Prevalence and Genetic Characteristics of TEM, SHV, and CTX-M in Clinical Klebsiella pneumoniae Isolates from Saudi Arabia von Tawfik, Abdulkader F., Alswailem, Abdulaziz M., Shibl, Atef M., Al-Agamy, Mohamed H.M.

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Hirshfeld Surface, Molecular Docking Study, Spectroscopic Characterization and NLO Profile of 2‐Methoxy‐4,6‐Diphenylnicotinonitrile von Gökce, Halil, Sert, Yusuf, Alpaslan, Gökhan, El‐Azab, Adel S., Alanazi, Mohammed M., Al‐Agamy, Mohamed H.M., Abdel‐Aziz, Alaa A.‐M.

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Synthesis, and characterization of a new series of sulfite and sulfate derivatives of d-Mannitol von Al Majid, Abdullah M.A., Barakat, Assem, Mabkhot, Yahia Nasser, Al-Agamy, Mohamed H.M.

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Carbonic Anhydrase Inhibition Activities of Schiff's Bases Based on Quinazoline-Linked Benzenesulfonamide von El-Azab, Adel S, Abdel-Aziz, Alaa A-M, Ghabbour, Hazem A, Bua, Silvia, Nocentini, Alessio, Alkahtani, Hamad M, Alsaif, Nawaf A, Al-Agamy, Mohamed H M, Supuran, Claudiu T

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Synthesis, antiproliferative and enzymatic inhibition activities of quinazolines incorporating benzenesulfonamide: Cell cycle analysis and molecular modeling study von El-Azab, Adel S., Alkahtani, Hamad M., AlSaif, Nawaf A., Al-Suwaidan, Ibrahim A., Obaidullah, Ahmad J., Alanazi, Mohammed M., Al-Obaid, Abdulrahman M., Al-Agamy, Mohamed H.M., Abdel-Aziz, Alaa A.-M.

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Synthesis, antitumor, and apoptosis-inducing activities of novel 5-arylidenethiazolidine-2,4-dione derivatives: Histone deacetylases inhibitory activity and molecular docking study von Hamdi, Abdelrahman, Elhusseiny, Walaa M., Othman, Dina I.A., Haikal, Abdullah, Bakheit, Ahmed H., El-Azab, Adel S., Al-Agamy, Mohamed H.M., Abdel-Aziz, Alaa A.-M.

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Synthesis, antitumor and antimicrobial activity of some new 6-methyl-3-phenyl-4(3H)-quinazolinone analogues: in silico studies von Alanazi, Amer M., Abdel-Aziz, Alaa A.-M., Shawer, Taghreed Z., Ayyad, Rezk R., Al-Obaid, Abdulrahman M., Al-Agamy, Mohamed H. M., Maarouf, Azza R., El-Azab, Adel S.

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Design, synthesis and antibacterial activity of fluoroquinolones containing bulky arenesulfonyl fragment: 2D-QSAR and docking study von Abdel-Aziz, Alaa A.-M., Asiri, Yousif A., Al-Agamy, Mohamed H.M.

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Synthesis, molecular structure investigations and antimicrobial activity of 2-thioxothiazolidin-4-one derivatives von Barakat, Assem, Al-Najjar, Hany J., Al-Majid, Abdullah Mohammed, Soliman, Saied M., Mabkhot, Yahia Nasser, Al-Agamy, Mohamed H.M., Ghabbour, Hazem A., Fun, Hoong-Kun

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Facile and Promising Method for Michael Addition of Indole and Pyrrole to Electron-Deficient trans-β-Nitroolefins Catalyzed by a Hydrogen Bond Donor Catalyst Feist’s Acid and Preli... von Naushad, M., al-Agamy, Mohamed H., Barakat, Assem, Islam, Mohammad Shahidul, Al Majid, Abdullah M. A.

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Synthesis, characterization, antimicrobial activity and molecular docking studies of combined pyrazol-barbituric acid pharmacophores von Barakat, Assem, Al-Qahtani, Bandar M., Al-Majid, Abdullah M., Shaik, M. Ali Mohammed Rafi, Al-Agamy, Mohamed H.M., Wadood, Abdul

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Synthesis, Characterization and Antimicrobial Activity of Novel Pharmacophores Incorporating Imidazoline-Oxazoline Scaffold von Barakat, Assem, Al-Majid, Abdullah Mohammed, Al-Qahatany, Faisal M., Islam, Mohammad Shahidul, Al-Agamy, Mohamed H.M.

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Structural, Spectroscopic, Electronic and Molecular Docking Studies on (11R,12 S)‐16‐Aminotetracyclo[6.6.2.02,7.09,14]hexadeca‐2(7),3,5,9(14),10,12‐hexaen‐15‐ol von Kaya, Serdal, Gökce, Halil, El‐Azab, Adel S., Sert, Yusuf, Alanazi, Mohammed M., Öztürk, Nuri, Al‐Agamy, Mohamed H. M., Abdel‐Aziz, Alaa A.‐M.

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Facile and promising method for Michael addition of indole and pyrrole to electron-deficient trans-[beta]-nitroolefins catalyzed by a hydrogen bond donor catalyst feist's acid and... von Majid, Abdullah M.A. Al, Islam, Mohammad Shahidul, Barakat, Assem, Agamy, Mohamed H.M. Al, Naushad, Mu

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Synthesis, Characterization and Antimicrobial Activity of Novel Pharmacophores Incorporating Imidazoline-Oxazoline Scaffold von Barakat, Assem, Al-Majid, Abdullah Mohammed, Al-Qahatany, Faisal M, Islam, Mohammad Shahidul, Al-Agamy, Mohamed H.M

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