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Assay Detail

CHEMBL5628548

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Inhibition of recombinant HDAC10 (unknown origin) using RHKK-Ac-AMC as substrate
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Polyamine deacetylase HDAC10 (CHEMBL5103)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Discovery of potent pyrrolo-pyrimidine and purine HDAC inhibitors for the treatment of advanced prostate cancer.
Moi D, Bonanni D, Belluti S, Linciano P, Citarella A, Franchini S, Sorbi C, Imbriano C, Pinzi L, Rastelli G.
Eur J Med Chem (2023) 260 : 115730 -115730
PubMed 37633202 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 5.66 5.66

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5631614 1 5.66

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5631614 IC50 = 2200.0 nM 5.66