Leuconicines A−G and (−)-Eburnamaline, Biologically Active Strychnan and Eburnan Alkaloids fromLeuconotis
Seven new indole alkaloids of the Strychnos type, leuconicines A-G (1-7), and a new eburnan alkaloid, (-)-eburnamaline (8), were isolated from the stem-bark extract of two Malayan Leuconotis species. The structures of these alkaloids were established using NMR and MS analysis and in the case of 8 al...
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my.um.eprints.256572020-12-14T05:34:10Z http://eprints.um.edu.my/25657/ Leuconicines A−G and (−)-Eburnamaline, Biologically Active Strychnan and Eburnan Alkaloids fromLeuconotis Gan, Chew Yan Low, Yun Yee Etoh, Tadahiro Hayashi, Masahiko Komiyama, Kanki Kam, Toh Seok Q Science (General) QD Chemistry Seven new indole alkaloids of the Strychnos type, leuconicines A-G (1-7), and a new eburnan alkaloid, (-)-eburnamaline (8), were isolated from the stem-bark extract of two Malayan Leuconotis species. The structures of these alkaloids were established using NMR and MS analysis and in the case of 8 also by partial synthesis. Alkaloids 1-5 reversed multidrug resistance in vincristine-resistant KB cells. © 2009 American Chemical Society and American Society of Pharmacognosy. American Chemical Society 2009 Article PeerReviewed Gan, Chew Yan and Low, Yun Yee and Etoh, Tadahiro and Hayashi, Masahiko and Komiyama, Kanki and Kam, Toh Seok (2009) Leuconicines A−G and (−)-Eburnamaline, Biologically Active Strychnan and Eburnan Alkaloids fromLeuconotis. Journal of Natural Products, 72 (12). pp. 2098-2103. ISSN 0163-3864 https://doi.org/10.1021/np900576b doi:10.1021/np900576b |
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Q Science (General) QD Chemistry Gan, Chew Yan Low, Yun Yee Etoh, Tadahiro Hayashi, Masahiko Komiyama, Kanki Kam, Toh Seok Leuconicines A−G and (−)-Eburnamaline, Biologically Active Strychnan and Eburnan Alkaloids fromLeuconotis |
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Seven new indole alkaloids of the Strychnos type, leuconicines A-G (1-7), and a new eburnan alkaloid, (-)-eburnamaline (8), were isolated from the stem-bark extract of two Malayan Leuconotis species. The structures of these alkaloids were established using NMR and MS analysis and in the case of 8 also by partial synthesis. Alkaloids 1-5 reversed multidrug resistance in vincristine-resistant KB cells. © 2009 American Chemical Society and American Society of Pharmacognosy. |
format |
Article |
author |
Gan, Chew Yan Low, Yun Yee Etoh, Tadahiro Hayashi, Masahiko Komiyama, Kanki Kam, Toh Seok |
author_facet |
Gan, Chew Yan Low, Yun Yee Etoh, Tadahiro Hayashi, Masahiko Komiyama, Kanki Kam, Toh Seok |
author_sort |
Gan, Chew Yan |
title |
Leuconicines A−G and (−)-Eburnamaline, Biologically Active Strychnan and Eburnan Alkaloids fromLeuconotis |
title_short |
Leuconicines A−G and (−)-Eburnamaline, Biologically Active Strychnan and Eburnan Alkaloids fromLeuconotis |
title_full |
Leuconicines A−G and (−)-Eburnamaline, Biologically Active Strychnan and Eburnan Alkaloids fromLeuconotis |
title_fullStr |
Leuconicines A−G and (−)-Eburnamaline, Biologically Active Strychnan and Eburnan Alkaloids fromLeuconotis |
title_full_unstemmed |
Leuconicines A−G and (−)-Eburnamaline, Biologically Active Strychnan and Eburnan Alkaloids fromLeuconotis |
title_sort |
leuconicines a−g and (−)-eburnamaline, biologically active strychnan and eburnan alkaloids fromleuconotis |
publisher |
American Chemical Society |
publishDate |
2009 |
url |
http://eprints.um.edu.my/25657/ https://doi.org/10.1021/np900576b |
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1687394112567771136 |