Table 2.
Proposed agents against COVID-19
| Classes | Drug | Pharmacologic categorya | Probable anti-COVID-19 mechanisma |
|---|---|---|---|
| Antiparasitic | Chloroquine | Antimalarials |
Alkalizes endosomal pH and interferes with virus-endosome fusion (Vincent et al. 2005; Yang et al. 2004) inhibits the glycosylation of ACE2 receptors (Vincent et al. 2005) possesses anti-inflammatory and immunomodulatory effects by inhibition of phospholipase A2 activity and blocking cytokine production and release (Al-Bari 2015) |
| Niclosamide | Anthelmintic | Inhibition of S-phase kinase-associated protein 2 (SKP2) and increase of autophagy (Gassen et al. 2019) | |
| Nitazoxanide | Anthelmintic, anti-protozoal | Amplifying host innate immune antiviral responses by triggering foreign cytoplasmic RNA sensing and type 1 interferon axis (Jasenosky et al. 2019). | |
| Antiviral agents | Indinavir | Anti-HIV | Protease inhibitor: inhibits cleavage of gag-pol polyprotein precursors, which in turn causes the formation of immature, non-infectious viral particles |
| Lopinavir | Anti-HIV | ||
| Ritonavir (typically used to boost levels of other protease inhibitors) | Anti-HIV | ||
| Atazanavir | Anti-HIV | ||
| Darunavir | Anti-HIV | ||
| Tipranavir | Anti-HIV | ||
| Fosamprenavir (prodrug) | Anti-HIV | Protease inhibitor: prevents processing of viral gag and gag-pol polyprotein precursors, resulting in the formation of immature noninfectious viral particle | |
| Abacavir | Anti-HIV | Nucleotide reverse transcriptase inhibitor: guanosine analog that inhibits HIV-1 reverse transcriptase by competing with dGTP as substrate, which in turn inhibits viral replication | |
| Elvitegravir | Anti-HIV | Integrase inhibitor: inhibits catalytic activity of HIV-1 integrase, in turn Inhibits viral replication | |
| Raltegravir | Anti-HIV | ||
| Remdesivir (prodrug) | research statement | RNA polymerase inhibitor: metabolized into an adenosine nucleotide analog that interferes with the action of virus RNA polymerase | |
| Favipiravir (prodrug) | Anti-influenza | ||
| Sofosbuvir (prodrug) | Anti-hepacivirus | RNA-dependent RNA polymerase: metabolized into uridine analog triphosphate, an inhibitor of HCV NS5B RNA-dependent polymerase; suppresses viral replication | |
| Ribavirin | Anti-hepacivirus | RNA-dependent RNA polymerase: inhibits the initiation and elongation of RNA fragments by inhibiting polymerase activity, inhibition of viral protein synthesis | |
| Antineoplastic agents | Carfilzomib | Proteasome inhibitor: binds to the n-terminal threonine-containing active sites of the 20s proteasome, the proteolytic core particle within the 26 s proteasome, causes cell cycle arrest and apoptosis | |
| Bortezomib | Proteasome inhibitor: reversible inhibitor of chymotrypsin-like activity at the 26-s proteasome, causes cell cycle arrest and apoptosis | ||
| Imatinib | Protein-tyrosine kinase inhibitor: ABL fusion kinase inhibitor (Ge et al. 2020) | ||
| Carrizumab | Programmed cell death protein 1 inhibitor: activate the immune system (Syn et al. 2017) | ||
| Antibiotics | Azithromycin | Macrolide | Antiviral and anti-inflammatory effects |
| Neutralizing monoclonal antibody | CR3022 | Research statement | Inhibits receptor-binding domain (RBD) of S1 subunit of viral spike glycoprotein (Tian et al. 2020) |
| Meplazumab | Anti-asthma | A monoclonal antibody against CD147 and inhibit the interaction of CD147 with spike protein of SARS-CoV2 | |
| Immunoglobulins | Human gamma globulin | Immunoglobulins | Improving passive immunity and modulating immune inflammation (Cao et al. 2020b; Zhang et al. 2020b). |
| Convalescent plasma | Research statement |
Contains neutralizing antibodies that suppress viremia acceleration of infected cell clearance (Chen et al. 2020) |
|
| Interferons | IFN β | Interferon type 1 | immunomodulatory cytokines (Lin and Young 2014) |
| IFN α -2a | |||
| IFN α | |||
| Cytokine storm inhibitors | Baricitinib | Disease-modifying anti-rheumatic drugs | Janus kinase (GAK) inhibitor that inhibits clathrin-mediated endocytosis, cytokine release, and inflammation (Richardson et al. 2020). |
| Tocilizumab | Monoclonal antibody targeting IL-6 (Zhang et al. 2020a) | ||
| Siltuximab | Antineoplastic | Monoclonal antibody targeting IL-6 (Gritti et al. 2020) | |
| CVL218 | Research statement | Poly-ADP-ribose polymerase 1 (PARP1) inhibition (Ge et al. 2020) |
Montelukast, deoxyrhapontin, polydatin, chalcone, disulfiram, carmofur, shikonin, ebselen, tideglusib, PX-12, TDZD-8, cyclosporin A, and cinanserin (Jin et al. 2020) are the other proposed agents against COVID-19 that are not included in the text and this table
ACE2, angiotensin-converting enzyme 2; dGTP, deoxyguanosine triphosphate
abased on www.medscape.com, April 2020; www.uptodate.com, March 5, 2020, and mentioned references