null

SMILES [#6]\[#6](-[#6])=[#6]\[#6]-c1ccc(\[#6]=[#6]\[#6](-[#8])=O)cc1-[#7]-[#6](=O)-[#6]-[#6]-c1ccccc1

InChI Key InChIKey=SMYHHZFAWOLAAX-RVDMUPIBSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 8 hits for monomerid = 50509753   

TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
Texas Tech University Health Sciences Center

Curated by ChEMBL
LigandPNGBDBM50509753(CHEMBL4470997)copy SMILEScopy InChI
Affinity DataIC50: 66nMAssay Description:Inhibition of recombinant human AKR1C3 expressed in Escherichia coli BL21 (D3) using S-tetralol as substrate in presence of NADP+ by UV-spectrophotom...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8X52PubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
Texas Tech University Health Sciences Center

Curated by ChEMBL
LigandPNGBDBM50509753(CHEMBL4470997)copy SMILEScopy InChI
Affinity DataIC50: 66nMAssay Description:Inhibition of recombinant human AKR1C3 expressed in Escherichia coli BL21 measured after 1.5 hrs by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8X52PubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
Texas Tech University Health Sciences Center

Curated by ChEMBL
LigandPNGBDBM50509753(CHEMBL4470997)copy SMILEScopy InChI
Affinity DataIC50: 7.20E+3nMAssay Description:Inhibition of recombinant human AKR1C2 expressed in Escherichia coli BL21 (D3) using S-tetralol as substrate in presence of NADP+ by UV-spectrophotom...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8X52PubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
Texas Tech University Health Sciences Center

Curated by ChEMBL
LigandPNGBDBM50509753(CHEMBL4470997)copy SMILEScopy InChI
Affinity DataIC50: 7.94E+3nMAssay Description:Inhibition of recombinant AKR1C2 (unknown origin) assessed as reduction in S-tetralol catalyzed oxidation in presence of NADPH by fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7MS2PubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
Texas Tech University Health Sciences Center

Curated by ChEMBL
LigandPNGBDBM50509753(CHEMBL4470997)copy SMILEScopy InChI
Affinity DataIC50: 530nMAssay Description:Inhibition of AKR1C3 in human HL60 cells assessed as potentiation of etoposide-induced cytotoxicity by measuring etoposide IC50 after 24 to 72 hrs by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7MS2PubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
Texas Tech University Health Sciences Center

Curated by ChEMBL
LigandPNGBDBM50509753(CHEMBL4470997)copy SMILEScopy InChI
Affinity DataIC50: 270nMAssay Description:Inhibition of AKR1C3 in human HL60 cells assessed as potentiation of etoposide-induced cytotoxicity by measuring etoposide IC50 pre-treated with comp...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7MS2PubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
Texas Tech University Health Sciences Center

Curated by ChEMBL
LigandPNGBDBM50509753(CHEMBL4470997)copy SMILEScopy InChI
Affinity DataIC50: 2.47E+3nMAssay Description:Inhibition of AKR1C3 in human KG1a cells assessed as potentiation of etoposide-induced cytotoxicity by measuring etoposide IC50 cotreated at 72 hrs b...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7MS2PubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
Texas Tech University Health Sciences Center

Curated by ChEMBL
LigandPNGBDBM50509753(CHEMBL4470997)copy SMILEScopy InChI
Affinity DataIC50: 63nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) assessed as reduction in S-tetralol catalyzed oxidation in presence of NADPH by fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7MS2PubMed