1. Academic Validation
  2. Novologues containing a benzamide side chain manifest anti-proliferative activity against two breast cancer cell lines

Novologues containing a benzamide side chain manifest anti-proliferative activity against two breast cancer cell lines

  • Bioorg Med Chem Lett. 2014 Aug 1;24(15):3633-7. doi: 10.1016/j.bmcl.2014.05.020.
Huiping Zhao 1 Mercy Anyika 1 Antwan Girgis 1 Brian S J Blagg 2
Affiliations

Affiliations

  • 1 Department of Medicinal Chemistry, The University of Kansas, 1251 Wescoe Hall Drive, Malott 4070, Lawrence, KS 66045-7563, United States.
  • 2 Department of Medicinal Chemistry, The University of Kansas, 1251 Wescoe Hall Drive, Malott 4070, Lawrence, KS 66045-7563, United States. Electronic address: [email protected].
Abstract

HSP90 represents a promising target for the development of both anti-cancer and neuroprotective agents. Structure-activity relationship studies on novobiocin and novobiocin analogues, led to the development of KU-32 and recently, KU-596, as lead compounds for the potential treatment of neurodegenerative diseases. Similar to KU-32, we have demonstrated that upon replacement of the acetamide side chain present in KU-32 with a benzamide, this neuroprotective agent was transformed into a scaffold that manifests anti-proliferative activity. To assess structure-activity relationships for this new scaffold, a library of benzamide-containing novologues was prepared and evaluated against two breast Cancer cell lines. Compound 14a manifested the most potent anti-proliferative activity from these studies and induced Hsp90-dependent client protein degradation in a concentration-dependent manner.

Keywords

Breast cancer; Heat shock protein 90; Hsp90 inhibitors; Novobiocin analogues.

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