Zobrazeno 1 - 10
of 414
pro vyhledávání: '"Rania B"'
Autor:
Jihene Feki, MD, Maissa Lajnef, MD, Mohamed Fourati, MD, Dhouha Sakka, MD, Rania B. Hassena, MD, Mourad H. Slimen, MD, Jamel Daoud, MD, Afef Khanfir, MD
Publikováno v:
Journal of Taibah University Medical Sciences, Vol 18, Iss 1, Pp 125-131 (2023)
الملخص: اهداف البحث: تعتبر الساركوما خلف الصفاق من اورام اللحمة المتوسطة النادرة. تهدف هذه الدراسة الى مناقشة مختلف الجوانب السريرية الع
Externí odkaz:
https://doaj.org/article/a5928212323f4814bec7e9aacdf967fb
Autor:
Nadia A. A. Elkanzi, Asmaa M. Kadry, Rasha M. Ryad, Rania B. Bakr, Mahmoud Abd El Aleem Ali Ali El-Remaily, Ali M. Ali
Publikováno v:
ACS Omega, Vol 7, Iss 26, Pp 22839-22849 (2022)
Externí odkaz:
https://doaj.org/article/5401af18471444edb82a6f707991ed75
Autor:
Mohamed A. Abdelgawad, Nadia A.A. Elkanzi, Arafa Musa, Mohammed M. Ghoneim, Waqas Ahmad, Mohammed Elmowafy, Ahmed M. Abdelhaleem Ali, Ahmed H. Abdelazeem, Syed N.A. Bukhari, Mohamed El-Sherbiny, Mohammed A.S. Abourehab, Rania B. Bakr
Publikováno v:
Arabian Journal of Chemistry, Vol 15, Iss 8, Pp 104015- (2022)
Background: Pyrazolopyrimidine heterocycle and its isosteres represent the main scaffold for many pharmacologically active drugs including anti-inflammatory agents. The COX-2 inhibitors are the principal gate for the design of new safe and potent ant
Externí odkaz:
https://doaj.org/article/66edb42224e740ee943a6b8d2da580ab
Autor:
Khairiah Nasser AL-Shammri, Nadia A.A. Elkanzi, Wael A.A. Arafa, Ibrahim O. Althobaiti, Rania B. Bakr, Shaima Mohamed Nabil Moustafa
Publikováno v:
Arabian Journal of Chemistry, Vol 15, Iss 5, Pp 103731- (2022)
An effective method for synthesizing series of twenty-two new compounds 1, 2a,b, 3, 4a,b, 5a-e, 7, 8, 9, 10, 12, 13a-d, 15a,b was performed starting from reaction of 1,2,3-indenetrione thiourea, and ethyl cyanoacetate under microwave irradiation and
Externí odkaz:
https://doaj.org/article/9d25d184d88447c39c96a75bb4371e3f
Autor:
Mohamed A. Abdelgawad, Nadia A.A. Elkanzi, A.A. Nayl, Arafa Musa, Nasser Hadal Alotaibi, W.A.A. Arafa, Sobhi M. Gomha, Rania B. Bakr
Publikováno v:
Arabian Journal of Chemistry, Vol 15, Iss 5, Pp 103781- (2022)
Pyrazolo[3,4-d]pyrimidine had been attracted awesome interest due to its pharmacological potential especially as an anticancer. Several mechanisms of action were accounted for the anticancer potential of this privileged scaffold. Previous researches
Externí odkaz:
https://doaj.org/article/5d1b4b4a4f594551a8ab7562ce8751a5
Autor:
Mohamed R. Mahdi, Rania B. Georges, Doaa M. Ali, Raouf F. Bedeer, Huda M. Eltahry, Abd-El Hakiem Z. Gabr, Martin R. Berger
Publikováno v:
Frontiers in Pharmacology, Vol 11 (2020)
Targeting of endothelin system genes is a promising strategy in cancer therapy. The modulation of these genes was explored in a model of colorectal cancer (CRC) liver metastasis and in a panel of CRC tumor cell lines that were exposed to the demethyl
Externí odkaz:
https://doaj.org/article/ae5ae01b0b0643ebbeb4a6047ab9b0a4
Publikováno v:
Journal of Taibah University for Science, Vol 12, Iss 6, Pp 774-782 (2018)
The present work is mainly dedicated to heterocyclic compounds as well as S-glycoside. 1,4-dihydroquinoxaline derivatives 3 were obtained from the reaction 2 with carbon disulfide in presence of potassium hydroxide. S-glycoside 4 was prepared from th
Externí odkaz:
https://doaj.org/article/5200364e27d94b92a365ce38ce9362d2
Publikováno v:
Molecules, Vol 26, Iss 11, p 3103 (2021)
Pyrazolothiazole-substituted pyridine conjugates are an important class of heterocyclic compounds with an extensive variety of potential applications in the medicinal and pharmacological arenas. Therefore, herein, we describe an efficient and facile
Externí odkaz:
https://doaj.org/article/32c6ca74b3bb4a1b9ab4bab1c0236bfb
Publikováno v:
Journal of Research in Interactive Marketing, 2024, Vol. 18, Issue 6, pp. 1136-1154.
Externí odkaz:
http://www.emeraldinsight.com/doi/10.1108/JRIM-06-2023-0192
Publikováno v:
Molecules, Vol 26, Iss 3, p 708 (2021)
In an effort to improve and achieve biologically active anticancer agents, a novel series of 1,2,3-triazole-containing hybrids were designed and efficiently synthesized via the Cu-catalyzed azide-alkyne cycloaddition (CuAAC) reaction of substituted-a
Externí odkaz:
https://doaj.org/article/a8fd5877bc6c4a53940306d395991859