BDBM50614606 CHEMBL5275102

SMILES CC(C)C[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](Cc1ccc2ccccc2c1)NC(=O)CCCCCNC(=O)c1ccc(C(O)=O)c(c1)-c1c2ccc(O)cc2oc2cc(=O)ccc12)C(=O)N[C@@H](C(C)C)P(=O)(Oc1ccccc1)Oc1ccccc1

InChI Key InChIKey=BGTJDAUVJGXIPX-UHFFFAOYSA-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 = 50614606   

TargetSerine protease HTRA1(Human)
Gwangju Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50614606(CHEMBL5275102)
Affinity DataIC50: 7.70E+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
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMed
TargetSerine protease HTRA2, mitochondrial(Human)
Gwangju Institute of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50614606(CHEMBL5275102)
Affinity DataIC50: 1.20E+4nMAssay 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
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMed