[HTML][HTML] Novel Tetrahydro-[1,2,4]triazolo[3,4-a]isoquinoline Chalcones Suppress Breast Carcinoma through Cell Cycle Arrests and Apoptosis

MIM Darwish, AM Moustafa, AM Youssef, M Mansour… - Molecules, 2023 - mdpi.com
Chalcones are interesting anticancer drug candidates which have attracted much interest
due to their unique structure and their extensive biological activity. Various functional …

Novel 1-(7-ethoxy-1-benzofuran-2-yl) substituted chalcone derivatives: synthesis, characterization and anticancer activity

D Coskun, M Erkisa, E Ulukaya, MF Coskun… - European journal of …, 2017 - Elsevier
Cancer treatment still requires new compounds to be discovered. Chalcone and its
derivatives exhibit anticancer potential in different cancer cells. A new series of benzofuran …

Chalcones incorporated pyrazole ring inhibit proliferation, cell cycle progression, angiogenesis and induce apoptosis of MCF7 cell line

MF Mohamed, MS Mohamed… - Anti-Cancer Agents …, 2014 - ingentaconnect.com
A Series of chalcone derivatives containing pyrazole ring was prepared and their cytotoxicity
against different human cell lines, including breast (MCF-7), colon (HCT-116) liver (HEPG2) …

Design, synthesis and biological evaluation of novel bischalcone derivatives as potential anticancer agents

S Burmaoglu, A Gobek, BO Aydin, E Yurtoglu… - Bioorganic …, 2021 - Elsevier
Building on our previous work that discovered chalcone as a promising pharmacophore for
anticancer activity, we have various other chalcone derivatives and have synthesized a …

Antiproliferative activity and p53 upregulation effects of chalcones on human breast cancer cells

MB Dos Santos, D Bertholin Anselmo… - Journal of enzyme …, 2019 - Taylor & Francis
Chalcones are valuable structures for drug discovery due to their broad bioactivity spectrum.
In this study, we evaluated 20 synthetic chalcones against estrogen-receptor-positive breast …

Synthesis and cytotoxic activity of chalcone analogues containing a thieno [2, 3-d] pyrimidin-2-yl group as the A-ring or B-ring

FC Wang, B Peng, SL Cao, HY Li, XL Yuan… - Bioorganic …, 2020 - Elsevier
Many natural or synthetic chalcones have potential anti-tumor activity. Here, we synthesized
two series of chalcone analogues containing a thieno [2, 3-d] pyrimidin-2-yl group and …

Novel 3′, 5′-diprenylated chalcones inhibited the proliferation of cancer cells in vitro by inducing cell apoptosis and arresting cell cycle phase

Z Wen, Y Zhang, X Wang, X Zeng, Z Hu, Y Liu… - European Journal of …, 2017 - Elsevier
A double Claisen rearrangements synthetic strategy was established for the total synthesis
of 4, 4′-dimethyl medicagenin (compound 6c). A series of its analogs also were prepared …

Cytotoxicity, molecular modeling, cell cycle arrest, and apoptotic induction induced by novel tetrahydro-[1, 2, 4] triazolo [3, 4-a] isoquinoline chalcones

MF Mohamed, HM Hassaneen… - European Journal of …, 2018 - Elsevier
Abstract Novel tetrahydro-[1, 2, 4] triazolo [3, 4-a] isoquinolin-3-yl)-3-arylprop-2-en-1-one
derivatives were synthesized and their structures were confirmed by different spectral tools …

[HTML][HTML] Design and Synthesis of Novel Chalcone Derivatives: Anti-Breast Cancer Activity Evaluation and Docking Study

W Lai, J Chen, X Gao, X Jin, G Chen, L Ye - International Journal of …, 2023 - mdpi.com
Chalcone is a common simple fragment of natural products with anticancer activity. In a
previous study, the research group discovered a series of chalcone derivatives with stronger …

[HTML][HTML] Chalcone derivatives: Role in anticancer therapy

Y Ouyang, J Li, X Chen, X Fu, S Sun, Q Wu - Biomolecules, 2021 - mdpi.com
Chalcones (1, 3-diaryl-2-propen-1-ones) are precursors for flavonoids and isoflavonoids,
which are common simple chemical scaffolds found in many naturally occurring compounds …