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Found 483 with Last Name = 'dreassi' and Initial = 'e'
TargetPolyamine oxidase 1(Zea mays)
Universit£

Curated by ChEMBL
LigandPNGBDBM50294105(1-(Guanidino)-17-(N1-(methylcyclopropyl)guanidino)...)
Affinity DataKi:  0.0800nMpH: 6.5Assay Description:Inhibition of maize PAO at pH 6.5 by spectrophotometry-based Dixon plot methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine oxidase 1(Zea mays)
Universit£

Curated by ChEMBL
LigandPNGBDBM50294107(1-(Guanidino)-17-(N1-(beta-methylallyl)guanidino)-...)
Affinity DataKi:  0.5nMpH: 6.5Assay Description:Inhibition of maize PAO at pH 6.5 by spectrophotometry-based Dixon plot methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine oxidase 1(Zea mays)
Universit£

Curated by ChEMBL
LigandPNGBDBM50294109(1-(Guanidino)-17-(N1-(propargyl)guanidino)-9-azahe...)
Affinity DataKi:  0.700nMpH: 6.5Assay Description:Inhibition of maize PAO at pH 6.5 by spectrophotometry-based Dixon plot methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine oxidase 1(Zea mays)
Universit£

Curated by ChEMBL
LigandPNGBDBM50294108(1-(Guanidino)-17-(N1-(benzyl)guanidino)-9-azahepta...)
Affinity DataKi:  1nMpH: 6.5Assay Description:Inhibition of maize PAO at pH 6.5 by spectrophotometry-based Dixon plot methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine oxidase 1(Zea mays)
Universit£

Curated by ChEMBL
LigandPNGBDBM50294106(1-(Guanidino)-17-(N1-(gamma-methylallyl)guanidino)...)
Affinity DataKi:  1.10nMpH: 6.5Assay Description:Inhibition of maize PAO at pH 6.5 by spectrophotometry-based Dixon plot methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChitotriosidase-1(Homo sapiens (Human))TBA
LigandPNGBDBM50541929(CHEMBL1738785)
Affinity DataKi:  1.40nMAssay Description:Inhibition of human CHIT1 using 4-methylumbelliferyl-beta-D-N,N',N''-triacetylchitotriose as substrate assessed as substrate hydrolysis by measuring ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails PubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
University Of Pisa

Curated by ChEMBL
LigandPNGBDBM50605682(CHEMBL5176915)
Affinity DataKi:  1.40nMAssay Description:Competitive inhibition of human recombinant MAGL using 4-nitrophenylacetate as substrate assessed as inhibition constant by Michaelis-Menten analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetPolyamine oxidase 1(Zea mays)
Universit£

Curated by ChEMBL
LigandPNGBDBM50294110(1,1'-(8,8'-azanediylbis(octane-8,1-diyl))bis(3-(3-...)
Affinity DataKi:  1.70nMpH: 6.5Assay Description:Inhibition of maize PAO at pH 6.5 by spectrophotometry-based Dixon plot methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine oxidase 1(Zea mays)
Universit£

Curated by ChEMBL
LigandPNGBDBM50294104(1-(Guanidino)-17-(N1-(gamma,gamma-dimethylallyl)gu...)
Affinity DataKi:  3nMpH: 6.5Assay Description:Inhibition of maize PAO at pH 6.5 by spectrophotometry-based Dixon plot methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50436581(CHEMBL2397805)
Affinity DataKi:  5nMAssay Description:Binding affinity to recombinant wild type human Abl using abitide as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50102904(CHEMBL3394091)
Affinity DataKi:  7nMAssay Description:Inhibition of human recombinant src kinase using KVEKIGEGTYGVVYK as substrate by filter binding assay in presence of [gamma-32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine oxidase 1(Zea mays)
Universit£

Curated by ChEMBL
LigandPNGBDBM50032500(1,1'-(8,8'-azanediylbis(octane-8,1-diyl))diguanidi...)
Affinity DataKi:  7.5nMpH: 6.5Assay Description:Inhibition of maize PAO at pH 6.5 by spectrophotometry-based Dixon plot methodMore data for this Ligand-Target Pair
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50102908(CHEMBL3393071)
Affinity DataKi:  10nMAssay Description:Inhibition of human recombinant src kinase using KVEKIGEGTYGVVYK as substrate by filter binding assay in presence of [gamma-32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine oxidase 1(Zea mays)
Universit£

Curated by ChEMBL
LigandPNGBDBM50294112(1-(5-aminopentyl)-3-(3-methylbut-2-enyl)guanidine ...)
Affinity DataKi:  10nMpH: 6.5Assay Description:Inhibition of maize PAO at pH 6.5 by spectrophotometry-based Dixon plot methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM13530(4-[(4-methylpiperazin-1-yl)methyl]-N-[4-methyl-3-[...)
Affinity DataKi:  13nMAssay Description:Inhibition of human recombinant c-Abl by filter-binding assayMore data for this Ligand-Target Pair
TargetPolyamine oxidase 1(Zea mays)
Universit£

Curated by ChEMBL
LigandPNGBDBM50294111(1-(4-aminobutyl)-3-(3-methylbut-2-enyl)guanidine |...)
Affinity DataKi:  15nMpH: 6.5Assay Description:Inhibition of maize PAO at pH 6.5 by spectrophotometry-based Dixon plot methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50354489(CHEMBL1836680)
Affinity DataKi:  18nMAssay Description:Inhibition human recombinant cSRC using KVEKIGEGTYGVVYK peptide substrate in presence of [gamma-32P]-ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50354489(CHEMBL1836680)
Affinity DataKi:  20nMAssay Description:Inhibition of human wild type full length N-terminal GST/6His-tagged SRC (M1 to L536 residues) expressed in baculovirus infected Sf9 cells using src ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50436582(CHEMBL2397804)
Affinity DataKi:  21nMAssay Description:Binding affinity to recombinant wild type human Abl using abitide as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine oxidase 1(Zea mays)
Universit£

Curated by ChEMBL
LigandPNGBDBM50294113(1-(6-aminohexyl)-3-(3-methylbut-2-enyl)guanidine |...)
Affinity DataKi:  22nMpH: 6.5Assay Description:Inhibition of maize PAO at pH 6.5 by spectrophotometry-based Dixon plot methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50354480(CHEMBL1836678)
Affinity DataKi:  25nMAssay Description:Inhibition human recombinant cSRC using KVEKIGEGTYGVVYK peptide substrate in presence of [gamma-32P]-ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50354481(CHEMBL1836679)
Affinity DataKi:  25nMAssay Description:Inhibition human recombinant cSRC using KVEKIGEGTYGVVYK peptide substrate in presence of [gamma-32P]-ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50102872(CHEMBL3394083)
Affinity DataKi:  30nMAssay Description:Inhibition of human recombinant src kinase using KVEKIGEGTYGVVYK as substrate by filter binding assay in presence of [gamma-32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50354485(CHEMBL412298)
Affinity DataKi:  40nMAssay Description:Binding affinity to recombinant wild type human Abl using abitide as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50101585(CHEMBL3393986)
Affinity DataKi:  40nMAssay Description:Inhibition of human recombinant src kinase using KVEKIGEGTYGVVYK as substrate by filter binding assay in presence of [gamma-32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50354485(CHEMBL412298)
Affinity DataKi:  40nMAssay Description:Inhibition human recombinant Abl using Abtide peptide substrate in presence of [gamma-32P]-ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50224371(1-(2-chloro-2-phenylethyl)-N-(3-chlorophenyl)-6-(e...)
Affinity DataKi:  40nMAssay Description:Inhibition of human recombinant AblMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50436570(CHEMBL2397818)
Affinity DataKi:  50nMAssay Description:Binding affinity to recombinant wild type human Abl using abitide as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50436590(CHEMBL2397796)
Affinity DataKi:  55nMAssay Description:Binding affinity to recombinant wild type human Abl using abitide as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50224388(CHEMBL238561 | N-(3-bromophenyl)-1-(2-chloro-2-phe...)
Affinity DataKi:  60nMAssay Description:Inhibition of human recombinant AblMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50436571(CHEMBL2397817)
Affinity DataKi:  60nMAssay Description:Binding affinity to recombinant wild type human Abl using abitide as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50436584(CHEMBL2397802)
Affinity DataKi:  60nMAssay Description:Inhibition of human wild type full length N-terminal GST/6His-tagged SRC (M1 to L536 residues) expressed in baculovirus infected Sf9 cells using src ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50354484(CHEMBL1629808)
Affinity DataKi:  64nMAssay Description:Inhibition human recombinant Abl using Abtide peptide substrate in presence of [gamma-32P]-ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50102878(CHEMBL3394082)
Affinity DataKi:  70nMAssay Description:Inhibition of human recombinant src kinase using KVEKIGEGTYGVVYK as substrate by filter binding assay in presence of [gamma-32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50089575(CHEMBL3578214)
Affinity DataKi:  70nMAssay Description:Inhibition of human recombinant full-length Fyn using Src substrate peptide after 15 mins incubation by MicroBeta liquid scintillation counting analy...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50343424(1-(2-chloro-2-(4-chlorophenyl)ethyl)-N-(4-fluorobe...)
Affinity DataKi:  80nMAssay Description:Inhibition of human recombinant c-Abl by filter-binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50224377(1-(2-chloro-2-phenylethyl)-N-(2-fluorobenzyl)-6-(m...)
Affinity DataKi:  80nMAssay Description:Inhibition of human recombinant AblMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50343424(1-(2-chloro-2-(4-chlorophenyl)ethyl)-N-(4-fluorobe...)
Affinity DataKi:  80nMAssay Description:Binding affinity to recombinant wild type human Abl using abitide as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50224377(1-(2-chloro-2-phenylethyl)-N-(2-fluorobenzyl)-6-(m...)
Affinity DataKi:  80nMAssay Description:Inhibition human recombinant Abl using Abtide peptide substrate in presence of [gamma-32P]-ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50354485(CHEMBL412298)
Affinity DataKi:  81nMAssay Description:Inhibition human recombinant cSRC using KVEKIGEGTYGVVYK peptide substrate in presence of [gamma-32P]-ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50224387(1-(2-chloro-2-phenylethyl)-N-(2-chlorobenzyl)-6-(m...)
Affinity DataKi:  89nMAssay Description:Inhibition human recombinant Abl using Abtide peptide substrate in presence of [gamma-32P]-ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50343427(CHEMBL1775039 | N-Benzyl-1-(2-chloro-2-phenylethyl...)
Affinity DataKi:  90nMAssay Description:Inhibition of human recombinant c-Abl by filter-binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50343427(CHEMBL1775039 | N-Benzyl-1-(2-chloro-2-phenylethyl...)
Affinity DataKi:  90nMAssay Description:Inhibition of AblMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50354476(CHEMBL1836673)
Affinity DataKi:  90nMAssay Description:Inhibition human recombinant cSRC using KVEKIGEGTYGVVYK peptide substrate in presence of [gamma-32P]-ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50224387(1-(2-chloro-2-phenylethyl)-N-(2-chlorobenzyl)-6-(m...)
Affinity DataKi:  90nMAssay Description:Inhibition of human recombinant AblMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50089569(CHEMBL3578215)
Affinity DataKi:  95nMAssay Description:Inhibition of human recombinant full-length Fyn using Src substrate peptide after 15 mins incubation by MicroBeta liquid scintillation counting analy...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
University Of Siena

Curated by ChEMBL
LigandPNGBDBM50606859(CHEMBL5219128)
Affinity DataKi:  100nMAssay Description:Binding affinity to DDX3X (unknown origin) assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50224372(1-(2-chloro-2-phenylethyl)-N-(4-fluorobenzyl)-6-(m...)
Affinity DataKi:  100nMAssay Description:Inhibition human recombinant Abl using Abtide peptide substrate in presence of [gamma-32P]-ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50102909(CHEMBL3394077)
Affinity DataKi:  100nMAssay Description:Inhibition of human recombinant src kinase using KVEKIGEGTYGVVYK as substrate by filter binding assay in presence of [gamma-32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent RNA helicase DDX3X(Homo sapiens (Human))
University Of Siena

Curated by ChEMBL
LigandPNGBDBM50606879(CHEMBL5220346)
Affinity DataKi:  100nMAssay Description:Binding affinity to DDX3X (unknown origin) assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
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