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Overview of Extraction, Isolation, and Bioavailability Enhancement of Resveratrol
Menezes, J. C., & Diederich, M. F. (2019). Natural dimers of coumarin, chalcones, and resveratrol and
the link between structure and pharmacology. European Journal of Medicinal Chemistry, 182, 111637.
doi:10.1016/j.ejmech.2019.111637 PMID:31494471
Niesen, D. B., Hessler, C., & Seeram, N. P. (2013). Beyond resveratrol: A review of natural stilbenoids
identified from 2009–2013. Journal of Berry Research, 3(4), 181–196. doi:10.3233/JBR-130062
Nunes, R., Baião, A., Monteiro, D., das Neves, J., & Sarmento, B. (2020). Zein nanoparticles as lowcost, safe, and effective carriers to improve the oral bioavailability of resveratrol. Drug Delivery and
Translational Research, 10(3), 826–837. doi:10.100713346-020-00738-z PMID:32207071
Polonini, H. C., de Almeida Bastos, C., de Oliveira, M. A. L., da Silva, C. G. A., Collins, C. H., Brandão,
M. A. F., & Raposo, N. R. B. (2014). In vitro drug release and ex vivo percutaneous absorption of resve-
ratrol cream using HPLC with zirconized silica stationary phase. Journal of Chromatography. B, Analyti-
cal Technologies in the Biomedical and Life Sciences, 947, 23–31. doi:10.1016/j.jchromb.2013.12.005
PMID:24381018
Romero-Pérez, A. I., Ibern-Gómez, M., Lamuela-Raventós, R. M., & de la Torre-Boronat, M. C. (1999).
Piceid, the major resveratrol derivative in grape juices. Journal of Agricultural and Food Chemistry,
47(4), 1533–1536. doi:10.1021/jf981024g PMID:10564012
Shrikanta, A., Kumar, A., & Govindaswamy, V. (2015). Resveratrol content and antioxidant properties
of underutilized fruits. Journal of Food Science and Technology, 52(1), 383–390. doi:10.100713197-
013-0993-z PMID:25593373
Şöhretoğlu, D., Baran, M. Y., Arroo, R., & Kuruüzüm-Uz, A. (2018). Recent advances in chemistry, therapeutic properties and sources of polydatin. Phytochemistry Reviews, 17(5), 973–1005. doi:10.100711101-
018-9574-0
Soleas, G. J., Angelini, M., Grass, L., Diamandis, E. P., & Goldberg, D. M. (2001). Absorption of
trans-resveratrol in rats. Methods in Enzymology, 335, 145–154. doi:10.1016/S0076-6879(01)35239-4
PMID:11400363
Soleas, G. J., Diamandis, E. P., & Goldberg, D. M. (1997). Resveratrol: A molecule whose time has come?
And gone? Clinical Biochemistry, 30(2), 91–113. doi:10.1016/S0009-9120(96)00155-5 PMID:9127691
Takaoka, M. J. (1940). Of the phenolic substances of white hellebore (Veratrum grandiflorum Loes.
fil.). Journal Faculty Science Hokkaido Imperial University, 3, 1–16.
Tian, B., & Liu, J. (2020). Resveratrol: A review of plant sources, synthesis, stability, modification and
food application. Journal of the Science of Food and Agriculture, 100(4), 1392–1404. doi:10.1002/
jsfa.10152 PMID:31756276
Tokuşoǧlu, Ö., Ünal, M. K., & Yemiş, F. (2005). Determination of the phytoalexin resveratrol (3, 5, 4
‘-trihydroxystilbene) in peanuts and pistachios by high-performance liquid chromatographic diode array (HPLC-DAD) and gas chromatography− mass spectrometry (GC-MS). Journal of Agricultural and
Food Chemistry, 53(12), 5003–5009. doi:10.1021/jf050496+ PMID:15941348
348
EBSCOhost - printed on 2/13/2023 11:18 AM via . All use subject to https://www.ebsco.com/terms-of-use

Overview of Extraction, Isolation, and Bioavailability Enhancement of Resveratrol
Tzanova, M., & Peeva, P. (2018). Rapid HPLC method for simultaneous quantification of trans-resveratrol
and quercetin in the skin of red grapes. Food Analytical Methods, 11(2), 514–521. doi:10.100712161-
017-1022-z
Udenigwe, C. C., Ramprasath, V. R., Aluko, R. E., & Jones, P. J. (2008). Potential of resveratrol in
anticancer and anti-inflammatory therapy. Nutrition Reviews, 66(8), 445–454. doi:10.1111/j.1753-
4887.2008.00076.x PMID:18667005
Venugopal, R., & Liu, R. H. (2012). Phytochemicals in diets for breast cancer prevention: The importance of resveratrol and ursolic acid. Food Science and Human Wellness, 1(1), 1–13. doi:10.1016/j.
fshw.2012.12.001
Wang, D. G., Liu, W. Y., & Chen, G. T. (2013). A simple method for the isolation and purification of resveratrol from Polygonum cuspidatum. Journal of Pharmaceutical Analysis, 3(4), 241–247. doi:10.1016/j.
jpha.2012.12.001 PMID:29403824
Wang, P., & Sang, S. (2018). Metabolism and pharmacokinetics of resveratrol and pterostilbene. BioFac-
tors (Oxford, England), 44(1), 16–25. doi:10.1002/biof.1410 PMID:29315886
Wang, W. X., Qian, J. Y., Wang, X. J., Jiang, A. P., & Jia, A. Q. (2014). Anti-HIV-1 activities of extracts and phenolics from Smilax china L. Pakistan Journal of Pharmaceutical Sciences, 27, 147–151.
PMID:24374442
Williams, L. D., Burdock, G. A., Edwards, J. A., Beck, M., & Bausch, J. (2009). Safety studies conducted on high-purity trans-resveratrol in experimental animals. Food and Chemical Toxicology, 47(9),
2170–2182. doi:10.1016/j.fct.2009.06.002 PMID:19505523
Yang, F., Zhang, T., & Ito, Y. (2001). Large-scale separation of resveratrol, anthraglycoside A and anthraglycoside B from Polygonum cuspidatum Sieb. et Zucc by high-speed counter-current chromatography.
Journal of Chromatography. A, 919(2), 443–448. doi:10.1016/S0021-9673(01)00846-9 PMID:11442052
Yu, W., Shu, B., & Zhao, Y. (2005). Supercritical CO
extraction of resveratrol and its glycoside piceid
2
from Chinese traditional medicinal herb Polygonum cuspidatum. Journal of the Science of Food and
Agriculture, 85(3), 489–492. doi:10.1002/jsfa.2007
Yücel, Ç., Karatoprak, G. Ş., & Atmar, A. (2018). Novel resveratrol-loaded nanocochleates and effectiveness in the treatment of diabetes. FABAD Journal of Pharmaceutical Sciences, 43(2), 35–44.
Zhi-fang, H., Jin-hai, Y. I., Qian-ling, L. I. U., Yun-hua, L. I. U., Yan, C., & Yu-hong, L. I. U. (2009).
Research of extracting and purifying process of resveratrol from Polygonum cuspidatum extract by en-
zymic hydrolysis. Natural Product Research & Development, 21(6).
Zhuang, X., Dong, X., Ma, S., & Zhang, T. (2008). Selective on-line extraction of trans-resveratrol and
emodin from Polygonum cuspidatum using molecularly imprinted polymer. Journal of Chromatographic
Science, 46(8), 739–742. doi:10.1093/chromsci/46.8.739 PMID:18796233
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350
Chapter 18
Phytochemicals From
Mangroves and Their Anti-
Viral Applications
Raghunath Satpathy
https://orcid.org/0000-0001-5296-8492
Gangadhar Meher University, India
Sonali Acharya
Gangadhar Meher University, India
ABSTRACT
Phytochemicals are recently gaining major attention for their therapeutic uses against several pathogenic viruses. Hence, searching for novel anti-viral molecules from plant sources is desirable as it is
having fewer side effects. The mangrove plants are considered as an excellent source of phytomedicine
due to production of several classes of phytochemicals. However, fewer studies have been conducted
regarding the extraction of the potential anti-viral compounds from mangrove sources. In this chapter,
an overview of isolation, extraction, and qualitative estimation of phytochemicals from the mangrove
plants have been described. The major representative mangrove plant and its extracts that have shown
potential anti-viral activity have been documented. Moreover, this chapter highlights the research-based
analysis of potential anti-viral compounds from the plants in the mangrove ecosystem.
INTRODUCTION
Plant-derived compounds are being used as an important natural source of drug molecules and have
gained importance in the medicinal chemistry. The parent molecules of most of the currently used
medications have been derived from the plant. Also, due to their less toxic, and minimum side effects
properties, the phytochemical is being preferred in therapeutic applications in comparison to synthetic
drug molecules (Heywood, 2002; Sofowora et al., 2013; Inoue et al., 2019; Ghildiyal et al., 2020).
So, the researchers are currently emphasizing deriving new knowledge based on natural plant-based
DOI: 10.4018/978-1-6684-5129-8.ch018
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Phytochemicals From Mangroves and Their Anti-Viral Applications
compounds for their potential use in the healing process of infectious diseases. The plants also contain
several types of secondary metabolites with diversity in their molecular structure and functional properties. Many of the plant’s secondary metabolites are effective in treating several metabolic diseases as
well as infectious diseases. An experimental basis of the study of these secondary metabolites of the
plants and their efficacy on the human disease treatment process has been performed. Several scientific
studies have revealed the promising use of phytochemicals for the treatment of viral infections (Inoue
& Craker, 2014; Satpathy, 2020; Kaur & Ahmed, 2021; Satpathy, 2021). The development of antiviral
drug molecules is an important task to combat the life-threatening disease caused by the deadliest virus
(Figure 31.1). Also, many of the viruses do not have established anti-viral treatment methods. Hence,
due to the urgency is concern, suitable phytochemicals are to be explored scientifically as effective and
inexpensive anti-viral inhibitor molecules (Ghorbanpour et al., 2017). To date, several viral diseases
have been reported and the mutant form of the deadly viruses are also occurring frequently. Among the
emerging viral diseases, most of them are caused by pathogenic viruses like Human Immunodeficiency
Virus (HIV), Influenza, Herpes simplex virus (HSV), Dengue, Chikungunya, Zika, Hepatitis B (HSB),
Hepatitis C (HCV), Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and so on. Viral
infections are associated with great health risks to human health. Also, the infection is difficult to control
as the origin of new mutant forms of the viral strains. In the past, deadly viruses caused pandemics in
the world thereby increasing the risk of spreading viral diseases between continents.
Very few drugs have been developed to date to effectively treat viral diseases. The majority of the
approved antiviral drugs possess adverse drug reactions and have also developed viral resistance in longterm therapy. The infectious virus is a major cause of mortality in the recent few years. For instance,
the infection by SARS–CoV-2 and influenza virus are responsible for over a million deaths throughout
the globe (Gasparini et al., 2012; Nováková et al., 2018; Ben-Shabat et al., 2020; Hafeez et al., 2020).
However, the repurposing method for the already reported phytochemical as an inhibitor for virus target
is possible to study the antiviral property of the molecule. Although most of the antiviral drugs approved
for the management of the viral disease are effective some of them have adverse reactions leading to
raise the need for the development of plant-based drug development (Bahadur et al., 2020; Anand et
al., 2021). Recently, the creation of SARS-CoV-2 virus-based pandemic situations and enhanced mortality rate in human beings have raised a serious global concern. Moreover, antiviral drugs also exhibit
adverse side effects, which directly and indirectly affect human health. This provides opportunities for
the development of plant-based drugs and herbal treatments with minimal side effects (Kapoor et al.,
2017; Irwin et al., 2016; Biswas et al., 2020).
Several targets in the viruses are available to which the specific phytochemicals are targeted and
block the metabolism of the virus (Kumar & Pandey, 2013; Ahmad et al., 2015; Lipson et al., 2017;
Subudhi et al., 2018).
1. Receptor –host cell interaction that interferes with the host cell receptors
2. Binding to the replication enzymes to stop the replications
3. Binding to the other non-structural proteins to inhibit the key metabolic pathway such as replication
and translation of the pathogenic viruses
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351

Phytochemicals From Mangroves and Their Anti-Viral Applications
Figure 1. Phytochemicals show activity against the target pathogenic virus
PLANT COMPOUNDS AS ANTIVIRAL AGENTS
As a treatment strategy, several categories of phytochemicals have been experimentally proved by researchers for showing their antiviral properties. For example, the activity of virus replication inhibitors
has been described by researchers that show potential inhibitory effects against several viruses like Herpes
Simplex Virus type 2 (HSV-2), HIV, Hepatitis B Virus (HBV), SARS–CoV. The crude extracts from the
plants like Andrographis paniculata (Burm. f.) Wall. ex Nees., Lindera chunii Merr., Dioscorea bulbifera
L., Wisteria floribunda. (Willd.) DC. have been shown to feature the antiviral feature (Mukhtar et al.,
2008; Bachar et al., 2021; Adhikari et al., 2021). The knowledge about the known bioactive compounds
from plant sources can be repurposed against other pathogenic viruses, the same has been successfully
evaluated by many researchers (Choi et al., 2019; Calabrese et al., 2000; Mpiana et al., 2020; El-Ansari
et al., 2020; Amparo et al., 2021).
METHOD OF ISOLATION OF PHYTOCHEMICALS FOR THERAPEUTIC USE
To enhance the scientific value, before isolation of bioactive constituents from the plants, it is essential
to identify the plant and the plant parts that produce the specific phytochemicals. The selection can be
based on the traditional knowledge about the use of the plant as anti-viral therapy. Also, sometimes the
ecological factor is taken into consideration since the plant can produce more specific categories of
secondary metabolites that can be used as antiviral agents. Additionally, the plant selection can be performed based on the published literature, toxic compounds that produce and therapeutic importance of
0
the plant and so on. The collected and identified plant material is initially kept for drying below 300
C
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Phytochemicals From Mangroves and Their Anti-Viral Applications
Figure 2. Standard procedure followed for identification of antiviral metabolites from the plants.
also it should be protected from exposure to direct sunlight to avoid the chemical change of the molecule
by electromagnetic radiation. Alternatively, the plant material can also be milled using the help of an
electric grinder or by mortar and pestle (Velavan, 2015).
The standard procedure that is followed in the screening of phytochemical extraction to antiviral
assay has been shown in Figure 2. The rate of success for the isolation of active phytochemicals is also
mostly dependent on the type of solvent used in the extraction process. Several chemical properties such
as low toxicity, evaporation at low heat, and high preservative potential of solvent are preferred during
the extraction process. In general, various solvent systems like acetone, alcohol, chloroform, ether, and
Dichloromethanol are used including water. Some of the popular extraction methods are being used in
the phytochemical extraction process are described in Table 1.
SCREENING METHODS OF PHYTOCHEMICALS
The bio-active phytochemicals are generally occurred in the plants in the form of different metabolites.
Hence, a preliminary qualitative mode of phytochemical analysis of the medicinal plants’ metabolites
is essential to confirm the presence of types of phytochemicals present in the extract (Starmans & Nijhuis, 1996; Savithramma & Suhrulatha, 2011). The methods adopted for qualitative analysis of major
phytochemicals have been described in Table 2.
APPLICATION AND IMPORTANCE OF MANGROVE PLANTS
AND PHYTOCHEMICALS IN ANTIVIRAL THERAPY
In consideration of the habit and habitat of different medicinal plant species, the mangroves exhibit special attention. These plants are perennial and usually grow in the tropical coastal wetlands area. These
plants (mostly trees and shrubs) grow in shallow water where the water is generally brackish. Since the
mangroves survive in harsh ecological conditions, they are highly adapted internally (anatomically,
physiologically, and morphologically). Due to their rich biodiversity, mangrove forests are considered
one of the hot spots of the wetland ecosystem (Kathiresan & Bingham, 2001).
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Phytochemicals From Mangroves and Their Anti-Viral Applications
Table 1. Major types of extraction methods of phytochemicals
Name of the method Description References
• In this process, the compound is isolated from the plant extract by a
repetitive procedure by using a nearly equal volume of solvent in each
cycle followed by solvent evaporation.
• This dried and plant sample is kept in the Soxhlet apparatus that
Soxhlet extraction
Accelerated solvent extraction
Supercritical fluid extraction
(SFE)
Microwave Assisted
Extraction (MAE)
Maceration
facilitates the extraction of the different phytochemicals based on the
types of the solvent used in the extraction method.
• After the end of each cycle of extraction, the solvent extract is
evaporated by a rotary evaporator in a vacuum environment.
• One of the major advantages of the use of the Soxhlet apparatus is
less amount of solvent is required.
• In this type of extraction method, the plant material is packed with
a solid support such as sand. The application of the organic solvents
with the high temperature and pressure accelerates the extraction
process by the process of diffusion.
• Since the method uses a small amount of solvents hence considered
more efficient as compared to the Soxhlet extraction method.
• This type of extraction method of phytochemicals involves the
principle of critical points, a particular condition in which the liquid
state and vapor state co-exists (properties of both states).
• In this method, the supercritical fluid (SCF) is applied to the plant
material at a high pressure contained in a cylinder and the extract is
collected in a separate chamber.
• This is mainly used to extract the non-polar and thermo-labile
phytochemicals.
• Microwave assisted extraction (MAE) is the best suitable for
thermolabile substances.
• The principle reveals, that microwaves cause a dipole rotation effect
in organic molecules and due to the subsequent heating process lead to
the destruction of hydrogen bonding.
• Destruction of hydrogen bonding also related to the enhanced
penetrating property of the solvents into the plant matrix
• The removal of moisture if any from the dried form of the plant
material is removed by high temperature and pressure generated due to
microwave radiation.
• Once the extraction process is completed, the separation of
compounds from the solvents is done by using the processes like
distillation.
• One cost-effective method is used for the extraction of bioactive
phytochemicals.
• The plant material is initially grounded into smaller particles to
enhance the surface area before the addition of the solvents
• The powdered plant material is then soaked in desired solvents for
kept for hours/ days to facilitate the diffusion process.
• The extract is prepared by filtration followed by the concentration in
a rotary evaporator by evaporating the solvent.
Mitra et al., (2021)
Sharma & Kaushik, (2021)
Arumugham et al., (2021)
Sharma et al., (2020)
Abubakar & Haque, (2020)
Research has been confirmed about the mangrove plants as an important source for the search for
novel drug molecules due to their ecological adaptation leads to the synthesis of large numbers of phytochemicals. Among these phytochemicals, many show significant pharmacological properties and are
used as active antiviral, antibacterial and antifungal compounds (Bandaranayake, 1998; Abeysinghe,
2010; Aljahdali et al., 2021). The biochemical investigations on several mangrove species have shown
that the plants are a rich source of a variety of bio-active compounds such as alkaloids, flavonoids,
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Phytochemicals From Mangroves and Their Anti-Viral Applications
Table 2. Qualitative assay methods of major phytochemicals
S.No. Phytochemical types Assay methods (reagents used)
1 Terpenoids
2 Tannins Addition drops of 1% lead acetate to the plant extract Yellowish precipitate
3 Saponins
4 Anthocyanins
5 Coumarins Plant aqueous extract is to be added with 10% NaOH
6 Emodins NH4OH and Benzene are to be added to the phyto extract. Appearance of red color
7 Steriods
Addition of the acetic anhydride to the plant extract
followed by concentrated H2 SO4 addition
The plant extract is mixed with distilled water followed by
agitation in a graduated cylinder for 15 minutes.
Aqueous plant extract is to be added with 2N Hydrochloric
acid (HCL) and ammonia.
Plant extract in the chloroform solvents is to be added with
an equal volume of concentrated sulphuric acid
Formation of blue, green rings
Formation of foam
Appearance of pink-red turns blueviolet
The formation of yellow color
indicates
The upper layer turns red and
Sulphuric acid layer shows yellowish
green fluorescence.
Observations
(Test of conformation)
triterpenoids, polyphenolic compounds, xanthones, coumarins, tannins, and so on (Vadlapudi & Naidu
2009; Abeysinghe et al., 2006). Hence, these bioactive compounds of mangrove plants are frequently
used as drugs against various critical human diseases (Kokpol et al., 1990; Reddy & Grace 2016; Ad-
Figure 3. Showing experimental determination of bioactive compounds from the mangrove plants
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355

Phytochemicals From Mangroves and Their Anti-Viral Applications
hikari et al., 2017). Many species of mangroves are frequently used in the traditional medicine systems
to treat several human health disorders. The therapeutic properties of the mangrove plant product are
based on its phytochemical composition and the mangroves are known to possess different categories of
secondary metabolites used to treat several human diseases (Premanathan et al., 1994; Mitter & Jadhav
2011; Piyusha et al., 2012). The common steps that are adapted for the extraction and characterization
of potential phytochemicals from the mangroves have been shown in Figure 31.3. Specifically, several
antimicrobial metabolites extracted from the mangrove plants have shown their antibiotic reactions on
many pathogenic microbial genera like Shigella, Staphylococcus, Escherichia, and Penicillium (Kokpal
et al., 1990).
Usually, the bioactive compounds of the mangrove plants are obtained in the form of primary or secondary metabolites. The knowledge of the chemical constituents of these plants is desirable to understand
the composition of the herbal drugs and their formulation (Premanathan et al., 1996; Poompozhil &
Kumarasamy, 2014). Several workers have evaluated the effectiveness of mangrove plants in traditional
medicine. For example, the qualitative and quantitative analysis of Laguncularia racemosa (L.) Gaertn.
f. leaves has indicated the presence of many phytochemicals (secondary metabolites) and can be tested
for their effectiveness against several diseases (Quraishi et al., 2015) . Meenakshi and Jayaprakash formulated a new type of pesticide from the mangrove plant Rhizophora mucronata Lam. that can be used
as a natural eco-friendly effective mosquito repellent to control vector-borne diseases (Meenakshi &
Jayaprakash, 2014). Similarly, Joel and Bhimba experimentally studied the antioxidant and thrombolytic
properties of the Rhizophora mucronata Lam. phytochemicals (Joel & Bhimba 2010). Eswaraiah et al.
(2020), studied the anti-microbial action of the leaf extract bioactive compounds of several mangrove
plants and proved their activity against pathogenic strains (Eswaraiah et al., 2020). Some more examples
have been documented in the table given below (Table 3).
CHALLENGES AND OPPORTUNITIES IN DISCOVERING THE
MANGROVE PHYTOCHEMICALS FOR THE ANTIVIRAL THERAPY
The global research strategies for the discovery of antiviral compounds from mangrove plant sources
are showing an increasing trend (Figure 4). The selection, identification and extraction procedure of
anti-viral phytochemicals from the mangrove plants are directly linked to the therapeutic applications.
The discovery of novel methods for the low-cost and safe extraction methods of bioactive compounds
from mangrove plants is a challenging task. Also, during the extraction process care should be taken
for the interference of other phyto-based contaminants with the target compound (Kwon et al., 2017;
Stéphane et al., 2021).
After successful isolation and extraction, another most challenging task is to successfully prove the
antiviral property of the compound and the formulation of the correct dose. Phytochemicals having antiviral activity can be nano-encapsulated for better delivery, prolonged action, and enhanced bioavailability.
Moreover, excessive research on different biodiversity-rich regions could be explored to get more potent
phytochemicals and metabolites as antiviral agents. Due to the presence of diverse phytochemicals in
the mangroves, it is expected that the mangroves contain the effective bioactive compound that may use
against several pathogenic viruses. Hence, the multiple virus target hitting nature of these compounds
is to be explored. In this aspect, the computational analysis might play a major role in the prediction
method due to its robustness and low-cost nature. Several computational analyses such as molecular
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Phytochemicals From Mangroves and Their Anti-Viral Applications
Table 3. Some of the representative mangrove plants produce phytochemicals are being used for Antiviral therapy.
Name of the plant Family Bioactive compounds Target virus References
Avicennia officinalis L. Acanthaceae Crude Plant extract
Aegiceras corniculatum (L.)
Blanco
Acanthus ilicifolius (L.) Acanthaceae 2-benzoxazoline hepatitis B virus (HBV)
Avicennia marina (Forssk.)
Vierh
Bruguiera cylindrica (L.)
Blume
Ceriops decandra
(Griff.) Ding Hou
Clerodendrum inerme (L.)
Gaertn
Callophylum inophyllum L. Callophyllaceae
Pistacia integerrima J. L.
Stewart ex Brandis (PI)
Pandanus odorifer
(Forssk.) Kuntze
Pongamia pinnata (L.) Pierre Fabaceae Seed extract Herpes Simplex Virus (HSV)
Rhizophora apiculata Blume Rhizophoracea Carbohydrate extract
Rhizophora mucronata Lam. Rhizophoracea Polysaccharide extract
Rhizophora lamarckii Montr Rhizophoracea Crude plant extract
Sonneratia apetala Buch.-
Ham
Sesuvium portulacastrum
L.
Salicornia brachiata Roxb. Amaranthaceae Crude Leaf, stem extract Hepatitis B virus (HBV)
Suaeda maritima (L.) Dumort. Amaranthaceae Steroid, triterpenes Hepatitis B virus (HBV)
Sonneratia paracaseolaris Lythraceae Triterpenoids Influenza A virus (H1N1) Gong et al., (2017)
Xylocarpus granatum J.
Koenig
Xylocarpus moluccensis (Lam)
M.Roem.
Primulaceae Cyclopentenone Influenza A virus (H1N1) Zhang et al., (2011)
Acanthaceae Crude plant extract
Rhizophoracea
Rhizophoraceae Phenolics and Flavonoids Hepatitis B virus (HBV)
Lamiaceae
Anacardiaceae
Pandanales
Lythraceae
Aizoaceae Crude Leaf extract Hepatitis B virus (HBV)
Meliaceae Limonoids
Meliaceae Limonoids Influenza A virus (H1N1) Li et al., (2015)
Extract from bark, fruit,
leaf, hypocotyl
Phenolic, steroids, di- and
triterpenes, flavonoids,
volatile oils
Benzopyrans, coumarins,
steroids, triterpenes,
xanthones
28-demethyl-betaamyrone, 24-Noroleana3,12-diene, and
stigmasterol
Anthroquinoid,
triterpenes and steroids,
gibberellins, carboxylic
acids and lactones,
polyphenols,
Severe Acute Respiratory
Syndrome Coronavirus 2 (SARSCoV2)
Human Immunodeficiency Virus,
Herpes Simplex Virus (HSV)
Hepatitis B virus (HBV)
Hepatitis B virus (HBV)
Human Immunodeficiency Virus
(HIV)
Severe Acute Respiratory
Syndrome Coronavirus 2 (SARSCoV2)
Human Immunodeficiency Virus
(HIV)
Human Immunodeficiency Virus
(HIV)
Human Immunodeficiency Virus
(HIV), hepatitis B virus (HBV)
Hepatitis B virus (HBV)
Human Immunodeficiency Virus
(HIV)
Mahmud et al., (2021)
Nabeelah Bibi et al.,
(2029)
Namazi et al., (2013)
Premnathan et al.,
(1992)
Krishnamoorthy et al.,
(2011)
Chakraborthy & Verma
(2013)
Govindappa et al.,
(2015)
Paul et al., (2022)
Elanchezhiyan et al.,
(1993)
Premanathan et al.,
(1999)
Premanathan et al.,
(1996)
Premanathan et al.,
(1996)
Bandaranayak, (2002)
Dhawan, (2012)
Dai et al., (2017)
docking and molecular dynamics simulation have been frequently used to establish phytochemicals as
anti-viral compounds. Many of the phytochemicals from the mangrove sources have been identified to
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