Compile Data Set for Download or QSAR
Report error Found 65 Enz. Inhib. hit(s) with all data for entry = 50044165
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007199(CHEMBL3237863)
Affinity DataIC50: 2.70nMAssay Description:Inhibition of chymotrypsin-like activity of human 20S proteasome using Suc-LLVY-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007198(CHEMBL3237862)
Affinity DataIC50: 3.90nMAssay Description:Inhibition of chymotrypsin-like activity of human 20S proteasome using Suc-LLVY-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007196(CHEMBL3237864)
Affinity DataIC50: 4.10nMAssay Description:Inhibition of chymotrypsin-like activity of human 20S proteasome using Suc-LLVY-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007206(CHEMBL3237867)
Affinity DataIC50: 4.10nMAssay Description:Inhibition of chymotrypsin-like activity of human 20S proteasome using Suc-LLVY-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007200(CHEMBL3237873)
Affinity DataIC50: 4.80nMAssay Description:Inhibition of chymotrypsin-like activity of human 20S proteasome using Suc-LLVY-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007193(CHEMBL3237865)
Affinity DataIC50: 5.10nMAssay Description:Inhibition of chymotrypsin-like activity of human 20S proteasome using Suc-LLVY-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007207(CHEMBL3237860)
Affinity DataIC50: 5.70nMAssay Description:Inhibition of chymotrypsin-like activity of human 20S proteasome using Suc-LLVY-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007195(CHEMBL3237866)
Affinity DataIC50: 5.70nMAssay Description:Inhibition of chymotrypsin-like activity of human 20S proteasome using Suc-LLVY-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007202(CHEMBL3237868)
Affinity DataIC50: 5.90nMAssay Description:Inhibition of chymotrypsin-like activity of human 20S proteasome using Suc-LLVY-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50069989(CHEMBL325041 | (R)-3-methyl-1-((S)-3-phenyl-2-(pyr...)
Affinity DataIC50: 7nMAssay Description:Inhibition of chymotrypsin-like activity of human 20S proteasome using Suc-LLVY-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007201(CHEMBL3237870)
Affinity DataIC50: 7.10nMAssay Description:Inhibition of chymotrypsin-like activity of human 20S proteasome using Suc-LLVY-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007205(CHEMBL3237871)
Affinity DataIC50: 7.5nMAssay Description:Inhibition of chymotrypsin-like activity of human 20S proteasome using Suc-LLVY-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007209(CHEMBL3237874)
Affinity DataIC50: 7.70nMAssay Description:Inhibition of chymotrypsin-like activity of human 20S proteasome using Suc-LLVY-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007197(CHEMBL3237869)
Affinity DataIC50: 7.80nMAssay Description:Inhibition of chymotrypsin-like activity of human 20S proteasome using Suc-LLVY-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007208(CHEMBL3237861)
Affinity DataIC50: 29nMAssay Description:Inhibition of chymotrypsin-like activity of human 20S proteasome using Suc-LLVY-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-8(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007199(CHEMBL3237863)
Affinity DataIC50: 31nMAssay Description:Inhibition of beta5i subunit of immunoproteasome (unknown origin) by active-site ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007206(CHEMBL3237867)
Affinity DataIC50: 46nMAssay Description:Inhibition of caspase-like activity of human 20S proteasome using Ac-nLPnLD-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007204(CHEMBL3237872)
Affinity DataIC50: 54nMAssay Description:Inhibition of chymotrypsin-like activity of human 20S proteasome using Suc-LLVY-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-8(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007200(CHEMBL3237873)
Affinity DataIC50: 59nMAssay Description:Inhibition of beta5i subunit of immunoproteasome (unknown origin) by active-site ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50007193(CHEMBL3237865)
Affinity DataIC50: 75nMAssay Description:Inhibition of caspase-like activity of human 20S proteasome using Ac-nLPnLD-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007195(CHEMBL3237866)
Affinity DataIC50: 76nMAssay Description:Inhibition of caspase-like activity of human 20S proteasome using Ac-nLPnLD-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-8(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50069989(CHEMBL325041 | (R)-3-methyl-1-((S)-3-phenyl-2-(pyr...)
Affinity DataIC50: 78nMAssay Description:Inhibition of beta5i subunit of immunoproteasome (unknown origin) by active-site ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007196(CHEMBL3237864)
Affinity DataIC50: 120nMAssay Description:Inhibition of caspase-like activity of human 20S proteasome using Ac-nLPnLD-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50069989(CHEMBL325041 | (R)-3-methyl-1-((S)-3-phenyl-2-(pyr...)
Affinity DataIC50: 120nMAssay Description:Inhibition of caspase-like activity of human 20S proteasome using Ac-nLPnLD-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007197(CHEMBL3237869)
Affinity DataIC50: 130nMAssay Description:Inhibition of caspase-like activity of human 20S proteasome using Ac-nLPnLD-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007198(CHEMBL3237862)
Affinity DataIC50: 140nMAssay Description:Inhibition of caspase-like activity of human 20S proteasome using Ac-nLPnLD-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-5(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007199(CHEMBL3237863)
Affinity DataIC50: 140nMAssay Description:Inhibition of beta5 subunit of immunoproteasome (unknown origin) by active-site ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-5(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50069989(CHEMBL325041 | (R)-3-methyl-1-((S)-3-phenyl-2-(pyr...)
Affinity DataIC50: 140nMAssay Description:Inhibition of beta5 subunit of immunoproteasome (unknown origin) by active-site ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007199(CHEMBL3237863)
Affinity DataIC50: 150nMAssay Description:Inhibition of caspase-like activity of human 20S proteasome using Ac-nLPnLD-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007200(CHEMBL3237873)
Affinity DataIC50: 170nMAssay Description:Inhibition of caspase-like activity of human 20S proteasome using Ac-nLPnLD-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007201(CHEMBL3237870)
Affinity DataIC50: 210nMAssay Description:Inhibition of caspase-like activity of human 20S proteasome using Ac-nLPnLD-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007202(CHEMBL3237868)
Affinity DataIC50: 250nMAssay Description:Inhibition of caspase-like activity of human 20S proteasome using Ac-nLPnLD-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-5(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007200(CHEMBL3237873)
Affinity DataIC50: 280nMAssay Description:Inhibition of beta5 subunit of immunoproteasome (unknown origin) by active-site ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-8(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007203(CHEMBL3237875)
Affinity DataIC50: 450nMAssay Description:Inhibition of beta5i subunit of immunoproteasome (unknown origin) by active-site ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007204(CHEMBL3237872)
Affinity DataIC50: 500nMAssay Description:Inhibition of caspase-like activity of human 20S proteasome using Ac-nLPnLD-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-5(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50432548(LACTACYSTIN)
Affinity DataIC50: 500nMAssay Description:Inhibition of beta5 subunit of immunoproteasome (unknown origin) by active-site ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-5(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007203(CHEMBL3237875)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of beta5 subunit of immunoproteasome (unknown origin) by active-site ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007205(CHEMBL3237871)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of caspase-like activity of human 20S proteasome using Ac-nLPnLD-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007198(CHEMBL3237862)
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of trypsin-like activity of human 20S proteasome using Ac-RLR-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50430990(BELACTOSIN A)
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibition of chymotrypsin-like activity of human 20S proteasome using Suc-LLVY-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50069989(CHEMBL325041 | (R)-3-methyl-1-((S)-3-phenyl-2-(pyr...)
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of trypsin-like activity of human 20S proteasome using Ac-RLR-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007200(CHEMBL3237873)
Affinity DataIC50: 2.17E+3nMAssay Description:Inhibition of trypsin-like activity of human 20S proteasome using Ac-RLR-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007193(CHEMBL3237865)
Affinity DataIC50: 2.40E+3nMAssay Description:Inhibition of trypsin-like activity of human 20S proteasome using Ac-RLR-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007195(CHEMBL3237866)
Affinity DataIC50: 2.50E+3nMAssay Description:Inhibition of trypsin-like activity of human 20S proteasome using Ac-RLR-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007199(CHEMBL3237863)
Affinity DataIC50: 2.70E+3nMAssay Description:Inhibition of trypsin-like activity of human 20S proteasome using Ac-RLR-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007197(CHEMBL3237869)
Affinity DataIC50: 2.70E+3nMAssay Description:Inhibition of trypsin-like activity of human 20S proteasome using Ac-RLR-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007196(CHEMBL3237864)
Affinity DataIC50: 2.70E+3nMAssay Description:Inhibition of trypsin-like activity of human 20S proteasome using Ac-RLR-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-8(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50432548(LACTACYSTIN)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of beta5i subunit of immunoproteasome (unknown origin) by active-site ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-7(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50007206(CHEMBL3237867)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of trypsin-like activity of human 20S proteasome using Ac-RLR-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin G(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50069989(CHEMBL325041 | (R)-3-methyl-1-((S)-3-phenyl-2-(pyr...)
Affinity DataIC50: 3.10E+3nMAssay Description:Inhibition of recombinant cathepsin G (unknown origin) using Suc-Ala-Ala-Pro-Phe-AMC as substrate by spectrofluorometer analysisMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
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