null
SMILES [#6]-[#6]\[#6](=[#6](\c1ccc(-[#8]-[#6]-[#6]-[#7]-2-[#6]-[#6]-[#6]-[#6]-[#6]-[#6]-2)cc1)-c1ccc(-[#8]-[#6]-[#6]-[#7]-2-[#6]-[#6]-[#6]-[#6]-[#6]-[#6]-2)cc1)-c1cccc(c1)-[#6](=O)-[#7]-[#6]-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]-[#7]-[#6](-[#7])=[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]-[#7]-[#6](-[#7])=[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]-[#7]-[#6](-[#7])=[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]-[#7]-[#6](-[#7])=[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]-[#7]-[#6](-[#7])=[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]-[#7]-[#6](-[#7])=[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]-[#7]-[#6](-[#7])=[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]-[#7]-[#6](-[#7])=[#7])-[#6](=O)-[#7]-[#6](-[#6])=O
InChI Key InChIKey=RYABNVMEDVLJEH-BOVVMFHJSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 12 hits for monomerid = 50458010
TargetProteasome subunit beta type-1(Homo sapiens (Human))
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of PGPH activity of human 26S proteasome using Z-LLE-MCA as substrate measured for 1 hr by fluorescence assayMore data for this Ligand-Target Pair
TargetProteasome subunit beta type-1(Homo sapiens (Human))
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Affinity DataIC50: 3.10E+3nMAssay Description:Inhibition of PGPH-like activity of 26S proteasome in human RPMI8226 cells using Z-LLE-MCA as substrate after 24 to 48 hrs by luminescence-based assa...More data for this Ligand-Target Pair
TargetProteasome subunit beta type-2(Homo sapiens (Human))
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Affinity DataIC50: 3.50E+3nMAssay Description:Inhibition of trypsin-like activity of human 20S proteasome using Boc-LRR-MCA as substrate measured for 1 hr by fluorescence assayMore data for this Ligand-Target Pair
TargetProteasome subunit beta type-2(Homo sapiens (Human))
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of trypsin-like activity of human 26S proteasome using Boc-LRR-MCA as substrate measured for 1 hr by fluorescence assayMore data for this Ligand-Target Pair
TargetProteasome subunit beta type-5(Homo sapiens (Human))
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of chymotrypsin-like activity of 26S proteasome in human RPMI8226 cells using Suc-LLVY-MCA as substrate after 24 to 48 hrs by luminescence...More data for this Ligand-Target Pair
TargetProteasome subunit beta type-2(Homo sapiens (Human))
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Affinity DataIC50: 4.10E+3nMAssay Description:Inhibition of trypsin-like activity of 26S proteasome in human KMS11 cells using Boc-LRR-MCA as substrate after 24 to 48 hrs by luminescence-based as...More data for this Ligand-Target Pair
TargetProteasome subunit beta type-5(Homo sapiens (Human))
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of chymotrypsin-like activity of human 20S proteasome using Suc-LLVY-MCA as substrate measured for 1 hr by fluorescence assayMore data for this Ligand-Target Pair
TargetProteasome subunit beta type-1(Homo sapiens (Human))
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of PGPH activity of human 20S proteasome using Z-LLE-MCA as substrate measured for 1 hr by fluorescence assayMore data for this Ligand-Target Pair
TargetProteasome subunit beta type-5(Homo sapiens (Human))
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Affinity DataIC50: 6.00E+3nMAssay Description:Inhibition of chymotrypsin-like activity of human 26S proteasome using Z-LLE-MCA as substrate measured for 1 hr in presence of ATPgammaS by fluoresce...More data for this Ligand-Target Pair
TargetProteasome subunit beta type-5(Homo sapiens (Human))
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of chymotrypsin-like activity of 26S proteasome in human KMS11 cells using Suc-LLVY-MCA as substrate after 24 to 48 hrs by luminescence-ba...More data for this Ligand-Target Pair
TargetProteasome subunit beta type-1(Homo sapiens (Human))
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Affinity DataIC50: 2.80E+3nMAssay Description:Inhibition of PGPH-like activity of 26S proteasome in human KMS11 cells using Z-LLE-MCA as substrate after 24 to 48 hrs by luminescence-based assayMore data for this Ligand-Target Pair
TargetProteasome subunit beta type-5(Homo sapiens (Human))
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Nagahama Institute of Bio-Science and Technology
Curated by ChEMBL
Affinity DataIC50: 9.40E+3nMAssay Description:Inhibition of chymotrypsin-like activity of human 26S proteasome using Suc-LLVY-MCA as substrate measured for 1 hr by fluorescence assayMore data for this Ligand-Target Pair