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Fardous F. El-Senduny

Researcher at Mansoura University

Publications -  53
Citations -  920

Fardous F. El-Senduny is an academic researcher from Mansoura University. The author has contributed to research in topics: Medicine & Chemistry. The author has an hindex of 11, co-authored 38 publications receiving 514 citations. Previous affiliations of Fardous F. El-Senduny include South Dakota State University & King Abdulaziz University.

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On the Neuroprotective Effects of Naringenin: Pharmacological Targets, Signaling Pathways, Molecular Mechanisms, and Clinical Perspective

TL;DR: The neuroprotective effects of naringenin, as well as its related pharmacological targets, signaling pathways, molecular mechanisms, and clinical perspective, are described and the need to develop novel naringanin delivery systems is discussed to solve its widespread pharmacokinetic limitation.
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Synthesis of new thiazolo-pyrrolidine-(spirooxindole) tethered to 3-acylindole as anticancer agents.

TL;DR: Compound 4k proved to retain a high cytotoxic activity and selectivity against colon cancer cells HCT-116, hepatocellular carcinoma, and prostate cancer cells PC-3 in comparison to cisplatin, and ligand Efficiency and Ligand Lipophilic Efficiency were evaluated and revealed that compound 4k had acceptable value.
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Approach for chemosensitization of cisplatin-resistant ovarian cancer by cucurbitacin B

TL;DR: Cucurbitacin B is a promising chemosensitizer for the cisplatin-resistant ovarian cancer and shows cytotoxicity against the ovarian cancer cell lines, and pretreatment of A2780CP cells leads to a significant increase in the cytotoxic effect of cisPlatin.
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Substituted spirooxindole derivatives as potent anticancer agents through inhibition of phosphodiesterase 1

TL;DR: A one-pot three-component reaction via a [3 + 2] cycloaddition/ring contraction sequence of a dipolarophile (activated alkene) with in situ-generated azomethine ylide (1,3-dipoles) without the use of any catalyst provides efficient access to synthetically useful and biologically important spirooxindoles in high yield with high diastereoselectivity.