BDBM50484018 CHEMBL223769

SMILES CCC1(Oc2ccccc2-n2cccc2C1=O)c1ccc(COc2ccccc2)cc1

InChI Key InChIKey=VPJVIMRYVJNTLM-UHFFFAOYSA-N

Data  4 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 4 hits for monomerid = 50484018   

TargetReverse transcriptase(Human immunodeficiency virus type 1)
2-Universit£

Curated by ChEMBL
LigandPNGBDBM50484018(CHEMBL223769)
Affinity DataIC50: 150nMAssay Description:Inhibition of HIV1 wild type reverse transcriptaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2020
Entry Details Article
PubMed
TargetReverse transcriptase protein(Human immunodeficiency virus type 1)
2-Universit£

Curated by ChEMBL
LigandPNGBDBM50484018(CHEMBL223769)
Affinity DataIC50: 400nMAssay Description:Inhibition of HIV1 reverse transcriptase K103N mutantMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2020
Entry Details Article
PubMed
TargetReverse transcriptase protein(Human immunodeficiency virus type 1)
2-Universit£

Curated by ChEMBL
LigandPNGBDBM50484018(CHEMBL223769)
Affinity DataIC50: 200nMAssay Description:Inhibition of HIV1 reverse transcriptase L100I mutantMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2020
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
University of Turin

Curated by ChEMBL
LigandPNGBDBM50484018(CHEMBL223769)
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of human wild type AK expressed in Escherichia coli using [2,8- 3H]-Ado and ATP as substrate by radiometric analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/18/2023
Entry Details
PubMed