Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Esam R. Ahmed"'
Autor:
Walaa M. El-Husseiny, Magda A.-A. El-Sayed, Naglaa I. Abdel-Aziz, Adel S. El-Azab, Esam R. Ahmed, Alaa A.-M. Abdel-Aziz
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 33, Iss 1, Pp 507-518 (2018)
New α,β-unsaturated ketones 4a,b; 5a–c; and 6a,b; as well as 4-H pyran 7; pyrazoline 8a,b; isoxazoline 9; pyridine 10–11; and quinoline-4-carboxylic acid 12a,b derivatives were synthesized and evaluated for in vitro antitumour activity against
Externí odkaz:
https://doaj.org/article/ffe7cb284bb742a5b8b4fb2fc4452d4a
Publikováno v:
Medicinal Chemistry Research. 28:2088-2098
Simple, small, drug-like molecules bearing aryl azide and aryl sulfonamide moieties were designed and synthesized. The cytotoxic activity of these compounds was measured on colon cancer HCT116, lung cancer A549, and normal fibroblast cells F180 cell
Autor:
Iman M Higazy, Ahmed M. Aboul-Enein, Witold Lojkowski, Samar A Shahein, Esam R Ahmed, Khaled AbouAitah, Shaker A. Mousa, Faten Abou-Elella
Publikováno v:
International Journal of Nanomedicine
Samar A Shahein1,*Ahmed M Aboul-Enein,1 Iman M Higazy,2 Faten Abou-Elella,1 Witold Lojkowski,3 Esam R Ahmed,4 Shaker A Mousa,5 Khaled AbouAitah3,6,*1Biochemistry Department, Faculty of Agriculture, Cairo University, Giza, Egypt; 2Department of Pharma
Autor:
Pradipta Ghosh, Alaa M. Hayallah, Esam R. Ahmed, Muhamad Mustafa, Gamal El-Din A. Abuo-Rahma, Amer Ali Abd El-Hafeez, Dalia Abdelhamid
Publikováno v:
Bioorg Med Chem Lett
Small molecule inhibitors of the focal adhesion kinase are regarded as promising tools in our armamentarium for treating cancer. Here, we identified four 1,2,4-triazole derivatives that inhibit FAK kinase significantly and evaluated their therapeutic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d734953e18de14d50a92e8ae22b854e6
https://escholarship.org/uc/item/2pc3s0tw
https://escholarship.org/uc/item/2pc3s0tw
Publikováno v:
MedChemComm. 9:1511-1528
A novel series of sulfonamide derivatives, coupled with a salicylamide scaffold, was designed and synthesized. The structures of the synthesized compounds were established using 1H NMR, 13C NMR and high-resolution mass spectroscopy. The synthesized c
Autor:
Esam R Ahmed, Anna Lucia Fallacara, Hatem A. Abdel-Aziz, Sahar M. Abou-Seri, Mahmoud M. Elaasser, Hany S. Ibrahim, Hazem A. Ghabbour, Maurizio Botta, Wagdy M. Eldehna
Publikováno v:
Future medicinal chemistry. 10(24)
Aim: Inhibition of P53-mdm2 interaction will lead to cancer cell apoptosis. This strategy was achieved by reported spiro-oxindole derivatives. Materials & methods: Spiro(indoline-3,4′-pyrazolo[3,4-b]pyridine)-5′-carbonitrile derivatives (4a–i a
Publikováno v:
MedChemComm. 9(9)
A novel series of sulfonamide derivatives, coupled with a salicylamide scaffold, was designed and synthesized. The structures of the synthesized compounds were established using (1)H NMR, (13)C NMR and high-resolution mass spectroscopy. The synthesiz
Autor:
Hend M Abo El-Atta, Esam R Ahmed
Publikováno v:
Journal of Clinical Toxicology.
Many environmental pollutants are considered to be obsogenes that are encountered to be one of the major nontraditional risk factors for induction of obesity. The aim of the present study is to determine role of malaoxon, malathion dicarboxylic acid
Autor:
Magda A.-A. El-Sayed, Esam R. Ahmed, Walaa M. El-Husseiny, Alaa A.-M. Abdel-Aziz, Adel S. El-Azab, Naglaa I. Abdel-Aziz
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 33, Iss 1, Pp 507-518 (2018)
Journal of Enzyme Inhibition and Medicinal Chemistry
Journal of Enzyme Inhibition and Medicinal Chemistry
New α,β-unsaturated ketones 4a,b; 5a–c; and 6a,b; as well as 4-H pyran 7; pyrazoline 8a,b; isoxazoline 9; pyridine 10–11; and quinoline-4-carboxylic acid 12a,b derivatives were synthesized and evaluated for in vitro antitumour activity against
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f110d3e3c5d1aef30e2e7d9928c64ea
Publikováno v:
Bioorganic chemistry. 76
In this research, three series of azole-hydrazone derivatives namely, benzimidazole, benzoxazole and benzothiazole were designed and synthesized. Their structures were confirmed by elemental analysis and spectroscopic techniques. Stereochemical confi