Author/Authors :
Jed L. Hubbs، نويسنده , , Hua Zhou، نويسنده , , Astrid M. Kral، نويسنده , , Judith C. Fleming، نويسنده , , William K. Dahlberg، نويسنده , , Bethany L. Hughes، نويسنده , , Richard E. Middleton، نويسنده , , Alexander A. Szewczak، نويسنده , , J. Paul Secrist، نويسنده , , Thomas A. Miller، نويسنده ,
Abstract :
Ongoing clinical studies indicate that inhibitors of Class I and Class II histone deacetylase (HDAC) enzymes show great promise for the treatment of cancer. Zolinza® (SAHA, Zolinza®) was recently approved by the FDA for the treatment of the cutaneous manifestations of cutaneous T-cell lymphoma. As a part of an ongoing effort to identify novel small molecules to target these important enzymes, we have prepared several classes of amino acid-derived HDAC1 inhibitors. The design rationale and in vitro activity against the HDAC1 enzyme and HCT116 cell line are described in this letter.
Keywords :
Histone deacetylase , cancer , Ugi reaction , lysine , amino acid , Benzothiophene