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Found 61 with Last Name = 'bernardini' and Initial = 'g'
Target4-hydroxyphenylpyruvate dioxygenase(Arabidopsis thaliana)
Universit£

Curated by ChEMBL
LigandPNGBDBM50264305(CHEMBL4102251)
Affinity DataKi:  5nMAssay Description:Inhibition of Arabidopsis thaliana HPPD expressed in Escherichia coli BL21(DE3) using HPPA as substrate after 10 mins by UV-Vis spectrometric analysi...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Arabidopsis thaliana)
Universit£

Curated by ChEMBL
LigandPNGBDBM50264306(CHEMBL4071950)
Affinity DataKi:  7nMAssay Description:Inhibition of Arabidopsis thaliana HPPD expressed in Escherichia coli BL21(DE3) using HPPA as substrate after 10 mins by UV-Vis spectrometric analysi...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Arabidopsis thaliana)
Universit£

Curated by ChEMBL
LigandPNGBDBM50264374(CHEMBL4069617)
Affinity DataKi:  7nMAssay Description:Inhibition of Arabidopsis thaliana HPPD expressed in Escherichia coli BL21(DE3) using HPPA as substrate after 10 mins by UV-Vis spectrometric analysi...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Arabidopsis thaliana)
Universit£

Curated by ChEMBL
LigandPNGBDBM50264350(CHEMBL4080249)
Affinity DataKi:  7nMAssay Description:Inhibition of Arabidopsis thaliana HPPD expressed in Escherichia coli BL21(DE3) using HPPA as substrate after 10 mins by UV-Vis spectrometric analysi...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Arabidopsis thaliana)
Universit£

Curated by ChEMBL
LigandPNGBDBM50264308(CHEMBL4061385)
Affinity DataKi:  7nMAssay Description:Inhibition of Arabidopsis thaliana HPPD expressed in Escherichia coli BL21(DE3) using HPPA as substrate after 10 mins by UV-Vis spectrometric analysi...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Arabidopsis thaliana)
Universit£

Curated by ChEMBL
LigandPNGBDBM50264309(CHEMBL4060588)
Affinity DataKi:  7nMAssay Description:Inhibition of Arabidopsis thaliana HPPD expressed in Escherichia coli BL21(DE3) using HPPA as substrate after 10 mins by UV-Vis spectrometric analysi...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Arabidopsis thaliana)
Universit£

Curated by ChEMBL
LigandPNGBDBM50264307(CHEMBL4093474)
Affinity DataKi:  7nMAssay Description:Inhibition of Arabidopsis thaliana HPPD expressed in Escherichia coli BL21(DE3) using HPPA as substrate after 10 mins by UV-Vis spectrometric analysi...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Arabidopsis thaliana)
Universit£

Curated by ChEMBL
LigandPNGBDBM50264336(TEMBOTRIONE)
Affinity DataKi:  13nMAssay Description:Inhibition of Arabidopsis thaliana HPPD expressed in Escherichia coli JM109 using HPPA as substrate after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Arabidopsis thaliana)
Universit£

Curated by ChEMBL
LigandPNGBDBM50264337(CHEBI:38321 | MESOTRIONE)
Affinity DataKi:  13nMAssay Description:Inhibition of Arabidopsis thaliana HPPD expressed in Escherichia coli BL21(DE3) using HPPA as substrate after 10 mins by UV-Vis spectrometric analysi...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Arabidopsis thaliana)
Universit£

Curated by ChEMBL
LigandPNGBDBM50264335(CHEMBL4080003)
Affinity DataKi:  31nMAssay Description:Inhibition of Arabidopsis thaliana HPPD expressed in Escherichia coli JM109 using HPPA as substrate after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Arabidopsis thaliana)
Universit£

Curated by ChEMBL
LigandPNGBDBM50264377(CHEMBL4069274)
Affinity DataKi:  31nMAssay Description:Inhibition of Arabidopsis thaliana HPPD expressed in Escherichia coli JM109 using HPPA as substrate after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Arabidopsis thaliana)
Universit£

Curated by ChEMBL
LigandPNGBDBM50264333(CHEMBL4082475)
Affinity DataKi:  31nMAssay Description:Inhibition of Arabidopsis thaliana HPPD expressed in Escherichia coli JM109 using HPPA as substrate after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Arabidopsis thaliana)
Universit£

Curated by ChEMBL
LigandPNGBDBM50264334(CHEMBL4090319)
Affinity DataKi:  31nMAssay Description:Inhibition of Arabidopsis thaliana HPPD expressed in Escherichia coli JM109 using HPPA as substrate after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224371(1-(2-chloro-2-phenylethyl)-N-(3-chlorophenyl)-6-(e...)
Affinity DataKi:  500nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50142887(1-(tert-butyl)-3-(4-chlorophenyl)-4-aminopyrazolo[...)
Affinity DataKi:  500nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224368(1-(2-chloro-2-phenylethyl)-N-(3-chlorophenyl)-6-(m...)
Affinity DataKi:  600nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50142880(1-(2-chloro-2-phenylethyl)-6-(methylthio)-N-phenet...)
Affinity DataKi:  700nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224385(1-(2-chloro-2-phenylethyl)-6-(methylthio)-N-phenyl...)
Affinity DataKi:  1.20E+3nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224376(1-(2-chloro-2-phenylethyl)-N-(3-chlorophenyl)-6-(p...)
Affinity DataKi:  1.20E+3nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224381(1-(2-chloro-2-phenylethyl)-N-(3-fluorophenyl)-6-(m...)
Affinity DataKi:  1.40E+3nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224388(CHEMBL238561 | N-(3-bromophenyl)-1-(2-chloro-2-phe...)
Affinity DataKi:  1.80E+3nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224383(1-(2-chloro-2-(4-chlorophenyl)ethyl)-6-(methylthio...)
Affinity DataKi:  2.80E+3nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224374(CHEMBL241749 | N-benzyl-1-(2-chloro-2-(4-chlorophe...)
Affinity DataKi:  3.00E+3nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224387(1-(2-chloro-2-phenylethyl)-N-(2-chlorobenzyl)-6-(m...)
Affinity DataKi:  3.10E+3nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50142885(Benzyl-[1-(2-chloro-2-phenyl-ethyl)-6-methylsulfan...)
Affinity DataKi:  3.70E+3nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224366(1-(2-chloro-2-phenylethyl)-N-(3-chlorophenyl)-1H-p...)
Affinity DataKi:  3.80E+3nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224386(CHEMBL399813 | N-(4-methoxyphenethyl)-1-(2-chloro-...)
Affinity DataKi:  4.00E+3nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224367(1-(2-chloro-2-phenylethyl)-N-(2-chlorophenethyl)-6...)
Affinity DataKi:  4.00E+3nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224382(CHEMBL399627 | N-(3-bromophenyl)-1-(2-chloro-2-(4-...)
Affinity DataKi:  4.10E+3nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224372(1-(2-chloro-2-phenylethyl)-N-(4-fluorobenzyl)-6-(m...)
Affinity DataKi:  4.60E+3nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224384(1-(2-chloro-2-phenylethyl)-N-(3-fluorobenzyl)-6-(m...)
Affinity DataKi:  5.20E+3nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224380(1-(2-chloro-2-phenylethyl)-N-(3-chlorophenethyl)-6...)
Affinity DataKi:  6.00E+3nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224369(1-(2-chloro-2-phenylethyl)-6-(ethylthio)-N-pheneth...)
Affinity DataKi:  7.50E+3nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224373(1-(2-chloro-2-phenylethyl)-N-(3-fluorophenethyl)-6...)
Affinity DataKi:  1.30E+4nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224379(1-(2-chloro-2-phenylethyl)-N-(4-methylphenethyl)-6...)
Affinity DataKi:  1.50E+4nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224377(1-(2-chloro-2-phenylethyl)-N-(2-fluorobenzyl)-6-(m...)
Affinity DataKi:  2.10E+4nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224378(CHEMBL239192 | N-(4-chlorobenzyl)-1-(2-chloro-2-ph...)
Affinity DataKi:  2.40E+4nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224375(CHEMBL401038 | N-(4-chlorophenethyl)-7-(2-chloro-2...)
Affinity DataKi:  2.50E+4nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50224370(CHEMBL241750 | N-benzyl-1-(2-chloro-2-(4-fluorophe...)
Affinity DataKi:  3.50E+4nMAssay Description:Inhibition of human recombinant SrcMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Universit£

Curated by ChEMBL
LigandPNGBDBM50403921(CHEMBL309664)
Affinity DataIC50:  15nMAssay Description:Inhibition of pig liver HPPD using 4-hydroxyphenylpyruvic acid as substrate after 15 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Arabidopsis thaliana)
Universit£

Curated by ChEMBL
LigandPNGBDBM50264344(CHEMBL4082652)
Affinity DataIC50:  19nMAssay Description:Inhibition of Arabidopsis thaliana HPPD expressed in Escherichia coli JM105 using 4-HPP as substrate preincubated for 15 mins followed by substrate a...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Universit£

Curated by ChEMBL
LigandPNGBDBM50403929(CHEMBL76394)
Affinity DataIC50:  28nMAssay Description:Inhibition of pig liver HPPD using 4-hydroxyphenylpyruvic acid as substrate after 15 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Universit£

Curated by ChEMBL
LigandPNGBDBM50089165(CHEMBL23622 | Cyclopropanecarboxylic acid 3-oxo-cy...)
Affinity DataIC50:  30nMAssay Description:Inhibition of pig liver HPPD using 4-hydroxyphenylpyruvic acid as substrate after 15 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Rattus norvegicus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50264347(CHEMBL4092919)
Affinity DataIC50:  36nMAssay Description:Inhibition of Wistar rat liver cytosol HPPD using HPP as substrate assessed as reduction in O2 consumptionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Rattus norvegicus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50264337(CHEBI:38321 | MESOTRIONE)
Affinity DataIC50:  37nMAssay Description:Inhibition of Wistar rat liver cytosol HPPD using HPP as substrate assessed as reduction in O2 consumptionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Rattus norvegicus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50088804(1,3-Cyclohexanedione, 2-(2-nitro-4-(trifluoromethy...)
Affinity DataIC50:  40nMAssay Description:Inhibition of Wistar rat liver cytosol HPPD using HPP as substrate assessed as reduction in O2 consumptionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Rattus norvegicus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50088804(1,3-Cyclohexanedione, 2-(2-nitro-4-(trifluoromethy...)
Affinity DataIC50:  40nMAssay Description:Inhibition of Wistar rat liver HPPD using 4-Hydroxyphenylpyruvate as substrate assessed as reduction in oxygen consumption preincubated for 3 mins fo...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Arabidopsis thaliana)
Universit£

Curated by ChEMBL
LigandPNGBDBM50056923((+)-usnic acid | (9bR)-2,6-diacetyl-3,7,9-trihydro...)
Affinity DataIC50:  70nMAssay Description:Inhibition of Arabidopsis thaliana HPPD expressed in Escherichia coli JM105 using HPPA as substrate after preincubated for 15 min followed by substra...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Universit£

Curated by ChEMBL
LigandPNGBDBM50403933(CHEMBL72081)
Affinity DataIC50:  70nMAssay Description:Inhibition of pig liver HPPD using 4-hydroxyphenylpyruvic acid as substrate after 15 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Universit£

Curated by ChEMBL
LigandPNGBDBM50403932(CHEMBL308315)
Affinity DataIC50:  110nMAssay Description:Inhibition of pig liver HPPD using 4-hydroxyphenylpyruvic acid as substrate after 15 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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