[HTML][HTML] Benzimidazole and its derivatives as cancer therapeutics: The potential role from traditional to precision medicine

YT Lee, YJ Tan, CE Oon - Acta Pharmaceutica Sinica B, 2023 - Elsevier
Cancer is the second leading cause of mortality globally which remains a continuing threat
to human health today. Drug insensitivity and resistance are critical hurdles in cancer …

Benzimidazole scaffold as anticancer agent: synthetic approaches and structure–activity relationship

N Shrivastava, MJ Naim, MJ Alam, F Nawaz… - Archiv der …, 2017 - Wiley Online Library
Cancer, also known as malignant neoplasm, is a dreadful disease which involves abnormal
cell growth having the potential to invade or spread to other parts of the body …

[HTML][HTML] Role of cellular cytoskeleton in epithelial-mesenchymal transition process during cancer progression

BO Sun, Y Fang, Z Li, Z Chen… - Biomedical …, 2015 - spandidos-publications.com
Currently, cancer metastases remain a major clinical problem that highlights the importance
of recognition of the metastatic process in cancer diagnosis and treatment. A critical process …

VOSO4 catalyzed highly efficient synthesis of benzimidazoles, benzothiazoles, and quinoxalines

CS Digwal, U Yadav, AP Sakla, PVS Ramya… - Tetrahedron …, 2016 - Elsevier
Herein, we describe a highly efficient and eco-friendly protocol for the synthesis of
benzimidazoles, benzothiazoles, and quinoxalines using VOSO 4 as a catalyst in ethanol …

Divergent Synthesis of Pyrazolo[1,5-a]pyridines and Imidazo[1,5-a]pyridines via Reagent-Controlled Cleavage of the C–N or C–C Azirine Bond in 2-Pyridylazirines

AV Agafonova, AA Golubev, IA Smetanin… - Organic …, 2023 - ACS Publications
The three-membered ring in 2-(2-pyridyl) azirine-2-carboxylic esters and thioesters can
undergo selective cleavage of either the N–C2 bond under copper (II) catalysis or the C–C …

Construction of Imidazole-Fused-Ring Systems by Iron-Catalyzed C(sp3)-H Amination–Cyclization under Aerobic Conditions

J Peng, S Li, J Huang, Q Meng, L Wang… - The Journal of …, 2023 - ACS Publications
An iron-catalyzed efficient C–H amination for the construction of imidazole-fused-ring
systems was developed under aerobic conditions. Compared to previous studies, this work …

Metal complexes of benzimidazole derived sulfonamide: Synthesis, molecular structures and antimicrobial activity

A Ashraf, WA Siddiqui, J Akbar, G Mustafa… - Inorganica Chimica …, 2016 - Elsevier
Benzimidazole and sulfonamide moieties are found in a number of pharmaceutically active
molecules. By incorporating the sulfonamide pharmacophore into the benzimidazole …

Synthesis and biological evaluation of cis-restricted triazole/tetrazole mimics of combretastatin-benzothiazole hybrids as tubulin polymerization inhibitors and …

AVS Rao, K Swapna, SP Shaik, VL Nayak… - Bioorganic & Medicinal …, 2017 - Elsevier
A series of colchicine site binding tubulin inhibitors were synthesized by the modification of
the combretastatin pharmacophore. The ring B was replaced by the pharmacologically …

Synthesis and biological evaluation of 1, 2, 3‐triazole tethered pyrazoline and chalcone derivatives

SMA Hussaini, P Yedla, KS Babu… - Chemical biology & …, 2016 - Wiley Online Library
A series of pyrazoline derivatives and corresponding chalcone intermediates with
substituents same as combretastatin‐A4 (CA‐4) conjugated with triazole nucleus has been …

Design, synthesis, and biological evaluation of imidazopyridine‐linked thiazolidinone as potential anticancer agents

MA Iqbal, A Husain, O Alam, SA Khan… - Archiv der …, 2020 - Wiley Online Library
In this study, two series of imidazopyridine‐linked thiazolidinone rings (5a–h and 6a–h)
constituting 16 new compounds were synthesized and tested for their antiproliferative …