bromo-7-oxa-5-aza-bicyclo[3.2.1]octan-6-...)
Affinity DataIC50: 5.82E+3nMAssay 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 B(Human)
The Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50201703((1S,2S)-2-bromo-7-oxa-5-aza-bicyclo[3.2.1]octan-6-...)
Affinity DataIC50: 158nMAssay 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