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Found 26 with Last Name = 'mcnae' and Initial = 'iw'
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1(Homo sapiens (Human))
Palacky£? University And Institute Of Experimental Botany Ascr

Curated by ChEMBL
LigandPNGBDBM50341878((2R)-2-{[7-(benzylamino)-3-(propan-2-yl)-1H-pyrazo...)
Affinity DataIC50:  40nMAssay Description:Inhibition of human recombinant CDK2/cyclin EMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-H/Cyclin-dependent kinase 7(Homo sapiens (Human))
Palacky£? University And Institute Of Experimental Botany Ascr

Curated by ChEMBL
LigandPNGBDBM50341878((2R)-2-{[7-(benzylamino)-3-(propan-2-yl)-1H-pyrazo...)
Affinity DataIC50:  160nMAssay Description:Inhibition of human recombinant CDK7/cyclin H/MAT1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Palacky£? University And Institute Of Experimental Botany Ascr

Curated by ChEMBL
LigandPNGBDBM50341878((2R)-2-{[7-(benzylamino)-3-(propan-2-yl)-1H-pyrazo...)
Affinity DataIC50:  200nMAssay Description:Inhibition of human recombinant CDK5/p35More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1(Homo sapiens (Human))
Palacky£? University And Institute Of Experimental Botany Ascr

Curated by ChEMBL
LigandPNGBDBM7533((2R)-2-[[6-(benzylamino)-9-isopropyl-purin-2-yl]am...)
Affinity DataIC50:  220nMAssay Description:Inhibition of human recombinant CDK2/cyclin EMore data for this Ligand-Target Pair
TargetCyclin-H/Cyclin-dependent kinase 7(Homo sapiens (Human))
Palacky£? University And Institute Of Experimental Botany Ascr

Curated by ChEMBL
LigandPNGBDBM7533((2R)-2-[[6-(benzylamino)-9-isopropyl-purin-2-yl]am...)
Affinity DataIC50:  480nMAssay Description:Inhibition of human recombinant CDK7/cyclin H/MAT1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Palacky£? University And Institute Of Experimental Botany Ascr

Curated by ChEMBL
LigandPNGBDBM7533((2R)-2-[[6-(benzylamino)-9-isopropyl-purin-2-yl]am...)
Affinity DataIC50:  940nMAssay Description:Inhibition of human recombinant CDK5/p35More data for this Ligand-Target Pair
TargetCyclin-T1/Cyclin-dependent kinase 9(Homo sapiens (Human))
Palacky£? University And Institute Of Experimental Botany Ascr

Curated by ChEMBL
LigandPNGBDBM50341878((2R)-2-{[7-(benzylamino)-3-(propan-2-yl)-1H-pyrazo...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of human recombinant CDK9/cyclin T1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-T1/Cyclin-dependent kinase 9(Homo sapiens (Human))
Palacky£? University And Institute Of Experimental Botany Ascr

Curated by ChEMBL
LigandPNGBDBM7533((2R)-2-[[6-(benzylamino)-9-isopropyl-purin-2-yl]am...)
Affinity DataIC50:  1.77E+3nMAssay Description:Inhibition of human recombinant CDK9/cyclin T1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent 6-phosphofructokinase(Trypanosoma brucei)
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50270350(2,5-Anhydro-1-deoxy-1-(3,4-dichlorobenzylamino)-D-...)
Affinity DataIC50:  2.30E+4nMAssay Description:Inhibition of Trypanosoma brucei phosphofructokinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase(Leishmania mexicana)
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50270352((2S,3S,4S,5R)-N-cycloheptyl-5-((cycloheptylamino)m...)
Affinity DataIC50:  2.60E+4nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent 6-phosphofructokinase(Trypanosoma brucei)
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50270447((2S,3S,4S,5R)-N-(3,4-dichlorobenzyl)-5-((cyclohept...)
Affinity DataIC50:  4.90E+4nMAssay Description:Inhibition of Trypanosoma brucei phosphofructokinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent 6-phosphofructokinase(Trypanosoma brucei)
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50270348((2S,3S,4S,5R)-5-((3,4-dichlorobenzylamino)methyl)-...)
Affinity DataIC50:  5.00E+4nMAssay Description:Inhibition of Trypanosoma brucei phosphofructokinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase(Leishmania mexicana)
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50270448((2S,3S,4S,5R)-5-((cycloheptylamino)methyl)-3,4-dih...)
Affinity DataIC50:  5.30E+4nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase(Leishmania mexicana)
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50270344(2,5-Anhydro-1-deoxy-1-(cycloheptylamino)-D-mannito...)
Affinity DataIC50:  7.10E+4nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent 6-phosphofructokinase(Trypanosoma brucei)
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50270351((2S,3S,4S,5R)-5-((3,4-dichlorobenzylamino)methyl)-...)
Affinity DataIC50:  8.00E+4nMAssay Description:Inhibition of Trypanosoma brucei phosphofructokinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent 6-phosphofructokinase(Trypanosoma brucei)
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50270460(2,5-Anhydro-1-deoxy-1-(3,4-dichlorobenzylamino)-D-...)
Affinity DataIC50:  4.10E+5nMAssay Description:Inhibition of Trypanosoma brucei phosphofructokinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase(Leishmania mexicana)
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50270341((2R,3S,4S,5R)-2-(hydroxymethyl)-5-(((R)-1-(4-metho...)
Affinity DataIC50:  9.00E+5nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase(Leishmania mexicana)
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50270338((2R,3S,4S,5R)-2-(hydroxymethyl)-5-((1,2,3,4-tetrah...)
Affinity DataIC50:  1.20E+6nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase(Leishmania mexicana)
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50270347((2R,3S,4S,5R)-2-(((1R,2S,4R)-bicyclo[2.2.1]heptan-...)
Affinity DataIC50:  1.50E+6nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase(Leishmania mexicana)
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50270343((2R,3S,4S,5R)-2-(hydroxymethyl)-5-(((S)-1-(naphtha...)
Affinity DataIC50:  1.50E+6nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase(Leishmania mexicana)
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50270349((2R,3S,4S,5R)-2-(hydroxymethyl)-5-(((R)-1-(naphtha...)
Affinity DataIC50:  1.50E+6nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase(Leishmania mexicana)
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50270345((2R,3S,4S,5R)-2-(hydroxymethyl)-5-(((S)-3-methylbu...)
Affinity DataIC50:  2.30E+6nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase(Leishmania mexicana)
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50270474((2R,3S,4S,5R)-2-(hydroxymethyl)-5-((pentan-2-ylami...)
Affinity DataIC50:  2.50E+6nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase(Leishmania mexicana)
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50270340((2R,3S,4S,5R)-2-(hydroxymethyl)-5-(((S)-1-(4-metho...)
Affinity DataIC50:  3.50E+6nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase(Leishmania mexicana)
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50270449((2R,3S,4S,5R)-2-((cyclopentylamino)methyl)-5-(hydr...)
Affinity DataIC50:  4.10E+6nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase(Leishmania mexicana)
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50270339((2R,3S,4S,5R)-2-((cyclobutylamino)methyl)-5-(hydro...)
Affinity DataIC50:  4.30E+6nMAssay Description:Inhibition of Leishmania mexicana pyruvate kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed