Structure and property based design, synthesis and biological evaluation of γ-lactam based HDAC inhibitors: Part II
C Lee, E Choi, M Cho, B Lee, SJ Oh, SK Park…
Index: Lee, Chulho; Choi, Eunhyun; Cho, Misun; Lee, Boah; Oh, Soo Jin; Park, Song-Kyu; Lee, Kiho; Kim, Hwan Mook; Han, Gyoonhee Bioorganic and Medicinal Chemistry Letters, 2012 , vol. 22, # 12 p. 4189 - 4192
Full Text: HTML
Citation Number: 13
Abstract
Histone deacetylases (HDACs) are involved in post-translational modification and epi- genetic expression, and have been the intriguing targets for treatment of cancer. In previous study, we reported synthesis and the biological preliminary results of γ-lactam based HDAC inhibitors. Based on the previous results, smaller γ-lactam core HDAC inhibitors are more active than the corresponding series of larger δ-lactam based analogues and the ...
Related Articles:
[Heckrodt, Thilo J.; Singh, Rajinder Synthetic Communications, 2012 , vol. 42, # 19 p. 2854 - 2865]
[Das, Asish R.; Medda, Arunima; Singha, Raghunath; Guchhait, Nikhil Journal of the Indian Chemical Society, 2009 , vol. 86, # 8 p. 841 - 848]
[Zhou, Lijun; Yang, Qingang; Wang, Yong; Hu, Youhong; Luo, Xiaomin; Bai, Donglu; Li, Shukun Chemical and Pharmaceutical Bulletin, 2008 , vol. 56, # 8 p. 1147 - 1152]
[Molander, Gary A.; Pack, Shawn K. Tetrahedron, 2003 , vol. 59, # 52 p. 10581 - 10591]
[Molander, Gary A.; Pack, Shawn K. Tetrahedron, 2003 , vol. 59, # 52 p. 10581 - 10591]