Cytotoxic Compounds from Aloe megalacantha
Abdissa Ayana N, Gohlke S, Frese M, Sewald N (2017)
Molecules 22(7): 1136.
Zeitschriftenaufsatz
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Abstract / Bemerkung
Phytochemical investigation of the ethyl acetate extract of the roots of Aloe megalacantha led to the isolation of four new natural products—1,8-dimethoxynepodinol (1), aloesaponarin III (2), 10-O-methylchrysalodin (3) and methyl-26-O-feruloyl-oxyhexacosanate (4)—along with ten known compounds. All purified metabolites were characterized by NMR, mass spectrometric analyses and comparison with literature data. The isolates were evaluated for their cytotoxic activity against a human cervix carcinoma cell line KB-3-1 and some of them exhibited good activity, with aloesaponarin II (IC50 = 0.98 µM) being the most active compound.
Stichworte
Asphodelaceae;
Aloe megalacantha;
roots;
quinone;
anthraquinone;
cytotoxicity
Erscheinungsjahr
2017
Zeitschriftentitel
Molecules
Band
22
Ausgabe
7
Art.-Nr.
1136
Urheberrecht / Lizenzen
ISSN
1420-3049
Finanzierungs-Informationen
Open-Access-Publikationskosten wurden durch die Deutsche Forschungsgemeinschaft und die Universität Bielefeld gefördert.
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https://pub.uni-bielefeld.de/record/2912699
Zitieren
Abdissa Ayana N, Gohlke S, Frese M, Sewald N. Cytotoxic Compounds from Aloe megalacantha. Molecules. 2017;22(7): 1136.
Abdissa Ayana, N., Gohlke, S., Frese, M., & Sewald, N. (2017). Cytotoxic Compounds from Aloe megalacantha. Molecules, 22(7), 1136. doi:10.3390/molecules22071136
Abdissa Ayana, Negera, Gohlke, Sebastian, Frese, Marcel, and Sewald, Norbert. 2017. “Cytotoxic Compounds from Aloe megalacantha”. Molecules 22 (7): 1136.
Abdissa Ayana, N., Gohlke, S., Frese, M., and Sewald, N. (2017). Cytotoxic Compounds from Aloe megalacantha. Molecules 22:1136.
Abdissa Ayana, N., et al., 2017. Cytotoxic Compounds from Aloe megalacantha. Molecules, 22(7): 1136.
N. Abdissa Ayana, et al., “Cytotoxic Compounds from Aloe megalacantha”, Molecules, vol. 22, 2017, : 1136.
Abdissa Ayana, N., Gohlke, S., Frese, M., Sewald, N.: Cytotoxic Compounds from Aloe megalacantha. Molecules. 22, : 1136 (2017).
Abdissa Ayana, Negera, Gohlke, Sebastian, Frese, Marcel, and Sewald, Norbert. “Cytotoxic Compounds from Aloe megalacantha”. Molecules 22.7 (2017): 1136.
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2019-09-06T09:18:50Z
MD5 Prüfsumme
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Daten bereitgestellt von European Bioinformatics Institute (EBI)
5 Zitationen in Europe PMC
Daten bereitgestellt von Europe PubMed Central.
Evaluation of Antimalarial Activity of the Leaf Latex and TLC Isolates from Aloe megalacantha Baker in Plasmodium berghei Infected Mice.
Hintsa G, Sibhat GG, Karim A., Evid Based Complement Alternat Med 2019(), 2019
PMID: 31110551
Hintsa G, Sibhat GG, Karim A., Evid Based Complement Alternat Med 2019(), 2019
PMID: 31110551
Antidiabetic and Antihyperlipidemic Activities of the Leaf Latex Extract of Aloe megalacantha Baker (Aloaceae) in Streptozotocin-Induced Diabetic Model.
Hammeso WW, Emiru YK, Ayalew Getahun K, Kahaliw W., Evid Based Complement Alternat Med 2019(), 2019
PMID: 31178917
Hammeso WW, Emiru YK, Ayalew Getahun K, Kahaliw W., Evid Based Complement Alternat Med 2019(), 2019
PMID: 31178917
Bioactive secondary metabolites from new endophytic fungus Curvularia. sp isolated from Rauwolfia macrophylla.
Kaaniche F, Hamed A, Abdel-Razek AS, Wibberg D, Abdissa N, El Euch IZ, Allouche N, Mellouli L, Shaaban M, Sewald N., PLoS One 14(6), 2019
PMID: 31247016
Kaaniche F, Hamed A, Abdel-Razek AS, Wibberg D, Abdissa N, El Euch IZ, Allouche N, Mellouli L, Shaaban M, Sewald N., PLoS One 14(6), 2019
PMID: 31247016
In vitro α-amylase inhibitory effect of TLC isolates of Aloe megalacantha baker and Aloe monticola Reynolds.
Tekulu GH, Araya EM, Mengesha HG., BMC Complement Altern Med 19(1), 2019
PMID: 31391018
Tekulu GH, Araya EM, Mengesha HG., BMC Complement Altern Med 19(1), 2019
PMID: 31391018
Aloe Genus Plants: From Farm to Food Applications and Phytopharmacotherapy.
Salehi B, Albayrak S, Antolak H, Kręgiel D, Pawlikowska E, Sharifi-Rad M, Uprety Y, Tsouh Fokou PV, Yousef Z, Amiruddin Zakaria Z, Varoni EM, Sharopov F, Martins N, Iriti M, Sharifi-Rad J., Int J Mol Sci 19(9), 2018
PMID: 30235891
Salehi B, Albayrak S, Antolak H, Kręgiel D, Pawlikowska E, Sharifi-Rad M, Uprety Y, Tsouh Fokou PV, Yousef Z, Amiruddin Zakaria Z, Varoni EM, Sharopov F, Martins N, Iriti M, Sharifi-Rad J., Int J Mol Sci 19(9), 2018
PMID: 30235891
31 References
Daten bereitgestellt von Europe PubMed Central.
The Taxonomy of Aloinella, Guillauminia and Lemee (Aloaceae)
Smith G.F., Vanwyk B.E., Mossmer M., Viljoen A.., 1995
Smith G.F., Vanwyk B.E., Mossmer M., Viljoen A.., 1995
Reynolds G.W.., 1966
Demisew S., Nordan I.., 2010
Carter S.., 1994
Folk uses and commercial exploitation of the Aloe leaf pulp
Morton J.F.., 1961
Morton J.F.., 1961
Neoaloesin A: a new C-glucofuranosyl chromone from Aloe barbadensis.
Park MK, Park JH, Shin YG, Kim WY, Lee JH, Kim KH., Planta Med. 62(4), 1996
PMID: 17252472
Park MK, Park JH, Shin YG, Kim WY, Lee JH, Kim KH., Planta Med. 62(4), 1996
PMID: 17252472
Aloe vera leaf gel: a review update.
Reynolds T, Dweck AC., J Ethnopharmacol 68(1-3), 1999
PMID: 10624859
Reynolds T, Dweck AC., J Ethnopharmacol 68(1-3), 1999
PMID: 10624859
Formation of tetrahydroanthracene glucosides by Callus tissue of Aloe saponaria
Yagi A., Shoyama Y., Nishioki I.., 1973
Yagi A., Shoyama Y., Nishioki I.., 1973
Antimalarial compounds from Kniphofia foliosa roots.
Wube AA, Bucar F, Asres K, Gibbons S, Rattray L, Croft SL., Phytother Res 19(6), 2005
PMID: 16114082
Wube AA, Bucar F, Asres K, Gibbons S, Rattray L, Croft SL., Phytother Res 19(6), 2005
PMID: 16114082
Antitumor properties and modulation of antioxidant enzymes' activity by Aloe vera leaf active principles isolated via supercritical carbon dioxide extraction.
El-Shemy HA, Aboul-Soud MA, Nassr-Allah AA, Aboul-Enein KM, Kabash A, Yagi A., Curr. Med. Chem. 17(2), 2010
PMID: 19941474
El-Shemy HA, Aboul-Soud MA, Nassr-Allah AA, Aboul-Enein KM, Kabash A, Yagi A., Curr. Med. Chem. 17(2), 2010
PMID: 19941474
Cytotoxic quinones from the roots of Aloe dawei.
Abdissa N, Induli M, Fitzpatrick P, Alao JP, Sunnerhagen P, Landberg G, Yenesew A, Erdelyi M., Molecules 19(3), 2014
PMID: 24642911
Abdissa N, Induli M, Fitzpatrick P, Alao JP, Sunnerhagen P, Landberg G, Yenesew A, Erdelyi M., Molecules 19(3), 2014
PMID: 24642911
Knipholonecyclooxanthrone and an anthraquinone dimer with antiplasmodial activities from the roots of Kniphofia foliosa
Abdissa N., Induli M., Akala H.M., Heydenreich M., Midiwo J.O., Ndakala A., Yenesew A.., 2013
Abdissa N., Induli M., Akala H.M., Heydenreich M., Midiwo J.O., Ndakala A., Yenesew A.., 2013
A xanthone and a phenylanthraquinone from the roots of Bulbine frutescens, and the revision of six seco-anthraquinones into xanthones
Abdissa N., Heydenreich M., Midiwo J.O., Ndakala A., Majer Z., Neumann B., Stammler H., Sewald N., Yenesew A.., 2014
Abdissa N., Heydenreich M., Midiwo J.O., Ndakala A., Majer Z., Neumann B., Stammler H., Sewald N., Yenesew A.., 2014
New bianthraquinone pigments from Kniphofia species
Dagne E., Berhanu E., Steglich W.., 1987
Dagne E., Berhanu E., Steglich W.., 1987
Bianthrones from Senna longiracemosa
Alemayehu G., Abegaz B., Snatzke G., Duddeck H.., 1993
Alemayehu G., Abegaz B., Snatzke G., Duddeck H.., 1993
7-Hydroxy-4-methoxy-5-methylcoumarin: A Further 5-Methylcoumarin from Toonaciliata (Meliaceae)
Chowdhury R., Ahmed A., Rahman M.Z.., 2004
Chowdhury R., Ahmed A., Rahman M.Z.., 2004
Anthraquinones as taxonomic markers in Ethiopian Kniphofia species
Berhanu E., Fetene M., Dagne E.., 1986
Berhanu E., Fetene M., Dagne E.., 1986
Studies on the constituents of Aloe saponaria
Yagi A., Makino K., Nishioka I.., 1977
Yagi A., Makino K., Nishioka I.., 1977
Chemistry of Aloe Species
Dagne E., Bisrat D., Viljoen A., Van B.E.., 2000
Dagne E., Bisrat D., Viljoen A., Van B.E.., 2000
Studies on the constituents of Aloe saponaria HAW. I. The structures of tetrahydroanthracene derivatives and the related anthraquinones
Yagi A., Makino K., Nishioki I.., 1974
Yagi A., Makino K., Nishioki I.., 1974
Aloechrysone, a dihydroanthracenone from Aloe berhana
Dagne E., Casser I., Steglich W.., 1992
Dagne E., Casser I., Steglich W.., 1992
Studies on the constituents of Aloe saponaria HAW. I. The structure of bianthraquinoid pigments
Yagi A., Makino K., Nishioki I.., 1978
Yagi A., Makino K., Nishioki I.., 1978
(R)-Prechrysophanol from Aloe graminicola
Yenesew A., Ogur J.A., Duddeck H.., 1993
Yenesew A., Ogur J.A., Duddeck H.., 1993
Anthraquinones, pre-anthraquinones and isoeleutherol in the roots of Aloe species
Dagne E., Yenesew A., Asmellash S., Demissew S., Mavi S.., 1994
Dagne E., Yenesew A., Asmellash S., Demissew S., Mavi S.., 1994
Chemistry of the Coccoidea: Synthesis of the ancient dyestuff kermesic acid and of related anthraquinones
Cameron D.W., Deutscher D.J., Feutrill G.I., Griffiths P.G.., 1981
Cameron D.W., Deutscher D.J., Feutrill G.I., Griffiths P.G.., 1981
Three dimeric anthracene derivatives from the fruits of Bulbine abyssinica
Wanjohi J.M., Yenesew A., Midiwo J.O., Heydenreich M., Peter M.G., Dreyer M., Reichert M., Bringmann G.., 2005
Wanjohi J.M., Yenesew A., Midiwo J.O., Heydenreich M., Peter M.G., Dreyer M., Reichert M., Bringmann G.., 2005
ω-Feruloyloxy acids: a novel class of polar lipids in peat soil
Ries-Kautt M., Kintzinger P.J., Albrecht P.., 1988
Ries-Kautt M., Kintzinger P.J., Albrecht P.., 1988
Anti-liver cancer constituents from the thorns of Gleditsia sinensis
Yu J.Q., Xian Y.X., Geng Y.L., Wang D.J., Zhoub H.L., Wang X.., 2015
Yu J.Q., Xian Y.X., Geng Y.L., Wang D.J., Zhoub H.L., Wang X.., 2015
Approaches for the synthesis of functionalized cryptophycins.
Sammet B, Bogner T, Nahrwold M, Weiss C, Sewald N., J. Org. Chem. 75(20), 2010
PMID: 20857920
Sammet B, Bogner T, Nahrwold M, Weiss C, Sewald N., J. Org. Chem. 75(20), 2010
PMID: 20857920
The metabolism and toxicity of quinones, quinonimines, quinone methides, and quinone-thioethers.
Monks TJ, Jones DC., Curr. Drug Metab. 3(4), 2002
PMID: 12093358
Monks TJ, Jones DC., Curr. Drug Metab. 3(4), 2002
PMID: 12093358
Nitrogen-containing heterocyclic quinones: a class of potential selective antitumor agents.
Garuti L, Roberti M, Pizzirani D., Mini Rev Med Chem 7(5), 2007
PMID: 17504183
Garuti L, Roberti M, Pizzirani D., Mini Rev Med Chem 7(5), 2007
PMID: 17504183
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