BDBM50480319 Nomilin

SMILES [H][C@]12O[C@@]11[C@@](C)(CC[C@]3([H])[C@@]4(C)[C@H](CC(=O)OC(C)(C)[C@]4([H])CC(=O)[C@@]13C)OC(C)=O)[C@H](OC2=O)c1ccoc1

InChI Key InChIKey=KPDOJFFZKAUIOE-UHFFFAOYSA-N

Data  3 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 3 hits for monomerid = 50480319   

TargetReverse transcriptase(Human immunodeficiency virus type 1)
University of Rome Tor Vergata

Curated by ChEMBL
LigandPNGBDBM50480319(Nomilin)
Affinity DataIC50: 6.65nMAssay Description:Inhibition of HIV1 3B reverse transcriptase activityMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2020
Entry Details Article
PubMed
TargetReverse transcriptase(Human immunodeficiency virus type 1)
University of Rome Tor Vergata

Curated by ChEMBL
LigandPNGBDBM50480319(Nomilin)
Affinity DataIC50: 6.92nMAssay Description:Inhibition of HIV1 3B reverse transcriptase activity infected in human H9 cells assessed as level of p24 antigenMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2020
Entry Details Article
PubMed
TargetReverse transcriptase(Human immunodeficiency virus type 1)
University of Rome Tor Vergata

Curated by ChEMBL
LigandPNGBDBM50480319(Nomilin)
Affinity DataIC50: 3.88E+5nMAssay Description:Inhibition of HIV1 RTMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/27/2020
Entry Details Article
PubMed