key: cord-0838363-oimg9zig
authors: Illian, Didi Nurhadi; Siregar, Etti Sartina; Sumaiyah, Sumaiyah; Utomo, Ahmad Rusdan; Nuryawan, Arif; Basyuni, Mohammad
title: Potential compounds from several Indonesian plants to prevent SARS-CoV-2 infection: A mini-review of SARS-CoV-2 therapeutic targets
date: 2021-01-16
journal: Heliyon
DOI: 10.1016/j.heliyon.2021.e06001
sha: 2b1cdf23020d6cc35fb7bebd95fd7376951b3054
doc_id: 838363
cord_uid: oimg9zig

The outbreak of coronaviruses (CoVs) presents an enormous threat to humans. To date, no new therapeutic drugs or vaccines licensed to treat human coronaviruses remain undiscovered. This mini-review briefly reports the number of potential plants widely distributed in Indonesia for further research and development as anti-SARS-CoV-2 agents and the critical targets for SARS-CoV-2 therapy, such as angiotensin-converting enzyme 2 (ACE-2) receptor, spike protein, 3-chymotrypsin-like protease (3CL(pro)), papain-like protease (PL(pro)), RNA-dependent RNA polymerase (RdRp), helicase, and serine protease. Indonesia is rich in medicinal plants (herbal); it also has a long history of using plants to treat various hereditary diseases. However, since SARS-CoV-2 is a new disease, it has no history of plant-based treatment anywhere in the world. This mini-review describes natural products from several Indonesian plants that contain compounds that could potentially prevent or reduce SARS-CoV-2 infection, act as potential targeted therapy, and provide new therapeutic strategies to develop SARS-CoV-2 countermeasures.

CoVs are a family of positive-stranded RNA viruses that cause lifethreatening breathing infections and severe pneumonia in humans (which resulted in a significant epidemic only two decades ago). Presently, three single-stranded RNA (ssRNA) beta-coronaviruses, including SARS (severe acute respiratory syndrome) virus, MERS (Middle East respiratory syndrome) virus, and SARS-CoV-2, have been detected (Masters, 2006; Gorbalenya et al., 2020; Huang et al., 2020) .

The World Health Organization (WHO) designated the coronavirus discovered in 2019 as 2019-novel coronavirus or SARS-CoV-2. It has been reported that SARS-CoV-2 is exceptionally homologous to SARS-CoV. Therefore, SARS-CoV-2 is believed to be a close relative of SARS-CoV. Accordingly, the International Virus Classification Commission (ICTV) identified SARS-CoV-2 as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), and concurrently, the WHO recognized the disease generated by 2019-nCoV as COVID-19 Chen et al., 2020a, b) . At the time this mini-review was written, the number of confirmed cases was 5,488,825, with a mortality rate of 349,095 people in 217 countries or territories (WHO, 2020) .

The Department of Clinical Microbiology, Faculty of Medicine, Universitas Indonesia, conducted a preliminary analysis on COVID-19 cases in Indonesia. The Laboratory of Clinical Microbiology (one of the reference laboratories for COVID-19 specimens) received 4167 specimens from March to April 2020, with 582 specimens showing positive results, indicating that the positivity rate was 12.6%. Demographic data revealed that the average age of COVID-19-positive patients was 44.5 years, with an age range of 2-85 years, and 59% were male. Approximately 17% of patients had comorbidities, predominantly cardiovascular disease (58%) and diabetes (37%). The average age of the COVID-19-positive patients reported in that work was similar to that reported in the Singapore case data (42.5 years) but younger than that reported in Wuhan (55.5 years).

However, the findings that male sex and cardiovascular disease are COVID-19 comorbidities are concordant with previous studies from other countries (Ibrahim et al., 2020) .

Moreover, 8% of the positive patients with COVID-19 were health workers. Another surprising finding was that approximately 22% of COVID-19 patients were asymptomatic, and 34% had mild symptoms, with the remaining 44% exhibiting moderate to serious signs. Although respiratory symptoms are common in patients with COVID-19 (found in 73% of cases), it has been shown that nonspecific symptoms of COVID-19, such as gastrointestinal complaints, lethargy and headaches, cannot be excluded. This fact should definitely be considered due to the transmission risk (Ibrahim et al., 2020) .

SARS-CoV-2 interacts with cell surface receptors named angiotensin converting enzyme 2 (ACE-2) once it enters the cells of humans (Li et al., 2003; Han et al., 2006; Ge et al., 2013) . The penetration of the virus into the human body triggers an immune system reaction with the aim of eliminating the virus. The working immune system consists of various cells, including macrophage cells, neutrophil cells, lymphocytes, dendrite cells, etc., which produce cytokines. These cytokines activate cells and trigger further mechanisms that elicit symptoms of the disease. Example mechanisms in the lungs ( Figure 1 ): S-ACE2 protein binding leads to viral entrytriggers the immune system: (1) Endothelial cell damage occurs, and fluid from the blood vessels enters the alveoli of the lungs, causing symptoms.

(2) The damaged endothelium triggers the coagulation system (blood clotting), and a blood clot can form, which is carried through the bloodstream and causes blockage of the blood vessels. (3) An inflammatory reaction (inflammation) occurs, which induces the production of cytokines and leads to a cytokine storm (Teuwen et al., 2020) .

Example mechanisms in the heart ( Figure 2 ): S-ACE2 protein binding leads to viral entrytriggers the immune system: Cytokines are released by macrophages, causing damage to endothelial cells and pericytes, as well as myocyte damage. The resulting damage can lead to myocarditis, acute coronary syndrome, arrhythmia, and heart failure. The symptoms are the same as those of a heart attack (Guzik et al., 2020) and can be mild, moderate, or severe, depending on the amount of cytokines formed. The more cytokines that are formed, the more severe the symptoms will be (illustration in Figure 3 ) (Zhou et al., 2020a, b) .

There are two therapeutic possibilities for anti-coronavirus therapy (depending on the target): enhancing the human immune system (human cells) and attacking the coronavirus itself. The innate immune response is associated with the human immune system and helps to control the infection by preventing coronavirus replication (Omrani et al., 2014) . If the human cell signaling pathways required for virus replication can be blocked, a certain antiviral effect could be achieved.

Coronavirus therapies include preventing viral RNA synthesis through the use of genetic virus material to prevent replication by acting on critical virus enzymes and preventing the binding of virus to human cells (ACE-2 receptor and spike protein) or inhibiting the process of selfassembly of the virus by acting on certain structural proteins, including viral papain-like protease (PL pro ), main protease (M pro /3CL pro , also recognized 3-chymotrypsin-like protease), RNA-dependent RNA polymerase (RdRp), helicase, and serine protease Clemente et al., 2019; Wu et al., 2020) .

Presently, in silico (computational model) techniques are being used to identify plant compounds that can prevent SARS-CoV-2 infection and replication by predicting their activity against disease targets (Gyebi et al., 2020) . For example, methoxyflavonoid compounds such as hesperetin, tangerine, naringenin, and nobiletin have been identified in oranges (Citrus sp.; fruit and skin) (Singh et al., 2020; Utomo et al., 2020) , and baikalin, scutellarin, glycyrrhizin, rhoifolin, herbacetin, pectolinarin and galangin compounds have been identified in galangal (Alpinia galanga; rhizome) (Tang et al., 2018; Haslberger et al., 2020; Utomo et al., 2020) . The similarity of the SARS-CoV-2 virus gene sequences with SARS-CoV reaches 79.5%, and the similarity in the manner in which the virus enters humans and passes through the ACE-2 receptor suggests common therapeutic targets (Jia et al., 2005; Zhou et al., 2020a, b) . The chemical content (compounds) of some plants has been widely studied, and their activity related to SARS-CoV therapy has been documented, which will speed up evaluations of the activity of these compounds against SARS-CoV-2. Some Indonesian plants contain active compounds that could restrict SARS-CoV-2 infection and replication based on their activity against relevant therapeutic targets. Potentially active compounds have been found in vegetables, crops, and mangroves (Indonesian plants) and show activity (binding) against protein targets such as RBD-S, PD-ACE2, and SARS-CoV-2 protease. These compounds (i.e., hesperidin, flavonoids, curcumin, brazilin, and galangin), show the potential for development as SARS-CoV-2 inhibitors that could be applied in daily life as prophylaxis for COVID-19 (Amin et al., 2019; Azminah et al., 2019; Utomo et al., 2020) .

Data on COVID-19, herbal medicine and dietary therapy were searched and collected for this miniature review and perspective. We used key search engines, namely, Google Scholar, PubMed, Science Direct and SciFinder. The search keywords used comprised coronavirus; etiology; signs; symptoms; allopathic therapy adjacent to COVID-19; immunomodulatory and anti-influenza herbal activity, SARS-CoV-1, and SARS-CoV-2. The authors appraised, evaluated, and interpreted the selected articles. This perspective reflects the opinion of the authors concerning the use of foods and herbs as preventatives and corresponding therapies against COVID-19.

3.1. Angiotensin-converting enzyme 2 (ACE-2) ACE-2 is a receptor that has been confirmed as the entry point for the SARS-CoV-2 virus to infect human cells. Scientists suggest a strong interaction exists between human ACE-2 molecules and SARS-CoV-2 . ACE-2 receptors are widely present in lung cells (especially lung endothelial cells) and in large numbers in type II alveolar cells in the lungs, epithelial cells in the upper esophagus, enterocytes in the ileum (the last part of the small intestine) and colon (large intestine), epithelial cells in the bile, heart muscle cells, proximal tubules in the kidneys, and urothelial cells in the bladder (Zou et al., 2020) , meaning that the SARS CoV-2 virus can attack any organ that has ACE-2 receptors. Symptoms that arise based on the target organ are as follows: in the lungs, it causes shortness-edema-respiratory failure; in the blood, it causes a reduction in the number of blood cells-coagulopathy; in the kidneys, it causes renal failure; and in the heart, it causes tachycardia-arrhythmia and heart failure ( Figure 4 ) (Zhou et al., 2020a, b) . ACE-2 is an integral membrane protein type I with an active site domain uncovered outside the cells and has been described in receptor function studies of SARS-CoV-2 (Kuhn binding between SARS-CoV-2 and ACE-2 in the host cell (Walls et al., 2020) . The interaction of ACE-2 and the viral S-protein enables SARS-CoV-2 to enter the circulation (Belouzard et al., 2009 ). The SARS-CoV-2 receptor-binding domain (RBD) successfully interacts human ACE2-expressing cells but not with any other receptors, ensuring that in the future, human ACE-2 will be required by the newly evolving SARS-CoV-2 for cell entry (Hoffmann et al., 2020; Letko et al., 2020) . This infection risk can be prevented or reduced with plant compounds that can interfere with these interactions. Molecular docking studies have shown that baicalin might bind strongly to the ACE-2 enzyme with an expected ΔG (kcal/mol) of -8.46 and potential binding sites at ASN-149, ARG-273, and HIS-505. These binding sites are situated in the hydrophobic area of ACE-2. Based on the potential binding to ACE-2, it can be suggested that baicalin is a promising candidate for 2019-nCoV treatment. Furthermore, molecular docking found that scutellarin has the potential to bind to ACE-2 with a projected ΔG (kcal/mol) of -14.9 and binding sites at GLU-495, UNK-957, and ARG-482 (Chen and Du, 2020) . The molecular docking studies of hesperidin with the ACE-2 enzyme demonstrated that hesperidin can bind to ACE-2 with a predicted ΔG (kcal/mol) of -8.3 and binding sites at TYR-613, SER-611, ARG-482, and GLU-479 (Chen and Du, 2020) . These results suggest that hesperidin may bind to ACE-2 and thus block 2019-nCoV infection.

A previous study (Takahashi et al., 2015) demonstrated that nicotianamine is a powerful inhibitor of ACE-2, with an IC 50 value of 84 nM. The molecular docking studies of nicotinamine to the ACE-2 enzyme showed that nicotinamine has a promising binding affinity to ACE-2, with an approximate ΔG (kcal/mol) of -5.1 and binding sites at ARG-518, GLU-406, SER-409, GLN-522, and GLN-442. These results indicate that nicotinamine might block 2019-nCoV infection by inhibiting ACE-2 (Chen and Du, 2020). The molecular docking results also showed that glycyrrhizin could bind to ACE-2 with an estimated ΔG (kcal/mol) of -9 and binding sites at ARG-559, GLN-388, ARG-393, and ASP-30. Based on the hydrophobic nature of the ACE-2 binding site, the prediction of the binding site of glycyrrhizin is near this site. GLN-388 and ARG-393 are close to the zinc metallopeptidase that might regulate the activity of ACE-2 in cells (Chen and Du, 2020) . The docking scores of the binding sites between natural compounds and ACE-2 of SARS-CoV-2 are presented in Table 1 . Several edible plants found across Indonesia contain emodin and luteolin compounds, which have the potential to prevent or reduce infection with this virus (Table 2 ). These compounds are capable of preventing interactions between ACE-2 receptors and the S-protein in SARS-CoV (Miean and Mohamed, 2001; Ho et al., 2007) . Edible Indonesian plants, used Several studies have reported several mangrove plants that contain emodin or luteolin, as shown in Table 3 . Two mangrove species, Kandelia candel and Lumnitzera racemosa, have been reported to contain emodin (Wu et al., 2008; Liu et al., 2010) . In Indonesia, K. candel is distributed in northeast Sumatera and west and north Kalimantan, while L. racemosa is widely available throughout Indonesia (Noor et al., 1999) . Indonesia is recognized as the major mangrove area in the world and has vast species diversity (Noor et al., 1999) . Similarly, luteolin is found in Avicennia marina leaves and aerial roots and in mangroves and is associated with Pongamia pinnata leaves and stems (Sharaf et al., 2000; Momtazi-borojeni et al., 2013) . A. marina and P. pinnata are found throughout Indonesia (Noor et al., 1999; Li et al., 2006; Ahmed et al., 2010; Shamsuddin et al., 2013) . This potential of these raw materials opens up several non-wood functions of mangrove plants that can help reduce and prevent SARS-CoV-2 infection.

The coronavirus (CoV) family has an abundance of similar spike proteins. This spike protein (S-protein) interacts with host cells, such as pulmonary and parabronchial epithelial cells, and aids in SARS-CoV-2 infection via the epithelial cell membrane . The surface spike (S) glycoprotein (S-protein) is an essential binding protein for fusion of the virus with the cell membrane of the target cells (host cells) via cellular receptor angiotensin-converting enzyme 2 (ACE-2) (Song et al., 2018) . The S-protein has two main functions: the first is binding to the target cell (host cells), which can be imagined as a key in a lock (it must fit or match), and the second is fusion of the viral membrane with the host cell (human), which allows the virus to enter the target cell. Once in the target cell, the RNA from SARS-CoV-2 can be transferred into the host cell to immediately begin virus propagation (Walls et al., 2020) , and then the virus will multiply (replicate) and be packaged into new viruses. The new copies of the virus will then leave the target cell and look for other target cells ( Figure 5 ) (Risitano et al., 2020) . SARS-CoV-2 is easily transmitted because the S-protein on the virus surface binds quite efficiently to ACE-2 on human cells.

As shown in a previous study of several potentially active compounds, the docking scores of cannabinoids, rhoifolin, pectolinarin, morin, kaempferol, epigallocatechin gallate, herbacetin, and hesperidin against the S-protein were -10.2, -9.5, -9.8, -8.8, -8.5, -9.8, -8.3, and -10.4, respectively (Tallei et al., 2020) . Another investigation showed that hesperidin had a docking score against the S-protein of -9.6 (Utomo et al., 2020) . The docking scores of these natural compounds with the binding sites (protein) of the S-protein of SARS-CoV-2 are shown in Table 4 .

3CL pro is a crucial enzyme for coronavirus replication . 3CL pro mediates Nsps (nonstructural protein) maturation directly, which is significant in the virus life cycle. Investigations into the structure and catalytic mechanism of 3CL pro have made it an enticing target for anti-coronavirus drug development. Peptide and small molecular inhibitors primarily contain inhibitors of SARS-CoV-2 3CL pro (Pillaiyar et al., 2016) .

As presented in a previous study of several potentially active compounds, the best docking scores of cannabinoids, rhoifolin, pectolinarin, morin, kaempferol, epigallocatechin gallate, herbacetin, and hesperidin against 3CL pro were -8, -8.2, -8.2, -7.8, -7.8, -7.8, -7.2, and -8.3, respectively (Tallei et al., 2020) .

Hesperidin was found to dose-dependently inhibit the cleavage activity of the 3-C-like protease (3CL pro ) of SARS coronavirus in cell-free and cell-based assays, with an IC 50 of 8.3 μM (Lin et al., 2005) . A previous study also showed that the docked hesperidin compound against 3CL pro was -13.51 (Utomo et al., 2020) , and according to a previous investigation, the best hesperidin position against SARS-CoV-2 3CL pro had a score of -10.1 (Chen et al., 2020a, b) .

Another investigation reported that the rhoifolin binding score for SARS-CoV 3CL pro was -9.565, and the induced-fit docking result of pectolinarin against SARS-CoV 3CL pro was -8.054. Based on a previous description, the best binding positions against SARS-CoV 3CL pro of morin, kaempferol, and herbacetin had scores of -8.930, -8.526, and -9.263, respectively (Jo et al., 2020) . Epigallocatechin gallate has also been reported to prevent the proteolytic property of SARS-CoV 3CL pro (Nguyen et al., 2012) . The docking scores of the binding sites of natural compounds towards 3CL pro of SARS-CoV-2 are presented in Table 5 . 

The polyproteins of the coronavirus are expressed after the papainlike protease (PL pro ) enzyme plays a critical function in cleaving the polyproteins into fewer products, which are utilized for replicating novel viruses (Wrapp et al., 2020) . PL pro controls the cleavage of the N-terminus of the replicase polyprotein to release Nsp1, Nsp2, and Nsp3, which is indispensable for modulating virus replication (Harcourt et al., 2004) .

The bioactive compounds from natural sources, including platycodin D, baicalin, sugetriol-3,9-diacetate (from Platycodon grandiflorus, Scutellaria baicalensis, Cyperus rotundus, respectively), phaitanthrin D and 2,2di (3-indolyl)-3-indolent from Isatis indigotica, catechin compounds ((e)-epigallocatechin gallate and 2 (3,4-dihydroxy phenyl)-2-[[2-(3,4dihydroxy phenyl)-3,4-dihydro5,7-dihydroxy-2H-1-benzopyran-3-yl] oxy]-3,4-dihydro-2H-1benzopyran-3,4,5,7-tetrol), exhibited strong binding affinity to PL pro protein, illustrating that these compounds could be used for SARS-CoV-2 therapeutics .

Furthermore, the screening results reported in a previous study revealed that a series of drugs, including antivirals (ribavirin, valganciclovir, and thymidine), antibacterials (chloramphenicol, cefamandole, and tigecycline), muscle relaxants (chlorphenesin carbamate), and antitussives (levodropropizine), might all have a high binding affinity to PL pro . According to the docking model results, ribavirin attached to the active site of the enzyme and was described as a SARS-PL pro inhibitor (PDB code 3e9s). The interaction between ribavirin and the enzyme (hydrophobic interaction and strong hydrogen bonding) signifies that it is a potent PL pro inhibitor .

Coronavirus expresses RNA-dependent RNA polymerase (RdRp) to generate the daughter RNA genome, which is an a significant replication step that catalyzes the synthesis of complementary RNA strands utilizing viral RNA templates (Mullard, 2018) . The conserved protein in coronavirus (Nsp12) is an RdRp and the vital enzyme of the coronavirus replication or transcription complex (Subissi et al., 2014) . According to a study on SARS-CoV and MERS-CoV inhibitors, Nsp12-RdRp has been shown to be a pivotal drug target. However, the targeted inhibition of Nsp12-RdRp might not induce significant toxicity and adverse impacts on host cells, and no particular inhibitors have been identified so far (Chu et al., 2006) . Some bioactive compounds from natural sources and derivatives with antiviral, anti-inflammatory, and antitumor activities have revealed major binding affinity to RdRp, including betulonal, 2β,30β-dihydroxy-3,4-seco-friedelolactone-27-lactone, 14-deoxy-11,12-didehydroandrographolide, 1,7-dihydroxy-3-methoxyxanthone, and theaflavin 3,3 0 -di-Ogallate (from Cassine xylocarpa, Andrographis paniculata, Swertia pseudochinensis, and Camellia sinensis, respectively); gnidicin and gniditrin (from Gnidia lamprantha); and andrographolide derivatives . It has been shown that RNA-dependent RNA polymerase was detected in a mangrove plant, Excoecaria agallocha (Li et al., 2012) . Aloe vera Leaves Emodin (Ahlawat and Khatkar, 2011) Rheum officinale Roots Emodin (Hsu and Chung, 2012) ; (Kuo et al., 2020) Cassia alata or Senna alata Leaves, stems, fruits Emodin (Hennebelle et al., 2009) ; (Das et al., 2019) Roots Emodin (Adedoyin et al., 2015) Stems Luteolin (Hennebelle et al., 2009) Cassia obtusifolia or Senna obtusifolia Seeds Emodin (Yang et al., 2003) Senna alexandrina Pods Emodin (Elkhidir et al., 2012) Cassia occidentalis Roots Emodin (Chukwujekwu et al., 2006) Apium graveolens Leaves Luteolin (Zhu and Row, 2011) ; (Shivashri et al., 2013) Elephantopus scaber The whole plant, aerial part, and roots

Luteolin (Zuo et al., 2016) ; (Chang et al., 2011) ; (Su et al., 2009) Allium cepa Bulbs Luteolin (Singh and Goel, 2015) Brassica oleracea Leaves Luteolin (Miean and Mohamed, 2001) ; (Schmidt et al., 2010) ; (Mageney et al., 2017) Capsicum annuum Fruits Luteolin (Miean and Mohamed, 2001) ; (Materska et al., 2015) Averrhoa bilimbi Fruits and leaves Luteolin (Miean and Mohamed, 2001) Aerial roots Luteolin (Sharaf et al., 2000) Pongamia pinnata Stem Luteolin Leaves study demonstrated that myricetin and scutellarin compounds are capable of inhibiting helicase enzyme activity . Several Indonesian plants contain myricetin and scutellarin compounds; myricetin was found in clove plants (Syzygium aromaticum; flowers), duwet plants (Syzygium cumini; leaves), Semarang guava (Syzygium samarangense; leaves), and rosella (Hibiscus sabdariffa; flower petals), while scutellarin was found in Jakatuwa plants (Scoparia dulcis; leaves) and senggugu (Clerodendron serratum; leaves) (Cai and Wu, 1996; Kuo et al., 2004; Ali et al., 2005; Ayyanar and Subash-Babu, 2012; Wu et al., 2012; Wang et al., 2017) . Some bioactive compounds from natural sources have revealed high binding affinity to helicase, including many flavanoids (a-glucosyl hesperidin, hesperidin, rutin, quercetagetin 6-O-bD-glucopyranoside, and homovitexin), xanthones such as 3,5-dimethoxy-1-[(6-O-bDxylopyranosyl-bD-glucopyranosyl)oxy]-9H-xanthen-9-one, kouitchenside H, kouitchenside A, 8, 4, oxy]-9H-xanthen-9one, kouitchenside D, 1-hydroxy-2,6-dimethoxy-8-[(6-O-bDxylopyranosyl-bD-glucopyranosyl)oxy]-9H-xanthen-9-one and triptexanthoside D from Swertia genus, phyllaemblicin B and phyllaemblinol from Phyllanthus emblica .

In addition, according to structure-modeling helicase proteins, as described previously, several drugs, including antibacterial (lymecycline, cefsulodine, and rolitetracycline), antifungal (itraconazole), anti-HIV-1 (saquinavir), anticoagulant (dabigatran), and diuretic (canrenoic acid) drugs, have been projected through virtual ligand screening to be helicase inhibitors with high mfScores.

As previously described, SARS-CoV-2 infection in humans not only requires ACE-2 receptors as an entry point but also involves the binding of the S-protein on the surface of the virus to ACE-2 receptors. At a later stage, the activity of the serine protease enzyme required by TMPRSS2 (a transmembrane glycol) allows for fusion and entry of the target cell to begin infection. The inhibition of serine protease activity is a target in the prevention of viral infections. Recently, it has been shown that in addition to inhibiting interactions with ACE-2 receptors, the inhibition of protease enzymes (especially serine proteases) is also an impending target for controlling SARS-CoV-2 infection. Compounds that inhibit proteases in serine residues (serine protease inhibitors, hereafter referred to as SPIs) are thought to be good candidate drugs to stop the viral life cycle. SARS-CoV-2 employs proteases to facilitate the infection of host cells, making proteases a significant therapeutic target, as they are involved in many vital processes in the propagation of coronaviruses (Clemente et al., 2019; Hoffmann et al., 2020). Plants are an abundant source of SPI and have been widely studied. SPI compounds derived from plants are generally in the form of proteins or molecules containing proteins (large molecules). Leguminous family plants (Fabaceae, Poaceae, and Solanaceae) are the primary sources of SPI-producing plants. The protein fraction derived from legumes is rich in SPI compounds. Examples of leguminous plants whose seeds contain SPI are peanuts (Arachis hypogaea), soybeans (Glycine max), beans (Phaseolus vulgaris), peas (Pisum sativum), and snore (Crotalaria juncea). In addition to legumes, several Indonesian plants contain SPI compounds, including moringa (Moringa oleifera; leaves and seeds), bitter melon (Momordica charantia; seeds), cucumber (Cucumis sativus; fruit), pumpkin (Cucurbita moschata; fruit), pineapple (Ananas comosus; fruit), sweet potato (Ipomoea batatas; tuber), and potato (Solanum tuberosum; tuber) (Bijina et al., 2011; Srikanth and Chen, 2016) . Furthermore, SPI has been reported in the mangrove plant Excoecaria agallocha (Li et al., 2012) and mangrove-associated Derris trifoliata (Bhattacharyya and Babu, 2009) .

The Indonesian government encourages the potential use of domestic resources to deal with COVID-19. The efficacy claims of the products available to combat COVID-19 are more focused on the function of maintaining and increasing the human immune system (Hartanti et al., 2020) . The future prospects of natural compounds on COVID-19 from Indonesian medicinal plants include, for example, trans-cinnamaldehyde and analogs of Cinnamomum verum as immunomodulators; 6-gingerol, 6-shogaol, and 8-shogaol of Zingiber officinale var. Rubrum as antioxidants (Qadir et al., 2018) ; curcumin and polysaccharide as immunomodulators; phyllanthin and the related phenolic compounds of Phyllanthus niruri as immunomodulators; and polysaccharides of Oryza sativa as immunomodulators (Yang et al., 2015) .

In conclusion, all the compounds and plants mentioned in this review have not yet been tested for effectiveness in experimental models relevant to SARS-CoV-2 because this virus was only identified at the beginning of 2020. However, these plants possess the potential to prevent infection or inhibit the replication of SARS-CoV-2 based on the identified therapeutic targets in SARS-CoV-2 and their reaction to SARS-CoV.

The results of the abovementioned computational model (in silico) predictions still need confirmation via laboratory testing and experimentation. Many strategies are being developed by researchers to seek out active antiviral compounds, including those derived from natural plant compounds. The rich biodiversity of Indonesian plants provides a variety of structural compounds from natural materials, providing major capital in the effort to identify suitable drug candidates to combat disease, including SARS-CoV-2. At the same time, this is a call for Indonesian researchers to support drug-independence programs.

All authors listed have significantly contributed to the development and the writing of this article. 

Data included in article/supplementary material/referenced in article.

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Anti-SARS coronavirus 3C-like protease effects of Isatis indigotica root and plant-derived phenolic compounds

The bioactive metabolites of the mangrove endophytic fungus Talaromyces sp. ZH-154 isolated from Kandelia candel (L.) Druce

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A guide to the variability of flavonoids in Brassica oleracea

The molecular biology of coronaviruses

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Antiproliferative activities of five Chinese medicinal herbs and active compounds in Elephantopus scaber

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Identification of myricetin and scutellarein as novel chemical inhibitors of the SARS coronavirus helicase, nsP13

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Box-Behnken design for optimizing extraction of luteolin from celery leaves

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Single-cell RNA-seq data analysis on the receptor ACE2 expression reveals the potential risk of different human organs vulnerable to 2019-nCoV infection

The authors declare no conflict of interest.

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