S. Mohamady

发表

Design, Synthesis, and Biological Evaluation of Novel 7H-[1,2,4]Triazolo[3,4-b][1,3,4]thiadiazine Inhibitors as Antitumor Agents

Muhammad I. Ismail, K. Abouzid, N. Samir, 2020, ACS omega.

Discovery of 5-aryl-3-thiophen-2-yl-1H-pyrazoles as a new class of Hsp90 inhibitors in hepatocellular carcinoma.

Scott D. Taylor, Muhammad I. Ismail, S. Mohamady, 2019, Bioorganic chemistry.

The effect of bisphosphonate acidity on the activity of a thymidylyltransferase.

D. Jakeman, S. Mohamady, S. Beaton, 2013, Organic & biomolecular chemistry.

Synthesis of nucleoside tetraphosphates and dinucleoside pentaphosphates via activation of cyclic trimetaphosphate.

Scott D. Taylor, S. Mohamady, 2013, Organic letters.

Synthesis of Nucleoside‐5′‐O‐Tetraphosphates from Activated Trimetaphosphate and Nucleoside‐5′‐O‐Monophosphates

Scott D. Taylor, S. Mohamady, 2018, Current protocols in nucleic acid chemistry.

An improved method for the synthesis of nucleoside triphosphate analogues.

D. Jakeman, S. Mohamady, 2005, The Journal of organic chemistry.

General procedure for the synthesis of dinucleoside polyphosphates.

Scott D. Taylor, S. Mohamady, 2011, The Journal of organic chemistry.

Design and novel synthetic approach supported with molecular docking and biological evidence for naphthoquinone-hydrazinotriazolothiadiazine analogs as potential anticancer inhibiting topoisomerase-IIB.

S. Mohamady, A. Gibriel, M. S. Hendy, 2020, Bioorganic chemistry.

Efficient One-Pot, Two-Component Modular Synthesis of 3,5-Disubstituted Pyrazoles

Scott D. Taylor, S. Mohamady, Braden Kralt, 2018, ACS omega.

Aryl azide-sulfonamide hybrids induce cellular apoptosis: synthesis and preliminary screening of their cytotoxicity in human HCT116 and A549 cancer cell lines

Yaser A. Mostafa, S. Mohamady, Muhamad Mustafa, 2019, Medicinal Chemistry Research.

Exploring the Potent Inhibition of CTP Synthase by Gemcitabine‐5′‐Triphosphate

Scott D. Taylor, S. Bearne, S. Mohamady, 2016, Chembiochem : a European journal of chemical biology.

One flask synthesis of 2′,3′-cyclic nucleoside monophosphates from unprotected nucleosides using activated cyclic trimetaphosphate

Scott D. Taylor, S. Mohamady, 2016 .

Synthesis of Nucleoside Triphosphates from 2'-3'-Protected Nucleosides Using Trimetaphosphate.

Scott D. Taylor, S. Mohamady, 2016, Organic letters.

Synthesis of nucleoside 5'-tetraphosphates containing terminal fluorescent labels via activated cyclic trimetaphosphate.

Scott D. Taylor, S. Mohamady, 2014, The Journal of organic chemistry.

Dual Targeting of VEGFR2 and C-Met Kinases via the Design and Synthesis of Substituted 3-(Triazolo-thiadiazin-3-yl)indolin-2-one Derivatives as Angiogenesis Inhibitors

Hamed I. Ali, Wagdy M. Eldehna, Hany S. Ibrahim, 2020, ACS omega.

Design, synthesis, and docking of novel thiazolidine‐2,4‐dione multitarget scaffold as new approach for cancer treatment

M. Ghoneim, Sahar Ahmed, Khaled El-Adl, 2023, Archiv der Pharmazie.

Aryl azide-sulfonamide hybrids induce cellular apoptosis: synthesis and preliminary screening of their cytotoxicity in human HCT116 and A549 cancer cell lines

Yaser A. Mostafa, S. Mohamady, Muhamad Mustafa, 2019, Medicinal Chemistry Research.

WITHDRAWN: First order derivative spectrophotometric technique and coefficients validation for contemporaneous determination of oral diabetes medicines

Tim Chen, S. Mohamady, John C. Y. Chen, 2018, Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy.

Isatin-pyrimidine hybrid derivatives as enoyl acyl carrier protein reductase (InhA) inhibitors against Mycobacterium tuberculosis.

M. Abdel-Aziz, S. Mohamady, A. Khalil, 2023, Bioorganic chemistry.

Sulfonyl imidazolium salts as reagents for the rapid and efficient synthesis of nucleoside polyphosphates and their conjugates.

Scott D. Taylor, S. Mohamady, Ahmed Y. Desoky, 2012, Organic letters.

Synthesis of nucleoside tetraphosphates and dinucleoside pentaphosphates via activation of cyclic trimetaphosphate.

Scott D. Taylor, S. Mohamady, 2013, Organic letters.

Anticancer evaluations of iodoquinazoline substituted with allyl and/or benzyl as dual inhibitors of EGFRWT and EGFRT790M: design, synthesis, ADMET and molecular docking

S. Mohamady, A. El-Morsy, Omar M. Alatawi, 2024, RSC advances.

Fragment-based design and synthesis of coumarin-based thiazoles as dual c-MET/STAT-3 inhibitors for potential antitumor agents.

Mohamed S. Nafie, S. Mohamady, Haytham O. Tawfik, 2024, Bioorganic chemistry.

Tailored horseshoe-shaped nicotinonitrile scaffold as dual promising c-Met and Pim-1 inhibitors: Design, synthesis, SAR and in silico study.

Mohamed S. Nafie, S. Mohamady, Haytham O. Tawfik, 2023, Bioorganic chemistry.