Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Nadia A. Khalil"'
Autor:
Nadia A. Khalil, Eman M. Ahmed, Ashraf F. Zaher, Eman A. Sobh, Samiha A. El-Sebaey, Mona S. El-Zoghbi
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 36, Iss 1, Pp 1839-1859 (2021)
A series of [1]benzothieno[2,3-c]pyridines was synthesised. Most compounds were chosen by NCI-USA to evaluate their anticancer activity. Compounds 5a–c showed prominent growth inhibition against most cell lines. 5c was selected at five dose concent
Externí odkaz:
https://doaj.org/article/7fd1385ad8224361afb139d530aa8210
Autor:
Nadia A. Khalil, Eman M. Ahmed, Ashraf F. Zaher, Shimaa M. Alhamaky, Nada Osama, Mona S. El-Zoghbi
Publikováno v:
Bioorganic Chemistry. 137:106638
Publikováno v:
Bangladesh Journal of Pharmacology, Vol 11, Iss 4 (2016)
The aim of the present study was to examine the involvement of skin bacteria in the pathogenesis of keratosis. Skin swab of five different sites (palm, dorsum of the hand, chest, axilla and alar crease) from arsenic unexposed volunteer (n = 15), arse
Externí odkaz:
https://doaj.org/article/424ab5c6596f46c1aee4b66ebb11ed43
Publikováno v:
Drug development researchREFERENCES. 83(5)
New cytotoxic agents based on benzothienopyrimidine scaffold were designed, synthesized, and evaluated against the MCF-7 breast cancer line in comparison to erlotinib and letrozole as reference drugs. Eight compounds demonstrated up to 20-fold higher
Publikováno v:
Pakistan Veterinary Journal, Vol 33, Iss 1, Pp 41-44 (2013)
The present study was carried out to investigate the hypoglycemic potential of herbal mixture (Citrullus Colocynthis and Cicer arietinum) in normal and alloxan induced diabetic rabbits. Hypoglycemic potential was evaluated through curative and preven
Externí odkaz:
https://doaj.org/article/480bdb212a824c9c8e30773cc6fa0f7f
Publikováno v:
International Design Journal. 10:437-450
The world is witnessing in the present era rapid developments forced societies to seek to keep up with these successive developments in various fields, and this by working to modernize their various systems, perhaps the most important in the field of
Publikováno v:
Chemical Papers. 74:2501-2514
In this work, 3-amino-4-cyano-2-thiophenecarboxamides 1a-k were used as versatile synthons for the preparation of thieno[3,2-d]pyrimidine-7-carbonitriles 2a-k and 4a-d as well as the unexpectedly prepared thieno[3,4-b]pyridine-7-carboxamides 5a-e. Th
Publikováno v:
Chemical Papers. 74:2491-2500
An efficient and atom economic modification of a previously reported synthetic pathway to tetrasubstituted thiophenes is described. The previously published synthetic methodology involved a one pot procedure starting with ketene dithioacetal and an a
Publikováno v:
Current Organic Chemistry. 23:2005-2015
This review summarizes the data published on the methods of preparation of β- keto amides as a versatile synthon for many heterocyclic rings and asymmetric urea derivatives. Based on the starting materials used for the synthesis of β-keto amides, e
Autor:
Mona S. El-Zoghbi, Eman M. Ahmed, Nadia A. Khalil, Eman A. Sobh, Ashraf F. Zaher, Samiha A. El-Sebaey
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry
article-version (VoR) Version of Record
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 36, Iss 1, Pp 1839-1859 (2021)
article-version (VoR) Version of Record
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 36, Iss 1, Pp 1839-1859 (2021)
A series of [1]benzothieno[2,3-c]pyridines was synthesised. Most compounds were chosen by NCI-USA to evaluate their anticancer activity. Compounds 5a–c showed prominent growth inhibition against most cell lines. 5c was selected at five dose concent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36d55cc159fc1feed728dc142f5c9851