Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Mona E, Aboutabl"'
Autor:
Alia Y. Ragheb, Marwa A. Masoud, Mona O. El Shabrawy, Mai M. Farid, Nesrine M. Hegazi, Reda S. Mohammed, Mona M. Marzouk, Mona E. Aboutabl
Publikováno v:
Scientific African, Vol 20, Iss , Pp e01672- (2023)
Although inflammation is a beneficial response to harmful triggers, the associated diseases develop the potential for death-threatening conditions. Citrus species are valuable sources of chemical compounds with diverse structural properties that coul
Externí odkaz:
https://doaj.org/article/aff057c1314344c7890e5021ef0b73ac
Publikováno v:
Bulletin of the National Research Centre, Vol 45, Iss 1, Pp 1-20 (2021)
Abstract Background Caffeine is a natural alkaloid present in a variety of highly consumed popular drinks such as coffee, tea and soft drinks as well as chocolate. Its consumption elicits beneficiary psychostimulant that has been linked to a reduced
Externí odkaz:
https://doaj.org/article/ba37efea833445eab5a3e61db40a13e3
Publikováno v:
Journal of Applied Pharmaceutical Science. :165-178
Autor:
Manal A. Hamed, Asmaa F. Aboul Naser, Amal M. El-Feky, Marwa M. Elbatanony, Sylvia E. Shaker, Dalia B. Fayed, Entesar E.S. Hassan, Sanaa A. Ali, Wagdy K.B. Khalil, Mona E. Aboutabl
Publikováno v:
Journal of Biologically Active Products from Nature. 12:254-275
Autor:
Asmaa F. Aboul Naser, Mona E Aboutabl, Wagdy K. B. Khalil, Ali M. El-Hagrassi, Wessam M Aziz, Entesar E. S. Hassan, Ayman A. Farghaly, Abeer F. Osman, Manal A. Hamed
Publikováno v:
Biomarkers. 26:788-807
Rheumatoid arthritis (RA) is a chronic, progressive autoimmune disease characterized by aggressive and systematic polyarthritis. Objective: The present study aimed to isolate and identify the phenolic constituents in Brassica oleracea L. (Brassicacea
Autor:
Mona E. Aboutabl, Waill A. Elkhateeb, Marwa A. Masoud, Ghoson M. Daba, Ahmed H. Afifi, Rehab A. Hussein
Publikováno v:
Biomedical Chromatography. 36
GC-MS and HPLC analyses of the hydromethanolic extracts of the truffles Tirmania nivea (TN) and Tirmania pinoyi (TP) revealed the presence of 18 metabolites and 11 polyphenols, respectively. In vivo, TP extract protected against subcutaneous pentylen
Autor:
Mohamed N. Aboul-Enein, Aida A. El-Azzouny, Mohamed I. Attia, Yousreya A. Maklad, Mona E. Aboutabl, Fatma Ragab, Walaa H. A. Abd El-Hamid
Publikováno v:
International Journal of Molecular Sciences, Vol 15, Iss 9, Pp 16911-16935 (2014)
Synthesis and anticonvulsant potential of certain new 6-aryl-9-substituted-6,9-diazaspiro[4.5]decane-8,10-diones (6a–l) and 1-aryl-4-substituted-1,4-diazaspiro[5.5] undecane-3,5-diones (6m–x) are reported. The intermediates 1-[(aryl)(cyanomethyl)
Externí odkaz:
https://doaj.org/article/c977f7f3c26845549ebee7dea07ee565
Autor:
Manal A, Hamed, Asmaa F, Aboul Naser, Mona E, Aboutabl, Abeer F, Osman, Entesar E S, Hassan, Wessam M, Aziz, Wagdy K B, Khalil, Ayman A, Farghaly, Ali M, El-Hagrassi
Publikováno v:
Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals. 26(8)
Rheumatoid arthritis (RA) is a chronic, progressive autoimmune disease characterized by aggressive and systematic polyarthritis.The present study aimed to isolate and identify the phenolic constituents inThe GC/MS profiling of the plant was determine
Autor:
Federica Vincenzoni, Mona E Aboutabl, Francesca Sciandra, Manuela Bozzi, Claudia Desiderio, Mohammed Farrag El-Behairy, Ahmed M. El Kerdawy, Beatrice Sampaolese, Iman A.Y. Ghannam, Rasha M. Hassan
In the current work, a series of novel 4-benzyloxy and 4-(2-phenylethoxy) chalcone fibrate hybrids (10a-o) and (11a-e) were synthesized and evaluated as new PPARα agonists in order to find new agents with higher activity and fewer side effects. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7b068875fe0f6e1bd5589110c75634c
http://hdl.handle.net/10807/184001
http://hdl.handle.net/10807/184001
Publikováno v:
Bioorganic Chemistry. 71:135-145
A series of (1-(benzyl (aryl) amino) cyclohexyl) methyl esters 7a-n were prepared and screened for their anticonvulsant profile. Screening of these esters 7a-n and their starting alcohols 6a and 6b revealed that compound 7k was the most potent one in