Simple 2 (5H)-furanone derivatives with selective cytotoxicity towards non-small cell lung cancer cell line A549–Synthesis, structure-activity relationship and biological …

A Byczek-Wyrostek, R Kitel, K Rumak… - European journal of …, 2018 - Elsevier
A series of 5-alkoxy derivatives of 3, 4-dichloro-5-hydroxyfuran-2-(5H)-one (mucochloric
acid, MCA) were obtained and subsequently subjected to modification in the C-4 position of …

Development of 3-methyl/3-(morpholinomethyl) benzofuran derivatives as novel antitumor agents towards non-small cell lung cancer cells

MM Al-Sanea, GH Al-Ansary, ZM Elsayed… - Journal of Enzyme …, 2021 - Taylor & Francis
As one of the most lethal malignancies, lung cancer is considered to account for
approximately one-fifth of all malignant tumours-related deaths worldwide. This study reports …

Synthesis, in vitro antitumor activity and molecular mechanism of novel furan derivatives and their precursors

D Lu, Y Zhou, Q Li, J Luo, Q Jiang… - Anti-Cancer Agents in …, 2020 - ingentaconnect.com
Background: Compounds featuring furan nucleus exhibit diverse biological properties. Lots
of furan derivatives have been explored as pharmaceutical compounds. Hence it is of great …

Novel Pyrazole‐Based Benzofuran Derivatives as Anticancer Agents: Synthesis, Biological Evaluation, and Molecular Docking Investigations

I Ameziane El Hassani, A Altay… - Chemistry & …, 2023 - Wiley Online Library
In this work, the design, synthesis, and mechanistic studies of novel pyrazole‐based
benzofuran derivatives 1–8 as anticancer agents were discussed. Cytotoxic potency of the …

Mucochloric Acid: A Useful Synthon for the Selective Synthesis of 4‐Aryl‐3‐chloro‐2(5H)‐furanones, (Z)‐4‐Aryl‐5‐[1‐(aryl)methylidene]‐3‐chloro‐2(5H)‐furanones and 3,4 …

F Bellina, C Anselmi, F Martina… - European Journal of …, 2003 - Wiley Online Library
Dichloro‐2 (5H)‐furanone, which has been prepared efficiently from mucochloric acid, has
been transformed selectively into 4‐aryl‐3‐chloro‐2 (5H)‐furanones either by Suzuki‐or …

3, 4, 5-Trisubstituted furan-2 (5H)-one derivatives: Efficient one-pot synthesis and evaluation of cytotoxic activity

WM Basyouni, KAM El-Bayouki, AS El-Sayed… - Drug …, 2015 - thieme-connect.com
A series of 3, 4, 5-trisubstituted 2 (5H)-furanone derivatives was synthesized through one-
pot reaction of amines, aldehydes and diethyl acetylenedicarboxylate. Silica sulfuric acid …

Bis‐2(5H)‐furanone derivatives as new anticancer agents: Design, synthesis, biological evaluation, and mechanism studies

YC Wu, L Cao, WJ Mei, HQ Wu, SH Luo… - Chemical Biology & …, 2018 - Wiley Online Library
New bis‐2 (5H)‐furanone derivatives containing a benzidine core were synthesized via a
one‐step transition‐metal‐free reaction of benzidine with 5‐substituted 3, 4‐dihalo‐2 (5H) …

Synthesis, molecular properties prediction and cytotoxic screening of 3-(2-aryl-2-oxoethyl) isobenzofuran-1 (3H)-ones

AF da Silva Maia, RP Siqueira, FM de Oliveira… - Bioorganic & Medicinal …, 2016 - Elsevier
In the present investigation, a collection of nineteen 3-(2-aryl-2-oxoethyl) isobenzofuran-1
(3H)-ones was synthesized and screened for their cytotoxic activity against a panel of three …

Anticancer therapeutic potential of benzofuran scaffolds

AA Abbas, KM Dawood - RSC advances, 2023 - pubs.rsc.org
Benzofuran moiety is the main component of many biologically active natural and synthetic
heterocycles. These heterocycles have unique therapeutic potentials and are involved in …

Synthesis and cytotoxicity of 3, 4-diaryl-2 (5H)-furanones

Y Kim, NH Nam, YJ You, BZ Ahn - Bioorganic & medicinal chemistry letters, 2002 - Elsevier
A series of 3, 4-diaryl-2 (5H)-furanone derivatives were synthesized and evaluated for their
cytotoxicity in a small panel of cancer cell lines. Four out of 10 compounds in this series, for …