Drug intelligence / Profile preview

Ocean Univ. of China HDAC3 compound B22

Development stage
Preclinical
Lead developer
Ocean University of China
Modality
PROTACs (E3 ligase recruitment) → Targeted Protein Degraders (TPDs) → Small Molecules
01

Overview

Ocean Univ. of China HDAC3 compound B22: sourced facts only. name: "Among these, representative compound B22 potently degraded HDAC3, with a DC50 of 30.73 nM and a Dmax of 82%." [PMID:41610583]; target: "Among these, representative compound B22 potently degraded HDAC3, with a DC50 of 30.73 nM and a Dmax of 82%." [PMID:41610583]; developer: "Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, 5 Yushan Road, Qingdao 266003, China." [PMID:41610583]; modality: "In this study, we designed a series of novel HDAC3 PROTACs based on our previously designed HDAC3 inhibitor as the POI ligand." [PMID:41610583]; stage: "B22 synergized with the clinically approved AML agent Venetoclax, demonstrating potent anti-proliferative effects and significantly promoting apoptosis in MV4-11 cells." [PMID:41610583]

02

Targets

HDAC3 (Histone Deacetylase 3)

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