Synthesis, antiproliferative and cytotoxic activities, DNA binding features and molecular docking study of novel enamine derivatives

M Burcu Gürdere, A Aydin, B Yencilek… - Chemistry & …, 2020 - Wiley Online Library
Novel enamine derivatives were synthesized from the reaction of lactone and chalcones and
their antiproliferative and cytotoxic activities against six cancer cell lines (eg, HeLa, HT29 …

Exploration of biological potency of carboxylic acid derivatives: designing, synthesis, characterizations and molecular docking study

M Sirajuddin, S Ali, A Shahnawaz, F Perveen… - Journal of Molecular …, 2020 - Elsevier
The carboxylic acid functional group plays a fundamental role in the biochemistry of living
systems as well as in drug design by enhancing the hydrophilicity of drugs as well as their …

New chalcones bearing isatin scaffold: synthesis, molecular modeling and biological evaluation as anticancer agents

YA Ammar, EA Fayed, AH Bayoumi, RR Ezz… - Research on Chemical …, 2017 - Springer
Derivatives of isatin have been reported to possess cytotoxic effects against different human
carcinoma cell lines. A series of new isatin-linked chalcones was synthesized starting from …

Polyaromatic ring containing β-diketone derivatives with antiproliferative activity toward human breast cancer cell lines: Synthesis, structure, DNA binding and …

MA Neelakantan, V Latha, S Thalamuthu - Journal of Molecular Structure, 2022 - Elsevier
The β-diketone derivatives in plants exhibit biological activity due to tautomerism and
extended conjugation with the aromatic ring system. β-diketone derivatives;(Z)-3-(4-(4 …

Design, synthesis, molecular docking, and biological evaluation of new emodin anthraquinone derivatives as potential antitumor substances

Y Li, F Guo, T Chen, L Zhang, Z Wang… - Chemistry & …, 2020 - Wiley Online Library
The emodin anthraquinone derivatives are generally used in traditional Chinese medicine
due to their various pharmacological activities. In the present study, a series of emodin …

3‐Aminomethyl pyridine chalcone derivatives: Design, synthesis, DNA binding and cytotoxic studies

SD Durgapal, R Soni, S Umar… - Chemical Biology & …, 2018 - Wiley Online Library
Herein we report design, synthesis, and anticancer activity of compounds 6a–h and 11a–j.
Compounds 6a–f were designed based on 3‐aminomethyl pyridine attached to different …

Synthesis, biological evaluation and molecular docking studies of pyridine incorporated chalcone derivatives as anticancer agents

S Madhavi, R Sreenivasulu… - Letters in Organic …, 2016 - ingentaconnect.com
Background: Cancer is a group of diseases characterized by the uncontrolled growth and
spread of abnormal cells. If the spread is not controlled, it can result in death. Cancer is …

Novel β‑hydroxy ketones: Synthesis, spectroscopic characterization, molecular docking, and anticancer activity studies

HB Kucuk, G Kanturk, S Yerlikaya, T Yildiz… - Journal of Molecular …, 2022 - Elsevier
In this study, a series of novel β‑hydroxy ketone derivatives 3a-o were designed,
synthesized, and evaluated for their anticancer activity. The structure of these compounds …

Synthesis, structure characterization, DFT calculations, and computational anticancer activity investigations of 1-phenyl ethanol derivatives

AM Senan, MT Muhammed, LA Al-Shuraym… - Journal of Molecular …, 2023 - Elsevier
Phenyl ethanol derivatives are well-known classes of drug molecules that play an important
role as effective substitute analogs to anticancer and antiviral agents. In this work …

Design, synthesis and molecular docking of chalcone derivatives as potential anticancer agents

HM Abosalim, MA Nael, TF El‐Moselhy - ChemistrySelect, 2021 - Wiley Online Library
Twenty derivatives of chalcones were synthesized and their anticancer activities were
estimated against both breast and liver cancer besides two human normal cell lines. Out of …