Design, synthesis, and evaluation of cyclic C7-bridged monocarbonyl curcumin analogs containing an o-methoxy phenyl group as potential agents against gastric cancer

Design, synthesis, and evaluation of cyclic C7-bridged monocarbonyl curcumin analogs containing an o-methoxy phenyl group as potential agents against gastric cancer

The structure-activity relationship (SAR) between toxicity and the types of linking ketones of C7 bridged monocarbonyl curcumin analogs (MCAs) was not clear yet. In the pursuit of effective and less cytotoxic chemotherapeutics, we conducted a SAR analysis using various diketene skeletons of C7-bridg...

Disgrifiad llawn

Manylion Llyfryddiaeth
Prif Awduron: Xin Gan, Yuna Wu, Min Zhu, Bo Liu, Miaomiao Kong, Zixuan Xi, Ke Li, Haibao Wang, Tiande Su, Jiali Yao, Fatehi Khushafah, Baozhu Yi, Jiabing Wang, Wulan Li, Jianzhang Wu
Fformat: Erthygl
Iaith:English
Cyhoeddwyd: Taylor & Francis Group 2024-12-01
Cyfres:Journal of Enzyme Inhibition and Medicinal Chemistry
Pynciau:
Cyclic C7 bridged monocarbonyl curcumin analogues
synthesis
anticancer activity
QSAR based on artificial intelligence
AKT/STAT3 inhibitor
Mynediad Ar-lein:https://www.tandfonline.com/doi/10.1080/14756366.2024.2314233

Rhyngrwyd

https://www.tandfonline.com/doi/10.1080/14756366.2024.2314233

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