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Found 5 of ic50 for monomerid = 50355116
TargetTransthyretin(Homo sapiens (Human))
The Board of Trustees of The Leland Stanford Junior University

US Patent
LigandPNGBDBM50355116(CHEMBL493923 | US10278929, Compound 22 | US1133793...)
Affinity DataIC50:  4.79E+3nMAssay Description:The FP assay was then adapted for HTS and used to screen ~120,000 small molecule library for compounds that displaced probe 5 from the T4 binding of ...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetTransthyretin(Homo sapiens (Human))
The Board of Trustees of The Leland Stanford Junior University

US Patent
LigandPNGBDBM50355116(CHEMBL493923 | US10278929, Compound 22 | US1133793...)
Affinity DataIC50:  4.79E+3nMAssay Description:Table 3: The FP assay was then adapted for HTS and used to screen 120,000 small molecule library for compounds that displaced probe 5 from the T4 bin...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetTransthyretin(Homo sapiens (Human))
The Board of Trustees of The Leland Stanford Junior University

US Patent
LigandPNGBDBM50355116(CHEMBL493923 | US10278929, Compound 22 | US1133793...)
Affinity DataIC50:  4.79E+3nMAssay Description:The FP assay was then adapted for HTS and used to screen a ˜120,000 member small molecule library for compounds that displaced the FP probe from the ...More data for this Ligand-Target Pair
In DepthDetails US Patent
Target4-diphosphocytidyl-2-C-methyl-D-erythritol kinase(Yersinia pestis)
University Of Utah

Curated by ChEMBL
LigandPNGBDBM50355116(CHEMBL493923 | US10278929, Compound 22 | US1133793...)
Affinity DataIC50:  9.00E+3nMAssay Description:Inhibition of His6-tagged Yersinia pestis KIM6 CDP-ME kinase assessed as ADP production after 30 mins by Kinase Glo luminescence-based assay or stand...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGalactokinase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50355116(CHEMBL493923 | US10278929, Compound 22 | US1133793...)
Affinity DataIC50:  1.20E+4nMAssay Description:Inhibition of human galactokinase after 30 mins by Kinase-GloTM assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed