Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Mohamed R. E. Aly"'
Autor:
El Sayed H. El Ashry, El Sayed H. El Tamany, Mohy El Din Abdel Fattah, Mohamed R. E. Aly, Ahmed T. A. Boraei, Axel Duerkop
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 135-146 (2013)
Glycosylations of 5-(1H-indol-2-yl)-1,3,4-oxadiazoline-2(3H)-thione delivered various degrees of S- and/or N-glycosides depending on the reaction conditions. S-Glycosides were obtained regiospecifically by grinding oxadiazolinethiones with acylated
Externí odkaz:
https://doaj.org/article/a279b548eef34b5ba297cf0665e24d0a
Improvement of Metabolic and Histological Changes of Adiposity in Rats by Synthetic Oleoyl Chalcones
Autor:
Azza A. M. AlKhathami, Hosam A. Saad, Fareed A. Fareed, Eman S. El‐Shafey, Eslam S. Elsherbiny, Mamdouh R. El Nahas, Mohamed R. E. Aly
Publikováno v:
Chemistry & Biodiversity. 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6a4d3fd833871590b15ad69abe79f6e
https://doi.org/10.1002/cbdv.202200670
https://doi.org/10.1002/cbdv.202200670
Autor:
Mohy El Din Abd El Fattah, El Sayed H. El Tamany, El Sayed H. El Ashry, Ahmed T. A. Boraei, Mohamed R. E. Aly, Axel Duerkop
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 135-146 (2013)
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 135-146 (2013)
Glycosylations of 5-(1H-indol-2-yl)-1,3,4-oxadiazoline-2(3H)-thione delivered various degrees of S- and/or N-glycosides depending on the reaction conditions. S-Glycosides were obtained regiospecifically by grinding oxadiazolinethiones with acylated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62e39ee83cd3d9fc7b40c643480c6d7b
https://doi.org/10.3762/bjoc.9.16
https://doi.org/10.3762/bjoc.9.16
Autor:
Mohy El Din Abd El Fattah, Samreen Soomro, Almas Jabeen, Ahmed T. A. Boraei, El Sayed H. El Ashry, Beenish Fatima, Mohamed R. E. Aly, El Sayed H. El Tamany, Ahmed Shukrulla, Omer Mohamed Abdalla, M. Ahmed Mesaik
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry. 28:105-112
A series of S- and N-alkylated indolyloxadiazoles 2-7 were prepared. All compounds were tested for their immunomodulatory activity against T-cell proliferation, oxidative burst and cytokine analysis. Compounds 1, 2a, 2b, 2c and 2k demonstrated highly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20919e5bb901fbecaed12febf049a3e0
https://doi.org/10.3109/14756366.2011.636361
https://doi.org/10.3109/14756366.2011.636361
Publikováno v:
Synlett. 2010:2247-2250
A new class of N-2-glycosyl thiosemicarbazides has been synthesized from N-3-glycosyl oxadiazoline-thiones. Glycosylation of 5-(1H-indol-2-yl)-1,3,4-oxadiazolin-2(3H)-thione with acetylated α-glycosyl halides by grinding in the presence of basic alu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fbd0d30d95788a6b8bdd15e99804d107
https://doi.org/10.1055/s-0030-1258024
https://doi.org/10.1055/s-0030-1258024
Autor:
El Sayed H. El Ashry, Ahmed T. A. Boraei, Mohy El Din Abd El Fattah, El Sayed H. El Tamany, Mohamed R. E. Aly
Publikováno v:
Letters in Organic Chemistry. 6:462-469
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e1aad5bbeeab85d4279da7e06fce5d3
https://doi.org/10.2174/157017809789124902
https://doi.org/10.2174/157017809789124902
Autor:
Barbara Windschiegl, Ludger Johannes, Graça Raposo, Pierre Sens, Claudia Steinem, Jean-Claude Florent, Patricia Bassereau, Valérie Chambon, Winfried Römer, David Perrais, Vincent Fraisier, Ludwig Berland, Mohamed R. E. Aly, Christophe Lamaze, Danièle Tenza, Katharina Gaus
Publikováno v:
Nature. 450:670-675
Clathrin seems to be dispensable for some endocytic processes and, in several instances, no cytosolic coat protein complexes could be detected at sites of membrane invagination. Hence, new principles must in these cases be invoked to account for the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aff6e3b177c771e1224641e93da6d7f1
https://doi.org/10.1038/nature05996
https://doi.org/10.1038/nature05996
Publikováno v:
Pure and Applied Chemistry. 79:2229-2242
The structural diversity as well as the biological significance of N-acetylglucosamine-containing glycans are exemplified. The problem of forming the respective glycosidic bonds of synthetic targets is addressed. Special emphasis has been given to hu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a74dc2ec503daa9277a578ec6f64a58
https://doi.org/10.1351/pac200779122229
https://doi.org/10.1351/pac200779122229
Autor:
Mohamed R. E. Aly, Richard R. Schmidt
Publikováno v:
European Journal of Organic Chemistry. 2005:4382-4392
Glucosamine was transformed into N-diphenylmaleoyl (DPM), N-(3,3-dimethylglutaryl) (DMG), and N-diglycolyl (DG) derivatives which furnished O-acetyl-protected O-glycosyl trichloroacetimidates 3, 12, and 20, respectively, as glycosyl donors. Their rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbf46ed3fb31e430df7021b025b65ba5
https://doi.org/10.1002/ejoc.200500107
https://doi.org/10.1002/ejoc.200500107
Publikováno v:
Carbohydrate Research. 331:129-142
tert -Butyldimethylsilyl 3,6-di- O -benzyl-2-deoxy-2-dimethylmaleimido-β- d -glucopyranoside was readily transformed into the disaccharide glycosyl donor, 3,4,6-tri- O -acetyl-2-deoxy-2-dimethylmaleimido-β- d -glucopyranosyl-(1→4)-3,6-di- O -benz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f2c500b76022c152ce682236ae5685e
https://doi.org/10.1016/s0008-6215(01)00024-6
https://doi.org/10.1016/s0008-6215(01)00024-6