null

SMILES OC(=O)Cn1c2c(CCN(Cc3ccc(cc3)C(F)(F)F)C2=S)c2ccccc12

InChI Key InChIKey=ZHCFANIYRYFINK-UHFFFAOYSA-N

  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 2 hits for monomerid = 50363058   

TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363058(CHEMBL1946963)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363058(CHEMBL1946963)copy SMILEScopy InChI
Affinity DataIC50: 3.80E+3nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed