The rationale behind drug design is the strategic utilization of heterocyclic fragments with specific physicochemical properties to form molecular targeted agents. Among the …
NM Ahmed, M Youns, MK Soltan… - Journal of Enzyme …, 2019 - Taylor & Francis
New anticancer agents are highly needed to overcome cancer cell resistance. A novel series of pyrimidine pyrazoline-anthracene derivatives (PPADs)(4a-t) were designed and …
A novel series of pyrimidine-5-carbonitrile derivatives was designed, synthesized, then evaluated for their cytotoxic activity as novel anti-cancer with dual EGFRWT/COX-2 …
Two series of chalcone and thiopyrimidine benzofuran derivatives were designed, synthesized and evaluated in vitro for their vascular endothelial growth factor receptor …
MS Mohamed, MM Youns, NM Ahmed - Medicinal Chemistry Research, 2014 - Springer
In the present study, a novel series of indolyl-pyrimidines (1–13) were synthesized starting from 4-hydrazinopyrimidine-5-carbonitrile 3. Elemental analysis, IR, 1 H-NMR, 13 C-NMR …
Abstract A new series of 6-(4-fluorophenyl)-2-(methylthio) pyrimidine-5-carbonitrile derivatives were designed and synthesized as EGFR/PI3K dual inhibitors, and potential …
NFH Mahmoud, EA Ghareeb - Journal of heterocyclic chemistry, 2019 - Wiley Online Library
Tetrahydropyrimidine derivative 1 was employed as intermediate compound, which in turn was allowed to react with different electrophilic and nucleophilic reagents to synthesize new …
MS Mohamed, MM Youns, NM Ahmed - European Journal of Medicinal …, 2013 - Elsevier
Abstract A series of 6-aryl-5-cyano thiouracil derivatives (2a-c to 11a-c) was synthesized from 6-aryl-4-hydrazino-2-thioxo-1, 2-dihydropyrimidine-5-carbonitriles (1a-c). The products …
NM Ahmed, MS Mohamed, SM Awad… - Journal of Enzyme …, 2024 - Taylor & Francis
Herein, a novel series of 6-amino-5-cyano-2-thiopyrimidines and condensed pyrimidines analogues were prepared. All the synthesized compounds (1a-c, 2a-c, 3a-c, 4a-r and 5a-c) …