Drug intelligence / Profile preview

Shandong Univ. HDAC8 compound 5b

Development stage
Unknown
Lead developer
Shandong University
01

Overview

Shandong Univ. HDAC8 compound 5b: sourced facts only. name: "Among them, the tetrahydroquinoline derivative 11k exhibited potent HDAC8 inhibitory activity (IC50 = 0.10 μM), and the indole derivative 5b also showed activity (IC50 = 0.28 μM), both with excellent selectivity." [PMID:41785528]; target: "Among them, the tetrahydroquinoline derivative 11k exhibited potent HDAC8 inhibitory activity (IC50 = 0.10 μM), and the indole derivative 5b also showed activity (IC50 = 0.28 μM), both with excellent selectivity." [PMID:41785528]; developer: "Department of Medicinal Chemistry, State Key Laboratory of Discovery and Utilization of Functional Components in Traditional Chinese Medicine, Shandong Key Laboratory of Druggability Optimization and Evaluation for Lead Compounds, Shandong Basic Science Academic Special Zone/ Research Center (Pharmacy), School of Pharmaceutical Sciences, Cheelo College of Medicine, Shandong University, Jinan, Shandong, PR China." [PMID:41785528]

02

Targets

HDAC8 (Histone Deacetylase 8)

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