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 C19stemofoline alkaloid, methylstemofoline (9), and the first glycosidated Stemona alkaloid, stemofolinoside (10), and three known alkaloid...

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Main Authors: Thanapat Sastraruji, Araya Jatisatienr, Stephen G. Pyne, Alison T. Ung, Wilford Lie, Morwenna C. Williams
Format: Journal
Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/62075
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-620752018-09-11T09:27:43Z Phytochemical studies on Stemona plants: Isolation of stemofoline alkaloids Thanapat Sastraruji Araya Jatisatienr Stephen G. Pyne Alison T. Ung Wilford Lie Morwenna C. Williams Biochemistry, Genetics and Molecular Biology Chemistry Medicine Pharmacology, Toxicology and Pharmaceutics Six new stemofoline alkaloids, (2′A)-hydroxystemofoline (5), (3′R)-stemofolenol (6), (3′S)-stemofolenol (7), 1′,2′- didehydrostemofoline-AT-oxide (8), the first C19stemofoline 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. 2018-09-11T09:21:37Z 2018-09-11T09:21:37Z 2005-12-01 Journal 01633864 2-s2.0-30544452979 10.1021/np050361y https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=30544452979&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/62075
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Biochemistry, Genetics and Molecular Biology
Chemistry
Medicine
Pharmacology, Toxicology and Pharmaceutics
spellingShingle Biochemistry, Genetics and Molecular Biology
Chemistry
Medicine
Pharmacology, Toxicology and Pharmaceutics
Thanapat Sastraruji
Araya Jatisatienr
Stephen G. Pyne
Alison T. Ung
Wilford Lie
Morwenna C. Williams
Phytochemical studies on Stemona plants: Isolation of stemofoline alkaloids
description Six new stemofoline alkaloids, (2′A)-hydroxystemofoline (5), (3′R)-stemofolenol (6), (3′S)-stemofolenol (7), 1′,2′- didehydrostemofoline-AT-oxide (8), the first C19stemofoline 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.
format Journal
author Thanapat Sastraruji
Araya Jatisatienr
Stephen G. Pyne
Alison T. Ung
Wilford Lie
Morwenna C. Williams
author_facet Thanapat Sastraruji
Araya Jatisatienr
Stephen G. Pyne
Alison T. Ung
Wilford Lie
Morwenna C. Williams
author_sort Thanapat Sastraruji
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 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=30544452979&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/62075
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