Nagwa M. Fawzy, Samira A. Swelam and Mohamed A. Farid
Biotechnology, 2008, 7(1), 43-50.
Synthesis of some 3,4-dihydroquinazolinone-4-one, quinoxaline, benzoxazine, benzothiazine, pyran and pyrrolidinedione derivatives using readily available starting materials were described. It has been found that compounds 4b, 8a and 8b were the most active compounds against the test organisms. Compound 8b was the most active against Gram positive and Gram negative bacteria (B. subtilus and E. coli) where compounds 4b and 8a were active against (St. aureus). Compound 12a is the least active member of this group. On the other hand, compound 14b showed a good activity compound against St. aureus.
ASCI-ID: 11-365
Biotechnology, 2008, 7(1), 129-133.
Antimicrobial Activities of Cajanus cajan, Garcinia kola and Xylopia aethiopica on Pathogenic MicroorganismsBiotechnology, 2004, 3(1), 41-43.
Tetrahedron Letters, 2012, 53(28), 3546. DOI: 10.1016/j.tetlet.2012.04.126
Synthesis of Quinazolinone Based Schiff Bases as Potential Anti-inflammatory and Analgesic AgentsJournal of Pharmacy and Allied Health Sciences, 2014, 4(1), 15. DOI: 10.3923/jpahs.2014.15.23
Functionalized 1,4‐Benzothiazine: A Versatile Scaffold with Diverse Biological PropertiesArchiv der Pharmazie, 2012, 345(11), 841. DOI: 10.1002/ardp.201200140
Anti-inflammatory Activity and PGE2 Inhibitory Properties of Novel Phenylcarbamoylmethyl Ester-Containing CompoundsMolecules, 2009, 14(2), 667. DOI: 10.3390/molecules14020667
Synthesis and biological evaluation of α-ketoamides as inhibitors of the Dengue virus protease with antiviral activity in cell-cultureBioorganic & Medicinal Chemistry, 2011, 19(13), 4067. DOI: 10.1016/j.bmc.2011.05.015