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Dimacrolide Sesquiterpene Pyridine Alkaloids from the Stems of Tripterygium regelii

Two new dimacrolide sesquiterpene pyridine alkaloids (DMSPAs), dimacroregelines A (1) and B (2), were isolated from the stems of Tripterygium regelii. The structures of both compounds were characterized by extensive 1D and 2D NMR spectroscopic analyses, as well as HRESIMS data. Compounds 1 and 2 are...

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Detalles Bibliográficos
Autores principales: Fan, Dongsheng, Zhu, Guo-Yuan, Li, Ting, Jiang, Zhi-Hong, Bai, Li-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273108/
https://www.ncbi.nlm.nih.gov/pubmed/27589701
http://dx.doi.org/10.3390/molecules21091146
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author Fan, Dongsheng
Zhu, Guo-Yuan
Li, Ting
Jiang, Zhi-Hong
Bai, Li-Ping
author_facet Fan, Dongsheng
Zhu, Guo-Yuan
Li, Ting
Jiang, Zhi-Hong
Bai, Li-Ping
author_sort Fan, Dongsheng
collection PubMed
description Two new dimacrolide sesquiterpene pyridine alkaloids (DMSPAs), dimacroregelines A (1) and B (2), were isolated from the stems of Tripterygium regelii. The structures of both compounds were characterized by extensive 1D and 2D NMR spectroscopic analyses, as well as HRESIMS data. Compounds 1 and 2 are two rare DMSPAs possessing unique 2-(3′-carboxybutyl)-3-furanoic acid units forming the second macrocyclic ring, representing the first example of DMSPAs bearing an extra furan ring in their second macrocyclic ring system. Compound 2 showed inhibitory effects on the proliferation of human rheumatoid arthritis synovial fibroblast cell (MH7A) at a concentration of 20 μM.
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spelling pubmed-62731082018-12-28 Dimacrolide Sesquiterpene Pyridine Alkaloids from the Stems of Tripterygium regelii Fan, Dongsheng Zhu, Guo-Yuan Li, Ting Jiang, Zhi-Hong Bai, Li-Ping Molecules Article Two new dimacrolide sesquiterpene pyridine alkaloids (DMSPAs), dimacroregelines A (1) and B (2), were isolated from the stems of Tripterygium regelii. The structures of both compounds were characterized by extensive 1D and 2D NMR spectroscopic analyses, as well as HRESIMS data. Compounds 1 and 2 are two rare DMSPAs possessing unique 2-(3′-carboxybutyl)-3-furanoic acid units forming the second macrocyclic ring, representing the first example of DMSPAs bearing an extra furan ring in their second macrocyclic ring system. Compound 2 showed inhibitory effects on the proliferation of human rheumatoid arthritis synovial fibroblast cell (MH7A) at a concentration of 20 μM. MDPI 2016-08-29 /pmc/articles/PMC6273108/ /pubmed/27589701 http://dx.doi.org/10.3390/molecules21091146 Text en © 2016 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
Fan, Dongsheng
Zhu, Guo-Yuan
Li, Ting
Jiang, Zhi-Hong
Bai, Li-Ping
Dimacrolide Sesquiterpene Pyridine Alkaloids from the Stems of Tripterygium regelii
title Dimacrolide Sesquiterpene Pyridine Alkaloids from the Stems of Tripterygium regelii
title_full Dimacrolide Sesquiterpene Pyridine Alkaloids from the Stems of Tripterygium regelii
title_fullStr Dimacrolide Sesquiterpene Pyridine Alkaloids from the Stems of Tripterygium regelii
title_full_unstemmed Dimacrolide Sesquiterpene Pyridine Alkaloids from the Stems of Tripterygium regelii
title_short Dimacrolide Sesquiterpene Pyridine Alkaloids from the Stems of Tripterygium regelii
title_sort dimacrolide sesquiterpene pyridine alkaloids from the stems of tripterygium regelii
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273108/
https://www.ncbi.nlm.nih.gov/pubmed/27589701
http://dx.doi.org/10.3390/molecules21091146
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