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30-, 31-, and 32-Hydroxybullatacinones: Bioactive Terminally Hydroxylated Annonaceous Acetogenins from Annona bullata

Authors :
Xin-ping Fang
David L. Smith
Zhe-Ming Gu
Jerry L. McLaughlin
Laura R. Miesbauer
Source :
Journal of Natural Products. 56:870-876
Publication Year :
1993
Publisher :
American Chemical Society (ACS), 1993.

Abstract

From Annona bullata, three more pairs of new ketolactone Annonaceous acetogenins were isolated by bioactivity-directed isolation. They are hydroxylated adjacent bistetrahydrofuran (THF) acetogenins and are named (2,4-cis and trans)-32-hydroxybullatacinone (1 and 2), (2,4-cis and trans)-31-hydroxybullatacinone (3 and 4), and (2,4-cis and trans)-30-hydroxybullatacinone (5 and 6). The structures were elucidated by analysis of the 1H- and 13C-nmr spectra of 1-6 and their acetates and the ms of their tri-trimethylsilyl (TMSi) derivatives as compared with bullatacinone [7]. This is the first time that Annonaceous acetogenins with OH groups at successive positions near the end of the aliphatic chain have been reported. All of the new compounds showed potent activities in the brine shrimp lethality test and against human solid tumor cells in culture, with selectivities exhibited especially toward the colon cancer cell line (HT-29).

Details

ISSN :
15206025 and 01633864
Volume :
56
Database :
OpenAIRE
Journal :
Journal of Natural Products
Accession number :
edsair.doi.dedup.....f02433ab430358688cc46cae831de4af
Full Text :
https://doi.org/10.1021/np50096a010