Publications

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Journal Article
Shabaan, M. A., A. T. Taher, and E. Omar, "Synthesis of novel 3,4‐dihydroquinoxalin‐2(1H)‐one derivatives", European Journal of Chemistry, vol. 3, issue 2, pp. 365-371, 2011. abstract_7.docx
Alhilal, M., Y. A. M. Sulaiman, S. Alhilal, S. M. Gomha, and S. A. Ouf, "Synthesis of Novel Acyclic Nucleoside Analogue Starting From 6-Aminouracil as Potent Antimicrobial Agent", Polycyclic Aromatic CompoundsPolycyclic Aromatic Compounds: Taylor & Francis, pp. 1 - 12, 2021. AbstractWebsite
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Badawy, M. A., N. H. Metwally, and D. S. Okpy, "Synthesis of some new 5-substituted-3-phenyl-4-thioxo-2-thiazolidinones and their fused thiopyrano[2,3- d ]thiazole derivatives", Journal of Sulfur Chemistry, vol. 36, issue 5, pp. 1-15 , 2015.
Rodrigues, L. {\'ıgiaM., C. S. Francisco, A. M. F. Oliveira-Campos, and A. M. Salaheldin, "Synthesis of Tacrine Analogs Derived from N-Aryl-5-amino-4-cyanopyrazoles", Synthetic Communications, vol. 38, no. 24: Taylor & Francis, pp. 4369–4378, 2008. Abstract
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Oliferenko, P. V., A. A.Oliferenko, A. S. Girgis, D. O. Saleh, A. M. Srour, R. F.George, G. G. Pillai, C. S. Panda, D. C. Hall, and A. R. Katritzky, "Synthesis, Bioassay, and Molecular Field Topology Analysis of Diverse Vasodilatory Heterocycles.", Journal of Chemical Information and Modeling, vol. 54, pp. 1103-1116, 2014. j._chem._inform._modeling_54_11031116_2014.pdf
Awadallah, F. M., T. A. El-Waei, M. M. Hanna, S. E. Abbas, M. Ceruso, B. E. Oz, O. O. Guler, and C. T. Supuran, "Synthesis, carbonic anhydrase inhibition and cytotoxic activity of novel chromone-based sulfonamide derivatives", European Journal of Medicinal Chemistry, vol. 96, pp. 425-435, 2015. Carbonic anhydrase_paper.pdf
Awadallah, F. M., T. A. El-Waei, M. M. Hanna, S. E. Abbas, M. Ceruso, B. E. Oz, O. O. Guler, and C. T. Supuran, "Synthesis, carbonic anhydrase inhibition and cytotoxic activity of novel chromone-based sulfonamide derivatives.", European journal of medicinal chemistry, vol. 96, pp. 425-35, 2015. Abstractpaper.pdf

Four series of sulfonamides incorporating chromone moieties were synthesized and assessed for their cytotoxic activity against MCF-7 and A-549 cell lines, considering the fact that some of these tumors overexpress isoforms of carbonic anhydrase (CA, EC 4.2.1.1) which is inhibited by sulfonamides. Most new sulfonamides showed weak inhibitory activity against the offtarget, cytosolic isoforms hCA I, II but effectively inhibited the tumor-associated hCA IX and XII. The most active compounds featured a primary SO2NH2 group and were active in the low micromolar range against MCF-7 and A-549 cell lines. Compound 4a showed IC50 of 0.72 and 0.50 μM against MCF-7 and A-549 cell lines, respectively, and was further evaluated for its proapoptotic activity which proved enhanced in both tumor types.

O, M., F. A, A. - R. M, and S. MA, "Synthesis, Charachterization and Optimization of PCL-based nanocapsules for Dilevery of Anticancer Chemotherapeutic Drugs", Journal of Scientific Research for Science , vol. 29, 2019.
Ahmed, Y. M., W. H. Mahmoud, M. M. Omar, and G. G. Mohamed, "Synthesis, Characterization and Biological Activity of Transition Metals Schiff Base Complexes Derived from 4,6-Diacetylresorcinol and 1,8-Naphthalenediamine", Journal of Inorganic and Organometallic Polymers and Materials, vol. 31, pp. 2339–2359 , 2021. ahmed2021_article_synthesischaracterizationandbi.pdf
Manar E. A. Elasasy, Dina H. Elnaggar, N. A. Abdel-Hafez, M. E. Azab, Abd El-Galil E. Amra, M. M. Omran, and A. M. Mohamed, "Synthesis, characterization and investigation of antiproliferative activity of novel hydrazono thiazolidene and thiazole Derivatives bearing Rhodanine moiety", Russian Journal of General Chemistry, vol. 91, issue 5, pp. 915–925, 2021.
Ahmed, M. A., N. Okasha, and B. Hussein, "Synthesis, characterization and studies on magnetic and electrical properties of LaAlyFe1-yO3 nanomultiferroic", Journal of Alloys and Compounds, vol. 553, pp. 308 - 315, 2013. AbstractWebsite

Multiferroic LaAlyFe1-yO3; 0.00 ≤ y ≤ 0.20 were successfully synthesized using citrate autocombustion method and their properties were systematically studied. All the samples were crystallized in a perovskite structure. The evaluation of the unit-cell parameters by X-ray diffraction technique revealed that the lattice constants and volume of the unit cell decreased along with increase of Al content, while the Fe-O octahedra became less distorted. The Goldschmidt tolerance factor for the perovskite increases from 0.905 for LaFeO3 to 0.914 for LaAl 0.2Fe0.8O3 confirming that the crystal structure is orthorhombic. All the magnetic parameters such as μeff, χM, and magnetization (MRT) decrease as Al content increases, while Néel temperature indicates the highest value (834 K) at y = 0.1. The magnetic measurements revealed that it has a superparamagnetic behavior with coercive field Hc nearly zero. Dielectric and activation energy results agree well with the other measurements. © 2012 Elsevier B.V. All rights reserved.

Ragheb, M. A., R. S. Omar, M. H. Soliman, A. H. M. Elwahy, and I. A. Abdelhamid, "Synthesis, characterization, DNA photocleavage, in silico and in vitro DNA/BSA binding properties of novel hexahydroquinolines", Journal of Molecular Structure, vol. 1267: Elsevier, pp. 133628, 2022. Abstract
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Ragheb, M. A., R. S. Omar, M. H. Soliman, A. H. M. Elwahy, and I. A. Abdelhamid, "Synthesis, characterization, DNA photocleavage, in silico and in vitro DNA/BSA binding properties of novel hexahydroquinolines", Journal of Molecular Structure, vol. 1267: Elsevier, pp. 133628, 2022. Abstract
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Ragheb, M. A., R. S. Omar, M. H. Soliman, A. H. M. Elwahy, and I. A. Abdelhamid, "Synthesis, characterization, DNA photocleavage, in silico and in vitro DNA/BSA binding properties of novel hexahydroquinolines", Journal of Molecular Structure, vol. 1267, pp. 133628, 2022.
Abou-Seri, S. M., A. A. M. Eissa, M. G. M. Behery, and F. A. Omar, "Synthesis, in vitro anticancer activity and in silico studies of certain isoxazole-based carboxamides, ureates, and hydrazones as potential inhibitors of VEGFR2.", Bioorganic chemistry, vol. 116, pp. 105334, 2021. Abstract

The ensuing research presents the results of in vitro anticancer activity of novel 28 compounds of isoxazole-based carboxamides 3(a-d); ureates 4(a-g), 5, 6, 7a,b, 8; and hydrazones 9(a-f), 10(a-d), 11a,b as potential inhibitors of VEGFR2. The carboxamides and ureates were synthesized by converting 5-(aryl)-isoxzaole-3-carbohydrazides 1a,b to the corresponding carbonylazides 2a,b followed by treatment with the appropriate amines. The hydrazones were directly obtained through condensation of the carbohydrazide 1a,b with aldehydes and/or ketones. The structures of the target compounds were confirmed by elemental and spectral analyses. A preliminary in vitro anticancer screening of solutions (10M) on 60 cancer cell lines (NCI, USA) revealed that the carboxamide 3c is the most promising growth inhibitor. Explicitly, 3c showed potent anticancer activity at 10µ M against leukemia (HL-60(TB), K-562 and MOLT-4), colon cancer (KM12) and melanoma (LOX IMVI) cell lines with %GI range = 70.79-92.21. Evaluation of growth inhibitory activity of the synthesized compounds against hepatocellular carcinoma (HepG2), that overexpresses VEGFR2, showed superior activity of compounds 8, 10a and 10c with IC in sub micromolar concentrations of 0.84, 0.79 and 0.69 μM, respectively, which is better than that of the reference drug, Sorafenib (IC = 3.99 µM). Moreover, these compounds displayed high selective cytotoxicity for HepG2 cancer cells over the nontumorigenic THLE2 liver cells (SI range = 26.37-38.60) which reflect their safety. The results of VEGFR2 kinase inhibition assay demonstrate that, compounds 8 and 10a are the most active inhibitors with IC = 25.7 and 28.2 nM, respectively, (Sorafenib IC = 28.1 nM). Molecular docking of the synthesized derivatives to VEGFR2 (PDB: 3WZE) showed similar binding modes to that of the co-crystallized ligand, sorafenib. Moreover, the results of computational assessment of ADME and drug-likeness characteristics inspire further investigations of the new isoxazole-based derivatives to afford more potent, safe and orally active VEGFR2 inhibitors as potential anticancer drug candidates.

Mohammed, E. Z., W. R. Mahmoud, R. F. George, G. S. Hassan, F. A. Omar, and H. H. Georgey, "Synthesis, in vitro anticancer activity and in silico studies of certain pyrazole-based derivatives as potential inhibitors of cyclin dependent kinases (CDKs)", Bioorganic Chemistry, vol. 116, pp. 105347, 2021.
Mohammed, E. Z., W. R. Mahmoud, R. F. George, G. S. Hassan, F. A. Omar, and H. H. Georgey, "Synthesis, in vitro anticancer activity and in silico studies of certain pyrazole-based derivatives as potential inhibitors of cyclin dependent kinases (CDKs)", Bioorganic Chemistry, vol. 116, pp. 105347-105361, 2021.
Mohammed, E. Z., W. R. Mahmoud, R. F. George, G. S. Hassan, F. A. Omar, and H. H. Georgey, "Synthesis, in vitro anticancer activity and in silico studies of certain pyrazole-based derivatives as potential inhibitors of cyclin dependent kinases (CDKs).", Bioorganic Chemistry, vol. 116, pp. 105347, 2021. Bioorganic_2021.pdf
Macky, T. A., C. Oelkers, U. Rix, M. L. Heredia, E. Künzel, M. Wimberly, B. Rohrer, C. E. Crosson, and J. Rohr, "Synthesis, pharmacokinetics, efficacy, and rat retinal toxicity of a novel mitomycin C-triamcinolone acetonide conjugate.", Journal of medicinal chemistry, vol. 45, issue 5, pp. 1122-7, 2002 Feb 28. Abstract

A novel conjugate of mitomycin C (MMC) and triamcinolone acetonide (TA) was synthesized using glutaric acid as a linker molecule. To determine the rate of hydrolysis, the conjugate was dissolved in aqueous solution and the rate of appearance of free MMC and TA was determined by high-performance liquid chromatography analysis. Antiproliferative activity of the MMC-TA conjugate and parent compounds was assessed using an NIH 3T3 fibroblast cell line. Cell growth was quantified using the MTT assay. Kinetic analysis of the hydrolysis rate demonstrated that the conjugate had a half-life of 23.6 h in aqueous solutions. The antiproliferative activities of the MMC-TA conjugate and MMC were both concentration dependent, with similar IC(50) values of 2.4 and 1.7 microM, respectively. However, individual responses at concentrations above 3 microM showed that the conjugate was less active than MMC alone. TA alone showed only limited inhibition of cell growth. Studies evaluating intravitreal injection of the conjugate demonstrate that this agent produced no measurable toxicity. Our data provide evidence that the MMC-TA conjugate could be used as a slow-release drug delivery system. This could in turn be used to modulate a posttreatment wound healing process or to treat various proliferative diseases.

El-halim, H. A. F., M. M. Omar, and G. G. Mohamed, "Synthesis, Structural, Thermal Studies and Biological Activity of A Tridentate Schiff Base Ligand and their Transition Metal Complexes", Spectrochimica Acta, 2011. Abstract

Schiff base (L) ligand is prepared via condensation of pyridine-2,6-dicarboxaldehyde with 2-aminopyridine. The ligand and its metal complexes are characterized based on elemental analysis, mass, IR, solid re?ectance, magnetic moment, molar conductance, and thermal analyses (TG, DTG and DTA). The molar conductance reveals that all the metal

Leon, H., H. Osman, M. Georgy, and M. Ibrahim, "System Dynamics Approach for Forecasting Performance of Construction Projects", Journal of Management in Engineering, vol. 34, issue 1, 2018.
Omran, L. N., A. M. El-Bialy, A. H. kandil, and S. A. Fawzy, "A System for Simulating the Orthodontic Treatment Plan", International Journal of Multidisciplinary Approach and Studies, vol. 2, issue 2348 – 537X, pp. 90-99, 2015. treatmentplan.pdf