Professor Ayman Sadek Ahmed El-Faham

أ. د. أيمن صادق احمد الفحام

Position : Faculty Member
Email : ayman.a@dau.edu.sa
Phone : 011-4949376
Fax :

Summary of his biography :

Prof. Ayman El-Faham focuses on the synthesis and characterization of peptides, peptide coupling reagents, green chemistry, medicinal chemistry, and biologically active small compounds based triazine moiety. He has more than 290 publications in highly cited journal, 14 US-patent. He received the B.Sc. degree in Chemistry in 1980 and M.Sc. in 1985 in Physical Organic Chemistry, from Faculty of Science, University of Alexandria, Egypt. In 1991 he received his Ph.D degree in organic chemistry as a joint project between the University of Massachusetts, Amherst, MA, U. S. A. and the University of Alexandria under the supervision of Prof. L. A. Carpino, where he worked on the synthesis of new protecting groups for both solution and solid phase peptide synthesis. In addition, he involved in the development of new coupling reagents based on 1-hydroxy-7-azabenzotriazole. He continued working on these new coupling reagents as a postdoctoral work at the University of Massachusetts in Prof. Carpino’s Lab (1992-1999). He shared many patents in peptide field. In 1999 he received the University of Alexandria award in Chemistry. He nominated to submit a proposal for Noble prize in 2003. Also, he has collaborated with Barcelona Science Park, Barcelona University, Spain from 2006 to present with Prof. Fernando Albericio in the development of a new family of immonium/uronium type coupling reagents and drug design based Triazine moiety. In 2000-2004, he worked as the Head of the Chemistry Department, Beirut Arab University, Lebanon. In 2004-2008, he worked as the Direct Manager of both the NMR Lab and the Central Lab at the Faculty of Science, Alexandria University, Egypt. 2008-2010, he worked at King Saud University, as a Professor of Organic Chemistry, College of Science, Chemistry Department, Saudi Arabia. In 2010, he received the D.Sc. degree in Peptide Synthesis. In 2010 he received the University of Alexandria a Medal award in Chemistry for scientific publication. 2010-2011, he worked as a Vice Dean of Community Service and Environment Development, in 2012 he received Award of Excellence in Scientific Publishing from Quality Authority (CIQAP) Egypt 2012. From 2011 to 2021, he worked at King Saud University, as a Professor of Organic Chemistry, College of Science, Chemistry Department, Saudi Arabia. He is Emeritus Professor of Organic and Peptide Chemistry, Faculty of Science, Alexandria. He recorded as top 2% Scientist around the world according to the published data by Stanford, five years in rolled 2024,2023, 2022, 2021, 2020. Currently, he is a Professor at College of Medicine, Dar Al Uloom University, Riyadh, Saudi Arabia. In addition he is the head of the Center of Entrepreneurship & Innovation and Knowlege Transfer at DAU.

Title Date Major Organization
BSc1980ChemistryAlexandria University
MSc1985Chemistry
PhD1991ChemistryAlexandria University
DSc2010ChemistryAlexandria University
Title Organization Date From Date To
ProfessorAlexandria University27-11-200130-08-2024
Associate ProfessorAlexandria University29-10-199626-11-2001
Assistant ProfessorAlexandria University24-09-199128-10-1996
Assistant LectureAlexandria University25-11-198523-09-1991
DemonstratorAlexandria University07-10-198024-11-1985
ProfessorKing Saud University01-09-200830-07-2010
ProfessorKing Saud University01-09-201118-07-2021
Professor, Head of Chemistry DepartmentBeirut Arab University, Faculty of Science, Lebanon01-09-200030-07-2004
Vice-Dean for Community Development & Environmental Affairs, University of Alexandria, Faculty of ScienceAlexandria University23-09-201008-10-2011
Post-Doctoral Research AssociateUniversity of Massachusetts, UMASS, Amherst01-09-199230-08-1994
Post-Doctoral Research AssociateUniversity of Massachusetts, UMASS, Amherst01-09-199630-08-1998
Visiting Research ProfessorUniversity of Barcelona, Barcelona Science Park01-07-200630-08-2011
Title Publish Date Journal
Synthesis, X-ray Crystal Structure and Antimicrobial Activity of Unexpected Trinuclear Cu(II) Complex from s-Triazine-Based Di-Compartmental Ligand via Self-Assembly2019Crystals 2019, 9, 661; doi:10.3390/cryst9120661
A Simple, Efficient, and Eco-Friendly Method for the Preparation of 3-Substituted-2,3-dihydroquinazolin-4(1H)-one Derivatives2019Molecules 2019, 24, 4052; doi:10.3390/molecules24224052
Investigating Triorthogonal Chemoselectivity. Effect of Azide Substitution on the Triazine Core2019Org. Lett. 2019, 21, 2459−2463; doi: 10.1021/acs.orglett.9b02878
γ-Valerolactone (GVL): An eco-friendly anchoring solvent for solid-phase peptide synthesis2019Tetrahedron Letters, 2019, 60, 151058; doi: 10.1016/j.tetlet.2019.151058
Bis-pyrazolyl-s-triazine Ni(II) pincer complexes as selective gram positive antibacterial agents; synthesis, structural and antimicrobial studies2019J. Mol. Str. 2019, 1195, 315-322; doi: 10.1016/j.molstruc.2019.05.103
Physico Chemical and Biological Evaluation of PLCL/SF Nanofibers Loaded with Oregano Essential Oil2019Pharmaceutics 2019, 11, 386 (1-18); doi:10.3390/pharmaceutics11080386
Pseudo-Wang Handle for the Preparation of Fully Protected Peptides. Synthesis of Liraglutide by Fragment Condensation2019Org. Lett. 2019, 21, 2459−2463; doi: 10.1021/acs.orglett.9b00813
Optimized Stepwise Synthesis of the API Liraglutide Using BAL Resin and Pseudoprolines2019ACS Omega 2019, 4, 8674−8680; doi: 10.1021/acsomega.9b00974.
Synthesis, X-ray structure and DFT studies of five- and eight-coordinated Cd(II) complexes with s-triazine N-pincer chelate2019J. Coord. Chem., 2019, 72, 1621-1636; doi: 10.1080/00958972.2019.1608360.
Cu(II)-promoted cyclization of Hydrazonophthalazine to triazolophthalazine; Synthesis and structure diversity of six novel copper(II) complexes2019Applied Organometallic Chemistry; 2019; e4992; doi.org/10.1002/aoc.4992
Cu(II)-promoted cyclization of Hydrazonophthalazine to triazolophthalazine; Synthesis and structure diversity of six novel copper(II) complexes2019Applied Organometallic Chemistry; 2019; e4992; doi.org/10.1002/aoc.4992
Synthesis, Molecular and Supramolecular Structures of New Cd(II) Pincer-Type Complexes with s- Triazine Core Ligand2019. Crystals 2019, 9, 226 (1-16); doi:10.3390/cryst9050226.
Bypassing Osmotic Shock Dilemma in a Polystyrene Resin Using the Green Solvent Cyclopentyl methyl Ether (CPME): A Morphological Perspective2019Polymers 2019, 11, 874 (1-13) ; doi:10.3390/polym11050874.
Synthesis, X-Ray Crystal Structures, and Preliminary Anti-proliferative Activities of News-Triazine-hydroxybenzylidene Hydrazone Derivatives2019Journal of Chemistry 2019, Volume 2019, Article ID 9403908, 10 pages ; doi: 10.1155/2019/9403908
Efficient Route for Synthesis of Enamines from 1,3-Alkyl-2-Thioxodihydropyrimidine-4,6(1H,5H)-dione Enols2019Lett. in Org. Chem., 2019, 16, 538-540; doi: 10.2174/1570178616666190409145118
Synthesis and structural DFT studies of Ni(II) and Co(II) complexes with s-triazine-based di-compartmental ligand2019Polyhedron 2019, 165, 162–170; doi: 10.1016/j.poly.2019.03.024
Synthesis, molecular structure and DFT studies of two heteroleptic nickel(II) s-triazine pincer type complexes2019J. Mol. Str., 2019, 1185, 461-468; doi: 10.1016/j.molstruc.2019.02.089
Design and synthesis of mono-and di-pyrazolyl-s-triazine derivatives, their anticancer profile in human cancer cell lines, and in vivo toxicity in zebrafish embryos2019Bioorg. Chem., 2019, 87, 457–464; doi: 10.1016/j.bioorg.2019.03.063
Green Transformation of Solid-Phase Peptide Synthesis2019ACS Sustainable Chem. Eng., 2019, 7, 3671−3683. doi: 10.1021/acssuschemeng.8b06520.
Synthesis and structure diversity of high coordination number Cd(II) complexes of large s-triazine bis-Schiff base pincer chelate2019Inorganica Chimica Acta 2019, 488, 131–140; doi: 10.1016/j.ica.2019.01.018.
Hunt Bacteria through an Intriguing Cyclic Peptide2019ChemMedChem, 2019, 14, 24 – 5; doi: 10.1002/cmdc.201800597.
A Facile and Eco-Friendly Method for the Synthesis of Sulfonamide and Sulfonate Carboxylic Acid Derivatives—X-ray Structure, Hirshfeld Analysis and Spectroscopic Characterizations2019Crystals 2019, 9, 35; doi:10.3390/cryst9010035.
Evaluation of clay-ionene nanocomposite carriers for controlled drug delivery: Synthesis, in vitro drug release, and kinetics2019Mater. Chem. Phy., 2019, 225, 122–132; dio: 10.1016/j.matchemphys.2018.12.054
Eco-friendly method for silver nanoparticles immobilized decorated silica: Synthesis & characterization and preliminary antibacterial activity2019J. Taiwan Inst. Chem. Eng., 2019, 95,423-331; doi.org/10.1016/j.jtice.2018.07.020
. Modified Epoxy with Chitosan Triazine Dihydrazide Derivatives for Mechanical and Corrosion Protection of Steel2020Coatings 2020, 10, 1256; doi:10.3390/coatings10121256 w.
Fe(III) Complexes Based on Mono- and Bispyrazolyl-s-triazine Ligands: Synthesis, Molecular Structure, Hirshfeld, and Antimicrobial Evaluations2020Molecules 2020, 25, 5750; doi:10.3390/molecules25235750
Ultrasonically Assisted N Cyanoacylation and Synthesis of Alkyl(4- (3-cyano-4,6-dimethyl-2-oxopyridin-1(2H) yl)benzoyl)amino Acid Ester Derivatives.2020. ACS Omega 2020, 5(47), 30671-30678; doi: 10.1021/acsomega.0c04730
Novel 4,6-disubstituted s-Triazin-2-yl Amino Acid 3 Derivatives as Promising Antifungal Agents2020J. Fungi 2020, 6, 237; doi:10.3390/jof6040237
Synthesis, X-ray Structure, Hirshfeld Analysis of Biologically Active Mn(II) Pincer Complexes Based on s-Triazine Ligands2020Crystals 2020, 10, 931; doi:10.3390/cryst10100931.
Exploiting azido-dichloro-triazine as a linker for regioselective incorporation of peptides through their N, O, S functional groups2020Bioorganic Chemistry 2020, 104, 104334; doi: 10.1016/j.bioorg.2020.104334
OxymaPure Coupling Reagents: Beyond Solid-Phase Peptide Synthesis2020Synthesis 2020, 52, 3189-3210; doi: 10.1055/s-0040-1706296.
1,3,5-Triazine as core for the preparation of dendrons2020Arkivoc 2020, part iii, doi: 10.24820/ark.5550190.p011.245
Synthesis, Anti-proliferative Activity, and Molecular Docking Study of New Series of 1,3-5-Triazine Schiff Base Derivatives2020Molecules 2020, 25, 4065; doi:10.3390/molecules25184065
Barbiturate- and Thiobarbituarte-Based s‑Triazine Hydrazone Derivatives with Promising Antiproliferative Activities2020ACS Omega 2020, 5, 15805−15811; doi.org/10.1021/acsomega.0c00468
Synthesis, structure and in vitro anticancer activity of Pd(II) complexes of mono- and bis-pyrazolyl-s-triazine ligands2020Polyhedron 2020, 187,114665; doi.org/10.1016/j.poly.2020.114665.
Chitosan-s-triazinyl-bis(2-aminomethylpyridine) and chitosan-s-triazinylbis(8-oxyquinoline) derivatives: New reagents for silver nanoparticles preparation and their effect of antimicrobial evaluation2020Journal of Chemistry, 2020, 2020, Article ID 9590120, 8 pages; doi: 10.1155/2020/9590120
Molecular and supramolecular structures of self-assembled Cu(II) and Co(II) complexes with 4,4’-[6-(3,5-dimethyl-1H-pyrazol-1-yl)-1,3,5- triazine-2,4-diyl]dimorpholine ligand2020J. Mol. Str. 2020, 1219, 128584; doi:10.1016/j.molstruc.2020.128584
Synthesis and Characterization of New Series of 1,3-5-Triazine Hydrazone Derivatives with Promising Antiproliferative Activity2020Molecules 2020, 25, 2708; doi:10.3390/molecules25112708
Crystal Structure and Theoretical Investigation of Thiobarbituric Acid Derivatives as Nonlinear Optical (NLO) Materials2020Crystals 2020, 10, 442; doi:10.3390/cryst10060442
Enamine Barbiturates and Thiobarbiturates as a New Class of Bacterial Urease Inhibitors2020Appl. Sci. 2020, 10(10), 3523; doi:10.3390/app10103523
Synthesis, X-ray structure, Hirshfeld analysis, and DFT studies of a new Pd(II) complex with an anionic s-triazine NNO donor ligand2020J.Mol. Str. 2020, 1217, 128463, doi:10.1016/j.molstruc.2020.128463
Novel one-dimensional polymeric Cu(II) complexes via Cu(II)-assisted hydrolysis of the 2,4-bis(3,5-dimethyl-1Hpyrazol- 1-yl)-6-methoxy-1,3,5-triazine pincer ligand: Synthesis, structure, and antimicrobial activities2020Appl Organomet Chem. 2020; e5941; DOI: 10.1002/aoc.5941
Syntheses, structure, Hirshfeld analysis and antimicrobial activity of four new Co(II) complexes with s-triazine-based pincer ligand2020Inorganica Chimica Acta. 2020, 510, 119753, doi:10.1016/j.ica.2020.119753
Synthesis, Characterization of sym-2,4,6-trisubstituted-s-Triazine Derivatives and Their Effects on Flame Retardancy of Polypropylene Composites2020Processes 2020, 8(5), 581; doi:10.3390/pr8050581
Multi-Functional Cardanol Triazine Schiff Base Polyimine Additives for Self-Healing and Super-Hydrophobic Epoxy of Steel Coating2020Coatings 2020, 10, 327; doi:10.3390/coatings10040327
Carpino's protecting groups, beyond the Boc and the Fmoc2020Pept Sci. 2020;e24164. Doi:10.1002/pep2.24164
Functionalization of Silica with Triazine Hydrazide to Improve Corrosion Protection and Interfacial Adhesion Properties of Epoxy Coating and Steel Substrate2020Coatings 2020, 10, 351; doi:10.3390/coatings10040351.
Simple approaches for the synthesis of AgNPs in solution and solid phase using modified methoxypolyethylene glycol and evaluation of their antimicrobial activity2020International Journal of Nanomedicine, 2020, 15, 2353–2362; doi: 10.2147/IJN.S244678.
Synthesis, structure and biological activity of zinc(II) pincer complexes with 2,4-bis(3,5-dimethyl-1H-pyrazol-1-yl)-6-methoxy-1,3,5-triazine2020Inorganica Chimica Acta 2020, 508, 119627; doi: 10.1016/j.ica.2020.119627.
Mono- and penta-nuclear self-assembled silver(I) complexes of pyrazolyl s-triazine ligand; synthesis, structure and antimicrobial studies2020Appl Organometal Chem. 2020;34:e5603.; Doi: 10.1002/aoc.5603
Protocol for synthesis of di- and tri-substituted s-triazine derivatives2020MethodsX, 2020, 7, 100825; doi: 0.1016/j.bioorg.2019.103397
Microwave-Assisted Synthesis of Cross-Linked Co-poly(itaconic anhydride-methyl methacrylate): The Effects of the Molar Ratio and Cross-Linking Agent on the Thermal Stability2020Int. J. Polym. Sci., 2020; Vol. 2020, Article ID 9706106, 11 pages; doi:10.1155/2020/9706106
Synthesis and characterisation of thiobarbituric acid enamine derivatives, and evaluation of their α-glucosidase inhibitory and anti-glycation activity2020” J. Enzy. Inhib. Med. Chem., 2020; 35:1, 692-701, DOI: 10.1080/14756366.2020.1737045.
Synthesis, crystal structure, DFT and biological activity of E-pyrene-1-carbaldehyde oxime and E-2-naphthaldehyde oxime2020J. Mol. Str., 2020, 1207, 127848; doi: 10.1016/j.molstruc.2020.127848.
Phenol as a Modulator in the Chemical Reactivity of 2,4,6-Trichloro-1,3,5-triazine: Rules of the Game II2020. Aust. J. Chem. 2020, 1-5, doi.org/10.1071/CH19524
A class of carbonic anhydrase IX/XII – selective carboxylate inhibitors2020J. ENZY. INHIB. MED. CHEM., 2020, 35(1), 549–554; doi: 10.1080/14756366.2020.1715388
Synthesis, crystal structure, evaluation of urease inhibition potential and the docking studies of cobalt(III) complex based on barbituric acid Schiff base ligand2020Inorganic Chimica Acta, 2020, 503, 119405; doi.org/10.1016/j.ica.2019.119405
Synthesis, characterization, thermal stability and kinetics of thermal degradation of novel polymers based-s-triazine Schiff base2020Journal of Polymer Research 2020, 27:10, 1-11; doi.org/10.1007/s10965-019-1961-8
Di- and tri-substituted s-triazine derivatives: Synthesis, characterization, anticancer activity in human breast-cancer cell lines, and developmental toxicity in zebrafish embryos2020Bioorg. Chem. 94 (2020) 103397 doi: 10.1016/j.bioorg.2019.103397
Three Multi-Components Reaction: Synthesis and X-Ray Single-Crystal of Hydroacridinone-Based Hydrazino-S-Triazine Derivative as a New Class of Urease Inhibitor2020Crystals 2020, 10, 14; doi:10.3390/cryst10010014.
Synthesis and Antimicrobial Activity of a New Series of Thiazolidine-2,4-diones Carboxamide and Amino Acid Derivatives2020Molecules 2020, 25, 105; doi:10.3390/molecules25010105
Synthesis, and Molecular Structure Investigations of a New s-Triazine Derivatives Incorporating Pyrazole/Piperidine/ Aniline Moieties2021Crystals 2021, 11, 1500; doi:10.3390/cryst11121500
Straightforward Regio- and Diastereoselective Synthesis, Molecular Structure, Intermolecular Interactions and Mechanistic Study of Spirooxindole-Engrafted Rhodanine Analogs2021Molecules 2021, 26, 7276; doi. 10.3390/molecules262372.
Synthesis, X-ray Structure, Conformational Analysis, and DFT Studies of a Giant s-Triazine bis-Schiff Base2021Crystals 2021, 11, 1418; doi: 10.3390/cryst11111418
Preparation of Multifunctional Plasma Cured Cellulose Fibers Coated with Photo-Induced Nanocomposite toward Self-Cleaning and Antibacterial Textiles2021Polymers 2021, 13, 3664; doi.org/10.3390/polym13213664
Minimizing Side-Reactions During Amide Formation using DIC and OxymaPure in Solid-Phase Peptide Synthesis2021Tetrahedron Lett. 2021, 153462; doi: 10.1016/j.tetlet.2021.153462.
Amide Formation: Choosing the Safer Carbodiimide in Combination with OxymaPure to Avoid HCN Release2021Org. Lett. 2021; 23, 6900−6904; doi:10.1021/acs.orglett.1c02466
Synthesis, characterization and comparative thermal degradation kinetics of s‑Triazine based polymers2021J. Poly. Res. 2021, 28(304); doi: 10.1007/s10965-021-02667-y.
Molecular and Supramolecular Structures of Cd(II) Complexes with Hydralazine-Based Ligands; A New Example for Cyclization of Hydrazonophthalazine to Triazolophthalazine.2021Crystals 2021, 11, 823; doi: 10.3390/cryst11070823.
A Novel Centrosymmetric Fe(III) Complex with Anionic Bis-pyrazolyl-s-triazine Ligand; Synthesis, Structural Investigations and Antimicrobial Evaluations2021Symmetry 2021, 13, 1247; doi: 10.3390/sym13071247
Latest Advances on Synthesis, Purification, and Characterization of Peptides and Their Applications2021Appl. Sci. 2021, 11, 5593; doi:10.3390/app11125593.
Syntheses and Structural Investigations of Penta-Coordinated Co(II) Complexes with Bis-Pyrazolo-S- Triazine Pincer Ligands, and Evaluation of Their Antimicrobial and Antioxidant Activities2021Molecules 2021, 26, 3633; doi: 10.3390/molecules26123633.
s-Triazine Pincer Ligands: Synthesis of their Metal Complexes, Coordination Behavior, and Applications2021Applied Organometallic Chemistry. 2021, 35:e6317; doi: 10.1002/aoc.6317.
Scope and Limitations of Barbituric and Thiobarbituric Amino Acid Derivatives as Protecting Groups for Solid-Phase Peptide Synthesis: Towards a Green Protecting Group2021ChemistrySelect., 2021, 6, 6626–6630; doi: 10.1002/slct.202101539.
Preparation and Characterization of Nanofibrous Scaffolds of Ag/Vanadate Hydroxyapatite Encapsulated into Polycaprolactone: Morphology, Mechanical, and In Vitro Cells Adhesion2021Polymers 2021, 13, 1327; doi. 10.3390/polym13081327
The Antiproliferative and Apoptotic Effect of a Novel Synthesized S-Triazine Dipeptide Series, and Toxicity Screening in Zebrafish Embryos2021Molecules 2021, 26, doi: 10.3390/molecules26041170.
Enhancing the Antifungal Activity of Griseofulvin by Incorporation a Green Biopolymer‐Based Nanocomposite2021Polymers, 2021, 13, 542; doi: 10.3390/polym13040542
Synthesis, Structure and In Vitro Anticancer Activity of Pd(II) Complex of Pyrazolyl-s-Triazine Ligand; A New Example of Metal-Mediated Hydrolysis of s-Triazine Pincer Ligand2021Crystals, 2021, 11, 119; doi: 10.3390/cryst11020119.
A Privileged Structure for Drug Discovery and Bioconjugation2021Molecules, 2021, 26, 864; doi: 10.3390/molecules26040864.
In situ preparation of composites based on trishydrazino-s-triazine (1,4-/1,3-) benzene dicarboxyaldehyde with reduced graphene oxide and their electrical conductivity performance2021J. Mater. Res. Technol. 2021, 10, 1280-1290; doi: 10.1016/j.jmrt.2020.12.075.
Synthesis and X-ray Structure Combined with Hirshfeld and AIM Studies on a New Trinuclear Zn(II)-Azido Complex with s-Triazine Pincer Ligand2022Crystals 2022, 12, 1786; doi: 10.3390/cryst12121786.
Pyrazolyl-s-Triazine with Indole Motif as a Novel of Epidermal Growth Factor Receptor/ Cyclin-Dependent Kinase 2 Dual Inhibitors2022Fornt. Chem, 2022, 10:1078163; doi: 10.3389/fchem.2022.1078163.
Synthesis, Molecular and Supramolecular Structures of Symmetric Dinuclear Cd(II) Azido Complex with bis-Pyrazolyl s-Triazine Pincer Ligand2022Symmetry 2022, 14, 2409. doi.org/10.3390/sym14112409
[3 + 2] Cycloadditions in Asymmetric Synthesis of Spirooxindole Hybrids Linked to Triazole and Ferrocene Units: X-ray Crystal Structure and MEDT Study of the Reaction Mechanism.2022Symmetry 2022, 14, 2071; doi 10.3390/sym14102071
Synthesis and Solid-State X-Ray Structure of the Mononuclear Palladium(II) Complex Based on 1,2,3-Triazole Ligand2022Crystals 2022, 12, 1335; doi:10.3390/cryst12101335
tert-Butylethylcarbodiimide as an Efficient Substitute for Diisopropylcarbodiimide in Solid-Phase Peptide Synthesis: Understanding the Side Reaction of Carbodiimides with OxymaPure2022Org. Process Res. Dev. 2022, 26, 2894−2899; doi: 10.1021/acs.oprd.2c00220.
Syntheses, X-ray structure and biological studies of binuclear μ-oxo diiron complexes with s-triazine pincer ligand2022Inorganica Chimica Acta. 2022, 543, 121196; doi: 10.1016/j.ica.2022.121196
Acetic Acid Mediated for One-Pot Synthesis of Novel Pyrazolyl s-Triazine Derivatives for the Targeted Therapy of Triple-Negative Breast Tumor Cells (MDA-MB-231) via EGFR/PI3K/AKT/mTOR Signaling Cascades2022Pharmaceutics 2022, 14, 1558; doi:10.3390/pharmaceutics14081558
Synthesis and Antiproliferative Activity of a New Series of Monoand Bis(dimethylpyrazolyl) s triazine Derivatives Targeting EGFR/ PI3K/AKT/mTOR Signaling Cascades2022ACS Omega, 2022, 7(28), 24858–24870, doi: 10.1021/acsomega.2c03079.
Synthesis, in vitro and in cell study of a new spirooxindoles based N-alkylated maleimides targeting HER2/3 signaling pathway2022POLYCYCLIC AROMATIC COMPOUNDS, 2022, 1-26, doi: 10.1080/10406638.2022.2101486
. X-ray Structure Analyses and Biological Evaluations of a New Cd(II) Complex with S-Triazine Based Ligand2022Crystals 2022, 12, 861. doi.10.3390/cryst12060861.
Synthesis, Structure and Biological Evaluations of Zn(II) Pincer Complexes Based on S-Triazine Type Chelator2022Molecules 2022, 27, 3625; doi. 10.3390/molecules27113625.
Co (II) Complexes Based on the Bis-Pyrazol-S-Triazine Pincer Ligand: Synthesis, X-ray Structure Studies, and Cytotoxic Evaluation2022Crystals 2022, 12, 741; doi: 10.3390/cryst12050741
Synthesis, X-ray structure and biological studies of new self-assembled Cu(II) complexes derived from s-triazine Schiff base ligand2022Molecules 2022, 27, 2989; doi. 10.3390/molecules27092989
A New Pt(II) Complex with Anionic s-Triazine Based NNO-Donor Ligand: Synthesis, X-ray Structure, Hirshfeld Analysis and DFT Studies2022Molecules 2022, 27, 1628; doi.10.3390/molecules27051628
Synthesis of New S-Triazine Bishydrazino and Bishydrazido-Based Polymers and Their Application in Flame-Retardant Polypropylene Composites2022Polymers 2022, 14, 784. doi. 10.3390/polym14040784
Understanding OxymaPure as a Peptide Coupling Additive: A Guide to New Oxyma Derivatives2022ACS Omega, 2022, 7, 6007−6023; doi. 10.1021/acsomega.1c06342 A.
Synthesis, molecular and supramolecular structure aspects and biological evaluations of a novel [Ag2(phthalazine)(NO3)2]n 3D coordination polymer2022J. Mol. Str. 2022, 1257, 132592; doi.10.1016/j.molstruc.2022.132592.
Synthesis, structure, X-ray photoelectron spectroscopy (XPS), and antimicrobial, anticancer, and antioxidant activities of Co (III) complexes based on the antihypertensive hydralazine2022Appl Organomet Chem. 2022; e6565; doi: 10.1002/aoc.6565.
Synthesis and Characterizations of Novel Isatin-s-Triazine Hydrazone Derivatives; X-ray Structure, Hirshfeld Analysis and DFT Calculations2023Crystals 2023, 13, 305; doi. 10.3390/cryst13020305.
Cytotoxicity and Apoptosis-Induction in MCF-7 Cells for New Pd(II) Complex Based on s-Triazine Ligand: Synthesis, Single Crystal X-Ray Diffraction Analysis and Structural Investigations2023Crystals 2023, 13, 1472; doi.10.3390/cryst13101472.
. Synthesis and X-ray Structure Analysis of the Polymeric [Ag2(4-Amino-4H-1,2,4-triazole)2(NO3)]n(NO3)n Adduct: Anticancer, and Antimicrobial Applications2023Inorganics 2023, 11, 395; dio. 10.3390/inorganics11100395
Synthesis, X-ray Structure, Hirshfeld Surface Analysis and Antimicrobial Assessment of Tetranuclear s-Triazine Hydrazine Schiff Base Ligand2023Inorganics 2023, 11, 357; doi:10.3390/inorganics11090357.
X-ray Structures and Hirshfeld Studies of Two Dinuclear Cd(II) Complexes with a s-Triazine/Pyrazolo Ligand and Pesudohalides as a Linker2023Crystals 2023, 13, 1198; doi.10.3390/cryst13081198
Synthesis, X-ray Structure and Hirshfeld Surface Analysis of Zn(II) and Cd(II) Complexes with s-Triazine Hydrazone Ligand2023Crystals 2023, 13, 1232; doi:10.3390/cryst13081232
Novel Proton Exchange Membranes Based on Sulfonated Poly(acrylonitrile-co-glycidyl methacrylate)/ Poly(vinyl chloride) Composite2023Sustainability 2023, 15, 11166; doi. 10.3390/su151411166
Supramolecular Structure and Antimicrobial Activity of Ni(II) Complexes with s-Triazine/Hydrazine Type Ligand2023Inorganics 2023, 11, 253; doi:10.3390/inorganics11060253
A Novel Na(I) Coordination Complex with s-Triazine Pincer Ligand: Synthesis, X-ray Structure, Hirshfeld Analysis, and Antimicrobial Activity2023Crystals 2023, 13, 890; doi: 10.3390/cryst13060890
Synthesis, X-ray Structure of Two Hexa-Coordinated Ni(II) Complexes with s-Triazine Hydrazine Schiff Base Ligand2023Inorganics 2023, 11, 222; doi: 10.3390/inorganics11050222
Synthesis, Structure and Antimicrobial Activity of New Co(II) Complex with bis-Morpholino/Benzoimidazole-s-Triazine Ligand2023Inorganics 2023, 11, 278; doi.10.3390/inorganics11070278
Synthesis, Characterizations, Antitumor and Antimicrobial Evaluations of Novel Mn(II) and Cu(II) Complexes with NNN-tridentate s-Triazine-Schiff base Ligand2023Inorganica Chimica Acta 2023, 555, 121586, doi.org/10.1016/j.ica.2023.121586
A New 1D Ni (II) Coordination Polymer of s-Triazine Type Ligand and Thiocyanate as Linker via Unexpected Hydrolysis of 2,4-Bis(3,5-dimethyl-1H-pyrazol-1-yl)-6-methoxy-1,3,5-triazine2023Inorganics 2023, 11(3), 135; doi.10.3390/inorganics11030135
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Exploring pyrrolidinyl-spirooxindole natural products as promising platforms for the synthesis of novel spirooxindoles as EGFR/ CDK2 inhibitors for halting breast cancer cells29-02-2024Frontiers in Chemistry
Bis(dimethylpyrazolyl)-aniline-s-triazine derivatives as efficient corrosion inhibitors for C-steel and computational studies12-03-2024Royal Soc.,Open Sci.
Synthesis, X-ray Structure, Cytotoxic, and Anti-Microbial Activities of Zn(II) Complexes with a Hydrazono s-Triazine Bearing Pyridyl Arm19-06-2024Inorganics
Synthesis of Co(II), Mn(II), and Ni(II) complexes with 4-(4,6-bis (3,5-dimethyl-1H-pyrazol-1-yl)-1,3,5-triazin-2-yl)morpholine; X-ray structure, Hirshfeld, AIM, and biological studies08-07-2024Inorganica Chimica Acta
Experimental and Computational Anticorrosion Behaviors of Pyrazole s Triazine/anilino-morpholino Derivatives for Steel in Acidic Solutions11-07-2024ACS Omega
Homoleptic Co(II) and Ni(II) complexes with promising anticancer and antimicrobial activities; Synthesis, X-ray structure, and DFT studies24-08-2024Journal of Molecular Structure
Novel Spirooxindole-Triazole Derivatives: Unveiling [3+2] Cycloaddition Reactivity Through Molecular Electron Density Theory and Investigating Their Potential Cytotoxicity Against HepG2 and MDA-MB-231 Cell Lines23-09-2024Frontiers in Chemistry, section Organic Chemistry. doi: 10.3389/fchem.2024.1460384
Structural and Biological Comparative Studies on M(II)-Complexes (M = Co, Mn, Cu, Ni, Zn) of Hydrazone-s-Triazine Ligand Bearing Pyridyl Arm14-10-2024Inorganics 2024, 12, 268; doi: 10.3390/inorganics12100268
A New Bromo-Mn(II) Complex with 1,3,5-Triazine derivative: Synthesis, Crystal Structure, DFT and Biological Studies28-10-2024Inorganics 2024, 12(11), 284; doi: 10.3390/inorganics12110284.
Title From To Note
Head of Scientific Research and Innovation Unit at College of Medicine08-09-2024
Member of the Scientific Research and Innovation Committee at DAU12-09-2024
Head of the Entrepreneurship& Innovation and Knowledge transfer Center at DAU12-09-2024
Title Donor Date
Unilever Sustainable Living Plan Prize for the best Article2016
Award of Excellence in Scientific Publishing from Quality Authority (CIQAP) Egypt2012
Prize of Administrative Excellence Alexandria University2012
Medal for Distinguish Scientific Publication in Chemistry, Alexandria University2010
Nominated to submit a proposal for Noble Prize in Chemistry2003
Alexandria University Award for Science1999