Anticancer compounds based on isatin-derivatives: Strategies to ameliorate selectivity and efficiency

RE Ferraz de Paiva, EG Vieira… - Frontiers in molecular …, 2021 - frontiersin.org
In this review we compare and discuss results of compounds already reported as anticancer
agents based on isatin-derivatives, metalated as well as non-metallated. Isatin compounds …

Recent advances in isatin hybrids as potential anticancer agents

Z Ding, M Zhou, C Zeng - Archiv der Pharmazie, 2020 - Wiley Online Library
The isatin framework is a useful template for the development of novel anticancer agents.
This is exemplified by the fact that several isatin‐based anticancer agents, such as …

An insight into the interaction between Indisulam and human serum albumin: Spectroscopic method, computer simulation and in vitro cytotoxicity assay

B Zhou, H Zhou, L Xu, R Cai, C Chen, B Chi, X Tuo - Bioorganic Chemistry, 2022 - Elsevier
Indisulam (IDM) is a sulfanilamide anticancer agent and has been identified as a molecular
glue recently. It shows potential for novel therapies development and brings more hope for …

Inhibition of Orai1‐mediated Ca2+ entry enhances chemosensitivity of HepG2 hepatocarcinoma cells to 5‐fluorouracil

BD Tang, X Xia, XF Lv, BX Yu, JN Yuan… - Journal of Cellular …, 2017 - Wiley Online Library
Increasing evidence supports that activation of store‐operated Ca2+ entry (SOCE) is
implicated in the chemoresistance of cancer cells subjected to chemotherapy. However, the …

Hydrazide-hydrazone/hydrazone as enabling linkers in anti-cancer drug discovery: A comprehensive review

S Murugappan, S Dastari, K Jungare, NM Barve… - Journal of Molecular …, 2024 - Elsevier
The burgeoning demand for novel cytotoxic drugs possessing improved bioavailability and
safety profiles has spurred the hybridization of various pharmacophores in the past decades …

The N-Substituted-4-Methylbenzenesulphonyl Hydrazone Inhibits Angiogenesis in Zebrafish Tg(fli1: EGFP) Model

M Gawrońska-Grzywacz, I Piątkowska-Chmiel… - Pharmaceuticals, 2022 - mdpi.com
One of the most important therapies of malignant neoplasms, which are the second cause of
death worldwide, is focused on the inhibition of pathological angiogenesis within the tumor …

Design, Synthesis, and In Vitro and In Vivo Bioactivity Studies of Hydrazide–Hydrazones of 2, 4-Dihydroxybenzoic Acid

Ł Popiołek, M Gawrońska-Grzywacz, A Dziduch… - International Journal of …, 2023 - mdpi.com
In this research, twenty-four hydrazide–hydrazones of 2, 4-dihydroxybenzoic acid were
designed, synthesized, and subjected to in vitro and in vivo bioactivity studies. The chemical …

[PDF][PDF] Synthesis and Biological Evaluation of Some Hydrazide-Hydrazone Derivatives as Anticancer Agents.

K Akdağ, F Tok, S Karakuş, Ö Erdoğan… - Acta Chimica …, 2022 - researchgate.net
In this study, a series of hydrazide-hydrazone derivatives (3a-3u) were synthesized and
evaluated for their anticancer activities against prostate cancer cell line (PC-3), breast …

A general strategy to add diversity to ruthenium arene complexes with bioactive organic compounds via a coordinated (4-hydroxyphenyl) diphenylphosphine ligand

L Biancalana, LK Batchelor, A De Palo, S Zacchini… - Dalton …, 2017 - pubs.rsc.org
Esterification of (4-hydroxyphenyl) diphenylphosphine, coordinated to the [Ru (η6-p-
cymene) Cl2] fragment, allows a series of bioactive carboxylic acids to be introduced directly …

The potential impact of 6PPD and its oxidation product 6PPD-quinone on human health: A case study on their interaction with human serum albumin

C Chen, L Gao, P Ding, S Zhang, X Wang, K Yang… - Chemosphere, 2024 - Elsevier
Abstract 6PPD and its oxidation product, 6PPD-quinone have garnered widespread
attention due to their adverse effects on aquatic ecosystems and human health, and are …