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Found 46 with Last Name = 'ennis' and Initial = 'c'
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552035(CHEMBL4792698)
Affinity DataIC50:  100nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552040(CHEMBL4764675)
Affinity DataIC50:  120nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552034(CHEMBL4743218)
Affinity DataIC50:  140nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552041(CHEMBL4744776)
Affinity DataIC50:  150nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50537058(CHEMBL4531719)
Affinity DataIC50:  300nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552022(CHEMBL4785115)
Affinity DataIC50:  400nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552031(CHEMBL4741968)
Affinity DataIC50:  490nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50014917(4-(2-Chloro-phenyl)-2-imidazol-1-ylmethyl-6-methyl...)
Affinity DataIC50:  500nMAssay Description:Inhibition of Thromboxane A2 synthase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50368043(CHEMBL1203671)
Affinity DataIC50:  600nMAssay Description:Inhibition of Thromboxane A2 synthase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552032(CHEMBL4742331)
Affinity DataIC50:  820nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552024(CHEMBL4741684)
Affinity DataIC50:  890nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552033(CHEMBL4787707)
Affinity DataIC50:  940nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552037(CHEMBL4784714)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50014907(4-(2-Difluoromethoxy-phenyl)-2-imidazol-1-ylmethyl...)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibition of Thromboxane A2 synthetase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552023(CHEMBL4799050)
Affinity DataIC50:  1.29E+3nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50368036(CHEMBL1203682)
Affinity DataIC50:  1.40E+3nMAssay Description:Inhibition of Thromboxane A2 synthetase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50368045(CHEMBL1203652)
Affinity DataIC50:  1.40E+3nMAssay Description:Inhibition of Thromboxane A2 synthetase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552038(CHEMBL4790390)
Affinity DataIC50:  1.51E+3nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50368040(CHEMBL1203686)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibition of Thromboxane A2 synthetase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552039(CHEMBL4795681)
Affinity DataIC50:  2.02E+3nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50368033(CHEMBL1203626)
Affinity DataIC50:  2.20E+3nMAssay Description:Inhibition of Thromboxane A2 synthase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50368037(CHEMBL1744226)
Affinity DataIC50:  2.30E+3nMAssay Description:Inhibition of Thromboxane A2 synthase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552036(CHEMBL4761720)
Affinity DataIC50:  2.49E+3nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM7962(4-(2-Imidazol-1-yl-ethoxy)-benzoic acid; hydrochlo...)
Affinity DataIC50:  2.50E+3nMAssay Description:Inhibition of Thromboxane A2 synthase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552027(CHEMBL4742051)
Affinity DataIC50:  2.90E+3nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50014918(2-Imidazol-1-ylmethyl-6-methyl-4-(2-nitro-phenyl)-...)
Affinity DataIC50:  3.20E+3nMAssay Description:Inhibition of Thromboxane A2 synthetase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50368034(CHEMBL1203674)
Affinity DataIC50:  5.00E+3nMAssay Description:Inhibition of Thromboxane A2 synthetase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552021(CHEMBL4764209)
Affinity DataIC50:  5.09E+3nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50368032(CHEMBL1203662)
Affinity DataIC50:  5.30E+3nMAssay Description:Inhibition of Thromboxane A2 synthase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50368031(CHEMBL1203654)
Affinity DataIC50:  1.10E+4nMAssay Description:Inhibition of Thromboxane A2 synthetase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552025(CHEMBL4786545)
Affinity DataIC50:  1.12E+4nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50368042(CHEMBL1203687)
Affinity DataIC50:  1.18E+4nMAssay Description:Inhibition of Thromboxane A2 synthetase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50368041(CHEMBL1203653)
Affinity DataIC50:  1.28E+4nMAssay Description:Inhibition of Thromboxane A2 synthetase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552026(CHEMBL4783844)
Affinity DataIC50:  1.30E+4nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50014919(4-(2,3-Dichloro-phenyl)-2-imidazol-1-ylmethyl-6-me...)
Affinity DataIC50:  1.30E+4nMAssay Description:Inhibition of Thromboxane A2 synthetase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50014908(4-(2-Chloro-3-trifluoromethyl-phenyl)-2-imidazol-1...)
Affinity DataIC50:  1.60E+4nMAssay Description:Inhibition of Thromboxane A2 synthetase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50368039(CHEMBL1202293)
Affinity DataIC50:  1.95E+4nMAssay Description:Inhibition of Thromboxane A2 synthase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50368044(CHEMBL1203649)
Affinity DataIC50:  2.30E+4nMAssay Description:Inhibition of Thromboxane A2 synthetase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50014902(4-(2-Difluoromethoxy-phenyl)-2-imidazol-1-ylmethyl...)
Affinity DataIC50:  2.50E+4nMAssay Description:Inhibition of Thromboxane A2 synthase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552028(CHEMBL4764635)
Affinity DataIC50:  4.01E+4nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552029(CHEMBL4758562)
Affinity DataIC50:  5.38E+4nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50552030(CHEMBL4743223)
Affinity DataIC50:  5.97E+4nMAssay Description:Inhibition of human DDX3X using dsRNA as substrate measured every 30 sec for 40 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50368038(CHEMBL1203655)
Affinity DataIC50:  7.20E+4nMAssay Description:Inhibition of Thromboxane A2 synthetase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50368035(CHEMBL1203656)
Affinity DataIC50:  1.15E+5nMAssay Description:Inhibition of Thromboxane A2 synthetase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50014915(4-(2-Chloro-3-trifluoromethyl-phenyl)-2-imidazol-1...)
Affinity DataIC50:  1.25E+5nMAssay Description:Inhibition of Thromboxane A2 synthase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50318494(3-ethyl 5-methyl 2,6-dimethyl-4-(3-nitrophenyl)-1,...)
Affinity DataIC50:  1.00E+6nMAssay Description:Inhibition of Thromboxane A2 synthase after oral administration of 0.03 mmol/kgMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed