Riham George
Professor of Pharmaceutical Chemistry
(email)
Publications
Classes
h index
Publications
Export 61 results:
RTF
Tagged
XML
BibTex
Sort by:
Author
[
Title
]
Type
Year
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
3
Ewida, M. A., H. A. Ewida, M. S. Ahmed, H. A. Allam, R. I. Elbagary, R. F. George, H. H. Georgey, and H. I. El-Subbagh,
"
3-Methyl-imidazo[2,1-b]thiazole derivatives as a new class of antifolates: Synthesis, in vitro/in vivo bio-evaluation and molecular modeling simulations
",
Bioorganic Chemistry
, vol. 115, pp. 105205, 2021.
A
Hassan, G. S., H. H. Georgey, R. F. George, and E. R. Mohamed,
"
Aurones and furoaurones: Biological activities and synthesis
",
Bulletin of Faculty of Pharmacy, Cairo University
, vol. 56, pp. 121-127, 2018.
B
El-Aleam, R. A. H., R. F. George, H. H. Georgey, and H. M. Abdel-Rahman,
"
Bacterial virulence factors: a target for heterocyclic compounds to combat bacterial resistance
",
RSC Advances
, vol. 11, pp. 36459–36482, 2021.
C
Hassan, G. S., H. H. Georgey, R. F. George, and E. R. Mohammed,
"
Construction of some cytotoxic agents with aurone and furoaurone scaffolds
",
Future Medicinal Chemistry
, vol. 18, issue 1, pp. 27-52, 2018.
D
El-Aleam, A. R. H., R. F. George, K. J. Lee, A. B. Keeton, G. A. Piazza, A. A. Kamel, M. E. El-Daly, G. S. Hassan, and H. M. Abdel-Rahman,
"
Design and synthesis of 1,2,4-triazolo[1,5-a]pyrimidine derivatives as PDE 4B inhibitors endowed with bronchodilator activity
",
Archiv der Pharmazie
, vol. 352, pp. 1900002, 2019.
El-Aleam, R. A. H., A. M. Sayed, M. N. Taha, R. F. George, H. H. Georgey, and H. M. Abdel-Rahman,
"
Design and synthesis of novel benzimidazole derivatives as potential Pseudomonas aeruginosa anti-biofilm agents inhibiting LasR: Evidence from comprehensive molecular dynamics simulation and in vitro investigation
",
European Journal of Medicinal Chemistry
, vol. 241, pp. 114629, 2022.
Ghanem, N. M., F. Farouk, R. F. George, S. E. S. Abbas, and O. M. El-Badry,
"
Design and synthesis of novel imidazo[4,5-b]pyridine based compounds as potent anticancer agents with CDK9 inhibitory activity
",
Bioorganic Chemistry
, vol. 80, pp. 565–576, 2018.
Osman, E. E. A., N. S. Hanafy, R. F. George, and S. M. El-Moghazy,
"
Design and synthesis of some barbituric and 1,3-dimethylbarbituric acid derivatives: A non-classical scaffold for potential PARP1 inhibitors
",
Bioorganic Chemistry
, vol. 104, pp. 104198, 2020.
Farouk, A. K. B. A. W., H. A. Allam, E. Rashwan, R. F. George, and S. E. - S. Abbas,
"
Design and synthesis of some new 6-bromo-2-(pyridin-3-yl)-4-substituted quinazolines as multi tyrosine kinase inhibitors
",
Bioorganic Chemistry
, vol. 128, pp. 106099, 2022.
Mohamed, A. R., A. E. M. Kerdawy, R. F. George, H. H. Georgey, and N. A. M. Gawad,
"
Design, synthesis and in silico insights of new 7,8-disubstituted-1,3-dimethyl-1H-purine-2,6(3H,7H)-dione derivatives with potent anticancer and multi-kinase inhibitory activities
",
Bioorganic Chemistry
, vol. 107, pp. 104569, 2021.
George, R. F., N. S. M. Ismail, J. Stawinski, and A. S. Girgis,
"
Design, synthesis and QSAR studies of dispiroindole derivatives as new antiproliferative agents
",
European Journal of Medicinal Chemistry
, vol. 68, pp. 339-351, 2013.
eur._j._med._chem._68_339-351_2013.pdf
Abo-Ashour, M. F., W. M. Eldehna, R. F. George, M. M. Abdel-Aziz, M. A. H. M. O. U. D. M. ELAASSER, N. A. M. Gawad, A. Gupta, S. Bhakta, and S. M. Abou-Seri,
"
Design, synthesis and whole cell phenotypic evaluation as a novel class of antimicrobial agents.
",
European Journal of Medicinal Chemistry
, vol. 160, pp. 49-60, 2018.
Amin, K. M., G. H. Hegazy, R. F. George, N. R. Ibrahim, and N. M. Mohamed,
"
Design, synthesis, and pharmacological characterization of some 2‐substituted‐3‐phenyl‐quinazolin‐4(3H)‐one derivatives as phosphodiesterase inhibitors
",
Archiv der Pharmazie
, vol. 354, pp. e2100051, 2021.
Seliem, I. A., S. S. Panda, A. S. Girgis, Y. I. Nagy, R. F. George, W. Fayed, N. G. Fawzy, T. S. Ibrahim, A. M. M. Al-Mahmoudy, R. Sakhuja, et al.,
"
Design, synthesis, antimicrobial, and DNA gyrase inhibitory properties of fluoroquinolone–dichloroacetic acid hybrids
",
Chemical Biology & Drug Design
, vol. 95, pp. 248-259, 2020.
Aziz, N. A. A. M., R. F. George, K. El-Adl, and W. R. Mahmoud,
"
Design, synthesis, in silico docking, ADMET and anticancer evaluations of thiazolidine-2,4-diones bearing heterocyclic rings as dual VEGFR-2/ EGFRT790M tyrosine kinase inhibitors
",
RSC Advances
, vol. 12, pp. 12913–12931, 2022.
F
Hanna, M. M., and R. F. George,
"
Facile Synthesis and Quantitative Structure–Activity Relationship Study of Antitumor Active 2-(4-Oxo-thiazolidin-2-ylidene)-3-oxo-propionitriles
",
Chem. Pharm. Bull
, vol. 60, issue 9, pp. 1195–1206, 2012.
George, R. F.,
"
Facile synthesis of simple 2-oxindole-based compounds with promising antiproliferative activity
",
Future Medicinal Chemistry
, vol. 10, issue 3, pp. 269-282, 2018.
Eid, N. M., and R. F. George,
"
Facile synthesis of some pyrazoline-based compounds with promising anti-inflammatory activity
",
Future Medicinal Chemistry
, vol. 10, issue 2, pp. 183-199, 2018.
Bokhita, R. M., S. S. Panda, A. S. Girgis, H. H. Honkanadavar, T. S. Ibrahim, R. F. George, M. O. N. A. T. KASHEF, W. A. L. I. D. FAYAD, R. Sakhuja, E. H. Abdel-Aal, et al.,
"
Flouroquinolone-3-carboxamide amino acid conjugates: Synthesis, antibacterial properties and molecular modeling studies
",
Medicinal Chemistry
, vol. 17, pp. 71-84, 2021.
H
Elwaie, T. A., S. E. Abbas, E. I. Aly, R. F. George, H. Ali, N. Kraiouchkine, K. S. Abdelwahed, T. E. Fandy, K. E. A. Sayed, Z. A. Y. Elmageed, et al.,
"
HER2 Kinase-Targeted Breast Cancer Therapy: Design, Synthesis, and In Vitro and In Vivo Evaluation of Novel Lapatinib Congeners as Selective and Potent HER2 Inhibitors with Favorable Metabolic Stability
",
Journal of Medicinal Chemistry
, vol. 63, issue 24, pp. 15906−15945, 2020.
I
Rashad, M. S., H. H. Georgey, R. F. George, and N. M. Abdel-Gawad,
"
Identification of some benzoxazepines as anticancer agents inducing cancer cell apoptosis
",
Future Medicinal Chemistry
, vol. 10, issue 14, pp. 1649–1664, 2018.
Mohamed, A. R., H. H. Georgey, R. F. George, W. I. El-Eraky, D. O. Saleh, and N. A. M. Gawad,
"
Identification of some novel xanthinebased derivatives with bronchodilator activity
",
Future Medicinal Chemistry
, vol. 9, issue 15, pp. 1731-1747, 2017.
M
Hassan, G. S., H. H. Georgey, E. Z. Mohammed, R. F. George, W. R. Mahmoud, and F. A. Omar,
"
Mechanistic selectivity investigation and 2D-QSAR study of some new antiproliferative pyrazoles and pyrazolopyridines as potential CDK2 inhibitors
",
European Journal of Medicinal Chemistry
, vol. 218, pp. 113389, 2021.
Tiwari, A. D., S. S. Panda, A. S. Girgis, S. Sahu, R. F.George, A. M. Srour, B. L. Starza, A. M. Asiri, D. C. Hall, and A. R. Katritzky,
"
Microwave assisted synthesis and QSAR study of novel NSAID acetaminophen conjugates with amino acid linkers
",
Organic & Biomolecular Chemistry
, vol. 12, issue 37, pp. 7238-7249, 2014.
N
Ewida, M. A., H. A. Ewida, M. S. Ahmed, H. A. Allam, R. I. Elbagary, R. F. George, H. H. Georgey, and H. I. El‐Subbagh,
"
Nanomolar potency of imidazo[2,1‐b]thiazole analogs as indoleamine 2,3‐dioxygenase inhibitors
",
Archiv der Pharmazie
, vol. 354, pp. e2100202, 2021.
1
2
3
next ›
last »
C.V.
Scientific activities
publications
Recent Publications
Design and synthesis of some new 6-bromo-2-(pyridin-3-yl)-4-substituted quinazolines as multi tyrosine kinase inhibitors
Design and synthesis of novel benzimidazole derivatives as potential Pseudomonas aeruginosa anti-biofilm agents inhibiting LasR: Evidence from comprehensive molecular dynamics simulation and in vitro investigation
Some 2-(4-bromophenoxymethyl)-6-iodo-3-substituted quinazolin-4(3H)ones: Synthesis, cytotoxic activity, EGFR inhibition and molecular docking
Design, synthesis, in silico docking, ADMET and anticancer evaluations of thiazolidine-2,4-diones bearing heterocyclic rings as dual VEGFR-2/ EGFRT790M tyrosine kinase inhibitors
Synthesis, molecular modelling and QSAR study of new N-phenylacetamide-2-oxoindole benzensulfonamide conjugates as carbonic anhydrase inhibitors with antiproliferative activity
more