BDBM1306 3-Aminopyridin-2(1H)-one analogue 26::5-ethyl-3-({furo[2,3-c]pyridin-2-ylmethyl}amino)-6-methyl-1,2-dihydropyridin-2-one::CHEMBL123968

SMILES CCc1cc(NCc2cc3ccncc3o2)c(=O)[nH]c1C

InChI Key InChIKey=ONFSYSYGCPKYCA-UHFFFAOYSA-N

Data  2 IC50

  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 = 1306   

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Organon Research and Development Group

Curated by ChEMBL
LigandPNGBDBM1306(5-ethyl-3-({furo[2,3-c]pyridin-2-ylmethyl}amino)-6...)
Affinity DataIC50: 1.05E+5nMAssay Description:Inhibition of HIV-1 reverse transcriptase (HIV-1 RT)More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/22/2013
Entry Details Article
PubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Merck Research Laboratories

LigandPNGBDBM1306(5-ethyl-3-({furo[2,3-c]pyridin-2-ylmethyl}amino)-6...)
Affinity DataIC50: 1.05E+5nMpH: 8.2Assay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/29/2004
Entry Details Article
PubMed