Mahmoud A. Ramadan
Assiut University
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Featured researches published by Mahmoud A. Ramadan.
Phytochemistry | 1998
Diaa T. A. Youssef; Mahmoud A. Ramadan; A.A. Khalifa
Abstract The ethanolic extract of fresh flowering bulbs of Pancratium maritimum L. yielded a new chromone, maritimin, two new polyoxygenated acetophenones, together with the flavonoids syzalterin, (−)-farrerol and (−)-liquiritigenin, and the chalcone isoliquiritigenin. The structures of the isolated compounds were determined through spectral analyses including NMR and MS studies.
Phytochemistry | 1981
A. A. Ali; Horst Kating; August W. Frahm; A.M. El-Moghazi; Mahmoud A. Ramadan
Abstract Several alkaloids were isolated from Crinum augustum grown in Assiut, Egypt. Two were identified as lycorine and buphanisine. In addition two new non-hydroxylated alkaloids of identical molecular formula C 17 H 19 NO 4 were investigated by spectroscopic methods. The gross structure of the first, termed augustine, belongs to the 1,2-epoxy-5, 10-b-ethanophenanthridine-type. In contrast the second could not be related to any of the known alkaloid types of the Amaryllidaceae.
Medicinal Chemistry Research | 2015
John Refaat; Mamdouh N. Samy; Samar Desoukey; Mahmoud A. Ramadan; Sachiko Sugimoto; Katsuyoshi Matsunami; Mohamed S. Kamel
From the flowers of Chorisia chodatii Hassl. (family: Bombacaceae), seventeen compounds were isolated and identified, including: two sterols, β-sitosterol (1) and β-sitosterol 3-O-β-D-glucopyranoside (10); two furanoids, 5-hydroxymethyl furfural (3) and (3R,4R,5S)-3,4-dihydroxy-5-methyl-dihydrofuran-2-one (12); two coumarins, scopoletin (8) and aesculetin (9); four phenolic acids and esters, ethyl vanillate (4), vanillic acid (5), protocatechuic acid ethyl ester (6) and p-hydroxy benzoic acid (7); five flavonoids, kaempferol 3-O-β-D-(6″-acetyl)-glucopyranoside (13), kaempferol 3-O-β-D-(6″-E-p-coumaroyl)-glucopyranoside (14), kaempferol 3-O-β-D-glucopyranoside (15), luteolin 7-O-β-D-glucopyranoside (16) and apigenin 7-O-neohesperidoside (17), in addition to mono-octyl phthalate (2) and succinic acid (11). All the isolated metabolites were reported for the first time from this plant, and among them, compounds (3), (4), (6), (7), (12) and (13) were isolated for the first time from family Bombacaceae. Besides, this is the first report for isolation of (2) in a pure form from a natural source. These phytochemical data revealed important chemotaxonomic value and may broaden the use of this plant in future phytotherapy. Moreover, all of the obtained phytocompounds were evaluated for their DPPH free radical scavenging properties and cytotoxic activities against the human lung cancer cell line A549.
Phytochemistry | 2000
Mahmoud A. Ramadan; Mohamed S. Kamel; Kazuhiro Ohtani; Ryoji Kasai; Kazuo Yamasaki
Planta Medica | 1991
M. A. Abd El Hafiz; Mahmoud A. Ramadan; M. L. Jung; J. P. Beck; R. Anton
Magnetic Resonance in Chemistry | 1985
August W. Frahm; A. A. Ali; Mahmoud A. Ramadan
Pharmaceutical Biology | 2013
John Refaat; Samar Y. Desoky; Mahmoud A. Ramadan; Mohamed S. Kamel
International Journal of Pharmaceutical Sciences and Research | 2012
John Refaat; Mohamed S. Kamel; Mahmoud A. Ramadan; A. A. Ali
Pharmacognosy Research | 2009
John Refaat; Ahmed Abdel-Lateff; Mohamed S. Kamel; A. A. Ali; Mahmoud A. Ramadan; Tatsufumi Okino; Yasuyuki Nogata
Phytochemistry Letters | 2015
John Refaat Fahim; Ghada Abd El-Moneim Hegazi; Reda El-Said Abo El-Fadl; Mohamed Reda Abd Almegid Abd Alhady; Samar Yehia Desoukey; Mahmoud A. Ramadan; Mohamed S. Kamel