The anti-breast cancer activity of indeno [1, 2-b] pyridin-5-one and their hydrazonal precursors endowed with anti-CDK-2 enzyme activity

SA Al-Hussain, TA Farghaly, MH Ibrahim… - Journal of Molecular …, 2024 - Elsevier
A new series of aza-indeno [1, 2-b] pyridin-5-one derivatives 6a-h was designed. The novel
pyridin-5-one derivatives were constructed via cyclization of their corresponding hydrazonal …

Organocatalytic [3+ 2] Cycloaddition reaction: synthesis of fully decorated sulfonyl-1, 2, 3-triazolyl pyrimidines as potent anticancer and EGFR inhibitors

JMR Velidandla, SK Koppula - Polycyclic Aromatic Compounds, 2024 - Taylor & Francis
A general strategy was developed for the synthesis of new fully decorated sulfonyl1, 2, 3-
triazolyl pyrimidines (6a–6j and 8a–8f) from 2-((6-methyl-2-(methylsulfonyl) pyrimidin-4-yl) …

Heterocycle-functional steroidal derivatives: Design, synthesis, bioevaluation and SARs of steroidal pyrazolo [1, 5-a] pyrimidines as potential ALK inhibitors

F Liu, S Wen, M Liu, Y Min, Z Zhang, L Shi, K Wang… - Bioorganic …, 2024 - Elsevier
Two series of heterocyclic steroidal pyrazolo [1, 5-a] pyrimidines derived from
dehydroepiandrosterone (DHEA) and epiandrosterone (EPIA) were designed and …

[HTML][HTML] New Pyrazole/Pyrimidine-Based Scaffolds as Inhibitors of Heat Shock Protein 90 Endowed with Apoptotic Anti-Breast Cancer Activity

LH Al-Wahaibi, MAI Elbastawesy, NE Abodya… - Pharmaceuticals, 2024 - mdpi.com
Background/Objectives: Supported by a comparative study between conventional, grinding,
and microwave techniques, a mild and versatile method based on the [1+ 3] cycloaddition of …

Novel tropane analogues as Hsp90 inhibitors targeting colon cancer: Synthesis, biological estimation, and molecular docking study

SJ Almehmadi, R Sabour, AF Kassem, EMH Abbas… - Bioorganic …, 2024 - Elsevier
New derivatives of tropane scaffold were prepared from the reaction of their thione or
thioamide derivatives with α-halocarbonyl compounds. The structures of all new derivatives …

Novel indeno-pyrazole and indeno-pyrimidine conjugates: Synthesis, DFT, anticancer screening and in silico studies as potent tubulin inhibitors

DH Elnaggar, SF Mohamed, HS Abd-Elghaffar… - Journal of Molecular …, 2025 - Elsevier
Background A leading procedure for creating innovative anticancer treatments that, in
theory, can address many of the pharmacokinetic drawbacks of conventional anticancer …

Novel Indene-[1, 3, 4] Oxadiazine hybrids: Design, construction, molecular docking, QSAR, ADME study and anticancer potential

MF Hussein, I Althobaiti, H Altaleb… - Egyptian Journal of …, 2024 - ejchem.journals.ekb.eg
In an attempt to improve and develop biologically potential anticancer agents, synthesis of
new anticancer agents are in progress. This study focused on the synthesis of novel …

Synthesis, Characterization, Anticancer, Pharmacokinetic, and Docking Studies of Vanillin-Benzimidazole Derivatives as Aromatase Inhibitors

AM Malebari, S Nazreen, SEI Elbehairi… - Polycyclic Aromatic …, 2024 - Taylor & Francis
The current work highlights the preparation and antitumor activity of new benzimidazole
derivatives of the natural product vanillin as a novel aromatase inhibitor. All the newly …

Comprehensive study for synthesis, antiviral activity, docking and ADME study for the new fluorinated hydrazonal and indeno [1, 2-b] pyridine derivatives

MH Ibrahim, A Rushdi, SJ Almehmadi, MEA Zaki… - Journal of Molecular …, 2024 - Elsevier
In this context, we synthesized a novel series of fluorinated-indeno [1, 2-b] pyridin-5-one
derivatives 6a-h and used spectral and elemental studies to demonstrate their structural …

Novel 1, 3-Indanedione-Thiazole Hybrids as Small-Molecule SARS-COV-2 Main Protease Inhibitors With Potential anti-Coronaviral Activity

TA Farghaly, GS Masaret… - Polycyclic Aromatic …, 2024 - Taylor & Francis
Since arising in 2019, COVID 19 has been causing rapidly-increasing mortality and
morbidity rates across the globe. Herein, novel 1, 3-indanedione-thiazole hybrids were …