Masouda E. Amer
Alexandria University
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Featured researches published by Masouda E. Amer.
Phytochemistry | 1999
Antonio Evidente; Amina H. Abou-Donia; Fikria A. Darwish; Masouda E. Amer; Fahima F. Kassem; Hal A.m Hammoda; Andrea Motta
Abstract Two masanane-type lactone alkaloids, named nobilisitine A and B, were isolated from Egyptian Clivia nobilis and characterized by spectroscopic and chemical methods. Both compounds showed contain the same [2]benzopyrano [3,4- g ]indole ring system and therefore belong to the same subgroup of Amaryllidaceae alkaloids. In particular, nobilisitine A and B, reported as two new alkaloids, proved to be the 5 β -hydroxy-3a,11c- epi -masan-7-one and the 3-hydroxybutanoyl ester of clivonine (5a-hydroxy-5a- epi -masan-7-one), the alkaloid previously extracted from Clivia miniata and belonging to the same alkaloid subgroup. Nobilisitine B appears to be an epimer at the acyl side chain of clivatine.
Phytochemistry | 1983
Zeinab F. Mahmoud; Sawsan El-Masry; Masouda E. Amer; Jürgen Ziesche; Ferdinand Bohlmann
Abstract The aerial parts of Sonchus macrocarpus afforded, in addition to known triterpenes, two new eudesmanolides.
Phytochemistry | 1984
Zeinab F. Mahmoud; Sawsan El-Masry; Masouda E. Amer; Jürgen Ziesche; Michael Grenz
Abstract Eight sesquiterpene lactones were isolated from the roots of Sonchus macrocarpus. The eudesmanolides 15-hydroxy-4β, 15-dihydroreynosin and 15-hydroxy-4β, 15, 11β, 13-tetrahydroreynosin were isolated for the first time.
Phytochemistry | 1990
Zeinab F. Mahmoud; Masouda E. Amer; Maged S. Abdel Kader; Nabil A. Abdel-Salam
Abstract 8-(γ,γ-dimethyl-allyl)-1-Methoxycoumestrol has been isolated for the first time from the roots of Lotus creticus along with some known compounds. The new structure was elucidated by spectroscopic methods.
Phytochemistry | 1989
Masouda E. Amer; Arokia M. Abdallah; J. Jakupovic; Nabil A. Abdel Aalam
Abstract The aerial part of Carthamus mareoticus afforded, in addition to know triterpenes, two new epimeric fueopyranosides of a sesquiterpene alcohol. The structures were elucidated by spectroscopic methods.
Fitoterapia | 2016
Samah M. El Sohafy; Aly M. Metwally; Abdalla A. Omar; Masouda E. Amer; Mohamed M. Radwan; Maged S. Abdel-Kader; Sayed A. El Toumy; Mahmoud A. ElSohly
The ethanol extract of Cynara cornigera L. was fractionated and the fractions were subjected to hepatoprotective assays using Wistar albino rats at a dose of 500 and 250mg/kg. The liver injury was induced in rats using carbon tetrachloride. Biochemical parameters such as aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP) and total bilirubin were estimated as reflections of the liver condition, with silymarin as a positive control. Phytochemical investigation and chromatographic separation of the hepatoprotective fractions led to the isolation of a new sesqui-lignan namely cornigerin (1), along with eight known compounds: apigenin (2), luteolin (3), β-sitosterol glycoside (4), apigenin 7-O-β-D-glucopyranoside (5), luteolin-7-O-β-D-glucopyranoside (6), apigenin-7-O-rutinoside (7), cynarin 1,5-di-O-caffeoylquinic acid (8), and apigenin-7-O-β-D-glucuronide (9). This is the first report for the isolation of 8 and 9 from this plant.
Journal of Natural Products | 1991
Masouda E. Amer; Alan J. Freyer
Phytochemistry | 2002
Sawsan El-Masry; Masouda E. Amer; Maged S. Abdel-Kader; Hala H. Zaatout
Journal of Natural Products | 1991
Masouda E. Amer; Sawsan El-Masry; Alan J. Freyer
Planta Medica | 2002
Amina H. Abou-Donia; Masouda E. Amer; Fikria A. Darwish; Fahima F. Kassem; Hala M. Hammoda; Maged S. Abdel-Kader; Bing-Nan Zhou; David G. I. Kingston