Technology ID
TAB-2224

Selective 12-Human Lipoxygenase Inhibitors for the Treatment of Diabetes and Clotting

E-Numbers
E-134-2010-0
Lead Inventor
Maloney, David (NHGRI)
Co-Inventors
Holman, Theodore (University of California, San Diego)
Nadler, Jerry
Holinstat, Michael (Thomas Jefferson University)
Simeonov, Anton (NHGRI)
Jadhav, Ajit (NHGRI)
Applications
Therapeutics
Research Materials
Diagnostics
Therapeutic Areas
Cardiology
Development Status
Pre-clinical
Lead IC
NCATS
ICs
NHGRI
This invention discloses small molecule inhibitors of human 12-lipoxygenase (12-hLO). 12-lipoxygenase expression, activation, and lipid metabolites have been implicated in type 1 and type 2 diabetes, cardiovascular disease, hypertension, Alzheimer’s, and Parkinson’s disease. The development of 12-hLO inhibitors may be a potent intracellular approach to decreasing the ability of platelets to form large clots in response to vessel injury or activation of the coagulation pathway. Thus, 12-hLO inhibition has the potential to attenuate platelet-mediated clot formation caused by diabetes and/or cardiovascular disease and significantly decrease the occurrence of myocardial infarction and death. Moreover, Type 1 and Type 2 diabetes are serious disorders that can lead to major complications and reduced lifespan. An unmet medical need is to identify new ways to protect beta cells in these metabolic disorders. A selective 12-hLO inhibitor could provide a new therapeutic approach to prevent or treat either form of diabetes.
Commercial Applications
  • Therapeutic developments (blood clots; Type 1 and Type 2 diabetes, cardiovascular disease, and neurodegenerative diseases)
  • Inflammatory responses
Competitive Advantages
  • Small molecule (series of analogs can be derived in search of improved performances and/or different functions)
  • Selective inhibitor of human 12-lipoxygenase
Licensing Contact:
Vepa, Suryanarayana
sury.vepa@nih.gov