Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Amany M. M. Al‐Mahmoudy"'
Autor:
Samar A. El-Kalyoubi, Ehab S. Taher, Tarek S. Ibrahim, Mohammed Farrag El-Behairy, Amany M. M. Al-Mahmoudy
Publikováno v:
Pharmaceuticals, Vol 15, Iss 5, p 494 (2022)
A series of quinoline–uracil hybrids (10a–l) has been rationalized and synthesized. The inhibitory activity against hCA isoforms I, II, IX, and XII was explored. Compounds 10a–l demonstrated powerful inhibitory activity against all tested hCA i
Externí odkaz:
https://doaj.org/article/ba1011e7b67d4fe2bed1d304b66199bf
Autor:
Riham M. Bokhtia, Adel S. Girgis, Tarek S. Ibrahim, Fatma Rasslan, Eman S. Nossier, Reham F. Barghash, Rajeev Sakhuja, Eatedal H. Abdel-Aal, Siva S. Panda, Amany M. M. Al-Mahmoudy
Publikováno v:
Pharmaceuticals, Vol 15, Iss 2, p 191 (2022)
The development of new antibiotics to treat multidrug-resistant (MDR) bacteria or possess broad-spectrum activity is one of the challenging tasks. Unfortunately, there are not many new antibiotics in clinical trials. So, the molecular hybridization a
Externí odkaz:
https://doaj.org/article/710c2b076dac4c72b7f1d5e460164be3
Autor:
Ahmad J. Almalki, Tarek S. Ibrahim, Ehab S. Taher, Mamdouh F. A. Mohamed, Mahmoud Youns, Wael A. H. Hegazy, Amany M. M. Al-Mahmoudy
Publikováno v:
Molecules, Vol 27, Iss 3, p 671 (2022)
Since the synthesis of prontosil the first prodrug shares their chemical moiety, sulfonamides exhibit diverse modes of actions to serve as antimicrobials, diuretics, antidiabetics, and other clinical applications. This inspiring chemical nucleus has
Externí odkaz:
https://doaj.org/article/6ee754bdb2fa47088366d9d8d924e12b
Autor:
Tarek S. Ibrahim, Ehab S. Taher, Ebtihal Samir, Azizah M. Malebari, Ahdab N. Khayyat, Mamdouh F. A. Mohamed, Riham M. Bokhtia, Mohammed A. AlAwadh, Israa A. Seliem, Hani Z. Asfour, Nabil A. Alhakamy, Siva S. Panda, Amany M. M. AL-Mahmoudy
Publikováno v:
Molecules, Vol 25, Iss 14, p 3125 (2020)
Two sets of diphenyl ether derivatives incorporating five-membered 1,3,4-oxadiazoles, and their open-chain aryl hydrazone analogs were synthesized in good yields. Most of the synthesized compounds showed promising in vitro antimycobacterial activity
Externí odkaz:
https://doaj.org/article/1a98e0d226f94938a261231fab034565
Autor:
Tarek S. Ibrahim, Israa A. Seliem, Siva S. Panda, Amany M. M. Al-Mahmoudy, Zakaria K. M. Abdel-Samii, Nabil A. Alhakamy, Hani Z. Asfour, Mohamed Elagawany
Publikováno v:
Molecules, Vol 25, Iss 11, p 2501 (2020)
A straightforward, mild and cost-efficient synthesis of various arylamides in water was accomplished using versatile benzotriazole chemistry. Acylation of various amines was achieved in water at room temperature as well as under microwave irradiation
Externí odkaz:
https://doaj.org/article/c4bbc310b1374f7996a3ac8da6e7d382
Autor:
Israa A. Seliem, Siva S. Panda, Adel S. Girgis, Queen L. Tran, Mona F. Said, Mohamed S. Bekheit, Anwar Abdelnaser, Soad Nasr, Walid Fayad, Ahmed A. F. Soliman, Rajeev Sakhuja, Tarek S. Ibrahim, Zakaria K. M. Abdel‐Samii, Amany M. M. Al‐Mahmoudy
Publikováno v:
ChemMedChem. 17(13)
Three sets of isatin-based Schiff bases were synthesized utilizing the molecular hybridization approach. Some of the synthesized Schiff bases show significant to moderate antiproliferative properties against MCF7 (breast), HCT116 (colon), and PaCa2 (
Autor:
Ahmad J, Almalki, Tarek S, Ibrahim, Ehab S, Taher, Mamdouh F A, Mohamed, Mahmoud, Youns, Wael A H, Hegazy, Amany M M, Al-Mahmoudy
Publikováno v:
Molecules (Basel, Switzerland). 27(3)
Since the synthesis of prontosil the first prodrug shares their chemical moiety, sulfonamides exhibit diverse modes of actions to serve as antimicrobials, diuretics, antidiabetics, and other clinical applications. This inspiring chemical nucleus has