Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Faida H. Bamanie"'
Autor:
Mohamed Ayman El-Zahabi, Faida H. Bamanie, Salah Ghareeb, Heba K. Alshaeri, Moudi M. Alasmari, Mohamed Moustafa, Zohair Al-Marzooki, Mohamed F. Zayed
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 17; Pages: 9605
New quinazoline-sulfonylurea hybrids were prepared and examined for their in vivo anti-hyperglycemic activities in STZ-induced hyperglycemic rats using glibenclamide as a reference drug. Compounds VI-6-a, V, IV-4, VI-4-c, IV-6, VI-2-a, IV-1, and IV-2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be933d6da9ae902f89cab1eae286fb22
Autor:
Diaa T. A. Youssef, Lamiaa A. Shaala, Gamal A. Mohamed, Jihan M. Badr, Faida H. Bamanie, Sabrin R. M. Ibrahim
Publikováno v:
Marine Drugs, Vol 12, Iss 4, Pp 1911-1923 (2014)
In our search for bioactive metabolites from marine organisms, we have investigated the polar fraction of the organic extract of the Red Sea sponge Theonella swinhoei. Successive chromatographic separations and final HPLC purification of the potent a
Externí odkaz:
https://doaj.org/article/dc8b5d685391428cb6cdd62e0ba51b87
Autor:
Faida H. Bamanie, Jihan M. Badr, Diaa T. A. Youssef, Gamal A. Mohamed, Sabrin R.M. Ibrahim, Lamiaa A. Shaala
Publikováno v:
Phytochemistry Letters. 13:212-217
Investigation of the Red Sea marine tunicate Symplegma rubra Monniot, 1972 gave three new purine alkaloids namely 6-methoxy-7,9-dimethyl-8-oxoguanine ( 1 ), 6-methoxy-9-methyl-8-oxoguanine ( 2 ), and 2-methoxy-7-methyl-8-oxoadenine ( 4 ) together wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::780f7ee3c7f60ba49d7b7487b9e29346
https://doi.org/10.1016/j.phytol.2015.06.012
https://doi.org/10.1016/j.phytol.2015.06.012
Publikováno v:
Phytochemistry Letters. 12:296-301
In continuation of our efforts to identify bioactive compounds from the Red Sea marine sponges, we have recently investigated the organic extract of the sponge Biemna ehrenbergi . This study resulted in the isolation of eight compounds including a ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee15b85cb011cd7c7d737aca7cfd97d4
https://doi.org/10.1016/j.phytol.2015.04.024
https://doi.org/10.1016/j.phytol.2015.04.024
Autor:
Mohamed El-Zahabi, Faida H. Bamanie, Eman R. El-Bendary, Salah A. Ghareib, Ibrahim H. Eissa, Mohamed F. Radwan
Publikováno v:
Bioorganic Chemistry. 91:103115
New series of phthalimide-sulfonylurea hybrids were prepared and examined for their in vivo anti-hyperglycemic activities in STZ-induced hyperglycemic rats using glibenclamide as a reference drug. Compounds 6c, 6d, 6g, 6h, 6j and 6k induced significa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da6690e7584f36793e4ab8a23c194c9e
https://doi.org/10.1016/j.bioorg.2019.103115
https://doi.org/10.1016/j.bioorg.2019.103115
Publikováno v:
Medicinal Chemistry Research. 21:75-84
Certain new nitrogen-substituted derivatives of cyclic imides phthalimide (a), 1,8-naphthalimide (b), and diphenimide (c), were synthesized aiming to obtain potent hypolipidemic agents. Thus, 2-(N-imido) propanoic acids, 2-(N-phthalimido)-2-methylpro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d17154e5f5961dacd068303ae32269ad
https://doi.org/10.1007/s00044-010-9492-1
https://doi.org/10.1007/s00044-010-9492-1
Autor:
Mohamed A. Moustafa, Faida H. Bamanie, Laila M. Gad, Abdulkhader M. Ismaiel, Salah A. Ghareib
Publikováno v:
Medicinal Chemistry Research. 20:381-387
Modeling studies demonstrate that aryl piperazines (I), aryloxyalkylamines (II), phenylalkykamines (III) and indolylalkylamines (VI) may interact at 5-HT receptors in a similar manner. Examination of these structures (I–VI) reveals that all possess
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01f1abc49ff1d40b6f6ff8bc61a43de3
https://doi.org/10.1007/s00044-010-9316-3
https://doi.org/10.1007/s00044-010-9316-3
Autor:
Laila M. Gad, Salah A. Ghareib, Abdulkhader M. Ismaiel, Mohamed A. Moustafa, Faida H. Bamanie
Publikováno v:
Medicinal Chemistry Research. 18:745-757
Most h5-HT1B serotonin subreceptors agonists bind with high affinity but low selectivity. Aryloxyalkylamines are a curious exception. In this investigation a new series of aryloxyalkylamines (4–7, 10, 11) was designed and synthesized in which the n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62f1996ab0ae7f5f01d770ea13585637
https://doi.org/10.1007/s00044-009-9164-1
https://doi.org/10.1007/s00044-009-9164-1
Autor:
El-Zahabi, Mohamed Ayman1 (AUTHOR) malzahaby@azhar.edu.eg, Bamanie, Faida H.2 (AUTHOR), Ghareeb, Salah3 (AUTHOR), Alshaeri, Heba K.4 (AUTHOR), Alasmari, Moudi M.5,6 (AUTHOR), Moustafa, Mohamed7 (AUTHOR), Al-Marzooki, Zohair2 (AUTHOR), Zayed, Mohamed F.1,4 (AUTHOR) malzahaby@azhar.edu.eg
Publikováno v:
International Journal of Molecular Sciences. Sep2022, Vol. 23 Issue 17, p9605. 23p.
Publikováno v:
Medicinal Chemistry Research; Dec2009, Vol. 18 Issue 9, p745-757, 13p