Newly synthesized series of oxoindole–oxadiazole conjugates as potential anti-SARS-CoV-2 agents: in silico and in vitro studies

Author:

El-Masry Rana M.1,Al-Karmalawy Ahmed A.2ORCID,Alnajjar Radwan34,Mahmoud Sara H.5,Mostafa Ahmed5ORCID,Kadry Hanan H.6,Abou-Seri Sahar M.7,Taher Azza T.68

Affiliation:

1. Organic Chemistry Department, Faculty of Pharmacy, October University for Modern Sciences and Arts (MSA), October 6 city, Giza, Egypt

2. Department of Pharmaceutical Medicinal Chemistry, Faculty of Pharmacy, Horus University-Egypt, New Damietta 34518, Egypt

3. Department of Chemistry, Faculty of Science, University of Benghazi, Benghazi, Libya

4. Department of Chemistry, University of Cape Town, Rondebosch 7701, South Africa

5. Center of Scientific Excellence for Influenza Viruses, National Research Centre (NRC), Dokki, Giza 12622, Egypt

6. Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, Cairo University, Cairo, Egypt

7. Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Cairo University, Cairo, Egypt

8. Department of Organic Pharmaceutical Chemistry, Faculty of Pharmacy, October 6 University (O6U), October 6 City, Giza, Egypt

Abstract

The pharmacophoric features of the novel series of 1,3,4-oxadiazole–oxoindole conjugates (IVa–g) as potential anti-SARS-CoV-2 agents based on the reported Mpro inhibitor (Ia) are presented.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

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