Synthesis and Importance of Bulky Aromatic Cap of Novel SAHA Analogs for HDAC Inhibition and Anticancer Activity 


Vol. 32,  No. 6, pp. 1891-1896, Jun.  2011
10.5012/bkcs.2011.32.6.1891


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  Abstract

On the basis of potent HDAC-inhibitory activity and anticancer activity of SAHA, novel SAHA derivatives 3a-d and 7 with a bulky cap such as p-dimethylaminophenyl, 4-phenylaminophenyl, 4-phenyloxyphenyl, 9Hfluorenyl or naphthalenyl ring were synthesized starting from the corresponding aryl amines or naphthalenyl acetic acid using an EDC-mediated amide coupling reaction in the presence of HOBt followed by a nucleophilic addition-elimination reaction with hydroxylamine. Compounds 3b, 3c and 3d showed more potent inhibitory activity on total HDACs (14~27-fold), HDAC1 (8~15-fold), HDAC2 (1.3~25-fold) and HDAC7 (1~3-fold) and more potent anticancer activity (2~22-fold) against MCF-7, MDA-MB-231, MCF-7/ Dox, MCF-7/Tam, SK-OV-3, LNCaP and PC3 human cancer cell lines than SAHA.

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  Cite this article

[IEEE Style]

P. Chun, W. H. Kim, J. Kim, J. Kang, H. J. Lee, J. Y. Park, M. Y. Ahn, H. S. Kim, H. R. Moon, "Synthesis and Importance of Bulky Aromatic Cap of Novel SAHA Analogs for HDAC Inhibition and Anticancer Activity," Bulletin of the Korean Chemical Society, vol. 32, no. 6, pp. 1891-1896, 2011. DOI: 10.5012/bkcs.2011.32.6.1891.

[ACM Style]

Pusoon Chun, Won Hee Kim, Jungsu Kim, Jin-Ah Kang, Hye Jin Lee, Ji Young Park, Mee Young Ahn, Hyung Sik Kim, and Hyung Ryong Moon. 2011. Synthesis and Importance of Bulky Aromatic Cap of Novel SAHA Analogs for HDAC Inhibition and Anticancer Activity. Bulletin of the Korean Chemical Society, 32, 6, (2011), 1891-1896. DOI: 10.5012/bkcs.2011.32.6.1891.

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ISSN(Print) 0253-2964
ISSN(Online) 1229-5949