Compile Data Set for Download or QSAR
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Report error Found 36 Enz. Inhib. hit(s) with all data for entry = 50047448
TargetProteasome subunit beta type-5(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50069985((S)-4-methyl-2-(3-phenyl-propionylamino)-pentanoic...)
Affinity DataIC50:  37nMAssay Description:Inhibition of chymotrypsin-like activity of 20S human proteasome assessed as Suc-LLVY-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedPDB3D3D Structure (crystal)

TargetProteasome subunit beta type-1(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50069985((S)-4-methyl-2-(3-phenyl-propionylamino)-pentanoic...)
Affinity DataIC50:  44nMAssay Description:Inhibition of caspase-like activity of 20S human proteasome assessed as Z-nLPnLD-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedPDB3D3D Structure (crystal)

TargetProteasome subunit beta type-2(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50069985((S)-4-methyl-2-(3-phenyl-propionylamino)-pentanoic...)
Affinity DataIC50:  52nMAssay Description:Inhibition of trypsin-like activity of 20S human proteasome assessed as Z-LRR-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated fo...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedPDB3D3D Structure (crystal)

TargetProteasome subunit beta type-5(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168037(CHEMBL3798365)
Affinity DataIC50:  9.88E+3nMAssay Description:Inhibition of chymotrypsin-like activity of 20S human proteasome assessed as Suc-LLVY-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-5(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168039(CHEMBL3798569)
Affinity DataIC50:  1.03E+4nMAssay Description:Inhibition of chymotrypsin-like activity of 20S human proteasome assessed as Suc-LLVY-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-5(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168055(CHEMBL3797781)
Affinity DataIC50:  1.19E+4nMAssay Description:Inhibition of chymotrypsin-like activity of 20S human proteasome assessed as Suc-LLVY-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-5(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168049(CHEMBL3798873)
Affinity DataIC50:  1.33E+4nMAssay Description:Inhibition of chymotrypsin-like activity of 20S human proteasome assessed as Suc-LLVY-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-5(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168048(CHEMBL3800382)
Affinity DataIC50:  1.38E+4nMAssay Description:Inhibition of chymotrypsin-like activity of 20S human proteasome assessed as Suc-LLVY-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-5(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168040(CHEMBL3799001)
Affinity DataIC50:  1.42E+4nMAssay Description:Inhibition of chymotrypsin-like activity of 20S human proteasome assessed as Suc-LLVY-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-5(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168054(CHEMBL3798107)
Affinity DataIC50:  1.61E+4nMAssay Description:Inhibition of chymotrypsin-like activity of 20S human proteasome assessed as Suc-LLVY-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-5(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168038(CHEMBL3799308)
Affinity DataIC50:  1.76E+4nMAssay Description:Inhibition of chymotrypsin-like activity of 20S human proteasome assessed as Suc-LLVY-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-5(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168053(CHEMBL3800196)
Affinity DataIC50:  2.15E+4nMAssay Description:Inhibition of chymotrypsin-like activity of 20S human proteasome assessed as Suc-LLVY-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-5(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168051(CHEMBL3800475)
Affinity DataIC50:  2.31E+4nMAssay Description:Inhibition of chymotrypsin-like activity of 20S human proteasome assessed as Suc-LLVY-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-5(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168050(CHEMBL3799436)
Affinity DataIC50:  2.61E+4nMAssay Description:Inhibition of chymotrypsin-like activity of 20S human proteasome assessed as Suc-LLVY-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-1(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168039(CHEMBL3798569)
Affinity DataIC50:  3.03E+4nMAssay Description:Inhibition of caspase-like activity of 20S human proteasome assessed as Z-nLPnLD-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-1(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168054(CHEMBL3798107)
Affinity DataIC50:  5.04E+4nMAssay Description:Inhibition of caspase-like activity of 20S human proteasome assessed as Z-nLPnLD-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-1(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168038(CHEMBL3799308)
Affinity DataIC50:  7.05E+4nMAssay Description:Inhibition of caspase-like activity of 20S human proteasome assessed as Z-nLPnLD-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-1(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168055(CHEMBL3797781)
Affinity DataIC50:  7.44E+4nMAssay Description:Inhibition of caspase-like activity of 20S human proteasome assessed as Z-nLPnLD-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-1(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168050(CHEMBL3799436)
Affinity DataIC50:  8.02E+4nMAssay Description:Inhibition of caspase-like activity of 20S human proteasome assessed as Z-nLPnLD-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-1(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168048(CHEMBL3800382)
Affinity DataIC50:  8.22E+4nMAssay Description:Inhibition of caspase-like activity of 20S human proteasome assessed as Z-nLPnLD-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-1(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168037(CHEMBL3798365)
Affinity DataIC50:  1.03E+5nMAssay Description:Inhibition of caspase-like activity of 20S human proteasome assessed as Z-nLPnLD-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-1(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168049(CHEMBL3798873)
Affinity DataIC50:  1.25E+5nMAssay Description:Inhibition of caspase-like activity of 20S human proteasome assessed as Z-nLPnLD-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-1(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168053(CHEMBL3800196)
Affinity DataIC50:  1.25E+5nMAssay Description:Inhibition of caspase-like activity of 20S human proteasome assessed as Z-nLPnLD-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-2(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168055(CHEMBL3797781)
Affinity DataIC50:  1.26E+5nMAssay Description:Inhibition of trypsin-like activity of 20S human proteasome assessed as Z-LRR-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated fo...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-1(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168040(CHEMBL3799001)
Affinity DataIC50:  1.31E+5nMAssay Description:Inhibition of caspase-like activity of 20S human proteasome assessed as Z-nLPnLD-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-1(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168051(CHEMBL3800475)
Affinity DataIC50:  1.33E+5nMAssay Description:Inhibition of caspase-like activity of 20S human proteasome assessed as Z-nLPnLD-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-2(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168039(CHEMBL3798569)
Affinity DataIC50:  1.52E+5nMAssay Description:Inhibition of trypsin-like activity of 20S human proteasome assessed as Z-LRR-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated fo...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-2(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168049(CHEMBL3798873)
Affinity DataIC50:  1.56E+5nMAssay Description:Inhibition of trypsin-like activity of 20S human proteasome assessed as Z-LRR-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated fo...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-2(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168037(CHEMBL3798365)
Affinity DataIC50:  2.20E+5nMAssay Description:Inhibition of trypsin-like activity of 20S human proteasome assessed as Z-LRR-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated fo...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-2(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168050(CHEMBL3799436)
Affinity DataIC50:  2.76E+5nMAssay Description:Inhibition of trypsin-like activity of 20S human proteasome assessed as Z-LRR-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated fo...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-2(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168040(CHEMBL3799001)
Affinity DataIC50:  3.90E+5nMAssay Description:Inhibition of trypsin-like activity of 20S human proteasome assessed as Z-LRR-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated fo...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-2(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168053(CHEMBL3800196)
Affinity DataIC50:  4.75E+5nMAssay Description:Inhibition of trypsin-like activity of 20S human proteasome assessed as Z-LRR-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated fo...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-2(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168038(CHEMBL3799308)
Affinity DataIC50:  5.58E+5nMAssay Description:Inhibition of trypsin-like activity of 20S human proteasome assessed as Z-LRR-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated fo...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-2(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168051(CHEMBL3800475)
Affinity DataIC50:  5.89E+5nMAssay Description:Inhibition of trypsin-like activity of 20S human proteasome assessed as Z-LRR-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated fo...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-2(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168054(CHEMBL3798107)
Affinity DataIC50:  6.43E+5nMAssay Description:Inhibition of trypsin-like activity of 20S human proteasome assessed as Z-LRR-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated fo...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProteasome subunit beta type-2(Human)
Peking University Health Science Center

Curated by ChEMBL
LigandPNGBDBM50168048(CHEMBL3800382)
Affinity DataIC50:  7.30E+5nMAssay Description:Inhibition of trypsin-like activity of 20S human proteasome assessed as Z-LRR-AMC hydrolysis at using Promega proteasome-Glo-3 substrate incubated fo...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed