A review on the role of cyclin dependent kinases in cancers

S Ghafouri-Fard, T Khoshbakht, BM Hussen… - Cancer Cell …, 2022 - Springer
The Cyclin-dependent kinase (CDK) class of serine/threonine kinases has crucial roles in
the regulation of cell cycle transition and is mainly involved in the pathogenesis of cancers …

Amino-pyrazoles in medicinal chemistry: A review

M Lusardi, A Spallarossa, C Brullo - International journal of molecular …, 2023 - mdpi.com
A pyrazole nucleus is an easy-to-prepare scaffold with large therapeutic potential.
Consequently, the search for new pyrazole-based compounds is of great interest to the …

The anticancer and EGFR-TK/CDK-9 dual inhibitory potentials of new synthetic pyranopyrazole and pyrazolone derivatives: X-ray crystallography, in vitro, and in silico …

A Musa, SK Ihmaid, DL Hughes, MA Said… - Journal of …, 2023 - Taylor & Francis
Abstract Treatment options for the management of breast cancer are still inadequate. This
inadequacy is attributed to the lack of effective targeted medications, often resulting in the …

Novel quinoxaline-based VEGFR-2 inhibitors to halt angiogenesis

MMF Ismail, TZ Shawer, RS Ibrahim, RM Allam… - Bioorganic …, 2023 - Elsevier
Vascular endothelial growth factor receptor-2 is a dynamic target for therapeutic intervention
in various types of cancer. This study was aimed at exploring the VEGFR-2 inhibitory activity …

[HTML][HTML] Characterization, DFT calculations and dyeing performance on polyester fabrics of some azo disperse dyes containing pyrazole ring

AZ Omar, MG Mohamed, EA Hamed… - Journal of Saudi Chemical …, 2023 - Elsevier
A number of azo pyrazole derivatives and novel Schiff bases derived from azo diamino
pyrazole were synthesized. These included 4-(2-arylhydrazono)-4H-pyrazole-3, 5-diamines …

[PDF][PDF] A comprehensive analysis of the role of molecular docking in the development of anticancer agents against the cell cycle CDK enzyme.

P Solanki, N Rana, PC Jha, A Manhas - Biocell, 2023 - cdn.techscience.cn
Cancer is considered one of the most lethal diseases responsible for causing deaths
worldwide. Although there have been many breakthroughs in anticancer development …

Laccase-mediated chemoselective C-4 arylation of 5-aminopyrazoles

M Shahedi, R Shahani, N Omidi, Z Habibi, M Yousefi… - Plos one, 2024 - journals.plos.org
Chemoselective arylation of 5-aminopyrazoles was performed through oxidative formation of
orthoquinones from catechols catalyzed by Myceliophthora thermophila laccase (Novozym …

Novel quinoxaline-3-propanamides as VGFR-2 inhibitors and apoptosis inducers

MMF Ismail, TZ Shawer, RS Ibrahim, MS Abusaif… - RSC …, 2023 - pubs.rsc.org
Vascular endothelial growth factor receptor-2 is a vital target for therapeutic mediation in
various types of cancer. This study was aimed at exploring the cytotoxic activity of seventeen …

Prodrugs of sulfacetamide: Synthesis, X-ray structure, Hirshfeld analysis, antibacterial assessment, and docking studies

MS Ayoup, SM Soliman, M Haukka, MF Harras… - Journal of Molecular …, 2022 - Elsevier
New prodrugs of sulfacetamide as azo compounds were synthesized and have been
evidenced through elemental and spectral analyses. Their synthesis were carried out by …

A new bithiophene inhibited amyloid-β accumulation and enhanced cognitive function in the hippocampus of aluminum-induced Alzheimer's disease in adult rats

K AbdElRaouf, HSH Farrag… - Journal of …, 2024 - journals.sagepub.com
Background Alzheimer's disease (AD) is a progressive and irreversible neurological
disorder that gradually deteriorates an individual's ability to carry out even the simplest …