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Alkaloids with Nitric Oxide Inhibitory Activities from the Roots of Isatis tinctoria

As our ongoing research project on Ban Lan Gen (Isatis tinctoria roots), a total of 23 alkaloids were obtained. Compounds 1 and 2 contain an unusual C–C bond between the 2(1H)-quinolinone moiety and the phenol moiety and between the 2(1H)-quinolinone moiety and the 1H-indole moiety, respectively. Co...

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Autores principales: Zhang, Dongdong, Shi, Yanhong, Li, Jingyi, Ruan, Deqing, Jia, Qi, Zhu, Weiliang, Chen, Kaixian, Li, Yiming, Wang, Rui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891263/
https://www.ncbi.nlm.nih.gov/pubmed/31703370
http://dx.doi.org/10.3390/molecules24224033
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author Zhang, Dongdong
Shi, Yanhong
Li, Jingyi
Ruan, Deqing
Jia, Qi
Zhu, Weiliang
Chen, Kaixian
Li, Yiming
Wang, Rui
author_facet Zhang, Dongdong
Shi, Yanhong
Li, Jingyi
Ruan, Deqing
Jia, Qi
Zhu, Weiliang
Chen, Kaixian
Li, Yiming
Wang, Rui
author_sort Zhang, Dongdong
collection PubMed
description As our ongoing research project on Ban Lan Gen (Isatis tinctoria roots), a total of 23 alkaloids were obtained. Compounds 1 and 2 contain an unusual C–C bond between the 2(1H)-quinolinone moiety and the phenol moiety and between the 2(1H)-quinolinone moiety and the 1H-indole moiety, respectively. Compound 3 possesses an unusual carbon skeleton and its putative biosynthetic pathway was discussed, and Compound 23 was deduced as a new indole alkaloid glycoside. Compounds 4–7 were identified as four new natural products by extensive spectroscopic experiments. Additionally, the anti-inflammatory activity was assessed based on nitric oxide (NO) production using Lipopolysaccharide-stimulated RAW264.7 macrophages. Compounds 9, 15, and 17 showed inhibitory effects with IC(50) values of 1.2, 5.0, and 74.4 μM.
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spelling pubmed-68912632019-12-12 Alkaloids with Nitric Oxide Inhibitory Activities from the Roots of Isatis tinctoria Zhang, Dongdong Shi, Yanhong Li, Jingyi Ruan, Deqing Jia, Qi Zhu, Weiliang Chen, Kaixian Li, Yiming Wang, Rui Molecules Article As our ongoing research project on Ban Lan Gen (Isatis tinctoria roots), a total of 23 alkaloids were obtained. Compounds 1 and 2 contain an unusual C–C bond between the 2(1H)-quinolinone moiety and the phenol moiety and between the 2(1H)-quinolinone moiety and the 1H-indole moiety, respectively. Compound 3 possesses an unusual carbon skeleton and its putative biosynthetic pathway was discussed, and Compound 23 was deduced as a new indole alkaloid glycoside. Compounds 4–7 were identified as four new natural products by extensive spectroscopic experiments. Additionally, the anti-inflammatory activity was assessed based on nitric oxide (NO) production using Lipopolysaccharide-stimulated RAW264.7 macrophages. Compounds 9, 15, and 17 showed inhibitory effects with IC(50) values of 1.2, 5.0, and 74.4 μM. MDPI 2019-11-07 /pmc/articles/PMC6891263/ /pubmed/31703370 http://dx.doi.org/10.3390/molecules24224033 Text en © 2019 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
Zhang, Dongdong
Shi, Yanhong
Li, Jingyi
Ruan, Deqing
Jia, Qi
Zhu, Weiliang
Chen, Kaixian
Li, Yiming
Wang, Rui
Alkaloids with Nitric Oxide Inhibitory Activities from the Roots of Isatis tinctoria
title Alkaloids with Nitric Oxide Inhibitory Activities from the Roots of Isatis tinctoria
title_full Alkaloids with Nitric Oxide Inhibitory Activities from the Roots of Isatis tinctoria
title_fullStr Alkaloids with Nitric Oxide Inhibitory Activities from the Roots of Isatis tinctoria
title_full_unstemmed Alkaloids with Nitric Oxide Inhibitory Activities from the Roots of Isatis tinctoria
title_short Alkaloids with Nitric Oxide Inhibitory Activities from the Roots of Isatis tinctoria
title_sort alkaloids with nitric oxide inhibitory activities from the roots of isatis tinctoria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891263/
https://www.ncbi.nlm.nih.gov/pubmed/31703370
http://dx.doi.org/10.3390/molecules24224033
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