[HTML][HTML] A comprehensive review on pyrazoline based heterocyclic hybrids as potent anticancer agents
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 …
every year due to cancer. Some clinically approved anticancer drugs play a riveting role in …
Recent advancements in the development of bioactive pyrazoline derivatives
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 …
been proven as a ubiquitous motif which is present in a number of pharmacologically …
Unveiling a versatile heterocycle: pyrazoline–a review
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 …
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 …
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 …
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
To exploit the advantageous properties of approved drugs to hasten anticancer drug
discovery, we designed and synthesized a series of fluoroquinolone (FQ) analogs via …
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 …
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 …
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
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 …
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 …
tetrahydrothiochromeno [4, 3-c] pyrazole derivatives were synthesized. Structures of all …