Design, synthesis, and antitumor evaluation of histone deacetylase inhibitors with L-phenylglycine scaffold

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Design, synthesis, and antitumor evaluation of histone deacetylase inhibitors with l-phenylglycine scaffold

In our previous research, a novel series of histone deacetylase (HDAC) inhibitors with L-phenylglycine scaffold were designed and synthesized, among which amides D3 and D7 and ureido D18 were far superior to the positive control (suberoylanilide hydroxamic acid [SAHA]) in HDAC inhibition, but were only comparable to SAHA in antiproliferation on tumor cell lines. Herein, further structural deriv...

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ژورنال

عنوان ژورنال: Drug Design, Development and Therapy

سال: 2015

ISSN: 1177-8881

DOI: 10.2147/dddt.s94037