BDBM50614605 CHEMBL5278663

SMILES CC(C)[C@H](NC(=O)[C@H](CC1CC1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](Cc1ccccc1)NC(=O)CCCCCNC(=O)c1ccc(C(O)=O)c(c1)-c1c2ccc(O)cc2oc2cc(=O)ccc12)P(=O)(Oc1ccccc1)Oc1ccccc1

InChI Key InChIKey=MQYFDMZWAQQKGI-WKIKYWDLSA-N

Data  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 2 hits for monomerid = 50614605   

LigandPNGBDBM50614605(CHEMBL5278663)
Affinity DataIC50:  8.30E+3nMAssay Description:Inhibition of recombinant human HTRA2 using H2-OPT as substrate assessed as increase in fluorescence and measured for 2 hrs by fluorescent plate read...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSerine protease HTRA1(Homo sapiens (Human))TBA
LigandPNGBDBM50614605(CHEMBL5278663)
Affinity DataIC50:  6.30E+3nMAssay Description:Inhibition of recombinant human HTRA1 using H2-OPT as substrate assessed as increase in fluorescence and measured for 2 hrs by fluorescent plate read...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed