Thoraya Farghaly
Professor of Chemistry
Cairo University, Giza, Egypt
(email)
Abbas, A. A., T. A. Farghaly, and K. M. Dawood,
"
Recent advances on anticancer and antimicrobial activities of directly-fluorinated five-membered heterocycles and their benzo-fused systems
",
RSC Adv
, vol. 14, pp. 19752–19779, 2024.
Abbas, A. A., T. A. Farghaly, and K. M. Dawood,
"
Recent progress in therapeutic applications of fluorinated five-membered heterocycles and their benzo-fused systems
",
RSC Adv.
, vol. 14, pp. 33864–33905, 2024.
Farghaly, T. A., A. Fawzy, H. H. Alsharief, and N. Alqarnic,
"
Investigation of inhibition efficiencies of Novel bis-oxindole and bis(spiro(triazole-oxindole)) for the corrosion of copper in sulfuric acid medium
",
POLYCYCLIC AROMATIC COMPOUNDS
, vol. 44, pp. 1258–1272, 2024.
Farghaly, T. A., G. S. Masaret, and H. G. Abdulwahab,
"
Novel 1,3-Indanedione-Thiazole Hybrids as Small-Molecule SARS-COV-2 Main Protease Inhibitors With Potential anti- Coronaviral Activity
",
POLYCYCLIC AROMATIC COMPOUNDS
, vol. 44, pp. 6941–6956, 2024.
Abdulwahab, H. G., R. E. - S. Mansour, T. A. Farghaly, and H. M. El-Sehrawi,
"
Discovery of novel benzimidazole derivatives as potent HDACs inhibitors against leukemia with (Thio)Hydantoin as zinc-binding moiety: Design, synthesis, enzyme inhibition, and cellular mechanistic study
",
Bioorganic Chemistry
, vol. 146, pp. 107284 , 2024.
Farghaly, T. A., E. M. H. Abbas, H. S. Abd-Elghaffar, M. A. Elsayed, D. H. Elnaggar, and A. F. El-Sayed,
"
Synthesis, characterization, molecular docking, pharmacokinetics, and molecular dynamics of new bis-thiazoles based on bis-thiosemicarbazone as anti-coxsackievirus
",
Scientific Reports
, vol. 14, pp. 29378, 2024.
Hakami, A. A., Hajar S. Alorfi, T. A. Farghaly, and M. A. Hussein,
"
Synthesis of new polyazomethine-based pyrazole moieties as promising biologically active macromolecules
",
POLYMER-PLASTICS TECHNOLOGY AND MATERIALS
, 2024.
Hakami, A. A., Hajar S. Alorfi1, T. A. Farghaly, and M. A. Hussein,
"
Synthesis, and antimicrobial activity of polyazomethine-pyrazole/multi-walled carbon nanotubes nanocomposite materials
",
Polymers and Polymer Composites
, vol. 32, pp. 1–12, 2024.
Farghaly, T. A., R. A. Pashameah, A. Bayazeed, A. M. Al-Soliemy, A. M. R. Alsaed, and M. F. Harras,
"
Design and Synthesis of New bis-oxindole and Spiro(triazole-oxindole) as CDK4 Inhibitors with Potent Anti-breast Cancer Activity
",
Medicinal Chemistry
, pp. 1-15, 2024.
Alkhatib, F. M., Thoraya A. Farghaly, M. F. Harras, and H. E. - A. Ghamry,
"
Copper(II) complexes based on 1,3,4- thiadiazolethiosemicarbazone NNS donor ligands: synthesis, molecular structure, DNA binding and in silico molecular docking approach
",
INORGANIC AND NANO-METAL CHEMISTRY
, vol. 54, pp. 18–29, 2024.
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Antimicrobial Activity of [1,2,4]Triazolo[4,3-a]pyrimidine and New Pyrido[3,2-f][1,4] thiazepine Derivatives
Antitumor activity of pyrrolizines and their Cu(II) complexes: Design, synthesis and cytotoxic screening with potential apoptosi
Biological evaluation of benzosuberones
Cholinesterase Inhibitory Activity of Some semi-Rigid Spiro Heterocycles: POM Analyses and Crystalline Structure of Pharmacophor
Indomethacin Analogs: Synthesis, Anti-inflammatory and Analgesic Activities of Indoline Derivatives
Microwave-Assisted Synthesis of Antimicrobial Agents Containing Carbazole and Thiazole Moieties
Synthesis of 8,10-disubstituted-triazoloperimidines from (E)-3-(dimethylamino)-1-(8- phenyl-8H-[1,2,4]triazolo[4,3-a]perimidin-1
Synthesis of New Bis-Spiropyrazoles as Antitumor Agents under Ultrasound Irradiation
Synthesis of Pyrazolone Derivatives and Their Nanometer Ag(I) Complexes and Physicochemical, DNA Binding, Antitumor, and Theoret
Terephthalaldehyde: An Effecient Key Precursor for Novel Synthesis of Some Interesting Bis-thiazoles and Bis-triazolopyrimidinon
file:///E:/Mostafa/Desktop/F/Thoraya/thoraya%20Reveiw/Papers%20Thoraya/2019/New%20folder/2019JHC391.pdf
file:///E:/Mostafa/Desktop/F/Thoraya/thoraya%20Reveiw/Papers%20Thoraya/2019/New%20folder/molecules-24-04009%20(1).pdf
http://www.eurekaselect.com/164007/article
http://www.eurekaselect.com/166944/article
http://www.eurekaselect.com/170178/article
http://www.eurekaselect.com/170369/article
http://www.eurekaselect.com/172873/article
https://link.springer.com/article/10.1007%2Fs11164-018-03714-y
https://link.springer.com/article/10.1007%2Fs11164-018-3594-7
https://onlinelibrary.wiley.com/doi/abs/10.1002/aoc.5099
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539608/
https://www.ncbi.nlm.nih.gov/pubmed/30207239
https://www.sciencedirect.com/science/article/abs/pii/S0022286019304077?via%3Dihub
https://www.sciencedirect.com/science/article/abs/pii/S0167732219322287
https://www.sciencedirect.com/science/article/pii/S2405844019310370
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