Two New Triterpenoids from Lysimachia heterogenea Klatt and Evaluation of Their Cytotoxicity

Two new 13,28-epoxy oleanane-type triterpenoids, namely heterogenoside E and F, were isolated from Lysimachia heterogenea Klatt, together with the eight known compounds: palmitic acid, β-stigmasterol, kaempferol, quercetin, hyperin, isorhamnetin, isorhamnetin-3-O-galactopyranoside and anagallisin C....

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Autores principales: Huang, Xin-An, Shen, Xiao-Ling, Hu, Ying-Jie, Liu, Ya-Ming, Liu, Kang-Lun, Zhang, Feng-Xue, Zhou, Xin-Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264703/
https://www.ncbi.nlm.nih.gov/pubmed/21934645
http://dx.doi.org/10.3390/molecules16098076
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author Huang, Xin-An
Shen, Xiao-Ling
Hu, Ying-Jie
Liu, Ya-Ming
Liu, Kang-Lun
Zhang, Feng-Xue
Zhou, Xin-Xin
author_facet Huang, Xin-An
Shen, Xiao-Ling
Hu, Ying-Jie
Liu, Ya-Ming
Liu, Kang-Lun
Zhang, Feng-Xue
Zhou, Xin-Xin
author_sort Huang, Xin-An
collection PubMed
description Two new 13,28-epoxy oleanane-type triterpenoids, namely heterogenoside E and F, were isolated from Lysimachia heterogenea Klatt, together with the eight known compounds: palmitic acid, β-stigmasterol, kaempferol, quercetin, hyperin, isorhamnetin, isorhamnetin-3-O-galactopyranoside and anagallisin C. Heterogenoside F possesses acetoxyl groups at the unusual C-21 and C-22 positions of its oleanane skeleton. The cytotoxic activities of anagallisin C, heterogenoside E and F were weak.
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spelling pubmed-62647032018-12-10 Two New Triterpenoids from Lysimachia heterogenea Klatt and Evaluation of Their Cytotoxicity Huang, Xin-An Shen, Xiao-Ling Hu, Ying-Jie Liu, Ya-Ming Liu, Kang-Lun Zhang, Feng-Xue Zhou, Xin-Xin Molecules Communication Two new 13,28-epoxy oleanane-type triterpenoids, namely heterogenoside E and F, were isolated from Lysimachia heterogenea Klatt, together with the eight known compounds: palmitic acid, β-stigmasterol, kaempferol, quercetin, hyperin, isorhamnetin, isorhamnetin-3-O-galactopyranoside and anagallisin C. Heterogenoside F possesses acetoxyl groups at the unusual C-21 and C-22 positions of its oleanane skeleton. The cytotoxic activities of anagallisin C, heterogenoside E and F were weak. MDPI 2011-09-20 /pmc/articles/PMC6264703/ /pubmed/21934645 http://dx.doi.org/10.3390/molecules16098076 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Communication
Huang, Xin-An
Shen, Xiao-Ling
Hu, Ying-Jie
Liu, Ya-Ming
Liu, Kang-Lun
Zhang, Feng-Xue
Zhou, Xin-Xin
Two New Triterpenoids from Lysimachia heterogenea Klatt and Evaluation of Their Cytotoxicity
title Two New Triterpenoids from Lysimachia heterogenea Klatt and Evaluation of Their Cytotoxicity
title_full Two New Triterpenoids from Lysimachia heterogenea Klatt and Evaluation of Their Cytotoxicity
title_fullStr Two New Triterpenoids from Lysimachia heterogenea Klatt and Evaluation of Their Cytotoxicity
title_full_unstemmed Two New Triterpenoids from Lysimachia heterogenea Klatt and Evaluation of Their Cytotoxicity
title_short Two New Triterpenoids from Lysimachia heterogenea Klatt and Evaluation of Their Cytotoxicity
title_sort two new triterpenoids from lysimachia heterogenea klatt and evaluation of their cytotoxicity
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264703/
https://www.ncbi.nlm.nih.gov/pubmed/21934645
http://dx.doi.org/10.3390/molecules16098076
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