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C19-Norditerpenoid Alkaloids from Aconitum szechenyianum

Three new C(19)-norditerpenoid alkaloids (1–3), along with two known C(19)-norditerpenoid alkaloids (4,5), have been isolated from Aconitum szechenyianum. Based on extensive spectroscopic techniques (1D, 2D-NMR, IR, and MS) and chemical methods, their structures were established as szechenyianine D...

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Autores principales: Song, Bei, Jin, Bingliang, Li, Yuze, Wang, Fei, Yang, Yifu, Cui, Yuwen, Song, Xiaomei, Yue, Zhenggang, Liu, Jianli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100137/
https://www.ncbi.nlm.nih.gov/pubmed/29738430
http://dx.doi.org/10.3390/molecules23051108
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author Song, Bei
Jin, Bingliang
Li, Yuze
Wang, Fei
Yang, Yifu
Cui, Yuwen
Song, Xiaomei
Yue, Zhenggang
Liu, Jianli
author_facet Song, Bei
Jin, Bingliang
Li, Yuze
Wang, Fei
Yang, Yifu
Cui, Yuwen
Song, Xiaomei
Yue, Zhenggang
Liu, Jianli
author_sort Song, Bei
collection PubMed
description Three new C(19)-norditerpenoid alkaloids (1–3), along with two known C(19)-norditerpenoid alkaloids (4,5), have been isolated from Aconitum szechenyianum. Based on extensive spectroscopic techniques (1D, 2D-NMR, IR, and MS) and chemical methods, their structures were established as szechenyianine D (1), szechenyianine E (2), szechenyianine F (3), 8-O-methyl-14-benzoylaconine (4), and spicatine A (5). The immunosuppressive effects of compounds 1–5 were studied using a ConA-induced or LPS-induced splenocyte proliferation model. In vitro tests showed that Compounds 2, 4, and 5 suppressed ConA-induced or LPS-induced splenocyte proliferation in a concentration-dependent manner. The CC(50)/IC(50) values of 2, 4, and 5 suggested that these compounds were potential immunosuppressive agents for the treatment of autoimmune diseases characterized by arthritis, such as rheumatoid arthritis.
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spelling pubmed-61001372018-11-13 C19-Norditerpenoid Alkaloids from Aconitum szechenyianum Song, Bei Jin, Bingliang Li, Yuze Wang, Fei Yang, Yifu Cui, Yuwen Song, Xiaomei Yue, Zhenggang Liu, Jianli Molecules Article Three new C(19)-norditerpenoid alkaloids (1–3), along with two known C(19)-norditerpenoid alkaloids (4,5), have been isolated from Aconitum szechenyianum. Based on extensive spectroscopic techniques (1D, 2D-NMR, IR, and MS) and chemical methods, their structures were established as szechenyianine D (1), szechenyianine E (2), szechenyianine F (3), 8-O-methyl-14-benzoylaconine (4), and spicatine A (5). The immunosuppressive effects of compounds 1–5 were studied using a ConA-induced or LPS-induced splenocyte proliferation model. In vitro tests showed that Compounds 2, 4, and 5 suppressed ConA-induced or LPS-induced splenocyte proliferation in a concentration-dependent manner. The CC(50)/IC(50) values of 2, 4, and 5 suggested that these compounds were potential immunosuppressive agents for the treatment of autoimmune diseases characterized by arthritis, such as rheumatoid arthritis. MDPI 2018-05-08 /pmc/articles/PMC6100137/ /pubmed/29738430 http://dx.doi.org/10.3390/molecules23051108 Text en © 2018 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Song, Bei
Jin, Bingliang
Li, Yuze
Wang, Fei
Yang, Yifu
Cui, Yuwen
Song, Xiaomei
Yue, Zhenggang
Liu, Jianli
C19-Norditerpenoid Alkaloids from Aconitum szechenyianum
title C19-Norditerpenoid Alkaloids from Aconitum szechenyianum
title_full C19-Norditerpenoid Alkaloids from Aconitum szechenyianum
title_fullStr C19-Norditerpenoid Alkaloids from Aconitum szechenyianum
title_full_unstemmed C19-Norditerpenoid Alkaloids from Aconitum szechenyianum
title_short C19-Norditerpenoid Alkaloids from Aconitum szechenyianum
title_sort c19-norditerpenoid alkaloids from aconitum szechenyianum
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100137/
https://www.ncbi.nlm.nih.gov/pubmed/29738430
http://dx.doi.org/10.3390/molecules23051108
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