Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mosaad Sayed Mohamed"'
Autor:
Doaa Samaha, Sawsan Mahmoud, Mosaad Sayed Mohamed, Rokaia S. Abdullah, Nageh A. Abou Taleb, Tomohisa Nagamatsu, Hamed I. Ali
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 39, Iss 1 (2024)
This study describes the development of novel alloxazine analogues as potent antitumor agents with enhanced selectivity for tumour cells. Twenty-nine out of 45 newly compounds were investigated in vitro for their growth inhibitory activities, against
Externí odkaz:
https://doaj.org/article/7e64012660c14ee68f7beb506c1e3ea9
Autor:
Samar Said, Fatahala, Mosaad Sayed, Mohamed, Jaqueline Youssef, Sabry, Yara Esam El-Deen, Mansour
Publikováno v:
Medicinal Chemistry. 18:1013-1043
Abstract: In the last several decades, interest in pyrrole and pyrrolopyrimidine derivatives has increased owing to their biological importance, such as anti-tumor, anti-microbial, anti-inflammatory, anti-diabetic, anti-histaminic, anti-malarial, ant
Publikováno v:
World Journal of Advanced Research and Reviews. 15:272-296
Pyrimidines represent an important class of heterocycles containing two nitrogen atoms at position 1 and 3 of the six membered ring show wide range of biological activities. Numerous methods for the synthesis of pyrimidine and their diverse reactions
Autor:
Mosaad Sayed Mohamed, Ahmed Mahmoud Alafify, Sami Gaber Abdel-Hamide, Mohamed Kamal Ibrahim, M Adel Mostafa
Publikováno v:
International Journal of Pharmacology. 1:261-266
Publikováno v:
Acta Pharmaceutica
Volume 61
Issue 2
Volume 61
Issue 2
A series of 6-aryl-5-cyano-2-thiouracil derivatives (1a-d) was synthesized by the reaction of ethyl cyanoacetate with thiourea and aldehydes. These products were used as intermediate compounds for the synthesis of a number of thiouracil derivatives (
Publikováno v:
Acta Pharmaceutica
Volume 59
Issue 2
Volume 59
Issue 2
In an effort to establish new pyrroles and pyrrolo[2,3-d]pyrimidines with improved antimicrobial activity we report here the synthesis and in vitro microbiological evaluation of a series of pyrrole derivatives. A series of new 2-aminopyrrole-3-carbon