Title of article :
Aminosuberoyl hydroxamic acids (ASHAs): A potent new class of HDAC inhibitors
Author/Authors :
Sandro Belvedere، نويسنده , , David J. Witter، نويسنده , , Jiaming Yan، نويسنده , , J. Paul Secrist، نويسنده , , Victoria Richon، نويسنده , , Thomas A. Miller، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Pages :
3
From page :
3969
To page :
3971
Abstract :
Histone deacetylase (HDAC) inhibitors that target Class I and Class II HDACs are currently in advanced clinical trials for the treatment of cancer. Vorinostat (Zolinza™, SAHA) is a hydroxamic acid approved for the treatment of patients with cutaneous T-cell lymphoma who have progressive, persistent or recurrent disease on or following two systemic therapies. As part of an on-going effort to better understand the nature of the HDAC enzyme/inhibitor interaction and design highly effective HDAC inhibitors, we herein report the design, synthesis and HDAC inhibitory activity of a vorinostat-derived series of substrate-based HDAC inhibitors.
Keywords :
hydroxamic acids , Histone deacetylase inhibitor , HDAC , anticancer drug , HDAC inhibitor , SAHA
Journal title :
Bioorganic & Medicinal Chemistry Letters
Serial Year :
2007
Journal title :
Bioorganic & Medicinal Chemistry Letters
Record number :
798349
Link To Document :
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