O. Salem

发表

Design, synthesis, and antiproliferative properties of new 1,2,3-triazole-carboximidamide derivatives as dual EGFR/VEGFR-2 inhibitors

M. A. Mahmoud, B. Youssif, Anber F. Mohammed, 2023, Journal of Molecular Structure.

New 1,3,4‐oxadiazoles linked with the 1,2,3‐triazole moiety as antiproliferative agents targeting the EGFR tyrosine kinase

H. Gomaa, Ola I A Salem, M. A. Mahmoud, 2022, Archiv der Pharmazie.

Design and synthesis of novel 2,3-dihydropyrazino[1,2-a]indole-1,4-dione derivatives as antiproliferative EGFR and BRAFV600E dual inhibitors.

A. Gouda, Hatem S. Farghaly, L. Trembleau, 2020, Bioorganic chemistry.

Design, synthesis, mechanistic and histopathological studies of small-molecules of novel indole-2-carboxamides and pyrazino[1,2-a]indol-1(2H)-ones as potential anticancer agents effecting the reactive oxygen species production.

M. Abdelgawad, S. N. Bukhari, A. Abdelazeem, 2018, European journal of medicinal chemistry.

Novel N-substituted 5-aminosalicylamides as dual inhibitors of cyclooxygenase and 5-lipoxygenase enzymes: Synthesis, biological evaluation and docking study.

H. Abdu-Allah, H. Farghaly, Ola I A Salem, 2018, Bioorganic chemistry.

New pyrimidine/thiazole hybrids endowed with analgesic, anti‐inflammatory, and lower cardiotoxic activities: Design, synthesis, and COX‐2/sEH dual inhibition

Ehab S. Taher, P. Lan, H. Gomaa, 2022, Archiv der Pharmazie.

Design and synthesis of some new theophylline derivatives with bronchodilator and antibacterial activities

Ola I A Salem, A. Hayallah, A. M. A. Abdel Alim, 2011, Archives of pharmacal research.

Novel fluoroquinolone hybrids as dual DNA gyrase and urease inhibitors with potential antibacterial activity: Design, synthesis, and biological evaluation

Katarina Cirnski, J. Herrmann, Ola I A Salem, 2022, Journal of Molecular Structure.

Novel 1,2,4-triazole derivatives as apoptotic inducers targeting p53: Synthesis and antiproliferative activity.

A. Gouda, K. S. Alharbi, H. Gomaa, 2020, Bioorganic chemistry.

Novel class of benzimidazole-thiazole hybrids: The privileged scaffolds of potent anti-inflammatory activity with dual inhibition of cyclooxygenase and 15-lipoxygenase enzymes.

Ola I A Salem, Asmaa Y. Ali, Mohammed T-E Maghraby, 2020, Bioorganic & medicinal chemistry.

Design, synthesis, and modelling study of new 1,2,3‐triazole/chalcone hybrids with antiproliferative action as epidermal growth factor receptor inhibitors

Ola I A Salem, B. Youssif, M. Sheha, 2022, Chemical biology & drug design.

Development of a hypoxia-selective near-infrared fluorescent probe for non-invasive tumor imaging.

H. Nagasawa, K. Okuda, S. Kizaka-Kondoh, 2012, Chemical & pharmaceutical bulletin.

Novel 5alpha-reductase inhibitors: synthesis, structure-activity studies, and pharmacokinetic profile of phenoxybenzoylphenyl acetic acids.

R. Hartmann, C. Scherer, K. Biemel, 2006, Journal of medicinal chemistry.

Prooxidant and antioxidant action of 4-(4-phenoxybenzoyl)benzoic acid derivatives.

T. Michalska, I. Kruk, R. Hartmann, 2004, Biopolymers.

6-Substituted 3,4-Dihydro-naphthalene-2-carboxylic Acids: Synthesis and Structure-Activity Studies in a Novel Class of Human 5α Reductase Inhibitors

R. Hartmann, Ola I A Salem, E. Baston, 2002, Journal of enzyme inhibition and medicinal chemistry.