BDBM17300 (2S,3R)-3-methyl-1-oxo-1-(1,3-thiazolidin-3-yl)pentan-2-aminium::allo isoleucyl thiazolidide, 2

SMILES CC[C@@H](C)[C@H]([NH3+])C(=O)N1CCSC1

InChI Key InChIKey=WCRLBFHWFPELKW-SFYZADRCSA-O

Data  4 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 4 hits for monomerid = 17300   

TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Merck Research Laboratories

LigandPNGBDBM17300((2S,3R)-3-methyl-1-oxo-1-(1,3-thiazolidin-3-yl)pen...)
Affinity DataIC50:  460nMpH: 7.5 T: 2°CAssay Description:The enzyme activity resulted in the formation of the fluorescent product amidomethylcoumarin (AMC), which was monitored by excitation at 360 nm and m...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 9(Homo sapiens (Human))
Merck Research Laboratories

LigandPNGBDBM17300((2S,3R)-3-methyl-1-oxo-1-(1,3-thiazolidin-3-yl)pen...)
Affinity DataIC50:  320nMAssay Description:The enzyme activity resulted in the formation of the fluorescent product amidomethylcoumarin (AMC), which was monitored by excitation at 360 nm and m...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 8(Homo sapiens (Human))
Merck Research Laboratories

LigandPNGBDBM17300((2S,3R)-3-methyl-1-oxo-1-(1,3-thiazolidin-3-yl)pen...)
Affinity DataIC50:  220nMAssay Description:The enzyme activity resulted in the formation of the fluorescent product, which was monitored by excitation at 400 nm and measurement of fluorescent ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 2(Homo sapiens (Human))
Merck Research Laboratories

LigandPNGBDBM17300((2S,3R)-3-methyl-1-oxo-1-(1,3-thiazolidin-3-yl)pen...)
Affinity DataIC50:  1.80E+4nMAssay Description:The enzyme activity resulted in the formation of the fluorescent product amidomethylcoumarin (AMC), which was monitored by excitation at 360 nm and m...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed