[HTML][HTML] A comprehensive review on pyrazoline based heterocyclic hybrids as potent anticancer agents

K Haider, M Shafeeque, S Yahya, MS Yar - European Journal of Medicinal …, 2022 - Elsevier
Cancer is one of the leading causes of death globally, around 10 million deaths are reported
every year due to cancer. Some clinically approved anticancer drugs play a riveting role in …

Recent advancements in the development of bioactive pyrazoline derivatives

B Nehra, S Rulhania, S Jaswal, B Kumar… - European journal of …, 2020 - Elsevier
Pyrazolines remain privileged heterocycles in drug discovery. 2-Pyrazoline scaffold has
been proven as a ubiquitous motif which is present in a number of pharmacologically …

Unveiling a versatile heterocycle: pyrazoline–a review

B Varghese, SN Al-Busafi, FEO Suliman… - RSC advances, 2017 - pubs.rsc.org
The design and synthesis of novel fluorescent heterocyclic dyes is a “hotspot” research area,
due to their favourable photophysical properties and crucial role in charge transfer …

Discovery of novel topoisomerase II inhibitors by medicinal chemistry approaches

W Hu, XS Huang, JF Wu, L Yang… - Journal of Medicinal …, 2018 - ACS Publications
DNA topoisomerase II (topo II) is an important enzyme involved in DNA replication,
recombination, and repair. Despite the popular applications of topo II inhibitors in cancer …

Recent progress in anticancer agents incorporating pyrazole scaffold

S Mor, M Khatri, R Punia… - Mini Reviews in Medicinal …, 2022 - benthamdirect.com
The search for new anticancer agents is considered a dynamic field of medicinal chemistry.
In recent years, the synthesis of compounds with anticancer potential has increased and a …

Design and synthesis of novel cytotoxic fluoroquinolone analogs through topoisomerase inhibition, cell cycle arrest, and apoptosis

MA Elanany, EEA Osman, EM Gedawy… - Scientific Reports, 2023 - nature.com
To exploit the advantageous properties of approved drugs to hasten anticancer drug
discovery, we designed and synthesized a series of fluoroquinolone (FQ) analogs via …

Unpacking the Pathogen Box—an open source tool for fighting neglected tropical disease

CGL Veale - ChemMedChem, 2019 - Wiley Online Library
Abstract The Pathogen Box is a 400‐strong collection of drug‐like compounds, selected for
their potential against several of the world's most important neglected tropical diseases …

[HTML][HTML] A series of isatin-hydrazones with cytotoxic activity and CDK2 kinase inhibitory activity: a potential type II ATP competitive inhibitor

HS Al-Salem, M Arifuzzaman, HM Alkahtani… - Molecules, 2020 - mdpi.com
Isatin derivatives potentially act on various biological targets. In this article, a series of novel
isatin-hydrazones were synthesized in excellent yields. Their cytotoxicity was tested against …

A medicinal chemist's perspective towards structure activity relationship of heterocycle based anticancer agents

B Nehra, B Mathew, PA Chawla - Current Topics in Medicinal …, 2022 - benthamdirect.com
Aim: This paper aims to describe the structure activity relationship of heterocyclic derivatives
with multi-targeted anticancer activity. Objectives: With the following goals in mind, this …

Synthesis and biological evaluation of novel pyrazoline derivatives containing indole skeleton as anti-cancer agents targeting topoisomerase II

Y Song, S Feng, J Feng, J Dong, K Yang, Z Liu… - European journal of …, 2020 - Elsevier
In order to develop potent anticaner agents, a novel series of 3-(1H-indol-3-yl)-2, 3, 3a, 4-
tetrahydrothiochromeno [4, 3-c] pyrazole derivatives were synthesized. Structures of all …