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Found 73 with Last Name = 'riou' and Initial = 'jf'
TargetDimer of Protein farnesyltransferase subunit beta(Homo sapiens (Human))
RhôNe-Poulenc Rorer

Curated by ChEMBL
LigandPNGBDBM50088001((+/-)-11-[2-(2-methoxyphenyl)acryloyl]-1-phenyl-(1...)
Affinity DataKi:  25nMAssay Description:Inhibition of farnesyltransferase by Ras/SPA assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDimer of Protein farnesyltransferase subunit beta(Homo sapiens (Human))
RhôNe-Poulenc Rorer

Curated by ChEMBL
LigandPNGBDBM50088009((+/-)-11-[2-(2-methoxyphenyl)acetyl]-1-phenyl-(1R,...)
Affinity DataKi:  140nMAssay Description:Inhibition of farnesyltransferase by Ras/SPA assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDimer of Protein farnesyltransferase subunit beta(Homo sapiens (Human))
RhôNe-Poulenc Rorer

Curated by ChEMBL
LigandPNGBDBM50088004(8-hydroxy-11-[2-(2-methoxyphenyl)acetyl]-1-phenyl-...)
Affinity DataKi:  250nMAssay Description:Inhibition of farnesyltransferase by Ras/SPA assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDimer of Protein farnesyltransferase subunit beta(Homo sapiens (Human))
RhôNe-Poulenc Rorer

Curated by ChEMBL
LigandPNGBDBM50088014(1-(2,3-dihydrobenzo[b]furan-5-yl)-11-[2-(2-methoxy...)
Affinity DataKi:  420nMAssay Description:Inhibition of farnesyltransferase by Ras/SPA assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDimer of Protein farnesyltransferase subunit beta(Homo sapiens (Human))
RhôNe-Poulenc Rorer

Curated by ChEMBL
LigandPNGBDBM50088008(11-[2-(2-methoxyphenyl)acetyl]-1-phenyl-(1R,8R,9S,...)
Affinity DataKi:  420nMAssay Description:Inhibition of farnesyltransferase by Ras/SPA assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDimer of Protein farnesyltransferase subunit beta(Homo sapiens (Human))
RhôNe-Poulenc Rorer

Curated by ChEMBL
LigandPNGBDBM50088013(2-[11-[2-(2-methoxyphenyl)acetyl]-1-phenyl-(1R,8R,...)
Affinity DataKi:  738nMAssay Description:Inhibition of farnesyltransferase by Ras/SPA assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDimer of Protein farnesyltransferase subunit beta(Homo sapiens (Human))
RhôNe-Poulenc Rorer

Curated by ChEMBL
LigandPNGBDBM50088002(1-(4-carboxymethoxyphenyl)-11-[2-(2-methoxyphenyl)...)
Affinity DataKi:  2.55E+4nMAssay Description:Inhibition of farnesyltransferase by Ras/SPA assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDimer of Protein farnesyltransferase subunit beta(Homo sapiens (Human))
RhôNe-Poulenc Rorer

Curated by ChEMBL
LigandPNGBDBM50088003(11-[2-(2-benzyloxyphenyl)acetyl]-1-phenyl-(1R,8R,9...)
Affinity DataKi:  3.20E+4nMAssay Description:Inhibition of farnesyltransferase by Ras/SPA assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDimer of Protein farnesyltransferase subunit beta(Homo sapiens (Human))
RhôNe-Poulenc Rorer

Curated by ChEMBL
LigandPNGBDBM50088005(2-(2-methoxyphenyl)-1-[1-phenyl-(1R,8S,9R,13R)-11-...)
Affinity DataKi:  4.00E+4nMAssay Description:Inhibition of farnesyltransferase by Ras/SPA assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDimer of Protein farnesyltransferase subunit beta(Homo sapiens (Human))
RhôNe-Poulenc Rorer

Curated by ChEMBL
LigandPNGBDBM50088006(6-hydroxy-11-[2-(2-methoxyphenyl)acetyl]-1-phenyl-...)
Affinity DataKi:  5.00E+4nMAssay Description:Inhibition of farnesyltransferase by Ras/SPA assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDimer of Protein farnesyltransferase subunit beta(Homo sapiens (Human))
RhôNe-Poulenc Rorer

Curated by ChEMBL
LigandPNGBDBM50088000((+/-)-11-[2-(2-methoxyphenyl)acryloyl]-1-(4-methyl...)
Affinity DataIC50:  8nMAssay Description:Inhibition of FarnesyltransferaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDimer of Protein farnesyltransferase subunit beta(Homo sapiens (Human))
RhôNe-Poulenc Rorer

Curated by ChEMBL
LigandPNGBDBM50088001((+/-)-11-[2-(2-methoxyphenyl)acryloyl]-1-phenyl-(1...)
Affinity DataIC50:  50nMAssay Description:Inhibition of FarnesyltransferaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50134030(9-[4-(N,N-dimethylamino)phenylamino]-3,6-bis(3-pyr...)
Affinity DataIC50:  90nMAssay Description:Inhibition of human telomerase in A549 cells by TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50298376(4,5-Bis[3-(N,N-dimethylamino)propylaminomethyl]acr...)
Affinity DataIC50:  150nMAssay Description:Inhibition of human telomerase in A549 cells by TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDimer of Protein farnesyltransferase subunit beta(Homo sapiens (Human))
RhôNe-Poulenc Rorer

Curated by ChEMBL
LigandPNGBDBM50088009((+/-)-11-[2-(2-methoxyphenyl)acetyl]-1-phenyl-(1R,...)
Affinity DataIC50:  200nMAssay Description:Inhibition of FarnesyltransferaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM2581(3,13,23-triazahexacyclo[14.7.0.0^{2,10}.0^{4,9}.0^...)
Affinity DataIC50:  2.45E+3nMAssay Description:Inhibition of Protein Kinase C(PKC)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50298371(2,2'-[4,5-Acridindiylbis(methyleneimino)]bis(N,N,N...)
Affinity DataIC50:  3.00E+3nMAssay Description:Inhibition of human telomerase in A549 cells by TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50054428(13-(3,4-dihydroxy-6-hydroxymethyl-5-methoxytetrahy...)
Affinity DataIC50:  3.70E+3nMAssay Description:Inhibition of Protein Kinase C(PKC)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50298372(2,2'-[4,5-Acridindiylbis(methyleneimino)]bis[N-met...)
Affinity DataIC50:  4.00E+3nMAssay Description:Inhibition of human telomerase in A549 cells by TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50298373(4,5-Bis[2-(N,N-dimethylamino)ethylaminomethyl]acri...)
Affinity DataIC50:  5.60E+3nMAssay Description:Inhibition of human telomerase in A549 cells by TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50298374(CHEMBL577150 | N,N'-[4,5-Acridindiylbis(methylene)...)
Affinity DataIC50:  6.00E+3nMAssay Description:Inhibition of human telomerase in A549 cells by TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50298375(2,2'-[4,5-Acridindiylbis(methyleneimino)]bis(N,N,N...)
Affinity DataIC50:  7.30E+3nMAssay Description:Inhibition of human telomerase in A549 cells by TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50298377(CHEMBL576188 | N,N'-[4,5-Acridindiylbis(methylene)...)
Affinity DataIC50:  1.20E+4nMAssay Description:Inhibition of human telomerase in A549 cells by TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50298378(CHEMBL573120 | N,N'-[4,5-Acridindiylbis(methylene)...)
Affinity DataIC50:  1.30E+4nMAssay Description:Inhibition of human telomerase in A549 cells by TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50054426(7-hydroxy-6,7,12,13-tetrahydro-5H-indolo[2,3-a]pyr...)
Affinity DataIC50:  2.21E+4nMAssay Description:Inhibition of Protein Kinase C(PKC)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50298379(2,2'-[4,5-Acridindiylbis(methyleneimino)]bis[N-met...)
Affinity DataIC50:  2.70E+4nMAssay Description:Inhibition of human telomerase in A549 cells by TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50054423(1,11-dichloro-13-(3,4-dihydroxy-6-hydroxymethyl-5-...)
Affinity DataIC50:  2.88E+4nMAssay Description:Inhibition of Protein Kinase C(PKC)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50298382(CHEMBL573353 | N,N'-[4,5-Acridindiylbis(methylene)...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human telomerase in A549 cells by TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50298386(4,5-Bis(aminomethyl)acridine dihydrochloride salt ...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human telomerase in A549 cells by TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50298385(CHEMBL573861 | N,N'-[4,5-Acridindiylbis(methylene)...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human telomerase in A549 cells by TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50298384(CHEMBL573387 | N,N'-[4,5-Acridindiylbis(methylene)...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human telomerase in A549 cells by TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50298383(CHEMBL575850 | N,N'-[4,5-Acridindiylbis(methylene)...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human telomerase in A549 cells by TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50298381(CHEMBL573386 | N,N'-[4,5-Acridindiylbis(methylene)...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human telomerase in A549 cells by TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50298380(2,2'-[4,5-Acridindiylbis(methyleneimino)]bis[N-met...)
Affinity DataIC50:  3.00E+4nMAssay Description:Inhibition of human telomerase in A549 cells by TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50054429(6-Hydroxy-12-(4-O-methyl-beta-D-glucopyrannosyl) -...)
Affinity DataIC50:  4.00E+4nMAssay Description:Inhibition of Protein Kinase C(PKC)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50054425(6-amino-6,7,12,13-tetrahydro-5H-indolo[2,3-a]pyrro...)
Affinity DataIC50:  4.35E+4nMAssay Description:Inhibition of Protein Kinase C(PKC)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM2672(3,13,23-triazahexacyclo[14.7.0.0^{2,10}.0^{4,9}.0^...)
Affinity DataIC50:  4.47E+4nMAssay Description:Inhibition of Protein Kinase C(PKC)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50060400(6-methyl-12-(3,4,5-trihydroxy-6-hydroxymethyltetra...)
Affinity DataIC50:  6.20E+4nMAssay Description:Inhibition of Protein kinase C alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50054432(1,11-Dichloro-6-hydroxy-12-(4-O-methyl-beta-D-gluc...)
Affinity DataIC50:  6.80E+4nMAssay Description:Inhibition of Protein Kinase C(PKC)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50054434(6-(4-Semicarbazido)-6,7,12,13-tetrahydro-5,7-dioxo...)
Affinity DataIC50:  7.80E+4nMAssay Description:Inhibition of Protein Kinase C(PKC)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50054422(6-hydroxy-6,7,12,13-tetrahydro-5H-indolo[2,3-a]pyr...)
Affinity DataIC50:  7.92E+4nMAssay Description:Inhibition of Protein Kinase C(PKC)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50060402(3,5-di(methylcarbonyloxy)-2-methylcarbonyloxymethy...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of Protein kinase C alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50060403(1,11-dichloro-12-(3,4-dihydroxy-6-hydroxymethyl-5-...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of Protein kinase C alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50054420(12-(3,4-dihydroxy-6-hydroxymethyl-5-methoxytetrahy...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of Protein kinase C alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50162287((Rebeccamycin)1,11-dichloro-12-(3,4-dihydroxy-6-hy...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of Protein kinase C alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50060401(6-methyl-12-(3,4,5-trihydroxy-6-methyltetrahydro-2...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of Protein kinase C alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50060404(12-(3,4-dihydroxy-6-hydroxymethyl-5-methoxytetrahy...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of Protein kinase C alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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