New Arylalkenyl α-Pyrones from Cryptocarya densiflora
- PMID: 39679660
- DOI: 10.1002/cbdv.202403120
New Arylalkenyl α-Pyrones from Cryptocarya densiflora
Abstract
Four previously undescribed arylalkenyl α-pyrones, designated as crydensiones A‒D (1‒4), were isolated from the twigs and leaves of Cryptocarya densiflora. Their structures were determined through comprehensive spectroscopic analyses together with quantum chemical calculations of electronic circular dichroism and nuclear magnetic resonance data. All isolates were assessed for cytotoxicity against HCT-116 (colon), A549 (lung), and MDA-MB-231 (breast) cancer cell lines; however, none demonstrated significant activity.
Keywords: Cryptocarya densiflora; cytotoxicity; quantum chemical calculations; spectroscopic data; α‐pyrones.
© 2024 Wiley‐VHCA AG, Zurich, Switzerland.
References
-
- Y. Cheng, N. Xia, and M. G. Gilbert, Flora of China, Vol. 7 (Zhongguo Zhiwu Zhi) (Beijing: Science Press, 2008).
-
- T. L. Meragelman, D. A. Scudiero, and R. E. Davis, “Inhibitors of the NF‐κB Activation Pathway From Cryptocarya rugulosa,” Journal of Natural Products 72 (2009): 336–339.
-
- R. A. Davis, O. Demirkiran, M. L. Sykes, et al., “7′,8′‐Dihydroobolactone, A Typanocidal α‐Pyrone From the Rainforest Tree Cryptocarya obovata,” Bioorganic & Medicinal Chemistry Letters 20 (2010): 4057–4059.
-
- R. Feng, T. Wang, W. Wei, R. X. Tan, and H. M. Ge, “Cytotoxic Constitutents From Cryptocarya maclurei,” Phytochemistry 90 (2013): 147–153.
-
- H.‐R. Lin, T.‐H. Chou, D.‐W. Huang, and I.‐S. Chen, “Cryptochinones From Cryptocarya chinensis Act as Farnesoid X Receptor Agonists,” Bioorganic & Medicinal Chemistry Letters 24 (2014): 4181–4186.
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous