Arylnapthalene Vacuolar-ATPase Inhibitors as Anti-viral Agents
A new drug treatment selectively inhibits viral entry and host proteins using a chemotype that targets the host vacuolar-ATPase, offering a potential path to treat deadly Ebola and Marburg viruses.
Ebola and Marburg viruses are a filamentous RNA virus that causes severe hemorrhagic fevers. Recovery from these viruses relies fully on the patient's immune response, because currently, there is no FDA-approved vaccine or medicine available to the public yet. These viruses are deadly and there is a need for a vaccine or some type of medicine that can treat these viruses better than what is available now.
Researchers at Purdue University have developed a potential drug treatment for virus infections including Ebola and Marburg. This technology relies on selective inhibition of virus entry by a chemotype that inhibits the host vacuolar-ATPase. This will allow for the inhibition of the viral cell. This technology also allows for the inhibition of a host protein which will be key in treating these two viruses, because protein is needed for the viruses to achieve infection and replication. This new technology could open the door for how Ebola and Marburg are treated.
Advantages:
-Inhibition of the viral cell
-Inhibition of a host
Potential Applications:
-Viral entry
-Antiviral agents
TRL: 3
Intellectual Property:
Provisional-Patent, 2018-03-19, United States | PCT-Patent, 2019-03-18, WO | NATL-Patent, 2020-09-18, United States | CIP-Patent, 2021-04-06, United States | CON-Patent, 2024-01-22, United States
Keywords: Ebola treatment, Marburg virus, hemorrhagic fever drug, RNA virus inhibition, viral entry inhibitor, host vacuolar-ATPase, chemotype inhibitor, antiviral agents, host protein inhibition, selective inhibition