BDBM50261659 CHEMBL4059725

SMILES CC(C)C[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@@H](N)CCC(O)=O)[C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(O)=O)C(O)=O

InChI Key InChIKey=XEUWOGGAUYQDDW-CCIJQOLZSA-N

Data  2 Kd

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50261659   

TargetProtein Mdm4(Homo sapiens (Human))
University of Maryland

Curated by ChEMBL
LigandPNGBDBM50261659(CHEMBL4059725)
Affinity DataKd:  614nMAssay Description:HIV Protease inhibitory activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetE3 ubiquitin-protein ligase Mdm2(Homo sapiens (Human))
University of Maryland

Curated by ChEMBL
LigandPNGBDBM50261659(CHEMBL4059725)
Affinity DataKd:  346nMAssay Description:Cross Resistance (antiviral activity) of the compound with L100I (Nonnucleoside reverse transcriptase inhibitor) resistant HIV isolatefrom cytopathic...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed