Drug repurposing and search of selective inhibitors for human dihydroorotate dehydrogenase as a strategy in fighting against COVID-19

  • Funded by Fundação de Amparo à Pesquisa do Estado de São Paulo [São Paulo Research Foundation] (FAPESP)
  • Total publications:0 publications

Grant number: 20/06190-0

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2021
    2023
  • Funder

    Fundação de Amparo à Pesquisa do Estado de São Paulo [São Paulo Research Foundation] (FAPESP)
  • Principal Investigator

    Maria Cristina Nonato
  • Research Location

    Brazil
  • Lead Research Institution

    Faculdade de Ciências Farmacêuticas de Ribeirão Preto (FCFRP). Universidade de São Paulo (USP). Ribeirão Preto , SP, Brazil
  • Research Priority Alignment

    N/A
  • Research Category

    Therapeutics research, development and implementation

  • Research Subcategory

    Pre-clinical studies

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

No longer than four months ago, the world was not aware of the existence of the virus SARS-CoV-2. Today, this virus, responsible for COVID-19, has already spread around the all planet, infecting more than 2 million people and killing more than 150 thousand. The pandemic caused by COVID-19 has led to the collapse of both economic and the health systems around the world. So far, social distance is the only weapon available to minimize the impact of the virus proliferation. There is no vaccine available to prevent the infection caused by SARS-CoV-2, neither an effective treatment for COVID-19. In this context, this proposal aims at contributing to the development of an innovative therapy against COVID-19, either through drug repurposing or by identifying new chemical identities, all based on the selective inhibition of the human enzyme dihydroorotate dehydrogenase (HsDHODH). HsDHODH, which, takes part of the de novo pyrimidine biosynthetic pathway, is the pharmacological validated target for proliferative and parasitic diseases, and have been considered an attractive target for the development of antivirais. The fact that the virus relies on the host cell biochemical machinery to provide nucleosides for its viral replication cycle makes enzymes involved in the biosynthesis of nucleosides, such as HsDHODH, potential targets for the development of broad spectrum antivirals. Our studies include enzymatic and biophysical assays, citotoxicity tests using different mammal cells, antiviral assays in cell culture using a biosafety level 3 laboratory and synthesis of drugs and analogues based on virtual screening studies. Our project put together research leaders in complementary areas, contributing not only to accomplish our goals, but also to consolidate a complex and multidisciplinary pipeline in drug discovery. (AU)