Publication: Structural relationships of stemona alkaloids: Assessment of species-specific accumulation trends for exploiting their biological activities
3
Issued Date
2011-09-23
Resource Type
ISSN
15206025
01633864
01633864
Other identifier(s)
2-s2.0-80053217145
Rights
Mahidol University
Rights Holder(s)
SCOPUS
Bibliographic Citation
Journal of Natural Products. Vol.74, No.9 (2011), 1931-1938
Suggested Citation
Sumet Kongkiatpaiboon, Johann Schinnerl, Susanne Felsinger, Vichien Keeratinijakal, Srunya Vajrodaya, Wandee Gritsanapan, Lothar Brecker, Harald Greger Structural relationships of stemona alkaloids: Assessment of species-specific accumulation trends for exploiting their biological activities. Journal of Natural Products. Vol.74, No.9 (2011), 1931-1938. doi:10.1021/np2004374 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/11470
Research Projects
Organizational Units
Authors
Journal Issue
Thesis
Title
Structural relationships of stemona alkaloids: Assessment of species-specific accumulation trends for exploiting their biological activities
Other Contributor(s)
Abstract
On the basis of a comparison of 42 Stemona samples, representing eight different species collected and cultivated in Thailand, species-specific accumulation trends of Stemona alkaloids were analyzed. An overview was achieved by comparative HPLC analyses of methanolic crude extracts of underground parts coupled with diode array or evaporative light scattering detectors. All major compounds were isolated and their structures elucidated by NMR and MS analyses. Protostemonine- and stichoneurine-type derivatives dominated, from which the latter characterize S. tuberosa and S. phyllantha accumulating species-specific isomers of tuberostemonine (3). The widespread S. curtisii and S. collinsiae clearly deviate by protostemonine-type derivatives dominated by stemofoline (10) and/or didehydrostemofoline (11). Further diversification within this structural type results from a mutual accumulation of derivatives with a pyrrolo - or pyridoazepine nucleus, leading to chemical variability in S. curtisii and S. aphylla. © 2011 The American Chemical Society and American Society of Pharmacognosy.