Phytochemical studies on Stemona plants: Isolation of stemofoline alkaloids
Six new stemofoline alkaloids, (2′A)-hydroxystemofoline (5), (3′R)-stemofolenol (6), (3′S)-stemofolenol (7), 1′,2′- didehydrostemofoline-AT-oxide (8), the first C19 stemofoline alkaloid, methylstemofoline (9), and the first glycosidated Stemona alkaloid, stemofolinoside (10), and three known alkaloi...
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th-cmuir.6653943832-49202014-08-30T02:55:57Z Phytochemical studies on Stemona plants: Isolation of stemofoline alkaloids Sastraruji T. Jatisatienr A. Pyne S.G. Ung A.T. Lie W. Williams M.C. Six new stemofoline alkaloids, (2′A)-hydroxystemofoline (5), (3′R)-stemofolenol (6), (3′S)-stemofolenol (7), 1′,2′- didehydrostemofoline-AT-oxide (8), the first C19 stemofoline alkaloid, methylstemofoline (9), and the first glycosidated Stemona alkaloid, stemofolinoside (10), and three known alkaloids, (2′S)-hydroxystemofoline (2), (HZ)-1′,2′-didehydrostemofoline (3), and (11E)-1′, 2′-didehydrostemofoline (4), have been isolated from a root extract of an unidentified Stemona species. The structure and relative configuration of these new alkaloids have been determined by spectral data interpretation and from semisynthetic studies. © 2005 American Chemical Society and American Society of Pharmacognosy. 2014-08-30T02:55:57Z 2014-08-30T02:55:57Z 2005 Article 01633864 10.1021/np050361y 16378370 JNPRD http://www.scopus.com/inward/record.url?eid=2-s2.0-30544452979&partnerID=40&md5=aafe7bec906e7cbbb4a2cfae8cafa4ed http://cmuir.cmu.ac.th/handle/6653943832/4920 English |
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Six new stemofoline alkaloids, (2′A)-hydroxystemofoline (5), (3′R)-stemofolenol (6), (3′S)-stemofolenol (7), 1′,2′- didehydrostemofoline-AT-oxide (8), the first C19 stemofoline alkaloid, methylstemofoline (9), and the first glycosidated Stemona alkaloid, stemofolinoside (10), and three known alkaloids, (2′S)-hydroxystemofoline (2), (HZ)-1′,2′-didehydrostemofoline (3), and (11E)-1′, 2′-didehydrostemofoline (4), have been isolated from a root extract of an unidentified Stemona species. The structure and relative configuration of these new alkaloids have been determined by spectral data interpretation and from semisynthetic studies. © 2005 American Chemical Society and American Society of Pharmacognosy. |
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Article |
author |
Sastraruji T. Jatisatienr A. Pyne S.G. Ung A.T. Lie W. Williams M.C. |
spellingShingle |
Sastraruji T. Jatisatienr A. Pyne S.G. Ung A.T. Lie W. Williams M.C. Phytochemical studies on Stemona plants: Isolation of stemofoline alkaloids |
author_facet |
Sastraruji T. Jatisatienr A. Pyne S.G. Ung A.T. Lie W. Williams M.C. |
author_sort |
Sastraruji T. |
title |
Phytochemical studies on Stemona plants: Isolation of stemofoline alkaloids |
title_short |
Phytochemical studies on Stemona plants: Isolation of stemofoline alkaloids |
title_full |
Phytochemical studies on Stemona plants: Isolation of stemofoline alkaloids |
title_fullStr |
Phytochemical studies on Stemona plants: Isolation of stemofoline alkaloids |
title_full_unstemmed |
Phytochemical studies on Stemona plants: Isolation of stemofoline alkaloids |
title_sort |
phytochemical studies on stemona plants: isolation of stemofoline alkaloids |
publishDate |
2014 |
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http://www.scopus.com/inward/record.url?eid=2-s2.0-30544452979&partnerID=40&md5=aafe7bec906e7cbbb4a2cfae8cafa4ed http://cmuir.cmu.ac.th/handle/6653943832/4920 |
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