Development of Hsp90 C-terminal inhibitors with noviomimetics that manifest anti-proliferative activities

Eva Amatya, Chitra Subramanian, Mark S. Cohen, Brian S.J. Blagg

Research output: Contribution to journalArticlepeer-review

Abstract

Inhibition of the Hsp90 C-terminal domain offers a promising opportunity to treat numerous diseases/indications. Furthermore, the development of Hsp90 C-terminal inhibitors (CTIs) is advantageous over N-terminal inhibitors because it avoids the detriments associated with induction of the heat shock response (HSR). However, the lack of co-crystal structures of small molecules bound to the C-terminus have hindered their development. Therefore, structure-activity relationship (SAR) studies have been pursued to optimize such inhibitors. Noviose sugar surrogates, also known as noviomimetics have been prepared to investigate the size and nature of the C-terminal domain binding pocket. Herein, we report the synthesis and anti-proliferative activity manifested by this new series of Hsp90 C-terminal inhibitors.

Original languageEnglish (US)
Pages (from-to)888-894
Number of pages7
JournalRSC Medicinal Chemistry
Volume15
Issue number3
DOIs
StatePublished - Jan 18 2024

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Medicine
  • Pharmacology
  • Pharmaceutical Science
  • Drug Discovery
  • Organic Chemistry

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