Back to Search
Start Over
5,6-Dihydro-α-pyrones from the leaves of Cryptocarya pulchinervia (Lauraceae).
- Source :
-
Journal of natural medicines [J Nat Med] 2020 Jun; Vol. 74 (3), pp. 584-590. Date of Electronic Publication: 2020 Mar 23. - Publication Year :
- 2020
-
Abstract
- Three new 5,6-dihydro-α-pyrones derivatives, named (S)-rugulactone (1) pulchrinervialactone A (2), and pulchrinervialactone B (4), along with one known pyrone, cryptobrachytone C (3), and three known amide derivatives (5-7) have been isolated from the leaves of Cryptocarya pulchrinervia. The structures of 1-7 were elucidated based on extensive spectroscopic data and comparison with literatures. The configurations of compounds 3 and 4 were established by single crystal X-ray diffraction analysis. This is also the first report in finding (S)-rugulactone (1) as a natural product. In addition, the preliminary cytotoxic activity of the isolated compounds was evaluated against P-388 cells using the [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] assay. All the pyrones, except compound 4, were active significantly inhibiting the growth of P-388 cells, while the amides derivatives (5-7) showed moderate to weak activities. Therefore, compounds 1-3 could be potentially examined further for anticancer agents.
- Subjects :
- Animals
Antineoplastic Agents isolation & purification
Cell Line, Tumor
Lactones isolation & purification
Mice
Molecular Structure
Neoplasms drug therapy
Plant Leaves chemistry
Pyrones isolation & purification
Antineoplastic Agents pharmacokinetics
Cell Proliferation drug effects
Cryptocarya chemistry
Lactones pharmacology
Pyrones pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1861-0293
- Volume :
- 74
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Journal of natural medicines
- Publication Type :
- Academic Journal
- Accession number :
- 32207026
- Full Text :
- https://doi.org/10.1007/s11418-020-01397-7