
Therapeutic applications in cancer, Alzheimer’s disease, and memory enhancement.
Alzheimer’s disease, memory impairment, and prostate cancer remain significant health challenges that require more effective treatment options. Current histone deacetylase inhibitors (HDAC inhibitors) have limitations, including poor blood-brain barrier permeability and undesirable toxicity, which can reduce their effectiveness and broader therapeutic use. There is a need for new HDAC-targeting compounds that can better support treatment of neurological disorders and cancer.
UWM researchers have developed next-generation HDAC inhibitor therapies that provide improved therapeutic performance by addressing key limitations of existing compounds, including poor blood-brain barrier permeability and toxicity. By offering novel HDAC inhibitor structures with demonstrated biological activity, the invention creates opportunities for more effective treatments targeting cancer, neurodegenerative diseases, and memory-related disorders.
The technology consists of novel HDAC inhibitor compounds and related pharmaceutical compositions. These compounds work by inhibiting histone deacetylase activity, which is associated with regulation of gene expression and cellular processes. The invention includes multiple compound classes, synthesis methods, pharmaceutical formulations, and therapeutic applications.
The compounds have been synthesized and evaluated through biological assays, including studies of HDAC inhibition, histone acetylation, cell viability, apoptosis, and reactive oxygen species generation.
The inventors have also launched a startup, Elafar, to further develop and bring this technology to real-world use and are looking for partner apps with pharmaceutical companies, biotechnology companies, and drug development organizations.
Issued US Patent, US20180258135
M Mahmun Hossain, UWM Professor, Chemistry & Biochemistry
Karyn Frick, UWM Distinguished Professor, Physiological & Brain Sciences