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Found 7 of ic50 for monomerid = 50206008
TargetPolyunsaturated fatty acid lipoxygenase ALOX15(Oryctolagus cuniculus (rabbit))
Tahitian Noni International

Curated by ChEMBL
LigandPNGBDBM50206008(6-hydroxy-7-methoxy-2H-chromen-2-one | CHEMBL39032...)
Affinity DataIC50:  1.51E+4nMAssay Description:Inhibition of 15LOX in rabbit reticulocytes by EIA assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetInduced myeloid leukemia cell differentiation protein Mcl-1(Homo sapiens (Human))
Dalian University Of Technology

Curated by ChEMBL
LigandPNGBDBM50206008(6-hydroxy-7-methoxy-2H-chromen-2-one | CHEMBL39032...)
Affinity DataIC50:  5.15E+4nMAssay Description:Displacement of FAM-Bid peptide from recombinant N-terminal His6x-tagged human Mcl-1 expressed in Escherichia coli BL21 (DE3) incubated for 30 mins b...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University Of Toyama

Curated by ChEMBL
LigandPNGBDBM50206008(6-hydroxy-7-methoxy-2H-chromen-2-one | CHEMBL39032...)
Affinity DataIC50:  5.62E+4nMAssay Description:Inhibition human recombinant aldose reductase 1 by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
Tahitian Noni International

Curated by ChEMBL
LigandPNGBDBM50206008(6-hydroxy-7-methoxy-2H-chromen-2-one | CHEMBL39032...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of 5LOX in human PBMC by EIA assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Tahitian Noni International

Curated by ChEMBL
LigandPNGBDBM50206008(6-hydroxy-7-methoxy-2H-chromen-2-one | CHEMBL39032...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human recombinant COX2 expressed in insect Sf21 cells by EIA assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50206008(6-hydroxy-7-methoxy-2H-chromen-2-one | CHEMBL39032...)
Affinity DataIC50:  1.38E+5nMAssay Description:Inhibition of xanthine oxidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
University Of Toyama

Curated by ChEMBL
LigandPNGBDBM50206008(6-hydroxy-7-methoxy-2H-chromen-2-one | CHEMBL39032...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition sorbitol dehydrogenase by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed