Antioxidant activity and molecular docking study of Erythrin neillii polyphenolics
dc.Affiliation | October University for modern sciences and Arts (MSA) | |
dc.contributor.author | Gabr S.K. | |
dc.contributor.author | Bakr R.O. | |
dc.contributor.author | Mostafa E.S. | |
dc.contributor.author | El-Fishawy A.M. | |
dc.contributor.author | El-Alfy T.S. | |
dc.contributor.other | Department of Pharmacognosy | |
dc.contributor.other | Faculty of Pharmacy | |
dc.contributor.other | October University for Modern Sciences and Arts | |
dc.contributor.other | Giza | |
dc.contributor.other | 11787 | |
dc.contributor.other | Egypt; Department of Pharmacognosy | |
dc.contributor.other | Faculty of Pharmacy | |
dc.contributor.other | Cairo University | |
dc.contributor.other | Cairo | |
dc.contributor.other | 11562 | |
dc.contributor.other | Egypt | |
dc.date.accessioned | 2020-01-09T20:40:40Z | |
dc.date.available | 2020-01-09T20:40:40Z | |
dc.date.issued | 2019 | |
dc.description | Scopus | |
dc.description | MSA Google Scholar | |
dc.description.abstract | Species of genus Erythrina have a great contribution in folk medicine; various species are utilized as a tranquilizer, to treat insomnia, inflammation and colic. Besides, Erythrina species have reported antioxidant, hepatoprotective and anxiolytic activities. Erythrina neillii is a hybrid obtained through a cross between E. herbacea L. and E. humeana Spreng. It has not been well-studied for its chemical or biological profile; therefore it represents an interesting field of study. In this study, seven phenolic compounds; two hydrolysable tannins (1,3), one phenolic acid (2) and four known flavonoids (4�7) were isolated and characterized for the first time in E neillii and Erythrina genus except for vitexin (7). Isolated compounds were assessed for their antioxidant activities using ORAC assay. 2?-O-galloyl orientin (6) exhibited the highest activity followed by 2?-O-galloyl vitexin (5). Flexible molecular docking on heme oxygenase, an important stress protein that is involved in cellular protection, antioxidant and anti-inflammatory activities, justified the antioxidant activity of the isolated compounds. The best scoring was observed with 2?-O-galloyl orientin forming four binding interactions with residues, Arg 136 (two interactions), Met34 and Gly139. Erythrina neillii offered powerful and available antioxidant beside significantly active phytoconstituents. 2018 South African Association of Botanists | en_US |
dc.description.uri | https://www.scimagojr.com/journalsearch.php?q=17257&tip=sid&clean=0 | |
dc.identifier.doi | https://doi.org/10.1016/j.sajb.2018.12.011 | |
dc.identifier.doi | PubMed ID : | |
dc.identifier.issn | 2546299 | |
dc.identifier.other | https://doi.org/10.1016/j.sajb.2018.12.011 | |
dc.identifier.other | PubMed ID : | |
dc.identifier.uri | https://t.ly/b2jYZ | |
dc.language.iso | English | en_US |
dc.publisher | Elsevier B.V. | en_US |
dc.relation.ispartofseries | South African Journal of Botany | |
dc.relation.ispartofseries | 121 | |
dc.subject | Docking | en_US |
dc.subject | Erythrina neillii | en_US |
dc.subject | Heme oxygenase | en_US |
dc.subject | ORAC | en_US |
dc.subject | Polyphenolics | en_US |
dc.subject | antioxidant | en_US |
dc.subject | biochemistry | en_US |
dc.subject | cell | en_US |
dc.subject | chemical binding | en_US |
dc.subject | enzyme | en_US |
dc.subject | enzyme activity | en_US |
dc.subject | herb | en_US |
dc.subject | molecular analysis | en_US |
dc.subject | phenolic compound | en_US |
dc.subject | protein | en_US |
dc.subject | tannin | en_US |
dc.subject | Erythrina herbacea | en_US |
dc.title | Antioxidant activity and molecular docking study of Erythrin neillii polyphenolics | en_US |
dc.type | Article | en_US |
dcterms.isReferencedBy | Agrawal, P.K., Bansal, M.C., Porter, L.J., Foo, L.Y., Carbon-13NMR of flavonoids (1989) Studies in Inorganic Chemistry.; Alves, C.Q., David, J.M., David, J.P., Villareal, C.F., Soares, M.B.P., De Queiroz, L.P., Aguiar, R.M., Flavonoids and other bioactive phenolics isolated from Cenostigma macrophyllum (Leguminosae) (2012) Quimica Nova, 35, pp. 1137-1140; Anupama, V., Narmadha, R., Gopalakrishnan, V.K., Devaki, K., Enzymatic alteration in the vital organs of streptozotocin diabetic rats treated with aqueous extract of Erythrina variegata bark (2012) International Journal of Pharmacy and Pharmaceutical Sciences, 4, pp. 134-147; Barbagallo, I., Galvano, F., Frigiola, A., Cappello, F., Riccioni, G., Murabito, P., D'Orazio, N., Li Volti, G., Potential therapeutic effects of natural heme oxygenase-1 inducers in cardiovascular diseases (2012) Antioxidants & Redox Signaling; Brewer, M.S., Natural antioxidants: sources, compounds, mechanisms of action, and potential applications (2011) Comprehensive Reviews in Food Science and Food Safety, 10, pp. 221-247; Callejon, D.R., Riul, T.B., Feitosa, L.G.P., Guaratini, T., Silva, D.B., Adhikari, A., Shrestha, R.L.S., Lopes, N.P., Leishmanicidal evaluation of tetrahydroprotoberberine and spirocyclic Erythrina-alkaloids (2014) Molecules, 19, pp. 5692-5703; Chacha, M., Bojase-Moleta, G., Majinda, R.R.T., Antimicrobial and radical scavenging flavonoids from the stem wood of Erythrina latissima (2005) Phytochemistry, 66, pp. 99-104; Chang, Q., Su, M.H., Chen, Q.X., Zeng, B.Y., Li, H.H., Wang, W., Physicochemical properties and antioxidant capacity of Chinese olive (Canarium album L.) Cultivars (2017) Journal of Food Science, 82, pp. 1369-1377; Chhabra, S.C., Uiso, F.C., Mshiu, E.N., Phytochemical screening of Tanzanian medicinal plants. I (1984) Journal of Ethnopharmacology, 11, pp. 157-179; Choi, A.M.K., Alam, J., Heme oxygenase-1: function, regulation, and implication of a novel stress-inducible protein in oxidant-induced lung injury (1996) American Journal of Respiratory Cell and Molecular Biology, 15, pp. 9-19; Dimitri? Markovi?, J.M., Pejin, B., Milenkovi?, D., Ami?, D., Begovi?, N., Mojovi?, M., Markovi?, Z.S., Antiradical activity of delphinidin, pelargonidin and malvin towards hydroxyl and nitric oxide radicals: the energy requirements calculations as a prediction of the possible antiradical mechanisms (2017) Food Chemistry, 218, pp. 440-446; El-Masry, S., Hammoda, H.M., Radwan, M.M., Ross, S.A., Zaatout, H.H., C-flavonoidal glycosides from Erythrina caffra flowers (2010) Natural Product Sciences, 16, pp. 217-222; Fortes, G.A.C., Carvalho, A.G., Ramalho, R.R.F., da Silva, A.J.R., Ferri, P.H., Santos, S.C., Antioxidant activities of hydrolysable tannins and flavonoid glycosides isolated from Eugenia uniflora L (2015) Records of Natural Products, 9, pp. 251-256; Gabr, S.K., Bakr, R.O., Elshishtawy, H.M., El-Fishawy, A.M., El-Alfy, T.S., Botanical and genetic characters of Erythrina neillii cultivated in Egypt (2017) Revista Brasileira de Farmacognosia, 27, pp. 273-281; Garca-Mateos, R., Soto-Hernndez, M., Vibrans, H., Erythrina americana miller (Colorn; Fabaceae), a versatile resource from Mexico: a review (2001) Economic Botany, 55, pp. 391-400; Ghosal, S., Dutta, S.K., Bhattacharya, S.K., Erythrina chemical and pharmacological evaluation II: alkaloids of Erythrina variegata L (1972) Journal of Pharmaceutical Sciences, 61, pp. 1274-1277; Huang, D., Ou, B., Hampsch-Woodill, M., Flanagan, J.A., Deemer, E.K., Development and validation of oxygen radical absorbance capacity assay for lipophilic antioxidants using randomly methylated B-cyclodextrin as the solubility enhancer (2002) Journal of Agricultural and Food Chemistry, 50, pp. 1815-1821; Kapitulnik, J., Gonzalez, F.J., Bilirubin: an endogenous product of heme degradation with both cytotoxic and cytoprotective properties (2004) Molecular Pharmacology, 66, pp. 773-779; Karamac, M., Kosiska, A., Pegg, R.B., Comparison of radical-scavenging activities for selected phenolic acids (2005) Polish Journal of Food and Nutrition Sciences, 14, pp. 165-169; Kosalec, I., Bakmaz, M., Pepeljnjak, S., Vladimir-Knezevi?, S., Quantitative analysis of the flavonoids in raw propolis from northern Croatia (2004) Acta Pharmaceutica, 54, pp. 65-72; Latt, K.P., Ferreira, D., Venkatraman, M.S., Kolodziej, H., O-galloyl-C-glycosylflavones from Pelargonium reniforme (2002) Phytochemistry, 59, pp. 419-424; Li, T., Bonkovsky, H.L., Guo, J., Structural analysis of heme proteins: implications for design and prediction (2011) BMC Structural Biology, 11, p. 13; Lian, T.W., Wang, L., Lo, Y.H., Huang, I.J., Wu, M.J., Fisetin, morin and myricetin attenuate CD36 expression and oxLDL uptake in U937-derived macrophages (2008) Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids, 1781, pp. 601-609; Majinda, R.R.T., Wanjala, C.C.W., Juma, B.F., Bioactive non-alkaloidal constituents from the genus Erythrina (2005) Studies in Natural Products Chemistry, 32, pp. 821-853; Marzouk, M.S., Moharram, F.A., El Dib, R.A., El-Shenawy, S.M., Tawfike, A.F., Polyphenolic profile and bioactivity study of Oenothera speciosa nutt. aerial parts (2009) Molecules, 14, pp. 1456-1467; Nawwar, M.A.M., Souleman, A.M.A., Buddrus, J., Linscheid, M., Flavonoids of the flowers of Tamarix nilotica (1984) Phytochemistry, 23, pp. 2347-2349; Nawwar, M.A.M., Hussein, S.A.M., Merfort, I., NMR spectral analysis of polyphenols from Punica granatum (1994) Phytochemistry, 36, pp. 793-798; Nawwar, M., Ayoub, N., Hussein, S., Hashim, A., El-Sharawy, R., Wende, K., Harms, M., Lindequist, U., A flavonol triglycoside and investigation of the antioxidant and cell stimulating activities of Annona muricata Linn (2012) Archives of Pharmacal Research, 35, pp. 761-767; Neill, D.A., Experimental studies on species relationships in Erythrina (Leguminosae: Papilionoideae) (1988) Annals of the Missouri Botanical Garden, 75, pp. 886-969; Nkengfack, A.E., Azebaze, A.G.B., Waffo, A.K., Fomum, Z.T., Meyer, M., Van Heerden, F.R., Cytotoxic isoflavones from Erythrina indica (2001) Phytochemistry, 58, pp. 1113-1120; Pae, H.O., Son, Y., Kim, N.H., Jeong, H.J., Chang, K.C., Chung, H.T., Role of heme oxygenase in preserving vascular bioactive NO (2010) Nitric Oxide Biology and Chemistry, 23, pp. 251-257; Prez, A.J., Hassan, E.M., Pecio, ?., Omer, E.A., Kucinska, M., Murias, M., Stochmal, A., Triterpenoid saponins and C-glycosyl flavones from stem bark of Erythrina abyssinica Lam and their cytotoxic effects (2015) Phytochemistry Letters, 13, pp. 59-67; Rabe, C., Steenkamp, J.A., Joubert, E., Burger, J.F.W., Ferreira, D., Phenolic metabolites from rooibos tea (Aspalathus linearis) (1994) Phytochemistry, 35, pp. 1559-1565; Rahman, M.N., Vukomanovic, D., Vlahakis, J.Z., Szarek, W.A., Nakatsu, K., Jia, Z., Structural insights into human heme oxygenase-1 inhibition by potent and selective azole-based compounds (2012) Journal of the Royal Society Interface, 10, p. 20120697; Repetto, G., del Peso, A., Zurita, J.L., Neutral red uptake assay for the estimation of cell viability/cytotoxicity (2008) Nature Protocols, 3, pp. 1125-1131; Sellappan, S., Akoh, C.C., Krewer, G., Phenolic compounds and antioxidant capacity of Georgia-grown blueberries and blackberries (2002) Journal of Agricultural and Food Chemistry, 50, pp. 2432-2438; Setti-Perdig�o, P., Serrano, M.A.R., Flausino, O.A., Bolzani, V.S., Guimar�es, M.Z.P., Castro, N.G., Erythrina mulungu alkaloids are potent inhibitors of neuronal nicotinic receptor currents in mammalian cells (2013) PLoS One, 8; Slimestad, R., Andersen, O.M., Francis, G.W., Marston, A., Hostettmann, K., Syringetin 3-O-(6?-acetyl)-beta-glucopyranoside and other flavonols from needles of Norway spruce, picea-abies (1995) Phytochemistry, 40, pp. 1537-1542; Son, Y., Lee, J.H., Chung, H.T., Pae, H.O., Therapeutic roles of heme oxygenase-1 in metabolic diseases: curcumin and resveratrol analogues as possible inducers of heme oxygenase-1 (2013) Oxidative Medicine and Cellular Longevity, 2013, p. 639541; Tanaka, T., Nonaka, G., Nishioka, I., Tannins and related compounds. XLII. Isolation and characterization of four new hydrolyzable tannins, terflavins A and B, tergallagin and tercatain from the leaves of Terminalia catappa L (1986) Chemical & Pharmaceutical Bulletin, 34, pp. 1039-1049; Valko, M., Leibfritz, D., Moncol, J., Cronin, M.T.D., Mazur, M., Telser, J., Free radicals and antioxidants in normal physiological functions and human disease (2007) The International Journal of Biochemistry & Cell Biology, 39, pp. 44-84; Wanjala, C.C.W., Majinda, R.R.T., Two novel glucodienoid alkaloids from Erythrina latissima seeds (2000) Journal of Natural Products, 63, pp. 871-873; Yenesew, A., Derese, S., Irungu, B., Midiwo, J.O., Waters, N.C., Liyala, P., Akala, H., Peter, M.G., Flavonoids and isoflavonoids with antiplasmodial activities from the root bark of Erythrina abyssinica (2003) Planta Medica, 69, pp. 658-661 | |
dcterms.source | Scopus |
Files
Original bundle
1 - 1 of 1
Loading...
- Name:
- avatar_scholar_128.png
- Size:
- 2.73 KB
- Format:
- Portable Network Graphics
- Description: