Discovery of a Potent and Selective ATAD2 Bromodomain Inhibitor with Antiproliferative Activity in Breast Cancer Models.
ATPases Associated with Diverse Cellular Activities
/ antagonists & inhibitors
Antineoplastic Agents
/ chemical synthesis
Breast Neoplasms
/ drug therapy
Cell Line, Tumor
Crystallography, X-Ray
DNA-Binding Proteins
/ antagonists & inhibitors
Drug Discovery
Drug Screening Assays, Antitumor
Female
Humans
Models, Molecular
Small Molecule Libraries
Structure-Activity Relationship
Substrate Specificity
Tumor Stem Cell Assay
Journal
Journal of medicinal chemistry
ISSN: 1520-4804
Titre abrégé: J Med Chem
Pays: United States
ID NLM: 9716531
Informations de publication
Date de publication:
24 02 2022
24 02 2022
Historique:
pubmed:
9
2
2022
medline:
11
3
2022
entrez:
8
2
2022
Statut:
ppublish
Résumé
ATAD2 is an epigenetic bromodomain-containing target which is overexpressed in many cancers and has been suggested as a potential oncology target. While several small molecule inhibitors have been described in the literature, their cellular activity has proved to be underwhelming. In this work, we describe the identification of a novel series of ATAD2 inhibitors by high throughput screening, confirmation of the bromodomain region as the site of action, and the optimization campaign undertaken to improve the potency, selectivity, and permeability of the initial hit. The result is compound
Identifiants
pubmed: 35133824
doi: 10.1021/acs.jmedchem.1c01871
doi:
Substances chimiques
Antineoplastic Agents
0
DNA-Binding Proteins
0
Small Molecule Libraries
0
ATAD2 protein, human
EC 3.6.1.3
ATPases Associated with Diverse Cellular Activities
EC 3.6.4.-
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM