BDBM50610496 CHEMBL441158

SMILES [H][C@@]12CCCCN1C(=O)[C@@]([H])(COC(=O)[C@]([H])(C(C)C)N(C)C(=O)CN(C)C(=O)CNC(=O)[C@]1([H])CCCCN1C(=O)[C@@]([H])(COC(=O)[C@]([H])(C(C)C)N(C)C(=O)CN(C)C(=O)CNC2=O)NC(=O)c1nc2ccccc2cc1O)NC(=O)c1nc2ccccc2cc1O

InChI Key InChIKey=WXIVYIYCEBUEHL-UHFFFAOYSA-N

Data  1 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 1 hit for monomerid = 50610496   

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Indo-Soviet Friendship College of Pharmacy (ISFCP)

Curated by ChEMBL
LigandPNGBDBM50610496(CHEMBL441158)
Affinity DataIC50: 0.130nMAssay Description:Inhibition of HIV-1 reverse transcriptase incubated for 90 mins by liquid scintillation counting analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/21/2024
Entry Details
PubMed