BDBM50432548 LACTACYSTIN

SMILES CC(C)[C@H](O)[C@]1(NC(=O)[C@H](C)[C@@H]1O)C(=O)SC[C@H](NC(C)=O)C(O)=O

InChI Key InChIKey=DAQAKHDKYAWHCG-UHFFFAOYSA-N

Data  11 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 11 hits for monomerid = 50432548   

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-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-5(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50432548(LACTACYSTIN)
Affinity DataIC50: 1.01E+4nMAssay Description:Inhibition of chymotrypsin-like activity of human beta-5 subunit of 20S proteasome using Suc-LLVY-AMC as substrate by fluorometer analysisMore 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: 370nMAssay Description:Inhibition of chymotrypsin-like activity of proteasome beta5 subunit in human MDA-MB-468 cells using Suc-Leu-Leu-Val-Tyr-AMC as substrate after 2 hrs...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-2(Human)
Nagahama Institute of Bio-Science and Technology

Curated by ChEMBL
LigandPNGBDBM50432548(LACTACYSTIN)
Affinity DataIC50: 3.25E+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
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-1(Human)
Nagahama Institute of Bio-Science and Technology

Curated by ChEMBL
LigandPNGBDBM50432548(LACTACYSTIN)
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
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-5(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50432548(LACTACYSTIN)
Affinity DataIC50: 160nMAssay 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
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-5(Human)
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50432548(LACTACYSTIN)
Affinity DataIC50: 4.96E+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
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-1(Human)
Nagahama Institute of Bio-Science and Technology

Curated by ChEMBL
LigandPNGBDBM50432548(LACTACYSTIN)
Affinity DataIC50: 8.00E+3nMAssay 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
In DepthDetails Article
PubMed
TargetProteasome subunit beta type-2(Human)
Nagahama Institute of Bio-Science and Technology

Curated by ChEMBL
LigandPNGBDBM50432548(LACTACYSTIN)
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
In DepthDetails Article
PubMed
LigandPNGBDBM50432548(LACTACYSTIN)
Affinity DataIC50: 259nMAssay Description:Inhibition of human 20S proteasomeMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed