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Discovery of a Novel HDAC3 Selective Inhibitor and its Evaluation in Lymphoma Model

Authors
Choi, Chang-JuKim, MiraHan, Sun YoungJeon, JiyoungLee, Jae HoOh, Jeong-InSuh, Kwee HyunSuh, Dong-ChurlLee, Kwang-Ok
Issue Date
Jan-2016
Publisher
WILEY-V C H VERLAG GMBH
Keywords
HDAC3 selective inhibitor; Lymphoma model
Citation
BULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.37, no.1, pp 42 - 47
Pages
6
Journal Title
BULLETIN OF THE KOREAN CHEMICAL SOCIETY
Volume
37
Number
1
Start Page
42
End Page
47
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/7422
DOI
10.1002/bkcs.10619
ISSN
0253-2964
1229-5949
Abstract
Histone deacetylase (HDAC) inhibition is a potentially attractive approach to cancer therapy. A number of HDAC inhibitors are in clinical development stages for the treatment of cancer as well as immune and inflammatory disorders. Although there are several approved HDAC inhibitors by the US FDA, they show a broad inhibitory spectrum against HDAC subfamily. Herein, we synthesized a series of novel hydroxamate analogs, and evaluated them with lymphoma cancer cell. Conclusively, we identified an HDAC3 selective inhibitor which shows good anticancer activity for the lymphoma model, as well as a good drug metabolism and pharmacokinetics (DMPK) profile.
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