This technology is a set of small molecule agonists of the Sigma non-opioid receptor for the treatment of Timothy Syndrome.
Activation of Sigma non-opioid receptor 1 (SIGMAR1) may treat Timothy Syndrome. Current Sigma non-opioid receptor 1 agonists include dextromethorphan and fluovoxamine. However, these agonists were designed to treat neurological disorders and thus are highly permeable to the blood-brain barrier (BBB). High BBB permeability of SIGMAR1 agonists can produce undesired side effects for the treatment of Timothy Syndrome.
This technology describes the development of small molecule SIGMAR1 agonists MY33-1 and MY33-2 that are “less permeable” through the blood-brain barrier (BBB) to treat Timothy Syndrome. These agonists rescue cardiac phenotypes in Timothy Syndrome stem cell models. Thus, MY33-1 and MY33-2 may be used to treat Timothy Syndrome and cardiac arrhythmias.
This technology has been tested in Timothy Syndrome patient-specific induced pluripotent stem cell models.
Masayuki Yazawa, Ph.D.
Patent Pending
IR CU23081
Licensing Contact: Kristin Neuman