p53 as a potential target for treatment of cancer: A perspective on recent advancements in small molecules with structural insights and SAR studies

R Bhatia, B Kumar - European Journal of Medicinal Chemistry, 2023 - Elsevier
Cancer represents one of the world's biggest hazardous diseases. p53 is the uttermost
researched tumour suppressor protein. It is commonly considered the “guardian of the …

Recent updates in click and computational chemistry for drug discovery and development

JH Cai, XZ Zhu, PY Guo, P Rose, XT Liu, X Liu… - Frontiers in …, 2023 - frontiersin.org
Drug discovery is a costly and time-consuming process with a very high failure rate.
Recently, click chemistry and computer-aided drug design (CADD) represent popular areas …

An updated overview on the synthesis and anticancer evaluation of quinazoline derivatives

J Kaur, S Kaur, A Anand, N Islam, S Singh… - …, 2023 - Wiley Online Library
Cancer, a leading global cause of death, necessitates the exploration of safer and more
effective anticancer drugs due to the adverse side effects associated with current cytotoxic …

Synthesis, biological evaluation and in silico investigations of benzotriazole derivatives as potential inhibitors of NIMA related kinase

T Qadri, M Aziz, PA Channar, SA Ejaz, M Hussain… - RSC …, 2023 - pubs.rsc.org
In the current study, a novel compound, bis (3-(2H-benzo [d][1, 2, 3] triazol-2-yl)-2-(prop-2-yn-
1-yloxy)-5-(2, 4, 4-trimethylpentan-2-yl) phenyl) methane (TAJ1), has been synthesized by …

Synthesis and Screening of Novel 2, 4-Bis Substituted quinazolines as Tubulin Polymerization Promotors and Antiproliferative Agents

AR Dwivedi, V Kumar, V Kumar, V Prashar… - RSC Medicinal …, 2025 - pubs.rsc.org
Twelve 2, 4-Bis substituted quinazoline based compounds were synthesized and screened
for antiproliferative and tubulin polymerization enhancing potential. In the series, compound …

Design, synthesis and biological evaluation of a novel colchicine-magnolol hybrid for inhibiting the growth of Lewis lung carcinoma in Vitro and in Vivo

Z Li, S Hu, LY Pu, Z Li, G Zhu, Y Cao, L Li, Y Ma… - Frontiers in …, 2022 - frontiersin.org
Colchicine is a bioactive alkaloid originally from Colchicum autumnale and possesses
excellent antiproliferative activity. However, colchicine-associated severe toxicity …

Design and Synthesis of 1-(4-Bromo-2-(Pyrrolidine-1-Yl) Benzyl) Piperidine-Based Derivatives as Anti-Tubulin Agents

R Guguloth, SK Gubbiyappa - Current Topics in Medicinal …, 2025 - benthamdirect.com
Background Piperidines are among the essential synthetic fragments for designing drugs
and play a significant role in the pharmaceutical industry. The synthesis of newer derivatives …

Review; Recent approaches on Tubulin Polymerization inhibitors (2018-2022)

AO El-Abd - Delta University Scientific Journal, 2024 - journals.ekb.eg
Cancer is a disease in which some of the body's cells grow uncontrollably and spread to
other parts of the body. Cancer treatment usually involves the use of single or combined …

Caesium carbonate promoted regioselective O-functionalization of 4, 6-diphenylpyrimidin-2 (1 H)-ones under mild conditions and mechanistic insight

V Kumar, PP Singh, AR Dwivedi, N Kumar, SC Sahoo… - RSC …, 2023 - pubs.rsc.org
A facile one-step catalyst free methodology has been developed for the regioselective
functionalization of 4, 6-diphenylpyrimidin-2 (1H)-ones under mild conditions. Selectivity …

[PDF][PDF] Design, Synthesis, Molecular Docking, In-vitro Anticancer and Antibacterial Evaluation of Novel Pyrazole Linked with Quinazoline Scaffolds.

M AFRO, G SHIvA kUMAR - Oriental Journal of Chemistry, 2023 - pdfs.semanticscholar.org
Design, Synthesis, Molecular Docking, In-vitro Anticancer and Antibacterial Evaluation of Novel
Pyrazole Linked with Quinazoline Page 1 ORIENTAL JOURNAL OF CHEMISTRY …