BDBM50132596 CHEMBL2370434::Dimeric peptide

SMILES NCCCC[C@H](NC(=O)[C@H](CSSC[C@H](NC(=O)[C@@H](N)Cc1c[nH]cn1)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(N)=O)NC(=O)[C@@H](N)Cc1c[nH]cn1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(N)=O

InChI Key InChIKey=MJWYOGSHVHNPBX-BLYCEMGBSA-N

Data  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50132596   

TargetIntegrase(Human immunodeficiency virus 1)
Nih

Curated by ChEMBL
LigandPNGBDBM50132596(CHEMBL2370434 | Dimeric peptide)
Affinity DataIC50:  8.10E+4nMAssay Description:In vitro inhibitory activity of the compound against HIV-1 integrase enzyme 3'-end processingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrase(Human immunodeficiency virus 1)
Nih

Curated by ChEMBL
LigandPNGBDBM50132596(CHEMBL2370434 | Dimeric peptide)
Affinity DataIC50:  5.80E+4nMAssay Description:In vitro inhibitory activity of the compound against HIV-1 integrase enzyme strand transfer processMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed