| Literature DB >> 32207026 |
Lia D Juliawaty1, Pramukti N Ra'idah2, Syawal Abdurrahman2, Elvira Hermawati2, Anita Alni2, Marselina I Tan3, Hayato Ishikawa4, Yana M Syah2.
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.Entities:
Keywords: (S)-rugulactone; Cryptobrachitone C; Cryptocarya pulchrinervia; P-388 cells; Pulchrinervialactone A; Pulchrinervialactone B
Year: 2020 PMID: 32207026 DOI: 10.1007/s11418-020-01397-7
Source DB: PubMed Journal: J Nat Med ISSN: 1340-3443 Impact factor: 2.343