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Found 14 with Last Name = 'ulrich' and Initial = 'rg'
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
Gilead Calistoga

US Patent
LigandPNGBDBM119781(US8691829, 4b)
Affinity DataKi:  5nMAssay Description:The relative efficacies of compounds as inhibitors of an enzyme activity (or other biological activity) can be established by determining the concent...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
Gilead Calistoga

US Patent
LigandPNGBDBM119780(US8691829, 3e)
Affinity DataKi:  6nMAssay Description:The relative efficacies of compounds as inhibitors of an enzyme activity (or other biological activity) can be established by determining the concent...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
Gilead Calistoga

US Patent
LigandPNGBDBM50403092(CHEMBL2216871 | US8691829, 4a)
Affinity DataKi:  7nMAssay Description:The relative efficacies of compounds as inhibitors of an enzyme activity (or other biological activity) can be established by determining the concent...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
Gilead Calistoga

US Patent
LigandPNGBDBM119779(US8691829, 3d)
Affinity DataKi:  40nMAssay Description:The relative efficacies of compounds as inhibitors of an enzyme activity (or other biological activity) can be established by determining the concent...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetProtein-tyrosine-phosphatase(Yersinia pestis)
National Cancer Institute-Frederick

Curated by ChEMBL
LigandPNGBDBM50342237((E)-5-((((3'-(Difluoro(phosphono)methyl)-[1,1'-bip...)
Affinity DataIC50:  190nMAssay Description:Inhibition of Yersinia pestis outer protein H expressed in Escherichia coli after 15 to 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-tyrosine-phosphatase(Yersinia pestis)
National Cancer Institute-Frederick

Curated by ChEMBL
LigandPNGBDBM50342236(CHEMBL1766711 | difluoro(4'-(((5-(hydroxymethyl)fu...)
Affinity DataIC50:  730nMAssay Description:Inhibition of Yersinia pestis outer protein H expressed in Escherichia coli after 15 to 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-tyrosine-phosphatase(Yersinia pestis)
National Cancer Institute-Frederick

Curated by ChEMBL
LigandPNGBDBM50342235(CHEMBL1766710 | difluoro(4'-(((5-methylfuran-2-yl)...)
Affinity DataIC50:  910nMAssay Description:Inhibition of Yersinia pestis outer protein H expressed in Escherichia coli after 15 to 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-tyrosine-phosphatase(Yersinia pestis)
National Cancer Institute-Frederick

Curated by ChEMBL
LigandPNGBDBM50342234(CHEMBL1766709 | difluoro(4'-((furan-2-ylmethylenea...)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibition of Yersinia pestis outer protein H expressed in Escherichia coli after 15 to 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
National Cancer Institute-Frederick

Curated by ChEMBL
LigandPNGBDBM50342237((E)-5-((((3'-(Difluoro(phosphono)methyl)-[1,1'-bip...)
Affinity DataIC50:  2.23E+3nMAssay Description:Inhibition of human PTP1BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-tyrosine-phosphatase(Yersinia pestis)
National Cancer Institute-Frederick

Curated by ChEMBL
LigandPNGBDBM50317073(16-(4-(benzyloxy)phenyl)-3,14-dioxa-2,15-diazahexa...)
Affinity DataIC50:  2.40E+3nMAssay Description:Inhibition of Yersinia pestis YopH after 15 mins by pNPP hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-tyrosine-phosphatase(Yersinia pestis)
National Cancer Institute-Frederick

Curated by ChEMBL
LigandPNGBDBM50342233(CHEMBL1766708 | difluoro(4'-((furan-3-ylmethylenea...)
Affinity DataIC50:  3.69E+3nMAssay Description:Inhibition of Yersinia pestis outer protein H expressed in Escherichia coli after 15 to 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein phosphatase F(Homo sapiens (Human))
National Cancer Institute-Frederick

Curated by ChEMBL
LigandPNGBDBM50342237((E)-5-((((3'-(Difluoro(phosphono)methyl)-[1,1'-bip...)
Affinity DataIC50: >4.00E+5nMAssay Description:Inhibition of human leukocyte antigen related phosphataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 14(Homo sapiens (Human))
National Cancer Institute-Frederick

Curated by ChEMBL
LigandPNGBDBM50342237((E)-5-((((3'-(Difluoro(phosphono)methyl)-[1,1'-bip...)
Affinity DataIC50: >4.00E+5nMAssay Description:Inhibition of human DUSP14More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 22(Homo sapiens (Human))
National Cancer Institute-Frederick

Curated by ChEMBL
LigandPNGBDBM50342237((E)-5-((((3'-(Difluoro(phosphono)methyl)-[1,1'-bip...)
Affinity DataIC50: >4.00E+5nMAssay Description:Inhibition of human DUSP22More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed