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طباعة هذه الصفحة
ا.د / منى منير كامل ميخائيل
الكيمياء العضوية الصيدلية
mona.kamel@pharma.cu.edu.eg

Latest List of Publications

1) Synthesis of Certain Quinazolinone derivatives of Pharmaceutical Interest
M. M. Kamel, M. Mohsen Ismail, B. Abd EL Fattah and N. A. Moneib Egypt. J. Pharm. Sci, 32(1-2), 191-204 (1991)

2) Synthesis of some Novel Tetracyclic Diazepines of Biological Interest
Mona M. Kamel, Mosaad S. Mohamed, Mohamed A. Shaban and Saad H.El-Zanfally Alex. J. Pharm. Sci, 9(2), 79-84 (1995)

3) Synthesis and Preliminary Pharmacological Evaluation of some Thieno-diazepines Derivatives as Sedatives and Anticonvusalnts Mona M. Kamel, Mosaad S. Mohamed, Mohamed A.Shaban and Saad H. El-Zanfally Alex.J.Pharm.sci, 9 (2), 95-98 (1995)

4) Synthetic approaches towards 3-pyridinecarbonitrile derivatives and antimicrobial properties. Mona M kamel & Manal M M Hussein Indian Journal of Chemistry, 42b, 2136-2141(2003)

5) Synthesis of certain substituted Pyridazines and Pyrimido[4,5-c]Pyridazines of Anticipated Antimicrobial Activity Rasha A. Mahmoud, Mona M. Kamel, Afaf K. El Ansary and Samir Botros Bull. Fac. Pharm.Cairo.Univ., 43(3), 35-41(2005)

6) Synthesis of certain substituted Pyridazine and Pyrazolo[3,4-c]Pyridazines of Anticipated Antimicrobial Activity Rasha A. Mahmoud, Mona M. Kamel*and Afaf K. El-Ansary Bull. Fac .Pharm.Cairo.Univ., 44(3), 35-41 (2006)

7) The reaction of 2-aminocyclohexeno[b]thiopene derivatives with ethoxycarbonylisothiocyanate: synthesis of Fused Thiopene Derivatives with antibacterial and antifungal activities Wagnat W. Wardakhan, Nadia A. Louca and Mona. M. Kamel Acta Chem. Slov., 54(2), 229-241 (2007)

8) One pot synthesis of Hydrazide-Hydrazone Derivatives and their uses to Synthesis Heterocyclic Compounds with Antimycobacterial and Antimicrobial Activities
Mona M. Kamel, Wagnat W.Wardakhan and S. A.Ouf Bull.Fac.Pharm.Cairo Univ., 45(2), 2007

9) Design, synthesis and blood pressure lowering activity of certain tetrahydrobenzo[b]thiopene derivatives with arylpiperarazinyl side chains Khaled Abouzid*, AzzaTaher and Mona M. Kamel Bull.Fac.Pharm.Cairo Univ., 45(2), 44-50 (2007)

10) Novel Thiophenes, Thienopyrimidines and Triazolothienopyrimidines for the Evaluation of Anticancer and Augmentation Effects of γ-Radiation
Mohamed A. Shaaban, Mostafa M. Ghorab, Helmy I. Heiba, Mona M. Kamel, Nashwa H. Zaher and Mohamed I. Mostafa Arch. Pharm. Chem. Life Sci. 343, 404 – 410 (2010)

11) Synthesis and antitumor activity of novel 6-aryl and 6-alkylpyrazolo[3,4-d]pyrimidin-4-one derivatives Mervat M. El-Enany, Mona M. Kamel, Omneya M. Khalil, Hala B. El-Nassan Eur. J. Med. Chem., 45, 5286-5291 (2010)

12) Synthesis and antitumor activity of novel pyrazolo[1,5‐a]pyrimidine derivatives
Mervat Mostafa El‐Enany, Mona Monir Kamel, Omneya Mahmoud Khalil and Hala Bakr El‐Nassan, Eur. J. of Chem., 2 (3), 331‐336 (2011)

13) Synthesis of New Indole Derivatives Structurally Related to Donepezil and Their Biological Evaluation as Acetylcholinesterase Inhibitors Mohamed M. Ismail, Mona M. Kamel, Lamia W. Mohamed * and Samar I. Faggal Molecules, 17, 4811-4823 (2012).

14) Synthesis and Biological Evaluation of Thiophene Derivatives as Acetylcholinesterase Inhibitors Mohamed M. Ismail, Mona M. Kamel, Lamia W. Mohamed, Samar I. Faggal and Mai A. Galal Molecules, 17, 7217-7231 (2012)

15) Design, Synthesis and Cytotoxicity of Pyridine, PyrazoleandThiazole Derivatives Derived From N-Alkyl-4,5,6,7-tetrahydro-1-benzothiophene M. M. Kamel, A. K. El-Ansary, Y. R. Milad Chemistry of Heterocyclic Compounds, Vol. 49, 392-403 (2013)

16) Synthesis of novel 1,2,4-triazoles, triazolothiadiazines and triazolothiadiazoles as potential anticancer agents Mona M. Kamel, Nadia Y. MegallyAbdo Eur. J. of Med. Chem., 86, 75-80 (2014)

17) Useful Four-Carbon Synthons en route to Monastrol Analogs Amr M. Abdou, S. Botros, Rasha A. Hassan, Mona M. Kamel, Douglass F. Taber and Azza T. Taher Tetrahedron 71, 139-146 (2015)

18) Convenient Synthesis, Characterization, Cytotoxicity and Toxicity of Pyrazole Derivatives Mona M. Kamel Acta Chim. Slov., 62, 136-151 (2015)
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