COMPOUNDS FOR THE TREATMENT OF SARS

A novel class of highly potent compounds inhibits a key viral protease (3CLpro) in coronaviruses like SARS-CoV-2, offering superior antiviral performance over existing emergency-authorized treatments.
Technology No. 2021-GHOS-69511

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: 3

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: novel compounds, 3-chymotrypsin like protease, 3CLpro inhibitor, coronavirus, SARS, COVID-19, antiviral activity, viral replication, protease inhibitor, therapeutic compounds

  • expand_more mode_edit Authors (2)
    Arun K Ghosh
    Monika Yadav
  • expand_more cloud_download Supporting documents (1)
    Product brochure
    COMPOUNDS FOR THE TREATMENT OF SARS.pdf
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