Compile Data Set for Download or QSAR
Report error Found 54 of ki data for polymerid = 50003459
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50069985BDBM50069985({1-[(S)-(S)-1-((S)-1-Formyl-3-methyl-butylcarbamoy...)
Affinity DataKi:  1nMAssay Description:Inhibition of 20S immuno proteosome beta2i subunit (unknown origin) assessed as substrate hydrolysis using Z-Leu-Leu-Leu-al as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMedPDB3D3D Structure (crystal)
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50069985BDBM50069985({1-[(S)-(S)-1-((S)-1-Formyl-3-methyl-butylcarbamoy...)
Affinity DataKi:  1nMAssay Description:Inhibition of 20s immunoproteasome beta2 trypsin-like activity in human spleen using Boc-Leu-Arg-Arg-AMC as substrate after 10 mins by fluorescence a...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/15/2020
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50644998BDBM50644998(CHEMBL5571110)
Affinity DataKi:  2.40nMAssay Description:Inhibition of 20S proteasome beta-2 in human erythrocytes using Boc-LRR-AMC as substrate by AK-740 assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50645001BDBM50645001(CHEMBL5573136)
Affinity DataKi:  36nMAssay Description:Inhibition of 20S proteasome beta-2 in human erythrocytes using Boc-LRR-AMC as substrate by AK-740 assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50644999BDBM50644999(CHEMBL5571666)
Affinity DataKi:  78nMAssay Description:Inhibition of 20S proteasome beta-2 in human erythrocytes using Boc-LRR-AMC as substrate by AK-740 assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50645000BDBM50645000(CHEMBL5576028)
Affinity DataKi:  136nMAssay Description:Inhibition of 20S proteasome beta-2 in human erythrocytes using Boc-LRR-AMC as substrate by AK-740 assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50644996BDBM50644996(CHEMBL5591317)
Affinity DataKi:  175nMAssay Description:Inhibition of 20S proteasome beta-2 in human erythrocytes using Boc-LRR-AMC as substrate by AK-740 assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50644993BDBM50644993(CHEMBL5563704)
Affinity DataKi:  226nMAssay Description:Inhibition of 20S proteasome beta-2 in human erythrocytes using Boc-LRR-AMC as substrate by AK-740 assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50069985BDBM50069985({1-[(S)-(S)-1-((S)-1-Formyl-3-methyl-butylcarbamoy...)
Affinity DataKi:  330nMAssay Description:Inhibition of trypsin-like proteasome activity of human 20S proteasomeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50550643BDBM50550643(CHEMBL4749207)
Affinity DataKi:  487nMAssay Description:Binding affinity to human 20S constitutive proteasome beta 2 subunit assessed as equilibrium constant using fluorogenic peptide Ac-WLR-AMC as substra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50644992BDBM50644992(CHEMBL5572583)
Affinity DataKi:  583nMAssay Description:Inhibition of 20S proteasome beta-2 in human erythrocytes using Boc-LRR-AMC as substrate by AK-740 assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50644987BDBM50644987(CHEMBL5571946)
Affinity DataKi:  688nMAssay Description:Inhibition of 20S proteasome beta-2 in human erythrocytes using Boc-LRR-AMC as substrate by AK-740 assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50644997BDBM50644997(CHEMBL5571783)
Affinity DataKi:  723nMAssay Description:Inhibition of 20S proteasome beta-2 in human erythrocytes using Boc-LRR-AMC as substrate by AK-740 assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50069989BDBM50069989(CHEMBL325041 | (R)-3-methyl-1-((S)-3-phenyl-2-(pyr...)
Affinity DataKi: >1.00E+3nMAssay Description:Inhibition of 20S proteasome beta-2 in human erythrocytes using Boc-LRR-AMC as substrate by AK-740 assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50410909BDBM50410909(CHEMBL207591 | PSI)
Affinity DataKi:  2.70E+3nMAssay Description:Inhibition of trypsin-like proteasome activity of human 20S proteasomeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50599554BDBM50599554(CHEMBL5172870)
Affinity DataKi:  3.00E+3nMAssay Description:Inhibition of 20S immuno proteosome beta2i subunit (unknown origin) assessed as substrate hydrolysis using Boc-Leu-Arg-Arg-AMC as fluorogenic substra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50599553BDBM50599553(CHEMBL5198329)
Affinity DataKi:  4.00E+3nMAssay Description:Inhibition of 20S immuno proteosome beta2i subunit (unknown origin) assessed as substrate hydrolysis using Boc-Leu-Arg-Arg-AMC as fluorogenic substra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50599556BDBM50599556(CHEMBL5182479)
Affinity DataKi:  4.00E+3nMAssay Description:Inhibition of 20S constitutive proteosome beta2c subunit (unknown origin) assessed as substrate hydrolysis using Boc-Leu-Arg-Arg-AMC as fluorogenic s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50453651BDBM50453651(CHEMBL4205881)
Affinity DataKi:  4.38E+3nMAssay Description:Inhibition of 20s immunoproteasome beta2 trypsin-like activity in human spleen using Boc-Leu-Arg-Arg-AMC as substrate after 10 mins by fluorescence a...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/15/2020
Entry Details Article
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50599554BDBM50599554(CHEMBL5172870)
Affinity DataKi:  5.00E+3nMAssay Description:Inhibition of 20S constitutive proteosome beta2c subunit (unknown origin) assessed as substrate hydrolysis using Boc-Leu-Arg-Arg-AMC as fluorogenic s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50069985BDBM50069985({1-[(S)-(S)-1-((S)-1-Formyl-3-methyl-butylcarbamoy...)
Affinity DataKi:  5.52E+3nMAssay Description:Inhibition of 20s constitutive proteasome beta2 trypsin-like activity in human erythrocytes using Boc-Leu-Arg-Arg-AMC as substrate after 10 mins by f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/15/2020
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50069985BDBM50069985({1-[(S)-(S)-1-((S)-1-Formyl-3-methyl-butylcarbamoy...)
Affinity DataKi:  5.52E+3nMAssay Description:Inhibition of 20S constitutive proteosome beta2c subunit (unknown origin) assessed as substrate hydrolysis using Z-Leu-Leu-Leu-al as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMedPDB3D3D Structure (crystal)
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50453650BDBM50453650(CHEMBL4213821)
Affinity DataKi:  5.57E+3nMAssay Description:Inhibition of 20s immunoproteasome beta2 trypsin-like activity in human spleen using Boc-Leu-Arg-Arg-AMC as substrate after 10 mins by fluorescence a...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/15/2020
Entry Details Article
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50126171BDBM50126171(CHEBI:80033 | CHEMBL1236043)
Affinity DataKi:  6.70E+3nMAssay Description:Inhibition of 20S proteasome beta-2 (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50453683BDBM50453683(CHEMBL4208777)
Affinity DataKi:  6.71E+3nMAssay Description:Inhibition of 20s immunoproteasome beta2 trypsin-like activity in human spleen using Boc-Leu-Arg-Arg-AMC as substrate after 10 mins by fluorescence a...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/15/2020
Entry Details Article
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50599552BDBM50599552(CHEMBL5195299)
Affinity DataKi:  9.00E+3nMAssay Description:Inhibition of 20S constitutive proteosome beta2c subunit (unknown origin) assessed as substrate hydrolysis using Boc-Leu-Arg-Arg-AMC as fluorogenic s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50644995BDBM50644995(CHEMBL5564813)
Affinity DataKi: >1.00E+4nMAssay Description:Inhibition of 20S proteasome beta-2 in human erythrocytes using Boc-LRR-AMC as substrate by AK-740 assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50645002BDBM50645002(CHEMBL5570955)
Affinity DataKi: >1.00E+4nMAssay Description:Inhibition of 20S proteasome beta-2 in human erythrocytes using Boc-LRR-AMC as substrate by AK-740 assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50644990BDBM50644990(CHEMBL5569145)
Affinity DataKi: >1.00E+4nMAssay Description:Inhibition of 20S proteasome beta-2 in human erythrocytes using Boc-LRR-AMC as substrate by AK-740 assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50599553BDBM50599553(CHEMBL5198329)
Affinity DataKi:  1.00E+4nMAssay Description:Inhibition of 20S constitutive proteosome beta2c subunit (unknown origin) assessed as substrate hydrolysis using Boc-Leu-Arg-Arg-AMC as fluorogenic s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50644989BDBM50644989(CHEMBL5571582)
Affinity DataKi: >1.00E+4nMAssay Description:Inhibition of 20S proteasome beta-2 in human erythrocytes using Boc-LRR-AMC as substrate by AK-740 assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50645004BDBM50645004(CHEMBL5574191)
Affinity DataKi: >1.00E+4nMAssay Description:Inhibition of 20S proteasome beta-2 in human erythrocytes using Boc-LRR-AMC as substrate by AK-740 assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50644988BDBM50644988(CHEMBL5569360)
Affinity DataKi: >1.00E+4nMAssay Description:Inhibition of 20S proteasome beta-2 in human erythrocytes using Boc-LRR-AMC as substrate by AK-740 assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50645003BDBM50645003(CHEMBL5567035)
Affinity DataKi: >1.00E+4nMAssay Description:Inhibition of 20S proteasome beta-2 in human erythrocytes using Boc-LRR-AMC as substrate by AK-740 assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50599555BDBM50599555(CHEMBL5192242)
Affinity DataKi:  1.00E+4nMAssay Description:Inhibition of 20S constitutive proteosome beta2c subunit (unknown origin) assessed as substrate hydrolysis using Boc-Leu-Arg-Arg-AMC as fluorogenic s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50644994BDBM50644994(CHEMBL5590795)
Affinity DataKi: >1.00E+4nMAssay Description:Inhibition of 20S proteasome beta-2 in human erythrocytes using Boc-LRR-AMC as substrate by AK-740 assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50644991BDBM50644991(CHEMBL5575929)
Affinity DataKi: >1.00E+4nMAssay Description:Inhibition of 20S proteasome beta-2 in human erythrocytes using Boc-LRR-AMC as substrate by AK-740 assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50599551BDBM50599551(CHEMBL5207762)
Affinity DataKi:  1.20E+4nMAssay Description:Inhibition of 20S immuno proteosome beta2i subunit (unknown origin) assessed as substrate hydrolysis using Boc-Leu-Arg-Arg-AMC as fluorogenic substra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50599551BDBM50599551(CHEMBL5207762)
Affinity DataKi:  1.50E+4nMAssay Description:Inhibition of 20S constitutive proteosome beta2c subunit (unknown origin) assessed as substrate hydrolysis using Boc-Leu-Arg-Arg-AMC as fluorogenic s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50453651BDBM50453651(CHEMBL4205881)
Affinity DataKi:  2.00E+4nMAssay Description:Inhibition of 20s constitutive proteasome beta2 trypsin-like activity in human erythrocytes using Boc-Leu-Arg-Arg-AMC as substrate after 10 mins by f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/15/2020
Entry Details Article
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50599556BDBM50599556(CHEMBL5182479)
Affinity DataKi:  2.00E+4nMAssay Description:Inhibition of 20S immuno proteosome beta2i subunit (unknown origin) assessed as substrate hydrolysis using Boc-Leu-Arg-Arg-AMC as fluorogenic substra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50069985BDBM50069985({1-[(S)-(S)-1-((S)-1-Formyl-3-methyl-butylcarbamoy...)
Affinity DataKi:  2.21E+4nMAssay Description:Competitive inhibition of trypsin-like activity of human 20S proteasome using Boc-Leu-Arg-Arg-AMC as substrate measured for 10 mins by fluorescence a...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/10/2018
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50599555BDBM50599555(CHEMBL5192242)
Affinity DataKi:  4.20E+4nMAssay Description:Inhibition of 20S immuno proteosome beta2i subunit (unknown origin) assessed as substrate hydrolysis using Boc-Leu-Arg-Arg-AMC as fluorogenic substra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50599557BDBM50599557(CHEMBL5196430)
Affinity DataKi:  4.20E+4nMAssay Description:Inhibition of 20S immuno proteosome beta2i subunit (unknown origin) assessed as substrate hydrolysis using Boc-Leu-Arg-Arg-AMC as fluorogenic substra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50410900BDBM50410900(CHEMBL207425)
Affinity DataKi:  5.10E+4nMAssay Description:Inhibition of trypsin-like proteasome activity of human 20S proteasomeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50644986BDBM50644986(CHEMBL1236118)
Affinity DataKi:  1.08E+5nMAssay Description:Inhibition of 20S proteasome beta-2 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50069984BDBM50069984((R)-1-((S)-2-((S)-2-(benzyloxycarbonyl)-4-methylpe...)
Affinity DataKi:  1.10E+5nMAssay Description:Inhibition of trypsin-like proteasome activity of human 20S proteasomeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50410898BDBM50410898(CHEMBL205757)
Affinity DataKi:  2.90E+5nMAssay Description:Inhibition of trypsin-like proteasome activity of human 20S proteasomeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50410899BDBM50410899(CHEMBL383674)
Affinity DataKi: >3.00E+5nMAssay Description:Inhibition of trypsin-like proteasome activity of human 20S proteasomeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProteasome subunit beta type-2(Human)
University of Messina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50410903BDBM50410903(CHEMBL207598)
Affinity DataKi: >3.00E+5nMAssay Description:Inhibition of trypsin-like proteasome activity of human 20S proteasomeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
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