BDBM50385299 CHEMBL2035464::US8592468, EbSe16

SMILES O=c1n(CCCCCCn2[se]c3ccccc3c2=O)[se]c2ccccc12

InChI Key InChIKey=PXGKVHIRSKZGDU-UHFFFAOYSA-N

Data  1 KI  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 = 50385299   

TargetThioredoxin reductase 1, cytoplasmic(Rat)
Peking University

Curated by ChEMBL
LigandPNGBDBM50385299(CHEMBL2035464 | US8592468, EbSe16)
Affinity DataIC50: 1.66E+3nMAssay Description:Inhibition of TrxR1 in rat liver homogenate preincubated for 5 mins measured by DNTB assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/7/2013
Entry Details Article
PubMed
TargetGlutaminase kidney isoform, mitochondrial(Human)
Sichuan University

Curated by ChEMBL
LigandPNGBDBM50385299(CHEMBL2035464 | US8592468, EbSe16)
Affinity DataIC50: 200nMAssay Description:Inhibition of C-terminal His-tagged human recombinant KGA transformed in Escherichia coli BL21 DE3 at pH 7.4 incubated for 3 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetThioredoxin reductase(Escherichia coli (strain K12))
Thioredoxin Systems

US Patent
LigandPNGBDBM50385299(CHEMBL2035464 | US8592468, EbSe16)
Affinity DataKi:  10nM IC50: 2.25E+3nMAssay Description:All the benzisoselenazol-3(2H)-one and bisbenzisoselenazol-3(2H)-one derivatives were tested as potential E. coli TrxR inhibitors by standard DTNB as...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/17/2014
Entry Details
Go to US Patent