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Found 111 with Last Name = 'sopkova-de oliveira santos' and Initial = 'j'
TargetPyroglutamylated RF-amide peptide receptor(Homo sapiens (Human))
Normandy University

Curated by ChEMBL
LigandPNGBDBM50469449(CHEMBL4277047)
Affinity DataIC50:  579nMAssay Description:Antagonist activity at human QRFPR expressed in CHO cells co-expressing Galpha16 assessed as inhibition of 26RFa-induced Ca2+ mobilization preincubat...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50103203(3-(3-Hydroxy-4-methoxy-phenyl)-thieno[2,3-b]pyrrol...)
Affinity DataIC50:  1.50E+3nMAssay Description:Inhibition of GSK3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267161((E/Z) 8-[3-(3-Hydroxy-4-methoxyphenyl) pyrrolo[2,3...)
Affinity DataIC50:  3.20E+3nMAssay Description:Inhibition of CDK5 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267161((E/Z) 8-[3-(3-Hydroxy-4-methoxyphenyl) pyrrolo[2,3...)
Affinity DataIC50:  3.80E+3nMAssay Description:Inhibition of CDK1/cyclin B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50103203(3-(3-Hydroxy-4-methoxy-phenyl)-thieno[2,3-b]pyrrol...)
Affinity DataIC50:  5.50E+3nMAssay Description:Inhibition of CDK1/cyclin B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267161((E/Z) 8-[3-(3-Hydroxy-4-methoxyphenyl) pyrrolo[2,3...)
Affinity DataIC50:  5.50E+3nMAssay Description:Inhibition of GSK3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyroglutamylated RF-amide peptide receptor(Homo sapiens (Human))
Normandy University

Curated by ChEMBL
LigandPNGBDBM50469440(CHEMBL4281854)
Affinity DataIC50:  6.06E+3nMAssay Description:Antagonist activity at human QRFPR expressed in CHO cells co-expressing Galpha16 assessed as inhibition of 26RFa-induced Ca2+ mobilization preincubat...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetPyroglutamylated RF-amide peptide receptor(Homo sapiens (Human))
Normandy University

Curated by ChEMBL
LigandPNGBDBM50469430(CHEMBL4279100)
Affinity DataIC50:  8.25E+3nMAssay Description:Antagonist activity at human QRFPR expressed in CHO cells co-expressing Galpha16 assessed as inhibition of 26RFa-induced Ca2+ mobilization preincubat...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267160((E/Z) 8-[3-(3-Benzyloxy-4-methoxyphenyl) pyrrolo[2...)
Affinity DataIC50:  9.00E+3nMAssay Description:Inhibition of CDK1/cyclin B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, brain(Rattus norvegicus (rat))
Universit£

Curated by ChEMBL
LigandPNGBDBM50390019(CHEMBL2071543)
Affinity DataIC50:  1.06E+4nMAssay Description:Inhibition of nNOS in rat cerebellum homogenates assessed as reduction in conversion of L-[3H]arginine to L-[3H]citrullineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267109(3-(3-hydroxy-4-methoxyphenyl)pyrrolo[2,3-b]pyrroli...)
Affinity DataIC50:  1.10E+4nMAssay Description:Inhibition of GSK3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267160((E/Z) 8-[3-(3-Benzyloxy-4-methoxyphenyl) pyrrolo[2...)
Affinity DataIC50:  1.40E+4nMAssay Description:Inhibition of CDK5 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267160((E/Z) 8-[3-(3-Benzyloxy-4-methoxyphenyl) pyrrolo[2...)
Affinity DataIC50:  1.70E+4nMAssay Description:Inhibition of GSK3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267109(3-(3-hydroxy-4-methoxyphenyl)pyrrolo[2,3-b]pyrroli...)
Affinity DataIC50:  2.20E+4nMAssay Description:Inhibition of CDK1/cyclin B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, brain(Rattus norvegicus (rat))
Universit£

Curated by ChEMBL
LigandPNGBDBM50390023(CHEMBL2071547)
Affinity DataIC50:  2.82E+4nMAssay Description:Inhibition of nNOS in rat cerebellum homogenates assessed as reduction in conversion of L-[3H]arginine to L-[3H]citrullineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267109(3-(3-hydroxy-4-methoxyphenyl)pyrrolo[2,3-b]pyrroli...)
Affinity DataIC50:  3.00E+4nMAssay Description:Inhibition of CDK5 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, brain(Rattus norvegicus (rat))
Universit£

Curated by ChEMBL
LigandPNGBDBM50390027(CHEMBL2071551)
Affinity DataIC50:  4.25E+4nMAssay Description:Inhibition of nNOS in rat cerebellum homogenates assessed as reduction in conversion of L-[3H]arginine to L-[3H]citrullineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267081(1-(3,4-dimethoxyphenyl)furo[2,3-e]pyrrolo[1,2-a]py...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of CDK5 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267080(1-(3,4-Dichlorophenyl)furo[2,3-e]pyrrolo [1,2-a]py...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of CDK5 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267040(1-(4-Chlorophenyl)-3,4-dihydro-5H-dipyrrolo [1,2-a...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of GSK3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267041(1-(3,4-Dimethoxyphenyl)-3,4-dihydro-5H-dipyrrolo [...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of GSK3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267076(1-(4-Bromophenyl)furo[2,3-e]pyrrolo[1,2-a] pyrazin...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of GSK3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267077(1-(4-Fluorophenyl)furo[2,3-e]pyrrolo[1,2-a] pyrazi...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of GSK3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267078(1-(4-Methylphenyl)furo[2,3-e]pyrrolo[1,2-a] pyrazi...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of GSK3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267079(1-(4-Methoxyphenyl)furo[2,3-e]pyrrolo [1,2-a]pyraz...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of GSK3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267080(1-(3,4-Dichlorophenyl)furo[2,3-e]pyrrolo [1,2-a]py...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of GSK3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267081(1-(3,4-dimethoxyphenyl)furo[2,3-e]pyrrolo[1,2-a]py...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of GSK3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50240449(3-(3-(benzyloxy)-4-methoxyphenyl)-8H-thieno[2,3-b]...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of GSK3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267079(1-(4-Methoxyphenyl)furo[2,3-e]pyrrolo [1,2-a]pyraz...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of CDK5 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267107(3-(4-chlorophenyl)pyrrolo[2,3-b]pyrrolizin-8(1H)-o...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of GSK3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50240446(3-(3,4-Dimethoxy-phenyl)-1H-1,3b-diaza-cyclopenta[...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of GSK3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267108(3-(3-(benzyloxy)-4-methoxyphenyl)pyrrolo[2,3-b]pyr...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of GSK3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267078(1-(4-Methylphenyl)furo[2,3-e]pyrrolo[1,2-a] pyrazi...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of CDK5 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50240447(3-(3,4-Dimethoxy-phenyl)-furo[2,3-b]pyrrolizin-8-o...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of GSK3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267077(1-(4-Fluorophenyl)furo[2,3-e]pyrrolo[1,2-a] pyrazi...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of CDK5 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267076(1-(4-Bromophenyl)furo[2,3-e]pyrrolo[1,2-a] pyrazin...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of CDK5 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50240449(3-(3-(benzyloxy)-4-methoxyphenyl)-8H-thieno[2,3-b]...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of CDK1/cyclin B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267041(1-(3,4-Dimethoxyphenyl)-3,4-dihydro-5H-dipyrrolo [...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of CDK5 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267107(3-(4-chlorophenyl)pyrrolo[2,3-b]pyrrolizin-8(1H)-o...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of CDK1/cyclin B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267108(3-(3-(benzyloxy)-4-methoxyphenyl)pyrrolo[2,3-b]pyr...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of CDK1/cyclin B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267040(1-(4-Chlorophenyl)-3,4-dihydro-5H-dipyrrolo [1,2-a...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of CDK5 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50240447(3-(3,4-Dimethoxy-phenyl)-furo[2,3-b]pyrrolizin-8-o...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of CDK5 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267107(3-(4-chlorophenyl)pyrrolo[2,3-b]pyrrolizin-8(1H)-o...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of CDK5 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50240446(3-(3,4-Dimethoxy-phenyl)-1H-1,3b-diaza-cyclopenta[...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of CDK5 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50267108(3-(3-(benzyloxy)-4-methoxyphenyl)pyrrolo[2,3-b]pyr...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of CDK5 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50240447(3-(3,4-Dimethoxy-phenyl)-furo[2,3-b]pyrrolizin-8-o...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of CDK1/cyclin B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, brain(Rattus norvegicus (rat))
Universit£

Curated by ChEMBL
LigandPNGBDBM50390021(CHEMBL2071545)
Affinity DataIC50:  5.17E+4nMAssay Description:Inhibition of nNOS in rat cerebellum homogenates assessed as reduction in conversion of L-[3H]arginine to L-[3H]citrullineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, brain(Rattus norvegicus (rat))
Universit£

Curated by ChEMBL
LigandPNGBDBM50390025(CHEMBL2071549)
Affinity DataIC50:  7.25E+4nMAssay Description:Inhibition of nNOS in rat cerebellum homogenates assessed as reduction in conversion of L-[3H]arginine to L-[3H]citrullineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyroglutamylated RF-amide peptide receptor(Homo sapiens (Human))
Normandy University

Curated by ChEMBL
LigandPNGBDBM50469431(CHEMBL4282568)
Affinity DataIC50: >1.00E+5nMAssay Description:Antagonist activity at human QRFPR expressed in CHO cells co-expressing Galpha16 assessed as inhibition of 26RFa-induced Ca2+ mobilization preincubat...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetPyroglutamylated RF-amide peptide receptor(Homo sapiens (Human))
Normandy University

Curated by ChEMBL
LigandPNGBDBM50469447(CHEMBL4291594)
Affinity DataIC50: >1.00E+5nMAssay Description:Antagonist activity at human QRFPR expressed in CHO cells co-expressing Galpha16 assessed as inhibition of 26RFa-induced Ca2+ mobilization preincubat...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
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