Novel fused imidazotriazines acting as promising top. II inhibitors and apoptotic inducers with greater selectivity against head and neck tumors: Design, synthesis, and …

AA Al-Karmalawy, M Rashed, M Sharaky… - European Journal of …, 2023 - Elsevier
Although the great effectiveness of doxorubicin (Dox) in the treatment of many types of
tumors, it showed limited effectiveness against the head and neck squamous cell carcinoma …

Novel 4-thiophenyl-pyrazole, pyridine, and pyrimidine derivatives as potential antitumor candidates targeting both EGFR and VEGFR-2; design, synthesis, biological …

SM Al-Muntaser, AA Al-Karmalawy, AM El-Naggar… - RSC …, 2023 - pubs.rsc.org
In this article, we continued our previous effort to develop new selective anticancer
candidates based on the basic pharmacophoric requirements of both EGFR and VEGFR-2 …

An overview of the mechanisms of cadmium-induced toxicity in the male Reproductive System

SA Antar, A Halouani, C Gad… - Pharmaceutical …, 2023 - ps.tbzmed.ac.ir
Cadmium (Cd) is a toxic heavy metal that is known to accumulate in various organs and
tissues in the body, including the testes. Exposure to Cd has been shown to cause …

Rational design and eco-friendly one-pot multicomponent synthesis of novel ethylidenehydrazineylthiazol-4 (5H)-ones as potential apoptotic inducers targeting wild …

EM Abbass, AA Al-Karmalawy, M Sharaky… - Bioorganic …, 2024 - Elsevier
A novel series of ethylidenehydrazineylthiazol-4 (5H)-ones were synthesized using various
eco-friendly one-pot multicomponent synthetic techniques. The anticancer activity of …

1-Benzyl-5-bromo-3-hydrazonoindolin-2-ones as novel anticancer agents: Synthesis, biological evaluation and molecular modeling insights

T Al-Warhi, H Almahli, RM Maklad, ZM Elsayed… - Molecules, 2023 - mdpi.com
Human health is experiencing several obstacles in the modern medical era, particularly
cancer. As a result, the cancer therapeutic arsenal should be continually expanded with …

A comprehensive overview of organ inflammatory responses: genesis, possible mechanisms, and mediators of inflammation

SA Antar, AM Mahmoud, W Abdo, C Gad… - Pharmaceutical …, 2023 - e-space.mmu.ac.uk
An immune system response known as inflammation can be carried on by a variety of things,
such as infections, damaged cells, and noxious substances. These factors may cause acute …

Identification of 3‐(5‐cyano‐6‐oxo‐pyridin‐2‐yl) benzenesulfonamides as novel anticancer agents endowed with EGFR inhibitory activity

MA Shaldam, AF Khalil, H Almahli… - Archiv der …, 2024 - Wiley Online Library
Abstract New 5‐cyano‐6‐oxo‐pyridine‐based sulfonamides (6a–m and 8a–d) were
designed and synthesized to potentially inhibit both the epidermal growth factor receptor …

Design and synthesis of novel pyrazolopyrimidine candidates as promising EGFR-T790M inhibitors and apoptosis inducers

AA Gaber, M Sharaky, AA Elmaaty… - Future Medicinal …, 2023 - Taylor & Francis
Aim: Our objective was to design and synthesize a new range of pyrazolopyrimidines while
maintaining the key pharmacophoric features of EGFR tyrosine kinase inhibitors. Materials & …

[HTML][HTML] Green synthesis of silver nanoparticles using curcumin: A comparative study of antimicrobial and antibiofilm effects on Acinetobacter baumannii against …

MA Abdelwahab, A Nabil, H El-Hosainy, R Tahway… - Results in …, 2024 - Elsevier
Acinetobacter baumannii (A. baumannii) is an important pathogen that causes hospital-
acquired illnesses worldwide. The biofilm-forming activity of the organism enhances its …

Computational Design, Synthesis, and Bioevaluation of 2-(Pyrimidin-4-yl) oxazole-4-carboxamide Derivatives: Dual Inhibition of EGFRWT and EGFRT790M with …

NR Khedkar, M Sindkhedkar, A Joseph - Bioorganic Chemistry, 2024 - Elsevier
The ongoing research in cancer treatment underscores the significance of dual epidermal
growth factor receptor (EGFR) kinase inhibitors targeting both mutant and wild-type variants …