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Bioorg Med Chem ; 53: 116523, 2022 01 01.
Artigo em Inglês | MEDLINE | ID: covidwho-1525708

RESUMO

Since the end of 2019, the outbreak of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) has evolved into a global pandemic. There is an urgent need for effective and low-toxic antiviral drugs to remedy Remdesivir's limitation. Hydroxychloroquine, a broad spectrum anti-viral drug, showed inhibitory activity against SARS-CoV-2 in some studies. Thus, we adopted a drug repurposing strategy, and further investigated hydroxychloroquine. We obtained different configurations of hydroxychloroquine side chains by using chiral resolution technique, and successfully furnished R-/S-hydroxychloroquine sulfate through chemical synthesis. The R configuration of hydroxychloroquine was found to exhibit higher antiviral activity (EC50 = 3.05 µM) and lower toxicity in vivo. Therefore, R-HCQ is a promising lead compound against SARS-CoV-2. Our research provides new strategy for the subsequent research on small molecule inhibitors against SARS-CoV-2.


Assuntos
Antivirais/farmacologia , Hidroxicloroquina/farmacologia , SARS-CoV-2/efeitos dos fármacos , Animais , Antivirais/síntese química , Antivirais/toxicidade , Chlorocebus aethiops , Reposicionamento de Medicamentos , Feminino , Hidroxicloroquina/síntese química , Hidroxicloroquina/toxicidade , Masculino , Camundongos , Testes de Sensibilidade Microbiana , Estereoisomerismo , Células Vero
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