Abstract
Recently, natural compounds have gained significant importance in health care, as they do not exhibit adverse effects compared to synthetic drugs. Since the dawn of civilization, plants have been one of the primary sources of medicine. Natural occurring medicinal plants, either alone or in combination, are widely used in the health care system. Medicinal plants can be a rich source of chemical substances with therapeutic potential. Coronavirus is an infectious disease that causes acute respiratory illness caused by a virus. Even a year after COVID-19’s first occurrence in Wuhan city, the number of cases is still rising daily throughout the world. SARS-CoV-2 infection spreads quickly and is distinct from other infections, probably due to variations in structural spike proteins. Patients suffering from critical conditions may die from acute respiratory distress syndrome (ARDS), which is characterized by rapid inflammatory reactions caused by the immune effector cells’ excessive production of cytokines and chemokines. This chapter reviews medicinal plants used against SARS-CoV or coronavirus infections, particularly emphasizing ethnopharmacology, chemistry, clinical, and preclinical studies. Various traditional herbs with medicinal values against coronavirus are discussed. AYUSH formulations that have advanced into pilot and full clinical trials against SAR-CoV-2 are also described. Phytoconstituents with potential against coronavirus were studied using activity miner studies, and cluster analysis; disparity and similarity scores were analyzed. To address the current problem, it is advised that promising AYUSH formulations and Indian medicinal plants be explored as soon as possible. This review can be utilized for both therapeutic and research purposes.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Abbreviations
- 3CLpro:
-
“3-chymotrypsin-like protease”
- ACE2:
-
Angiotensin-converting enzyme 2
- IL:
-
Interleukin-6
- MERS-CoV:
-
Middle East respiratory syndrome coronavirus
- N:
-
Nucleocapsid
- PLpro:
-
Papain-like protease
- pp.:
-
Polyprotein
- RAAS:
-
Renin-angiotensin-aldosterone system;
- RBD:
-
Receptor binding domain
- RdRp:
-
“RNA-dependent RNA polymerase”
- S :
-
Spike
- SARS-CoV:
-
Severe Acute Respiratory Syndrome
- SoC:
-
Standard of care (SoC)
- TM:
-
Traditional medicine
- TMPRSS2:
-
Transmembrane protease serine
- TNF-alpha:
-
Tumor necrosis factor-alpha
- VoC:
-
Variant of concern
References
Islam MM (2013) Biochemistry, medicinal and food values of jute (Corchorus capsularis L. and C. olitorius L.) leaf: a review. Int J Enhanc Res Sci Technol En 2:135–144. https://doi.org/10.3390/antiox11071358
Bouyahya A, Bakri Y, Khay EO, Edaoudi F, Talbaoui A, Et-Touys A, Abrini J, Dakka N (2017) Antibacterial, antioxidant and antitumor properties of Moroccan medicinal plants: a review. Asian Pac J Trop Dis 7:57–64. https://doi.org/10.12980/apjtd.7.2017d6-294
Tabish SA (2008) Complementary and alternative healthcare: is it evidence-based? Int. J. Health Sci 2:1–143. https://doi.org/10.1155/2014/525340
Kamboj VP (2000) Herbal medicine. Curr Sci 78:35–39. https://doi.org/10.2307/24103844
Calixto JB (2000) Efficacy, safety, quality control, marketing and regulatory guidelines for herbal medicines (phytotherapeutic agents). Braz J Med Biol Res 33:179–189. https://doi.org/10.1590/s0100-879x2000000200004
Khan M, Adil SF, Alkhathlan HZ, Tahir MN, Saif S, Khan M, Khan ST (2020) COVID-19: a global challenge with old history, epidemiology and progress so far. Molecules 26:39. https://doi.org/10.3390/molecules26010039
Schneider E (2012) Severe Acute Respiratory Syndrome (SARS). Netter’s Inf Dis:537–543. https://doi.org/10.1016/B978-1-4377-0126-5.00089-6
Atzrodt CL, Maknojia I, McCarthy RD, Oldfield TM, Po J, Ta KT, Stepp HE, Clements TP (2020) A Guide to COVID-19: a global pandemic caused by the novel coronavirus SARS-CoV-2. FEBS J 287:3633–3650. https://doi.org/10.1111/febs.15375
Safari I, Elahi E (2021) Evolution of the SARS-CoV-2 genome and emergence of variants of concern. Arch Virol 167:293–305. https://doi.org/10.1007/s00705-021-05295-5
Zoccola R, Beltramo C, Magris G, Peletto S, Acutis P, Bozzetta E, Radovic S, Zappulla F, Porzio AM, Gennero MS, Dondo A (2021) First detection of an Italian human-to-cat outbreak of SARS-CoV-2 Alpha variant–lineage B. 1.1. 7. One. Health 13:100295. https://doi.org/10.1016/j.onehlt.2021.100295
Kannan S, Ali PS, Sheeza A (2021) Evolving biothreat of variant SARS-CoV-2-molecular properties, virulence and epidemiology. Eur Rev Med Pharmacol Sc 25:4405–4412. https://doi.org/10.26355/eurrev_202106_26151
La Rosa G, Brandtner D, Mancini P, Veneri C, Bonanno Ferraro G, Bonadonna L, Lucentini L, Suffredini E (2021) Key SARS-CoV-2 mutations of alpha, gamma, and eta variants detected in urban wastewaters in Italy by long-read amplicon sequencing based on nanopore technology. Water. 13:2503. https://doi.org/10.3390/w13182503
Mohapatra RK, Kandi V, Verma S, Dhama K (2022) Challenges of the Omicron (B. 1.1. 529) variant and its lineages: a global perspective. Chembiochem 23:e202200059. https://doi.org/10.1002/cbic.202200059
Petersen E, Ntoumi F, Hui DS, Abubakar A, Kramer LD, Obiero C, Tambyah PA, Blumberg L, Yapi R, Al-Abri S, Pinto TD (2022) Emergence of new SARS-CoV-2 Variant of Concern Omicron (B. 1.1. 529)-highlights Africa’s research capabilities, but exposes major knowledge gaps, inequities of vaccine distribution, inadequacies in global COVID-19 response and control efforts. Int. J. Infect. Dis. 114:268–272. https://doi.org/10.1016/j.ijid.2021.11.040
Chen J, Wang R, Gilby NB, Wei GW (2022) Omicron variant (B. 1.1. 529): infectivity, vaccine breakthrough, and antibody resistance. J Chem Inf Mode 62(2):412–422. https://doi.org/10.1021/acs.jcim.1c01451
Bentur SA, Mishra A, Kumar Y, Thakral S, Sanjiv S, Garg R (2021) Integrative Therapy based on Yoga, Ayurveda and Modern Western Medicine for treatment of high-risk cases of COVID-19: a telemedicine-based case series. IJTK 21. https://doi.org/10.56042/ijtk.v21i3.55516
Clark AM (1996) Natural products as a resource for new drugs. Pharm Res 13:1133–1141. https://doi.org/10.1023/a:1016091631721
Fuzimoto AD, Isidoro C (2020) The antiviral and coronavirus-host protein pathways inhibiting properties of herbs and natural compounds – additional weapons in the fight against the COVID-19 pandemic? J Tradit Complement Med 10:405–419. https://doi.org/10.1016/j.jtcme.2020.05.003
Siddiqui AJ, Danciu C, Ashraf SA, Moin A, Singh R, Alreshidi M, Patel M, Jahan S, Kumar S, Alkhinjar MI, Badraoui R (2020) Plants-derived biomolecules as potent antiviral phytomedicines: new insights on ethnobotanical evidences against coronaviruses. Plants (Basel) 9. https://doi.org/10.3390/plants9091244
Heinrich M (2010) Ethnopharmacology in the 21st century-grand challenges. Front Pharmacol 1:8. https://doi.org/10.3389/fphar.2010.00008
Wang J-b, Andrade-Cetto A, Echeverria J, Wardle J, Yen H-R, Heinrich M (2022) Ethnopharmacological responses to the coronavirus disease 2019 pandemic. Front Pharmacol 7. https://doi.org/10.3389/fphar.2021.798674
Okoro EE, Maharjan R, Jabeen A, Ahmad MS, Azhar M, Shehla N, Zaman W, Shams S, Osoniyi OR, Onajobi FD, Choudhary MI (2021) Isoflavanquinones from Abrus precatorius roots with their antiproliferative and anti-inflammatory effects. Phytochemistry 187:112743. https://doi.org/10.1016/j.phytochem.2021.112743
Dutta T, Ghorai S, Khan AA, Baildya N, Ghosh NN (2021) Screening of potential anti-HIV compounds from Achyranthes aspera extracts for SARS-CoV-2: an insight from molecular docking study. J Phys Conf Ser 1797. https://doi.org/10.1088/1742-6596/1797/1/012042
Donma MM, Donma O (2020) The effects of allium sativum on immunity within the scope of COVID-19 infection. Med Hypotheses 144:109934. https://doi.org/10.1016/j.mehy.2020.109934
Moghadamtousi SZ, Fadaeinasab M, Nikzad S, Mohan G, Ali HM, Kadir HA (2015) Annona muricata (Annonaceae): a review of its traditional uses, isolated acetogenins and biological activities. Int. J. Mol. Sci 16:15625–15658. https://doi.org/10.3390/ijms160715625
Balderrama-Carmona AP, Silva-Beltrán NP, Gálvez-Ruiz JC, Ruíz-Cruz S, Chaidez-Quiroz C, Morán-Palacio EF (2020) Antiviral, antioxidant, and antihemolytic effect of Annona muricata L. leaves extracts. Plant 9(1650). https://doi.org/10.3390/plants9121650
Balkrishna A, Pokhrel S, Singh H, Joshi M, Mulay VP, Haldar S, Varshney A (2021) Withanone from Withania somnifera attenuates SARS-CoV-2 RBD and host ACE2 interactions to rescue spike protein induced pathologies in humanized zebrafish model. Drug Des Devel Ther 15:1111. https://doi.org/10.2147/DDDT.S292805
Koulgi S, Jani V, Uppuladinne VNM, Sonavane U, Joshi R (2021) Natural plant products as potential inhibitors of RNA dependent RNA polymerase of Severe Acute Respiratory Syndrome Coronavirus-2. PLoS One 16:e0251801. https://doi.org/10.1371/journal.pone.0251801
Khalifa SA, Yosri N, El-Mallah MF, Ghonaim R, Guo Z, Musharraf SG, Du M, Khatib A, Xiao J, Saeed A, El-Seedi HH (2021) Screening for natural and derived bio-active compounds in preclinical and clinical studies: One of the frontlines of fighting the coronaviruses pandemic. Phytomedicine 85:153311. https://doi.org/10.1016/j.phymed.2020.153311
Shahhamzehei N, Abdelfatah S, Efferth T (2022) In Silico and In Vitro Identification of Pan-Coronaviral Main Protease Inhibitors from a Large Natural Product Library. Pharmaceuticals (Basel) 15:308. https://doi.org/10.3390/ph15030308
Kanjanasirirat P, Suksatu A, Manopwisedjaroen S, Munyoo B, Tuchinda P, Jearawuttanakul K, Seemakhan S, Charoensutthivarakul S, Wongtrakoongate P, Rangkasenee N, Pitiporn S (2020) High-content screening of Thai medicinal plants reveals Boesenbergia rotunda extract and its component Panduratin a as anti-SARS-CoV-2 agents. Sci Rep 10:1–12. https://doi.org/10.1038/s41598-020-77003-3
Thakur A, Gautam S, Kaushal K, Kumari A, Thakur A, Bhatt K, Jasta S (2022) A review on therapeutic potential of Indian medicinal plants against COVID-19 pandemic. Ann. Phytomed. 11:36–47. https://doi.org/10.47070/ijapr.v9i7.2001
Kataria S, Sharma P, Ram JP, Deswal V, Singh M, Rana R, Singhal R, Tripathi A, Kumar K, Trehan N (2022) A pilot clinical study of an add-on Ayurvedic formulation containing Tinospora cordifolia and Piper longum in mild to moderate COVID-19. J Ayurveda Integr Med 13:100454. https://doi.org/10.1016/j.jaim.2021.05.008
Wanjarkhedkar P, Sarade G, Purandare B, Kelkar DA (2022) A prospective clinical study of an Ayurveda regimen in COVID 19 patients. J Ayurveda Integr Med 13:100365. https://doi.org/10.1016/j.jaim.2020.10.008
Wylie MR, Merrell DS (2022) The antimicrobial potential of the neem tree Azadirachta indica. Front Pharmacol 13:891535. https://doi.org/10.3389/fphar.2022.891535
Godatwar PK, Deshpande S, JoshiDeshmukh PS, Deshpande VS, Ghungralekar R, Tamoli S, Gupta A, Vedula S, Rugvedi P, Rai RK (2021) Clinical evaluation of Chyawanprash as a preventive measure during the COVID-19 pandemic: an open-label, multicentric, randomized, comparative, prospective, and interventional community-based clinical study on healthy individuals. J Indian Syst Med 9:104–113. https://doi.org/10.4103/jism.jism_27_21
Gupta A, Madan A, Yadav B, Mundada P, Singhal R, Pandey YK, Agarwal R, Tripathi A, Rana R, Sharma BS, Rao BC (2021) Chyawanprash for the prevention of COVID-19 infection among healthcare workers: a randomized controlled trial. medRxiv. https://doi.org/10.1101/2021.02.17.21251899
Jindal N, Rajput S, Yadav B, Mundada P, Singhal R, Varshney S, Nimbalkar K, Rana R, Khanduri S, Rao BC, Mata S (2021) Chyawanprash as add on to the standard of care in preventing COVID-19 infection among apparently healthy health care workers a single arm, longitudinal study. AAM 10:204–219. https://doi.org/10.5455/AAM.73639
Natarajan S, Anbarasi C, Sathiyarajeswaran P, Manickam P, Geetha S, Kathiravan R, Prathiba P, Pitchiahkumar M, Parthiban P, Kanakavalli K, Balaji P (2021) Kabasura Kudineer (KSK), a poly-herbal Siddha medicine, reduced SARS-CoV-2 viral load in asymptomatic COVID-19 individuals as compared to vitamin C and zinc supplementation: findings from a prospective, exploratory, open-labeled, comparative, randomized controlled trial, Tamil Nadu, India. Trials 22:1–11. https://doi.org/10.1186/s13063-021-05583-0
Srivastava A, Rengaraju M, Srivastava S, Narayan V, Gupta V, Upadhayay R (2021) A double blinded placebo controlled comparative clinical trial to evaluate the effectiveness of Siddha medicines, Kaba Sura Kudineer (KSK) & Nilavembu Kudineer (NVK) along with standard Allopathy treatment in the management of symptomatic COVID 19 patients – a structured summary of a study protocol for a randomized controlled trial. Trials. 22:130. https://doi.org/10.1186/s13063-021-05041-x
Singh H, Srivastava S, Yadav B, Rai AK, Jameela S, Muralidharan S, Mohan R, Chaudhary S, Singhal R, Rana R, Khanduri S (2022) AYUSH-64 as an adjunct to Standard Care in mild to moderate COVID-19: an open-label randomized controlled trial in Chandigarh, India. Complement Ther Me 66:102814. https://doi.org/10.1016/j.ctim.2022.102814
Srivastava S, Singh H, Muralidharan S, Mohan R, Chaudhary S, Rani P, Payyappalli U, Srikanth N (2021) A retrospective analysis of Ayurvedic clinical management of mild COVID-19 patients. 5(2):80–86. https://doi.org/10.4103/jras.jras_15_21
Surve A, Sharma R, Mata S, Rana R, Singhal R (2020) AYUSH 64, a polyherbal Ayurvedic formulation in Influenza-like illness–results of a pilot study. https://doi.org/10.1016/j.jaim.2020.05.010
Gundeti MS, Bhurke LW, Mundada PS, Murudkar S, Surve A, Sharma R, Mata S, Rana R, Singhal R, Vyas N, Khanduri S (2020) AYUSH 64, a polyherbal Ayurvedic formulation in influenza-like illness – results of a pilot study. J Ayurveda Integr Med 13. https://doi.org/10.1016/j.jaim.2020.05.010
Pawar KS, Mastud RN, Pawar SK, Pawar SS, Bhoite RR, Bhoite RR, Kulkarni MV, Deshpande AR (2021) Oral curcumin with piperine as adjuvant therapy for the treatment of COVID-19: a randomized clinical trial. Front. Pharmacol. 12:1056. https://doi.org/10.3389/fphar.2021.669362
Varnasseri M, Siahpoosh A, Hoseinynejad K, Amini F, Karamian M, Yad MJ, Cheraghian B, Khosravi AD (2022) The effects of add-on therapy of Phyllanthus Emblica (Amla) on laboratory confirmed COVID-19 cases: a randomized, double-blind, controlled trial. Complement Ther Med 65:102808. https://doi.org/10.1016/j.ctim.2022.102808
Nikhat S, Fazil M (2020) Overview of Covid-19; its prevention and management in the light of Unani medicine. Sci Total Environ 728:138859. https://doi.org/10.3389/fphar.2021.669362
Haggag YA, El-Ashmawy NE, Okasha KM (2020) Is hesperidin essential for prophylaxis and treatment of COVID-19 infection? Med Hypotheses 144:109957. https://doi.org/10.1016/j.mehy.2020.109957
Trieu V, Saund S, Rahate PV, Barge VB, Nalk KS, Windlass H, Uckun FM (2021) Targeting TGF-b pathway with COVID-19 drug candidate ARTIVeda/PulmoHeal accelerates recovery from mild-moderate COVID-19. medRxiv. https://doi.org/10.1101/2021.01.24.21250418
Hu K, Guan WJ, Bi Y, Zhang W, Li L, Zhang B, Liu Q, Song Y, Li X, Duan Z, Zheng Q (2021) Efficacy and safety of Lianhuaqingwen capsules, a repurposed Chinese herb, in patients with coronavirus disease 2019: a multicenter, prospective, randomized controlled trial. Phytomedicine 85:153242. https://doi.org/10.1016/j.phymed.2020.153242
Sarah M, Khadidja H, Keltoum D, Asma T (2022) The use of Syzygium aromaticum L. to avoid and control the SARS-CoV-2 related complications. Egypt. Acad. J. Biol. Sci 14:77–89. https://doi.org/10.21608/eajbsc.2022.215048
Senthil Kumar KJ, Gokila Vani M, Wang CS, Chen CC, Chen YC, Lu LP, Huang CH, Lai CS, Wang SY (2020) Geranium and lemon essential oils and their active compounds downregulate angiotensin-converting enzyme 2 (ACE2), a SARS-CoV-2 spike receptor-binding domain, in epithelial cells. Plan Theory 9:770. https://doi.org/10.3390/plants9060770
Natarajan S, Anbarasi C, Sathiyarajeswaran P, Manickam P, Geetha S, Kathiravan R, Prathiba P, Pitchiahkumar M, Parthiban P, Kanakavalli K, Balaji P (2021) Kabasura Kudineer (KSK), a poly-herbal Siddha medicine, reduced SARS-CoV-2 viral load in asymptomatic COVID-19 individuals as compared to vitamin C and zinc supplementation: findings from a prospective, exploratory, open-labeled, comparative, randomized controlled trial, Tamil Nadu. India. Trials. 22:623. https://doi.org/10.1186/s13063-021-05583-0
Balkrishna A, Bhatt AB, Singh P, Haldar S, Varshney A (2021) Comparative retrospective open-label study of Ayurvedic medicines and their combination with allopathic drugs on asymptomatic and mildly-symptomatic COVID-19 patients. J Herb Med 29:1–8. https://doi.org/10.1016/j.hermed.2021.100472
Sharifi-Rad M, Varoni EM, Salehi B, Sharifi-Rad J, Matthews KR, Ayatollahi SA, Kobarfard F, Ibrahim SA, Mnayer D, Zakaria ZA, Sharifi-Rad M (2017) Plants of the genus Zingiber as a source of bioactive phytochemicals. Molecules 22:2145. https://doi.org/10.3390/molecules22122145
Tripathi S, Maier KG, Bruch D, Kittur DS (2007) Effect of 6-gingerol on pro-inflammatory cytokine production and costimulatory molecule expression in murine peritoneal macrophages. J Surg Res 138:209–213. https://doi.org/10.1016/j.jss.2006.07.051
Rathinavel T, Palanisamy M, Palanisamy S, Subramanian A, Thangaswamy S (2020) Phytochemical 6-Gingerol–a promising drug of choice for COVID-19. Int J Adv Sci Eng 6:1482–1489. https://doi.org/10.29294/IJASE.6.4.2020.1482-1489
Raaben M, Einerhand AW, Taminiau LJ, Van Houdt M, Bouma J, Raatgeep RH, Büller HA, De Haan CA, Rossen JW (2007) Cyclooxygenase activity is important for efficient replication of mouse hepatitis virus at an early stage of infection. J. Virol 4:1–5. https://doi.org/10.1186/1743-422X-4-55
Akbay P, Basaran AA, Undeger U, Basaran N (2003) In vitro immunomodulatory activity of flavonoid glycosides from Urtica dioica L. Phytother Res 17:34–37. https://doi.org/10.1002/ptr.1068
Semalty M, Adhikari L, Semwal D, Chauhan A, Mishra A, Kotiyal R, Semalty A (2017) A comprehensive review on phytochemistry and pharmacological effects of stinging nettle (Urtica dioica). Curr Tradit Med 3:156–167. https://doi.org/10.2174/2215083803666170502120028
Dibazar SP, Fateh S, Daneshmandi S (2015) Immunomodulatory effects of clove (Syzygium aromaticum) constituents on macrophages: in vitro evaluations of aqueous and ethanolic components. J Immunotoxicol 12:124–131. https://doi.org/10.3109/1547691x.2014.912698
Rahayu RP, Prasetyo RA, Purwanto DA, Kresnoadi U, Iskandar RP, Rubianto M (2018) The immunomodulatory effect of green tea (Camellia sinensis) leaves extract on immunocompromised Wistar rats infected by Candida albicans. Vet World 11:765–770. https://doi.org/10.14202/vetworld.2018
Martel J, Ko YF, Ojcius DM, Lu CC, Chang CJ, Lin CS, Lai HC, Young JD (2017) Immunomodulatory properties of plants and mushrooms. TIPS 38:967–981. https://doi.org/10.1016/j.tips.2017.07.006
Kim HY, Shin HS, Park H, Kim YC, Yun YG, Park S, Shin HJ, Kim K (2008) In vitro inhibition of coronavirus replications by the traditionally used medicinal herbal extracts, Cimicifuga rhizoma, Meliae cortex, Coptidis rhizoma, and Phellodendron cortex. J Clin Virol 41:122–128. https://doi.org/10.1016/j.jcv.2007.10.011
Dhanasekaran S, Pradeep P (2020) Scope of phytotherapeutics in targeting ACE2 mediated host- SARS-CoV-2. ChemRxiv. https://doi.org/10.26434/chemrxiv.12089730.v1
Varma A, Padh H, Shrivastava N (2011) Andrographolide: a new plant-derived antineoplastic entity on horizon. eCAM 2011. https://doi.org/10.1093/ecam/nep135
Wang W, Wang J, Dong SF, Liu CH, Italiani P, Sun SH, Xu J, Boraschi D, Ma SP, Qu D (2010) Immunomodulatory activity of andrographolide on macrophage activation and specific antibody response. Acta Pharmacol Sin 2010(31):191–201. https://doi.org/10.1038/aps.2009.205
Lu J, Ma Y, Wu J, Huang H, Wang X, Chen Z, Chen J, He H, Huang C (2019) A review for the neuroprotective effects of andrographolide in the central nervous system. Biomed Pharmacother 117. https://doi.org/10.1016/j.biopha..109078
Arreola R, Quintero-Fabián S, López-Roa RI, Flores-Gutiérrez EO, Reyes-Grajeda JP, Carrera-Quintanar L, Ortuño-Sahagún D (2015) Immunomodulation and anti-inflammatory effects of garlic compounds. J Immunol Res 2015:1–14. https://doi.org/10.1155/2015/401630
Lang A, Lahav M, Sakhnini E, Barshack I, Fidder HH, Avidan B, Bardan E, Hershkoviz R, Bar-Meir S, Chowers Y (2004) Allicin inhibits spontaneous and TNF-α induced secretion of proinflammatory cytokines and chemokines from intestinal epithelial cells. Clin Nutr 23:1199–1208. https://doi.org/10.1016/j.clnu.2004.03.011
Djakpo O, Yao W (2010) Rhus chinensis and Galla Chinensis–folklore to modern evidence. Phytother Res 24:1739–1747. https://doi.org/10.1002/ptr.3215
Yi L, Li Z, Yuan K, Qu X, Chen J, Wang G, Zhang H, Luo H, Zhu L, Jiang P, Chen L (2004) Small molecules blocking the entry of severe acute respiratory syndrome coronavirus into host cells. J Virol 78:11334–11339. https://doi.org/10.1128/JVI.78.20.11334-11339.2004
Wen CC, Shyur LF, Jan JT, Liang PH, Kuo CJ, Arulselvan P, Wu JB, Kuo SC, Yang NS (2011) Traditional Chinese medicine herbal extracts of Cibotium barometz, Gentiana scabra, Dioscorea batatas, Cassia tora, and Taxillus chinensis inhibit SARS-CoV replication. J Tradit Complement Med 1:41–50. https://doi.org/10.1016/S2225-4110(16)30055-4
Liu L (2020) Traditional Chinese medicine contributes to the treatment of COVID-19 patients. Chin Herb Med 12:95–96. https://doi.org/10.1016/j.chmed.2020.04.003
Yang Y, Islam MS, Wang J, Li Y, Chen X (2020) Traditional Chinese medicine in the treatment of patients infected with 2019-new coronavirus (SARS-CoV-2): a review and perspective. Int J Biol Sci 16:1708–1717. https://doi.org/10.7150/ijbs.45538
Yang Y, Lee GJ, Yoon DH, Yu T, Oh J, Jeong D, Lee J, Kim SH, Kim TW, Cho JY (2013) ERK1-and TBK1-targeted anti-inflammatory activity of an ethanol extract of Dryopteris crassirhizoma. J Ethnopharmacol 145:499–508. https://doi.org/10.1016/j.jep.2012.11.019
Jezova D, Karailiev P, Karailievova L, Puhova A, Murck H (2021) Food enrichment with glycyrrhiza glabra extract suppresses ACE2 mRNA and protein expression in rats-possible implications for COVID-19. Nutrients 13:2321. https://doi.org/10.3390/nu13072321
Chen F, Chan KH, Jiang Y, Kao RY, Lu HT, Fan KW, Cheng VC, Tsui WH, Hung IF, Lee TS, Guan Y (2004) In vitro susceptibility of 10 clinical isolates of SARS coronavirus to selected antiviral compounds. J Clin Virol 31:69–75. https://doi.org/10.1016/j.jcv.2004.03.003
Zhao H, Zhao M, Wang Y, Li F, Zhang Z (2016) Glycyrrhizic acid prevents sepsis-induced acute lung injury and mortality in rats. J Histochem Cytochem 64:125–137. https://doi.org/10.1369/0022155415610168
Kanchibhotla D, Subramanian S, Kumar RM, Hari KV, Pathania M (2022) An in-vitro evaluation of a polyherbal formulation, against SARS-CoV-2. J Ayurveda Integr Med 13:100581. https://doi.org/10.1016/j.jaim.2022.100581
Barretto N, Jukneliene D, Ratia K, Chen Z, Mesecar AD, Baker SC (2005) The papain-like protease of severe acute respiratory syndrome coronavirus has deubiquitinating activity. J Virol. 79:15189–15198. https://doi.org/10.1128/JVI.79.24.15189-15198.2005
Amin SA, Banerjee S, Gayen S, Jha T (2021) Protease targeted COVID-19 drug discovery: what we have learned from the past SARS-CoV inhibitors? Eur J Med Chem. 215:113294. https://doi.org/10.1016/j.ejmech.2021.113294
Lin SC, Ho CT, Chuo WH, Li S, Wang TT, Lin CC (2017) Effective inhibition of MERS-CoV infection by resveratrol. BMC Infect Dis. 17:1–10. https://doi.org/10.1186/s12879-017-2253-8
Müller C, Schulte FW, Lange-Grünweller K, Obermann W, Madhugiri R, Pleschka S, Ziebuhr J, Hartmann RK, Grünweller A (2018) Broad-spectrum antiviral activity of the eIF4A inhibitor silvestrol against corona-and picornaviruses. Antivir Res 150:123–129. https://doi.org/10.1016/j.antiviral.2017.12.010
Millet JK, Séron K, Labitt RN, Danneels A, Palmer KE, Whittaker GR, Dubuisson J, Belouzard S (2016) Middle East respiratory syndrome coronavirus infection is inhibited by griffithsin. Antivir Res. 133:1–8. https://doi.org/10.1016/j.antiviral.2016.07.011
Li SY, Chen C, Zhang HQ, Guo HY, Wang H, Wang L, Zhang X, Hua SN, Yu J, Xiao PG, Li RS (2005) Identification of natural compounds with antiviral activities against SARS-associated coronavirus. Antivir Res 67:18–23. https://doi.org/10.1016/j.antiviral.2016.07.011
Yu MS, Lee J, Lee JM, Kim Y, Chin YW, Jee JG, Keum YS, Jeong YJ (2012) Identification of myricetin and scutellarein as novel chemical inhibitors of the SARS coronavirus helicase, nsP13. Bioorg Med Chem 22:4049–4054. https://doi.org/10.1016/j.bmcl.2012.04.081
Park JY, Yuk HJ, Ryu HW, Lim SH, Kim KS, Park KH, Ryu YB, Lee WS (2017) Evaluation of polyphenols from Broussonetia papyrifera as coronavirus protease inhibitors. J Enzyme Inhib Med Chem 32:504–512. https://doi.org/10.1080/14756366.2016.1265519
Kim DW, Seo KH, Curtis-Long MJ, Oh KY, Oh JW, Cho JK, Lee KH, Park KH (2014) Phenolic phytochemical displaying SARS-CoV papain-like protease inhibition from the seeds of Psoralea corylifolia. J Enzyme Inhib Med Chem 29:59–63. https://doi.org/10.3109/14756366.2012.753591
Hoever G, Baltina L, Michaelis M, Kondratenko R, Baltina L, Tolstikov GA, Doerr HW, Cinatl J (2005) Antiviral activity of glycyrrhizic acid derivatives against SARS− coronavirus. J Med Chem 48:1256–1259. https://doi.org/10.1021/jm0493008
Cho JK, Curtis-Long MJ, Lee KH, Kim DW, Ryu HW, Yuk HJ, Park KH (2013) Geranylated flavonoids displaying SARS-CoV papain-like protease inhibition from the fruits of Paulownia tomentosa. Bioorg Med Chem 21:3051–3057. https://doi.org/10.1016/j.bmc.2013.03.027
Keyaerts E, Vijgen L, Pannecouque C, Van Damme E, Peumans W, Egberink H, Balzarini J, Van Ranst M (2007) Plant lectins are potent inhibitors of coronaviruses by interfering with two targets in the viral replication cycle. Antivir Res 75:179–187. https://doi.org/10.1016/j.antiviral.2007.03.003
Lin CW, Tsai FJ, Tsai CH, Lai CC, Wan L, Ho TY, Hsieh CC, Chao PD (2005) Anti-SARS coronavirus 3C-like protease effects of Isatis indigotica root and plant-derived phenolic compounds. Antivir Res 68:36–44. https://doi.org/10.1016/j.antiviral.2005.07.002
Ryu YB, Jeong HJ, Kim JH, Kim YM, Park JY, Kim D, Naguyen TT, Park SJ, Chang JS, Park KH, Rho MC (2010) Biflavonoids from Torreya nucifera displaying SARS-CoV 3CLpro inhibition. Bioorg Med Chem 18:7940–7947. https://doi.org/10.1016/j.bmc.2010.09.035
Chiang LC, Ng LT, Liu LT, Shieh D-E, Lin CC (2003) Cytotoxicity and anti-hepatitis B virus activities of saikosaponins from Bupleurum species. Planta Med 69:705–709. https://doi.org/10.1055/s-2003-42797
Zamboni A, Vrhovsek U, Kassemeyer HH, Mattivi F, Velasco R (2006) Elicitor-induced resveratrol production in cell cultures of different grape genotypes (Vitis spp.). Vitis 45:63–68. https://doi.org/10.5073/vitis.2006.45.63-68
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2024 Springer Nature Switzerland AG
About this entry
Cite this entry
Andole, S. et al. (2024). Medicinal Plants Against SARS-CoV/Corona Virus Infections: Ethnopharmacology, Chemistry, and Clinical and Preclinical Studies. In: Pal, D. (eds) Anti-Viral Metabolites from Medicinal Plants. Reference Series in Phytochemistry. Springer, Cham. https://doi.org/10.1007/978-3-031-12199-9_15
Download citation
DOI: https://doi.org/10.1007/978-3-031-12199-9_15
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-031-12198-2
Online ISBN: 978-3-031-12199-9
eBook Packages: Chemistry and Materials ScienceReference Module Physical and Materials ScienceReference Module Chemistry, Materials and Physics