BDBM50484808 CHEMBL1958233::NSC-205497

SMILES COc1ccccc1C(=O)N\N=C\c1c(O)ccc2ccccc12

InChI Key InChIKey=SGIUPSNOFYYWMP-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 = 50484808   

TargetIndoleamine 2,3-dioxygenase 1(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50484808(NSC-205497 | CHEMBL1958233)
Affinity DataIC50: 1.13E+4nMAssay Description:Inhibition of IDO1 in IFN-gamma stimulated human HeLa cells assessed as reduction in kynurenine production using L-tryptophan as substrate incubated ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/25/2021
Entry Details Article
PubMed
TargetReverse transcriptase(Human immunodeficiency virus type 1)
Magna Graecia University of Catanzaro

Curated by ChEMBL
LigandPNGBDBM50484808(NSC-205497 | CHEMBL1958233)
Affinity DataIC50: 2.10E+4nMAssay Description:Inhibition of ribonuclease H activity of HIV1 reverse transcriptase using as poly(dC)-[3H]poly(rG) as substrateMore 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)
Magna Graecia University of Catanzaro

Curated by ChEMBL
LigandPNGBDBM50484808(NSC-205497 | CHEMBL1958233)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of RNA-dependent DNA polymerase activity of Human immunodeficiency virus 1 reverse transcriptaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2020
Entry Details Article
PubMed