Skip to main content

Table 3 Antiviral Drugs or Compounds against Viruses have Similarities in the Type/Group, Genomic Composition, and Structure of SARS-CoV-2

From: Recent progress on drugs discovery study for treatment of COVID-19: repurposing existing drugs and current natural bioactive molecules

Viruses

Compounds

Plant Sources

Assays

Activities

Refs.

Human coronavirus type

 Human coronavirus strains OC43 (HCoV-OC43)

Tetrandrine (TET)

Fangchinoline (FAN)

Cepharanthine (CEP)

Stephania tetrandra

In vitro: in MRC-5 cells

IC50 of TET = 0.33 ± 0.03 μM; FAN = 1.01 ± 0.07 μM; CEP = 0.83 ± 0.07 μM

[91]

 HCoV-OC43

MERS-CoV

HCoV-NL63

MHV-A59

Lycorine (standard)

Amaryllidaceae

In vitro: in BHK-21, Vero E6, LLC-MK2, DBT cells

In vivo: in mice against HCoV-OC43

EC50 = 0.15 – 1.63 μM

[78]

  Coronavirus MHV-A59

Essential oils of the ethanol extracts (Ah extract) containing carvacrol (38.4%) and α-pinene (30.9%)

Anthemis hyaline (Ah)

In vitro using quantitative analysis by enzyme-linked immunosorbent assay (ELISA) in HeLa-CEACAM1a cells

After 6 and 8 h post infections, no detected virus was evaluated with TCID50 values at 1/10 dilution of Ah extracts

[79]

 HCoV-229E

Saikosaponin B2

Bupleurum spp., Heteromorpha spp., Scrophularia scorodonia

In vitro using XTT assay

IC50 = 1.7 ± 0.1 μmol/L

[92, 93]

Genomic similarities

 SARS-CoV strains 39,849

Baicalin

Scutellaria baicalensis (Huang Qin)

In vitro antiviral susceptibility testing on fRhK4 and Vero-E6 cell lines

EC50 in fRhK4 and Vero-E6 cell lines = 12.5 and 100 μg/mL at 48 h

[94]

 Recombinant SARS-CoV PLpro

Papyriflavonol A (prenylated quercetin derivative)

Broussonetia papyrifera (dried roots)

In vitro using viral protease inhibition assay on SARS-CoV based on the FRET method

IC50 = 3.7 μM

[80]

 MERS-CoV

Resveratrol

Vitis vinifera (grape), Polygonum cuspidatum (Huzhang), Vaccinium macrocarpon (cranberry)

In vitro using MTT assay, NRU (neural red uptake) assay, and plaque reduction assay in Vero E6 cells

Resveratrol reduced cell death in a range concentration of 250–125 μM for 48 h after infection

[81]

 SARS-CoV 3CLpro

Curcumin

 

In vitro using FRET method

IC50 40 μM

[95]

 SARS-CoV 3CLpro

Savinin

Chamaceyparis obtusa var. formosana

In vitro using FRET method

IC50 25 μM

Ki = 9.1 ± 2.4 μM

[95]

 SARS-CoV 3CLpro and PLpro

Xanthoangelol E

Angelica keiskei (Miq.) Koidz (ethanolic leaf extract)

In vitro using cell-free based assay

IC50 of 11.4 and 1.2 μM

[82]

 SARS-CoV PLpro

Coumestrol, isobavachalcone, and psoralidin

Psoralea corylifolia L. (ethanol extract of the seeds)

In vitro using the fluorogenic substrate Ub-AMC

IC50 of 4.2; 7.3 and 10.1 μM

[96]

 Recombinant SARS-CoV 3CLpro

Dieckol

Ecklonia cava (brown algae)

In vitro using FRET method (for cell-free transcleavage assay) and luciferase activity (for Vero cell-based cis-cleavage assay)

IC50 of trans- and cis- cleavage inhibitory: 2.7 and 68.1 μM, respectively

[83]

Enveloped viruses

  HIV-1

Baicalin and baicalein

Scutellaria baicalensis Georgi

In vitro using ELISA on fresh normal peripheral blood mononuclear cells (PBMC)

IC50 = 0.5 μg/mL

[97]

  HIV-1

Baicalin

Scutellaria baicalensis Georgi

In vitro using quantitative colorimetric assays

IC50 = 4 μM

[98]

 Murine cytomegalovirus (MCV)

Black seed oil (BSO) or habatussaudah

Nigella sativa

In vivo using a viral plaque-forming assay of BALB/c mice spleen and liver

Undetected virus at the ratio of the effector to target cells was 20:1

[99]

 HSV-1 and HSV-2

Ethanol extracts of flower buds of E. caryophyllus containing eugenol

Eugenia caryophyllus (Spreng.) Bullock & S.G. Harrison

In vitro using plaque reduction assay on green monkey kidney (GMK)

ED50 against HSV-1 and HSV-2: 72.8 and 74.4 μg/mL

[84]

 HSV-1

Isoborneol

Salvia fruticosa

In vitro using viral plaque assay on Vero cells

0.1% isoborneol inactivated 86% of the infectious virus within 30 min

[85]

 HSV-1

Star anise oil (SAO) contains trans-anethole (80%), eugenol, b-caryophyllene, eugenol

Illicium verum (star anise)

In vitro using plaque reduction assay

IC50 SAO = 1 ± 0.1 μg/mL

IC50 beta-caryophyllene = 0.25 ± 0.0 μg/mL

[86]

  Hepatitis B Virus (HBV)

Phyacidusin B and phllanthacidoid A1

Phyllantus acidus (stem)

In vitro using the cytopathic end-point assay in HepG2.2.2.15 cells

IC50 of HBsAg is 11.2 ± 0.01 μM by Phyacidusin B and HBeAg is 57.1 ± 0.02 μM by phllanthacidoid

[100]

 HSV-1 (F strain ATCC VR733)

J. oxycedrus berries oil containing α-pinene, β-myrcene

Juniperus oxycedrus ssp.

In vitro, using visually scoring of the virus-induced cytopathogenic effect (CPE) for 72 h post-infection on Vero cells

IC50: 200 μg/mL; SI of 5

[101]

Respiratory diseases

  Influenza virus A/Germany/27, str. Weybrigde (H7N7) and A/Germany/34, str. Rostock (H7N1)

(-)-thalimonine (Thl)

Thalictrum simplex L (aerial parts)

In vitro in cell cultures of chicken embryo fibroblasts

Inhibit viral reproduction at non-toxic concentration 0.1–6.4 μM with a selectivity index = 640

[87]

 Influenza type A (A/Betezda/63/10/H2N2) and type B (B/Lee/40)

Essential oil from fruits containing pinene, limonene, a complex of ethers of octanol and hexanol

Heracleum L species, such as H. aconitifolium Woronow. H. antasiaticum Manden., etc

In vivo using intrasanal and oral treatments on mice

LD50 of 0.2–0.4 mL

[102]

  Influenza A/PR/8/34 (PR8) virus (H1N1 subtype)

Cinnamaldehyde (CA)

Cinnamomi cortex

In vitro using plaque reduction assay on MCDK cells

In vivo based on therapeutic efficacy in mice

CA inhibits all of the virus growth at 200 μM. Application of CA in the airways led to the significant rescue of infected mice

[88]