2,6-Bis-arylmethyloxy-5-hydroxychromones |
Aryl diketoacids |
Not available |
SARS-Cov, HCV |
Inhibits ATPase and helicase activities |
Preclinical |
Kim et al. (2011) |
6′-Fluorinated-Aristeromycin Analogs |
Nucleoside analogs |
C11H15N5O3 (Aristeromycin) |
SARS-CoV, MERS-CoV, CHIKV, ZIKV |
RdRp and host cell SAH hydrolase inhibitors |
Preclinical studies |
Yoon et al. (2019) |
Abacavir |
Nucleoside analog |
C14H18N6O |
HIV |
Reverse transcriptase inhibitor |
Approved as HIV drug |
Beck et al. (2020) |
Acyclovir |
Doubly flexible synthetic nucleoside analogue |
C8H11N5O3
|
HSV, HCoV-NL63, MERS-CoV |
RNA polymerase inhibitor (RdRp) |
Preclinical studies |
Beck et al. (2020) |
Alisporivir |
Cyclosporin A-analog |
C63H113N11O12
|
HCV, HIV, SARS-CoV, MERS-CoV |
Non-immunosuppressive, Cyclophilin inhibitor |
HCV infection in phase III clinical trial (NCT01860326) |
de Wilde et al. (2017) |
Umifenovir (Arbidol) |
Indole derivative |
C22H25BrN2O3S |
SARS-CoV-2; SARS-CoV, Influenza virus |
Block viral fusion and replication |
Approved for influenza. Phase 4 for 2019-nCoV, (NCT04260594) |
Zhang and Liu (2020) |
Aryl diketoacids |
Enoic acids |
C10H8O4
|
HIV, SARS-Cov, HCV |
NTPase/helicase inhibitors, RdRp inhibitors |
Inhibit HIV-1 and HCV Preclinical |
Kim et al. (2011) |
ASC09F |
Not available |
Not available |
HIV, SARS-CoV-2 |
Inhibits 3CLpro |
Phase 3 for 2019-nCoV, ASC09F/oseltamivir (NCT04261270) |
Li and De Clercq (2020) |
Asunaprevir (BMS-650032) |
Oligopeptide |
C35H46ClN5O9S |
HCV |
NS3 protease inhibitor |
Approved for HCV, Phase III clinical trials |
Beck et al. (2020) |
Atazanavir |
Aza-dipeptide analogue |
C38H52N6O7
|
HIV, HBV, HCV, SARS-CoV-2 |
Protease inhibitor, inhibits 3CLpro |
Treat infection of HIV. Preclinical for 2019-nCoV |
Beck et al. (2020) |
Bevacizumab (Avastin) |
Immunoglobulin G 1 |
C6638H10160N1720O2108S44
|
SARS-CoV-2 |
VEGF inhibitor |
Approved in clinical oncotherapy Promising drug for COVID-19. Phase 2/3 trials (NCT04275414) |
Pang et al. (2021) |
Carmofur |
Pyrimidine analogue |
C11H16FN3O3
|
SARS-CoV-2 |
Inhibits THE protease (Mpro) |
Induce leukoencephalopathy |
Jin et al. (2020) |
Chloroquine |
Aminoquinoline |
C18H26ClN3
|
Broad spectrum: HCoV-229E HCoV-OC43, HIV, Ebola, SARS-CoV, MERS-CoV, SARS-CoV-2 |
S protein ACE2 inhibitor, Endosomal acidification |
Approved for malaria. Open-label trial for 2019-nCoV (ChiCTR2000029609) |
(Zhang and Liu, 2020; Zumla et al., 2016) |
Chloroquine Phosphate |
Phosphate salt of chloroquine |
C18H32ClN3O8P2
|
SARS-CoV-2 |
Inhibits autophagy and toll-like receptors (TLRs) |
An antimalarial drug, FDA approved drug for COVID. |
(Zhang and Liu, 2020; Zumla et al., 2016) |
Hydroxychloroquine |
Derivative of chloroquine |
C18H26ClN3O |
SARS-CoV, MERS-CoV, SARS-CoV-2 |
Antiparasitic agent |
Used to treat autoimmune disease, antimalarial |
Dyall et al. (2014) |
Triflupromazine (1), Fluphenazine (2), Promethazine (3) |
Phenothiazine derivative |
(1). C18H19F3N2S (2). C22H26F3N3OS (3). C17H20N2S |
SARS-CoV, MERS-CoV |
Antipsychotic that shows clathrin-mediated endocytosis |
First two approved as antipsychotic agents |
Li and De Clercq (2020) |
Chlorpromazine |
Phenothiazine |
C17H19ClN2S |
SARS-CoV, MERS-CoV, HCV |
An antipsychotic affects the assembly of clathrin-coated pits at the plasma membrane |
Approved as antipsychotic agents |
Zumla et al. (2016) |
Cobicistat (GS-9350) |
Monocarboxylic acid amide |
C40H53N7O5S2
|
HIV, SARS-CoV-2 |
Protease inhibitor, inhibits 3CLpro |
Approved for HIV and clinical trial at phase 3 for 2019-nCoV |
Li and De Clercq (2020) |
Compound 6 |
Pyrimidine derivative |
C12H14CIN3O3S |
MERS-CoV |
Inhibits papain-like protease |
Preclinical |
Lee et al. (2019) |
Cyclosporine A |
Cyclic non-ribosomal peptide |
C62H111N11O12
|
SARS-CoV, MERS-CoV, HIV, HCV |
Binds to nucleocapsid protein (NP), inhibits viral replication |
Approved as immunosuppressive drug in organ transplantation |
Zhang and Liu (2020) |
Darunavir |
Furofuran |
C27H37N3O7S |
HIV, SARS-CoV-2 |
Protease inhibitor, inhibits 3CLpro |
Approved for HIV and clinical trial at phase 3 for 2019-nCoV |
Li and De Clercq (2020) |
Disulfiram |
Carbamoyl derivative |
C10H20N2S4
|
MERS-CoV, SARS-CoV |
Papain-like protease inhibitor |
Approved for treat chronic alcoholism |
Lin et al. (2018) |
Dolutegravir |
Monocarboxylic acid amide |
C20H19F2N3O5
|
HIV, SARS-CoV-2 |
Second-generation integrase inhibitor |
Approved for HIV and Preclinical for 2019-nCoV |
Beck et al. (2020) |
Ebselen (SPI-1005) |
Organoselenium compound |
C13H9NOSe |
HIV, SARS-CoV-2 |
Potently inhibits Mpro and viral replication |
Used to treat Diabetes Mellitus |
Jin et al. (2020) |
Efavirenz |
Non-nucleoside |
C14H9ClF3NO2
|
HIV, SARS-CoV-2 |
Reverse transcriptase (RT) inhibitor, 3CLpro inhibitor |
Approved for HIV and Preclinical for 2019-nCoV |
Beck et al. (2020) |
Entecavir |
Guanosine nucleoside analogue |
C12H15N5O3
|
HBV, SARS-CoV-2 |
inhibits the reverse transcriptase (RT) viral RNA-dependent HBV DNA polymerase |
Approved for HBV and Preclinical for 2019-nCoV |
Beck et al. (2020) |
Favipiravir (T-705) |
Pyrazine carboxamide |
C5H4FN3O2
|
Influenza, SARS-CoV-2 |
RNA polymerase inhibitor (RdRp) |
Approved as influenza drug in Japan. China approved for 2019-nCoV |
Zhang and Liu (2020) |
Fingolimod (FTY720) |
Aminodiol |
C19H33NO2
|
2019-nCoV |
Sphingosine-1-phosphate receptor agonist and a CB1 receptor antagonist |
Approved for treatment of relapsing forms of multiple sclerosis. Phase 2 for 2019-nCoV, NCT04280588. |
Wang (2020) |
Galidesivir (BCX4430) |
Adenosine analog |
C11H15N5O3
|
SARS-CoV, MERS-CoV, IAV, Ebola |
RNA polymerase inhibitor (RdRp) |
Clinical trials as Phase 1 for yellow fever and Phase 1 for Marburg virus |
Warren et al. (2014) |
GC376 |
Bisulfite adduct |
C21H30N3NaO6S |
TGEV, FIPV and PTV, MERS-CoV, SARS-CoV |
Inhibits 3CLpro, Inhibits the replication of viruses |
Preclinical studies |
Kim et al. (2012) |
GC813 |
Pyrrolidinone based peptide |
C22H31ClN3NaO8S |
MERS-CoV |
Inhibits 3CLpro |
Preclinical studies |
Pillaiyar et al. (2020) |
Imatinib |
Benzamide |
C29H31N7O |
SARS-CoV, MERS-CoV |
Abelson tyrosine-protein kinase 2 (Abl2) inhibitor |
Approved for cancer |
Coleman et al. (2016) |
Trametinib |
Pyridopyrimidine |
C26H23FIN5O4
|
MERS-CoV, SARS-CoV |
Inhibits the ERK/MAPK and PI3K/AKT/mTOR signalling pathways |
Approved for cancer treatment |
Li and De Clercq (2020) |
Dasatinib |
Benzimidazole |
C22H26ClN7O2S |
MERS-CoV, SARS-CoV |
BCR/ABL and Src family tyrosine kinase inhibitor |
Approved for cancer treatment |
Li and De Clercq (2020) |
Selumetinib |
Benzimidazole |
C17H15BrClFN4O3
|
MERS-CoV, SARS-CoV |
Inhibits the ERK/MAPK and PI3K/AKT/mTOR signaling pathways |
Approved for cancer treatment |
Li and De Clercq (2020) |
Rapamycin |
Antibiotic |
C51H79NO13
|
MERS-CoV |
Inhibits the ERK/MAPK and PI3K/AKT/mTOR pathways, block early viral entry and/or post-entry |
Approved as antifungal agent |
Pillaiyar et al. (2020) |
Laninamivir |
Octanoyl ester |
C13H22N4O7
|
Influenza virus A and B |
Neuraminidase inhibitor |
Approved as influenza A and B drug |
Samson et al. (2014) |
Loperamide |
Phenyl-butanamide |
C29H33ClN2O2
|
MERS-CoV, SARS-CoV, HCoV-229E |
Inhibits viral replication. Opioid receptor binding |
Approved as synthetic antidiarrheal agent |
de Wilde et al. (2014) |
Lopinavir |
Dicarboxylic acid amide |
C37H48N4O5
|
HIV, HPV, HCoV-229E, MERS-CoV, SARS-CoV, SARS-CoV-2 |
Protease inhibitor, inhibits 3CLpro |
Approved for HIV, Phase 3 for 2019-nCoV, Phase 2/3 for MERS |
(Chu, 2004; Li and De Clercq, 2020) |
Methylprednisolone |
Corticosteroid |
C22H30O5
|
MERS-CoV, SARS-CoV |
Protease Inhibitor |
Treat arthritis and severe allergic reactions. Randomized trial for 2019-nCoV, NCT04323592
|
(Huang et al., 2020; Pillaiyar et al., 2020) |
Mucroporin-M1 |
Scorpion venom-derived peptide |
Not available |
HBV, H5N1, SARS-CoV |
Inhibiting viral replication |
Drug design to target COVID-19 |
Zhang and Liu (2020) |
Mycophenolic acid |
Antibiotic |
C17H20O6
|
MERS-CoV, HBV, HCV |
Inhibits viral replication, Inhibits IMPDH and guanine monophosphate synthesis |
Approved as immunosuppressant during organ transplantation |
Hart et al. (2014) |
Nafamostat |
Synthetic p-Guanidinobenzoic acid ester |
C19H17N5O2
|
SARS-CoV-2, MERS-CoV |
Serine protease inhibitor, Inhibits spike-mediated membrane fusion |
Approved as an anticoagulant therapy |
Li and De Clercq (2020) |
Nelfinavir |
Aryl sulfide |
C32H45N3O4S |
HIV, HBV, HCV, SARS-CoV |
Protease inhibitor |
Responsible for post-translational in HIV propeptides. Preclinical trials for 2019-nCoV |
Zhang and Liu (2020) |
Neuraminidase inhibitor analogs (compound 3k) |
Chlorobenzoic acid derivatives |
Not available |
SARS-CoV, MERS-CoV |
3CL protease inhibitor |
Preclinical |
Kumar et al. (2016) |
Niclosamide |
Benzamide |
C13H8Cl2N2O4
|
SARS-CoV |
ACE2 inhibitor, Inhibit replication of virus |
Antihelminthic drug Inhibits IFV-A in A549 cells. |
Li et al. (2019) |
Nicotianamine |
Metal ligand |
C12H21N3O6
|
SARS-CoV-2 |
S protein and ACE2 inhibitor |
Preclinical |
Zhang and Liu (2020) |
Oseltamivir |
Ethyl ester of oseltamivir acid |
C16H28N2O4
|
SARS-CoV-2; Influenza virus |
Influenza neuraminidase inhibitor |
Approved for influenza, Phase 3 and 4 for 2019-nCoV, NCT04261270
|
Lu (2020) |
Penciclovir |
Nucleoside analogue |
C10H15N5O3
|
HCV, SARS-CoV-2 |
RNA polymerase inhibitor (RdRp) |
Approved for HSV. Randomized trial for 2019-nCoV |
(M. Wang et al., 2020) |
Peptidomimetic inhibitors (Compound 6) |
Aldehyde derivatives |
Not available |
MERS-CoV, SARS-CoV |
3CL protease inhibitor |
Preclinical |
Kumar et al. (2016) |
Peramivir |
Cyclopentane derivative |
C15H28N4O4
|
Influenza A and B |
Neuraminidase inhibitor |
Approved as influenza A and B drug |
(De Clercq and Li, 2016; Lu, 2020) |
Promazine |
Phenothiazine derivative |
C17H20N2S |
SARS-CoV |
Blocking the interaction of S protein and ACE2 |
Alternative for the treatment of COVID-19 |
Zhang and Liu (2020) |
Pyrithiobac derivatives (6-5) |
Benzoic acids |
C13H11ClN2O4S (Pyrithiobac) |
SARS-CoV, |
3CL protease inhibitor |
Preclinical |
Wu et al. (2019) |
Remdesivir (GS-5734) |
Nucleoside analogue |
C27H35N6O8P |
Ebola, MERS-CoV, SARS-CoV, SARS-CoV-2 |
RNA polymerase inhibitor (RdRp) |
Randomized trials for SARS-CoV-2 |
(Sheahan et al., 2020a; M. Wang et al., 2020) |
Ribavirin |
Nucleoside analogue |
C8H12N4O5
|
HCV, RSV, MERS-CoV, SARS-CoV, SARS-CoV-2 |
Inhibits viral RNA replication and mRNA capping |
Approved for HCV and RSV. Randomized trials for SARS and SARS-CoV-2 |
(Chan et al., 2013; Lu, 2020) |
Ritonavir |
L-valine derivative |
C37H48N6O5S2
|
HIV, MERS-CoV, SARS-CoV-2 |
Protease inhibitor, inhibits 3CLpro |
Approved for HIV, Phase 3 for SARS-CoV-2, Phase 2/3 for MERS |
(Chu, 2004; Li and De Clercq, 2020) |
SK80 |
Phenylisoserine derivative |
C31H32N2O4
|
SARS-CoV |
3CL protease inhibitor |
Preclinical |
Konno et al. (2017) |
SSYA10-001 |
Triazole derivative |
C12H12N4O2S2
|
SARS-CoV, MERS-CoV, MHV |
Inhibits helicase without affecting ATPase activity |
Preclinical |
Adedeji et al. (2014) |
Losartan (Cozaar) |
Monopotassium salt |
C22H23ClN6O |
MERS-CoV, SARS-CoV, SARS-CoV-2 |
Angiotensin-receptor blocker |
Phase 2 for SARS-CoV-2 (NCT04312009) |
(Yan et al., 2020.) |
Verdinexor (KPT-335) |
Synthesized chemical compound |
C18H12F6N6O |
Influenza A and B virus, Respiratory syncytial virus (RSV) |
Blocking XPO1-mediated nuclear export of viral ribonucleoprotein complexes |
Inhibitor of Nuclear Export, Under clinical trial FOR Influenza (NCT02431364) |
Perwitasari et al. (2014) |
Zanamivir |
Sialic acid-analogue |
C12H20N4O7
|
Influenza virus |
Neuraminidase inhibitor |
Approved for influenza virus |
Lu (2020) |
Gemcitabine hydrochloride |
Deoxycytidine analog |
C9H12ClF2N3O4
|
MERS-CoV, SARS-CoV nfluenza virus |
DNA metabolism inhibitor, Inhibiting pyrimidine biosynthesis |
FDA-approved anticancer agent |
(Li et al., 2019; Pillaiyar et al., 2020) |
Amodiaquine |
Quinoline derivative |
C20H22ClN3O |
MERS-CoV, SARS-CoV, Ebola, ZIKA virus |
Targets early events of the viral replication cycle |
Approved as antimalarial drug |
(Dyall et al., 2014; Li and De Clercq, 2020) |
Mefloquine |
Quinoline derivative |
C17H16F6N2O |
MERS-CoV, SARS-CoV |
Targets early events of the viral replication cycle |
Approved as antimalarial drug |
(Dyall et al., 2014; Li and De Clercq, 2020) |
Dihydroartemisinin |
Sesquiterpene lactone |
C15H24O5
|
HIV, HCMV, HBV, influenza virus A |
Inhibits replication of virion |
Used as antimalarial and anticancer agent |
Krishna et al. (2008) |
E-64-D (Aloxistatin) |
L-leucine derivative |
C17H30N2O5
|
MERS-CoV, SARS-CoV |
Cathepsin protease inhibitor |
Inhibit calpain activity in intact platelets. |
Dyall et al. (2014) |
Recombinant interferons |
Signalling proteins |
Not available |
SARS-CoV-2; SARS-CoV; MERS-CoV |
Interferon response, Inhibiting the viral protein synthesis, disables viral replication |
Approved for melanoma (IFN-α2b), metastatic renal cell carcinoma (IFN-α2a), multiple sclerosis (IFN- β1a, 1b), chronic granulomatous disease (IFN-γ) |
Li and De Clercq (2020) |
SAB-301 |
Polyclonal antibody |
Not available |
MERS-CoV |
Prevent the virus from infecting and entering cells |
Phase 2/3 trial for MERS endemic in Kingdom of Saudi Arabia |
Beigel et al. (2018) |
REGN3048 and REGN 3051 |
Monoclonal antibodies |
Not available |
MERS-CoV |
Prevent the virus replication in cell |
Phase 1 trial for MERS-CoV (NCT03301090) |
de Wit et al. (2018) |
Nitazoxanide |
Thiazolides |
C12H9N3O5S |
Influenza viruses, HBV, HCV, HIV, SARS-CoV, MERS-CoV, SARS-CoV-2 |
Interferon response in host cell |
Approved for Diarrhea treatment. Phase III clinical development for Influenza virus -A and B strains |
(Li et al., 2019; Pillaiyar et al., 2020) |
Saracatinib |
Anilinoquinazoline |
C27H32ClN5O5
|
MERS-CoV |
Suppression of the SFK signalling pathways, Inhibits viral replication |
Approved for treating cancers |
Pillaiyar et al. (2020) |
Camostat |
Benzoic acid derivative |
C20H22N4O5
|
SARS-CoV MERS-CoV HCoV-229E |
Cysteine protease inhibitor, blocks endosomal protease mediated cleavage and the endosomal entry pathway |
Preclinical |
(Pillaiyar et al., 2020; Zumla et al., 2016) |
K11777 |
Piperazine derivative |
C32H38N4O4S |
SARS-CoV MERS-CoV HCoV-229E Ebola |
Cysteine protease inhibitor, targeting endosomal proteases involved in viral entry |
Preclinical |
Zhou et al. (2015) |
Nafamostat |
Benzoic acids derivative |
C19H17N5O2
|
SARS-CoV Influnza-A MERS-CoV |
Serine protease inhibitor |
FDA-approved to treat pancreatitis, approved as an anticoagulant therapy |
Li et al. (2019) |
K22 |
Benzamide |
C27H25BrN2O3
|
SARS-CoV, MERS-CoV, HCoV-229E |
Inhibits membrane-bound RNA synthesis and membrane vesicle formation |
Preclinical |
Lundin et al. (2014) |
Teicoplanin derivatives |
Glycopeptide antibiotic |
C80H81Cl2N9O33
|
Broad-spectrum (influenza virus, HCoV, Ebola, HIV, HCV) |
Inhibits peptidoglycan polymerization |
Effective drug against gram-positive infections |
(Li and De Clercq, 2020; Szűcs et al., 2018) |
FA-613 |
Carboxylic acid |
C18H14BrNO3
|
Influenza A and B, RSV, HCoV) SARS-CoV, MERS-CoV |
Inhibits DHODH, interferes intracellular pyrimidine synthesis pathways |
Preclinical |
(Cheung et al., 2017; Li and De Clercq, 2020) |
Convalescent plasma |
Immunoglobulins |
Not available |
SARS-CoV-2, SARS-CoV, MERS-CoV, influenza |
Inhibits virus entry to the target cells |
Phase 2 (NCT02190799) |
(Chen et al., 2020; Li and De Clercq, 2020) |
Mycophenolate mofetil |
Ester of mycophenolic acid |
C23H31NO7
|
HCoV-OC43, HCoV-NL63, MERS-CoV MHV-A59 |
Inhibits viral replication |
Approved as immunosuppressant |
Shen et al. (2019) |
Monensin sodium |
Antibiotic salt |
C36H61NaO11
|
MERS-CoV, HCoV-OC43, and HCov-NL63 |
Inhibits viral replication |
Antibacterial drug |
Shen et al. (2019) |
Phenazopyridine |
Pyridine derivative |
C11H12ClN5
|
MERS-CoV, HCoV-OC43, and HCov-NL63 |
Inhibits viral replication |
Urinary tract analgesic, Removed by FDA |
Shen et al. (2019) |
Pyrvinium pamoate |
Quinoline derivative |
C49H43N3O6
|
MERS-CoV, HCoV-OC43, and HCov-NL63 |
Inhibits viral replication |
DA-approved antihelmintic drug, inhibits WNT pathway signaling. |
Shen et al. (2019) |
Hexamethylene amiloride |
Pyrazines |
C12H18ClN7O |
SARS-CoV, HCoV-229E, and some animal CoVs |
Viroporin inhibitor that inhibits the ion channel activity of CoV E |
Preclinical |
Zumla et al. (2016) |
Indomethacin |
Indole derivative |
C19H16ClNO4
|
SARS-CoV |
COX1 and COX2 inhibitor, Blocking viral RNA synthesis |
Approved as anti-Inflammatory, used to treat gout |
Amici et al. (2006) |
Azithromycin |
Azalide |
C38H72N2O12
|
Zika, Ebola, SARS-CoV-2 |
Inhibit replication of virus |
Approved as antibiotic |
Gautret et al. (2020) |
Tocilizumab |
Monoclonal antibody |
C6428H9976N1720O2018S42
|
SARS-CoV-2 |
Treatment of cytokine storms induced by COVID-19 |
Phase III clinical development for COVID-19, NCT04361552
|
Luo et al. (2020) |
EIDD-2801 |
Prodrug of NHC |
C13H19N3O7
|
SARS-CoV-2, MERS-CoV, SARS-CoV |
Inhibit replication of virus |
Preclinical |
Sheahan et al. (2020b) |
β-D-N4 hydroxycytidine (NHC, EIDD-1931) |
Ribonucleoside analog |
C9H13N3O6
|
Influenza, Ebola, SARS-CoV-2, MERS-CoV, SARS-CoV |
Inhibit replication of virus |
Preclinical |
Sheahan et al. (2020b) |
Bromhexine hydrochloride |
Hydrochloride |
C14H21Br2ClN2
|
Influenza, SARS-CoV-2 |
Inhibit transmembrane serine protease 2 |
Mucolytic and prophylactic drug |
Habtemariam et al. (2020) |
Triazavirin |
Guanine nucleotide |
C5H4N6O3S |
SARS-CoV-2, H5N1, Ebola |
RNA polymerase inhibitor |
Antiviral drug |
Shahab and Sheikhi (2020) |
Carfilzomib |
Epoxomicin derivate |
C40H57N5O7
|
SARS-CoV-2 |
Protease inhibitor |
Approved anticancer drug |
Wang (2020) |
Eravacycline |
Antibiotic |
C27H31FN4O8
|
SARS-CoV-2 |
Protease inhibitor |
Broad spectrum antibacterial |
Wang (2020) |
Ruxolitinib |
Pyrazole |
C17H18N6
|
SARS-CoV-2 |
JAK inhibitor |
Anti-arthritic drugs |
Stebbing et al. (2020) |
Fedratinib |
Anilinopyrimidine derivative |
C27H36N6O3S |
SARS-CoV-2 |
JAK inhibitor |
Anti-arthritic drugs |
Stebbing et al. (2020) |
Baricitinib (Olumiant) |
Pyrazole |
C16H17N7O2S |
SARS-CoV-2 |
JAK and NAK inhibitor |
Anti-arthritic drugs |
Stebbing et al. (2020) |
Pirfenidone |
Pyridinone derivative |
C12H11NO
|
SARS-CoV-2 |
Inhibits DNA synthesis |
Antifibrotic agent, phase 3 for COVID-19 NCT04282902
|
(Su et al., 2020) |
Nintedanib |
Indolinone derivative |
C31H33N5O4
|
SARS-CoV-2 |
Kinase inhibitor |
Antifibrotic agent, phase 2 for COVID-19 NCT04338802
|
(Su et al., 2020) |
Sofosbuvir |
Nucleoside analogue |
C22H29FN3O9P |
Hepatitis C SARS-CoV-2 |
Bind to RdRp, Inhibits RNA synthesis |
Preclinical |
Shah et al. (2020) |
Tenofovir |
Acyclic nucleotide analogue of adenosine |
C9H14N5O4P |
HIV, HBV, SARS-CoV-2 |
Bind to RdRp, Inhibits reverse transcriptase |
Preclinical |
Shah et al. (2020) |
Tideglusib |
Thiadiazolidinone |
C19H14N2O2S |
SARS-CoV-2 |
non-ATP competitive inhibitor of glycogen synthase kinase 3, inhibits Mpro
|
Potent anti-inflammatory and neuroprotective |
Jin et al. (2020) |
Azvudine |
Cystidine analogue |
C9H11FN6O4
|
HIV, SARS-CoV-2 |
Reverse transcriptase inhibitor |
Clinical trial for COVID ChiCTR2000029853 |
Zhai et al. (2020) |
Danoprevir (R7227) |
Macrocyclic peptidomer |
C35H46FN5O9S |
HCV, SARS-CoV-2 |
Protease inhibitor |
Antiviral agent, phase 2 for COVID-19 NCT04338802NCT04291729 |
Shah et al. (2020) |
Baloxavir marboxil |
Synthesized compound |
C27H23F2N3O7S |
Influenza |
Inhibits mRNA and protein synthesis |
ChiCTR2000029544 |
Li and De Clercq (2020) |
Ciclesonide |
Glucocorticoid |
C32H44O7
|
SARS-CoV-2 |
Inhibits virus replication |
Treat obstructive airway diseases, under clinical trial for COVID -19 NCT04330586
|
Iwabuchi et al. (2020) |
Paritaprevir (ABT-450) |
Synthesized compound |
C40H43N7O7S |
HCV, SARS-CoV-2 |
Protease inhibitor |
Preclinical |
Shah et al. (2020) |
Amprenavir |
Derivative of hydroxyethylamine sulfonamide |
C25H35N3O6S |
HIV-1, SARS-CoV-2 |
Protease inhibitor |
Preclinical |
Wu et al. (2020) |
Adefovir |
Acyclic nucleotide analogue of adenosine |
C8H12N5O4P |
HIV, HBV, SARS- CoV |
Reverse transcriptase and Protease inhibitor |
Preclinical |
Shah et al. (2020) |
Ivermectin |
Macrocyclic lactone |
C48H74O14
|
Flavivirus, HIV, dengue, influenza, SARS-CoV-2 |
Inhibit the non-structural 3 (NS3) helicase |
FDA-approved broad-spectrum anti-parasitic drug. |
Kumar et al. (2020) |
Artesunate |
Semi-synthetic derivative artemisinin |
C19H28O8
|
Hepatitis, HCMV, SARS-CoV-2 |
Inhibit NF-kB (Nuclear Factor kappa B) |
Antimalarial drug |
Uzun and Toptas (2020) |
Dexamethasone |
Corticosteroid |
C22H29FO5
|
SARS-CoV-2 |
Potent anti-inflammatory drug treat arthritis |
Phase 6 clinical trial for COVID-19, NCT04325061
|
Villar et al. (2020) |
Siltuximab |
Monoclonal antibody |
C6450H9932N1688O2016S50
|
HIV, SARS-CoV-2 |
Interleukin-6 Inhibitors |
Phase 3 clinical trial for COVID-19 NCT04330638
|
Saini et al. (2020) |
Hydrocortisone |
Corticosteroid |
C21H30O5
|
SARS-CoV-2 |
Anti-inflammatory and immunosuppressive, |
Phase 3 clinical trials, NCT04348305
|
Saini et al. (2020) |
Boceprevir |
Synthetic tripeptide |
C27H45N5O5
|
HCV, SARS-CoV-2 |
Inhibits protease and viral replication |
Approved as antiviral agent |
Ma et al. (2020) |
GC-376 |
Synthetic compound |
C21H30N3NaO8S |
SARS, MERS, SARS-CoV-2 |
3C-like protease inhibitor |
Treatment for feline infectious peritonitis |
Ma et al. (2020) |
Thalidomide |
Synthetic derivative of glutamic acid |
C13H10N2O4
|
H1N1, SARS-CoV-2 |
Inhibits virus replication |
Phase 2 clinical trial for COVID-19, NCT04273529
|
Saini et al. (2020) |
Lenalidomide (Revlimid) |
Thalidomide analog |
C13H13N3O3
|
SARS-CoV-2 |
Inhibits virus replication |
Phase 4 clinical trial for COVID-19, NCT04361643
|
Saini et al. (2020) |
Acalabrutinib |
Synthetic compound |
C26H23N7O2
|
SARS-CoV-2 |
Inhibitor of Bruton's tyrosine kinase (BTK), and viral replication |
Phase 2 clinical trial for COVID-19, NCT03863184
|
Saini et al. (2020) |
Duvelisib |
Synthetic compound |
C22H17ClN6O |
HIV, hepatitis B, and C SARS-CoV-2 |
Inhibitor of phosphatidylinositol 3-kinase (PI3K) and viral replication |
Phase 2 clinical trial for COVID-19, NCT04372602
|
Saini et al. (2020) |
ML188 |
Acetamide |
C₂₆H₃₁N₃O₃ |
SARS-CoV, SARS-CoV-2 |
3CLpro inhibitor |
Noncovalent small molecule inhibitor |
(Loffredo et al., 2021) |
Famotidine |
Propanimidamide |
C8H15N7O2S3
|
SARS-CoV-2 |
Protease inhibitor |
Histamine H2-receptor antagonist |
(Loffredo et al., 2021) |
Tilorone |
Fluoren-9-ones |
C25H34N2O3
|
MERS-CoV, Ebola |
Inhibit viral replication |
Broad-spectrum antiviral and immunomodulator |
Ekins and Madrid (2020) |