|Year : 2016 | Volume
| Issue : 20 | Page : 123-138
A complete profile on blind-your-eye mangrove Excoecaria agallocha L. (Euphorbiaceae): Ethnobotany, phytochemistry, and pharmacological aspects
Sumanta Mondal1, Debjit Ghosh2, K Ramakrishna2
1 Department of Pharmaceutical Chemistry, GITAM Institute of Pharmacy, GITAM University, Visakhapatnam, Andhra Pradesh, India
2 Department of Chemistry, GITAM Institute of Science, GITAM University, Visakhapatnam, Andhra Pradesh, India
|Date of Web Publication||14-Nov-2016|
GITAM Institute of Pharmacy, GITAM University, Visakhapatnam - 530 045, Andhra Pradesh
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Traditional system of medicine consists of large number of plants with various medicinal and pharmacological importances. This article provides a comprehensive review of the complete profile of an important mangrove plant Excoecaria agallocha L. (Euphorbiaceae) and elaborately describing the ethnobotany, phytochemistry, and pharmacological properties. It is used traditionally in the treatment of various diseases such as epilepsy, ulcers, leprosy, rheumatism, and paralysis. The latex obtained from the bark is poisonous in nature and may cause temporary blindness, thus it is also known as the blind-your-eye mangrove plant. Many phytoconstituents were isolated from the plant, which were mainly diterpenoids, triterpenoids, flavonoids, sterols, and few other compounds. The plant also showed many pharmacological activities such as antioxidant, antimicrobial, anti-inflammatory, analgesic, antiulcer, anticancer, antireverse transcriptase, antihistamine-release, antifilarial, DNA damage protective, antidiabetic, and antitumor protecting activities. Hence, this review could help guide researchers anticipating to undertake further investigations in these directions.
Keywords: Diterpenoids, Euphorbiaceae, Excoecaria agallocha, mangrove, pharmacology, phytoconstituents
|How to cite this article:|
Mondal S, Ghosh D, Ramakrishna K. A complete profile on blind-your-eye mangrove Excoecaria agallocha L. (Euphorbiaceae): Ethnobotany, phytochemistry, and pharmacological aspects. Phcog Rev 2016;10:123-38
|How to cite this URL:|
Mondal S, Ghosh D, Ramakrishna K. A complete profile on blind-your-eye mangrove Excoecaria agallocha L. (Euphorbiaceae): Ethnobotany, phytochemistry, and pharmacological aspects. Phcog Rev [serial online] 2016 [cited 2017 Jul 26];10:123-38. Available from: http://www.phcogrev.com/text.asp?2016/10/20/123/194049
| Introduction|| |
Medicinal plants are considered an important component of flora and are distributed widely throughout India. From the dawn of civilization, medicinal plants are considered part and parcel of human society to combat diseases. Majority of the world's population rely wholly or partially on traditional system of medicine for their principle health care needs. A survey conducted by the World Health Organization (1993), the traditional medicinal practitioners deals with about 80% patients in India, 90% patients in Bangladesh, and 85% patients in Burma. In the recent past years, there has been an increase in the use of health products derived from plants in developed as well as developing countries which resulted in an exponential growth of herbal products globally. An upward trend has been observed in the research on herbals. In the present scenario, most of the drugs are obtained from plants sources such as morphine from the dried latex of unripe seedpods of Papaver somniferum poppy, atropine is obtained from Atropa belladonna, ephedrine obtained from Ephedra vulgaris, and reserpine from Rauvolfia serpentine. The secondary metabolites found in the medicinal plants are regarded as the potential source of drugs and thus are of immense therapeutic value. Medicines derived from medicinal plants are also easily available, safer, economical, and effective.
Mangroves have long been a source of astonishment to the layman and of interest for the scientists. The word “mangrove” may be derived by conjunction of the English word “grove” with Portuguese word “mangue,” the Spanish word “mangle,” “manglier” which is a French word or the Malay word “manggi-manggi.” A book named “The Mangroves and Us” by Marta Vannucci (1989) explains that the word is neither Portuguese nor Spanish, but the word 'mangue' derives from the national language of Senegal. It is possible that the Portuguese first adapted the word, later to be modified by the Spanish, as a result of their exploration of the coast of west Africa.
Mangroves are woody halophytic plants which are ecologically of great importance. They act as a source of energy in coastal food chain and also protects against various natural calamities such as cyclone and tsunami. Many drugs, dyes, and tannins are obtained from the mangroves. Mangroves usually constitute from about eighty families of shrubs and trees which inhabits the shoreline and estuaries in the tropical and subtropical coastal regions of the world. They also function as natural nutrient filters and recyclers, protect coastal areas from seawater intrusion, and also helps in floodwater mitigation.
The genus Excoecaria comprises nearly forty species which are distributed in the mangrove region of Asia, Africa, and northwest Australia. The milky latex discharged from Excoecaria agallocha bark is poisonous and may cause temporary blindness and blistering of the skin. The latex is also well known for its biocidal effects on marine organisms and phytoplankton, causes metabolic depression of the rice field crab, Oziotelphusa senex and is used as an uterotonic, fish poison, dart poison, and contains novel chalcones and piperidine alkaloids.E. agallocha usually shed their leaves annually. Unlike most mangrove species, they do not have specialized aerial roots called pneumatophores that extend above the soil surface and supply the underground roots with oxygen.
This review article gives a critical description about the complete profile of the mangrove plant E. agallocha L., and mainly highlighting the various ethnobotanical uses, phytochemical constituents isolated, and pharmacological studies conducted on this plant.
the details of the taxonomic position of Excoecaria agallocha L. is given in [Table 1].
Vernacular Names of Excoecaria Agallochal
Excoecaria agallocha L. is also known by several vernacular names as it is distributed in the mangrove region of various parts of India. The details of the vernacular names are mentioned in [Table 2].
E. agallocha L. is widely distributed in mangrove forests throughout Asia, Australia, and Southern pacific region of the world. Details are given in [Table 3].
E. agallocha L. is a mangrove plant belonging to family Euphorbiaceae. It is a small tree which usually grows up to 15 m in height [Figure 1]. The full description of its botanical features has been tabulated in [Table 4].,
|Figure 1: Branch of Excoecaria agallocha L. showing leaves and twigs (Sundarban, October 2015)|
Click here to view
The plant is known to play an important economical, ecological as well as medicinal role. It is traditionally used in the treatment of ulcers, sores, and stings from poisonous marine creatures, and also functions as an emetic and purgative. Treatment of rheumatism, leprosy, and paralysis is also cured by the bark oil obtained from E. agallocha. It is also used traditionally in the treatment of conjunctivitis, dermatitis, and hematuria. The latex exuded from this plant has been used as an abortifacient and as a purgative, and also used in treatment of ulcers, leprosy, paralysis, and rheumatism. The leaves and latex of this plant are used as fish poison by the people of Malaysia, India, and New Caledonia. In Thailand, the wood and bark is used as a cure for flatulence. In Sri Lanka, the root pounded with ginger has been used to treat swellings of hands and feet, and the smoke obtained from the burning wood is used to cure leprosy. A milky sap or latex exuded from the plant can cause temporary blindness if it comes in contact with the eye and can also cause skin blisters and irritation, thus also showing the poisonous nature of the plant. The latex being poisonous in nature is used as a fish poison as well as a dart poison. According to the Indian “materia medica,” a soft reddish substance (“Tejbala”) which is obtained from the lower part of the trunk of E. agallocha was used as a reputed “aphrodisiac tonic.” The people of Burma use the leaves to treat epilepsy. In Solomon Islands, the latex exuded from the plant is mixed with coconut milk which is used as a powerful emetic and purgative. The Malays treat itching and skin infection by the oil distilled from the woods. The roots of the plant are used to treat toothache and swellings  as well as used as an ingredient of embrocations.
The chemical constituents of E. agallocha L., include mainly diterpenoids, terpenoids, flavonoids, alkaloids, tannins, and some other compounds.,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,, The details of their names are given in [Table 5]. The chemical structures of some isolated compounds are given in [Figure 2].
|Figure 2: Chemical structures of phyto-constituents isolated from Excoecaria agallocha L.|
Click here to view
Diterpenes are the most abundantly isolated secondary metabolite from E. agallocha.
Labdane-type diterpenes are the dominant class of diterpenes isolated. About 41 labdane-type diterpenes 1–41 were isolated from E. agallocha.,,,,,,,,,,,,, Two new bis seco-labdane diterpenes 17 and 18 were isolated from resinous woods. Several seco-labdane diterpenes were also isolated from the same plant. New class of secolabdanoid compounds 37–40 with an unprecedented skeleton were isolated from the stems.
Fourteen isopimarane-type diterpenes 42–55 were isolated from E. agallocha.,,,,,,,, Roots yielded four isopimarane diterpenes 42–45,, five isopimarane diterpenes 47–51 were isolated from stems and leaves,, compounds 46 and 53–55 were isolated from woods,, and compound 52 was isolated from the whole plant. Two isopiramane diterpenes 53 and 54 contains a seven membered lactone moieties.
So far, 12 kaurane-type diterpenes 56–67 were isolated from different parts of E. agallocha. Most of the kaurane diterpenes are ent-kaurane derivatives., 34, ,,, Fifteen Beyerane-type diterpenes 68–82 were also isolated from different parts of the plant.,,,,,
Fourteen artisane-type diterpenes 83–96 were isolated from different parts of E. agallocha,,,,,,, out of which compounds 83 and 84 are isolated from woods,, compounds 85–88 were isolated from bark, compound 89 was isolated from the twigs and stems, and compound 96 was isolated from stems only  and stems and leaves yielded five artisane diterpene 90–95.,,
Seven daphnane-type diterpenes 97–103 as cryptic and free skin irritant were isolated from the latex. These diterpenes are named as Excoecaria factor (A1–A7) out of which Excoecaria factor (A1–A3) are known.,
A novel phorbol ester 104 was isolated from stems and leaves as the anti-HIV principle. In 1994, Karalai et al. isolated two new tigilane-type diterpenes 105 and 106 from the latex of E. agallocha.
Four diterpenoids excoagallochaols A–D 107–110 with an unprecedented skeleton were also isolated from stems and leaves of the plant.,
Seventeen triterpenoids 111–127 were isolated from various parts of E. agallocha. The terpenoids isolated are oleanane, taraxerone, cycloartane, and lupane derivatives.,,
Two flavonoids 2',4',6',4-tetramethoxychalcone 128 and 3, 5, 7, 3, 5-pentahydroxy-2R,3R-flavanonol 3-O-α-L-rhamnopyranoside 129 were isolated from this mangrove species.
A piperidine alkaloid 2,4-dimethoxy-3-ψ,ψ-dimethylallyl-trans-cinnamoylpiperidide 130 was isolated from E. agallocha.
Three steroidal components such as β–sitostenone 131, (24R)-24-ethylcholesta-4,22-dien-3-one 132, and β–sitosterol 133 were isolated from the stems and twigs.
In 2003, Konishi et al. isolated a known tannin 3, 4, 5-trimethoxyphenol 1-O-β-D-(6-galloyl)-glucopyranoside 134 from the fresh stem of the plant.
Ten other compounds 135-144 were isolated from the woods. They were mainly organic acids, organic acid esters and alcohol derivatives.,,,,,
| Pharmacological Activities|| |
Hossain et al. performed the antioxidant activity of dried powder of E. agallocha bark using various antioxidant models such as reducing power, 1,1-diphenyl-2-picryl-hydrazil (DPPH) free radical scavenging activity, and measurement of total antioxidant activity. The result showed that distilled water and ethanol fractions had high antioxidative activities compared to other fractions such as hexane, chloroform, and ethyl acetate. Antioxidant activities using DPPH radical scavenging assay were performed by Rajaram Panneerselvam et al. on field and micropropagated plant leaves of E. agallocha. The result revealed that DPPH radical scavenging effect was greater in micropropagated plants (IC50 value of 10.2, 10.8, and 17.4) than in the field grown plants. Ascorbic acid content was more in micropropagated plants 18/mg/plant when compared to field grown plants. Highest total phenolic content was also recorded in micropropagated plant (207 and 205 mg/GAE/g) than in field grown plant. Antioxidant activities were further determined on the aqueous extract which revealed that the antioxidant activity using DPPH radical scavenging activity, reducing power, and hydrogen peroxide scavenging activity increases in a dose-dependent manner. The phenol content was also determined which was 2.215 ± 0.049, 1.625 ± 0.006, 1.405 ± 0.006, and 1.109 ± 0.049 for acetone, ethanol, methanol, and aqueous extract, respectively. Poorna et al. performed the antioxidant activity on the leaves, and the result revealed that the methanol extract has a strong DPPH free radical scavenging activity (IC50 value 67.50 µg/µl). The methanolic extract also showed potent nitric oxide radical inhibition (IC50 value 4.8 µg/µl), lipid peroxidation inhibition (IC50 value 100 µg/µl), and metal chelating effect (IC50 value 2.47 µg) in a dose-dependent manner. In 2012, Patra et al. reported the antioxidant activity of thin layer chromatography fraction of E. agallocha, leaves which showed that 23.36% DPPH radical scavenging activity at 40 µl concentration.
Antimicrobial activity was evaluated by Varaprasad Bobbarala et al. on hexane, chloroform, and methanol extracts of E. agallocha leaves. Twelve microorganisms were taken to study antibacterial and antifungal activity, i.e. for antifungal – Acremonium strictum, Aspergillus flavus, Aspergillus niger, Candida albicans, Curvularia lunata, Fusarium oxysporum, Macrophomina phaseolina, Penicillium expansum, Rhizoctonia solani, Ustilago maydis, and Xanthomonas campestris and for antibacterial – Lactobacillus fermentum and Staphylococcus aureus. The result revealed that methanol extract exhibited higher activity compared to hexane and chloroform extract. Antimicrobial activities of the mangrove plant were further evaluated against selected fish pathogens such as Chryseobacterium indologenes, Flavobacterium indicum, Chryseobacterium gleum, and Elizabethkingia meningoseptica previously named Flavobacterium meningosepticum. Minimum inhibitory concentration (MIC) and minimum bactericidal concentration of the methanolic extract were 3.12 mg/ml and 6.25 mg/ml, respectively. Zone of inhibition was significantly different (P < 0.05) according to the doses (100, 300, and 500 mg/ml) of the crude extracts. The highest activity (LC50) recorded was 94.19 mg/ml. Thus, E. agallocha methanolic leaves extract showed high antimicrobial activity against these fish pathogens. Eighty percent methanolic extract of wild grown plants, leaf derived callus, and in vitro raised plant leaves of E. agallocha were prepared and evaluated for antibacterial activity against Bacillus cereus, Bacillus subtilis, Klebsiella pneumoniae, Proteus vulgaris, S. aureus, Salmonella typhi. The result revealed that methanolic extract of leaf derived callus showed more antibacterial activity than the wild grown and in vitro raised plants. Antimicrobial properties of E. agallocha fatty acid methyl esters (FAMEs) extracts were studied by Agoramoorthy et al., and the results showed that FAME extracts exhibited strong antimicrobial activities against 11 selected microorganisms of which seven were bacteria such as B. subtilis, Bacillus pumilus, S. aureus, Micrococcus luteus, K. pneumoniae, Pseudomonas aeruginosa, and Escherichia coli and four were yeast such as C. albicans, Candida tropicalis, Candida krusei, and Candida parapsilosis. The mean zone of inhibition of the extract calculated ranged between 7.3 and 16.6 mm. Ethanol extracts of fresh and dried leaves, roots, and stems were screened for antibacterial activity against Vibrio cholerae, S. aureus, S. typhi, Proteus sp., and Enterobacter sp. The result showed that in the dried plant sample, the leaf part showed more antibacterial activity against all the test organisms compared to the fresh plant extracts. Chloroform leaves extract were screened for antibacterial activity against various fish pathogens such as B. subtilis, Aeromonas hydrophila, Vibrio parahaemolyticus, Vibrio harveyi, and Serratia sp. The result showed that the third fraction exhibited the maximum activity which was 12 mm against V. parahaemolyticus, followed by V. harveyi (10 mm), B. subtilis (10 mm), and A. hydrophila (8 mm). The antibacterial activity of the aqueous leaf extracts was assayed in vitro by disc diffusion method against five bacterial strains. The Gram-negative bacterial strains revealed the zone of inhibition, i.e. E. coli (17 mm), P. aeruginosa (15 mm), K. pneumoniae (16 mm), and Gram-positive bacterial strains showed S. aureus (15 mm), B. subtilis (14 mm) at 128 μg concentration. The MIC of Gram-negative and Gram-positive organisms were analyzed by microtiter plate technique. The MIC values for E. coli was <2 μg, B. subtilis was 128 μg, S. aureus was 256 μg, P. aeruginosa was 128 μg, and K. pneumoniae was 32 μg.E. agallocha leaves extracts also showed significant antifungal activity against four fungal pathogens R. solani, Fusarium udum, M. phaseolina, Sclerotium rosii, whereas there was no activity shown in fungal pathogen Alternaria alternata. Ethanol:methanol (5.6:1) extract of leaves, stem, and root was screened for antifungal activity by the spore formation inhibition in Alternaria tenuis, Helminthosporium oryzae, F. oxysporum, and inhibition of budding in yeast (Saccharomyces cerevisiae). The result showed significant antifungal activity in a dose dependent manner. In 2012, Patra et al. reported the antimicrobial activity of the leaves against various bacterial pathogens such as S. aureus and B. subtilis, Shigella flexneri, P. aeruginosa, and E. coli. The result showed positive for S. aureus and P. aeruginosa.
Babuselvam et al. studied the acute inflammatory properties of ethanol in water (3:1) extract of different parts such as latex, leaves, and seed of E. agallocha which showed statistically significant activity at a dose of 500 mg/kg in carrageenan induced rat paw edema model at 4 h as compared to the control causing an inhibition of 63.15%, 62.15%, and 69.69% in latex, leaves, and seeds, respectively. Whereas in cotton pellet-induced granuloma test, the seed extract showed maximum activity at the dose of 500 mg/kg which was 57.03% compared to control.
The analgesic effect of ethanol:water (3:1) extract of leaves, seeds, and latex of E. agallocha was studied by Babuselvam et al., out of which the seed extract significantly decreased the number of writhes in 20 min and also increased the percentage of inhibition in acetic acid writhing test in test animals. Moreover, in the tail immersion model, the seed extract at the concentration of 500 mg/kg possesses maximum activity (80.29%) as compared to control. Crude alcoholic bark extract at 300 mg/kg dose showed maximum time needed for the response against thermal stimuli 6.72 ± 0.43 s compared to diclofenac sodium 8.20 ± 0.21 s in the hot plate test. In acetic acid-induced Writhings test in mice, 500 mg/kg dose of the bark extract showed maximum reduction (53.87%). In the tail immersion method, 300 mg/kg dose of the alcoholic bark extract showed the highest activity.
Antiulcer activity of E. agallocha leaves was studied in nonsteroidal anti-inflammatory drug induced ulcer in rats where the result showed that the leaves extract increases the mucosal defense in the gastric area as well as able to lower the acidity. Thus, the leaves of the plant can be used as an antiulcerogenic agent. The alcoholic extract of the bark showed significant antiulcer activity against acetylsalicylic acid induced ulceration.
In 2011, Patil et al. reported anticancer activity using MTS in vitro assay on activity-guided fraction of ethanol extract of E. agallocha stem, and the result revealed strong activity against pancreatic cancer cell lines Capan-1 and Miapaca-2 with IC50 values of 4 µg/ml and 7 µg/ml, respectively. In 2012, anticancer activity on human lung cancer cell lines of the ethanol stem extract were reported by Patil et al. where the result showed potent cytotoxic activities in a dose-dependent manner and also caused p21-mediated G1 arrest in p53-/-cells and apoptotic programmed cell death in p53+/+ cells.
Anticancer activity was also tested on leaf extract by Batsa and Periyasamy in cell line model, and the result revealed high activity at lower concentration when compared to higher concentration. At a particular higher concentration, the cell viability was more in methanol extract than the chloroform extract.
Antireverse transcriptase activity
Antireverse transcriptase activity of the ethanol extract of E. agallocha stems was reported by Patil et al. in 2011. The result showed that activity guided ethanol fraction of stem ethanol extract has a potent antireverse transcriptase activity. A novel phorbol ester was isolated which was a potent in vitro inhibitor of HIV-1 replication as measured by the inhibition of supernatant reverse transcriptase and p24 levels (IC50 6 nm).
Antihistamine-release activity of E. agallocha bark on ionophore A23187-induced histamine-release assay model was studied by Hossain et al., and the result revealed that distilled water and ethanol showed high antihistamine-release activity compared to other fractions such as hexane, chloroform, and ethyl acetate.
E. agallocha methanolic leaves extract showed significant antifilarial activity in a dose dependent response which was evident by death caused in the stages of development of Setaria digitate, which is a metazoan filarial parasite. After 24 h of treatment with the methanolic leaves extracts at a concentration of 10, 50, and 100 μg/ml about 30%, 75%, and 90% of the developmental stages of S. digitata were found dead, respectively.
DNA damage protective activity
DNA damage protective activity of E. agallocha leaves was reported by Poorna et al. in 2012, where significant activity were shown by the water fraction of the leaves extract which was successful in protecting DNA damage.
Antidiabetic activity of leaves of E. agallocha was studied by Thirumurugan et al. in alloxan-induced diabetic mice, and the result revealed that the ethanolic leaves extract at the dose of 500 mg/kg has significant hypoglycemic activity in both the normal and alloxan-induced diabetic mice.
Antitumor protecting activity
Seven diterpenoids were isolated from E. agallocha resinous woods which showed significant inhibitory effects on Epstein–Barr virus (EBV) activation which were induced by 12-O-tetradecanoylphorbol-13-acetate (TPA) a tumor promoter. Furthermore, ent-3 β-hydroxy-15-beyeren-2-one (82) exhibited remarkable antitumor promoting activity in vivo in a two-stage carcinogenesis test of mouse tumor using 7,12-dimethylbenz[a] anthracene (DMBA) as an initiator and TPA as a promoter.
Several diterpenoids were isolated from mangrove plant E. agallocha and their inhibitory effects on the induction of EBV early antigen (EBVEA) in Raji cells were also examined. Of these diterpenes, the seco-labdane-type diterpenoid, Excoecarin T1 (15) exhibited a potent inhibitory effect on EBVEA induction and a significant antitumor-promoting effect in the two-stage carcinogenesis test in mouse using DMBA as an initiator and TPA as a promoter.
| Conclusion|| |
Different parts of E. agallocha L., including the leaves, roots, woods, stems, bark, latex, and seeds have been reported to have therapeutic potential in traditional medicine for the treatment of various diseases. These include antioxidant, antimicrobial, anti-inflammatory, analgesic, antiulcer, anticancer, antireverse transcriptase, antihistamine-release, antifilarial, DNA damage protective, antidiabetic, and antitumor protecting activities. Several bioactive compounds belonging to various chemical groups were isolated from different parts of the plant. Mostly diterpenoids were isolated and they were mainly labdane, isopimarane, kaurane, beyerane, artisane, daphnane, tigilane type diterpenoids. Other phytoconstituents isolated are mainly triterpenoids, flavonoids, alkaloids, sterols, tannins, and few other miscellaneous compounds (Organic acids, organic acid esters, and alcohol derivatives). This review highlights several pharmacological and phytochemical studies that have demonstrated the therapeutic potential and phytochemical constituents of E. agallocha L.
The authors are thankful to GITAM University, Visakhapatnam, Andhra Pradesh, India, for providing financial support and facilities to carry out this review.
Financial support and sponsorship
This study was supported by GITAM University, Visakhapatnam, Andhra Pradesh, India.
Conflicts of interest
There are no conflicts of interest.
| References|| |
Kaushik P, Kaushik D, Khokra S, Chaudhary B. Abutilon indicum
(Atibala): Ethno-botany, phytochemistry and pharmacology – A review. Int J Pharm Clin Res 2009;1:4-9.
Biswas K, Chattopadhyay I, Banerjee RK, Bandyopadhyay U. Biological activities and medicinal properties of neem (Azadirachta indica
). Curr Sci 2002;82:1336-45.
Rahman S, Islam R, Kamruzzaman M, Alam K, Jamal AH. Ocimum sanctum
L.: A review of phytochemical and pharmacological profile. Am J Drug Discov Dev 2011;1-15. [DOl: 1O.3923/ajdd.2011].
Srivastav S, Singh P, Mishra G, Jha KK, Khosa RL. Achyranthes aspera –
An important medicinal plant: A review. J Nat Prod Plant Resour 2011;1:1-14.
Bandaranayake WM. Economic, Traditional and Medicinal Uses of Mangroves. AIMS Report 28. Australian Institute of Marine Science, Townsville, Australia; 1999.
Arumugam M, Panneerselvam R. Micropropagation and phenolic exudation protocol for Excoecaria agallocha
– An important mangrove. Asian Pac J Trop Biomed 2012;2:S1096-101.
Poorna CA, Resmi MS, Soniya EV. In vitro
Antioxidant analysis and the DNA Damage protective activity of leaf extract of the Excoecaria agallocha
Linn. mangrove plant. Int J Agric Chem 2012;1:1-6.
Gowri PM, Srirangaraja SV, Bhattara R, Reddy PG, Rakesh Y, Basha SJ, et al
. Three New ent-Labdane diterpenoids from the wood of Excoecaria agallocha
Linn. Helv Chim Acta 2009;92:1419-27.
Bandaranayake WM. Bioactivities, bioactive compounds and chemical constituents of mangrove plants. Wetlands Ecol Manage 2002;10:421-52.
Clough B. Continuing the Journey Amongst Mangroves. ISME Mangrove Educational Book Series No. 1. International Society for Mangrove Ecosystems (ISME), Okinawa, Japan, and International Tropical Timber Organization (ITTO), Yokohama, Japan; 2013.
. [Last accessed 2015 Oct 26].
Patil RC, Manohar SM, Katchi VI, Rao AJ, Moghe A. Ethanolic stem extract of Excoecaria agallocha
induces G1 arrest or apoptosis in human lung cancer cells depending on their P53 Status. Taiwania 2012;57:89-98.
Arumugam M, Pawar UR, Gomathinayagam M, Lakshmanan GM, Panneerselvam R. Antibacterial and antioxidant activity between micropropagated and field grown plants of Excoecaria agallocha
L. Int Res J Pharm 2012;3:235-40.
Agoramoorthy G, Chandrasekaran M, Venkatesalu V, Hsu MJ. Antibacterial and antifungal activities of fatty acid methyl esters of the blind-your-eye mangrove from India. Braz J Microbiol 2007;38:739-42.
Subhan N, Alam MA, Ahmed F, Shahid IJ, Nahar L, Sarker SD. Bioactivity of Excoecaria agallocha
. Braz J Pharmacogn 2008;18:521-6.
Agarwal VS. Drug plants of India. 1st
ed. New Delhi: Kalyani Publishers; 1997. p. 373.
Anjaneyulu AS, Rao VL. Five diterpenoids (agallochins A-E) from the mangrove plant Excoecaria agallocha
Linn. Phytochemistry 2000;55:891-901.
Anjaneyulu AS, Rao VL. Seco diterpenoids from Excoecaria agallocha
L. Phytochemistry 2003;62:585-9.
Kang J, Chen RY, Yu DQ. A new isopimarane-type diterpene and a new natural atisane-type diterpene from Excoecaria agallocha
. J Asian Nat Prod Res 2005;7:729-34.
Konishi T, Yamazoe K, Konoshima T, Fujiwara Y. Seco-labdane type diterpenes from Excoecaria agallocha
. Phytochemistry 2003;64:835-40.
Konishi T, Yamazoe K, Konoshima T, Maoka T, Fujiwara Y, Miyahara K. New bis-secolabdane diterpenoids from Excoecaria agallocha
. J Nat Prod 2003;66:108-11.
Konishi T, Konoshima T, Fujiwara Y, Kiyosawa S, Miyahara K, Nishi M. Stereostructures of new labdane-type diterpenes, excoecarins F, G1, and G2 from the wood of Excoecaria agallocha
. Chem Pharm Bull 1999;47:456-8.
Konishi T, Azuma M, Itoga R, Kiyosawa S, Fujiwara Y, Shimada Y. Three new labdane-type diterpenes from wood, Excoecaria agallocha.
Chem Pharm Bull 1996;44:229-31.
Konishi T, Kiyosawa S, Konoshima T, Fujiwara Y. Chemical structures of Excoecarins A, B, and C: Three new labdane-type diterpenes from wood, Excoecaria agallocha
. Chem Pharm Bull 1996;44:2100-2.
Konishi T, Konoshima T, Fujiwara Y, Kiyosawa S. Stereostructure of excoecarin H, a novel seco-labdane-type diterpene from Excoecaria agallocha
. Chem Pharm Bull 1998;46:721-2.
Konishi T, Fujiwara Y, Konoshima T, Kiyosawa S. Five new labdane-type diterpenes from Excoecaria agallocha
. IV. Chem Pharm Bull 1998;46:1393-8.
Li X, Lei J, Zheng YN, Sattler I, Lin WH. New ent-Isopimarane diterpene from mangrove Excoecaria agallocha
L. Chem Res Chin Univ 2007;23:541-3.
Annam SCh, Ankireddy M, Sura MB, Ponnapalli MG, Sarma AV, S JB. Epimeric excolides from the stems of Excoecaria agallocha
and structural revision of rhizophorin A. Org Lett 2015;17:2840-3.
Konishi T, Yamazoe K, Kanzato M, Konoshima T, Fujiwara Y. Three diterpenoids (excoecarins V1-V3) and a flavanone glycoside from the fresh stem of Excoecaria agallocha
. Chem Pharm Bull (Tokyo) 2003;51:1142-6.
Anjaneyulu AS, Rao VL, Sreedhar K. Agallochins J-L, new isopimarane diterpenoids from Excoecaria agallocha
L. Nat Prod Res 2003;17:27-32.
Wang JD, Li ZY, Guo YW. Secoatisane- and isopimaran-type diterpenoids from the Chinese mangrove Excoecaria agallocha
L. Helv Chim Acta 2005;88:979-85.
Wang JD, Guo YW. Agallochaols A and B, two new diterpenes from the Chinese mangrove Excoecaria agallocha
. Helv Chim Acta 2004;87:2829-33.
Ponnapalli MG, Ankireddy M, Annam SC, Ravirala S, Sukki S, Tuniki VR. Unusual ent-isopimarane-type diterpenoids from the wood of Excoecaria agallocha
. Tetrahedron Lett 2013;54:2942-5.
Anjaneyulu AS, Rao VL, Sreedhar K. ent-Kaurane and beyerane diterpenoids from Excoecaria agallocha
. J Nat Prod 2002;65:382-5.
Konishi T, Konoshima T, Maoka T, Fujiwara Y. Novel diterpenes, excoecarins M and N
from the resinous wood of Excoecaria agallocha
. Tetrahedron Lett 2000;41:3419-22.
Li Y, Liu J, Yu S, Proksch P, Gu J, Lin W. TNF-a inhibitory diterpenoids from the Chinese mangrove plant Excoecaria agallocha
L. Phytochemistry 2010;71:2124-31.
Konishi T, Konoshima T, Fujiwara Y, Kiyosawa S. Excoecarins D, E, and K, from Excoecaria agallocha
. J Nat Prod 2000;63:344-6.
Wang ZC, Lin YM, Feng DQ, Ke CH, Lin P, Yan CL, et al.
A new atisane-type diterpene from the bark of the mangrove plant Excoecaria agallocha
. Molecules 2009;14:414-22.
Wang JD, Li ZY, Xiang WS, Guo YW. Further new secoatisane diterpenoids from the Chinese mangrove Excoecaria agallocha
L. Helv Chim Acta 2006;89:1367-72.
Karalai C, Wiriyachitra P, Opferkuch HJ, Hecker E. Cryptic and free skin irritants of the daphnane and tigliane types in latex of Excoecaria agallocha
. Planta Med 1994;60:351-5.
Erickson KL, Beutler JA, Cardellina JH 2nd
, McMahon JB, Newman DJ, Boyd MR. A novel phorbol ester from Excoecaria agallocha
. J Nat Prod 1995;58:769-72.
Wang JD, Zhang W, Li ZY, Xiang WS, Guo YW, Krohn K. Elucidation of excogallochaols A-D, four unusual diterpenoids from the Chinese mangrove Excoecaria agallocha
. Phytochemistry 2007;68:2426-31.
Zou JH, Dai J, Chen X, Yuan JQ. Pentacyclic triterpenoids from leaves of Excoecaria agallocha
. Chem Pharm Bull (Tokyo) 2006;54:920-1.
Tian MQ, Bao GM, Ji NY, Li XM, Wang BG. Triterpenoids and steroids from Excoecaria agallocha
. Zhongguo Zhong Yao Za Zhi 2008;33:405-8.
Liu Z, Jiang W, Deng ZW, Lin WH. Assignment of the absolute stereochemistry of an unusual diterpenoid from the mangrove plant Excoecaria agallocha
L. J Chin Pharm Sci 2010;19:387-92.
Prakash S, Khan MA, Khan H, Zaman A. A piperidine alkaloid from Excoecaria agallocha
. Phytochemistry 1983;22:1836-7.
Popp M. Chemical composition of Australian mangroves II. Low molecular weight carbohydrates. Z Pflanzenphysiol 1984;113:411-21.
Masuda T, Yonemori S, Oyama Y, Takeda Y, Tanaka T, Andoh T, et al
. Evaluation of the antioxidant activity of environmental plants: Activity of the leaf extracts from seashore plants. J Agric Food Chem 1999;47:1749-54.
Li Y, Yu S, Liu D, Proksch P, Lin W. Inhibitory effects of polyphenols toward HCV from the mangrove plant Excoecaria agallocha
L. Bioorg Med Chem Lett 2012;22:1099-102.
Wiriyachitra P, Hajiwangoh H, Boonton P, Adolf W, Opferkuch HJ, Hecker E. Investigations of medicinal plants of euphorbiaceae and thymelaeaceae occurring and used in Thailand; II. Cryptic irritants of the diterpene ester type from three Excoecaria
species. Planta Med 1985;51:368-71.
Hossain SJ, Aoshima H, El-Sayed M, Ahmed F. Antioxidative and anti-histamine-release activities of Excoecaria agallocha
L. Pharmacologyonline 2009;2:927-36.
Patra JK, Mohapatra AD, Rath SK, Dhal NK, Thatoi H. Screening of antioxidant and antifilarial activity of leaf extracts of Excoecaria agallocha
L. Int J Integr Biol 2009;7:9-15.
Patra JK, Gouda S, Sahoo SK, Thatoi HN. Chromatography separation, 1H NMR analysis and bioautography screening of methanol extract of Excoecaria agallocha
L. from Bhitarkanika, Orissa, India. Asian Pac J Trop Biomed 2012;2:S50-6.
Vadlapudi V, Bobbarala V, Penumajji S, Naidu KC. Excoecaria agallocha
L. Antimicrobial properties against important pathogenic microorganisms. Int J ChemTech Res 2009;1:865-7.
Laith AA, Najiah M. Antimicrobial activities of blinding tree, Excoecaria agallocha
against selected bacterial pathogens. J Microbiol Antimicrob 2014;6:29-36.
Prakash M, Sivakumar T. A study on antibacterial activity of mangrove plant Excoecaria agallocha
L. Int J Curr Microbiol Appl Sci 2013;2:260-2.
Ravikumar S, Muthuraja M, Sivaperumal P, Gnanadesigan M. Antibacterial activity of the mangrove leaves Excoecaria agallocha
against selected fish pathogens. Asian J Med Sci 2010;2:211-3.
Packialakshmi N, Kanimozhi P. Bioautography screening of a mangrove Excoecaria agallocha
L. Int J Phytopharmacol 2014;5:1-5.
Kumar P, John SA. In vitro
Anti-fungal activity of Excoecaria agallocha
. L. from Pichavaram mangrove forest. Int J Plant Environ Sci 2013;3:32-4.
Deepa M, Padmaja CK. Effect of the extracts of Excoecaria agallocha
on spore formation and budding in fungi. Asian J Plant Sci Res 2013;3:14-9.
Babuselvam M, Ravikumar S, Mohamed Farook KA, Abideen S, Peer Mohamed M, Uthiraselvam M. Evaluation of anti-inflammatory and analgesic effects on the extracts of different parts of Excoecaria agallocha
L. J Appl Pharm Sci 2012;2:108-12.
Subhan N, Alam A, Ahmed F, Shahid IZ. Antinociceptive and gastroprotective effect of the crude ethanolic extracts of Excoecaria agallocha
linn. Turk J Pharm Sci 2008;5:143-54.
Thirunavukkarasu P, Ramkumar L, Ramanathan T. Anti-ulcer activity of Excoecaria agallocha
bark on NSAID-induced gastric ulcer in albino rats. Glob J Pharmacol 2009;3:123-6.
Patil RC, Manohar SM, Upadhye MV, Katchi VI, Rao AJ, Mule A, et al
. Anti reverse transcriptase and anticancer activity of stem ethanol extracts of Excoecaria agallocha
(Euphorbiaceae). Ceylon J Sci (Biol Sci) 2011;40:147-55.
Batsa AJ, Periyasamy K. Anticancer activity of Excoecaria agallocha
leaf extract in cell line model. Int J Pharm Biol Sci 2013;3:392-8.
Thirumurugan G, Vijayakumar TM, Poovi G, Senthilkumar K, Sivaraman K, Dhanaraju MD. Evaluation of antidiabetic activity of Excoecaria agallocha
L. in alloxan induced diabetic mice. Nat Prod Indian J 2010;6:1-5.
Konishi T, Takasaki M, Tokuda H, Kiyosawa S, Konoshima T. Anti-tumor-promoting activity of diterpenes from Excoecaria agallocha
. Biol Pharm Bull 1998;21:993-6.
Konoshima T, Konishi T, Takasaki M, Yamazoe K, Tokuda H. Anti-tumor-promoting activity of the diterpene from Excoecaria agallocha
. II. Biol Pharm Bull 2001;24:1440-2.
| Authors|| |
Dr. Sumanta Mondal , (Lecturer & NSS Programme Officer of GITAM Institute of Pharmacy, GITAM University, Andhra Pradesh, India). His research involves bioactivity and phytochemical studies of various medicinal plant species. He has published more than 48 research articles in various international and national journals. He has guided more than 20 M. Pharm students and presently seven students are pursuing PhD under his guidance.
Mr. Debjit Ghosh, pursuing PhD from Department of Chemistry, GITAM Institute of Science, GITAM University, Visakhapatnam, Andhra Pradesh, India, under the guidance of Prof. K. Rama Krishna and Dr. S. Mondal. His research interest includes isolation and structural elucidation of phyto-constituents, chromatographic and phytochemical analysis, toxicological studies and pharmacological screening.
Dr. K. Ramakrishna, (Professor, Department of Chemistry, Institute of Science, GITAM University, Visakhapatnam, Andhra Pradesh, India). His research interests are: pharmaceutical analysis, micellar catalysis, computational quantum chemical (CQC) and phytochemical studies. He published more than 100 research articles in various international and national journals. He trained 16 students for Ph.D. and seven students for M.Phil. Six students are pursuing PhD under his guidance.
[Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5]