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Found 176 with Last Name = 'schumacher' and Initial = 'am'
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50246998(CHEMBL505558 | benzyl (R)-1-((2S,4R)-2-(((S)-6-ami...)
Affinity DataKi:  12nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50246999(CHEMBL500474 | benzyl (R)-1-((2S,4R)-2-(((S)-6-ami...)
Affinity DataKi:  19nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50246997(CHEMBL505738 | benzyl (R)-1-((2S,4R)-2-(((S)-6-ami...)
Affinity DataKi:  27nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50246995(CHEMBL505048 | benzyl (R)-1-((2S,4R)-2-(((S)-6-ami...)
Affinity DataKi:  28nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50247004((3R,5S)-5-(((S)-6-amino-1-(benzo[d]oxazol-2-yl)-1-...)
Affinity DataKi:  29nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50246992(CHEMBL498914 | benzyl (R)-1-((2S,4R)-2-(((S)-6-ami...)
Affinity DataKi:  40nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50246994(CHEMBL443101 | benzyl (R)-1-((2S,4R)-2-(((S)-6-ami...)
Affinity DataKi:  41nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50246996(CHEMBL506226 | {(R)-1-[(2S,4R)-2-[(S)-5-Amino-1-(b...)
Affinity DataKi:  45nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50246991(CHEMBL509770 | benzyl (R)-1-((2S,3S)-2-(((S)-6-ami...)
Affinity DataKi:  49nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50247002(((R)-1-{(2S,4R)-2-[(S)-5-Amino-1-(benzooxazole-2-c...)
Affinity DataKi:  60nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50247000(CHEMBL446259 | benzyl (R)-1-((2S,4R)-2-(((S)-6-ami...)
Affinity DataKi:  65nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50247005((3R,5S)-5-(((S)-6-amino-1-(benzo[d]oxazol-2-yl)-1-...)
Affinity DataKi:  101nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50247001(CHEMBL448873 | Phenyl-carbamic acid (3R,5S)-5-[(S)...)
Affinity DataKi:  130nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50247003(CHEMBL501945 | {(R)-1-[(2S,4R)-2-[(S)-5-Amino-1-(b...)
Affinity DataKi:  176nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50246990(CHEMBL454436 | benzyl (R)-1-((2S,3R)-2-(((S)-6-ami...)
Affinity DataKi:  267nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50247006((3R,5S)-5-((S)-6-amino-1-(benzo[d]oxazol-2-yl)-1-o...)
Affinity DataKi:  510nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50246993(CHEMBL507245 | benzyl (R)-1-((2S,4R)-2-(((S)-6-ami...)
Affinity DataKi:  1.04E+3nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50246989(CHEMBL501802 | benzyl (R)-1-((S)-2-(((S)-6-amino-1...)
Affinity DataKi:  1.40E+3nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50247007(((R)-1-{(2S,4R)-2-[(S)-5-Amino-1-(benzooxazole-2-c...)
Affinity DataKi:  1.55E+3nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50246988(CHEMBL503925 | benzyl (S)-1-((S)-1-((S)-6-amino-1-...)
Affinity DataKi:  2.10E+3nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50246986(CHEMBL507205 | benzyl (S)-1-((S)-1-((S)-6-amino-1-...)
Affinity DataKi:  5.72E+3nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50246987(CHEMBL504394 | benzyl (S)-6-amino-1-((S)-1-((S)-6-...)
Affinity DataKi:  5.78E+3nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50246985(CHEMBL507704 | benzyl (S)-6-amino-1-((S)-1-((S)-6-...)
Affinity DataKi:  1.52E+4nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50246984(CHEMBL508055 | benzyl (S)-1-((S)-6-amino-1-(benzo[...)
Affinity DataKi: >1.00E+5nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstasin(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50246983(CHEMBL509923 | benzyl (S)-1-((S)-6-amino-1-(benzo[...)
Affinity DataKi: >1.00E+5nMAssay Description:Binding affinity to human prostasinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity tyrosine-phosphorylation-regulated kinase 1A(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation (Gnf)

Curated by ChEMBL
LigandPNGBDBM50538098(CHEMBL4640031)
Affinity DataIC50:  3nMAssay Description:Inhibition of recombinant human N-terminal GST-tagged DYRK1A (1 to 763 residues) expressed in Sf21 cells using Ulight-glycogen synthase as substrate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDual specificity tyrosine-phosphorylation-regulated kinase 1A(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation (Gnf)

Curated by ChEMBL
LigandPNGBDBM50538084(CHEMBL4647659)
Affinity DataIC50:  6nMAssay Description:Inhibition of recombinant human DYRK1A (129 to 509 residues) expressed in mammalian expression system by Kinomescan methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity tyrosine-phosphorylation-regulated kinase 1A(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation (Gnf)

Curated by ChEMBL
LigandPNGBDBM50538099(CHEMBL4636064)
Affinity DataIC50:  6.20nMAssay Description:Inhibition of recombinant human N-terminal GST-tagged DYRK1A (1 to 763 residues) expressed in Sf21 cells using Ulight-glycogen synthase as substrate ...More data for this Ligand-Target Pair
TargetDual specificity tyrosine-phosphorylation-regulated kinase 1A(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation (Gnf)

Curated by ChEMBL
LigandPNGBDBM50538095(CHEMBL4649473)
Affinity DataIC50:  12nMAssay Description:Inhibition of recombinant human N-terminal GST-tagged DYRK1A (1 to 763 residues) expressed in Sf21 cells using Ulight-glycogen synthase as substrate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDual specificity tyrosine-phosphorylation-regulated kinase 1A(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation (Gnf)

Curated by ChEMBL
LigandPNGBDBM50538090(CHEMBL4648742)
Affinity DataIC50:  13nMAssay Description:Inhibition of recombinant human N-terminal GST-tagged DYRK1A (1 to 763 residues) expressed in Sf21 cells using Ulight-glycogen synthase as substrate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDual specificity tyrosine-phosphorylation-regulated kinase 1A(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation (Gnf)

Curated by ChEMBL
LigandPNGBDBM50538093(CHEMBL4645474)
Affinity DataIC50:  15nMAssay Description:Inhibition of recombinant human N-terminal GST-tagged DYRK1A (1 to 763 residues) expressed in Sf21 cells using Ulight-glycogen synthase as substrate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50022322(CHEMBL3298923)
Affinity DataIC50:  15nMAssay Description:Antagonist activity at human TRPA1 expressed in CHO-TREX cells assessed as inhibition of cinnamaldehyde-induced calcium flux incubated 10 mins prior ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation (Gnf)

Curated by ChEMBL
LigandPNGBDBM50538084(CHEMBL4647659)
Affinity DataIC50:  16nMAssay Description:Inhibition of recombinant human GSK3beta (1 to 433 residues) expressed in mammalian expression system by Kinomescan methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity tyrosine-phosphorylation-regulated kinase 1A(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation (Gnf)

Curated by ChEMBL
LigandPNGBDBM50538094(CHEMBL4641631)
Affinity DataIC50:  17nMAssay Description:Inhibition of recombinant human N-terminal GST-tagged DYRK1A (1 to 763 residues) expressed in Sf21 cells using Ulight-glycogen synthase as substrate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDual specificity tyrosine-phosphorylation-regulated kinase 1A(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation (Gnf)

Curated by ChEMBL
LigandPNGBDBM50538091(CHEMBL4640465)
Affinity DataIC50:  17nMAssay Description:Inhibition of recombinant human N-terminal GST-tagged DYRK1A (1 to 763 residues) expressed in Sf21 cells using Ulight-glycogen synthase as substrate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50022322(CHEMBL3298923)
Affinity DataIC50:  18nMAssay Description:Antagonist activity at human TRPA1 expressed in CHO-TREX cells assessed as inhibition of allyl isothiocyanate-induced calcium flux incubated 10 mins ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50022322(CHEMBL3298923)
Affinity DataIC50:  20nMAssay Description:Antagonist activity at human TRPA1 expressed in CHO-TREX cells assessed as inhibition of dibenzo[b,f ][1,4]oxazepine-4-carboxamide-induced calcium fl...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50022321(CHEMBL3298922)
Affinity DataIC50:  24nMAssay Description:Antagonist activity at human TRPA1 expressed in CHO-TREX cells assessed as inhibition of cinnamaldehyde-induced calcium flux incubated 10 mins prior ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity tyrosine-phosphorylation-regulated kinase 1A(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation (Gnf)

Curated by ChEMBL
LigandPNGBDBM50538096(CHEMBL4641672)
Affinity DataIC50:  25nMAssay Description:Inhibition of recombinant human N-terminal GST-tagged DYRK1A (1 to 763 residues) expressed in Sf21 cells using Ulight-glycogen synthase as substrate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50022327(CHEMBL3299019)
Affinity DataIC50:  26nMAssay Description:Antagonist activity at human TRPA1 expressed in CHO-TREX cells assessed as inhibition of cinnamaldehyde-induced calcium flux incubated 10 mins prior ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50022347(CHEMBL3299022)
Affinity DataIC50:  26nMAssay Description:Antagonist activity at human TRPA1 expressed in CHO-TREX cells assessed as inhibition of cinnamaldehyde-induced calcium flux incubated 10 mins prior ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50022349(CHEMBL3299024)
Affinity DataIC50:  36nMAssay Description:Antagonist activity at human TRPA1 expressed in CHO-TREX cells assessed as inhibition of cinnamaldehyde-induced calcium flux incubated 10 mins prior ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50022328(CHEMBL3299020)
Affinity DataIC50:  39nMAssay Description:Antagonist activity at human TRPA1 expressed in CHO-TREX cells assessed as inhibition of cinnamaldehyde-induced calcium flux incubated 10 mins prior ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation (Gnf)

Curated by ChEMBL
LigandPNGBDBM50538083(CHEMBL4638292)
Affinity DataIC50:  40nMAssay Description:Inhibition of recombinant human GSK3beta (1 to 433 residues) expressed in mammalian expression system by Kinomescan methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDual specificity tyrosine-phosphorylation-regulated kinase 1A(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation (Gnf)

Curated by ChEMBL
LigandPNGBDBM50538097(CHEMBL4641839)
Affinity DataIC50:  43nMAssay Description:Inhibition of recombinant human N-terminal GST-tagged DYRK1A (1 to 763 residues) expressed in Sf21 cells using Ulight-glycogen synthase as substrate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDual specificity tyrosine-phosphorylation-regulated kinase 1A(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation (Gnf)

Curated by ChEMBL
LigandPNGBDBM50538085(CHEMBL4634969)
Affinity DataIC50:  43nMAssay Description:Inhibition of recombinant human N-terminal GST-tagged DYRK1A (1 to 763 residues) expressed in Sf21 cells using Ulight-glycogen synthase as substrate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50022317(CHEMBL3298251)
Affinity DataIC50:  48nMAssay Description:Antagonist activity at human TRPA1 expressed in CHO-TREX cells assessed as inhibition of cinnamaldehyde-induced calcium flux incubated 10 mins prior ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50022323(CHEMBL3298924)
Affinity DataIC50:  50nMAssay Description:Antagonist activity at human TRPA1 expressed in CHO-TREX cells assessed as inhibition of cinnamaldehyde-induced calcium flux incubated 10 mins prior ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50022389(CHEMBL3299025)
Affinity DataIC50:  50nMAssay Description:Antagonist activity at human TRPA1 expressed in CHO-TREX cells assessed as inhibition of cinnamaldehyde-induced calcium flux incubated 10 mins prior ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily A member 1(Mus musculus)
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50022322(CHEMBL3298923)
Affinity DataIC50:  53nMAssay Description:Antagonist activity at mouse TRPA1 expressed in CHO-TREX cells assessed as inhibition of cinnamaldehyde-induced calcium flux incubated 10 mins prior ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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