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Fatma E. Goda

Researcher at Mansoura University

Publications -  20
Citations -  394

Fatma E. Goda is an academic researcher from Mansoura University. The author has contributed to research in topics: Antimicrobial & Chemical synthesis. The author has an hindex of 9, co-authored 18 publications receiving 333 citations. Previous affiliations of Fatma E. Goda include Georgia State University.

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Synthesis, antimicrobial activity and conformational analysis of novel substituted pyridines: BF3-promoted reaction of hydrazine with 2-alkoxy pyridines

TL;DR: Some new 2-alkoxy-3-cyano-4,6-diarylpyridines 3,4 were synthesized by condensation of different alpha,beta-unsaturated ketones 1 with malononitrile 2, followed by cyclization in sodium alkoxide/alcohol system.
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Synthesis and biological evaluation of novel 6-nitro-5-substituted aminoquinolines as local anesthetic and anti-arrhythmic agents: molecular modeling study

TL;DR: A series of 6-nitro-5-[1-oxo-2-(substituted amino)ethylamino] quinoline was synthesized and evaluated for their local anesthetic and anti-arrhythmic activity and the superposition of the stable conformations of these compounds was studied using the HyperChem 5.11 program.
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Synthesis and evaluation of some novel quinazolinone derivatives as diuretic agents.

TL;DR: The results showed that 2‐[2‐(4‐chlorophenyl)vinyl]‐7‐chloro‐3‐(2‐sulfamoyl‐1, 3, 4‐thiadiazol‐5‐yl)quinazolin‐4(3H)‐one 7b exhibited significant diuretic activity.
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Exploration of larger central ring linkers in furamidine analogues: Synthesis and evaluation of their DNA binding, antiparasitic and fluorescence properties

TL;DR: The effects of replacing the central furan ring of furamidine with indole and benzimidazole on their DNA binding affinity, antiparasitic activity and fluorescence are reported and the fluorescence properties of the new analogues are similar to that of DAPI.
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[1,2,4]Triazolo[4,3-a]quinoxaline: synthesis, antiviral, and antimicrobial activities

TL;DR: In vitro antimicrobial screening against different pathogenic organisms using agar diffusion method demonstrated that compounds 4d, 6c, 7b, and 8a exhibit antibacterial and/or antifungal activities.