Angustilobine and andranginine type indole alkaloids and an uleine–secovallesamine bisindole alkaloid from Alstonia angustiloba
A total of 20 alkaloids were isolated from the leaf and stem-bark extracts of Alstonia angustiloba, of which two are hitherto unknown. One is an alkaloid of the angustilobine type (angustilobine C), while the other is a bisindole alkaloid angustiphylline, derived from the union of uleine and secoval...
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my.um.eprints.103912014-10-15T01:52:21Z http://eprints.um.edu.my/10391/ Angustilobine and andranginine type indole alkaloids and an uleine–secovallesamine bisindole alkaloid from Alstonia angustiloba Kam, T.S. Ku, W.F. Tan, S.J. Low, Y.Y. Komiyama, K. QD Chemistry A total of 20 alkaloids were isolated from the leaf and stem-bark extracts of Alstonia angustiloba, of which two are hitherto unknown. One is an alkaloid of the angustilobine type (angustilobine C), while the other is a bisindole alkaloid angustiphylline, derived from the union of uleine and secovallesamine moieties. The structures of these alkaloids were established using NMR and MS analysis. Angustilobine C showed moderate cytotoxicity towards KB cells. Elsevier 2011 Article PeerReviewed application/pdf en http://eprints.um.edu.my/10391/1/Angustilobine_and_andranginine_type_indole_alkaloids_and_an.pdf Kam, T.S. and Ku, W.F. and Tan, S.J. and Low, Y.Y. and Komiyama, K. (2011) Angustilobine and andranginine type indole alkaloids and an uleine–secovallesamine bisindole alkaloid from Alstonia angustiloba. Phytochemistry, 72. pp. 2212-2218. ISSN 0031-9422 doi:10.1016/j.phytochem.2011.08.001 |
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QD Chemistry Kam, T.S. Ku, W.F. Tan, S.J. Low, Y.Y. Komiyama, K. Angustilobine and andranginine type indole alkaloids and an uleine–secovallesamine bisindole alkaloid from Alstonia angustiloba |
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A total of 20 alkaloids were isolated from the leaf and stem-bark extracts of Alstonia angustiloba, of which two are hitherto unknown. One is an alkaloid of the angustilobine type (angustilobine C), while the other is a bisindole alkaloid angustiphylline, derived from the union of uleine and secovallesamine moieties. The structures of these alkaloids were established using NMR and MS analysis. Angustilobine C showed moderate cytotoxicity towards KB cells. |
format |
Article |
author |
Kam, T.S. Ku, W.F. Tan, S.J. Low, Y.Y. Komiyama, K. |
author_facet |
Kam, T.S. Ku, W.F. Tan, S.J. Low, Y.Y. Komiyama, K. |
author_sort |
Kam, T.S. |
title |
Angustilobine and andranginine type indole alkaloids and an
uleine–secovallesamine bisindole alkaloid from Alstonia angustiloba |
title_short |
Angustilobine and andranginine type indole alkaloids and an
uleine–secovallesamine bisindole alkaloid from Alstonia angustiloba |
title_full |
Angustilobine and andranginine type indole alkaloids and an
uleine–secovallesamine bisindole alkaloid from Alstonia angustiloba |
title_fullStr |
Angustilobine and andranginine type indole alkaloids and an
uleine–secovallesamine bisindole alkaloid from Alstonia angustiloba |
title_full_unstemmed |
Angustilobine and andranginine type indole alkaloids and an
uleine–secovallesamine bisindole alkaloid from Alstonia angustiloba |
title_sort |
angustilobine and andranginine type indole alkaloids and an
uleine–secovallesamine bisindole alkaloid from alstonia angustiloba |
publisher |
Elsevier |
publishDate |
2011 |
url |
http://eprints.um.edu.my/10391/1/Angustilobine_and_andranginine_type_indole_alkaloids_and_an.pdf http://eprints.um.edu.my/10391/ |
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1643688787631407104 |
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13.214268 |