Novel Compositions for Cancer Therapy (Proteasomes Inhibitors)
Simple synthesis Unique structure differentiate claimed compositions from other, known compositions of matter in vitro, in vivo and clinical studies Potent activity with low cytotoxicity Mechanism of action well understood through
While most enabled for the treatment of diverse cancers e.g., myeloma, denocarcinoma, pancreatic cancer, B cell-related cancer and lymphomas, proteasomes inhibitors have also demonstrated utility for the treatment of diverse human diseases, including but not limited to retroviral infections such as human immunodeficiency virus-1 (HIV-1) infection, immune disorders, inflammation (epoxomicin), Stroke and neurodegenerative disease (via promotion of neurite outgrowth as described for lactacystin, omurolide, tyropeptin A, curcumin, capsaicin, and TMC-95A).
Within mammalian cells, proteasome inhibitors block the ability of proteasomes to degrade unneeded or damaged proteins. When administered, proteasome inhibitors have been shown to be effective for treatment of cancer, HIV infection and autoimmune diseases. UC inventors have isolated, characterized and synthesized a natural proteasome inhibitor, discovered from a tropical marine cyanobacteria. Proprietary compositions (parent and analogs), which have intriguing and unique structural features, are claimed for treatment of cancer and other diseases responsive to proteasome inhibition.
诊断/治疗
人类免疫缺陷病毒
9409944
State Of Development Assay-guided purification was used to identify and isolate the parent compounds, carmaphycins A and B work has demonstrated potent efficacy vs. human lung adenocarcinoma and colon cancer cells. The structures were elucidated by means of NMR and HRESIMS data and absolute and relative configurations were determined by total synthesis. A straightforward synthetic method has generated material sufficient to support in vivo assessment of efficacy of compositions. Intellectual Property Info Worldwide rights available; pending patents available under confidentiality. Related Materials Pereira, AR, et al., The Carmaphycins: New Proteasome Inhibitors Exhibiting an a, ß-Epoxyketone Warhead from a Marine Cyanobacterium Additional Technologies by these Inventors Tech ID/UC Case 22376/2011-354-0 Related Cases 2011-354-0, 2010-351-0
Inventor's Bio
Inventor information
美国
