Skip to main content
Evidence-based Complementary and Alternative Medicine : eCAM logoLink to Evidence-based Complementary and Alternative Medicine : eCAM
. 2021 Jun 4;2021:6622410. doi: 10.1155/2021/6622410

Candidate Anti-COVID-19 Medicinal Plants from Ethiopia: A Review of Plants Traditionally Used to Treat Viral Diseases

Dires Tegen 1, Kindalem Dessie 1, Destaw Damtie 2,
PMCID: PMC8219417  PMID: 34221083

Abstract

Background

Emerging viral infections are among the major global public health concerns. The pandemic COVID-19 is a contagious respiratory and vascular disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). There are no medicines that can treat SARS-CoV-2 except the vaccines. Therefore, searching for plant-originated therapeutics for the treatment of COVID-19 is required. Consequently, reviewing medicinal plants used to treat different viral infections is mandatory. This review article aims to review the ethnobotanical knowledge of medicinal plants traditionally used to treat different viral diseases by the Ethiopian people and suggests those plants as candidates to fight COVID-19.

Methods

Articles written in English were searched from online public databases using searching terms like “Traditional Medicine,” “Ethnobotanical study,” “Active components,” “Antiviral activities,” and “Ethiopia.” Ethnobotanical data were analyzed using the Excel statistical software program.

Result

From the 46 articles reviewed, a total of 111 plant species were claimed to treat viral infections. Fifty-six (50.4%) of the plant species had reported to have antiviral active components that are promising to treat COVID-19. Lycorine, gingerol shogaol, resveratrol, rhoifolin, oleanolic acid, kaempferol, rosmarinic acid, almond oil, ursolic acid, hederagenin, nigellidine, α-hederin, apigenin, nobiletin, tangeretin, chalcone, hesperidin, epigallocatechin gallate, allicin, diallyl trisulfide, ajoene, aloenin, artemisinin, glucobrassicin, curcumin, piperine, flavonoids, anthraquinone, hydroxychloroquine, and jensenone were some of them.

Conclusion

The Ethiopian traditional knowledge applies a lot of medicinal plants to treat different viral infections. Reports of the chemical components of many of them confirm that they can be promising to fight COVID-19.

1. Introduction

Viral diseases are responsible for the global morbidity and mortality of human beings [1]. The pandemic COVID-19 is among such viral outbreaks challenging the healthcare systems around the world [2]. From 31 December 2019 to 31 October 2020, this pandemic resulted in 45,667,780 cases and 1,189,499 deaths globally and 95,789 cases and 1,464 deaths in Ethiopia [3]. However, no specific medications and drugs are known to treat this viral disease. Consequently, reports show that people from different countries use medicinal plants for the prevention and treatment of COVID-19, although not confirmed by the World Health Organization (WHO) for safety issues [4]. Because they contain various active components, medicinal plants can be alternatives to prevent and combat COVID-19 [5].

Plant secondary metabolites like lycorine [6], gingerol shogaol [7], resveratrol rhoifolin [8], oleanolic acid [9], kaempferol [10], rosmarinic acid [11], almond oil [12], ursolic acid [11], hederagenin, nigellidine, and α-hederin [11, 13], apigenin, ethyl cholate, nobiletin, tangeretin, chalcone, and hesperidin [10, 14, 15], epigallocatechin gallate [16], allicin, diallyl trisulfide ajoene, and apigenin [14, 17], aloenin [18], artemisinin [6, 19], glucobrassicin [10, 11], apigenin [11], curcumin [20], piperine [12], flavonoids, anthraquinone, and hydroxychloroquine [21], and jensenone [22] are reported to have antiviral activities. The mechanism of action of these secondary metabolites may be due to their greater binding affinity for SARS-CoV-2 6LU7 and 6Y2E proteases and inhibition of SARS-CoV-2 M protease (Mpro) and Spike (S) glycoprotein [622].

Globally, millions of people rely on medicinal plants not only for their primary healthcare systems but also for income generation and livelihood improvement [23]. Moreover, at least 25% and 50% of the pharmacopeia are derived from plant products and are originated from natural products, respectively [24]. Nowadays, traditional healers from different habitats and geographical locations are showing new candidate combinations for the treatment of viral infections such as SARS-CoV [5].

Using traditional medicine has a long history in Ethiopia. About 80% of the Ethiopian population is still dependent on the use of folk medicine [2527], due to its cultural acceptability, economic affordability, and efficacy against certain types of diseases compared to modern medicine [28]. However, the plants and the associated indigenous knowledge in the country are gradually declining because of environmental degradation, deforestation, lack of documentation, and potential acculturation [29].

Common cold, influenza, and COVID-19 share common characteristics. All of them affect the respiratory tract and have modes of transmission: direct contact, droplets, and fomites. Cough, sneezes, fever, shortness of breath, sore throat, and headache are among the common symptoms of these diseases [30]. Traditional healers from Ethiopia use medicines of plant origin to treat viral infections like the common cold, rabies, influenza, herpes simplex, herpes zoster, and hepatitis. Due to their fewer side effects, better patient tolerance, and relatively low cost, the use of medicinal plants is a common practice by the Ethiopian people.

Due to its ecological and cultural diversity, Ethiopia is a rich source of herbal medicine [31]. Plant extracts contain a lot of active components, so they have a wide range of activities against microorganisms. That is, they act on multiple active sites of the pathogen [32]. Therefore, a medicinal plant used to treat one viral infection may serve to fight other viral infections. This review, therefore, focuses on the identification of medicinal plants used by traditional healers of Ethiopia to treat viral diseases and extrapolates this knowledge for the fight of COVID-19.

2. Methods

2.1. Study Design and Setting

The location of Ethiopia is in the horn of Africa. Its boundaries are Eritrea to the North, Djibouti and Somalia to the East, Sudan and South Sudan to the West, and Kenya to the South. The current UN report shows that the Ethiopian population is estimated to be 115,855,859. Ethiopia's population is equivalent to 1.47% of the world's population. Around 21.3% of the population is an urban community. The population density in Ethiopia is 115/km2 (298 people/mi2) [33].The total land area is 1,104,300 km2 [34].

2.2. Search Strategies

The authors explored articles from PubMed, ScienceDirect, and Web of Science search engines using the following core search terms and phrases: “Traditional Medicine,” “Ethnobotanical study,” “Active components,” “Antiviral activities,” and “Ethiopia.” We used the search terms separately and in combination with Boolean operators like “OR” or “AND.” Besides, we searched for gray literature through the review of available references. Searching for relevant literature included in this systematic review was conducted from September 2020 to October 2020.

2.3. Inclusion and Exclusion Criteria

Studies that were written in the English language, reporting about the antiviral activity of traditional medicines, phytochemical analysis of medicinal plants, and candidate anti-COVID-19 medicinal plants in Ethiopia, Africa, China, Europe, and Western countries, were retrieved and included in this study. However, we excluded studies that did not contain antiviral medicinal plants.

2.4. Data Extraction

All authors contributed to the data extraction protocol preparation and evaluation. The data extraction protocol consists of the scientific, family, and local names, parts used, preparation methods, administration routes, diseases treated, and references.

2.5. Data Analysis

Ethnobotanical data were entered in an Excel spreadsheet and analyzed using Excel statistical software program. We tabulated and compiled quantitative data using descriptive statistics to identify the number and percentage of species and families of antiviral plants and expressed them in tables.

3. Results and Discussion

3.1. Search Results

From the total of 260 articles retrieved, only 46 (17.7%) of the studies met the eligibility criteria (Figure 1).

Figure 1.

Figure 1

PRISMA flowchart of the reviewed articles on antiviral medicinal plants from Ethiopia.

3.2. Identified Plants with Antiviral Activities

From the 46 articles reviewed, 111 plant species claimed to treat eleven viral infections. The most frequently reported viral diseases to be treated by the 111 plants were rabies (reported 36 times), hepatitis (30 times), common cold (26 times), herpes zoster (17 times), influenza (10 times), Herpes simplex virus (8 times), Wart (6 times), HIV-1 (5 times), Bursal viral diseases (once), flu (once), and Smallpox (once) (Table 1).

Table 1.

The medicinal plants used to treat viral diseases in different parts of Ethiopia.

No. Scientific name Family Local name Parts used and preparation method RA DT Ref.
1 Acacia abyssinica Hochst. ex Benth. Fabaceae Memona (Tig) Crush the bark and apply on the affected part Dermal H. zoster [35]
2 Acacia etbaica Schweinf. Fabaceae Seraw (Amh) Crushed bark Oral Wart [36]
3 Acacia nigra Fabaceae Tikur grar (Amh) Crush or pound and squeeze the leaf and apply on allergic skin Dermal H. zoster [37]
4 Acanthus polystachyus Acanthaceae Kucheshile (Amh) Crush the root and pound and give with water Oral Rabies [36, 38]
5 Acokanthera schimperi (A. DC.) Schweinf. Apocynaceae Meriz (Amh) Roots are burned on fire and fumigated Dermal Hepatitis [38, 39]
6 Allium sativum Alliaceae Nechsenkret (Amh) (i) Crushed rhizomes are pounded and eaten with honey
(ii) Crush the bulb and drink with water
Oral Influenza virus [36, 38]
(i) Bulb is pounded and mixed with meat soup and used as a drink
(ii) Boiled bulb vapor is inhaled orally and nasally
(iii) Cloves ground up and mixed with honey, take first thing in the morning on an empty stomach
(i) Oral
(ii) Oral and nasal
(iii) Oral
C. cold [4043]
7 Allium cepa Alliaceae QeY shikurt (Amh) Eat the part of the bulb with other foods Oral Rabies [35]
Crush the bulb and drink with water Oral HSV [44]
8 Aloe macrocarpa Tod. Aloaceae Eret (Amh) Leaf of A. macrocarpa is powdered and mixed with honey Oral Wart [45]
9 Amaranthus hybridus Linn. Amaranthaceae Tenbelel (Amh) Crush the fruit and leaf of Amaranthus hybridus Oral Hepatitis [36]
10 Argemone mexicana L. Papaveraceae Yahyaeshoh (Amh) (i) Crush the leaf
(ii) Crush the root and give with water
Oral Influenza, Rabies [36, 38]
11 Artemisia afra Jack. ex Willd. and Artemisia annua L. Asteraceae Chikugn (Amh) Grind leaves and apply topically Dermal Smallpox [40]
Crushed and powdered leaf Nasal, oral Influenza [36]
12 Azadirachta indica. A. Juss. Meliaceae Neem (Amh) Leaves Oral HIV-1 [46]
13 Bersama abyssinica Boyle Melianthaceae Azamer (Amh) Bark/leaves/roots Rabies, HIV-1 [47]
14 Brassica carinata A. Br. Herb Brassicaceae Gomen (Amh) The dried leaf was powdered and mixed with water then drunk Oral C. cold [48]
15 Brucea antidysenterica J. F. Mill Simaroubaceae Waginos (Aballo)(Amh) Fresh parts of the stem are boiled in water and the steam is inhaled through the mouth and nose Oral & nasal Hepatitis [49]
Squeeze the whole part of the plant and bake with teff flour and give for 3 days (together with Croton macrostachyus and Rumexnervosus) Oral Rabies [50]
16 Calpurnia aurea (Ait.) Benth. Fabaceae Digita (Amh) Crush the seeds of Calpurnia aurea and mix with water Orally Rabies [51]
17 Camellia sinensis Theaceae Shay kitel (Amh) Drink the leaves with tea Oral HBV, HCV, influenza, HIV, BCV [52, 53]
18 Capsicum annuum L. Solanaceae Berbere (Amh) Pounded being mixed with the leaf of V. sinaiticum, O. quadripartita, C. aurea (concoction), then bandage on the wound Dermal H. zoster [37]
19 Carica papaya L. Caricaceae Papaya (Amh) Fresh fruit and leaf pounded and crushed, add water Oral H. zoster, [37, 44]
20 Carissa edulis Vahl. Apocynaceae Agam (Amh) The root is powdered and mixed with food Oral Rabies [54]
21 Cayratia ibuensis (Hook.f.) Suess. Vitaceae Udusalim Rumiyi (Oro) The roots crushed and pounded, then boiled and drink 2-3 cups of coffee in the morning 5–7 of tea spoons drink (oral) Hepatitis [55]
22 Centella asiatica L. Apiaceae Yeait joro (Amh) A quarter of a finger-sized root is ground, mixed with water, filtered, and taken orally Oral Rabies [39]
23 Citrus aurantium L. Rutaceae Bahir Lome (Amh) Squeezing fruit (juice) Oral C. cold [43]
24 Citrus limon (L.) Burm. f. Rutaceae Lome (Amh) Squeezed fruit (juice) Oral C. cold [36]
25 Clematis hirsute Perr. & Guill. Ranunculaceae Hareg (Tig) Burn leaves in oven with leaves of Dodonaea angustifolia, grind, mix with butter and apply on the affected part. Dermal H. zoster [35]
26 Clutia abyssinica Jaub. & Spach. Euphorbiaceae Tewshealalito (Tig) Fiyle feji (Amh) Dry and mix leaves with dried leaves of Calpurnia aurea and Datura stramonium, grind, add butter, and spread the paste on the affected part
(i) Crush the root and boiled with water (Decoction)
Dermal
Oral
H. zoster, hepatitis [35, 37]
27 Coffea arabica L. Rubiaceae Bunna (Amh) Boil the leaf, decant then drink the juice Oral C. cold [38]
28 Combretum collinum Combretaceae Abalo (Amh) The seed of Combretum collinum with the seed of Solanumda syphyllum are crushed together powdered, mixed with “tella” and drunk for 3 days Oral Rabies [50]
29 Coriandrum sativum Apiaceae Dimblal (Amh) Potential anti-COVID-19 [56]
30 Cordia africana Boraginaceae Wanza (Amh) Boiled with sorghum (decoction) and drinking Oral Hepatitis [37]
31 Crinum abyscinicum Hochst. ex A. Rich. Amaryllidaceae Yejib shinkurt (Amh) Bulb of Crinum abyscinicum is used to treat rabies Oral Rabies [57]
32 Crotalaria incana L. Fabaceae Atarii Kuruphee (Oro) Sap from the whole part of the plant is directly creamed on affected area Dermal Hepatitis [41]
33 Croton macrostachyus Del. Euphorbiaceae Bisana (Amh) (i) Shoots are crushed with water, filtered and the solution is taken orally (for hepatitis)
(ii) The fresh root bark is crushed, pounded, mixed with water, and given orally (for rabies)
Oral Hepatitis, rabies [39, 44, 51]
34 Cucumis ficifolius A. Rich. Cucurbitaceae Yemidir Embuay (Amh) Crushed fresh root with water fermented for 3 days is taken with honey early morning before breakfast orally until the cure Oral Rabies [49]
35 Cucurbita pepo L. Cucurbitaceae Hamham (Tig) Fresh leaf boiled with water and given orally Oral Influenza [44]
36 Curcuma longa Zingiberaceae Erd (Amh) HBV, HCV [58]
37 Cussonia ostinii Chiov. Araliaceae Harfattu (Oro) Bark (root) of Cussonia ostinii, leaf Asplenium monathes and the leaf of Calpurnia subdecandra were pounded together, and 2 cups were given to cattle Orally Hepatitis [41]
38 Cyphostemma adenocaula (A. Rich.) Vitaceae Asserkush (Amh) The root was boiled with milk and filtered and the filtrate was taken in an empty stomach full of a coffee cup daily for 3 consecutive days Orally Rabies [50]
39 Datura stramonium L. Solanaceae Atsefaris (Amh) Leafy stem is squeezed and its drop prepared with butter Dermal Wart [35]
Leafy stem is squeezed and its drop prepared with butter Dermal cream Wart [36]
Crushed and homogenized leaves drunk with water Oral Rabies [50, 59]
Dried leaves of the plant and Calpurnia aurea and Clutia abyssinica are ground, mix powder with butter, and apply on the affected part Dermal H. zoster [35]
40 Diplolophium africanum Turcz. Apiaceae Zegerawta (Amh) Pound the root and give with water Orally Rabies [38]
41 Dipsacus pinnatifidus Steud. ex A. Rich. Dipsacaceae Fereze ng/kelem (Amh) Pound the leaf and give with water Nasal Rabies [38]
42 Dodonaea angustifolia L.f. Sapindaceae Kitkita (Amh) Dry the leaf of the plant alone or mix with the leaf of Clematis hirsuta on a hot stove, grind, add butter and rub the affected part Dermal H. zoster [35]
43 Dorstenia barnimiana Schweinf. Moraceae Work Bemeda (Amh) Root powder with shimmed milk or nug is taken orally early morning until a cure Orally Rabies [49]
Root powder with shimmed milk or nug is taken orally early morning until a cure Orally Hepatitis [49]
44 Dregea rubicunda Schum. Asclepiadaceae Kuandira (Amh) Crush and drink with milk Orally Rabies [38]
45 Dregea schimperi (Decne.) Bullock. Asclepiadaceae Shanqoq (Tig) Crush and drink the fluid Orally Rabies [35]
46 Echinops amplexicaulis Oliv. Asteraceae Kosorru Hare (Oro) The root of Echinops amplexicaulis is dried, powdered, and mixed with water The concoction is given to cattle Orally Hepatitis [41]
47 Ekebergia capensis Meliaceae The leaf of Ekebergia capensis is crushed and add water Orally C. cold [36]
48 Eucalyptus globulus Labill. Myrtaceae Nech bahirzaf (Amh) Boil and fumigate with the fume Nasal, oral, and dermal C. cold [36]
(i) Leaf of Eucalyptus globulus is chopped and boiled; the steam bath is taken by humans; vapor inhaled orally and nasally
(ii) Boil Eucalyptus and Damakasse in water and inhale
(iii) Leaf of E. globulus is boiled in water
Nasal, orally Influenza [35, 4042, 45]
49 Euphorbia abyssinica G.F.Gmel. Euphorbiaceae Kulkual (Amh) Stems are burned on fire and fumigated Dermal Hepatitis [39]
Mix the latex of Euphorbia abyssinica with milk and drink it Orally Rabies [38]
50 Ficus sycomorus L. Moraceae Sholla (Amh) (i) The sap of Ficus sycomorus is creamed directly on the skin (for hepatitis)
(ii)The bark of Ficus sycomorus and root of Prunus africana are powdered together and backed with teff flour and eaten (for rabies)
Dermal Oral Hepatitis, rabies [41, 45]
51 Ficus sp. Moraceae Warka (Amh) The stem bark and the latex are mixed with Phytolacca dodecandra (leaf) and given Oral Rabies [51]
52 Gnidia stenophylla Gilg. Trymalaceae Katarichaa (Oro) The decoction of the root is taken with goat milk 1 teaspoon drink orally Hepatitis [55]
53 Hypoestes forskaolii (Vahl) R.Br. Acanthaceae Girbia (Tig) A bunch of leaves was collected from 7 different sites, mixed with 10 tin cans of water, stored for 7 days, and washed for 7 consecutive days Dermal H. zoster [60]
54 Jasminum abyssinicum Hochst. Oleaceae Tembelel (Amh) Pounded being mixed with the leaf of V. sinaiticum, O. quadripartita, C. aurea, S. uliginosa, D. stramonium, and P. schmperi Dermal H. zoster [37]
55 Jatropha curcas L. Euphorbiaceae Yesudan-gulo (Amh) Crush the seed of Jatropha curcas mixed with water Orally Rabies [51]
56 Justicia schimperiana (Hochst. ex Nees) T. Anders Acanthaceae Smiza (Amh) (i) Root and leaf of Justica schimperiana are pounded together and mixed with water and 2-3 cups of tella are used as a drink
(ii) Seed of J. Schimperiana is crushed and mixed with water and filtered
(iii) The Justicia schimperiana and Brucea antidysenterica leaves are used to treat rabies
Oral Rabies [36, 41, 45, 59, 61]
Sniff unprocessed or after rubbing Nasal C. cold [36]
(i) Juice of seven shoot meristems that can be mixed with fresh water and drink a cup of the mixture
(ii) Juvenile leaf of Justicia schimperiana boiled with milk (decoction)
Orally Hepatitis [37, 62]
57 Laggera integrifolia Sch. Bip. ex A. Rich Asteraceae Gimmie (Amh) The leaf is inhaled sometimes through the nose Nasal (nostril) C. cold [63]
58 Lens culinaris Medic. Fabaceae Misir (Amh) Dry seeds are ground, powder is soaked in water, and cream is smeared on the affected part Dermal H. zoster [39]
59 Lippia abyssinica Lamiaceae Koseret (Amh) Nasal C. cold [59]
60 Lobelia rhynchopetalum Hemsl. Lobeliaceae Jibara (Amh) Roots are ground, mixed with milk, and solution drunk for five days Orally Rabies [39]
61 Lycopersicon esculentum (L.) Mill. Solanaceae Timaatima (Oro) Fresh fruit put in the fire and eaten when getting hot in order to get relief from the common cold Oral C. cold [48]
62 Mangifera indica Anacardiaceae Mango (Amh) Bark/leaves Oral C. cold, HSV-1/2 [46]
63 Millettia ferruginea (Hochst.) Bak. Fabaceae Birbira (Amh) Heat stick, then touch their body with hot part Dermal Rabies [38]
64 Moringa borziana Mattei Mawe Moringaceae Tamergnaw ketel (Shiferaw) (Amh) Leaf chewing Chewing Oral C. cold [36]
65 Musa spp. Musaceae Muz (Amh) SARS-CoV-2, influenza [64, 65]
66 Myrica salicifolia Hochst. ex A. Rich. Myricaceae Shinet (Amh) Crush, powder, then sniff Nasal C. cold [38]
67 Nicandra physalodes (L.) Gaertn Solanaceae Hawwixii (Oro) Nicandra physalodes (L.) Gaertn roots are pounded and mixed with cold water; 2–4 cups of tella are used as a drink Oral Hepatitis [41]
68 Nicotiana tabacum Solanaceae Tamiba (Had) Dry leaves are pounded and powdered, then drunk or smelled through the nose of humans Nasal C. cold [43]
69 Nigella sativa Ranunculaceae Tikur Azmud (Amh) Fried seeds wrapped in a piece of cloth and sniffed three times daily, wrap in small leaf, stick up nose Orally Nasal C. cold [40, 62]
70 Ocimum basilicum L. Herb Lamiaceae Bessobla (Amh) Fresh leaves together with the root of Aloe macrocarpa concocted together and drink the solution Oral Flu, CVB1 [48]
71 Ocimum lamiifolium Hochst. ex Benth. Lamiaceae Damakassie (Amh) Crushed and mixed/concocted/with coffee and take Orally C. cold [59]
(i) Squeeze leaves and drink the juice with coffee, or apply the rubbed leaves into the nose Nasal Influenza and acute viral infection [42, 66]
72 Ocimum urticifolium Roth. Lamiaceae Dama kesie (Amh) Boil with tea and drink Orally C. cold [38]
73 Olea europaea subsp. cuspidate Oleaceae Weyra (Amh) Boiled, adding salt for the night and isolate the residue (decoction) Orally Hepatitis [37]
74 Olinia rochetiana A. Juss Oliniaceae Noole (Sid) The leaf is heated slightly, rubbed by the hands, and then inhaled through nostrils Nasal Viral common cold [66]
75 Osyris quadripartita Decn. Santalaceae Keret (Amh) Dried and pounded then 2 spoonsful powder is mixed with a cup of water, drink for 3 consecutive days Orally Hepatitis [37]
Pounded being mixed with the leaf of C. annuum, V. sinaiticum, C.aurea, J. abyssinicum (concoction) Dermal H. zoster [37]
76 Otostegia integrifolia Benth. Lamiaceae Tunjut (Amh) Smoking and fumigating the house Smoking, oral C. cold [36, 38]
77 Piper nigrum Piperaceae Kundo berbere (Amh) VSV, PIV, CVB3 [67]
78 Phaseolus vulgaris Fabaceae Bakela (Amh) HIV-1, RSV, and HSV-1 [68, 69]
79 Phytolacca dodecandra Phytolaccaceae Endod (Amh) (i) Root is crushed and pounded, mixed with water; one-third of the tella cup is given to humans (liver problem); Phytolacca dodecandra root is crushed and pounded, mixed with water; one-third of a cup is given to humans
(ii) Dried root of Phytolacca dodecandra powder and one-two cups of domestic alcohol (malakia) are taken orally (for rabies)
(iii) Chopped root and leaves mixed with honey are given orally (for rabis)
(iv) Fresh root of Phytolacca dodecandra is pounded, mixed with water, one arake glass of the solution is given for 7–10 days (for humans)
Oral (i) Liver problem (hepatitis), (ii) Rabies [41, 42, 48, 70]
(v) Squeeze and apply on the wounded part Dermal H. zoster [37]
Juice extracted by pounded fresh root mixed with milk of similar cow and calf Roots are chewed and fluid swallowed; as an antidote, Guizotia abyssinica solution is taken orally Orally Rabies [39]
Juice of crushed fresh root taken with skimmed milk Oral Rabies [44]
Juice of crushed fresh root taken with skimmed milk Orally Hepatitis “wef beshita' [49]
80 Plantago lanceolata L. Plantaginaceae Korxobi (Oro) (i) The leaf is squeezed and apply on the affected dermal part
(ii) The squeezed leaf is pasted with butter and made to ointment
Dermal Wart, herpes wounds [54]
81 Podocarpus falcatus Podocarpaceae Birbirsa (Oro) Fresh stem barks boiled and filtered and then drunk in the middle of the night for three days; dry stem bark crushed and pounded then parted on the wound Oral Jaundice (hepatitis) or rabies [43]
82 Podocarpus gracilior Podocarpaceae Zigba (Amh) Combined Zigba (Podocarpus gracilior) of Dokuma (Syzgium guineense, listed next) in a cold maceration; drink on an empty stomach first thing in the morning, this induces vomiting which is thought to help treat Yellelitwofe (hepatitis) Oral Yellelito wofe (hepatitis) [40]
83 Polygala obtusissima Chod. Polygalaceae Calmala (Afa) The fresh leaves are pounded, kept in a handkerchief, and inhaled Inhalation (nasal) C. cold [71]
84 Prunus dulcis Rosaceae Lewuz (Amh) Drink with tea Oral HSV-1/ 2 [72]
85 Rhus natalensis Anacardiaceae Debobosha (Amh) Pounded being mixed with J. abyssinicum, D. stramonium, and S. nigrum (concoction); wash the entire body first and apply the remedy on the wound Dermal H. zoster [37]
86 Ricinus communis L. Euphorbiacea Kabosimbiro (Oro) Fresh leaves are crushed and mixed with water and one cup of tea is taken for 3 consecutive days Orally Rabies [50]
(i) The root is pounded, well-spiced, and mixed with food
(ii) Freshly pounded and squeezed leaves of Ricinus communis L. with milk for treating patients of rabies
Oral Rabies [54, 73]
87 Rosa abyssinica Rosaceae Qega (Amh) Oral Enteric coronavirus. [74]
88 Rosmarinus officinalis Lamiaceae Tibs kitel (Amh) RSV-A and B [75]
89 Rumex abyssinicus Polygonaceae Mekmoko (Amh) Root decocted, drunk or chewed Oral Hepatitis [40]
90 Rumex crispus Polygonaceae Enbacho (Amh) Roots chewed and juice swallowed Oral Hepatitis [40]
91 Ruta chalepensis L. Rutaceae Tena adam (Amh) Leaf of Ruta chalepensisis pounded with the bulb of Allium sativum mixed with soup and used as a drink Oral Influenza [41]
92 Saccharum officinarum L. Herb Poaceae Shankora ageda (Amh) Fresh steam is put in the fire and eaten when gets hot to get relief from the common cold Oral C. cold [48]
93 Salix subserrata Willd Salicaceae Crushed leaves of Salix subserrata Willd. and Afrocarpus falcatus (Thunb.) C. N. Page was also used in fresh form, mixed with water and milk, to treat rabies Oral Rabies [73]
94 Sesamum indicum Pedaliaceae Selit (Amh) two drops of sesame oil in each nostril each morning are suggested to prevent COVID-19 Nasal COVID-19 CCRH, 2020
95 Schinus molle Anacardiaceae Selit (Amh) Kendo berberie (Amh) Pounded Crushed Fruit Oral Cough (C. cold) [36]
Crushed fresh leaves of Schinus mole with water Oral H. zoster [44]
96 Solanecio gigas (Vatke) C. Jeffrey Asteraceae Boz (Amh) Leaves are collected from seven different areas, grounded with Guizotia abyssinica seeds, mixed with water and solution have taken orally Orally Hepatitis [39]
97 Sorghum bicolor (L.) Moench. Poaceae Boz (Amh) Boil it in water and wash the body with it Dermal H. zoster [35]
98 Spinacia oleracea Amaranthaceae Keyh leqa (Tig) SARS-CoV-2 [10]
99 Stephania abyssinica (Dillon & A. Rich.) Walp. Menispermaceae Kosta (Amh) Crushed and given with milk and water Orally Rabies [38]
100 Syzygium aromaticum Myrtaceae Chewchawit (Amh) HSV-1 and 2 [9]
101 Trichilia dregeana Meliaceae Kirnfud (Amh) Soaked, cooked, and put on tooth surface dermal Wound Warts [36]
102 Triumfetta heterocarpa Sprague and Hutch. Tiliaceae Anunu (Oro) The crushed fresh root is mixed with water and taken orally without food Orally Hepatitis [49]
103 Verbascum sinaiticum Benth. Scrophulariaceae Yelam tut (Amh) Roots are burned on fire and the smoke inhaled Nasal Hepatitis [39]
104 Vitis vinifera Vitaceae Qetetina (Amh) Fruits Oral HSV-1, PIV [8]
105 Vernonia amygdalina Del. Asteraceae Weyin fire (Amh) Leaves/roots Oral hepatitis, H. zoster, HSV, cough, HIV [46]
106 Warburgia ugandensis Sprague Canellaceae Befit (Oro) The smoke of 2-3 stick vascular part is inhaled to relieve cough Nasal Cough (C. cold) [55]
107 Withania somnifera Solanaceae Giziewa or Kumo (Amh) IBDV, HSV-1 [76]
Fresh leaf and root will be crushed Orally Hepatitis [36]
Leaf and root crushed and drunk after boiling, powdered, juiced and drunk for 4 days, squeezed with leaves Oral Cough (C. cold) [36]
108 Ximenia americana L. Oleaceae Enkuay (Amh) Soaking bark in water and the water is taken orally Orally Rabies [49]
109 Zehneria scabra (l.f.) Sond Cucurbitaceae Qorii Sinbiraa (Oro) The pounded root of Zehneria scabra is concocted with the pounded root of Ricinus communis One feast of the pond is given to cattle and pack animals Oral Rabies [41]
110 Zingiber officinale Roscoe. Zingiberaceae Zinjibile (Amh) The stem is pounded well and boiled with water and drink Orally, nasal Influenza [36, 37, 45]
2–5 medium roots crushed and boiled with tea or water and then taken Oral Cough and c. cold [43, 55]
111 Ziziphus abyssinica Hochst. ex A. Rich. Rhamnaceae Kurkura (Amh) Fresh leaves and root are crushed and mixed with water and taken orally Orally Hepatitis [49]

Notes: H. zoster = herpes zoster; C. cold = common cold; BCV = bovine coronavirus; HSV-1 = herpes simplex virus type 1; CVB1 = Coxsackie B virus type 1; IBDV = infectious bursal disease virus; RA = route of administration; DT = disease treated; Amh = Amharic; Oro = Oromo; Tig = Tigrinya; Afa = Afar; Had = Hadiyya; Sid = Sidaamu-afoo.

3.3. Taxonomic Diversity of Medicinal Plants Used for the Treatment of Viral Diseases in Ethiopia

We reviewed 162 plants which were grouped under 111 species and 57 families (Table 2). Among the families, Fabaceae was represented by 8 (7.2%) species, Solanaceae and Lamiaceae by 6 (5.4%) species each, Euphorbiaceae and Asteraceae by 5 (4.5%) species each, and Meliaceae, Vitaceae, Apiaceae, Anacardiaceae, Moraceae, Oleaceae, Cucurbitaceae, Rutaceae, and Acanthaceae by 3 (2.73%) species each, and the remaining 43 families were represented by 1 to 2 species (Table 2).

Table 2.

Family and species groups of the reviewed medicinal plants.

No. Family Species per family Medicinal plants per family
No. (%) Rank No. (%) Rank
1. Fabaceae 8 (7.2) 1 9 (5.6) 3
2. Lamiaceae 6 (5.4) 2 9 (5.6) 3
3. Alliaceae 2 (1.8) 8 (4.9) 4
4. Phytolaccaceae 1 (0.9) 8 (4.9) 4
5. Acanthaceae 3 (2.73) 4 7 (4.3) 5
6. Myrtaceae 2 (1.8) 6 (3.7) 6
7. Zingiberaceae 2 (1.8) 6 (3.7) 6
8. Asteraceae 5 (4.5) 3 5 (3.09) 7
9. Moraceae 3 (2.73) 4 5 (3.09) 7
10. Anacardiaceae 3 (2.73) 4 4 (2.5) 8
11. Apiaceae 3 (2.73) 4 3 (1.85)
12. Cucurbitaceae 3 (2.73) 4 3 (1.85)
13. Meliaceae 3 (2.73) 4 3 (1.85)
14. Oleaceae 3 (2.73) 4 3 (1.85)
15. Rutaceae 3 (2.73) 4 3 (1.85)
16. Vitaceae 3 (2.73) 4 3 (1.85)
17. Apocynaceae 2 (1.8) 3 (1.85)
18. Ranunculaceae 2 (1.8) 3 (1.85)
19. Amaranthaceae 2 (1.8) 2 (1.23)
20. Asclepiadaceae 2 (1.8) 2 (1.23)
21. Poaceae 2 (1.8) 2 (1.23)
22. Podocarpaceae 2 (1.8) 2 (1.23)
23. Polygonaceae 2 (1.8) 2 (1.23)
24. Rosaceae 2 (1.8) 2 (1.23)
25. Caricaceae 1 (0.9) 2 (1.23)
26. Musaceae 1 (0.9) 2 (1.23)
27. Papaveraceae 1 (0.9) 2 (1.23)
28. Santalaceae 1 (0.9) 2 (1.23)
29. Simaroubaceae 1 (0.9) 2 (1.23)
30. Theaceae 1 (0.9) 2 (1.23)
31. Solanaceae 6 (5.4)∗2 12 (7.41) 1
32. Euphorbiaceae 5 (4.5)∗3 11 (6.8) 2
33. Aloaceae 1 (0.9) 1 (0.6)
34. Amaryllidaceae 1 (0.9) 1 (0.6)
35. Araliaceae 1 (0.9) 1 (0.6)
36. Boraginaceae 1 (0.9) 1 (0.6)
37. Brassicaceae 1 (0.9) 1 (0.6)
38. Canellaceae 1 (0.9) 1 (0.6)
39. Combretaceae 1 (0.9) 1 (0.6)
40. Dipsacaceae 1 (0.9) 1 (0.6)
41. Lobeliaceae 1 (0.9) 1 (0.6)
42. Melianthaceae 1 (0.9) 1 (0.6)
43. Menispermaceae 1 (0.9) 1 (0.6)
44. Moringaceae 1 (0.9) 1 (0.6)
45. Myricaceae 1 (0.9) 1 (0.6)
46. Oliniaceae 1 (0.9) 1 (0.6)
47. Pedaliaceae 1 (0.9) 1 (0.6)
48. Piperaceae 1 (0.9) 1 (0.6)
49. Plantaginaceae 1 (0.9) 1 (0.6)
50. Polygalaceae 1 (0.9) 1 (0.6)
51. Rhamnaceae 1 (0.9) 1 (0.6)
52. Rubiaceae 1 (0.9) 1 (0.6)
53. Salicaceae 1 (0.9) 1 (0.6)
54. Sapindaceae 1 (0.9) 1 (0.6)
55. Scrophulariaceae 1 (0.9) 1 (0.6)
56. Tiliaceae 1 (0.9) 1 (0.6)
57. Trymalaceae 1 (0.9) 1 (0.6)
Total 111 162

Solanaceae was represented by n = 12, 7.41% plants, followed by Euphorbiaceae (by n = 11, 6.8% plants), Fabaceae and Lamiaceae (by n = 9, 5.6% plants each), Alliaceae and Phytolaccaceae (by n = 8, 4.9% plants each), Acanthaceae (by n = 7, 4.3% plants), Myrtaceae and Zingiberaceae (by n = 6, 3.7% plants each), Asteraceae and Moraceae (by n = 5, 3.09% plants each), and the remaining 43 families by 1 to 4 plants (Table 2).

3.4. Medicinal Plants with Antiviral Active Components

A range of active compounds with potential antiviral agents for future drug development has been identified from plants [77]. People in Ethiopia use different medicinal plants to treat different viral infections even without knowing their active components (Table 1). However, different literature shows that 56 (50.4%) of the plants reviewed contained components with antiviral activity (Table 3).

Table 3.

Medicinal plants with antiviral components.

No. Scientific name Family Local name Active components References
1 Acacia abyssinica Hochst.ex Benth. Fabaceae Bazra grar (Am) Flavonoid, tannin, terpenoids, polyphenolic [5]
2 Acacia etbaica Schweinf. Fabaceae Seraw (Am) Flavonoid, tannin, terpenoids, polyphenolic [5]
3 Acacia nigra Fabaceae Tikur grar (Am) Flavonoid, tannin, terpenoids, and polyphenolic [5]
4 Acanthus polystachyus Acanthaceae Kucheshile (Am) Tannins, flavonoids, saponins, polyphenols, and anthraquinones [78]
5 Acokanthera schimperi Apocynaceae Meriz (Am) Oleanolic acid and ursolic acid [79]
6 Allium cepa Alliaceae QeY shikurt (Am) Quercetinand epigallocatechin gallate [16]
7 Allium sativum Alliaceae Nechsenkret (Am) Allicin, diallyl trisulfide ajoene, and apigenin [14, 17]
8 Aloe macrocarpa Tod. Aloaceae Eret (Am) Aloenin, aloesin, aloe-emodin, aloin chrysophanol, catechin, and isoaloresin [18]
9 Amaranthus hybridus Linn. Amaranthaceae Tenbelel (Am) Amaranthine, quercetin, and kaempferol glycosides [80]
10 Artemisia afra Jack. ex Willd. and Artemisia annua L. Asteraceae Chikugn (Am) Artemisinin [6, 19]
11 Azadirachta indica Meliaceae Neem (Am) Quercetin and ß sitosterol, polyphenolic flavonoids [81]
12 Bersama abyssinica Melianthaceae Azamer (Am) Anthraquinones [82]
13 Brassica carinata A. Br. Herb Brassicaceae Gommon (Am) Kaempferol [10, 11]
14 Camellia sinensis Theaceae Shay kitel (Am) Epigallocatechin gallate [10]
15 Capsicum annuum L. Solanaceae Berbere (Am) Apigenin [11]
16 Carissa edulis Apocynaceae Agam (Am) Kaempferol and quercetin [83]
17 Citrus aurantium L Rutaceae Bahir Lome (Am) Apigenin, ethyl cholate, nobiletin, tangeretin, chalcone, and hesperidin [5, 10, 14, 15]
18 Citrus limon (L.) Burm. f. Rutaceae Lome (Am) Apigenin, ethyl cholate, nobiletin, tangeretin, chalcone, and hesperidin [5, 10, 14, 15]
19 Clematis hirsute Ranunculaceae Hareg (Tg) Kaempferol and quercetin [84]
20 Clutia abyssinica Euphorbiaceae Tewshealalito (Tg) Fiyle feji (Am) Anthraquinones [85]
21 Coriandrum sativum Apiaceae Dimblal (Am) Linalool, geranyl acetate [56]
22 Crinum abyscinicum Hochst. ex A. Rich Amaryllidaceae Yejib shinkurt (Am) Lycorine [57]
23 Curcuma longa Zingiberaceae Erd (Am) Curcumin [20]
24 Dodonia angustifolia Sapindaceae Kitkita (Am) Anthraquinones [86]
25 Dregea schimperi Asclepiadaceae Shanqoq (Tg) Anthraquinones [87]
26 Ekebergia capensis Meliaceae Sembo (Am) Oleanolic acid [88]
27 Eucalyptus globulus Myrtaceae Nech bahirzaf (Am) Jensenone [22]
28 Euphorbia abyssinica G.F.Gmel Euphorbiaceae Kulkual (Am) Oleanolic acid [89]
29 Lepidium sativum Brassicaceae feto (Am) Kaempferol and quercetin [22]
30 Lycopersicon esculentum (L.) Mill. Solanaceae Timaatima (Or) Rhoifolin [64]
31 Moringa borziana Mattei Mawe Moringaceae Tamergnaw ketel (Shiferaw) (Am) Flavonoids, anthraquinone, and hydroxychloroquine [21]
32 Musa spp. Musaceae Muz (Am) Rhoifolin [64]
33 Nigella sativa Ranunculaceae Tikur Azmud (Am) Hederagenin, nigellidine, and α-hederin [11, 90]
34 Ocimum basilicum L. Herb Lamiaceae Bessobla (Am) Oleanolic acid and ursolic acid [11]
35 Ocimum lamiifolium Hochst. Ex Benth. Lamiaceae Damakassie (Am) Oleanolic acid and ursolic acid [11]
36 Ocimum urticifolium Roth Lamiaceae Dama kesie (Am) Oleanolic acid and ursolic acid [11]
37 Olea europaea subsp. cuspidate Oleaceae Weyra (Am) Oleanolic acid and ursolic acid [11]
38 Osyris quadripartite Santalaceae Keret (Am) Ursolic acid, oleanolic acid (triterpenes), kaempferol-3-O-rutinoside, quercetin-3-O-rutinoside or rutoside, and quercetin-3-O-β-D-glucopyranoside (flavonoids) [91]
39 Phaseolus vulgaris Fabaceae Bakela (Am) Kaempferol [92]
40 Phytolacca dodecandra Phytolaccaceae Endod (Am) Oleanolic acid [93]
41 Piper nigrum Piperaceae Kundo berbere (Am) Piperine [12]
42 Prunus dulcis Rosaceae Lewuz (Am) Almond oil [94]
43 Ricinus communis L. Euphorbiacea Kabosimbiro (Or) Kaempferol and quercetin [95]
44 Rosa abyssinica Rosaceae Qega (Am) Unknown [74]
45 Rosmarinus officinalis Lamiaceae Tibs kitel (Am) Rosmarinic acid [11]
46 Rumex abyssinicus Polygonaceae Mekmoko (Am) Anthraquinones [96]
47 Rumex crispus Polygonaceae Enbacho (Am) Anthraquinones [96]
48 Ruta chalepensis L. Rutaceae Tena adam (Am) Kaempferol and quercetin [13]
49 Schinus molle Anacardiaceae Kendo berbera (Am) Piperine [12]
50 Spinacia oleracea Amaranthaceae Kosta (Am) Kaempferol [10]
51 Syzygium aromaticum Myrtaceae Kirnfud (Am) Oleanolic acid [9]
52 Vernonia amygdalina Asteraceae Grawa (Am) Anthraquinones [97]
53 Vitis vinifera Vitaceae Weyin fire (Am) Resveratrol rhoifolin [8]
54 Withania somnifera Solanaceae Giziewa or Kumo (Am) [76]
55 Ximenia americana Oleaceae Enkuay (Am) Anthraquinones [98]
56 Zingiber officinale Roscoe. Zingiberaceae Zinjibile (Am) Gingerol shogaol [7]

Flavonoids are secondary metabolites with antiviral properties [99]. The Ethiopian medicinal plants Acacia abyssinica, Acacia etbaica, and Acacia nigra [5], Moringa borziana [21], Acanthus polystachyus [78], Azadirachta indica [81], and Osyris quadripartite [91] were reported to contain flavonoids.

Reports show that tannins block virus attachment, entry, and cell-to-cell spread by binding to viral glycoproteins on viruses and the surfaces of infected cells [100]. The Ethiopian medicinal plants Acacia abyssinica, Acacia etbaica, and Acacia nigra [5] and Acanthus polystachyus [78] are reported to have tannins so that they can be good candidates to fight COVID-19.

Many terpenoids of plant origin have antiviral activities against severe acute respiratory syndrome coronavirus [101]. Medicinal plants reviewed in the present study may possess terpenoids. Studies among some of these medicinal plants show that they possess these secondary metabolites. Some of the medicinal plants with terpenoid active components were Acacia abyssinica, Acacia etbaica, and Acacia nigra [5] and Osyris quadripartite [91].

Polyphenols have demonstrated potent antiviral activities. For example, the polyphenol in green tea controls viruses such as hepatitis C, chikungunya, hepatitis B, herpes simplex virus type 1, influenza A, vaccinia, adenovirus, reovirus, vesicular stomatitis, and Zika (ZIKV) [102]. Acacia abyssinica, Acacia etbaica, and Acacia nigra [5], Acanthus polystachyus [78], and Azadirachta indica [81] of the present review contained polyphenols in their extracts.

Acanthus polystachyus [78] contained saponins that possess various biological activities, including antiviral action [103]. Ocimum basilicum, Ocimum lamiifolium, Ocimum urticifolium, and Olea europaea subsp. cuspidate [11], Osyris quadripartite [91], and Acokanthera schimperi [79] contain ursolic acid which is a pentacyclic triterpenoid with potent antiviral activities [104].

Another plant secondary metabolite with antiviral activity is oleanolic acid [105]. It is reported from Syzygium aromaticum [9], Ocimum basilicum, Ocimum lamiifolium, Ocimum urticifolium, and Olea europea subsp cuspidate [11], Osyris quadripartite [91], Acokanthera schimperi [78], Dregea schimperi [88], Euphorbia abyssinica [89], and Phytolacca dodecandra [93]. Oleanolic acid has a binding affinity for SARS-CoV-2 M protease and Spike (S) glycoprotein [106].

The plant metabolite quercetin inhibits viral entry into target cells via interaction with viral HA protein [107]. Medicinal plants from Ethiopia, Allium cepa [16], Lepidium sativum [22], Azadirachta indica [81], Osyris quadripartite [91], Amaranthus hybridus Linn [80], Clematis hirsute [84], Carissa edulis [90], Ricinus communis [95], and Ruta chalepensis [13], are reported to contain quercetin.

Epigallocatechin-3-O-gallate (EGCG) is known to inhibit a variety of DNA and RNA viruses [108]. It is found in Camellia sinensis [10] and Allium cepa [16]. Allicin exhibits antiviral, antifungal, and antiparasitic activities [109]. This phytochemical is reported from Allium sativum [14, 17], a medicinal plant used to treat viral infections by people in Ethiopia.

In vitro and in vivo results show that apigenin exhibits antiviral activities [110]. It is found in Capsicum annuum [11], Citrus aurantium [5, 10, 14, 15], Citrus limon [5, 10, 14, 15], and Allium cepa [14, 17]. Reports show that kaempferol has antiviral activities against influenza A virus (H1N1 and H9N2), human immunodeficiency virus (HIV) 1, and JEV [111]. Many medicinal plants used to treat viral infections in Ethiopia such as Citrus aurantium L., Citrus limon (L.) Burm. f., Capsicum annuum L., Eucalyptus globulus, Osyris quadripartite, Amaranthus hybridus Linn., Clematis hirsute, Ricinus communis L., Ruta chalepensis L., Carissa edulis, Phaseolus vulgaris also contain this active component [10, 11, 13, 22, 80, 83, 84, 91, 92, 95].

Lycorine is a compound with broad antiviral activity. It is reported to possess anti-SARS-CoV activity [6]. It is possessed in Ethiopian medicinal plants traditionally used to treat viral infections, for example, in Crinum abyscinicum Hochst. ex A. Rich. [57].

4. Conclusions

Traditional healers in Ethiopia have knowledge of medicinal plants with potential antiviral activity. Literature shows that the majority of the plants prescribed by traditional healers in Ethiopia have antiviral compounds. Therefore, these medicinal plants should be researched for anti-COVID-19 properties.

Data Availability

All related data have been presented within the manuscript. The dataset supporting the conclusions of this article is available from the authors on request.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

References

  • 1.Al-Ali K. H., El-Badry A. A. Anti-viral activity of two labiatae plants [Naana (Hassoi, Habak) and basil (Rahan)] of Al-Madiah Al-Munawarah. Journal of Medical and Biomedical Sciences. 2010;2:67–73. [Google Scholar]
  • 2.Tillu G., Chaturvedi S., Chopra A., Patwardhan B. Public health approach of Ayurveda and Yoga for COVID-19 prophylaxis. The Journal of Alternative and Complementary Medicine. 2020;26(5):360–364. doi: 10.1089/acm.2020.0129. [DOI] [PubMed] [Google Scholar]
  • 3.European Centre for Disease Prevention and Control. COVID-19 Situation Update Worldwide. Solna, Sweden: European Centre for Disease Prevention and Control; 2020. https://www.ecdc.europa.eu/en/geographical-distribution-2019-ncov-cases. [Google Scholar]
  • 4.Gupta Y. K., Briyal S., Gulati A. Therapeutic potential of herbal drugs in cerebral ischemia. Indian Journal of Physiology and Pharmacology. 2010;54(2):99–122. [PubMed] [Google Scholar]
  • 5.Mirzaie A., Halaji M., Dehkordi F. S., Ranjbar R., Noorbazargan H. A narrative literature review on traditional medicine options for treatment of corona virus disease 2019 (COVID-19) Complementary Therapies in Clinical Practice. 2020;40 doi: 10.1016/j.ctcp.2020.101214.101214 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Li S., Chen C., Zhang H., et al. Identification of natural compounds with antiviral activities against SARS-associated coronavirus. Antiviral Research. 2005;67(1):18–23. doi: 10.1016/j.antiviral.2005.02.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Rathinavel T., Palanisamy M., Palanisamy S., Subramanian A., Thangaswamy S. Phytochemical 6-Gingerol–A promising Drug of choice for COVID-19. International Journal of Advanced Science and Engineering. 2020;6(4) doi: 10.29294/IJASE.6.4.2020.1482-1489. [DOI] [Google Scholar]
  • 8.Orhan D. D., Orhan N., Ozcelik B., Ergun F. Biological activities of Vitis vinifera L. leaves. Turkish Journal of Biology. 2009;33:341–348. [Google Scholar]
  • 9.Diego C.-r. F., Wanderley O. P. Clove (Syzygium aromaticum): a precious spice. Asian Pacific Journal of Tropical Biomedicine. 2014;2:90–96. doi: 10.1016/S2221-1691(14)60215-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Tallei T. E., Tumilaar S. G., Niode N. J., et al. Potential of plant bioactive compounds as SARS-CoV-2 main protease (Mpro) and spike (S) glycoprotein inhibitors: a molecular docking study. Scientifica. 2020;2020:18. doi: 10.1155/2020/6307457.6307457 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Sampangi-Ramaiah M. H., Vishwakarma R., Shaanker R. U. Molecular docking analysis of selected natural products from plants for inhibition of SARS-CoV-2 main protease. Current Science. 2020;118(7):1087–1092. [Google Scholar]
  • 12.Mishra R. C., Kumari R., Yadav S., Yadav J. P. Antiviral potential of phytoligands against chymotrypsin-like protease of COVID‐19 virus using molecular docking studies: an optimistic approach. 2020.
  • 13.Alotaibi S. M., Saleem M. S., Al-humaidi J. G. Phytochemical contents and biological evaluation of Ruta chalepennsis L. growing in Saudi Arabia. Saudi Pharmaceutical Journal. 2018;26(4):504–508. doi: 10.1016/j.jsps.2018.02.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Ziaei S., Heidari M., Amin G., Kochmeshki A., Heidari M. Inhibitory effects of germinal angiotensin converting enzyme by medicinal plants used in Iranian traditional medicine as antihypertensive. Journal of Kerman University of Medical Sciences. 2009;16(2):134–143. [Google Scholar]
  • 15.Utomo R. Y., Meiyanto E. Revealing the potency of citrus and galangal constituents to Halt SARS-CoV-2 infection. Preprints. 2020. [DOI]
  • 16.Polansky H., Lori G. Coronavirus (COVID-19), first indication of efficacy of Gene-Eden-VIR/Novirin in SARS-CoV-2 infections. International Journal of Antimicrobial Agents. 2020;55(6) doi: 10.1016/j.ijantimicag.2020.105971.105971 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Thuy B. T. P., My T. T. A., Hai N. T. T., et al. Investigation into SARS-CoV-2 resistance of compounds in garlic essential oil. ACS Omega. 2020;5(14):8312–8320. doi: 10.1021/acsomega.0c00772. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Pandit M., Latha N. In silico studies reveal potential antiviral activity of phytochemicals from medicinal plants for the treatment of COVID-19 infection. Research Square. 2020. [DOI]
  • 19.Sehailia M., Chemat S. In-silico studies of antimalarial-agent artemisinin and derivatives portray more potent binding to Lys353 and Lys31-binding hotspots of SARS-CoV-2 Spike protein than hydroxychloroquine: potential repurposing of artenimol for COVID-19. Journal of Biomolecular Structure and Dynamics. 2020 doi: 10.1080/07391102.2020.1796809. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Jena A. B., Kanungo N., Nayak V., Chainy G., Dandapat J. 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. Research Square. 2020. [DOI]
  • 21.Hamza M., Ali A., Khan S., et al. nCOV-19 peptides mass fingerprinting identification, binding, and blocking of inhibitors flavonoids and anthraquinone of Moringa oleifera and hydroxychloroquine. Journal of Biomolecular Structure and Dynamics. 2020:1–11. doi: 10.1080/07391102.2020.1778534. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Sharma A. D., Kaur I. Jensenone from eucalyptus essential oil as a potential inhibitor of COVID 19 Coronavirus infection. Research & Reviews in Biotechnology & Biosciences. 2020;7(1):59–66. [Google Scholar]
  • 23.Uprety Y., Asselin H., Dhakal A., Julien N. Traditional use of medicinal plants in the boreal forest of Canada: review and perspectives. Journal of Ethnobiology and Ethnomedicine. 2012;8(1):p. 7. doi: 10.1186/1746-4269-8-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Borokini T. I., Omotayo F. O. Phytochemical and ethnobotanical study of some selected medicinal plants from Nigeria. Journal of Medicinal Plants Research. 2012;6(7):1106–1118. doi: 10.5897/jmpr09.430. [DOI] [Google Scholar]
  • 25.Abebe D., Hagos E. The traditional health practices of Ethiopia. Plant Genetic Resources of Ethiopia. 1991;101 [Google Scholar]
  • 26.World Health Organization. Legal Status of Traditional Medicine and Complementary/alternative Medicine: A Worldwide Review. Geneva, Switzerland: WHO; 2001. [Google Scholar]
  • 27.Fullas F. The role of indigenous medicinal plants in Ethiopian healthcare. African Renaissance. 2007;4(1):76–80. [Google Scholar]
  • 28.Omoruyi B., Bradley G., Afolayan A. Ethnomedicinal survey of medicinal plants used for the management of HIV/AIDS infection among local communities of Nkonkobe Municipality, Eastern Cape, South Africa. Journal of Medicinal Plants Research. 2012;6(19):3603–3608. doi: 10.5897/jmpr12.541. [DOI] [Google Scholar]
  • 29.Giday M., Asfaw Z., Woldu Z., Teklehaymanot T. Medicinal plant knowledge of the Bench ethnic group of Ethiopia: an ethnobotanical investigation. Journal of Ethnobiology and Ethnomedicine. 2009;5(1):p. 34. doi: 10.1186/1746-4269-5-34. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.World Health Organization. Coronavirus Disease (COVID-19): Similarities and Differences with Influenza. Geneva, Switzerland: WHO; 2020. https://www.who.int/emergencies/diseases/novel-coronavirus-2019/question-and-answers-hub/q-a-detail/coronavirus-disease-covid-19-similarities-and-differences-with-influenza. [Google Scholar]
  • 31.Doffana Z. D. Sacred natural sites, herbal medicine, medicinal plants and their conservation in Sidama, Ethiopia. Cogent Food & Agriculture. 2017;3(1) doi: 10.1080/23311932.2017.1365399.1365399 [DOI] [Google Scholar]
  • 32.Joshi B., Panda S. K., Jouneghani R. S., et al. Antibacterial, antifungal, antiviral, and anthelmintic activities of medicinal plants of Nepal selected based on ethnobotanical Evidence. Evidence-Based Complementary and Alternative Medicine. 2020;2020:14. doi: 10.1155/2020/1043471.1043471 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Worldometer. Ethiopia population (LIVE) 2020. https://www.worldometers.info/world-population/ethiopia-population/
  • 34. Information technology associates, 2020, https://theodora.com/wfbcurrent/ethiopia/ethiopia_geography.html.
  • 35.Teklay A., Abera B., Giday M. An ethnobotanical study of medicinal plants used in Kilte Awulaelo District, Tigray Region of Ethiopia. Journal of Ethnobiology and Ethnomedicine. 2013;9(1):p. 65. doi: 10.1186/1746-4269-9-65. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Worku A. A review on significant of traditional medicinal plants for human use in case of Ethiopia. Plant Pathology and Microbiology. 2019;10:p. 484. [Google Scholar]
  • 37.Seid M. A., Tsegay B. A. Ethnobotanical survey of traditional medicinal plants in Tehuledere district, South Wollo, Ethiopia. Journal of Medicinal Plants Research. 2011;5(26):6233–6242. doi: 10.5897/jmpr11.1070. [DOI] [Google Scholar]
  • 38.Chekole G., Asfaw Z., Kelbessa E. Ethnobotanical study of medicinal plants in the environs of Tara-gedam and Amba remnant forests of Libo Kemkem District, northwest Ethiopia. Journal of Ethnobiology and Ethnomedicine. 2015;11(1):p. 4. doi: 10.1186/1746-4269-11-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Simegniew Birhan Y., Leshe Kitaw S., Minuye Mengesha Y., Mengesha N. Ethnobotanical study of medicinal plants used to treat human diseases in Enarj Enawga district, East Gojjam zone, Amhara region, Ethiopia. SM Journal of Medicinal Plant Studies. 2017;1(1):1–20. doi: 10.36876/smjmps.1006. [DOI] [Google Scholar]
  • 40.Busse H., Tefera G. Handbook of Sidama Traditional Medicinal Plants. Madison, WI, USA: A Service Learning Project School of Medicine and Public Health, University of Wisconsin-Madison, School of Medicine & Public Health, Department of Surgery; 2013. [Google Scholar]
  • 41.Amenu E. Addis Ababa, Ethiopia: Addis Ababa University; 2007. Use and management of medicinal plants by indigenous people of Ejaji area (Chelya Woreda) West Shoa, Ethiopia: an ethnobotanical approach. M.Sc. thesis. [Google Scholar]
  • 42.Atnafu H., Awas T., Alemu S., Wube S. Ethnobotanical study of medicinal plants in selale mountain ridges, North Shoa, Ethiopia. International Journal of Biodiversity. 2018;2(6):567–577. [Google Scholar]
  • 43.Kebebew M., Mohamed E. Indigenous knowledge on use of medicinal plants by indigenous people of Lemo district, Hadiya zone, Southern Ethiopia. International Journal of Herbal Medicine. 2017;5(4):124–135. [Google Scholar]
  • 44.Zenebe G., Zerihun M., Solomon Z. An ethnobotanical study of medicinal plants in Asgede Tsimbila district, Northwestern Tigray, northern Ethiopia. Ethnobotany Research and Applications. 2012;10:305–320. doi: 10.17348/era.10.0.305-320. [DOI] [Google Scholar]
  • 45.Abera B. Medicinal plants used in traditional medicine by Oromo people, Ghimbi District, Southwest Ethiopia. Journal of Ethnobiology and Ethnomedicine. 2014;10(1):40–15. doi: 10.1186/1746-4269-10-40. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Maroyi A. Alternative medicines for HIV/AIDS in resource-poor settings: insight from traditional medicines use in sub- saharan Africa. Tropical Journal of Pharmaceutical Research. 2014;13(9):1527–1536. doi: 10.4314/tjpr.v13i9.21. [DOI] [Google Scholar]
  • 47.Asres K., Bucar F., Kartnig T., Witvrouw M., Pannecouque C., De Clercq E. Antiviral activity against human immunodeficiency virus type 1 (HIV-1) and type 2 (HIV-2) of ethnobotanically selected Ethiopian medicinal plants. Phytotherapy Research. 2001;15(1):62–69. doi: 10.1002/1099-1573(200102)15:1<62::aid-ptr956>3.0.co;2-x. [DOI] [PubMed] [Google Scholar]
  • 48.Beyi M. W. Ethnobotanical investigation of traditional medicinal plants in dugda district, Oromia regio. SM Journal of Medicinal Plant Studies. 2018;2(1):p. 1007. doi: 10.36876/smjmps.1007. [DOI] [Google Scholar]
  • 49.Teklehaymanot T. Ethnobotanical study of knowledge and medicinal plants use by the people in Dek Island in Ethiopia. Journal of Ethnopharmacology. 2009;124(1):69–78. doi: 10.1016/j.jep.2009.04.005. [DOI] [PubMed] [Google Scholar]
  • 50.Meresa A., Degu S., Tadele A., et al. Medicinal plants used for the management of rabies in Ethiopia–a review. Medicinal Chemistry (Los Angeles) 2017;7:795–806. [Google Scholar]
  • 51.Giday M., Teklehaymanot T., Animut A., Mekonnen Y. Medicinal plants of the shinasha, agew-awi and amhara peoples in northwest Ethiopia. Journal of Ethnopharmacology. 2007;110(3):516–525. doi: 10.1016/j.jep.2006.10.011. [DOI] [PubMed] [Google Scholar]
  • 52.Mahmood M. S., Mártinez J. L., Aslam A., et al. Antiviral effects of green tea (Camellia sinensis) against pathogenic viruses in human and animals (a mini-review) African Journal of Traditional, Complementary and Alternative Medicines. 2016;13(2):176–184. doi: 10.4314/ajtcam.v13i2.21. [DOI] [Google Scholar]
  • 53.Zaher K. S., Ahmed W., Zerizer S. N. Observations on the biological effects of black cumin seed (Nigella sativa) and green tea (Camellia sinensis) Global Veterinaria. 2008;2(4):198–204. [Google Scholar]
  • 54.Ayele T. T., Regasa M. B., Delesa D. A. Evaluation of antimicrobial activity of some traditional medicinal plants and herbs from Nekemte district against wound causing bacterial pathogens. Science, Technology and Arts Research Journal. 2015;4(2):199–203. [Google Scholar]
  • 55.Jima T. T., Megersa M. Ethnobotanical study of medicinal plants used to treat human diseases in Berbere district, Bale zone of Oromia regional state, south east Ethiopia. Evidence-Based Complementary and Alternative Medicine. 2018;2018:16. doi: 10.1155/2018/8602945.8602945 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Hussain F., Jahan N., Rahman K.-u., Sultana B., Jamil S. Identification of hypotensive biofunctional compounds of Coriandrum sativum and evaluation of their angiotensin-converting enzyme (ACE) inhibition potential. Oxidative Medicine and Cellular Longevity. 2018;2018:11. doi: 10.1155/2018/4643736.4643736 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Tamiru F., Terfa W., Kebede E., Dabessa G., Roy R. K., Sorsa M. Ethnoknowledge of plants used in veterinary practices in dabo hana district, west Ethiopia. Journal of Medicinal Plants Research. 2013;7(40):2960–2971. [Google Scholar]
  • 58.Kim K., Kim K. H., Kim H. Y., Cho H. K., Sakamoto N., Cheong J. Curcumin inhibits hepatitis C virus replication via suppressing the Akt-SREBP-1 pathway. FEBS Letters. 2010;584(4):707–712. doi: 10.1016/j.febslet.2009.12.019. [DOI] [PubMed] [Google Scholar]
  • 59.Agisho H., Osie M., Lambore T. Traditional medicinal plants utilization, management and threats in Hadiya Zone, Ethiopia. Journal of Medicinal Plants. 2014;2(2):94–108. [Google Scholar]
  • 60.Beyene T. Addis Ababa, Ethiopia: Addis Ababa University; 2015. Ethnobotany of medicinal plants in Erob and Gulomahda districts, Eastern zone of Tigray region, Ethiopia. PhD. dissertation. [Google Scholar]
  • 61.Yirga G., Zeraburk S. Ethnobotanical study of traditional medicinal plants in Gindeberet District, western Ethiopia. Mediterranean Journal of Social Sciences. 2011;2(4):49–54. [Google Scholar]
  • 62.Reta H. An Ethnobotanical Study of Useful Plants of the Farming Site in Gozamen Wereda, East Gojjam Zone of Amhara Region, Ethiopia. Addis Ababa, Ethiopia: Addis Ababa University; 2010. [Google Scholar]
  • 63.Amsalu N., Bezie Y., Fentahun M., Alemayehu A., Amsalu G. Use and conservation of medicinal plants by indigenous people of Gozamin Wereda, East Gojjam Zone of Amhara region, Ethiopia: an ethnobotanical approach. Evidence-Based Complementary and Alternative Medicine. 2018;2018:23. doi: 10.1155/2018/2973513.2973513 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.Peterson L. COVID-19 and flavonoids: in silico molecular dynamics docking to the active catalytic site of SARS-CoV and SARS-CoV-2 main protease. Preprint. 2020.
  • 65.Covés-Datson E. M., King S. R., Legendre M., et al. A molecularly engineered antiviral banana lectin inhibits fusion and is efficacious against influenza virus infection in vivo. Proceedings of the National Academy of Sciences. 2020;117(4):2122–2132. doi: 10.1073/pnas.1915152117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Tuasha N., Petros B., Asfaw Z. Medicinal plants used by traditional healers to treat malignancies and other human ailments in Dalle District, Sidama Zone, Ethiopia. Journal of Ethnobiology and Ethnomedicine. 2018;14(1):p. 15. doi: 10.1186/s13002-018-0213-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Priya N., Saravana Kumari P. Antiviral activities and cytotoxicity assay of seed extracts of Piper longum and Piper nigrum on human cell lines. International Journal of Pharmaceutical Sciences Review and Research. 2017;44(1):197–202. [Google Scholar]
  • 68.Ekowati H., Arai J., Damana Putri A. S., Nainu F., Shiratsuchi A., Nakanishi Y. Protective effects of Phaseolus vulgaris lectin against viral infection in Drosophila. Drug Discoveries & Therapeutics. 2017;11(6):329–335. doi: 10.5582/ddt.2017.01071. [DOI] [PubMed] [Google Scholar]
  • 69.Hafidh R. R., Abdulamir A. S., Abu Bakar F., Sekawi Z., Jahansheri F., Jalilian F. A. Novel antiviral activity of mung bean sprouts against respiratory syncytial virus and herpes simplex virus −1: an in vitro study on virally infected Vero and MRC-5 cell lines. BMC Complementary and Alternative Medicine. 2015;15(1):p. 179. doi: 10.1186/s12906-015-0688-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70.Abera B. Medicinal plants used in traditional medicine in Jimma Zone, Southwest Ethiopia. Ethiopian Journal of Health Sciences. 2003;13(2) [Google Scholar]
  • 71.Seifu T., Asres K., Gebre-Mariam T. Ethnobotanical and ethnopharmaceutical studies on medicinal plants of Chifra district, Afar region, North Eastern Ethiopia. Ethiopian Pharmaceutical Journal. 2006;24(1):41–58. doi: 10.4314/epj.v24i1.35097. [DOI] [Google Scholar]
  • 72.Musarra-Pizzo M., Ginestra G., Smeriglio A., Pennisi R., Sciortino M. T., Mandalari G. The antimicrobial and antiviral activity of polyphenols from almond (Prunus dulcis L.) skin. Nutrients. 2019;11(10):p. 2355. doi: 10.3390/nu11102355. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 73.Yineger H., Yewhalaw D., Teketay D. Ethnomedicinal plant knowledge and practice of the Oromo ethnic group in southwestern Ethiopia. Journal of Ethnobiology and Ethnomedicine. 2008;4(1):11–10. doi: 10.1186/1746-4269-4-11. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 74.Jassim S. A. A., Naji M. A. Novel antiviral agents: a medicinal plant perspective. Journal of Applied Microbiology. 2003;95(3):412–427. doi: 10.1046/j.1365-2672.2003.02026.x. [DOI] [PubMed] [Google Scholar]
  • 75.Shin H. B., Choi M. S., Ryu B., et al. Antiviral activity of carnosic acid against respiratory syncytial virus. Virology Journal. 2013;10(1):303–311. doi: 10.1186/1743-422X-10-303. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76.Nandan A., Tiwari S., Sharma V. Exploring alternative medicine options for the prevention or treatment of Coronavirus disease 2019 (COVID-19)-a systematic scoping Review. medRxiv. 2020:1–40. doi: 10.1101/2020.05.14.20101352. [DOI] [Google Scholar]
  • 77.Sohail M. N., Rasul F., Karim A., Kanwal U., Attitalla I. H. Plant as a source of natural antiviral agents. Asian Journal of Animal and Veterinary Advances. 2011;6(12):1125–1152. doi: 10.3923/ajava.2011.1125.1152. [DOI] [Google Scholar]
  • 78.Demilew W. Evaluation of the antibacterial and wound healing activity of the crude and solvent fractions of leaves of Acanthus polystachus Delile. 2017. https://nadre.ethernet.edu.et/record/1791#.X-Gbi9gzbIU.
  • 79.Matebie W. A., Zhang W., Zhang S., Xie G. Triterpenoids from Acokanthera schimperi in Ethiopia. Records of Natural Products. 2019;13(3):182–188. doi: 10.25135/rnp.94.18.07.324. [DOI] [Google Scholar]
  • 80.Zeashan H., Amresh G., Singh S., Rao C. V. Hepatoprotective activity of Amaranthus spinosus in experimental animals. Food and Chemical Toxicology. 2008;46(11):3417–3421. doi: 10.1016/j.fct.2008.08.013. [DOI] [PubMed] [Google Scholar]
  • 81.Alzohairy M. A. Therapeutics role of Azadirachta indica (Neem) and their active constituents in diseases prevention and treatment. Evidence-Based Complementary and Alternative Medicine. 2016;2016:11. doi: 10.1155/2016/7382506.7382506 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 82.Asian J. In-vitro antihelmentic evaluaion of leaf extract of bersama abyssinica (mellanthaceae) on Haemonchus contortus. Asian Journal of Medical and Pharmaceutical Researches. 2018;8(2):5–14. [Google Scholar]
  • 83.Al-Youssef H. M., Hassan W. H. B. Chemical constituents of Carissa edulis vahl. Arabian Journal of Chemistry. 2017;10(1):109–113. doi: 10.1016/j.arabjc.2014.01.004. [DOI] [Google Scholar]
  • 84.Sun F., Yang D. Advance in chemical constituents of genus Clematis. Zhongguo Zhong Yao Za Zhi. 2009;34(20):2660–2668. [PubMed] [Google Scholar]
  • 85.Terefe E. M., Shibeshi W., Terefe G., Teklehaymanot T. Evaluation of in vivo antitrypanosomal activity of aqueous and methanol leaf extracts of clutia abyssinica (Euphorbiaceae) against Trypanosoma Congolense field isolate. Natural Products Chemistry Research. 2014;2:p. 138. doi: 10.4172/2329-6836.1000138. [DOI] [Google Scholar]
  • 86.Anode S. O., Abraha T., Araya S. Phytochemical analysis of Dodonaea angustifolia plant extracts. Internajional Journal of Herbal Medicine. 2018;6:37–42. [Google Scholar]
  • 87.Onyancha J. M., Wakori E., Moriasi G. A., et al. In vitro antibacterial activities, safety studies and phytochemical screening of dregea schimperi clark (Asclepiadaceae) Extracts. World Journal of Pharmaceutical Research. 2017;6(7):169–178. [Google Scholar]
  • 88.Irungu B., Orwa J., Gruhonjic A., et al. Constituents of the roots and leaves of Ekebergia capensis and their potential antiplasmodial and cytotoxic activities. Molecules. 2014;19(9):14235–14246. doi: 10.3390/molecules190914235. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 89.El-Fiky F., Asres K., Gibbons S., Hammoda H., Badr J., Umer S. Phytochemical and antimicrobial investigation of latex from Euphorbia abyssinica Gmel. Natural Product Communications. 2008;3(9) doi: 10.1177/1934578x0800300922. [DOI] [Google Scholar]
  • 90.Salim B., Noureddine M. Identification of compounds from Nigella sativa as new potential inhibitors of 2019 novel Coronavirus (Covid-19): Molecular docking study. ChemRxiv. 2020 doi: 10.26434/chemrxiv.12055716.v1. [DOI] [Google Scholar]
  • 91.Shyaula S. A review on genusOsyris: phytochemical constituents and traditional uses. Journal of Natural Pharmaceuticals. 2012;3(2):p. 61. doi: 10.4103/2229-5119.102747. [DOI] [Google Scholar]
  • 92.Jo S., Kim S., Shin D. H., Kim M.-S. Inhibition of SARS-CoV 3CL protease by flavonoids. Journal of Enzyme Inhibition and Medicinal Chemistry. 2020;35(1):145–151. doi: 10.1080/14756366.2019.1690480. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 93.Kariuki S. T., Kariuki J. M., Mailu B. M., Muchiri D. R. Isolation and characterisation of chemical compounds from the plants, Phytolacca octandra (L.), Phytolacca dodecandra (LHerit) and Balanites aegyptiaca (L.) commonly used to control schistosomiasis transmitting snails in Kenya. African Journal of Pure and Applied Chemistry. 2018;12(6):38–41. doi: 10.5897/ajpac2018.0749. [DOI] [Google Scholar]
  • 94.Xu J., Zhang Y. Traditional Chinese medicine treatment of COVID-19. Complementary Therapies in Clinical Practice. 2020;39 doi: 10.1016/j.ctcp.2020.101165.101165 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 95.Singh R., Geetanjali G. Phytochemical and pharmacological investigations of Ricinus communis Linn. Algerian Journal of Natural Products. 2015;3:120–129. [Google Scholar]
  • 96.Augustin N., Nuthakki V. K., Abdullaha M., Hassan Q. P., Gandhi S. G., Bharate S. B. Discovery of Helminthosporin, an anthraquinone isolated from Rumex abyssinicus Jacq as a dual cholinesterase inhibitor. ACS Omega. 2020;5(3):1616–1624. doi: 10.1021/acsomega.9b03693. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 97.Tona L., Cimanga R. K., Mesia K., et al. In vitro antiplasmodial activity of extracts and fractions from seven medicinal plants used in the Democratic Republic of Congo. Journal of Ethnopharmacology. 2004;93(1):27–32. doi: 10.1016/j.jep.2004.02.022. [DOI] [PubMed] [Google Scholar]
  • 98.Ogunleye D., Ibitoye S. Studies of antimicrobial activity and chemical constituents of Ximenia americana. Tropical Journal of Pharmaceutical Research. 2003;2(2):239–241. [Google Scholar]
  • 99.Lalani S., Poh C. L. Flavonoids as antiviral agents for Enterovirus A71 (EV-A71) Viruses. 2020;12(2):p. 184. doi: 10.3390/v12020184. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 100.Lin L.-T., Chen T.-Y., Lin S.-C., et al. Broad-spectrum antiviral activity of chebulagic acid and punicalagin against viruses that use glycosaminoglycans for entry. BMC Microbiology. 2013;13(1):p. 187. doi: 10.1186/1471-2180-13-187. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 101.Wen C.-C., Kuo Y.-H., Jan J.-T., et al. Specific plant terpenoids and lignoids possess potent antiviral activities against severe acute respiratory syndrome coronavirus. Journal of Medicinal Chemistry. 2007;50(17):4087–4095. doi: 10.1021/jm070295s. [DOI] [PubMed] [Google Scholar]
  • 102.Vázquez-Calvo Á., Jiménez de Oya N., Martín-Acebes M. A., Garcia-Moruno E., Saiz J.-C. Antiviral properties of the natural polyphenols delphinidin and epigallocatechin gallate against the flaviviruses West Nile virus, Zika virus, and dengue virus. Frontiers in Microbiology. 2017;8:p. 1314. doi: 10.3389/fmicb.2017.01314. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 103.Simões C. M. O., Amoros M., Girre L. Mechanism of antiviral activity of triterpenoid saponins. Phytotherapy Research. 1999;13(4):323–328. doi: 10.1002/(sici)1099-1573(199906)13:4<323::aid-ptr448>3.0.co;2-c. [DOI] [PubMed] [Google Scholar]
  • 104.Tohmé M. J., Giménez M. C., Peralta A., Colombo M. I., Delgui L. R. Ursolic acid: a novel antiviral compound inhibiting rotavirus infection in vitro. International Journal of Antimicrobial Agents. 2019;54(5):601–609. doi: 10.1016/j.ijantimicag.2019.07.015. [DOI] [PubMed] [Google Scholar]
  • 105.Khwaza V., Oyedeji O., Aderibigbe B. Antiviral activities of oleanolic acid and its analogues. Molecules. 2018;23(9):p. 2300. doi: 10.3390/molecules23092300. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 106.Kumar A., Choudhir G., Shukla S. K., et al. Identification of phytochemical inhibitors against main protease of COVID-19 using molecular modeling approaches. Journal of Biomolecular Structure and Dynamics. 2020:1–11. doi: 10.1080/07391102.2020.1772112. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 107.Wu W., Li R., Li X., et al. Quercetin as an antiviral agent inhibits influenza A virus (IAV) entry. Viruses. 2016;8(1):p. 6. doi: 10.3390/v8010006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 108.Kaihatsu K., Yamabe M., Ebara Y. Antiviral mechanism of action of epigallocatechin-3-O-gallate and its fatty acid esters. Molecules. 2018;23(10):p. 2475. doi: 10.3390/molecules23102475. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 109.Nakamoto M., Kunimura K., Suzuki J. I., Kodera Y. Antimicrobial properties of hydrophobic compounds in garlic: allicin, vinyldithiin, ajoene and diallyl polysulfides. Experimental and Therapeutic Medicine. 2020;19(2):1550–1553. doi: 10.3892/etm.2019.8388. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 110.Qian S., Fan W., Qian P., et al. Apigenin restricts FMDV infection and inhibits viral IRES driven translational activity. Viruses. 2015;7(4):1613–1626. doi: 10.3390/v7041613. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 111.Care C., Sornjai W., Jaratsittisin J., et al. Discordant activity of kaempferol towards dengue virus and Japanese Encephalitis virus. Molecules. 2020;25(5):p. 1246. doi: 10.3390/molecules25051246. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

All related data have been presented within the manuscript. The dataset supporting the conclusions of this article is available from the authors on request.


Articles from Evidence-based Complementary and Alternative Medicine : eCAM are provided here courtesy of Wiley

RESOURCES