Acylated flavonol diglucosides from Ammania auriculata
dc.Affiliation | October University for modern sciences and Arts (MSA) | |
dc.contributor.author | Nawwar M. | |
dc.contributor.author | Ayoub N. | |
dc.contributor.author | El-Raey M. | |
dc.contributor.author | Zaghloul S. | |
dc.contributor.author | Hashem A. | |
dc.contributor.author | Mostafa E. | |
dc.contributor.author | Eldahshan O. | |
dc.contributor.author | Lindequist U. | |
dc.contributor.author | Linscheid M.W. | |
dc.contributor.other | National Research Center | |
dc.contributor.other | Department of Phytochemistry and Plant Systematics | |
dc.contributor.other | El Bohooth Str. | |
dc.contributor.other | P.O. 12622 | |
dc.contributor.other | Dokki | |
dc.contributor.other | Cairo | |
dc.contributor.other | Egypt; Faculty of Pharmacy | |
dc.contributor.other | Department of Pharmacognosy | |
dc.contributor.other | Ain-Shams University | |
dc.contributor.other | Cairo | |
dc.contributor.other | Egypt; October University for Modern Sciences and Arts | |
dc.contributor.other | 6th October City | |
dc.contributor.other | Egypt; Department of Pharmacognosy | |
dc.contributor.other | Faculty of Pharmacy | |
dc.contributor.other | Institute of Pharmacy | |
dc.contributor.other | Pharmaceutical Biology | |
dc.contributor.other | Ernst-Moritz-Arndt-Universit�t Greifswald | |
dc.contributor.other | Greifswald | |
dc.contributor.other | Germany; Laboratory of Applied Analytical and Environmental Chemistry | |
dc.contributor.other | Department of Chemistry | |
dc.contributor.other | Humboldt-Universit�t zu Berlin | |
dc.contributor.other | Berlin | |
dc.contributor.other | Germany | |
dc.date.accessioned | 2020-01-09T20:42:01Z | |
dc.date.available | 2020-01-09T20:42:01Z | |
dc.date.issued | 2015 | |
dc.description | Scopus | |
dc.description.abstract | Chemical investigation of the extract of the whole Ammania auriculata plant resulted in the identification of 13 polyphenols, including the hitherto unknown flavonoids, kaempferol 3-O-?-(6?-galloylglucopyranoside)- 7-O-?-glucopyranoside, and its quercetin analogue. The structures of all isolates were elucidated by conventional methods, spectroscopic analysis, including 1D and 2D NMR, and by HRESI-MS as well. | en_US |
dc.description.uri | https://www.scimagojr.com/journalsearch.php?q=14954&tip=sid&clean=0 | |
dc.identifier.doi | https://doi.org/10.1515/znc-2014-4165 | |
dc.identifier.doi | PubMed ID 25854842 | |
dc.identifier.issn | 9395075 | |
dc.identifier.other | https://doi.org/10.1515/znc-2014-4165 | |
dc.identifier.other | PubMed ID 25854842 | |
dc.identifier.uri | https://t.ly/xREdg | |
dc.language.iso | English | en_US |
dc.publisher | Verlag der Zeitschrift fur Naturforschung | en_US |
dc.relation.ispartofseries | Zeitschrift fur Naturforschung - Section C Journal of Biosciences | |
dc.relation.ispartofseries | 70 | |
dc.subject | October University for Modern Sciences and Arts | |
dc.subject | جامعة أكتوبر للعلوم الحديثة والآداب | |
dc.subject | University of Modern Sciences and Arts | |
dc.subject | MSA University | |
dc.subject | Craniofacial Bone Engineering | |
dc.subject | Bone Engineering | |
dc.subject | Tissue Engineering | |
dc.subject | 3-O-?-(6?-O-galloylglucoside)-7-O-?-glucoside | en_US |
dc.subject | Ammania auricultata (Lythraceae) | en_US |
dc.subject | Flavonols | en_US |
dc.subject | flavonol derivative | en_US |
dc.subject | glucoside | en_US |
dc.subject | acylation | en_US |
dc.subject | carbon nuclear magnetic resonance | en_US |
dc.subject | chemical structure | en_US |
dc.subject | chemistry | en_US |
dc.subject | electrospray mass spectrometry | en_US |
dc.subject | isolation and purification | en_US |
dc.subject | Lythraceae | en_US |
dc.subject | medicinal plant | en_US |
dc.subject | phytotherapy | en_US |
dc.subject | ultraviolet spectrophotometry | en_US |
dc.subject | Acylation | en_US |
dc.subject | Carbon-13 Magnetic Resonance Spectroscopy | en_US |
dc.subject | Flavonols | en_US |
dc.subject | Glucosides | en_US |
dc.subject | Lythraceae | en_US |
dc.subject | Molecular Structure | en_US |
dc.subject | Phytotherapy | en_US |
dc.subject | Plants, Medicinal | en_US |
dc.subject | Spectrometry, Mass, Electrospray Ionization | en_US |
dc.subject | Spectrophotometry, Ultraviolet | en_US |
dc.title | Acylated flavonol diglucosides from Ammania auriculata | en_US |
dc.type | Article | en_US |
dcterms.isReferencedBy | Nawwar, M.A., Hussein, S.A., Ayoub, N.A., Hashim, A.N., El-Sharawy, R.T., Lindequist, U., Constitutive phenolics of Harpephyllum caffrum (2011) Fitoterapia, 82, pp. 1265-1271; Nawwar, M.A., Ayoub, N.A., El-Rae, M.A., Bassyouny, F., Mostafa, E.S., Al-Abd, A., Cytotoxic ellagitannins from Reaumuria vermiculata (2012) Fitoterapia, 83, pp. 1256-1266; Nawwar, M.A., Ayoub, N.A., Hussein, S.A., Hashim, A.N., El-Sharawy, R.T., Wende, K., A flavonol triglycoside and investigation of the antioxidant and cell stimulating activities of Annona muricata Linn (2012) Arch Pharmacol Res, 35, pp. 761-767; Nawwar, M.A., Swilam, N.F., Hashim, A.N., Al-Abd, A.M., Abdel-Naim, A., Lindequist, U., Cytotoxic isoferulic acid amide from Myricaria germanica (Tamaricaceae) (2013) Plant Sign Behav, 8, pp. 33-41; Taeckholm, V., (1974) Student Flora of Egypt, p. 177. , 2nd ed. Published by Cairo University; Gohar, A.A., Maatooq, G.T., Mrawan, E.M., Zaki, A.A., Takaya, Y., Two oleananes from Ammannia auriculata Willd (2012) Nat Prod Res, 26, pp. 1328-1333; Nawwar, M.A., Ayoub, N.A., El-Raey, M.A., Zaghloul, S., Hashem, A.N., Mostafa, E.S., Polyphenols in Ammania auriculata: Structures, antioxidative activity and cytotoxicity (2014) Pharmazie, 69, pp. 860-864; Parekh, J., Chanda, S., Antibacterial and phytochemical studies on twelve species of Indian medicinal plants (2007) African J Biomed Res, 10, pp. 175-181; Harborne, J.B., Williams, C.A., Identification (1975) The Flavonoids, p. 383. , Harborne JB, Mabry TJ, Mabry H, editors.. London: Chapman & Hall; Mabry, T.J., Markham, K.R., Thomas, M.B., (1969) The Systematic Identification of the Flavonoids, , New York: Springer; Collins, F.W., Bohm, B.A., Wilkins, C.K., Flavonol glycoside gallates from Tellima grandiflora (1975) Phytochemistry, 14, pp. 1099-1102; Markham, K.R., Ternai, B., Stanley, R., Geiger, H., Mabry, T.J., 13C NMR studies of flavonoids-III. Naturally occurring flavonoid glycosides and their acylated derivatives (1978) Tetrahedron, 34, pp. 1389-1397; Nawwar, M.A., Buddrus, J., Bauer, H., Dimeric phenolic constituents from the roots of Tamarix nilotica (1982) Phytochemistry, 21, pp. 1755-1758; Nawwar, M.A., Ishak, M.S., Linscheid, M.W., Buddrus, J., Leaf flavonoids of Ziziphus spina-christi (1984) Phytochemistry, 23, pp. 2110-2111; Nawwar, M.A., Hussein, S.A., Gall polyphenolics of Tamarix aphylla (1994) Phytochemistry, 36, pp. 1035-1037; Matsuda, H., Studies on the constituents of the leaves of Rhus and of some species of related genera in Japan (1966) Chem Pharm Bull, 14, pp. 877-883; Ikramov, M.T., Mavasheva, F.A., Batirov, E.K.H., Myricetin-3-O-�-dglucopyranoside (isomyricetin) (1990) Chem Nat Comp, 26, p. 226; Liu, H., Yan, M., Zhao, J., Wang, J., Zhou, L., Wang, M., Flavonoids from Halostachys caspica and antioxidant activities (2010) Molecules, 15, pp. 7933-7945; Adam, K.P., Phenolic constituents of the fern Phegopetris connectilis (1999) Phytochemistry, 52, pp. 929-934; Panthama, N., Kanokmedhakul, S., Kanokmedhakul, K., Galloyl and hexahydroxydiphenoyl esters of phenylpropanoid glucosides. Phenyl propanoids and phenylpropanoid glucosides from Rhizome of Balanophora fungosa (2009) Chem Pharm Bull, 57, pp. 1352-1355; Hatano, T., Hattori, S., Okuda, T., Coriariin A and B, new dimeric and monomeric hydrolysable tannins (1986) Chem Pharm Bull, 34, pp. 4092-4097; Nishizawa, K., Nakata, I., Kishida, Aver, W.A., Browne, L.M., Some biologically active tannins of Nuphar variegatum (1990) Phytochemistry, 29, pp. 2491-2494 | |
dcterms.source | Scopus |
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