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Synthesis and evaluation of 8,9-amido analogs of geldanamycin
Authors:Merritt B. Andrus  Yong Wong  Kristin Beebe
Affiliation:a Department of Chemistry and Biochemistry, Brigham Young University, C100 BNSN, Provo, UT 84602, USA
b National Cancer Institute, Building 10-Hatfield CRC, Room 1-5952, 10 Center Drive, Rockville, MD 20892, USA
Abstract:Amido analogs of geldanamycin, an ansamycin anticancer agent, were designed, synthesized, and assayed with SKBR3 cells, in which stability of HER2 receptor tyrosine kinase is dependent on the chaperone Hsp90. An amide was employed as a trisubstituted alkene isostere at the C8,9 position, which provided for a simplified, convergent synthesis through two major fragments, an aniline-amine left-hand portion and a dicarboxylic acid right-hand piece.
Keywords:Glycolate aldol   Ansamycin   Geldanamycin   Amide isostere   Heat-shock protein
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