| Literature DB >> 27037933 |
Katherine M Byrd1, Chitra Subramanian2, Jacqueline Sanchez2, Hashim F Motiwala2, Weiya Liu3, Mark S Cohen2, Jeffrey Holzbeierlein3, Brian S J Blagg4.
Abstract
Development of heat shock protein 90 (Hsp90) C-terminal inhibitors has emerged as an exciting strategy for the treatment of cancer. Previous efforts have focused on modifications to the natural products novobiocin and coumermycin. Moreover, variations in both the sugar and amide moieties have been extensively studied, whereas replacements for the coumarin core have received less attention. Herein, 24 cores were synthesized with varying distances and angles between the sugar and amide moieties. Compounds that exhibited good anti-proliferative activity against multiple cancer cell lines and Hsp90 inhibitory activity, were those that placed the sugar and amide moieties between 7.7 and 12.1 Å apart along with angles of 180°.Entities:
Keywords: C-terminal inhibitors; Hsp90; antitumor agents; luciferase refolding; medicinal chemistry
Mesh:
Substances:
Year: 2016 PMID: 27037933 PMCID: PMC4962924 DOI: 10.1002/chem.201504955
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236