BDBM50140536 (S)-2-Amino-2-cyclohexyl-1-thiazolidin-3-yl-ethanone::CHEMBL23223

SMILES N[C@@H](C1CCCCC1)C(=O)N1CCSC1

InChI Key InChIKey=NEBWHDJOHHYIFW-UHFFFAOYSA-N

Data  1 KI  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50140536   

TargetDipeptidyl peptidase 4(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50140536((S)-2-Amino-2-cyclohexyl-1-thiazolidin-3-yl-ethano...)
Affinity DataIC50: 89nMAssay Description:Inhibitory activity against human Dipeptidylpeptidase IVMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetDipeptidyl peptidase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50140536((S)-2-Amino-2-cyclohexyl-1-thiazolidin-3-yl-ethano...)
Affinity DataIC50: 2.80E+3nMAssay Description:Inhibitory activity against human quiescent cell proline dipeptidase (QPP) enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50140536((S)-2-Amino-2-cyclohexyl-1-thiazolidin-3-yl-ethano...)
Affinity DataKi:  2.80E+4nMAssay Description:Binding affinity towards human ERG potassium ion channel was determinedMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed