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Found 51 with Last Name = 'winston-mcpherson' and Initial = 'gn'
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50535693(CHEMBL4572783)
Affinity DataIC50:  202nMAssay Description:Inhibition of human PCSK9 in HepG2 cells incubated for 24 hrs followed by medium replenishment and measured after 24 hrs by ELISAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50535683(CHEMBL4549362)
Affinity DataIC50:  250nMAssay Description:Inhibition of human PCSK9 in HepG2 cells incubated for 48 hrs by AlphaLISA assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50535686(CHEMBL4562557)
Affinity DataIC50:  300nMAssay Description:Inhibition of human PCSK9 in HepG2 cells incubated for 48 hrs by AlphaLISA assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50535688(CHEMBL4585306)
Affinity DataIC50:  900nMAssay Description:Inhibition of human PCSK9 in HepG2 cells incubated for 48 hrs by AlphaLISA assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50535690(CHEMBL4528279)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibition of human PCSK9 in HepG2 cells incubated for 48 hrs by AlphaLISA assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50535687(CHEMBL4435394)
Affinity DataIC50:  1.40E+3nMAssay Description:Inhibition of human PCSK9 in HepG2 cells incubated for 48 hrs by AlphaLISA assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50535689(CHEMBL4462933)
Affinity DataIC50:  1.50E+3nMAssay Description:Inhibition of human PCSK9 in HepG2 cells incubated for 48 hrs by AlphaLISA assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50535685(CHEMBL4531399)
Affinity DataIC50:  2.30E+3nMAssay Description:Inhibition of human PCSK9 in HepG2 cells incubated for 48 hrs by AlphaLISA assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50535691(CHEMBL4461546)
Affinity DataIC50:  2.30E+3nMAssay Description:Inhibition of human PCSK9 in HepG2 cells incubated for 48 hrs by AlphaLISA assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50535692(CHEMBL4545753)
Affinity DataIC50:  2.80E+3nMAssay Description:Inhibition of human PCSK9 in HepG2 cells incubated for 48 hrs by AlphaLISA assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50535684(CHEMBL4446521)
Affinity DataIC50:  5.60E+3nMAssay Description:Inhibition of human PCSK9 in HepG2 cells incubated for 48 hrs by AlphaLISA assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50049059(CHEMBL3319503 | US10730833, Compound 10a | US99696...)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibition of human PCSK9 in HepG2 cells incubated for 48 hrs by AlphaLISA assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049062(CHEMBL3319500 | US10730833, Compound 11c | US99696...)
Affinity DataEC50:  230nMAssay Description:AhR readily binds to various endogenous and xenobiotic polyaromatic heterocycles.More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049061(CHEMBL3319501 | US10730833, Compound 11d | US99696...)
Affinity DataEC50:  55nMAssay Description:AhR readily binds to various endogenous and xenobiotic polyaromatic heterocycles.More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049060(CHEMBL3319502 | US10730833, Compound 6' | US996968...)
Affinity DataEC50:  215nMAssay Description:AhR readily binds to various endogenous and xenobiotic polyaromatic heterocycles.More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049059(CHEMBL3319503 | US10730833, Compound 10a | US99696...)
Affinity DataEC50: >6.70E+3nMAssay Description:AhR readily binds to various endogenous and xenobiotic polyaromatic heterocycles.More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049058(CHEMBL3319504 | US10730833, Compound 10c | US99696...)
Affinity DataEC50:  94nMAssay Description:AhR readily binds to various endogenous and xenobiotic polyaromatic heterocycles.More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049057(CHEMBL3319505 | US10730833, Compound 10d | US99696...)
Affinity DataEC50:  86nMAssay Description:AhR readily binds to various endogenous and xenobiotic polyaromatic heterocycles.More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049065(CHEMBL3319497 | US10730833, Compound 6 | US9969686...)
Affinity DataEC50:  270nMAssay Description:This assay measures the induction of cytochrome P450-1A1 (CYP1A1), which is a major outcome of AhR activation. Whyte, J. J.; Jung, R. E.; Schmitt, C....More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049064(CHEMBL3319498 | US10730833, Compound 11a | US99696...)
Affinity DataEC50:  93nMAssay Description:This assay measures the induction of cytochrome P450-1A1 (CYP1A1), which is a major outcome of AhR activation. Whyte, J. J.; Jung, R. E.; Schmitt, C....More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049063(CHEMBL3319499 | US10730833, Compound 11b | US99696...)
Affinity DataEC50:  320nMAssay Description:This assay measures the induction of cytochrome P450-1A1 (CYP1A1), which is a major outcome of AhR activation. Whyte, J. J.; Jung, R. E.; Schmitt, C....More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049062(CHEMBL3319500 | US10730833, Compound 11c | US99696...)
Affinity DataEC50:  230nMAssay Description:This assay measures the induction of cytochrome P450-1A1 (CYP1A1), which is a major outcome of AhR activation. Whyte, J. J.; Jung, R. E.; Schmitt, C....More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049061(CHEMBL3319501 | US10730833, Compound 11d | US99696...)
Affinity DataEC50:  55nMAssay Description:This assay measures the induction of cytochrome P450-1A1 (CYP1A1), which is a major outcome of AhR activation. Whyte, J. J.; Jung, R. E.; Schmitt, C....More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049060(CHEMBL3319502 | US10730833, Compound 6' | US996968...)
Affinity DataEC50:  215nMAssay Description:This assay measures the induction of cytochrome P450-1A1 (CYP1A1), which is a major outcome of AhR activation. Whyte, J. J.; Jung, R. E.; Schmitt, C....More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049059(CHEMBL3319503 | US10730833, Compound 10a | US99696...)
Affinity DataEC50: >6.70E+3nMAssay Description:This assay measures the induction of cytochrome P450-1A1 (CYP1A1), which is a major outcome of AhR activation. Whyte, J. J.; Jung, R. E.; Schmitt, C....More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049058(CHEMBL3319504 | US10730833, Compound 10c | US99696...)
Affinity DataEC50:  94nMAssay Description:This assay measures the induction of cytochrome P450-1A1 (CYP1A1), which is a major outcome of AhR activation. Whyte, J. J.; Jung, R. E.; Schmitt, C....More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049057(CHEMBL3319505 | US10730833, Compound 10d | US99696...)
Affinity DataEC50:  86nMAssay Description:This assay measures the induction of cytochrome P450-1A1 (CYP1A1), which is a major outcome of AhR activation. Whyte, J. J.; Jung, R. E.; Schmitt, C....More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50541261(CHEMBL4646273)
Affinity DataEC50:  0.260nMAssay Description:Agonist activity at AhR in human HepG2 cells assessed as induction of CYP1A1 expression after 24 hrs by ethoxyresorufin-O-deethylase assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50541262(6-Formylindolo[3,2-B]Carbazole | CHEMBL472031)
Affinity DataEC50:  2nMAssay Description:Agonist activity at AhR in human HepG2 cells assessed as induction of CYP1A1 expression after 24 hrs by ethoxyresorufin-O-deethylase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50565588(CHEMBL4779430)
Affinity DataEC50:  348nMAssay Description:Modulation of PCSK9 in human HepG2 cells assessed as reduction in PCSK9 expression incubated for 24 hrs prior to compound washout followed by compoun...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50565589(CHEMBL4789986)
Affinity DataEC50:  2.5nMAssay Description:Modulation of PCSK9 in human HepG2 cells assessed as reduction in PCSK9 expression incubated for 24 hrs prior to compound washout followed by compoun...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50565590(CHEMBL4780905)
Affinity DataEC50:  0.150nMAssay Description:Modulation of PCSK9 in human HepG2 cells assessed as reduction in PCSK9 expression incubated for 24 hrs prior to compound washout followed by compoun...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50565591(CHEMBL4783308)
Affinity DataEC50:  1.20nMAssay Description:Modulation of PCSK9 in human HepG2 cells assessed as reduction in PCSK9 expression incubated for 24 hrs prior to compound washout followed by compoun...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50565592(CHEMBL4788701)
Affinity DataEC50:  11nMAssay Description:Modulation of PCSK9 in human HepG2 cells assessed as reduction in PCSK9 expression incubated for 24 hrs prior to compound washout followed by compoun...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50565593(CHEMBL4779800)
Affinity DataEC50:  40nMAssay Description:Modulation of PCSK9 in human HepG2 cells assessed as reduction in PCSK9 expression incubated for 24 hrs prior to compound washout followed by compoun...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50565594(CHEMBL4783828)
Affinity DataEC50:  88nMAssay Description:Modulation of PCSK9 in human HepG2 cells assessed as reduction in PCSK9 expression incubated for 24 hrs prior to compound washout followed by compoun...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50565595(CHEMBL4785006)
Affinity DataEC50:  0.280nMAssay Description:Modulation of PCSK9 in human HepG2 cells assessed as reduction in PCSK9 expression incubated for 24 hrs prior to compound washout followed by compoun...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50565596(CHEMBL4797870)
Affinity DataEC50:  0.690nMAssay Description:Modulation of PCSK9 in human HepG2 cells assessed as reduction in PCSK9 expression incubated for 24 hrs prior to compound washout followed by compoun...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049063(CHEMBL3319499 | US10730833, Compound 11b | US99696...)
Affinity DataEC50:  320nMAssay Description:AhR readily binds to various endogenous and xenobiotic polyaromatic heterocycles.More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049064(CHEMBL3319498 | US10730833, Compound 11a | US99696...)
Affinity DataEC50:  93nMAssay Description:AhR readily binds to various endogenous and xenobiotic polyaromatic heterocycles.More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049065(CHEMBL3319497 | US10730833, Compound 6 | US9969686...)
Affinity DataEC50:  270nMAssay Description:AhR readily binds to various endogenous and xenobiotic polyaromatic heterocycles.More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049065(CHEMBL3319497 | US10730833, Compound 6 | US9969686...)
Affinity DataEC50:  270nMAssay Description:Activation of AhR in human HepG2 cells assessed as fluorescence after 24 hrs incubation by EROD assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049064(CHEMBL3319498 | US10730833, Compound 11a | US99696...)
Affinity DataEC50:  93nMAssay Description:Activation of AhR in human HepG2 cells assessed as fluorescence after 24 hrs incubation by EROD assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049063(CHEMBL3319499 | US10730833, Compound 11b | US99696...)
Affinity DataEC50:  320nMAssay Description:Activation of AhR in human HepG2 cells assessed as fluorescence after 24 hrs incubation by EROD assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049062(CHEMBL3319500 | US10730833, Compound 11c | US99696...)
Affinity DataEC50:  230nMAssay Description:Activation of AhR in human HepG2 cells assessed as fluorescence after 24 hrs incubation by EROD assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049061(CHEMBL3319501 | US10730833, Compound 11d | US99696...)
Affinity DataEC50:  55nMAssay Description:Activation of AhR in human HepG2 cells assessed as fluorescence after 24 hrs incubation by EROD assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049060(CHEMBL3319502 | US10730833, Compound 6' | US996968...)
Affinity DataEC50:  215nMAssay Description:Activation of AhR in human HepG2 cells assessed as fluorescence after 24 hrs incubation by EROD assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049059(CHEMBL3319503 | US10730833, Compound 10a | US99696...)
Affinity DataEC50: >6.70E+3nMAssay Description:Activation of AhR in human HepG2 cells assessed as fluorescence after 24 hrs incubation by EROD assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProprotein convertase subtilisin/kexin type 9(Homo sapiens (Human))
University Of Wisconsin

Curated by ChEMBL
LigandPNGBDBM50565597(CHEMBL4783880)
Affinity DataEC50:  161nMAssay Description:Modulation of PCSK9 in human HepG2 cells assessed as reduction in PCSK9 expression incubated for 24 hrs prior to compound washout followed by compoun...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
Wisconsin Alumni Research Foundation

US Patent
LigandPNGBDBM50049057(CHEMBL3319505 | US10730833, Compound 10d | US99696...)
Affinity DataEC50:  86nMAssay Description:Activation of AhR in human HepG2 cells assessed as fluorescence after 24 hrs incubation by EROD assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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