Fadi M. Awadallah

El Kasr El Eini Street
Cairo, C 11562, Egypt

Last Updated: 09/26/2026

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Found 23 publications

Discovery of novel progesterone-heterocyclic conjugates and their encapsulated polymeric nanoparticles as potential CDK8 inhibitors: lung cytotoxicity evaluation, gene expression, and molecular docking.

Discovery of novel progesterone-heterocyclic conjugates and their encapsulated polymeric nanoparticles as potential CDK8 inhibitors: lung cytotoxicity evaluation, gene expression, and molecular docking.

Journal: RSC medicinal chemistry

Published: September 09, 2025

Development of novel amino-benzenesulfonamide derivatives and their analogues as carbonic anhydrase inhibitors: Design, synthesis, anticancer activity assessment, and pharmacokinetic studies using UPLC-MS/MS.

Development of novel amino-benzenesulfonamide derivatives and their analogues as carbonic anhydrase inhibitors: Design, synthesis, anticancer activity assessment, and pharmacokinetic studies using UPLC-MS/MS.

Journal: Bioorganic chemistry

Published: January 06, 2025

Corrigendum to "Sulfonamides as anticancer agents: A brief review on sulfonamide derivatives as inhibitors of various proteins overexpressed in cancer" [Bioorg. Chem. 147 (2024) 107409].

Corrigendum to "Sulfonamides as anticancer agents: A brief review on sulfonamide derivatives as inhibitors of various proteins overexpressed in cancer" [Bioorg. Chem. 147 (2024) 107409].

Journal: Bioorganic chemistry

Published: July 02, 2024

Sulfonamides as anticancer agents: A brief review on sulfonamide derivatives as inhibitors of various proteins overexpressed in cancer.

Sulfonamides as anticancer agents: A brief review on sulfonamide derivatives as inhibitors of various proteins overexpressed in cancer.

Journal: Bioorganic chemistry

Published: December 20, 2023

Design and synthesis of some new benzoylthioureido benzenesulfonamide derivatives and their analogues as carbonic anhydrase inhibitors.

Design and synthesis of some new benzoylthioureido benzenesulfonamide derivatives and their analogues as carbonic anhydrase inhibitors.

Journal: Journal of enzyme inhibition and medicinal chemistry

Published: October 28, 2022

Design and synthesis of some new benzoylthioureido phenyl derivatives targeting carbonic anhydrase enzymes.

Design and synthesis of some new benzoylthioureido phenyl derivatives targeting carbonic anhydrase enzymes.

Journal: Journal of enzyme inhibition and medicinal chemistry

Published: September 28, 2022

Assessment of vaccination with gamma radiationattenuated infective Toxocara canis eggs on murine toxocariasis.

Assessment of vaccination with gamma radiationattenuated infective Toxocara canis eggs on murine toxocariasis.

Journal: Tropical biomedicine

Published: February 22, 2021

Synthesis of some N-aroyl-2-oxindole benzenesulfonamide conjugates with carbonic anhydrase inhibitory activity.

Synthesis of some N-aroyl-2-oxindole benzenesulfonamide conjugates with carbonic anhydrase inhibitory activity.

Journal: Bioorganic chemistry

Published: November 30, 2019

Design and synthesis of novel PARP-1 inhibitors based on pyridopyridazinone scaffold.

Design and synthesis of novel PARP-1 inhibitors based on pyridopyridazinone scaffold.

Journal: Bioorganic chemistry

Published: February 25, 2019

Inhibition studies on a panel of human carbonic anhydrases with N1-substituted secondary sulfonamides incorporating thiazolinone or imidazolone-indole tails.

Inhibition studies on a panel of human carbonic anhydrases with N1-substituted secondary sulfonamides incorporating thiazolinone or imidazolone-indole tails.

Journal: Journal of enzyme inhibition and medicinal chemistry

Published: March 15, 2018

Design, synthesis and molecular modeling study for some new 2-substituted benzimidazoles as dual inhibitors for VEGFR-2 and c-Met.

Design, synthesis and molecular modeling study for some new 2-substituted benzimidazoles as dual inhibitors for VEGFR-2 and c-Met.

Journal: Future medicinal chemistry

Published: February 13, 2018

Molecular docking simulation, synthesis and 3D pharmacophore studies of novel 2-substituted-5-nitro-benzimidazole derivatives as anticancer agents targeting VEGFR-2 and c-Met.

Molecular docking simulation, synthesis and 3D pharmacophore studies of novel 2-substituted-5-nitro-benzimidazole derivatives as anticancer agents targeting VEGFR-2 and c-Met.

Journal: Bioorganic chemistry

Published: November 05, 2017

Showing 1-12 of 23

Last Updated: 09/26/2026