A. El-Azab

发表

Synthesis, cytotoxic evaluation, and molecular docking studies of novel quinazoline derivatives with benzenesulfonamide and anilide tails: Dual inhibitors of EGFR/HER2.

H. Alkahtani, Ashraf N. Abdalla, A. Y. Ahmed, 2019, Bioorganic chemistry.

Chapter 8 - Tadalafil

M. Al-Omar, Y. Asiri, A. Abdel-Aziz, 2011 .

Synthesis, spectroscopic analyses (FT-IR and NMR), vibrational study, chemical reactivity and molecular docking study and anti-tubercular activity of condensed oxadiazole and pyrazine derivatives

P. Miniyar, Y. Mary, Stevan Armaković, 2018 .

Spectroscopic and reactive properties of a newly synthesized quinazoline derivative: Combined experimental, DFT, molecular dynamics and docking study

Y. Mary, Y. Mary, C. Alsenoy, 2017 .

Design, synthesis, and antitumor activity of novel compounds based on 1,2,4-triazolophthalazine scaffold: Apoptosis-inductive and PCAF-inhibitory effects.

A. El-Azab, Hamada S. Abulkhair, Adel H. Ghiaty, 2020, Bioorganic chemistry.

Lipase-Mediated Preparation of Sugar Building Blocks

T. Taniguchi, K. Ogasawara, A. El-Azab, 1999 .

N-(12-Amino-9,10-dihydro-9,10-ethanoanthracen-11-yl)-4-methylbenzenesulfonamide

J. Mague, A. Abdel-Aziz, A. El-Azab, 2014, Acta crystallographica. Section E, Structure reports online.

2,6-Bis[(S)-1-phenylethyl]-1H,5H-pyrrolo[3,4-f]isoindole-1,3,5,7(2H,6H)-tetrone

E. Tiekink, S. Ng,, A. Alanazi, 2012, Acta crystallographica. Section E, Structure reports online.

(11R,12S)-16-Aminotetracyclo[6.6.2.02,7.09,14]hexadeca-2(7),3,5,9(14),10,12-hexaen-15-ol

E. Tiekink, A. Abdel-Aziz, A. El-Azab, 2012, Acta crystallographica. Section E, Structure reports online.

Inhibition of carbonic anhydrase isoforms I, II, IV, VII and XII with carboxylates and sulfonamides incorporating phthalimide/phthalic anhydride scaffolds.

C. Supuran, M. Ceruso, A. Abdel-Aziz, 2016, Bioorganic & medicinal chemistry.

Design, synthesis, antitumor, and VEGFR-2 inhibition activities of novel 4-anilino-2-vinyl-quinazolines: Molecular modeling studies.

A. Abdel-Aziz, A. El-Azab, Nawaf A. Alsaif, 2022, Bioorganic chemistry.

Synthesis, anticancer, apoptosis-inducing activities and EGFR and VEGFR2 assay mechanistic studies of 5,5-diphenylimidazolidine-2,4-dione derivatives: Molecular docking studies

H. Alkahtani, F. Alqahtani, F. Aleanizy, 2019, Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society.

AMANTADINE AMIDES PRODRUGS AS HEPATIC DELIVERY SYSTEMS TO ENHANCE ITS ACTIVITY AGAINST HCV

H. Abdel‐Aziz, T. Aboul-Fadl, A. El-Azab, 2011 .

Experimental and theoretical investigations on structural, spectroscopic, electronic and thermodynamic properties of (adamantan-1-yl)(phenylsulfanyl)methanone

A. Abdel-Aziz, A. El-Azab, H. Gökce, 2018, Journal of Molecular Structure.

Acacia senegal gum exudate offers protection against cyclophosphamide-induced urinary bladder cytotoxicity

A. R. Abd-Allah, O. Al‐Shabanah, Ali M. Gado, 2009, Oxidative medicine and cellular longevity.

Development and validation of an ELISA with high sensitivity for therapeutic monitoring of afatinib.

A. El-Azab, I. Darwish, M. Al-Shehri, 2018, Bioanalysis.

Synthesis, anti-inflammatory, analgesic, COX-1/2 inhibitory activities and molecular docking studies of substituted 2-mercapto-4(3H)-quinazolinones.

L. Abou-zeid, M. A. El-Sayed, A. Abdel-Aziz, 2016, European journal of medicinal chemistry.

Synthesis, antitumor, and apoptosis-inducing activities of novel 5-arylidenethiazolidine-2,4-dione derivatives: Histone deacetylases inhibitory activity and molecular docking study.

M. Al-agamy, A. Abdel-Aziz, A. El-Azab, 2022, European journal of medicinal chemistry.

Design and synthesis of novel 7-aminoquinazoline derivatives: antitumor and anticonvulsant activities.

A. El-Azab, K. Eltahir, 2012, Bioorganic & medicinal chemistry letters.

Synthesis, anti-inflammatory, cytotoxic, and COX-1/2 inhibitory activities of cyclic imides bearing 3-benzenesulfonamide, oxime, and β-phenylalanine scaffolds: a molecular docking study

H. Alkahtani, M. Alanazi, Ahmad J. Obaidullah, 2020, Journal of enzyme inhibition and medicinal chemistry.

Synthesis and potential antitumor activity of 7-(4-substituted piperazin-1-yl)-4-oxoquinolines based on ciprofloxacin and norfloxacin scaffolds: in silico studies

A. Alanazi, Y. Asiri, A. Abdel-Aziz, 2016, Journal of enzyme inhibition and medicinal chemistry.

Synthesis, antitumor activity, and molecular docking study of 2-cyclopentyloxyanisole derivatives: mechanistic study of enzyme inhibition

M. Alanazi, M. A. El-Sayed, A. Abdel-Aziz, 2020, Journal of enzyme inhibition and medicinal chemistry.

Synthesis, molecular modeling study, preliminary antibacterial, and antitumor evaluation of N-substituted naphthalimides and their structural analogues

A. Alanazi, M. A. El-Sayed, A. Abdel-Aziz, 2013, Medicinal Chemistry Research.

Crystal structure of 6-iodo-3-phenyl-2-propylquinazolin-4(3H)-one, C17H15IN2O

H. Alkahtani, H. Ghabbour, A. Abdel-Aziz, 2019 .

Design, synthesis and biological evaluation of some novel substituted 2-mercapto-3-phenethylquinazolines as antitumor agents

A. Alanazi, M. Mohamed, A. Abdel-Aziz, 2013, Medicinal Chemistry Research.

Synthesis and human/bacterial carbonic anhydrase inhibition with a series of sulfonamides incorporating phthalimido moieties.

C. Supuran, Silvia Bua, M. Mohamed, 2017, Bioorganic & medicinal chemistry.

Novel 4(3H)-quinazolinone analogs: synthesis and anticonvulsant activity

Ghada S. Hassan, M. Sayed-Ahmed, O. Al‐Shabanah, 2013, Medicinal Chemistry Research.

A New Route to (-)-aphanorphine Using a Dioxabicyclo[3.2.1]octane Chiral Building Block

T. Taniguchi, K. Ogasawara, A. El-Azab, 2002 .

Lewis acid-promoted direct synthesis of N-unsubstituted hydrazones via the reaction of hydrazine with acetophenone and isatin derivatives

M. Mohamed, H. Ghabbour, A. Abdel-Aziz, 2016, Russian Journal of General Chemistry.

2-Methoxy-4,6-diphenylnicotinonitrile

J. Mague, A. Abdel-Aziz, A. El-Azab, 2014, Acta crystallographica. Section E, Structure reports online.

Design, synthesis of 2,3-disubstitued 4(3H)-quinazolinone derivatives as anti-inflammatory and analgesic agents: COX-1/2 inhibitory activities and molecular docking studies.

M. Mohamed, L. Abou-zeid, A. Abdel-Aziz, 2016, Bioorganic & medicinal chemistry.

Design, synthesis and biological evaluation of novel quinazoline derivatives as potential antitumor agents: molecular docking study.

M. Al-Omar, M. Sayed-Ahmed, Adel S El-Azab, 2010, European journal of medicinal chemistry.

Non-classical antifolates. Part 2: synthesis, biological evaluation, and molecular modeling study of some new 2,6-substituted-quinazolin-4-ones.

M. Al-Omar, L. Abou-zeid, A. Abdel-Aziz, 2010, Bioorganic & medicinal chemistry.

Substituted quinazolines, part 3. Synthesis, in vitro antitumor activity and molecular modeling study of certain 2-thieno-4(3H)-quinazolinone analogs.

H. El-kashef, A. Abdel-Aziz, A. El-Azab, 2009, European journal of medicinal chemistry.

Synthesis and antitumor evaluation of trimethoxyanilides based on 4(3H)-quinazolinone scaffolds.

M. Mohamed, A. Abdel-Aziz, A. El-Azab, 2016, European journal of medicinal chemistry.

Newly synthesized dihydroquinazoline derivative from the aspect of combined spectroscopic and computational study

Y. Mary, Y. Mary, C. Alsenoy, 2017 .

Structure-based design of phthalimide derivatives as potential cyclooxygenase-2 (COX-2) inhibitors: anti-inflammatory and analgesic activities.

A. Alanazi, Y. Asiri, A. Abdel-Aziz, 2015, European journal of medicinal chemistry.

Design, synthesis and anticonvulsant evaluation of novel 8-substituted-4(3H)-quinazolines

A. El-Azab, K. Eltahir, 2011, Medicinal Chemistry Research.

Synthesis, antitumour and antioxidant activities of novel α,β-unsaturated ketones and related heterocyclic analogues: EGFR inhibition and molecular modelling study

M. A. El-Sayed, A. Abdel-Aziz, A. El-Azab, 2018, Journal of enzyme inhibition and medicinal chemistry.

Design, synthesis and biological evaluation of some novel substituted quinazolines as antitumor agents.

A. Alanazi, A. Abdel-Aziz, A. El-Azab, 2014, European journal of medicinal chemistry.

Synthesis, anticancer and apoptosis-inducing activities of quinazoline–isatin conjugates: epidermal growth factor receptor-tyrosine kinase assay and molecular docking studies

H. Alkahtani, L. Abou-zeid, A. Abdel-Aziz, 2017, Journal of enzyme inhibition and medicinal chemistry.

Design, synthesis, and biological evaluation of substituted hydrazone and pyrazole derivatives as selective COX-2 inhibitors: Molecular docking study.

Y. Asiri, M. A. El-Sayed, A. Abdel-Aziz, 2011, Bioorganic & medicinal chemistry.

Synthesis, Analgesic and Anti‐Inflammatory Evaluation of Some New 3H‐Quinazolin‐4‐one Derivatives

A. Kadi, A. Alafeefy, A. El-Azab, 2008, Archiv der Pharmazie.

Synthesis and anticonvulsant evaluation of some new 2,3,8-trisubstituted-4(3H)-quinazoline derivatives.

Adel S El-Azab, Kamal E H Eltahir, A. El-Azab, 2012, Bioorganic & medicinal chemistry letters.

Synthesis, Cytotoxic Evaluation, and Structure-Activity Relationship of Substituted Quinazolinones as Cyclin-Dependent Kinase 9 Inhibitors

H. Alkahtani, F. Alqahtani, F. Aleanizy, 2022, Molecules.

Synthesis, biological evaluation and molecular modeling study of pyrazole and pyrazoline derivatives as selective COX-2 inhibitors and anti-inflammatory agents. Part 2.

M. A. El-Sayed, A. Abdel-Aziz, A. El-Azab, 2012, Bioorganic & medicinal chemistry.

Synthesis and anticonvulsant evaluation of some novel 4(3H)-quinazolinones

S. Attia, A. El-Azab, K. Eltahir, 2011 .

Synthesis, antiproliferative and enzymatic inhibition activities of quinazolines incorporating benzenesulfonamide: Cell cycle analysis and molecular modeling study

H. Alkahtani, M. Alanazi, M. Al-agamy, 2023, Journal of Molecular Structure.

Carbonic Anhydrase Inhibition Activities of Schiff’s Bases Based on Quinazoline-Linked Benzenesulfonamide

C. Supuran, H. Alkahtani, Silvia Bua, 2022, Molecules.

Synthesis, Anticancer Screening of Some Novel Trimethoxy Quinazolines and VEGFR2, EGFR Tyrosine Kinase Inhibitors Assay; Molecular Docking Studies

Mubarak A. Alamri, M. Mohamed, A. Alabbas, 2021, Molecules.

Remarkable Conversion of 2-Thioxo-2,3-dihydroquinazolin-4(1H)-ones into the Corresponding Quinazoline-2,4(1H,3H)-diones: Spectroscopic Analysis and X-Ray Crystallography

A. Abdel-Aziz, A. El-Azab, N. Khalil, 2021 .

Synthesis, potential antitumor activity, cell cycle analysis, and multitarget mechanisms of novel hydrazones incorporating a 4-methylsulfonylbenzene scaffold: a molecular docking study

Ahmad J. Obaidullah, A. Abdel-Aziz, A. El-Azab, 2021, Journal of enzyme inhibition and medicinal chemistry.

Design, synthesis, and analysis of antiproliferative and apoptosis-inducing activities of nitrile derivatives containing a benzofuran scaffold: EGFR inhibition assay and molecular modelling study

M. A. El-Sayed, K. Selim, A. Abdel-Aziz, 2021, Journal of enzyme inhibition and medicinal chemistry.

S-substituted 2-mercaptoquinazolin-4(3H)-one and 4-ethylbenzensulfonamides act as potent and selective human carbonic anhydrase IX and XII inhibitors

C. Supuran, Hany E. A. Ahmed, M. Alanazi, 2020, Journal of enzyme inhibition and medicinal chemistry.

Exploring structure-activity relationship of S-substituted 2-mercaptoquinazolin-4(3H)-one including 4-ethylbenzenesulfonamides as human carbonic anhydrase inhibitors

C. Supuran, Hany E. A. Ahmed, A. Nocentini, 2020, Journal of enzyme inhibition and medicinal chemistry.

Synthesis and comparative carbonic anhydrase inhibition of new Schiff's bases incorporating benzenesulfonamide, methanesulfonamide, and methylsulfonylbenzene scaffolds.

C. Supuran, M. Alanazi, Silvia Bua, 2019, Bioorganic chemistry.

Synthesis of benzensulfonamides linked to quinazoline scaffolds as novel carbonic anhydrase inhibitors.

C. Supuran, M. Mohamed, A. Nocentini, 2019, Bioorganic chemistry.

Structural alterations based on naproxen scaffold: Synthesis, evaluation of antitumor activity and COX-2 inhibition, and molecular docking.

Y. Asiri, M. A. El-Sayed, A. Abdel-Aziz, 2018, European journal of medicinal chemistry.

Synthesis, antitumour activities and molecular docking of thiocarboxylic acid ester-based NSAID scaffolds: COX-2 inhibition and mechanistic studies

L. Abou-zeid, M. A. El-Sayed, A. Abdel-Aziz, 2018, Journal of enzyme inhibition and medicinal chemistry.

Synthesis, in vitro antitumour activity, and molecular docking study of novel 2-substituted mercapto-3-(3,4,5-trimethoxybenzyl)-4(3H)-quinazolinone analogues

H. Ghabbour, A. Abdel-Aziz, A. El-Azab, 2017, Journal of enzyme inhibition and medicinal chemistry.

Synthesis, antitumor and antimicrobial activity of some new 6-methyl-3-phenyl-4(3H)-quinazolinone analogues: in silico studies

A. Alanazi, M. Al-agamy, A. Abdel-Aziz, 2016, Journal of enzyme inhibition and medicinal chemistry.

Synthesis, anti-inflammatory, analgesic and COX-1/2 inhibition activities of anilides based on 5,5-diphenylimidazolidine-2,4-dione scaffold: Molecular docking studies.

L. Abou-zeid, A. Abdel-Aziz, A. El-Azab, 2016, European journal of medicinal chemistry.

Design, synthesis and biological evaluation of 2-mercapto-3-phenethylquinazoline bearing anilide fragments as potential antitumor agents: molecular docking study.

A. Alanazi, M. Mohamed, A. Abdel-Aziz, 2013, Bioorganic & medicinal chemistry letters.

Molecular design, synthesis and biological evaluation of cyclic imides bearing benzenesulfonamide fragment as potential COX-2 inhibitors. Part 2.

A. Alanazi, Adel S El-Azab, Ibrahim A Al-Suwaidan, 2013, Bioorganic & medicinal chemistry letters.

Design, synthesis and biological evaluation of some novel substituted 2-mercapto-3-phenethylquinazolines as antitumor agents

A. Alanazi, M. Mohamed, A. Abdel-Aziz, 2013, Medicinal Chemistry Research.

Synthesis of some new substituted iodoquinazoline derivatives and their antimicrobial screening

A. Alafeefy, M. Mohamed, S. Abdel-Hamid, 2011 .

Design, synthesis, single-crystal and preliminary antitumor activity of novel arenesulfonylimidazolidin-2-ones.

A. Alanazi, M. Al-Omar, A. Abdel-Aziz, 2012, Bioorganic & medicinal chemistry letters.

Novel 4(3H)-quinazolinone analogs: synthesis and anticonvulsant activity

Ghada S. Hassan, M. Sayed-Ahmed, O. Al‐Shabanah, 2013, Medicinal Chemistry Research.

Synthesis of Some New Substituted 2-Mercaptoquinazoline Analogs as Potential Antimicrobial Agents

A. El-Azab, 2007 .

Synthesis, antitumor activity and molecular docking study of some novel 3-benzyl-4(3H)quinazolinone analogues

A. Alanazi, M. Mohamed, M. A. El-Sayed, 2016, Journal of enzyme inhibition and medicinal chemistry.

Synthesis and biological evaluation of some novel cyclic-imides as hypoglycaemic, anti-hyperlipidemic agents.

M. Al-Omar, S. Attia, A. Abdel-Aziz, 2011, European journal of medicinal chemistry.

Conformational preferences of sterically congested 2-imidazolidinone using X-ray analysis and computational studies. Part 1: Trans-1-acetyl-4,5-di-tert-butyl-2-imidazolidinone

M. Al-Omar, A. Abdel-Aziz, A. El-Azab, 2010 .

An Alternative Route for Synthesis of Chiral 4-Substituted 1-Arenesulfonyl-2-imidazolidinones: Unusual Utility of (4S,5S)- and (4R,5R)-4,5-Dimethoxy-2-imidazolidinones and X-Ray Crystallography

A. Alanazi, I. Alswaidan, A. Abdel-Aziz, 2013 .

Synthesis, single-crystal, in vitro antitumor evaluation and molecular docking of 3-substitued 5,5-diphenylimidazolidine-2,4-dione derivatives

A. Alanazi, A. Abdel-Aziz, A. El-Azab, 2013, Medicinal Chemistry Research.

Synthesis and biological evaluation of cyclic imides incorporating benzenesulfonamide moieties as carbonic anhydrase I, II, IV and IX inhibitors.

C. Supuran, A. Angeli, A. Abdel-Aziz, 2017, Bioorganic & medicinal chemistry.

Trends in monoliths: Packings, stationary phases and nanoparticles.

M. Alanazi, Huda S. A Al-Salem, Ahmad J. Obaidullah, 2023, Journal of chromatography. A.

Synthesis and Conformational Analysis of Sterically Congested (4R)-(−)-1-(2,4,6-Trimethylbenzenesulfonyl)-3-n-butyryl-4-tert-butyl-2-imidazolidinone: X-Ray Crystallography and Semiempirical Calculations

A. Alanazi, I. Alswaidan, A. Abdel-Aziz, 2014 .

Spectroscopic analysis (FT-IR, FT-Raman and NMR) and molecular docking study of ethyl 2-(4-oxo-3-phenethyl-3,4-dihydroquinazolin-2-ylthio)-acetate

Y. Mary, K. Jalaja, C. Alsenoy, 2016 .

FT-IR, FT-Raman and molecular docking study of ethyl 4-(2-(4-oxo-3-phenethyl-3,4-dihydroquinazolin-2-ylthio)acetamido)benzoate

Y. Mary, C. Alsenoy, A. Abdel-Aziz, 2016 .

Bisoprolol: A comprehensive profile.

A. El-Azab, A. Bakheit, Raisuddin Ali, 2021, Profiles of drug substances, excipients, and related methodology.

Synthesis and anticonvulsant activity of some new thiazolo[3,2-a][1,3]diazepine, benzo[d]thiazolo[5,2-a][12,6]diazepine and benzo[d]oxazolo[5,2-a][12,6]diazepine analogues.

A. Kadi, Ghada S. Hassan, M. Sayed-Ahmed, 2011, European journal of medicinal chemistry.

DFT and experimental (FT-IR and FT-Raman) investigation of vibrational spectroscopy and molecular docking studies of 2-(4-oxo-3-phenethyl-3,4-dihydroquinazolin-2-ylthio)-N-(3,4,5-trimethoxyphenyl) acetamide

Y. Mary, C. Alsenoy, A. Abdel-Aziz, 2016 .

Design, synthesis, and carbonic anhydrase inhibition activity of benzenesulfonamide-linked novel pyrazoline derivatives.

C. Supuran, M. Alanazi, Silvia Bua, 2019, Bioorganic chemistry.

Co-Inhibition of P-gp and Hsp90 by an Isatin-Derived Compound Contributes to the Increase of the Chemosensitivity of MCF7/ADR-Resistant Cells to Doxorubicin

T. Tuccinardi, H. Alkahtani, R. Ahmad, 2021, Molecules.

Investigation of arenesulfonyl-2-imidazolidinones as potent carbonic anhydrase inhibitors

C. Supuran, D. Ekinci, M. Şentürk, 2015, Journal of enzyme inhibition and medicinal chemistry.

Synthesis of novel isoindoline-1,3-dione-based oximes and benzenesulfonamide hydrazones as selective inhibitors of the tumor-associated carbonic anhydrase IX.

C. Supuran, A. Nocentini, A. Abdel-Aziz, 2018, Bioorganic chemistry.

New anthranilic acid-incorporating N-benzenesulfonamidophthalimides as potent inhibitors of carbonic anhydrases I, II, IX, and XII: Synthesis, in vitro testing, and in silico assessment.

C. Supuran, M. Alanazi, Silvia Bua, 2019, European journal of medicinal chemistry.

Synthesis and carbonic anhydrase inhibition of polycyclic imides incorporating N-benzenesulfonamide moieties.

C. Supuran, A. Angeli, A. Nocentini, 2017, Bioorganic & medicinal chemistry.

Synthesis and biological evaluation of 2-styrylquinolines as antitumour agents and EGFR kinase inhibitors: molecular docking study

Hatem A. Abuelizz, M. A. El-Sayed, A. Abdel-Aziz, 2017, Journal of enzyme inhibition and medicinal chemistry.

Thiadiazolodiazepine analogues as a new class of neuromuscular blocking agents: Synthesis, biological evaluation and molecular modeling study.

Ghada S. Hassan, A. Abdel-Aziz, A. El-Azab, 2017, European journal of medicinal chemistry.

S-Phenyl 4-methoxybenzothioate

H. Fun, A. Abdel-Aziz, A. El-Azab, 2012, Acta crystallographica. Section E, Structure reports online.

An Efficient Synthesis of Thioesters Via TFA-Catalyzed Reaction of Carboxylic Acid and Thiols: Remarkably Facile C–S Bond Formation

A. Abdel-Aziz, A. El-Azab, 2012 .

Carbonic anhydrase inhibitory activity of sulfonamides and carboxylic acids incorporating cyclic imide scaffolds.

C. Supuran, M. Ceruso, A. Abdel-Aziz, 2014, Bioorganic & medicinal chemistry letters.

4-Substituted benzenesulfonamides featuring cyclic imides moieties exhibit potent and isoform-selective carbonic anhydrase II/IX inhibition.

C. Supuran, A. Nocentini, P. Gratteri, 2019, Bioorganic chemistry.

Molecular structure, Hirshfeld surface analysis, spectroscopic (FT-IR, Laser-Raman, UV–vis. and NMR), HOMO-LUMO and NBO investigations on N-(12-amino-9,10-dihydro-9,10-ethanoanthracen-11-yl)-4-methylbenzenesulfonamide

C. Alaşalvar, A. Abdel-Aziz, A. El-Azab, 2018, Journal of Molecular Structure.

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

M. Alanazi, M. Al-agamy, A. Abdel-Aziz, 2019, ChemistrySelect.

Hirshfeld Surface, Molecular Docking Study, Spectroscopic Characterization and NLO Profile of 2‐Methoxy‐4,6‐Diphenylnicotinonitrile

M. Alanazi, M. Al-agamy, A. Abdel-Aziz, 2019, ChemistrySelect.

Synthesis and anti-inflammatory activity of sulfonamides and carboxylates incorporating trimellitimides: Dual cyclooxygenase/carbonic anhydrase inhibitory actions.

C. Supuran, A. Angeli, A. Abdel-Aziz, 2019, Bioorganic chemistry.

An Expedient Route to the Calabar Bean Alkaloids (‐)‐Physovenine and (‐)‐Physostigmine.

T. Taniguchi, K. Ogasawara, A. El-Azab, 2001 .

Synergistic Anti Leukemia Effect of a Novel Hsp90 and a Pan Cyclin Dependent Kinase Inhibitors

H. Alkahtani, Ashraf N. Abdalla, A. Gouda, 2020, Molecules.

Antitumor activity, multitarget mechanisms, and molecular docking studies of quinazoline derivatives based on a benzenesulfonamide scaffold: Cell cycle analysis.

H. Alkahtani, M. Alanazi, Ahmad J. Obaidullah, 2020, Bioorganic chemistry.

1-Acetyl-5-methoxy-4-(phenylsulfanyl)imidazolidin-2-one

J. Mague, A. Alanazi, A. Abdel-Aziz, 2014, Acta Crystallographica Section E.

1-Acetyl-4-(phenylsulfanyl)imidazolidin-2-one

E. Tiekink, S. Ng,, A. Alanazi, 2012, Acta Crystallographica Section E.

4-[(1, 3-Dioxoisoindolin-2-yl)methyl]benzenesulfonamide: Full Structural and Spectroscopic Characterization and Molecular Docking with Carbonic Anhydrase II

A. Abdel-Aziz, A. El-Azab, H. Gökce, 2018, ChemistrySelect.

Crystal, molecular structure, and conformational preferences of 3-(2-(4-morpholinophenyl)-2-oxoethyl)-5,5-diphenylimidazolidine-2,4-dione

H. Fun, H. Ghabbour, A. Abdel-Aziz, 2016 .

Methyl 3-[(6-nitro-4-oxo-3-phenyl-3,4-dihydroquinazolin-2-yl)sulfanyl]propanoate

C. S. Chidan Kumar, H. Fun, A. Abdel-Aziz, 2013, Acta crystallographica. Section E, Structure reports online.

5-Isopropylimidazolidine-2,4-dione monohydrate

H. Fun, M. Hemamalini, A. Abdel-Aziz, 2012, Acta crystallographica. Section E, Structure reports online.

An expedient route to the Calabar bean alkaloids (-)-physovenine and (-)-physostigmine.

T. Taniguchi, K. Ogasawara, A. Elazab, 2000, Organic letters.

Applicable pharmacokinetic study: Development and validation of bioanalytical LC-MS/MS method for the simultaneous quantification of cytarabine and glasdegib used for the treatment of acute myeloid leukemia

M. Alanazi, A. Abdel-Aziz, A. El-Azab, 2023, Arabian Journal of Chemistry.

A Liquid Chromatography Tandem Mass Spectrometry Method for the Simultaneous Estimation of the Dopamine Receptor Antagonist LE300 and Its N-methyl Metabolite in Plasma: Application to a Pharmacokinetic Study

A. El-Azab, Mohamed W. Attwa, Manal El-Gendy, 2023, Molecules.

Antitumor evaluation and molecular docking study of substituted 2-benzylidenebutane-1,3-dione, 2-hydrazonobutane-1,3-dione and trifluoromethyl-1H-pyrazole analogues

A. Alanazi, M. A. El-Sayed, A. Abdel-Aziz, 2015, Journal of enzyme inhibition and medicinal chemistry.

A Rapid and Sensitive Liquid Chromatography-Tandem Mass Spectrometry Bioanalytical Method for the Quantification of Encorafenib and Binimetinib as a First-Line Treatment for Advanced (Unresectable or Metastatic) Melanoma—Application to a Pharmacokinetic Study

M. Alanazi, A. El-Azab, Mohamed W. Attwa, 2022, Molecules.

3-Amino-5,5-diphenylimidazolidine-2,4-dione

J. Mague, A. Abdel-Aziz, A. El-Azab, 2014, Acta crystallographica. Section E, Structure reports online.

3-[2-(4-Fluorophenyl)-2-oxoethyl]-5,5-diphenylimidazolidine-2,4-dione

J. Mague, A. Abdel-Aziz, A. El-Azab, 2014, Acta crystallographica. Section E, Structure reports online.

Synthesis, anticancer and apoptosis-inducing activities of quinazoline–isatin conjugates: epidermal growth factor receptor-tyrosine kinase assay and molecular docking studies

H. Alkahtani, L. Abou-zeid, A. Abdel-Aziz, 2017, Journal of enzyme inhibition and medicinal chemistry.

Synthesis of novel spirochromane incorporating Schiff's bases, potential antiproliferative activity, and dual EGFR/HER2 inhibition: Cell cycle analysis and in silico study

A. Abdel-Aziz, A. El-Azab, A. Bakheit, 2023, Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society.

Tadalafil.

M. Al-Omar, Y. Asiri, A. Abdel-Aziz, 2011, Profiles of drug substances, excipients, and related methodology.

Synthesis, Analgesic and Anti‐Inflammatory Evaluation of Some New 3H‐Quinazolin‐4‐one Derivatives

A. Kadi, A. Alafeefy, A. El-Azab, 2008, Archiv der Pharmazie.