key: cord-0889794-5ivngyl7 authors: Fakhri, Sajad; Nouri, Zeinab; Moradi, Seyed Zachariah; Akkol, Esra Küpeli; Piri, Sana; Sobarzo-Sánchez, Eduardo; Farzaei, Mohammad Hosein; Echeverría, Javier title: Targeting Multiple Signal Transduction Pathways of SARS-CoV-2: Approaches to COVID-19 Therapeutic Candidates date: 2021-05-14 journal: Molecules DOI: 10.3390/molecules26102917 sha: d9d33c1aa77383870b0833ad467b9a121d5b2928 doc_id: 889794 cord_uid: 5ivngyl7 Due to the complicated pathogenic pathways of coronavirus disease 2019 (COVID-19), related medicinal therapies have remained a clinical challenge. COVID-19 highlights the urgent need to develop mechanistic pathogenic pathways and effective agents for preventing/treating future epidemics. As a result, the destructive pathways of COVID-19 are in the line with clinical symptoms induced by severe acute coronary syndrome (SARS), including lung failure and pneumonia. Accordingly, revealing the exact signaling pathways, including inflammation, oxidative stress, apoptosis, and autophagy, as well as relative representative mediators such as tumor necrosis factor-α (TNF-α), nuclear factor erythroid 2-related factor 2 (Nrf2), Bax/caspases, and Beclin/LC3, respectively, will pave the road for combating COVID-19. Prevailing host factors and multiple steps of SARS-CoV-2 attachment/entry, replication, and assembly/release would be hopeful strategies against COVID-19. This is a comprehensive review of the destructive signaling pathways and host–pathogen interaction of SARS-CoV-2, as well as related therapeutic targets and treatment strategies, including potential natural products-based candidates. As a global pandemic, an outbreak of novel coronavirus, named severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), caused the coronavirus disease 2019 . It has been a serious leading cause of morbidity and mortality worldwide [1, 2] . Coronaviruses (CoVs) are a group of single-stranded enveloped ribonucleic acid viruses with the activity of ACE2. Since this enzyme is enriched in the lungs, heart, brain, kidneys, intestine, testes, and placenta [70] [71] [72] , there is a higher rate of virus presence and pathogenesis [73] . These results indicated that Ag II is likely to be the primary target of SARS-CoV-2 in the lungs [68] . Moreover, there are sex differences in the expression of ACE2. Sex hormones in males made a higher expression of ACE2 than in females, with a greater infectious rate [68, 74] . The ACE/ACE2 activity ratio in male serum is higher than in females. Individuals with coexisting disorders, including pneumonia [73] , diabetes [75] , along with aging [74, 76, 77] , cigarette use [78] , pregnancy [71, 79] , hypoxia, and HIF-1α [62, 80] , were shown to be more susceptible to the dysregulation of the ACE/ACE2 ratio. Overall, the molecular mechanisms and signaling pathways by which SARS-CoV-2 elicits its harmful effects are incompletely understood, and a few molecules have been identified as a target of SARS-CoV-2. For instance, it has been shown that SARS-CoV-2 reinforces chemokine-associated inflammation and fibrosis through IFN, with ACE2-induced Ras/Raf/mitogen-activated protein kinase kinase (MEK)/ERK/ activating protein 1 (AP1) and casein kinase (CK)2-p21-activated kinase 1 (PAK1) signaling pathways [81] . It has been reported that the aforementioned pathway offers the potential for pulmonary vascular remodeling and exaggerated hypoxia [82] . Aberrant activation of PAK1 hinders immune systems and participates in the promotion of viral infection [83] . Therefore, the suppression of PAK1 or it is upstream potentially repressed SARS-CoV-2 infection. In cases of SARS-CoV-2 infection, ACE2 has attracted substantial attention in COVID-19 pathogenicity [69] . Inappropriate regulation of ACE2/Ag (1-7)/Mas receptor and ACE1/Ag II type 1 receptor pathways could enhance ACE2, and thereby increase the chances of viral entry [69, 84] . On the other hand, downregulation of ACE2 by SARS-CoV-2 infection inhibits the degradation of Ag II into Ag (1-7), exacerbates inflammation, and leads to vascular permeability and cardiovascular complications [69] . It has been well-established that the proteolytic cleavage of the viral envelope glycoprotein by either intracellular or extracellular proteases, such as trypsin, furin, cathepsin, or transmembrane protease serine 2 (TMPRSS2), plays an important role in SARS-CoV entry [85] . Among them, TMPRSS2 has been shown to activate the spike-protein of COVID-19 for viral fusion and infectivity [86] . An accumulation of findings highlighted that the host protease TMPRSS2, employed for the entry of SARS-CoV-2 into lung epithelium, is an attractive target for pharmacologic intervention. It has been shown that pharmacologic inhibition of TMPRSS2 blocks SARS-CoV-2 entry into human lung cells. Additionally, inhibition of TMPRSS2 prevented SARS-CoV-1 infection in animal models. The TMPRSS2 gene expresses a protein of 492 amino acids which anchors to the plasma membrane. It can be divided into the catalytic chain and noncatalytic chain parts through autocatalytic cleavage between Arg255 and Ile256. After cleavage, the majority of mature proteases are membrane-bound, but their substantial portions can be released into the extracellular space [87] . It has been revealed that TMPRSS2 gene promoter possesses 15-bp androgen response element, and TMPRSS2 transcription is upregulated in the presence of androgens [88] . The activation of SARS-CoV by TMPRSS2 suppresses the blockage of SARS-CoV by IFN-induced transmembrane proteins, a class of IFN-stimulated host cell proteins that participate in inhibiting the entry of various enveloped viruses [89] . TMPRSS2 is known as a key gene in prostate cancer [90] . The hepatocyte growth factor (HGF)/c-Met cell is activated by TMPRSS2, provoking the survival pathway of HGF/c-Met receptor tyrosine kinase signaling and stimulating a pro-invasive role in prostate cancer cells. TMPRSS2 also induces inflammation by proteolytically activating the protease-activated receptor-2 (PAR-2) in the prostate. Additionally, the upregulation of PAR-2 promotes matrix metalloproteinase-2 (MMP-2) and MMP-9, both of which play a key role in the metastasis of tumor cells [89, 91] . Glucose-regulated protein 78 (GRP78), which belongs to the heat shock protein 70 family, is the master chaperone protein present in the lumen of the ER [92, 93] . Under cell stress, overexpressed GRP78 can escape ER retention and translocate to the cell membrane [94] . Once localized in the plasma membrane, GRP78 is susceptible to virus recognition, thereby facilitating the viral entry to the host cells. It has been reported that GRP78 is a target receptor of the MERS-CoV spike protein and bat coronavirus HKU9 (bCoV-HKU9) [95] . Recently, the existence of a SARS-CoV-2 spike protein-GRP78 binding site has been predicted using the computational method [96] , thus paving the route to design suitable inhibitors to prevent binding and infection. The cluster of differentiation 147 (CD147), also known as extracellular matrix metalloproteinase inducer, has recently emerged as an important receptor for SARS-CoV-2 [97] . CD147 possesses the ability to interact with various extracellular and intracellular partners which play a key role in the infection process of the human immunodeficiency virus (HIV), measles, and SARS-CoV [98, 99] . It has been reported that CD147 can bind with multiple ligands, including cyclophilins, monocarboxylate transporters, caveolin-1, and integrins [100] . As extracellular interactive partners, cyclophilins A and B can bind to CD147 and activate it, thereby increasing the chance of infection of CD147-expressing cells [101] . It has been reported that cyclophilins A and B can interact with nsp1 of SARS-CoV [98] ; however, it is yet not understood whether cyclophilins can bind to SARS-CoV-2. In an in vitro study, Wang et al. [102] revealed that meplazumab, an anti-CD147 antibody, significantly hindered the invasion of host cells by SARS-CoV-2. Surprisingly, this report has been supported by a clinical trial in which the anti-CD147 antibody inhibited SARS-CoV-2 spike protein binding and subsequently facilitated a viral clearance [103] . CD147 also participated in the regulation of nuclear factor-kappa B (NF-κB). Moreover, upregulation of CD147 leads to the activation of NF-κB which, in turn, involves inflammation and proliferative responses [104] . Additionally, cyclophilin-CD147 interaction can recruit the immune cells to the sites of inflammation via chemokine-like activity [105] . Cyclophilin 60 is identified as an important contributor protein in the expression and translocation of CD147 to the cell surface [106] . Several other proteins which bind to CD147 may affect its localization. For instance, the interaction of CD147 with the proton-coupled transporters of monocarboxylate, including MCT1 and MCT4 in the cell membrane, is highly dependent on glutamic acid residue 218 in the CD147 transmembrane domain. However, the mutation of this glutamic acid prevents the access of both CD147 and MCT to the cell membrane [107] . It has been also reported that caveolin-1 binds to CD147 on a cell surface, through which it plays a key role in the regulation of clustering and activity of CD147 [108] . As an interacting partner of CD147, integrin β1 interacts with CD147 to regulate integrin-dependent signaling and focal adhesion kinase (FAK) activation, leading to ignition of the downstream signaling Rac/Ras/Raf/ERK and phosphoinositide 3-kinases (PI3K)/Akt pathways and an increase in the metastatic potential of hepatocellular carcinoma [109] . It has been demonstrated that CD147 increases MMPs expression through several signaling pathways, including Janus kinase (JAK)/signal transducer and activator of transcription (STAT), Ras-MEK1-MAPK, and PI3K/Akt signaling pathway [110] . Dipeptidyl peptidase (DPP4), also known as CD26, was considered as the main entry receptor for MERS-CoV [111] . The S protein of MERS-CoV specifically interacts with DPP4 receptors, thereby inducing proteolytic activation of viral entrance and viral membrane fusion with the cell membrane [112] . There is about an 80% genome sequence similarity between MERS-CoV and SARS-CoV with SARS-CoV-2. Recent evidence has shown that DPP4/CD26 can also bind to the S1 domain of the SARS-CoV-2 spike glycoprotein, indicating the potential role of DPP4/CD26 in SARS-CoV-2 adhesion/virulence [113] . The potential interaction between SARS-CoV-2 spike glycoproteins and DPP4 has been demonstrated by docking studies and needs in-depth clarification in experimental models [114] . Intriguingly, there is also evidence suggesting that DPP4 is implicated in the induction of cytokine storm, oxidative stress, the immune system, and apoptosis [115] . DPP4 has been widely studied because of its proteolytic activity on various cytokines and peptides that participate in different medical conditions [116] . In the case of proteolytic activity, DPP4 reduces incretins such as glucagon-like peptide 1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), subsequently leading to a declined insulin secretion and abnormal glucose level [116] . Additionally, DPP4 proteolysis leads to partial or total alteration in signaling and functionality of its substrates, including peptide tyrosine-tyrosine (PYY), neuropeptide Y (NPY), and stromal-derived factor 1 (e.g., SDF-1 and CXCL12) [117] . Intriguingly, there is also evidence suggesting that DPP4 is implicated in the induction of cytokine storm, activation of NF-κB pathway, oxidative stress, the immune system, and apoptosis [115] . It has been revealed that CD26/DPP4 possesses the ability to directly trigger T cell activation through CARMA1-mediated NF-κB activation in T cells which, in turn, leads to T cell proliferation and pro-inflammatory interleukin (IL)-2 cytokine production [118] . People with diabetes are at higher risk of developing the serious clinical events caused by COVID-19 because chronic hyperglycemia and inflammation contribute to an ineffective immune response [119] . In this line, DPP4 inhibitors and/or GLP-1 receptor analogs are widely used for the control of hyperglycemia in type 2 diabetes [120] . The potential role of DPP4 inhibitors in COVID-19-infected patients with type 2 diabetes is not completely clarified. However, DPP4 may illustrate a potential target for decreasing the progression of the complications of type 2 diabetes in those infected with COVID-19 [119] . Therefore, DPP4 inhibition may hinder the infection and/or development of the COVID-19. Patients infected with SARS-CoV-2 exhibited various clinical manifestations such as fever, dyspnea, myalgia, and viral pneumonia [121] . In complicated patients, ARDS, acute kidney injury, cardiovascular complications, neurological side effects, and multiple organ failure have also been shown to be associated with increased mortality [49, 122, 123] . While the pathobiology of SARS-CoV-2 and molecular mechanisms behind the aforementioned clinical manifestations are not yet entirely known, the roles of inflammation, oxidative stress, apoptosis, and autophagy are undeniable. As previously mentioned, inflammatory pathways play important roles in the highly inflammatory conditions of pathogenesis in COVID-19 [124] . As such, in severe cases of COVID-19, patients showed higher serum levels of inflammatory cytokines, including TNF-α, IL-2, IL-6, IL-7, IL-10, IFN-γ, IL-1β, IL-12, IL-18, IL-33, tumor growth factor-β (TGFβ), macrophage inflammatory protein-1α (MIP-1α), monocyte chemoattractant protein-1 (MCP-1), granulocyte-colony stimulating factor (G-CSF), interferon-inducible protein-10 (IP-10), chemokines (e.g., CXCL8, CXCL9, CXCL10, CCL2, CCL3, CCL5) [13, [125] [126] [127] [128] , and c-reactive protein (CRP) [129] [130] [131] in the early phase as major causes of ARDS [132] . Extensive immunological responses, high levels of circulating inflammatory cytokines, substantial lymphopenia, and immune-cell infiltration are closely correlated to immunepathological changes of targeted organs [133] . In COVID-19 patients, increased neutrophils/CRP and decreased lymphocytes were revealed; this was in direct correlation with disease severity [13] . Releasing the aforementioned inflammatory factors is also called a cytokine storm, which, in turn, leads to various pathogenic complications in COVID-19 [134] [135] [136] . The innate immune system also employs IFN type I, IFN-α and IFN-β, and IFN-stimulated response element (ISRE) as downstream mediators in exerting a critical response against viral infection, while a reduced IFN leads to rapid viral replication [137, 138] . Consequently, IFN-α/β suppresses viral dissemination/replication in the early stage of viral infection. COVID-19 employs multiple ways toward interfering with the aforementioned pathways of type I IFN production [127, 139] , including JAK-STAT/ISRE pathway phosphorylation [140] . Following the production of type I IFN, COVID-19 is equipped to suppress the inflammatory pathways [65, 140, 141] , time-dependently [127] . Additionally, any dysregulation in the pathway leads to neutrophil/monocyte/macrophage activation and lethal pneumonia or acute respiratory distress syndrome [127] . A disturbance in the regulation of IFNs generation of pro-inflammatory cytokines produced by macrophages contributes to the apoptosis of T cells, which further hampers viral elimination [142] . During viral infection and activation of the adaptive immune response, the engagement of the T cell receptor provokes intracellular calcium overload which, in turn, induces calmodulin binding to calcineurin. Calcineurin activation participates in the nuclear factor of activated T-cell (NFAT) dephosphorylation [143] . The calcium-calcineurin-NFAT pathway boosts the generation of pro-inflammatory cytokines, thereby maintaining chronic inflammation conditions [144] . As other involved receptors, TLR-7 and TLR-3 activate the downstream signaling cascade, including NF-κB and IFN regulatory factor 3 (IRF3) [140] . Enhanced levels of pro-inflammatory cytokines and the migration of inflammatory cells into the lung tissues are the postulated mechanisms for acute lung injury. Cytokine storm disrupts tissue integrity and subsequently leads to pneumonitis [145] . Activation of various inflammatory cytokines involved in the cytokine storm is controlled by the intracellular signaling pathway JAK/STAT [146] . For instance, IL-6 which has been proven as a pivotal inflammatory cytokine, employs the JAK/STAT pathway to perform its biological functions such as immune response, inflammation, and oxidative stress. The inhibition of the IL-6/JAK/STAT pathway appears a promising therapeutic option for the alleviation of COVID-19 [147] . Oxidative stress is considered a key contributor to the severity and pathogenesis of SARS-CoV-2. Over-generation of reactive oxygen species (ROS) and antioxidant depletion drive a pivotal role in viral replication and viral-related complications [148, 149] . Some populations of innate immune cells, such as macrophages and neutrophils, would generate ROS to clear the pathogens [150, 151] . Despite the necessity of ROS production by macrophages and monocytes for modulating immune responses and eliminating viral infection, related over-production contributes to the oxidation of cellular proteins/lipids and corrupts both infected and normal cells, thereby leading to multiple organ dysfunctions [152] . Moreover, compelling studies have shown that viral infections such a SARS-CoV are linked to the inhibition of Nrf2 and augmentation of NF-κB signaling, leading to antioxidant deprivation and inflammation [153] . Nrf2, and its downstream target antioxidant enzyme heme oxygenase-1 (HO-1), serves as a crucial signaling pathway for cytoprotection against inflammation through inhibiting critical inflammatory regulatory pathways such as NF-κB [148] . Interestingly, Nrf2-keap1/HO-1 activation accompanied by an increase in enzymatic/non-enzymatic antioxidant activities, including superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione (GSH), thiobarbituric acid reductase (TBARS), NAD(P)H:quinone oxidoreductase 1 (NQO-1), which, in turn, suppress oxidative mediators and lipid peroxidation, thereby alleviating the hallmarks of viral infection [154, 155] . Therefore, the Nrf2 pathway is an auspicious therapeutic target for combating SARS-CoV pathogenesis. Apoptosis is a determiner pathway involved in COVID-19 complications. As a pathogenic pathway, apoptosis induction in infected cells can directly lead to viral pathogenesis [156] . In SARS-CoV-infected patients, lymphopenia may occur due to T cell diminution through the activation of apoptosis [157] . Apoptosis activation mediated by human COVID-19 infection contributes to the spread of the virus [158] . Apoptosis activation is associated with numerous abnormalities in virally infected organs. In this line, SARS-CoV-2 infection stimulated apoptosis in lung epithelial/endothelial cells, which causes vascular leakage and alveolar edema, as well as acute lung injury [29] . Several mechanisms are involved in apoptosis activation by human COVID-19. It has been reported that human COVID-19 stimulates apoptosis via ER, caspase-mediated, p38MAPK, and c-Jun N-terminal kinase (JNK) dependent pathways, which are needed for viral replication [159, 160] . From another point of view, SARS-CoV triggers apoptosis through decreasing anti-apoptotic B-cell lymphoma 2 (Bcl)-2 members (e.g., Bcl-2 and Bcl-xL) and key survival signaling pathways such as Akt. The upregulation of Akt inactivated several pro-apoptotic molecules such as glycogen synthase kinase-3β (GSK-3β), caspase-9, Bad, and forkhead transcription factor Foxo1 (FKHR), thereby hampering apoptotic pathways [161] . Virus infection can trigger poly (ADP ribose) polymerase (PARP) and ultimately result in apoptosis. PARP drives an important role in programmed cell death and cytokine release [162, 163] . Therefore, PARP inhibitors can be served as supportive treatments for alleviating the hallmarks of COVID-19. Besides, viral infections disrupt mitochondrial membrane potential and provoke pro-apoptotic factors such as cytochrome C, caspase-9, and caspase-3 [164, 165] . Therefore, targeting particular mediators and enzymes of the apoptotic pathway is an attractive strategy for fighting a viral infection. As another critical pathway for COVID-19, autophagy is an intracellular regulated process that plays a pivotal role in the maintenance of cellular homeostasis [166] . Considering mechanistic changes in COVID-19, autophagy is a fundamental cell process in the pathogenicity of disease. This process is characterized by the formation of the double-membrane autophagosomes that subsequently fuse with acidic lysosomes to form autolysosomes through a pH-dependent mechanism. The engulfed components are then degraded with lysosomal enzymes [167] . There is increasing evidence that dysregulated autophagy seems to play an essential role in the pathogenesis of SARS-CoV, as well as its arising complications. Altered autophagy caused by viral infection is strongly associated with severe tissue damage. On the other hand, autophagy could be considered a doubleedged sword in the pathogenesis of SARS-CoV. The pro-viral or antiviral role of autophagy remains unclear [149] . The virus that enters the host cell can either be eliminated via autophagy or escape autophagic degradation and replicate in the host cell [168] . A central aspect of the pro-viral role of autophagy is to boost viral replication by the formation of double-membrane vesicles in the host cells. In fact, virus replication in the host cell begins at the ER-Golgi intermediate compartment, which is connected to autophagosome biogenesis, where the viral genome possesses a critical interaction with the proteins that are necessary to assemble a complete virus [169, 170] . It has been identified that viral nsp6 protein was found to co-localize with the endogenous autophagy marker, LC3, suggesting a possible collaboration between autophagy and COVID-19 replication [168] . Therapeutics such as chloroquine and hydroxychloroquine elicit antiviral effects by inhibiting the fusion of autophagosomes and lysosomes, and blocks the later stages of autophagic flux [171] . On the other hand, the induction of autophagy may combat viral infection by the degradation of viral components and the augmentation of innate and adaptive immunity [172] . Induction of autophagy and inflammatory responses induced by viral infection contribute to lung injury [173] . It has been reported that the inhibition of S-phase kinase-associated protein 2 (SKP2), which is responsible for proteasomal degradation of Beclin 1, enhanced autophagy, and subsequently attenuated the replication of MERS-CoV [174] . A novel analysis has also highlighted the relation between autophagy mechanisms and antiviral/inflammatory responses in COVID-19. In this sense, PI3K/Akt/ mammalian target of rapamycin (mTOR) is a key control signaling pathway for autophagy that regulates various autophagy mediators, such as Beclin, microtuble-associated protein light chain 3 (LC3), and autophagy-related (Atg). Human COVID-19-infected hepatocytes could induce autophagy through ERK/MAPK and inhibition of the PI3K/Akt/mTOR pathway [175] . Additionally, JNK, AMP-activated protein kinase (AMPK), p38MAPK control the balance of the autophagy response to viral infection [176] [177] [178] . Considering the role of the afore-mentioned mediators in autophagy, modulating autophagic pathways could pave the road for combating SARS-CoV-2 infection [170] . Overall, the inhibition of autophagy during the first phase of COVID-19 could prevent the replication of SARS-CoV-2 and negatively regulate the IFN response. On the other hand, autophagic pathways are in a near link to inflammation and immune responses in COVID-19. Accordingly, dysregulation in autophagic pathways could lead to cytokine storm and immune dysfunction. Consequently, autophagy modulation restores homeostasis in the immune response of COVID-19 to represent an important challenge, indicating the ability to improve antiviral response, restrict inflammation, and prevent other complications [179] . Therefore, a mechanistic targeting of autophagy should be considered a new strategy in combating SARS-CoV-2. Shortly after the identification of COVID-19 in China, many studies demonstrated the effectiveness and advantages of different classes of drugs when hoping to find a suitable agent with promising effects in the prevention, control, recovery, and improvement of related pathological conditions. It has been well-established that inflammation, apoptosis, oxidative stress, autophagy, and host factors, as well as destructive signaling pathways, play a crucial role in the pathogenesis of SARS-CoV-2. Therefore, modulation of the dysregulated therapeutic targets and pathways is an attractive therapeutic avenue for COVID-19. Prevailing evidence has highlighted the cross-talk and the balanced interplay between autophagy and apoptosis [180] . The over-accumulation of autophagosome promotes the apoptotic pathway that eventually causes apoptotic death of the virally infected cells and represses the virus replication cycle [181] . Therefore, providing alternative therapies that potentially interfere with SARS-CoV-2 and lead to autophagy regulation is of great importance. To date, there are no proven effective therapies to prevent or cure COVID-19. An accumulation of findings suggests that several drugs under clinical trials for SARS-COV-2 are autophagy/apoptosis modulators. For instance, chloroquine/hydroxychloroquine, emtricitabine/tenofovir, IFN-α-2b, lopinavir/ritonavir, and ruxolitinib contribute to autophagosome accumulation through inhibiting autolysosome formation and thereby disrupt the replication of SARS-CoV-2 [182] . Additionally, corticosteroids suppress autophagy by inhibiting LC3 recruitment [183] . Besides, ruxolitinib, as a JAK inhibitor can induce autophagy through blocking mTORC [184] . Altogether, modulating apoptosis and autophagy seems to be a hopeful strategy in combating COVID-19. Viral infections provoke cytokine storm, which in turn leads to oxidative damage. Therefore, alleviation and management of oxidative damages can be achieved by a large dose of antioxidants [185] . Vitamin C possesses well-characterized antioxidant properties, being able to scavenge free radicals and thereby prevent cells and tissues from oxidative damage [186] . Apart from its antioxidant property, evidence is accumulating that vitamin C exhibits antiviral activity by augmenting IFN-α production, decreasing inflammation, ameliorating endothelial dysfunction, and also direct virucidal activity [187] . A randomized placebo-controlled trial revealed that the high dose of intravenous vitamin C can improve pulmonary function and decrease the risk of ARDS in 308 patients diagnosed with COVID-19 and transferred into the intensive care unit [188] . Vitamin E is a key lipophilic antioxidant that mitigates lipid peroxidation [189] . This vitamin also regulates immune response and stabilizes membrane cells. The important effects of vitamin E make it a potential candidate for the alleviation of oxidative damage and inflammation induced by SARS-COV-2 [190] . More importantly, astaxanthin, a lipid-soluble carotenoid that possesses a higher antioxidant effect than vitamin E and vitamin C, can be considered as a potential option in counteracting COVID-19 complications [191] . Targeting the lifecycle steps of SARS-CoV-2, including virus attachment and endocytosis, viral replication, and transcription, as well as virus assembly and release, provides a promising therapeutic approach. The auspicious drug targets encompass host factors (e.g., ACE2, TMPRSS2, and CD147), and NSPs (e.g., RNA-dependent RNA polymerase, and 3-chymotrypsin-like protease), along with structural proteins. Interestingly, serine protease inhibitors, such as camostat, were identified as suppressing TMPRSS2 and effectively decreasing mortality following SARS-CoV infection [11] . More importantly, Hoffmann et al. revealed that this drug possesses the ability to abrogate SARS-CoV-2 entry into lung cells by suppressing ACE2 and TMPRSS2 [192] . Based on preclinical investigations, a doubleblind randomized controlled clinical study was performed with 114 COVID-19 infected patients to find whether camostat mesylate at a dose of 200 mg/3 times a day can diminish a SARS-COV-2 viral load in early COVID-19 disease (NCT04353284). In an open-label phase 2 clinical trial, meplazumab, an anti-CD147 antibody, inhibited SARS-CoV-2 spike protein binding and could block the infection of SARS-CoV-2 in 20 COVID-19 patients with pneumonia [103] . It has been reported that arbidol possesses an attractive mechanism of action that affects the S protein/ACE2 interaction, halting viral membrane fusion [193] . A nonrandomized study revealed that treatment with arbidol for nine days decreased mortality rates and enhanced discharge rates in 67 patients infected with COVID-19 [194] . As antiviral chances, combined lopinavir/ritonavir combination as 3-chymotrypsin-like protease inhibitors of anti-retroviral drugs was suggested as an effective drug against MERS-CoV and SARS-CoV [195, 196] . For this reason, several clinical trials have been performed to investigate its effects on COVID-19. The results of those studies were not sufficient and did not recommend combination therapy as a suitable medication [1, 197] . The advantages of new studies emphasized that arbidol monotherapy was more impressive than lopinavir/ritonavir in the treatment of patients with COVID-19. About 14 days after the treatment, viral load was not identified in the arbidol group, and the duration of the positive RNA test was shorter in this group [198] . Favipiravir is a broad-spectrum RNA polymerase inhibitor, an antiviral compound that showed a suitable activity versus the Crimean-Congo hemorrhagic fever, rabies, oseltamivir-resistant, and wild-type influenza B virus in mice [199] [200] [201] . For this reason, an open-label control study was performed to investigate the advantages of favipiravir on COVID-19, and results showed improvement in the chest imaging in comparison with the control group and might be a useful agent in the treatment of COVID-19 [202] . Moreover, remdesivir is a new nucleotide analog and RNA-dependent polymerase inhibitor that showed considerable in vitro activity versus SARS-CoV-2 [203] . An emergency use authorization for remdesivir was issued to adults and children hospitalized with COVID-19. Wang et al. designed a double-blind, randomized trial to investigate the effect of remdesivir in 237 patients with severe COVID-19. Compared with placebo, remdesivir could not significantly reduce the duration of hospitalized time in patients with COVID-19 [204] . Besides, another RNA-dependent polymerase inhibitor, ribavirin, which is routinely used in combination with IFN for hepatitis C virus infection, could not find enough evidence to treat COVID-19 [205] . Darunavir is a protease inhibitor that has shown beneficial effects in treating HIV-1 infection. In February 2020, a clinical trial was registered in China to peruse the advantages of this drug in combination with cobicistat, a human cytochrome P-450 3A enzyme inhibitor; thus far, no data support the efficacy and safety of this agent in humans diagnosed with COVID-19 (NCT04252274). There is inadequate and insufficient information thus far to know whether chloroquine or hydroxychloroquine has a remarkable role in the treatment of COVID-19. Both hydroxychloroquine and chloroquine have been documented to inhibit SARS-CoV-2 in vitro; how-ever, it seems that the antiviral potential of hydroxychloroquine is more than chloroquine. The antiviral mechanisms of hydroxychloroquine and chloroquine are not fully realized, but inhibiting viral fusion, changing the pH at the cell membrane surface, inhibiting and suppressing the replication of nucleic acid, preventing viral assembly and release, and decreasing the glycosylation of viral proteins are amongst their important possible antiviral mechanism [203, 206] . Even so, the obtained clinical data on either of the two compounds are limited and have serious methodological problems. In an open-label study performed in March 2020, the administration of 200 mg hydroxychloroquine three times per day for ten days increased the rate of undetectable SARS-CoV-2 RNA in samples obtained from nasopharyngeal in comparison with the placebo group [207] . Significant methodologic problems reduced the value of those studies and made the results unreliable [208] . Another randomized trial with a statistical population of 30 adults with COVID-19 was performed in Shanghai. The results of those studies did not show a significant difference between the group receiving hydroxychloroquine and the group receiving standard care [209] . Furthermore, adverse effects due to high doses of chloroquine and increased mortality prevented patients from continuing the studies [210] . From an inflammatory point of view, the critical role of inflammatory responses and enhanced inflammatory cytokines in COVID-19 are the most critical factors. In this regard, the level of IL-6 showed a considerable correlation with the severity of COVID-19, and the measure of this cytokine can be used as an important factor in predicting disease severity [211] . Tocilizumab is a selective antagonist of the IL-6 receptor, which prevented cytokine release syndrome and led to improving the conditions of a patient with severe COVID-19 [212] . Several clinical studies have been conducted in various countries, including the United States, Spain, Nepal, Malaysia, and Belgium, to investigate the effects of this drug, but the full results of these studies have not yet been published (NCT04332094, NCT04377659, NCT04331795, NCT04330638, NCT04317092, NCT04345445). Siltuximab and sarilumab are other receptor antagonists of IL-6 that are in the early stages of clinical research (NCT04329650, NCT04322188, NCT04341870, NCT04357808). Consistently, it seems that the IFN-β Subtype may be a suitable option for COVID-19 treatment. IFN-β properly decreased the MERS-CoV in vitro and has had pleasant outcomes in an animal model of MERS-CoV infection, but no data evaluated the advantages of IFN-β on SARS-CoV-2 [195, 213, 214] . As the importance of JAK/STAT in the pathogenesis of COVID-19 was shown previously, baricitinib is a JAK inhibitor that leads to the inactivation of STATs and a decrease in the serum levels of IgG, IgA, IgM, and CRP. The limited data demonstrated that the administration of baricitinib may modify cytokine-release syndrome due to COVID-19. The results suggested this agent as a useful drug for damascening to the COVID-19 therapy regimen [215] ; for this reason, several clinical trials are in progress to sift the effect of baricitinib in COVID-19 (NCT04340232, NCT04321993, NCT04362943). Glucocorticoids are of the main classes of drugs possessing immunosuppressive, antiinflammatory, and antiproliferative activities through blocking IL-1α and β, NF-κB, TNF-α, AP-1, and increasing the synthesis of, IκB-α. The administration of glucocorticoids in patients with influenza led to a delay in viral clearance and enhanced risk for mortality; this was similar in patients with a MERS-CoV infection [216, 217] . Furthermore, the administration of glucocorticoid drugs on patients with COVID-19 did not provide adequate and acceptable results [218] . Nonsteroidal anti-inflammatory drugs (NSAIDs) have for a long time been considered effective therapies against inflammatory diseases [219] . To determine the efficacy of ibuprofen, a commonly prescribed NSAID, in COVID-19, a randomized phase 4 clinical study was applied in 230 severe COVID-19 patients to treat them with ibuprofen at a daily dose of 200 mg (NCT04334629). Additionally, a randomized phase 3 clinical trial was registered to assess the effectiveness of naproxen (250 mg twice a day) in patients (n = 584) infected with SARS-CoV2 (NCT04325633) [220] . Pre-clinical evidence has previously been presented on the use of NSAIDs during COVID-19 [221] . In addition to the aforementioned agents, antibiotics are used for possible effectiveness in combating COVID-19. Azithromycin is a macrolide antibiotic with conflicting information about its concomitant use with hydroxychloroquine for COVID-19 treatment. However, a study conducted in May 2020 in France showed that the use of azithromycin in combination with hydroxychloroquine before the beginning of COVID-19 complications may be safe and led to a very low fatality rate in patients [222] . The significant potential of both drugs for corrected QT interval prolongation, as well as the possibility for the exacerbation of this complication in their simultaneous use, prevents their concomitant administration, and it is not recommended [223, 224] . As another antibiotic, teicoplanin was shown to be effective against former coronaviruses and demonstrated an in vitro activity against the novel coronavirus, but enough information and convincing evidence are not available from clinical trials [225] . As another class of drugs, an anti-parasitic drug, ivermectin, showed a suitable in vitro effect on SARS-CoV-2 [226] . For this reason, the authors advised investigating the possible benefits of ivermectin in humans with COVID-19, and several clinical trials began in the hope of achieving convincing results (NCT04360356, NCT04343092, and NCT04374279). From another point of view, oseltamivir, a neuraminidase inhibitor, indicated for prophylaxis and treatment of influenza, did not show any significant effect for treatment or prophylaxis of COVID-19 [205] . From other drugs used against COVID-19, the Bacillus Calmette-Guérin (BCG) vaccine could be mentioned for its use in the immunization against tuberculosis and the prevention of leprosy. The BCG vaccine showed in vitro and in vivo non-specific protective activities versus other respiratory tract infections. Statistical analysis was conducted to investigate the effects of vaccine BCG in countries with and without national vaccination programs in preventing and reducing COVID-19's mortality. The results showed that, in countries with vaccination programs, the prevalence and mortality rate was estimated at 38.4 and 4.28 people per million, respectively. The death rate was 40/million in countries without BCG programs [227] . Therefore, it is hypothesized that the vaccine may reduce the incidence and severity of COVID-19 in healthcare workers. In this regard, several clinical trials are being conducted to investigate these effects (NCT04348370, NCT04373291, NCT04327206, NCT04350931, NCT04328441). Increasing evidence has shown that vitamin D deficiency is correlated with COVID-19-associated coagulopathy, inflammation, immune response dysfunction, and mortality [228] . From a mechanistic angle, vitamin D displays antiviral activity through immunomodulation and induction of autophagy [229] . It has been reported that vitamin D supplementation mitigates liver disease progression and augments responses to therapy in hepatitis C virus patients [230] . Other miscellaneous compounds, antioxidation, immune-modulatory, and anti-inflammatory activity of melatonin, as a neurohormone, made this compound one of the drugs with the potential to be added to the therapeutic regimen of patients with COVID-19 [231] . There is some other information on the protective effects of melatonin in viral diseases, which may display these advantages in patients with COVID-19 [231] . Phytochemicals are a consequential source of active chemicals constructed by plants, with potential effects against pathogens. They have been introduced as influential resources for drug discovery, possessing various human health benefits. Besides, a substantial spectrum of biological activities is reported for phytochemicals, such as anticancer, antibacterial, neuroprotective, cardioprotective, immune-modulatory, anti-inflammatory, and antioxidant effects [232, 233] . Several steps in viral replication and infection can be also suppressed by natural products [50] . Although many of these compounds have been shown to have broad-spectrum antiviral effects, the mechanisms behind these effects have not yet been fully elucidated. Besides their potent antioxidant activities, inhibiting the synthesis of DNA and RNA, suitable scavenging capacities, prevention of the virus entry, or reproduction of the virus are some of the critical reported antiviral mechanisms of these compounds [234] . The immune-modulatory effect of natural products and the significant potential for suppressing the inflammatory reaction, as one of the major reasons for mortality and morbidity of SARS-CoV-2 infection, are other promising mechanisms of phytochemicals in the treatment of SARS-CoV-2 [235] . We have previously reported the modulatory roles of natural products on inflammatory, apoptotic, and oxidative stress pathways involved in the pathogenesis of COVID-19-associated lung injury [35, 236] . We have also shown that the neuronal manifestations of COVID-19 could be potentially targeted by phytochemicals [35] . Therefore, in the present study, we have focused on the inflammatory, apoptotic, oxidative stress and autophagic pathways, and virus life cycle, as well as the phytochemical effects. Flavonoids, polyphenolics, alkaloids, terpenoids, coumarins, and carotenoids are some of the important groups of phytochemicals with antiviral, antioxidant, and anti-inflammatory activities towards developing a suitable therapeutic option for COVID-19 [35] . As a group of multi-targeted agents, flavonoids and polyphenols are already recognized as potential therapeutic agents for the treatment of viral infections. Numerous studies have shown that curcumin (a phenolic compound) possesses anti-inflammatory and antioxidant roles, and interrupts the viral infection process via several mechanisms, including hindering virus entry, replication, and budding, directly interfering with viral proteins and repressing the gene expression of the virus [237] [238] [239] [240] . From another point of view, curcumin reduced the pro-inflammatory cytokines and virus-induced cytokine storm, as well as alleviating lung injury, thereby indicating potential effects in the treatment of COVID-19 [237, 241] . According to computational methods, curcumin offers the ability to inhibit the spike protein of SARS-CoV-2 and disrupts viral entry [242] . Another in silico approach also revealed that curcumin and catechin were used as potential antiviral polyphenols through the dual inhibition of host cell receptors to the virus (mediated by ACE2) and viral protein entry (S-protein). It should be mentioned that the binding affinity of catechin was more than that of curcumin [243] . It has been previously documented that the bioactive flavonoid baicalein blocks influenza A virus H3N2 through suppressing autophagy markers, Atg-5, Atg-12, and LC3-II [244] . Baicalein could effectively abrogate the replication of SARS-CoV-2 in Vero cells through diminishing 3C-like proteases (3CL pro ) SARS-CoV-2 [245] . In another study, baicalein mitigated Vero E6 cell damage induced by SARS-CoV-2. Additionally, this nutraceutical agent alleviated the lesions of lung tissue and suppressed replication of SARS-CoV-2 in mice. Furthermore, this compound improved respiratory function and reduced inflammation, corroborated by decreasing the level of IL-1β and TNF-α in lipopolysaccharide (LPS)-induced acute lung injury of mice [246] . Docking evidence revealed that flavonoids biochanin A and silymarin strongly interact with the active site of SARS-CoV-2 spike glycoprotein and ACE2, respectively [247] . Further in vitro studies should be carried out on these flavonoids against SARS-CoV-2. As a best-docked bioflavonoid, naringin exhibited a high-affinity binding at the binding site of main protease (M pro ) and spike glycoprotein of SARS-CoV-2 [248, 249] . It has been recently reported that two-pore channel 2 (TPC2) is a key requirement for SARS-CoV-2 entry [250] . Surprisingly, naringenin exhibited the capacity of potent antiviral activity against SARS-CoV-2 and could successfully abrogate TPC2 in vitro [251] . Further in vivo studies are needed to confirm the beneficial effect of naringenin. It has been previously documented that phytoactive flavonoid taxifolin ameliorated sepsis-induced pulmonary damage and edema by inhibiting the NF-κB pathway [252] . According to the molecular docking approach, taxifolin was found a potential inhibitor against M pro SARS-CoV-2 [253] . As an effective candidate against SARS-CoV-2, the flavonoid silibinin declined immune response and inflammation by inhibiting STAT3, thereby facilitating effects on the early stage SARS-CoV-2 infection [254] . A computational study proposed that silibinin hinders the replication of SARS-CoV-2 via abrogating RNA-dependent RNA polymerase (RdRp) [255] . Silibinin offers excellent opportunities for further investigations in preclinical and clinical trials as an anti-SARS-CoV-2 agent. It has been reported that the flavonoid luteolin can disrupt the viral fusion and entry process and can also mitigate SARS-CoV infection with EC 50 values of 10.6 µM in a dose-dependent manner [256] . Resveratrol is a phenolic compound that appreciably inhibited MERS-CoV infection and could enhance cellular survival behind virus infection. It could notably decrease an essential protein expression for MERS-CoV replication (nucleocapsid N), and downregulated the in vitro apoptosis induced through MERS-CoV [257] . It has been also shown that resveratrol potentially suppressed SARS-CoV-2 infection in vitro [258] . Emodin is another chemical compound that belongs to the anthraquinone category. It was shown to block and suppress the S protein and ACE2 interaction, leading to beneficial effects in the treatment of SARS-CoV [259] . Hirsutenone, as a bioactive diarylheptanoid polyphenol isolated from Alnus japonica (Thunb.) Steud. (Betulaceae), exerted strong antiviral activity through diminishing papain-like protease (PL pro ) of SARS-CoV. It has been reported that catechol and α, β-unsaturated carbonyl moiety play critical roles in protease blocking activity [260] . Alkaloids are an important class of natural products with antiviral activities, which have been extensively studied [261, 262] . Molecular docking evidence proved the promising potential of such alkaloids in targeting SARS-CoV-2 RdRp, including 10 -hydroxyusambarensine, cryptospirolepine, and strychnopentamine [263] . The bioactive alkaloid emetine, as a viral entry inhibitor, has previously been shown to block MERS-CoV-mediated infection [264] . Interestingly, emetine inhibits SARS-CoV-2 replication in vitro, and a synergistic effect between the combination of remdesivir and emetine was observed [265] . As another alkaloid compound, lycorine was strongly able to diminish the spread and replication of human coronavirus OC43 (HCoV-OC43) in a mouse central nervous system [264] . It has also been shown that two alkaloids lycorine and oxysophoridine possess the ability to suppress the replication of SARS-CoV-2 in vitro [266] . Consequently, tylophorine, a natural alkaloid, has shown promising beneficial effects against coronavirus porcine transmissible gastroenteritis virus (TGEV) through suppressing JAK2 mediated NF-κB activation related to the inflammatory response. It also inhibited viral replication by interfering with the viral RNA complex [267] . As broad-spectrum antiviral agents, tylophorine based derivatives also blocked SARS-CoV-2, with EC 50 values of 2.5-14 nM [268] . Such results indicated the potential of tylophorine as a novel therapeutic intervention for COVID-19 infection. In addition to phenolic compounds and alkaloids, terpenoids could also contain auspicious natural plant-derived secondary metabolites for combating COVID-19 [269] . As a triterpenoid compound, glycyrrhizin has been successfully applied to mitigate virusinduced inflammatory cascades and viral replication [270, 271] . It has been well-established that high-mobility group B1 (HMGB1) protein plays a key role in viral infection and replication [272, 273] . Interestingly, an in silico study performed by Bailly et al. revealed that glycyrrhizin is a potential binder of HMG box protein, and could thereby be a promising candidate to be evaluated against COVID-19 [274] . Cumulative evidence has demonstrated that natural coumarin compounds possess antioxidant, antiapoptosis, and antiinflammatory activities toward antiviral effects. Additionally, these agents effectively disrupt various stages in the virus replication cycle, and could thereby be beneficial agents for tackling SARS-CoV-2 [275] . Regarding coumarins, a recent in silico study revealed that some naturally occurring coumarins, including corymbocoumarin, methylgalbanate, and heraclenol, displayed potential antiviral activity through inhibiting M pro [276] . Molecular docking approaches indicated that natural coumarin compound toddacoumaquinone possesses a significant suppressing ability against M pro of SARS-CoV-2, which is necessary for viral replication [277] . Another in silico study also illustrated that the bioactive coumarin inophyllum A remarkably targets M pro [278] . Consequently, of other natural products, carotenoids seem to be of potential interest in targeting various steps of the viral life cycle and host proteins [279] . As one of the most potent/efficient carotenoids, astaxanthin has been a promising source of antioxidation and anti-inflammatory agents, with promising potential to combat viral infections and related complications through targeting several destructive signaling mediators [191] . Altogether, several findings revealed that phytochemicals possess the ability to suppress SARS-CoV-2 infection. Unfortunately, almost all of the current evidence focused on the efficacy of phytoactive compounds in silico and in vitro models of COVID-19, and the main antiviral mechanisms remain elusive. Therefore, the beneficial effects of phytochemical against COVID-19 and main mechanisms require in-depth research to be verified by preclinical and clinical studies. Toxicological aspects, pharmacokinetics and pharmacodynamics properties and possible side effects, and structure-activity relationship (SAR) analyses need appropriate assessment. In silico studies indicated limonin [280] , berberine [281] , and fisetin [282] inhibited ACE2 and spike protein [280] , bound to ACE2, and increased Nrf2, HO-1, and TGF-β [281] ; also led to the reduction of TNF-α, IL-6, IL-1β [282] . Other compounds such as tetrandrine, lycorine, kazinol A [283] , and sinigrin [284] inhibited the early stage in HCoV-OC43infection, and also inhibited the effects against different species of CoV [283] , as well as inhibited SARS-CoV 3CL pro and PL pro [283, 284] . The results of in silico studies also demonstrated that methyl rosmarinate, calceolarioside B, myricetin 3-O-beta-D-glucopyranoside, betulinic acid, cryptotanshinone, dihomo-γ-linolenic acid, kaempferol, quercetin, sugiol, licoleafol, and amaranthine may have striking potential against COVID-19 [285, 286] . Based on in silico evidence, different flavonoids, likely tomentin A-E [287] , chrysin [288] , narcissin [289] , cyaniding [290] , and hesperetin [291] , interacted with ACE2 and declined its neurological manifestation in COVID-19 [288] [289] [290] [291] , and also inhibited papain-like protease in COVID-19 [287] . Docking evidence indicated that baicalin binds to TMPRSS2 and leads to the inhibition of COVID-19 [204] . An in vitro study also indicated that geraniol has inhibitory effects against viral spike protein and is a useful agent for therapy against COVID-19 [292] . Additionally, other natural compounds have important roles in modulating those signaling pathways, such as malvidin, which leads to the reduction of Bax/Bcl-2, caspase-3, IL-β, and TNF-α [50] . Additionally, osthole alleviated lung injury and inflammation through preventing the downregulation of ACE2 and Ang1-7 expression, thereby possessing anti-inflammatory effects [293] . Moreover, daidzein reduced TLR4, MyD88, NF-κB, MPO, IL-6, and TNF-α [294] , thymol reduced the level of NF-κB, IL-6, TNF-α, and IL-1β [295] , hyperin reduced TNF-α, IL-6, IL-1β, and NF-κB [296] , and cannabidiol declined the levels of MPO, TNF-α, and IL-6 [297] . These natural products declined the level of important mediators in signaling pathways of COVID-19, and have a vital function in reducing the symptoms of COVID-19. Several phytochemicals with promising antiviral effects are presented in Table 1 . Figure 1 shows the proposed targets and related therapeutic candidates for SARS-CoV-2. ↓Spread and replication of HCoV-OC43, ↓SARS-CoV-2 replication [264, 266] In vitro ↓Different species of CoV [283] Oxysophoridine In vitro ↓SARS-CoV-2 replication [266, 298] Strychnopentamine In silico ↓RdRp [263] Tetrandrine In vitro ↓HCoV-OC43-infected [283] Tylophorine In vitro ↓JAK2, ↓NF-κB, ↓inflammation, ↓replication [267, 268] Anthocyanin Malvidin In vitro ↓Bax/Bcl-2, Caspase-3, IL-1β, TNF-α [50] Cannabinoid Cannabidiol In vitro ↓MPO, TNF-α, IL-6 [297] Coumarin Inophyllum A In silico ↓M pro , ↓replication [278] Methylgalbanate In silico ↓M pro , ↓replication [276] Osthole In vitro ↓IL-6, TNF-α, ↑ACE2 and Ang1-7 [293] Toddacoumaquinone In silico ↓M pro , ↓replication [277] Diarylheptanoid Hirsutenone In vitro ↓PL pro , ↓replication [260] Flavonoid Baicalein In vitro In vivo ↓3CL pro ↓Vero E6 cells damage, ↓lesions of lung tissue, ↓replication, ↓IL-1β, ↓TNF-α, ↓inflammation [245, 246] Biochanin A In silico ↓spike glycoprotein [247] Kaempferol In vitro In silico ↓3CL pro , ↓replication [299] Luteolin In vitro In silico ↓Viral entry ↓SARS-CoV infection ↓TNF-α, IL-1β, IL-6, IL-18, NF-κB [256, 300] Naringenin In vitro In silico ↓TPC2, ↓viral infection ↓TNF-α, IL-1β, IL-6, IL-18, NF-κB [251, 300] Naringin In silico ↓M pro , ↓replication [249] In silico ↓Spike glycoprotein [248] Silibinin In silico ↓RdRp [255] Silymarin In silico ↓ACE2 ↓IL-6, IL-1β, TNF-α, p46-p54, p42, p38, p44, NF-κB, and JNK. [247] In silico ↓M pro [253] Flavonoid Cyanidin In silico ↓ACE2 and RdRp [290] Kazinol A In vitro ↓SARS-CoV 3CL pro and PL pro [283] Narcissin In silico Bind to ACE2 [289] Tomentin A-E In silico ↓PL pro in COVID-19 [287] Flavone Baicalin In silico ↓TMPRSS2 and lead to inhibition of COVID-19 [204] Chrysin In silico ↓ACE2 and decline neurological manifestation in COVID-19 [288] Geraniol In vitro ↓Spike protein, ↓TNF-α, IL-1β, IL-6, iNOS, COX-2 [292] Limonin In silico ↓ACE2, 3CL pro , PL pro , RdRp and spike protein [280] Thymol In vitro ↓NF-κB, IL-6, TNF-α, IL-1β, ↑SOD [295] ACE2: angiotensin-converting enzyme 2; Bcl-2: B-cell lymphoma 2; COX-2: cyclooxygenase; ERK: extracellular-regulated kinase; GPx: glutathione peroxidase; HCoV: human coronavirus; HO-1: heme oxygenase-1; IL: interleukin; iNOS: inducible nitric oxide synthase; JAK: Janus kinase; JNK: c-Jun N-terminal kinase; M pro : main protease; MERS-CoV: Middle East respiratory syndrome coronavirus; MIP: macrophage inflammatory protein; MPO: myeloperoxidase; NF-κB: nuclear factor-kappa B; PL pro : papain-like protease; RdRp: RNA-dependent RNA polymerase; Nrf2: nuclear factor erythroid 2-related factor 2; ROS: reactive oxygen species; SARS-CoV-2: severe acute respiratory syndrome coronavirus 2; SOD: superoxide dismutase; TGF-β: tumor grows factor-β; TLRs: toll-like receptors; TNF-α: tumor necrosis factor-α; TPC2: two-pore channel 2. Due to the complex pathological mechanisms behind COVID-19, revealing its precise signaling pathways may open new roads for providing efficient therapies. COVID-19 employs various signaling pathways/mediators, including inflammation, oxidative stress, apoptotic, and autophagy, to overcome the immune system. It has also been shown to alter the expression of some host factors, including enzymes/mediators and co-receptors such as ACE2, as well as ILs, TNF-α, IFN-γ, Nrf2, Bax/caspases, and Beclin/LC3 to facilitate cellular infection and subsequent complications (Figure 2 ). Despite advances, medicinal therapy against COVID-19 remains challenging. Besides, considering the multiple mediators involved in the pathogenesis of COVID-19, and providing multi-target agents, could be a more serious step toward controlling an infection. We previously reported the conventional therapeutic agents which potentially target the inflammatory signaling pathways in COVID-19 [124] . The current review introduces candidate therapeutic targets/treatment in COVID-19, as well as the evidence of using candidate phytochemicals. In this regard, phenolic compounds, alkaloids, terpenoids, coumarins, and carotenoids Due to the complex pathological mechanisms behind COVID-19, revealing its precise signaling pathways may open new roads for providing efficient therapies. COVID-19 employs various signaling pathways/mediators, including inflammation, oxidative stress, apoptotic, and autophagy, to overcome the immune system. It has also been shown to alter the expression of some host factors, including enzymes/mediators and co-receptors such as ACE2, as well as ILs, TNF-α, IFN-γ, Nrf2, Bax/caspases, and Beclin/LC3 to facilitate cellular infection and subsequent complications (Figure 2 ). Despite advances, medicinal therapy against COVID-19 remains challenging. Besides, considering the multiple mediators involved in the pathogenesis of COVID-19, and providing multi-target agents, could be a more serious step toward controlling an infection. We previously reported the conventional therapeutic agents which potentially target the inflammatory signaling pathways in COVID-19 [124] . The current review introduces candidate therapeutic targets/treatment in COVID-19, as well as the evidence of using candidate phytochemicals. In this regard, phenolic compounds, alkaloids, terpenoids, coumarins, and carotenoids showed potential anti-SARS-CoV-2 effects by targeting viral life cycle, virus entry/replication, spike proteins, ACE2, RdRP, PL pro , and M pro . It is worth mentioning that, despite preclinical mechanistic studies on the effects of phytochemicals on SARS-CoV-2, more clinical investigations are needed to confirm the results. More studies/methods are also needed to design a novel drug delivery system that counteracts the pharmacokinetic limitations of phytochemicals in showed potential anti-SARS-CoV-2 effects by targeting viral life cycle, virus entry/replication, spike proteins, ACE2, RdRP, PL pro , and M pro . It is worth mentioning that, despite preclinical mechanistic studies on the effects of phytochemicals on SARS-CoV-2, more clinical investigations are needed to confirm the results. More studies/methods are also needed to design a novel drug delivery system that counteracts the pharmacokinetic limitations of phytochemicals in COVID-19. Further areas of research on novel pathophysiological signaling pathways of COVID-19, especially on inflammatory, oxidative stress, apoptotic, and autophagic pathways, will show more potential candidates in the management, prevention, and treatment of COVID-19 complications. That said, more reports are still needed to confirm the benefits of targeting the aforementioned pathways in COVID-19. The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. Further areas of research on novel pathophysiological signaling pathways of COVID-19, especially on inflammatory, oxidative stress, apoptotic, and autophagic pathways, will show more potential candidates in the management, prevention, and treatment of COVID-19 complications. That said, more reports are still needed to confirm the benefits of targeting the aforementioned pathways in COVID-19. The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. Clinical characteristics of 138 hospitalized patients with 2019 novel coronavirus-infected pneumonia in Wuhan Risk factors associated with acute respiratory distress syndrome and death in patients with coronavirus disease Preliminary identification of potential vaccine targets for the COVID-19 coronavirus (SARS-CoV-2) based on SARS-CoV immunological studies Clinical characteristics of 138 hospitalized patients with 2019 novel coronavirus-infected pneumonia in Wuhan, China Risk factors associated with acute respiratory distress syndrome and death in patients with coronavirus disease 2019 pneumonia in Wuhan, China Preliminary identification of potential vaccine targets for the COVID-19 coronavirus (SARS-CoV-2) based on SARS-CoV immunological studies COVID-19) epidemics, the newest and biggest global health threats: What lessons have we learned? Diagnosis, treatment, and prevention of 2019 novel coronavirus infection in children: Experts' consensus statement State of knowledge and data gaps of Middle East respiratory syndrome coronavirus (MERS-CoV) in humans Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and corona virus disease-2019 (COVID-19): The epidemic and the challenges Plausibility of therapeutic effects of Rho kinase inhibitors against Severe Acute Respiratory Syndrome Coronavirus 2 (COVID-19) The continuous evolution and dissemination of 2019 novel human coronavirus COVID-19: Consider cytokine storm syndromes and immunosuppression Targeting the endocytic pathway and autophagy process as a novel therapeutic strategy in covid-19 A hypothesis for pathobiology and treatment of COVID-19: The centrality of ACE1/ACE2 imbalance Clinical features of patients infected with 2019 novel coronavirus in Wuhan Features, evaluation and treatment coronavirus (COVID-19). In Statpearls The possible of immunotherapy for COVID-19: A systematic review Sanjurjo-Sáez, M. Effectiveness, safety, and costs of a treatment switch to dolutegravir plus rilpivirine dual therapy in treatment-experienced HIV patients Tissue damage from neutrophilinduced oxidative stress in COVID-19 Delving beneath the surface of hyperinflammation in COVID-19 COVID-19 cytokine storm: The interplay between inflammation and coagulation SARS-CoV-2 receptor ACE2 gene expression and RAAS inhibitors The COVID-19 pandemic: A comprehensive review of taxonomy, genetics, epidemiology, diagnosis, treatment, and control An updated insight into the molecular pathogenesis, secondary complications and potential therapeutics of COVID-19 pandemic Genomic characterization of the 2019 novel human-pathogenic coronavirus isolated from a patient with atypical pneumonia after visiting Wuhan Genome composition and divergence of the novel coronavirus (2019-nCoV) originating in China COVID-2019: The role of the nsp2 and nsp3 in its pathogenesis Processing of the SARS-CoV pp1a/ab nsp7-10 region Genomic variance of the 2019-nCoV coronavirus A contemporary review on pathogenesis and immunity of COVID-19 infection The pathogenesis and treatment of the Cytokine Storm'in COVID-19 First case of 2019 novel coronavirus disease with Encephalitis Self-reported olfactory and taste disorders in patients with severe acute respiratory coronavirus 2 infection: A cross-sectional study There Is A New Symptom of Coronavirus, Doctors Say: Sudden Loss of Smell or Taste The neuroinvasive potential of SARS-CoV2 may play a role in the respiratory failure of COVID-19 patients Virus infections in the nervous system Targeting neurological manifestation of coronaviruses by candidate phytochemicals: A mechanistic approach Interaction brain-lungs. Ann. Fr. D'anesthesie et de Reanim COVID-19-associated acute hemorrhagic necrotizing encephalopathy: CT and MRI features Neuroinfection may contribute to pathophysiology and clinical manifestations of COVID-19 COVID-19 and liver dysfunction: Current insights and emergent therapeutic strategies The renin-angiotensin system in cardiovascular autonomic control: Recent developments and clinical implications Cardiovascular complications in COVID-19 Cardiovascular Complications in Patients with COVID-19: Consequences of Viral Toxicities and Host Immune Response COVID-19 pandemic: Cardiovascular complications and future implications Gastrointestinal symptoms associated with COVID-19: Impact on the gut microbiome COVID-19 and Gastrointestinal Symptoms-A Case Report Identification of a potential mechanism of acute kidney injury during the COVID-19 outbreak: A study based on single-cell transcriptome analysis Collapsing glomerulopathy in a COVID-19 patient COVID-19 and Kidney Failure in the Acute Care Setting: Our Experience from Seattle Acute kidney injury in SARS-CoV-2 infected patients The signaling pathways, and therapeutic targets of antiviral agents: Focusing on the antiviral approaches and clinical perspectives of anthocyanins in the management of viral diseases Tyrosine kinase inhibitors play an antiviral action in patients affected by chronic myeloid leukemia: A possible model supporting their use in the fight against SARS-CoV-2. Front The antiviral activity of Toll-like receptor 7 and 7/8 agonists Current and future antiviral drug therapies of hepatitis B chronic infection The interplay between viruses and TRIM family proteins Inhibitory receptor molecules in chronic hepatitis B and C infections: Novel targets for immunotherapy? The novel coronavirus 2019 (2019-nCoV) uses the SARS-coronavirus receptor ACE2 and the cellular protease TMPRSS2 for entry into target cells ACE2 Nascence, trafficking, and SARS-CoV-2 pathogenesis: The saga continues Modulation of TNF-α-converting enzyme by the spike protein of SARS-CoV and ACE2 induces TNF-α production and facilitates viral entry Angiotensin-converting enzyme 2: The first decade Role of angiotensin-converting enzyme 2 (ACE2) in COVID-19 Angiotensin II up-regulates angiotensin I-converting enzyme (ACE), but down-regulates ACE2 via the AT1-ERK/p38 MAP kinase pathway Role of HIF-1α in the regulation ACE and ACE2 expression in hypoxic human pulmonary artery smooth muscle cells ACE2 at the centre of COVID-19 from paucisymptomatic infections to severe pneumonia A novel coronavirus from patients with pneumonia in China Immunopathogenesis of coronavirus infections: Implications for SARS ACE2: Its potential role and regulation in severe acute respiratory syndrome and COVID-19 Physiological and pathological regulation of ACE2, the SARS-CoV-2 receptor Single-cell RNA expression profiling of ACE2, the receptor of SARS-CoV-2 Controversies of renin-angiotensin system inhibition during the COVID-19 pandemic Distribution of angiotensin-(1-7) and ACE2 in human placentas of normal and pathological pregnancies ACE2 expression and activity are enhanced during pregnancy Prevalence of complementary therapy use by women with breast cancer: A population-based survey Clinical characteristics of coronavirus disease 2019 in China Sex differences in the aging pattern of renin-angiotensin system serum peptidases High glucose-induced Nox1-derived superoxides downregulate PKC-βII, which subsequently decreases ACE2 expression and ANG (1-7) formation in rat VSMCs Sex-specific changes in renal angiotensin-converting enzyme and angiotensinconverting enzyme 2 gene expression and enzyme activity at birth and over the first year of life Early transmission dynamics in Wuhan, China, of novel coronavirus-infected pneumonia Nicotine and the renin-angiotensin system Age-and gender-related difference of ACE2 expression in rat lung MiRNA let-7b promotes the development of hypoxic pulmonary hypertension by targeting ACE2 PAK1-blockers: Potential Therapeutics against COVID-19 Raf/ERK drives the proliferative and invasive phenotype of BMPR2-silenced pulmonary artery endothelial cells Herbal therapeutics that block the oncogenic kinase PAK1: A practical approach towards PAK1-dependent diseases and longevity Outcomes in Patients with COVID-19 Infection Taking ACEI/ARB Cleavage of the SARS coronavirus spike glycoprotein by airway proteases enhances virus entry into human bronchial epithelial cells in vitro Moschüring-Alieva, E. TMPRSS2-inhibitors play a role in cell entry mechanism of COVID-19: An insight into camostat and nafamostat Gene of the month: TMPRSS2 (transmembrane serine protease 2) Inhibition of SARS-CoV-2 entry through the ACE2/TMPRSS2 pathway: A promising approach for uncovering early COVID-19 drug therapies TMPRSS2: A potential target for treatment of influenza virus and coronavirus infections New insights into genetic susceptibility of COVID-19: An ACE2 and TMPRSS2 polymorphism analysis The role of type II transmembrane serine protease-mediated signaling in cancer Peptide-binding heat shock protein GRP78 protects cardiomyocytes from hypoxia-induced apoptosis The ER chaperone and signaling regulator GRP78/BiP as a monitor of endoplasmic reticulum stress COVID-19 spike-host cell receptor GRP78 binding site prediction Middle East respiratory syndrome coronavirus and bat coronavirus HKU9 both can utilize GRP78 for attachment onto host cells Predicted therapeutic targets for COVID-19 disease by inhibiting SARS-CoV-2 and its related receptors CD147 as a target for COVID-19 treatment: Suggested effects of azithromycin and stem cell engagement Distribution of ACE2, CD147, CD26 and other SARS-CoV-2 associated molecules in tissues and immune cells in health and in asthma, COPD, obesity, hypertension, and COVID-19 risk factors CD147/EMMPRIN acts as a functional entry receptor for measles virus on epithelial cells CD147: A novel modulator of inflammatory and immune disorders Suppression of coronavirus replication by cyclophilin inhibitors SARS-CoV-2 invades host cells via a novel route: CD147-spike protein Meplazumab treats COVID-19 pneumonia: An open-labelled Low-salt diet and cyclosporine nephrotoxicity: Changes in kidney cell metabolism CD147 is a novel interaction partner of integrin αMβ2 mediating leukocyte and platelet adhesion Cell surface expression of CD147/EMMPRIN is regulated by cyclophilin 60 Cyclophilin-CD147 interactions: A new target for anti-inflammatory therapeutics Caveolin-1 regulates matrix metalloproteinases-1 induction and CD147/EMMPRIN cell surface clustering N-glycosylation by Nacetylglucosaminyltransferase V enhances the interaction of CD147/basigin with integrin β1 and promotes HCC metastasis The Role of FAK in the Secretion of MMP9 after CD147 Stimulation in Macrophages. Int Exposure to DPP-4 inhibitors and COVID-19 among people with type 2 diabetes. A case-control study Molecular basis of binding between novel human coronavirus MERS-CoV and its receptor CD26 Dipeptidyl peptidase-4 (DPP4) inhibition in COVID-19 DPP4 inhibition: Preventing SARS-CoV-2 infection and/or progression of COVID-19? The Potential Role of Renin Angiotensin System (RAS) and Dipeptidyl Peptidase-4 (DPP-4) in COVID-19: Navigating the Uncharted Unravelling the immunological roles of dipeptidyl peptidase 4 (DPP4) activity and/or structure homologue (DASH) proteins Chemokines: A new classification system and their role in immunity Cut to the chase: A review of CD26/dipeptidyl peptidase-4 s (DPP4) entanglement in the immune system COVID-19 and diabetes: Can DPP4 inhibition play a role? Diabetes and COVID-19 Epidemiology, causes, clinical manifestation and diagnosis, prevention and control of coronavirus disease (COVID-19) during the early outbreak period: A scoping review A Recovered Case of COVID-19 Myocarditis and ARDS Treated with Corticosteroids, Tocilizumab, and Experimental AT-001. Jacc: Case Rep Targeting pivotal inflammatory pathways in COVID-19: A mechanistic review Comparative and kinetic analysis of viral shedding and immunological responses in MERS patients representing a broad spectrum of disease severity The mercurial nature of neutrophils: Still an enigma in ARDS? Pathogenic human coronavirus infections: Causes and consequences of cytokine storm and immunopathology Human immunopathogenesis of severe acute respiratory syndrome (SARS) sCD163 in AOSD: A biomarker for macrophage activation related to hyperferritinemia The hyperferritinemic syndrome: Macrophage activation syndrome, Still's disease, septic shock and catastrophic antiphospholipid syndrome Eppur Si Muove: Ferritin is essential in modulating inflammation Into the eye of the cytokine storm. Microbiol Pathological inflammation in patients with COVID-19: A key role for monocytes and macrophages MERS-CoV infection in humans is associated with a pro-inflammatory Th1 and Th17 cytokine profile Plasma inflammatory cytokines and chemokines in severe acute respiratory syndrome Lung pathology of fatal severe acute respiratory syndrome Dysregulated type I interferon and inflammatory monocyte-macrophage responses cause lethal pneumonia in SARS-CoV-infected mice IFN-I response timing relative to virus replication determines MERS coronavirus infection outcomes Interaction of SARS and MERS coronaviruses with the antiviral interferon response Recent insights into emerging coronaviruses Middle East respiratory syndrome Macrophage-expressed IFN-β contributes to apoptotic alveolar epithelial cell injury in severe influenza virus pneumonia Calcineurin-NFAT signalling in myeloid leucocytes: New prospects and pitfalls in immunosuppressive therapy The Role of Calcium-Calcineurin-NFAT Signaling Pathway in Health and Autoimmune Diseases Lung biopsy cells transcriptional landscape from COVID-19 patient stratified lung injury in SARS-CoV-2 infection through impaired pulmonary surfactant metabolism Targeting JAK-STAT Signaling to Control Cytokine Release Syndrome in COVID-19 The potential of JAK/STAT pathway inhibition by ruxolitinib in the treatment of COVID-19 Oxidative Stress as Key Player in Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV) infection Antiviral activity of silymarin against Mayaro virus and protective effect in virus-induced oxidative stress The reactive oxygen species in macrophage polarization: Reflecting its dual role in progression and treatment of human diseases Reactive oxygen species localization programs inflammation to clear microbes of different size An anti-oxidative therapy for ameliorating cardiac injuries of critically ill COVID-19-infected patients Respiratory viral infections and subversion of cellular antioxidant defenses Aldose reductase inhibitor protects against hyperglycemic stress by activating Nrf2-dependent antioxidant proteins The Nrf2 Activator (DMF) and Covid-19: Is there a Possible Role Influenza virus directly infects human natural killer cells and induces cell apoptosis Overexpression of 7a, a protein specifically encoded by the severe acute respiratory syndrome coronavirus, induces apoptosis via a caspase-dependent pathway Viral infection and apoptosis A SARS-CoV protein, ORF-6, induces caspase-3 mediated, ER stress and JNK-dependent apoptosis Phosphorylation of p38 MAPK and its downstream targets in SARS coronavirus-infected cells Importance of Akt signaling pathway for apoptosis in SARS-CoVinfected Vero E6 cells Role of poly (ADP) ribose polymerase-1 inhibition by nicotinamide as a possible additive treatment to modulate host immune response and prevention of cytokine storm in COVID-19 Rho-kinase signaling pathway promotes the expression of PARP to accelerate cardiomyocyte apoptosis in ischemia/reperfusion Rabies virus matrix protein induces apoptosis by targeting mitochondria The SARS-Coronavirus Membrane protein induces apoptosis through modulating the Akt survival pathway A novel autophagy enhancer as a therapeutic agent against metabolic syndrome and diabetes Autophagy as a regulated pathway of cellular degradation Modulation of Autophagy by SARS-CoV-2: A Potential Threat for Cardiovascular System The SARS-CoV-2 cytopathic effect is blocked with autophagy modulators Autophagy as an emerging target for COVID-19: Lessons from an old friend, chloroquine Autophagy inhibitor, antimalarial, bitter taste receptor agonist in fight against COVID-19, a reality check? Digesting the crisis: Autophagy and coronaviruses Autophagy is involved in the acute lung injury induced by H9N2 influenza virus SKP2 attenuates autophagy through Beclin1-ubiquitination and its inhibition reduces MERS-Coronavirus infection Antiviral potential of ERK/MAPK and PI3K/AKT/mTOR signaling modulation for Middle East respiratory syndrome coronavirus infection as identified by temporal kinome analysis Bortezomib promotes KHSV and EBV lytic cycle by activating JNK and autophagy PRKAA/AMPK restricts HBV replication through promotion of autophagic degradation Escin induces caspase-dependent apoptosis and autophagy through the ROS/p38 MAPK signalling pathway in human osteosarcoma cells in vitro and in vivo Taming the Autophagy as a Strategy for Treating COVID-19. Cells 2020 Life and death partners: Apoptosis, autophagy and the cross-talk between them Simvastatin increases temozolomide-induced cell death by targeting the fusion of autophagosomes and lysosomes Autophagy and SARS-CoV-2 infection: A possible smart targeting of the autophagy pathway Corticosteroids block autophagy protein recruitment in Aspergillus fumigatus phagosomes via targeting dectin-1/Syk kinase signaling Mechanisms for mtorc1 activation and synergistic induction of apoptosis by ruxolitinib and bh3 mimetics or autophagy inhibitors in jak2-v617f-expressing leukemic cells including newly established pvtl-2 Targeting the heme-heme oxygenase system to prevent severe complications following COVID-19 infections Vitamin C as prophylaxis and adjunctive medical treatment for COVID-19? Quercetin and vitamin C: An experimental, synergistic therapy for the prevention and treatment of SARS-CoV-2 related disease (COVID-19). Front Intravenous high-dose vitamin C for the treatment of severe COVID-19: Study protocol for a multicentre randomised controlled trial Vitamin E deficiency and lipoperoxidation during adult respiratory distress syndrome Is Antioxidant Therapy a Useful Complementary Measure for Covid-19 Treatment? An Algorithm for Its Application COVID-19 and immune response: Focus on oxidative stress, apoptosis and autophagy SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor Pharmacologic treatments for coronavirus disease 2019 (COVID-19): A review Clinical features of 69 cases with coronavirus disease 2019 in Wuhan, China Treatment With Lopinavir/Ritonavir or Interferon-beta1b Improves Outcome of MERS-CoV Infection in a Nonhuman Primate Model of Common Marmoset Treatment and vaccines for severe acute respiratory syndrome A trial of lopinavir-ritonavir in adults hospitalized with severe Covid-19 Arbidol monotherapy is superior to lopinavir/ritonavir in treating COVID-19 Favipiravir (T-705) but not ribavirin is effective against two distinct strains of Crimean-Congo hemorrhagic fever virus in mice Reevaluation of the efficacy of favipiravir against rabies virus using in vivo imaging analysis Effectiveness of favipiravir (T-705) against wild-type and oseltamivir-resistant influenza B virus in mice Experimental Treatment with Favipiravir for COVID-19: An Open-Label Control Study Remdesivir and chloroquine effectively inhibit the recently emerged novel coronavirus (2019-nCoV) in vitro Remdesivir in adults with severe COVID-19: A randomised, double-blind, placebo-controlled, multicentre trial Review of therapeutic agents for the treatment of COVID-19 In vitro antiviral activity and projection of optimized dosing design of hydroxychloroquine for the treatment of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Hydroxychloroquine and azithromycin as a treatment of COVID-19: Results of an open-label non-randomized clinical trial Anticancer Agents from Natural Products A pilot study of hydroxychloroquine in treatment of patients with common coronavirus disease-19 (COVID-19) Effect of High vs Low Doses of Chloroquine Diphosphate as Adjunctive Therapy for Patients Hospitalized With Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection: A Randomized Clinical Trial Prognostic value of interleukin-6, C-reactive protein, and procalcitonin in patients with COVID-19 Tocilizumab, an anti-IL6 receptor antibody, to treat Covid-19-related respiratory failure: A case report Interferon-beta and mycophenolic acid are potent inhibitors of Middle East respiratory syndrome coronavirus in cell-based assays Type 1 interferons as a potential treatment against COVID-19 Baricitinib therapy in COVID-19: A pilot study on safety and clinical impact Corticosteroid therapy for critically ill patients with Middle East respiratory syndrome The effect of corticosteroids on mortality of patients with influenza pneumonia: A systematic review and meta-analysis Clinical evidence does not support corticosteroid treatment for 2019-nCoV lung injury Disease-modifying effects of long-term and continuous use of nonsteroidal anti-inflammatory drugs (NSAIDs) in spondyloarthritis Non-steroidal anti-inflammatory drugs in management of COVID-19; a systematic review on current evidence Associations between immune-suppressive and stimulating drugs and novel COVID-19-A systematic review of current evidence Early treatment of COVID-19 patients with hydroxychloroquine and azithromycin: A retrospective analysis of 1061 cases in Marseille, France An evaluation of co-use of chloroquine or hydroxychloroquine plus azithromycin on cardiac outcomes: A pharmacoepidemiological study to inform use during the COVID19 pandemic Safety signals for QT prolongation or Torsades de Pointes associated with azithromycin with or without chloroquine or hydroxychloroquine Teicoplanin: An alternative drug for the treatment of COVID-19? The FDA-approved drug ivermectin inhibits the replication of SARS-CoV-2 in vitro BCG vaccination may be protective against Covid-19 Vitamin D in prevention and treatment of COVID-19: Current perspective and future prospects Vitamin D for COVID-19: A case to answer? Vitamin D for your patients with chronic hepatitis C? COVID-19: Melatonin as a potential adjuvant treatment Nanoformulations of Herbal Extracts in Treatment of Neurodegenerative Disorders. Front Modulation of dysregulated cancer metabolism by plant secondary metabolites: A mechanistic review Antiviral activity of phytochemicals: A comprehensive review Candidate drugs against SARS-CoV-2 and COVID-19 Phytochemicals: Potential therapeutic interventions against coronaviruses-associated lung injury The inhibitory effect of curcumin on virus-induced cytokine storm and its potential use in the associated severe pneumonia Curcumin is a promising inhibitor of genotype 2 porcine reproductive and respiratory syndrome virus infection Anti-infective properties of the golden spice curcumin Antiviral potential of natural compounds against influenza virus hemagglutinin Potential effects of curcumin in the treatment of COVID-19 infection Virtual screening of curcumin and its analogs against the spike surface glycoprotein of SARS-CoV-2 and SARS-CoV Catechin and Curcumin interact with corona (2019-nCoV/SARS-CoV2) viral S protein and ACE2 of human cell membrane: Insights from Computational study and implication for intervention Baicalin inhibits autophagy induced by influenza A virus H3N2 Scutellaria baicalensis extract and baicalein inhibit replication of SARS-CoV-2 and its 3C-like protease in vitro The comprehensive study on the therapeutic effects of baicalein for the treatment of COVID-19 in vivo and in vitro Lead Finding from Selected Flavonoids with Antiviral (SARS-CoV-2) Potentials against COVID-19: An in-silico Evaluation In silico evaluation of flavonoids as effective antiviral agents on the spike glycoprotein of SARS-CoV-2 Docking Study of Naringin Binding with COVID-19 Main Protease Enzyme Characterization of spike glycoprotein of SARS-CoV-2 on virus entry and its immune cross-reactivity with SARS-CoV Naringenin is a powerful inhibitor of SARS-CoV-2 infection in vitro Inactivation of Nf-kb Pathway by Taxifolin Attenuates Sepsis-Induced Acute Lung Injury Computational guided identification of a citrus flavonoid as potential inhibitor of SARS-CoV-2 main protease Silibinin is a direct inhibitor of STAT3 Silibinin and SARS-CoV-2: Dual targeting of host cytokine storm and virus replication machinery for clinical management of COVID-19 patients Small molecules blocking the entry of severe acute respiratory syndrome coronavirus into host cells Effective inhibition of MERS-CoV infection by resveratrol Resveratrol inhibits the replication of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in cultured Vero cells Emodin blocks the SARS coronavirus spike protein and angiotensinconverting enzyme 2 interaction Diarylheptanoids from Alnus japonica inhibit papain-like protease of severe acute respiratory syndrome coronavirus Isoquinoline alkaloids and their antiviral, antibacterial, and antifungal activities and structure-activity relationship In vitro antiviral effects of Peganum harmala seed extract and its total alkaloids against Influenza virus Alkaloids and flavonoids from African phytochemicals as potential inhibitors of SARS-Cov-2 RNA-dependent RNA polymerase: An in silico perspective High-throughput screening and identification of potent broad-spectrum inhibitors of coronaviruses Remdesivir, lopinavir, emetine, and homoharringtonine inhibit SARS-CoV-2 replication in vitro lycorine and oxysophoridine inhibit novel coronavirus (SARS-CoV-2) in cell culture Targeting coronaviral replication and cellular JAK2 mediated dominant NF-κB activation for comprehensive and ultimate inhibition of coronaviral activity Inhibition of SARS-CoV-2 by highly potent broad-spectrum anti-coronaviral tylophorine-based derivatives The Potential Therapeutic Effect of RNA Interference and Natural Products on COVID-19: A Review of the Coronaviruses Infection Glycyrrhizin exerts antioxidative effects in H5N1 influenza A virus-infected cells and inhibits virus replication and pro-inflammatory gene expression Symptomatic protective action of glycyrrhizin (Licorice) in Covid-19 infection? Front High mobility group box 1 influences HSV1716 spread and acts as an adjuvant to chemotherapy High mobility group box protein-1 in HIV-1 infection Glycyrrhizin: An alternative drug for the treatment of COVID-19 infection and the associated respiratory syndrome? Therapeutic potential of coumarins as antiviral agents In silico screening of naturally occurring coumarin derivatives for the inhibition of the main protease of SARS-CoV-2 In silico molecular docking: Evaluation of coumarin based derivatives against SARS-CoV-2 Synthesis of novel coumarin analogues: Investigation of molecular docking interaction of SARS-CoV-2 proteins with natural and synthetic coumarin analogues and their pharmacokinetics studies Antiviral compounds obtained from microalgae commonly used as carotenoid sources In silico ADMET and molecular docking study on searching potential inhibitors from limonoids and triterpenoids for COVID-19 Anti-influenza activity of berberine improves prognosis by reducing viral replication in mice The plant flavonoid, fisetin alleviates cigarette smoke-induced oxidative stress, and inflammation in Wistar rat lungs Natural products and their derivatives against coronavirus: A review of the non-clinical and pre-clinical data Antiviral natural products and herbal medicines Structural basis of SARS-CoV-2 3CLpro and anti-COVID-19 drug discovery from medicinal plants † In silico screening of Chinese herbal medicines with the potential to directly inhibit 2019 novel coronavirus Geranylated flavonoids displaying SARS-CoV papain-like protease inhibition from the fruits of Paulownia tomentosa Molecular docking study of potential phytochemicals and their effects on the complex of SARS-CoV2 spike protein and human ACE2 Molecular docking reveals the potential of Salvadora persica flavonoids to inhibit COVID-19 virus main protease Computational selection of flavonoid compounds as inhibitors against SARS-CoV-2 main protease, RNA-dependent RNA polymerase and spike proteins: A molecular docking study Citrus fruits are rich in flavonoids for immunoregulation and potential targeting ACE2 Structure-based drug designing for potential antiviral activity of selected natural products from Ayurveda against SARS-CoV-2 spike glycoprotein and its cellular receptor Osthole protects lipopolysaccharide-induced acute lung injury in mice by preventing down-regulation of angiotensin-converting enzyme 2 Comparison of the antiviral activity of flavonoids against murine norovirus and feline calicivirus Preventive and therapeutic effects of thymol in a lipopolysaccharide-induced acute lung injury mice model The protective effect of hyperin on LPS-induced acute lung injury in mice Potential of cannabidiol for the treatment of viral hepatitis Structure-based virtual screening of bioactive compounds from Indonesian medical plants against severe acute respiratory syndrome coronavirus-2 In silico and in vitro evaluation of kaempferol as a potential inhibitor of the SARS-CoV-2 main protease (3CLpro) Active Compounds Activity from the Medicinal Plants against SARS-CoV-2 using in Silico Assay Polyphenols could prevent SARS-CoV-2 infection by modulating the expression of miRNAs in the host cells An in-silico evaluation of dietary components for structural inhibition of SARS-Cov-2 main protease