BDBM50099378 CHEMBL3344165

SMILES OC(=O)C(F)(F)F.CC[C@H](C)[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)OCc1ccccc1)C(=O)N[C@@H](CC(C)C)[C@@H](O)CC(=O)NC1CCCCC1

InChI Key InChIKey=JROVVTMLFYHVFM-CXYWKTTNSA-M

Data  3 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 = 50099378   

TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter And Eliza Hall Institute Of Medical Research

Curated by ChEMBL
LigandPNGBDBM50099378(CHEMBL3344165)
Affinity DataIC50:  26nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
The Walter And Eliza Hall Institute Of Medical Research

Curated by ChEMBL
LigandPNGBDBM50099378(CHEMBL3344165)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human BACE1 assessed as cleavage of TRF substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin D(Homo sapiens (Human))
The Walter And Eliza Hall Institute Of Medical Research

Curated by ChEMBL
LigandPNGBDBM50099378(CHEMBL3344165)
Affinity DataIC50:  447nMAssay Description:Inhibition of human cathepsin D assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed