BDBM50608544 CHEMBL3392741

SMILES Cc1ccc(cc1)S(=O)(=O)Nc1cc(ccc1C(=O)Nc1nc(cs1)-c1ccccc1)C(F)(F)F

InChI Key InChIKey=QZUGMNXETPARLI-UHFFFAOYSA-N

Data  2 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 6 hits for monomerid = 50608544   

TargetUbiquitin carboxyl-terminal hydrolase 8(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50608544(CHEMBL3392741)
Affinity DataIC50: 950nMAssay Description:Inhibition of USP8 (unknown origin) using Di-Ub IQF K48-02 as substrate preincubated for 30 mins followed by substrate addition by high-throughput as...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/11/2025
Entry Details
PubMed
TargetUbiquitin carboxyl-terminal hydrolase 8(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50608544(CHEMBL3392741)
Affinity DataIC50: 950nMAssay Description:Inhibition of human USP8 using Di-Ub IQF as substrate incubated for 15 mins by K63-2 assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/19/2024
Entry Details
PubMed
TargetUbiquitin carboxyl-terminal hydrolase 2(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50608544(CHEMBL3392741)
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of USP2 (unknown origin) using Di-Ub IQF K48-4 as substrate preincubated for 10 mins followed by substrate addition by high-throughput ass...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/11/2025
Entry Details
PubMed
TargetUbiquitin carboxyl-terminal hydrolase 2(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50608544(CHEMBL3392741)
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of human USP2 using Di-Ub IQF as substrate incubated for 15 mins by K63-2 assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/19/2024
Entry Details
PubMed
TargetUbiquitin carboxyl-terminal hydrolase 2(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50608544(CHEMBL3392741)
Affinity DataIC50: 3.60E+3nMAssay Description:Inhibition of USP2 (267 to 599 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3) cells using ubiquitin-rhodamine-110 as substrate p...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/11/2025
Entry Details
PubMed
TargetUbiquitin carboxyl-terminal hydrolase 8(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50608544(CHEMBL3392741)
Affinity DataIC50: 4.70E+3nMAssay Description:Inhibition of N-terminal His6 tagged USP8 (734 to 1110 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3) cells using ubiquitin-rhod...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/11/2025
Entry Details
PubMed