COMPOUNDS FOR THE TREATMENT OF SARS
Broad-spectrum antivirals effective against SARS, COVID-19, and future coronavirus strains.
Purdue University researchers have developed a series of compounds that potently inhibit an enzyme, 3-chymotrypsin like protease (3CLpro), essential for various coronaviruses, including those causing severe acute respiratory syndrome (SARS) and COVID-19. While the COVID-19 respiratory illness is specifically caused by the SARS-CoV-2 strain, various other coronaviruses also pose significant health threats. Despite the existence of therapeutics authorized for emergency use against coronaviruses, challenges remain with efficacy, ease of administration, and recurrence of illnesses.
Purdue researchers have created a novel class of compounds capable of inhibiting 3CLpro, a key protease found in many coronaviruses essential for efficient viral replication, including SARS and SARS-CoV-2. The compounds presented are chemically distinct from the current FDA-approved 3CLpro inhibitors for SARS-CoV-2. Moreover, they demonstrate enhanced potency in inhibiting 3CLpro and exhibit superior antiviral activity when compared to approved compounds.
TRL: Pharmaceuticals
Intellectual Property:
Provisional-Gov. Funding, 2021-05-28, United States
NATL-Patent, 2022-05-22, Europe
PCT-Gov. Funding, 2022-05-27, WO
NATL-Patent, 2023-11-28, United States
Keywords: 3CLpro, Coronavirus, COVID, COVID-19, Protease Inhibitor, SARS-CoV-2