|Year : 2020 | Volume
| Issue : 2 | Page : 192-200
Phytochemical screening and enzymatic and antioxidant activities of Erythrina suberosa (Roxb) bark
Zubair Ahmed1, Sohail Aziz2, Muhammad Hanif1, Syed Ghouse Mohiuddin2, Sayed Hurmat Ali Khan1, Rizwan Ahmed3, Siti Maisharah Sheikh Ghadzi2, Ahmad Naoras Bitar2
1 Department of Pharmacy, COMSATS University Islamabad, Islamabad, Pakistan
2 Department of Clinical Pharmacy, School of Pharmaceutical Sciences, Universiti Sains Malaysia (USM), George Town, Malaysia
3 Department of Natural Products and Alternative Medicines, College of Clinical Pharmacy, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia
|Date of Submission||26-Sep-2019|
|Date of Decision||24-Nov-2019|
|Date of Acceptance||26-Dec-2019|
|Date of Web Publication||15-Apr-2020|
Dr. Sohail Aziz
School of Pharmaceutical Sciences, Universiti Sains Malaysia (USM), George Town 11800, Pulau Pinang.
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Background: This study aimed to evaluate the phytochemicals screening of Erythrina suberosa (Roxb) bark and to analyze the enzymatic activities of its various organic fractions. Materials and Methods: Crude methanolic fraction of E. suberosa (Roxb) bark and its respective fractions were screened for the presence of different phytochemicals with different reagents. On the basis of increasing order of polarity, different organic solvents were used to obtain different fractions. Enzymatic studies were performed on crude methanolic extract of the plant. All the assays were performed under standard in vitro conditions. Results: The phytochemical analysis shows the presence of alkaloids, phenols, triterpenoids, phytosterols, and flavonoids. Phenolic compounds and flavonoids are the major constituents of the plant. In anticholinesterase assay, the percent inhibition of standard drug (eserine) was 91.27 ± 1.17 and the half maximal inhibitory concentration (IC50) was 0.04 ± 0.0001. For α-glucosidase inhibition, the IC50 value for Dichloromethane fraction was 8.45 ± 0.13, for Methanol fraction it was 64.24 ± 0.15, and for aqueous fraction it was 42.62 ± 0.17 as compared with standard IC50 that is 37.42 (acarbose). Furthermore, results show that all fractions have potential against anti-urease enzyme, but DCM fraction of crude aqueous extract has significant IC50 value (45.26 ± 0.13) than other fractions. Conclusion: Keeping in view all the results, it is evident that the plant can be used in future for formulating effective drugs against many ailments. Secondary metabolites and their derivatives possess different biological activities, for example, .g. flavonoids in cancer, asthma, and Alzheimer. Furthermore, the extracts of this plant can be used in their crude form, which is an addition to the complementary and alternative treatment strategies.
Keywords: Antioxidant activity, enzymatic activities, Erythrina suberosa (Roxb), phytochemicals
|How to cite this article:|
Ahmed Z, Aziz S, Hanif M, Mohiuddin SG, Ali Khan SH, Ahmed R, Sheikh Ghadzi SM, Naoras Bitar A. Phytochemical screening and enzymatic and antioxidant activities of Erythrina suberosa (Roxb) bark. J Pharm Bioall Sci 2020;12:192-200
|How to cite this URL:|
Ahmed Z, Aziz S, Hanif M, Mohiuddin SG, Ali Khan SH, Ahmed R, Sheikh Ghadzi SM, Naoras Bitar A. Phytochemical screening and enzymatic and antioxidant activities of Erythrina suberosa (Roxb) bark. J Pharm Bioall Sci [serial online] 2020 [cited 2021 Jan 16];12:192-200. Available from: https://www.jpbsonline.org/text.asp?2020/12/2/192/282487
| Introduction|| |
Medicinal plants have been used for different ailments throughout the world in different human civilizations. Medicinal herbs are the pillar of traditional medicine and herbal medicines industries. More than 3.3 billion people from less-developed countries use medicinal plants usually for different diseases. These medicinal herbs are regarded as plentiful source of elements that can be used in drug synthesis and development.
Traditional or complementary medicinal system has been of great global value since the past few years. Traditional medicine is generally considered highly available and accessible to people in developing countries but comparatively to poor and marginalized people are commonly assumed to be most reliant on traditional medicines for their healthcare. There are major differences in acceptability which have also been observed between rural and urban areas. However, those patterns have rarely been studied in Asia, and little is known on the determinants of traditional medicine use. Medicinal herbs are mostly used as crude matter for extraction of active elements that are used in the synthesis of different chemicals and drugs, for example, laxatives, blood thinners, antibiotics, and antimalarial medications. For instance, taxol, vincristine, and morphine are isolated from pacific yew, periwinkle (Catharanthus roseus), and poppy (Papaver somniferum), respectively.,
One of the locally used medicinal plants, Erythrina suberosa (Roxb), known as Indian Coral Tree, Corky Coral Tree, Pangra, and Toti gul belonging to Fabaceae family, usually known as the legume, pea, or bean family, is diverse and an important economic family of flowering herbs. It consists of trees, shrubs, and perennial or annual herbaceous plants, which can be identified easily by their fruit (legume) and the compound stipulated leaves. Distribution of this family is wide and is the third largest on land herbs family in terms of number of species, having approximately 751 genera and almost 19,000 known species. Erythrina suberosa (Roxb) is a medium-sized perennial tree dominant in Indian region whose leaves, flowers, fruits, and bark have significant medicinal uses.
Four isoflavonoids have been isolated from E. suberosa (Roxb) roots, which are designated as α-hydroxyerysotrine, 4′-methoxy lico-flavanone (MLF), alpinumiso-flavone, and wighteone. Moreover, a new derivative alkaloid of erythrinia, (+)-11α-hydroxyerythravine was isolated from the flowers of E. mulungu. Also, from the flowers of E. mulungu, the known derivatives (+)-erythravine and (+)-α-hydroxyerysotrine were isolated. In the phytochemical investigation, various alkaloidal constituents were isolated from the seeds of E. suberosa (Roxb). These alkaloids include erythraline, erysodine, erysotrine, and hypaphorine. Erysotrine was found to occur naturally and was isolated for the first time from natural source.
The bark of E. suberosa (Roxb) is locally used in India for diarrhea as a paste along with other plants. The bark of E. suberosa (Roxb) has been used as antitumor agent and along with that its bark has also been used for some liver disorders from early ages. Alkaloids isolated from the flowers of E. suberosa (Roxb) were investigated for anxiolytic properties in a research and the results showed significant effect that was performed on Swiss albino male mice. Compound known as erythraline is α4, β2-nicotinic receptors antagonist and has prominent anxiolytic effect. The crude aqueous extract of flowers of E. suberosa (Roxb) shows potential spasmolytic, bronchodilatory, and antioxidant effect. From the alcoholic extract of stem bark of E. suberosa (Roxb), certain flavonoids were isolated. Human promyelocytic leukemia HL-60 cells were used to investigate their biological activity, showing apoptosis-inducing effect. In this study, flavonoids from E. suberosa (Roxb) bark were found to be the most potent cytotoxic agent with the half maximal inhibitory concentration (IC50) of 20 IM in human leukemia HL-60 cells. In spite of apoptosis, these flavonoids significantly inhibited nuclear transcription factor (NF-κB) and STAT (signal transducer and activator of transcription) signaling pathway.
| Materials and Methods|| |
The plant was collected locally and identified by botanist. Voucher specimen was taken and kept in the university herbarium. The total weight of the freshly collected bark was 10kg, which was subjected to shade drying and powdered by grinding mill.
Powder drug (950g) was extracted with 80% methanol for 21 days. The extract was filtered using fourfold muslin sheath followed by Whatman filter paper no. 42 (125mm). The process of extraction was repeated thrice. Major portion of solvent was evaporated at 40°C using water bath, whereas the remaining solvent was completely evaporated using rotary evaporator under reduced pressure. A dark brown semisolid extract was obtained weighing 100g.
Fractions extracted with different organic solvents
Crude bark extract of E. suberosa (Roxb) was subjected to fractionation with different organic solvents depending upon increasing order of polarity, for example, dichloromethane, ethyl acetate, and methanol.
Phytochemical screening of Erythrina suberosa (Roxb) bark
Crude methanolic fraction of E. suberosa (Roxb) bark and its respective organic fractions were screened for the presence of different phytochemicals, for example, alkaloids, saponins, glycosides, phenols, and tannins with the help of different reagents as mentioned.,,
Tests for alkaloids
1 mL solution of extracts/fractions were acidified with 10% dilute acetic acid in two separate test tubes. To the first test tube few drops of freshly prepared Mayer’s reagent were added, whereas to the second test tube few drops of Dragendorff’s reagent were added. The appearance of cream-colored precipitates with Mayer’s reagent or reddish-brown precipitate with Dragendorff’s reagent confirmed the presence of alkaloids.
Tests for saponins
Lead acetate test
Few drops of lead acetate were added to the test tubes containing 2 mL of methanolic extract of E. suberosa (Roxb) bark and its organic fractions. Appearance of white precipitates confirmed the presence of saponins.
Crude methanolic extract of E. suberosa (Roxb) bark and its organic fractions were dissolved in methanol. Sample solutions were shaken well and allowed to stand for 15min. Persistent froths were observed, which confirmed the presence of saponins.
Tests for tannins
Ferric chloride test
Few drops of 5% ferric chloride (FeCl3) solution were added to crude methanolic extract of E. suberosa (Roxb) bark and its organic fractions, respectively, resulting in bluish black color, which confirmed the presence of tannins.
Test for cardiac glycosides (Keller–Killani’s test)
Crude methanolic extract of E. suberosa (Roxb) bark and its fractions were taken in a test tube separately and treated with 2 mL of glacial acetic acid, respectively. To the test tubes, 1 mL FeCl3 followed by 1 mL of concentration sulfuric acid were added, resulting in the formation of reddish black layer that indicated the presence of cardiac glycosides.
Test for terpinoids (Salkowski’s test)
Crude methanolic extract of E. suberosa (Roxb) bark and its organic fractions were taken separately in test tubes (5 mL each); 3 mL chloroform was added, respectively, to each test tube followed by addition of 3 mL concentrated sulfuric acid (H2SO4) carefully. The presence of terpenoids was confirmed by the reddish-brown color of the interface.
Test for flavonoids
Crude methanolic extract of E. suberosa (Roxb) bark and its organic fractions were taken separately in test tubes. 5 mL of dilute ammonia solution was added to the aqueous filtrate of each extract. Then concentrated H2SO4 was added carefully. Appearance of yellow color was observed indicating the presence of flavonoids.
Test for phenols
Crude methanolic extract of E. suberosa (Roxb) bark and its organic fractions were taken separately in test tubes. Few drops of 5% FeCl3 were added to each test tube, which resulted in bluish black color, thus confirming the presence of phenols.
Tests for reducing sugars
Crude methanolic extract of E. suberosa (Roxb) bark and its organic fractions were taken separately in test tubes (5 mL each). To each test tube, 5 mL of Benedict’s reagent was added; the mixture was placed over hot water bath to boil for 5min. Resulting in reddish-brown precipitates indicated the presence of carbohydrates.
Crude methanolic extract of E. suberosa (Roxb) bark and its organic fractions were taken separately in test tubes (1 mL each), to which few drops of Fehling reagent were added and boiled over hot water bath giving brick red precipitates, which indicated the presence of reducing sugars.
Test for phytosterols
Crude methanolic extract of E. suberosa (Roxb) bark and its organic fractions were taken separately in test tubes (2 mL each). Each fraction was treated first with chloroform (2mL) and then concentrated sulfuric acid (2mL). To this solution, dilute acetic acid (few drops) and 3 mL of acetic anhydride were added. Appearance of bluish green color showed the presence of phytosterols.
Crude extract of E. suberosa (Roxb) bark was studied for the inhibition of following enzymes: (1) acetyl cholinesterase inhibition assay, (2) urease inhibition assay, and (3) α-glucosidase inhibition assay.
Acetyl cholinesterase inhibition assay
The study was performed on crude methanolic extract of E. suberosa (Roxb) bark and its organic fractions. All equipment used in the following study were clean and incubated for 5min at 37°C. A total volume of 100 μL reaction mixture was prepared containing 60 µL of disodium phosphate of 50-mM concentration (as a buffer with 7.7 pH value), test sample having volume of 10 μL with 0.5mM concentration and enzyme having volume of 10 μL with 0.005 concentration
All the above were added to well-1, respectively, followed by prereading at 405nm. The mixture of the contents was incubated for 10min at 37°C after which reaction was initiated by the addition of 10 μL of 0.5-mM substrate acetylthiocholine iodide for Acetylcholine. At the end, 10 μL dithio nitrobenzoic acid with 0.5mM concentration was added and incubated for further 15min at 37°C. At 405nm, absorbance was measured again through 96-well plate reader (Synergy HT, BioTek, Winooski, USA). Eserine of 0.5-mM concentration was applied as positive control. The following formula was used to calculate percent inhibition (% inhibition):
Through serial dilutions from 0.5, 0.25, 0.125, 0.625, 0.03125, up to 0.015625mM of the compound, IC50 values were determined. With the help of graph, using EZ-Fit enzyme kinetics software (Perrella Scientific, MA, Amherst), the concentrations showing 50% or more inhibition were considered as IC50. All the values were presented as mean of three independent replicates.
Urease inhibition assay
This assay was performed on crude bark extract of E. suberosa (Roxb) bark and its organic fractions. All the equipment used were rinsed and incubated for at least 5min at 37°C.
An assay mixture of 85 μL was prepared by adding the following:
1. Phosphate buffer solution (PBS) 10 μL (pH 7.0).
2. Sample solution of 10 μL volume.
3. 25 μL of enzyme solution concentration 0.135 units.
All these contents were added, respectively, in 96-well plate, followed by preincubation at 37°C for 5min. To the aforementioned 96-well plate, 40 μL stock solution of 20mM concentration was added and incubated once again at 37°C for 10min. After incubation, 115 μL of phenol-hyper-chlorite reagent was added in each well, which was freshly prepared by mixing 70 μL alkali with 45 μL phenol. Incubation was done for further 10min to develop color. Absorbance was measured by using 96-well plate reader (Synergy HT, BioTek) at 625nm. For calculation of IC50 and %age inhibition, the same method was followed as mentioned for choline-esterase assay. Thiourea was taken as positive control.
α-Glucosidase inhibition assay
This assay was performed on crude bark extract of E. suberosa (Roxb) and its organic fractions. All the equipment used were rinsed and incubated for at least 5min at 37°C.
Sample solution of 60 μL and 50 μL of 0.1 M PBS having pH 6.8 containing α-glucosidase solution of 0.2 U/ mL concentrations was put in 96-well plate and placed in an incubator for 20min at 37°C. To the aforementioned each 96-well plate, 50 μL of 5mM ρ-nitrophenyl-α-D-glucopyranoside (PNPG) solution in 0.1 M PBS having pH 6.8 was added and incubated again at 37°C for 20min. After incubation process, reaction was stopped by the addition of 160 mL of 0.2-M sodium carbonate into all wells of the plate. At 405nm, absorbance was recorded by microplate reader (Synergy HT, BioTek). Percent inhibition and IC50 of samples were calculated by using the following formula: inhibition (%) = control – test / control × 100.
IC50 of samples were calculated with the help of EZ-Fit enzyme kinetic software (Perrella Scientific, MA, Amherst). By serial dilutions of compounds to different concentrations, that is, from 0.5, 0.25, 0.125, 0.625, 0.03125, up to 0.015625mM, IC50 values were calculated. With the help of graph, the concentration at which the inhibition was 50% or more was calculated as IC50. Acarbose was positive control in the study. All values are mean of three independent variables.
Antioxidant activity of Erythrina suberosa (Roxb) bark
Antioxidant activity of E. suberosa (Roxb) bark was performed on crude extract and its fractions. For each fraction, 1mg per mL stock solution was prepared in methanol. Dilutions from 1000 μg/ mL to 500, 250, 125, 62.5, 31.25, 15.62, and 7.81 μg/ mL were prepared by serial dilution method. 1 mL methanol solution of Diphenyl picrylhydrazyl in concentration of (1mg/mL) was mixed with each 1 mL of diluted solutions. After incubation for 30min at 25°C in darkness, absorbance was recorded at 517nm. The assay was performed in triplicates and %age inhibition was measured by using following formula:
Quercetin and propyl gallate were used as positive control.,
Results phytochemical analysis
Crude bark extract of E. suberosa (Roxb) bark and its organic fractions were studied for phytochemical screening with different reagents. Results are mentioned in [Table 1][Table 2][Table 3].
|Table 1: Phytochemical analysis of crude extract of Erythrina suberosa (Roxb) bark|
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Anti-urease assay of Erythrina suberosa (Roxb) bark
Methanolic extract of E. suberosa (Roxb) bark and its organic fractions were analyzed against urease enzyme; their % inhibition at 0.5mg/ mL and IC50 (µg/mL) were calculated. Results are shown in [Figure 1].
|Figure 1: Graph plotted between % inhibition on the x-axis and the half maximal inhibitory concentration (IC50) on the y-axis in comparison with thiourea as standard drug|
Click here to view
Anticholinesterase assay of Erythrina suberosa (Roxb) bark
Crude methanolic extract of E. suberosa (Roxb) bark and its organic fractions were subjected to in vitro anticholinesterase assay in comparison with standard drug eserine. Their % inhibition as well as IC50 (µg/mL) were calculated as shown in [Figure 2].
|Figure 2: Graph plotted between % inhibition on the x-axis and the half maximal inhibitory concentration (IC50) on the y-axis in comparison with eserine as standard drug|
Click here to view
In vitro α-glucosidase assay of Erythrina suberosa (Roxb) bark
Methanolic extract of E. suberosa (Roxb) bark and its organic fractions were subjected to α-glucosidase enzyme; their % inhibition at 0.5mg/ mL and IC50 (μg/mL) were calculated as given in [Figure 3].
|Figure 3: Graph plotted between % inhibition on the x-axis and the half maximal inhibitory concentration (IC50) on the y-axis in comparison with acarbose as standard drug|
Click here to view
Antioxidant activities of crude aqueous methanol extract of E. suberosa (Roxb) bark and its organic fractions were performed following DPPH method; their % inhibition at 0.5mg/ mL and IC50 (μg/mL) were calculated as shown in [Figure 4].
|Figure 4: Graph plotted between % inhibition on the x-axis and the half maximal inhibitory concentration (IC50) on the y-axis|
Click here to view
| Discussion|| |
Phytochemical analysis of crude methanolic extract of bark as well as its various organic fractions showed that it is rich in alkaloids, phenols, and saponins, whereas reducing sugars, flavonoids, tannins, and triterpenoids are also present. Secondary metabolites and their derivatives possess different biological activities; for example, flavonoids provide protection against cancer, heart attack, asthma, and Alzheimer’s diseases.,,
Because of complicated and diversified nature of phytoconstituents of plants, it is difficult to evaluate the nature of compound responsible for antioxidant activity of a crude extract and different organic fractions of plants. Phenolic compounds and flavonoids are present as major constituents in plants and are very important medicinally. The constituents belonging to this class mainly possess antioxidant activity and are, therefore, assessed for the said activity. Phenolic compounds express their antioxidant potential by scavenging radicals, taking the singlet oxygen, and donating a hydrogen atom. For screening of antioxidant potential of samples, DPPH assay was used, which is a well-known, fast and sensitive method. In this technique, purple-colored DPPH solution is reduced into yellow-colored diphenyl-picrylhydrazine in the presence of hydrogen-donating antioxidants. The antioxidant potential of the samples is directly proportional to the hydrogen-donating capacity of the sample resulting in less absorbance. The crude methanolic extract of E. suberosa (Roxb) bark and its organic fractions were also tested for antioxidant activities. The IC50 calculated for aqueous extract was 335.3 ± 0.21, and organic fractions has shown negligible values as compared with a standard (propyl gallate) IC50 that was 46.38 ± 0.11 µM.
In vitro enzymatic assays, that is, anticholinesterase, anti-urease, and α-glucosidase, were carried out on crude as well as different organic fractions of E. suberosa (Roxb) bark. The most important enzyme responsible for the carbohydrates digestion is α-glucosidase, which is present in the intestinal membrane surface. The inhibitors of α-glucosidase cause the retardation of D-glucose liberation of lipopolysaccharides and disaccharides from dietary complex carbohydrates resulting in suppression of postprandial hyperglycemia, which ultimately causes delay in the absorption of glucose., The inhibitory activity of crude aqueous extract of E. suberosa (Roxb) bark and its fractions toward α-glucosidase was significant, whereas DCM fraction showed a very strong inhibitory activity more than standard. The IC50 value for DCM fraction was 8.45 ± 0.13, for MeOH fraction it was 64.24 ± 0.15, and for aqueous fraction it was 42.62 ± 0.17 as compared with standard IC50 that is 37.42 (acarbose). From this, it can be concluded that molecules in DCM fraction can be considered against diabetes, which needs further investigation.
In anticholinesterase assay, the % inhibition of standard drug (eserine) was 91.27 ± 1.17 and IC50 was 0.04 ± 0.0001, whereas result of crude aqueous methanol extract and its different organic fraction were negligible. An enzyme urease helps to hydrolyze urea to ammonia and carbon dioxide, hence used medically against bacteria (Helicobacter pylori), which are one of the major causes of peptic ulcer. Crude aqueous methanol extract of bark as well as their organic fractions were subjected to anti-urease activity and results were compared with standard drug thiourea. Percent inhibition and IC50 were calculated and compared with standard drug. Percent inhibition of crude aqueous extract of bark, its methanol fraction, and DCM fraction are 94.48 ± 0.16, 67.31 ± 0.21, 96.23 ± 0.17, and 98.21 ± 0.18 (standard), respectively. IC50 of crude aqueous methanol extract, DCM fraction, and MeOH fraction are 72.35 ± 0.12, 45.26 ± 0.13, and 134.82 ± 0.16, respectively, which were compared with standard IC50 (21.25 ± 0.15). Result shows that all fractions have potential against this enzyme, but DCM fraction of crude aqueous extract has significant IC50 value (45.26 ± 0.13) than other fractions.
This research was carried out using financial support by COMSATS University Islamabad, Abbottabad Campus, Islamabad, Pakistan but due to short time period and limited resources we were not able to further study this plant for its cytotoxic behavior.
Alkaloids are widely used for the treatment of various ailments; for example, vincristine and taxols are used as anticancer drugs. Phytochemical analysis suggested that E. suberosa (Roxb) has enough number of these compounds, which can guide us to interesting new lead compounds. Looking at the IC50 value of DCM fraction against α-glucosidase inhibition assay, it can be concluded that molecules in DCM fraction can be considered against diabetes, which needs further investigation. DCM fraction of methanolic extract has potential to treat ulcer and gout, which needs to investigate molecule(s) responsible for such activity. Erythrina suberosa (Roxb) bark showed significant antioxidant activity, which offers potential opportunities for the future anticancer studies of this plant.
| Conclusion|| |
Keeping in view all the results, it is evident that the plant can be used in future for formulating effective drugs against many ailments. These results need further elaborative and higher scale studies, which can be of prime importance in introducing these chemicals for treatment of various diseases. Furthermore, the extracts of this plant can be used in their crude form, which is an addition to the complementary and alternative treatment strategies.
Data availability statement
The data related to the research are provided in the article.
We would like to thank COMSATS staff for their support. Furthermore, SA appreciates Universiti Sains Malaysia fellowship for their support.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Cordell GA. Phytochemistry and traditional medicine––a revolution in process. Phytochem Lett 2011;4:391-8.
Zhou LG, Wu JY. Development and application of medicinal plant tissue cultures for production of drugs and herbal medicinals in China. Nat Prod Rep 2006;23:789-810.
Chen SL, Yu H, Luo HM, Wu Q, Li CF, Steinmetz A. Conservation and sustainable use of medicinal plants: problems, progress, and prospects. Chin Med 2016;11:37.
Sharma AK, Kumar R, Mishra A, Gupta R. Problems associated with clinical trials of Ayurvedic medicines. Rev Brasil Farmacog 2010;20:276-81.
Li FS, Weng JK. Demystifying traditional herbal medicine with modern approach. Nat Plants 2017;3:17109.
Gutiérrez RM. Orchids: a review of uses in traditional medicine, its phytochemistry and pharmacology. J Med Plants Res 2010;4:592-638.
Kumar S, Pathania AS, Saxena AK, Vishwakarma RA, Ali A, Bhushan S. The anticancer potential of flavonoids isolated from the stem bark of Erythrina suberosa
through induction of apoptosis and inhibition of STAT signaling pathway in human leukemia HL-60 cells. Chem Biol Interact 2013;205:128-37.
Rahman MZ, Sultana SJ, Faruquee CF, Ferdous F, Rahman MS, Islam MS, et al
. Phytochemical and biological investigations of Erythrina variegata
. Saudi Pharma J 2007;15:140.
Flausino O Jr, Santos Lde A, Verli H, Pereira AM, Bolzani Vda S, Nunes-de-Souza RL. Anxiolytic effects of erythrinian alkaloids from Erythrina mulungu
. J Nat Prod 2007;70:48-53.
Janbaz KH, Nisar U, Ashraf M, Qadir MI. Spasmolytic, bronchodilatory and antioxidant activities of Erythrina superosa
Roxb. Acta Pol Pharm 2012;69:1111-7.
Nawaz AH, Hossain M, Karim M, Khan M, Jahan R, Rahmatullah M. An ethnobotanical survey of Rajshahi district in Rajshahi division, Bangladesh. Am Eurasian J Sustain Agric 2009;3:143-50.
Agrawal SK, Agrawal M, Sharma PR, Gupta BD, Arora S, Saxena AK. Induction of apoptosis in human promyelocytic leukemia HL60 cells by an extract from Erythrina suberosa
stem bark. Nutr Cancer 2011;63:802-13.
Serrano MA, Batista AN, Bolzani VD, Santos LD, Nogueira PJ, Nunes-de-Souza RL, et al
. Anxiolytic-like effects of erythrinian alkaloids from Erythrina suberosa
. Química Nova 2011;34:808-11.
Juma BF, Majinda RR. Erythrinaline alkaloids from the flowers and pods of Erythrina lysistemon
and their DPPH radical scavenging properties. Phytochemistry 2004;65:1397-404.
Mohanta YK, Panda SK, Jayabalan R, Sharma N, Bastia AK, Mohanta TK. Antimicrobial, antioxidant and cytotoxic activity of silver nanoparticles synthesized by leaf extract of Erythrina suberosa
(roxb.). Front Mol Biosci 2017;4:14.
Savithramma N, Rao ML, Suhrulatha D. Screening of medicinal plants for secondary metabolites. Middle-East J Sci Res 2011;8:579-84.
Mojab F, Kamalinejad M, Ghaderi N, Vahidipour HR. Phytochemical screening of some species of Iranian plants. Iran J Pharm Res 2010;20:77-82.
Otoide JE, Kayode J. Phytochemical study of some plants commonly used as herbal remedies in southern Nigeria. Bull Pure Appl Sci 2011;30:33.
Ayoola GA, Coker HA, Adesegun SA, Adepoju-Bello AA, Obaweya K, Ezennia EC, et al
. Phytochemical screening and antioxidant activities of some selected medicinal plants used for malaria therapy in Southwestern Nigeria. Trop J Pharm Res 2008;7:1019-24.
Ashraf M, Ismail T, Arshad S, Khalid N, Khan M. Synthesis, characterization and biological evaluation of m-Phenetidine derivatives. J Chem Soc Pak 2015;37:122.
Kaskoos RA. In-vitro
α-glucosidase inhibition and antioxidant activity of methanolic extract of Centaurea calcitrapa
from Iraq. Am J Essent Oils Nat Prod 2013;1:122-5.
Ali MA, Devi LI, Nayan V, Chanu KV, Ralte L. Antioxidant activity of fruits available in Aizawl market of Mizoram, India. World J Agric Sci 2011;7:327-32.
Kawai M, Hirano T, Higa S, Arimitsu J, Maruta M, Kuwahara Y, et al
. Flavonoids and related compounds as anti-allergic substances. Allergol Int 2007;56:113-23.
Ahmed A. Apple phytochemicals for human benefits. IJPR 2011;1:40.
Bezerra-Santos CR, Vieira-de-Abreu A, Vieira GC, Filho JR, Barbosa-Filho JM, Pires AL, et al
. Effectiveness of Cissampelos sympodialis
and its isolated alkaloid warifteine in airway hyperreactivity and lung remodeling in a mouse model of asthma. Int Immunopharmacol 2012;13:148-55.
Bansal S, Bharati AJ, Bansal YK. In vitro
callogenesis and phytochemical screening of harsingar (Nyctanthes arbor-tristis
) a multipotent medicinal tree. Int J PharmTech Res 2013;5:1786-93.
Kim DM, Nam BW. Extracts and essential oil of Ledum palustre
L. leaves and their antioxidant and antimicrobial activities. Prev Nutr Food Sci 2006;11:100-4.
Shridhar M, Gopal S. Radical scavenging potential of Terminalia arjuna bark
. Int J Biotechnol Biochem 2009;5:307-17.
Boath AS, Stewart D, McDougall GJ. Berry components inhibit α-glucosidase in vitro
: synergies between acarbose and polyphenols from black currant and rowanberry. Food Chem 2012;135:929-36.
[Figure 1], [Figure 2], [Figure 3], [Figure 4]
[Table 1], [Table 2], [Table 3]