BDBM50261658 CHEMBL4099164

SMILES CC(C)C[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)[C@@H](N)[C@@H](C)O)C(=O)N[C@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(O)=O

InChI Key InChIKey=ZYPYAXPTWKNCLK-LPSCLBFBSA-N

Data  2 Kd

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50261658   

TargetE3 ubiquitin-protein ligase Mdm2(Homo sapiens (Human))
University of Maryland

Curated by ChEMBL
LigandPNGBDBM50261658(CHEMBL4099164)
Affinity DataKd:  14nMAssay Description:Agonist activity at human beta-2 adrenergic receptor expressed in human H292 cells assessed as accumulation of intracellular cAMP after 1 hr by Alpha...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein Mdm4(Homo sapiens (Human))
University of Maryland

Curated by ChEMBL
LigandPNGBDBM50261658(CHEMBL4099164)
Affinity DataKd:  61nMAssay Description:Cross Resistance (antiviral activity) of the compound with Y188C (Nonnucleoside reverse transcriptase inhibitor) resistant HIV isolate from cytopathi...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed