Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Sherif A. F. Rostom"'
Autor:
Diana K. Ghobrial, Nefertiti El-Nikhely, Eman Sheta, Hanan M. Ragab, Sherif A. F. Rostom, Hesham Saeed, Ahmed Wahid
Publikováno v:
Antioxidants, Vol 12, Iss 3, p 637 (2023)
Liver Fibrosis can be life-threatening if left untreated as it may lead to serious, incurable complications. The common therapeutic approach is to reverse the fibrosis while the intervention is still applicable. Celecoxib was shown to exhibit some an
Externí odkaz:
https://doaj.org/article/2599163c563449319823adfd395d4604
Publikováno v:
Journal of Chemistry, Vol 2016 (2016)
The synthesis of polysubstituted pyridines, in addition to some derived pyrido[2,3-d]pyrimidine ring systems supported with chemotherapeutically active functionalities, is described. They were evaluated for their in vitro cytotoxic effects against th
Externí odkaz:
https://doaj.org/article/06a85e532d1b40c6987246ddf7d50625
Autor:
Ahmed H. Moustafa, Sherif A. F. Rostom, Maan T. Khayat, Ayat K Saad El-Deen, Tarek S. Ibrahim, Siva S. Panda, Hassan A. El-Sayed, Amany M.M. Al-Mahmoudy
Publikováno v:
Medicinal Chemistry. 14:791-808
Background Viral diseases are considered main threats that face the humanity worldwide. The emergence of new viruses like influenza viruses emphasizes the significance of designing novel antiviral drugs. Method The aim of this work is to synthesize a
Autor:
Hoda G. Daabees, Sherif A. F. Rostom, Aya Y. Rashad, Ahmed E. Abdel Moneim, Shaymaa E. Kassab
Publikováno v:
Bioorganic Chemistry. 113:104948
Various febuxostat derivatives comprising carboxamide functionalities and different substituted heterocycles were synthesized and evaluated for their biological activities as xanthine oxidase (XO) and cyclooxygenase (COX) inhibitors. All the tested c
Publikováno v:
CHEMICAL & PHARMACEUTICAL BULLETIN. 65:442-454
Two series of novel alkoxylated 2-oxo(imino)-3-pyridinecarbonitriles (structurally-relevant to some reported anticancer pyridines with phosphodiesterase 3A (PDE3A) inhibitory activity) were synthesized and evaluated for their in vitro differential tu
Publikováno v:
Current Topics in Medicinal Chemistry. 16:3569-3581
There has been considerable interest in azole-containing compounds as promising antiinflammatory agents. Designed compounds with five-membered nitrogen-containing nuclei have demonstrated good anti-inflammatory activity, indicating their potential fo
Publikováno v:
Archiv der Pharmazie. 348:824-834
A series of novel 1,4,6-trisubstituted-2-oxo-1,2-dihydropyridine-3-carbonitriles supported with some functionalities reported to contribute to significant chemotherapeutic potential were synthesized and evaluated for their antimicrobial and/or cytoto
Autor:
Sherif A. F. Rostom, Adnan A. Bekhit
Publikováno v:
European Journal of Medicinal Chemistry. 92:712-722
The synthesis of 18 novel pyrrolylpyridines and some derived bi-, tri- and tetracyclic ring systems using both the conventional heating and MW irradiation techniques is described. Fourteen compounds; 2 – 9 , 10 – 12 , 14 , 17 and 18 were evaluate
Publikováno v:
European journal of medicinal chemistry. 139
Synthesis of twenty nine new 1,2,4-triazoles and some derived thiazolothiadiazoles (structurally-relevant to some reported triazoles with anticancer and/or Cdc25A/B inhibitory activities) is described in this study. The obtained NCI's in vitro antitu
Publikováno v:
Archiv der Pharmazie. 350(5)
The synthesis and evaluation of the anti-inflammatory activity of some structure hybrids comprising basically the 5-hydroxy-3-methyl-1-phenyl-4-substituted-1H-pyrazole scaffold directly linked to a variety of heterocycles and functionalities, or annu