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Found 106 with Last Name = 'li' and Initial = 'zm'
TargetAcetolactate synthase, chloroplastic(Arabidopsis thaliana)
Nankai University

Curated by ChEMBL
LigandPNGBDBM50486243(MONOSULFURON ESTER)
Affinity DataKi:  260nMAssay Description:Inhibition of wild type Arabidopsis thaliana acetohydroxyacid synthase colorimetric assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Chinese Academy Of Medical Sciences And Peking Union Medical College

Curated by ChEMBL
LigandPNGBDBM50470518(CHEMBL4294523)
Affinity DataKi:  740nMAssay Description:Inhibition of Cy5-labeled double-strand DNA probe binding to STAT3 (unknown origin) expressed in H1299 cell lysates assessed as decrease in DNA bindi...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Chinese Academy Of Medical Sciences And Peking Union Medical College

Curated by ChEMBL
LigandPNGBDBM50470513(CHEMBL4290712)
Affinity DataKi:  1.01E+3nMAssay Description:Inhibition of Cy5-labeled double-strand DNA probe binding to STAT3 (unknown origin) expressed in H1299 cell lysates assessed as decrease in DNA bindi...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Chinese Academy Of Medical Sciences And Peking Union Medical College

Curated by ChEMBL
LigandPNGBDBM50470517(CHEMBL4294114)
Affinity DataKi:  1.18E+3nMAssay Description:Inhibition of Cy5-labeled double-strand DNA probe binding to STAT3 (unknown origin) expressed in H1299 cell lysates assessed as decrease in DNA bindi...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Chinese Academy Of Medical Sciences And Peking Union Medical College

Curated by ChEMBL
LigandPNGBDBM50470512(CHEMBL1416382)
Affinity DataKi:  1.40E+3nMAssay Description:Inhibition of Cy5-labeled double-strand DNA probe binding to STAT3 (unknown origin) expressed in H1299 cell lysates assessed as decrease in DNA bindi...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAcetolactate synthase, chloroplastic(Arabidopsis thaliana)
Nankai University

Curated by ChEMBL
LigandPNGBDBM50486242(CHEMBL2230130)
Affinity DataKi:  1.70E+3nMAssay Description:Inhibition of wild type Arabidopsis thaliana acetohydroxyacid synthase colorimetric assayMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Chinese Academy Of Medical Sciences And Peking Union Medical College

Curated by ChEMBL
LigandPNGBDBM50470515(CHEMBL4291509)
Affinity DataKi:  2.50E+3nMAssay Description:Inhibition of Cy5-labeled double-strand DNA probe binding to STAT3 (unknown origin) expressed in H1299 cell lysates assessed as decrease in DNA bindi...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetKetol-acid reductoisomerase (NADP(+))(Escherichia coli)
Nankai University

LigandPNGBDBM82145(N-hydroxy-N-isopropyloxamate, IpOHA)
Affinity DataKi:  2.75E+3nM ΔG°:  -32.3kJ/molepH: 8.0 T: 2°CAssay Description:Inhibition of E. coli KARI (ketol-acid reductoisomerase) is time dependent, and activity was measured by the decrease in A340 at 30 C in solutions co...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetolactate synthase, chloroplastic(Arabidopsis thaliana)
Nankai University

Curated by ChEMBL
LigandPNGBDBM50486241(CHEBI:5869 | IMAZAQUIN)
Affinity DataKi:  3.00E+3nMAssay Description:Inhibition of wild type Arabidopsis thaliana acetohydroxyacid synthase colorimetric assayMore data for this Ligand-Target Pair
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Chinese Academy Of Medical Sciences And Peking Union Medical College

Curated by ChEMBL
LigandPNGBDBM50470514(CHEMBL4283640)
Affinity DataKi:  3.92E+3nMAssay Description:Inhibition of Cy5-labeled double-strand DNA probe binding to STAT3 (unknown origin) expressed in H1299 cell lysates assessed as decrease in DNA bindi...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAcetolactate synthase, chloroplastic(Arabidopsis thaliana)
Nankai University

Curated by ChEMBL
LigandPNGBDBM50486245(CHEMBL2230131)
Affinity DataKi:  4.69E+3nMAssay Description:Inhibition of wild type Arabidopsis thaliana acetohydroxyacid synthase colorimetric assayMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetAcetolactate synthase, chloroplastic(Arabidopsis thaliana)
Nankai University

Curated by ChEMBL
LigandPNGBDBM50486244(CHEMBL2229985)
Affinity DataKi:  5.57E+3nMAssay Description:Inhibition of wild type Arabidopsis thaliana acetohydroxyacid synthase colorimetric assayMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetAcetolactate synthase, chloroplastic(Arabidopsis thaliana)
Nankai University

Curated by ChEMBL
LigandPNGBDBM50486243(MONOSULFURON ESTER)
Affinity DataKi:  8.53E+3nMAssay Description:Inhibition of Arabidopsis thaliana acetohydroxyacid synthase W574L mutant colorimetric assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Chinese Academy Of Medical Sciences And Peking Union Medical College

Curated by ChEMBL
LigandPNGBDBM50470516(CHEMBL4282824)
Affinity DataKi:  8.87E+3nMAssay Description:Inhibition of Cy5-labeled double-strand DNA probe binding to STAT3 (unknown origin) expressed in H1299 cell lysates assessed as decrease in DNA bindi...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAcetolactate synthase, chloroplastic(Arabidopsis thaliana)
Nankai University

Curated by ChEMBL
LigandPNGBDBM50486242(CHEMBL2230130)
Affinity DataKi:  2.45E+4nMAssay Description:Inhibition of Arabidopsis thaliana acetohydroxyacid synthase W574L mutant colorimetric assayMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetAcetolactate synthase, chloroplastic(Arabidopsis thaliana)
Nankai University

Curated by ChEMBL
LigandPNGBDBM50486245(CHEMBL2230131)
Affinity DataKi:  2.57E+4nMAssay Description:Inhibition of Arabidopsis thaliana acetohydroxyacid synthase W574L mutant colorimetric assayMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetAcetolactate synthase, chloroplastic(Arabidopsis thaliana)
Nankai University

Curated by ChEMBL
LigandPNGBDBM50486244(CHEMBL2229985)
Affinity DataKi:  2.71E+4nMAssay Description:Inhibition of Arabidopsis thaliana acetohydroxyacid synthase W574L mutant colorimetric assayMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetKetol-acid reductoisomerase (NADP(+))(Escherichia coli)
Nankai University

LigandPNGBDBM82144(Cyclopropane, 5)
Affinity DataKi:  3.12E+4nM ΔG°:  -26.2kJ/molepH: 8.0 T: 2°CAssay Description:Inhibition of E. coli KARI (ketol-acid reductoisomerase) is time dependent, and activity was measured by the decrease in A340 at 30 C in solutions co...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKetol-acid reductoisomerase (NADP(+))(Escherichia coli)
Nankai University

LigandPNGBDBM82142(Cyclopropane, 3)
Affinity DataKi:  7.66E+4nM ΔG°:  -23.9kJ/molepH: 8.0 T: 2°CAssay Description:Inhibition of E. coli KARI (ketol-acid reductoisomerase) is time dependent, and activity was measured by the decrease in A340 at 30 C in solutions co...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKetol-acid reductoisomerase (NADP(+))(Escherichia coli)
Nankai University

LigandPNGBDBM82143(Cyclopropane, 4)
Affinity DataKi:  9.53E+4nM ΔG°:  -23.3kJ/molepH: 8.0 T: 2°CAssay Description:Inhibition of E. coli KARI (ketol-acid reductoisomerase) is time dependent, and activity was measured by the decrease in A340 at 30 C in solutions co...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetolactate synthase, chloroplastic(Arabidopsis thaliana)
Nankai University

Curated by ChEMBL
LigandPNGBDBM50486241(CHEBI:5869 | IMAZAQUIN)
Affinity DataKi:  4.70E+5nMAssay Description:Inhibition of Arabidopsis thaliana acetohydroxyacid synthase W574L mutant colorimetric assayMore data for this Ligand-Target Pair
TargetProteasome subunit beta type-5(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50259656(CHEMBL4089402)
Affinity DataIC50:  0.000200nMAssay Description:Dissociation constant against galectin-3 using competitive fluorescence polarizationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProteasome subunit beta type-5(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50259645(CHEMBL4070336)
Affinity DataIC50:  0.300nMAssay Description:Inhibition of chymotrypsin-like activity of 20S proteasome in human HL60 cells using Suc-LLVYaminoluciferin as substrate after 2 hrs by fluorescence ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProteasome subunit beta type-5(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50259647(CHEMBL4100727)
Affinity DataIC50:  2nMAssay Description:Inhibition of chymotrypsin-like activity of 20S proteasome in human HL60 cells using Suc-LLVYaminoluciferin as substrate after 2 hrs by fluorescence ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProteasome subunit beta type-5(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50259657(CHEMBL4068221)
Affinity DataIC50:  2nMAssay Description:Dissociation constant against galectin-3 using competitive fluorescence polarizationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProteasome subunit beta type-5(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50259659(CHEMBL4076838)
Affinity DataIC50:  3nMAssay Description:Dissociation constant against galectin-3 using competitive fluorescence polarizationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProteasome subunit beta type-5(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50069989((R)-3-methyl-1-((S)-3-phenyl-2-(pyrazine-2-carboxa...)
Affinity DataIC50:  4nMAssay Description:Inhibition of chymotrypsin-like activity of 20S proteasome in human HL60 cells using Suc-LLVYaminoluciferin as substrate after 2 hrs by fluorescence ...More data for this Ligand-Target Pair
TargetProteasome subunit beta type-5(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50259642(CHEMBL4077037)
Affinity DataIC50:  4nMAssay Description:Inhibition of chymotrypsin-like activity of 20S proteasome in human HL60 cells using Suc-LLVYaminoluciferin as substrate after 2 hrs by fluorescence ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetE3 ubiquitin-protein ligase Mdm2(Homo sapiens (Human))
Roche Pharma Research

Curated by ChEMBL
LigandPNGBDBM50446191(CHEMBL3109036)
Affinity DataIC50:  5nMAssay Description:Binding affinity to GST-tagged MDM2 (unknown origin) assessed as inhibition of interaction with biotinylated p53 after 1 hr by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetE3 ubiquitin-protein ligase Mdm2(Homo sapiens (Human))
Roche Pharma Research

Curated by ChEMBL
LigandPNGBDBM50437206(CHEMBL2402737)
Affinity DataIC50:  6nMAssay Description:Binding affinity to GST-tagged MDM2 (unknown origin) assessed as inhibition of interaction with p53 after 1 hr by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetE3 ubiquitin-protein ligase Mdm2(Homo sapiens (Human))
Roche Pharma Research

Curated by ChEMBL
LigandPNGBDBM50446197(CHEMBL3109042)
Affinity DataIC50:  6nMAssay Description:Binding affinity to GST-tagged MDM2 (unknown origin) assessed as inhibition of interaction with biotinylated p53 after 1 hr by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetE3 ubiquitin-protein ligase Mdm2(Homo sapiens (Human))
Roche Pharma Research

Curated by ChEMBL
LigandPNGBDBM50446195(CHEMBL3109040)
Affinity DataIC50:  7nMAssay Description:Binding affinity to GST-tagged MDM2 (unknown origin) assessed as inhibition of interaction with biotinylated p53 after 1 hr by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetE3 ubiquitin-protein ligase Mdm2(Homo sapiens (Human))
Roche Pharma Research

Curated by ChEMBL
LigandPNGBDBM50446196(CHEMBL3109041)
Affinity DataIC50:  7nMAssay Description:Binding affinity to GST-tagged MDM2 (unknown origin) assessed as inhibition of interaction with biotinylated p53 after 1 hr by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProteasome subunit beta type-5(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50259655(CHEMBL4080306)
Affinity DataIC50:  10nMAssay Description:Dissociation constant against galectin-3 using competitive fluorescence polarizationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProteasome subunit beta type-5(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50259641(CHEMBL484701)
Affinity DataIC50:  10nMAssay Description:Inhibition of chymotrypsin-like activity of 20S proteasome in human HL60 cells using Suc-LLVYaminoluciferin as substrate after 2 hrs by fluorescence ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetE3 ubiquitin-protein ligase Mdm2(Homo sapiens (Human))
Roche Pharma Research

Curated by ChEMBL
LigandPNGBDBM50446204(CHEMBL3109055)
Affinity DataIC50:  11nMAssay Description:Binding affinity to GST-tagged MDM2 (unknown origin) assessed as inhibition of interaction with biotinylated p53 after 1 hr by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProteasome subunit beta type-5(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50259646(CHEMBL4075225)
Affinity DataIC50:  12nMAssay Description:Inhibition of chymotrypsin-like activity of 20S proteasome in human HL60 cells using Suc-LLVYaminoluciferin as substrate after 2 hrs by fluorescence ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetE3 ubiquitin-protein ligase Mdm2(Homo sapiens (Human))
Roche Pharma Research

Curated by ChEMBL
LigandPNGBDBM50446207(CHEMBL3109051)
Affinity DataIC50:  17nMAssay Description:Binding affinity to GST-tagged MDM2 (unknown origin) assessed as inhibition of interaction with biotinylated p53 after 1 hr by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetE3 ubiquitin-protein ligase Mdm2(Homo sapiens (Human))
Roche Pharma Research

Curated by ChEMBL
LigandPNGBDBM50446205(CHEMBL3109049)
Affinity DataIC50:  18nMAssay Description:Binding affinity to GST-tagged MDM2 (unknown origin) assessed as inhibition of interaction with biotinylated p53 after 1 hr by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetE3 ubiquitin-protein ligase Mdm2(Homo sapiens (Human))
Roche Pharma Research

Curated by ChEMBL
LigandPNGBDBM50434287(CHEMBL2386346)
Affinity DataIC50:  18nMAssay Description:Binding affinity to GST-tagged MDM2 (unknown origin) assessed as inhibition of interaction with p53 after 1 hr by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProteasome subunit beta type-5(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50259649(CHEMBL4077282)
Affinity DataIC50:  20nMAssay Description:Dissociation constant against galectin-3 using competitive fluorescence polarizationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetE3 ubiquitin-protein ligase Mdm2(Homo sapiens (Human))
Roche Pharma Research

Curated by ChEMBL
LigandPNGBDBM50437209(CHEMBL2402734)
Affinity DataIC50:  20nMAssay Description:Binding affinity to GST-tagged MDM2 (unknown origin) assessed as inhibition of interaction with p53 after 1 hr by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProteasome subunit beta type-1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50259656(CHEMBL4089402)
Affinity DataIC50:  20nMAssay Description:Inhibition of caspase-like activity of 20S proteasome in human HL60 cells using Z-nLPnLDaminoluciferin as substrate after 2 hrs by fluorescence analy...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProteasome subunit beta type-5(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50259658(CHEMBL4096371)
Affinity DataIC50:  20nMAssay Description:Dissociation constant against galectin-3 using competitive fluorescence polarizationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetE3 ubiquitin-protein ligase Mdm2(Homo sapiens (Human))
Roche Pharma Research

Curated by ChEMBL
LigandPNGBDBM50437208(CHEMBL2402735)
Affinity DataIC50:  21nMAssay Description:Binding affinity to GST-tagged MDM2 (unknown origin) assessed as inhibition of interaction with p53 after 1 hr by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetE3 ubiquitin-protein ligase Mdm2(Homo sapiens (Human))
Roche Pharma Research

Curated by ChEMBL
LigandPNGBDBM50437210(CHEMBL2402733)
Affinity DataIC50:  22nMAssay Description:Binding affinity to GST-tagged MDM2 (unknown origin) assessed as inhibition of interaction with p53 after 1 hr by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetE3 ubiquitin-protein ligase Mdm2(Homo sapiens (Human))
Roche Pharma Research

Curated by ChEMBL
LigandPNGBDBM50437212(CHEMBL2402731)
Affinity DataIC50:  22nMAssay Description:Binding affinity to GST-tagged MDM2 (unknown origin) assessed as inhibition of interaction with p53 after 1 hr by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetE3 ubiquitin-protein ligase Mdm2(Homo sapiens (Human))
Roche Pharma Research

Curated by ChEMBL
LigandPNGBDBM50437211(CHEMBL2402732)
Affinity DataIC50:  23nMAssay Description:Binding affinity to GST-tagged MDM2 (unknown origin) assessed as inhibition of interaction with p53 after 1 hr by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetE3 ubiquitin-protein ligase Mdm2(Homo sapiens (Human))
Roche Pharma Research

Curated by ChEMBL
LigandPNGBDBM50446201(CHEMBL3109046)
Affinity DataIC50:  25nMAssay Description:Binding affinity to GST-tagged MDM2 (unknown origin) assessed as inhibition of interaction with biotinylated p53 after 1 hr by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetE3 ubiquitin-protein ligase Mdm2(Homo sapiens (Human))
Roche Pharma Research

Curated by ChEMBL
LigandPNGBDBM50437207(CHEMBL2402736)
Affinity DataIC50:  25nMAssay Description:Binding affinity to GST-tagged MDM2 (unknown origin) assessed as inhibition of interaction with p53 after 1 hr by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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