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Three New Benzophenone Derivatives from Selaginella tamariscina

Six compounds including three new benzophenones, selagibenzophenones D-F (1–3), two known selaginellins (4–5) and one known flavonoid (6), were isolated from Selaginella tamariscina. The structures of new compounds were established by 1D-, 2D-NMR and HR-ESI-MS spectral analyses. Compound 1 represent...

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Autores principales: Long, Jiayin, Mao, Qingqing, Peng, Yujie, Liu, Lei, Hong, Yin, Xiang, Honglin, Ma, Ming, Zou, Hui, Kuang, Junwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10304954/
https://www.ncbi.nlm.nih.gov/pubmed/37375139
http://dx.doi.org/10.3390/molecules28124582
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author Long, Jiayin
Mao, Qingqing
Peng, Yujie
Liu, Lei
Hong, Yin
Xiang, Honglin
Ma, Ming
Zou, Hui
Kuang, Junwei
author_facet Long, Jiayin
Mao, Qingqing
Peng, Yujie
Liu, Lei
Hong, Yin
Xiang, Honglin
Ma, Ming
Zou, Hui
Kuang, Junwei
author_sort Long, Jiayin
collection PubMed
description Six compounds including three new benzophenones, selagibenzophenones D-F (1–3), two known selaginellins (4–5) and one known flavonoid (6), were isolated from Selaginella tamariscina. The structures of new compounds were established by 1D-, 2D-NMR and HR-ESI-MS spectral analyses. Compound 1 represents the second example of diarylbenzophenone from natural sources. Compound 2 possesses an unusual biphenyl-bisbenzophenone structure. Their cytotoxicity against human hepatocellular carcinoma HepG2 and SMCC-7721 cells and inhibitory activities on lipopolysaccharide-induced nitric oxide (NO) production in RAW264.7 cells were evaluated. Compound 2 showed moderate inhibitory activity against HepG2 and SMCC-7721 cells, and compounds 4 and 5 showed moderate inhibitory activity to HepG2 cells. Compounds 2 and 5 also exhibited inhibitory activities on lipopolysaccharide-induced nitric oxide (NO) production.
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spelling pubmed-103049542023-06-29 Three New Benzophenone Derivatives from Selaginella tamariscina Long, Jiayin Mao, Qingqing Peng, Yujie Liu, Lei Hong, Yin Xiang, Honglin Ma, Ming Zou, Hui Kuang, Junwei Molecules Article Six compounds including three new benzophenones, selagibenzophenones D-F (1–3), two known selaginellins (4–5) and one known flavonoid (6), were isolated from Selaginella tamariscina. The structures of new compounds were established by 1D-, 2D-NMR and HR-ESI-MS spectral analyses. Compound 1 represents the second example of diarylbenzophenone from natural sources. Compound 2 possesses an unusual biphenyl-bisbenzophenone structure. Their cytotoxicity against human hepatocellular carcinoma HepG2 and SMCC-7721 cells and inhibitory activities on lipopolysaccharide-induced nitric oxide (NO) production in RAW264.7 cells were evaluated. Compound 2 showed moderate inhibitory activity against HepG2 and SMCC-7721 cells, and compounds 4 and 5 showed moderate inhibitory activity to HepG2 cells. Compounds 2 and 5 also exhibited inhibitory activities on lipopolysaccharide-induced nitric oxide (NO) production. MDPI 2023-06-06 /pmc/articles/PMC10304954/ /pubmed/37375139 http://dx.doi.org/10.3390/molecules28124582 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Long, Jiayin
Mao, Qingqing
Peng, Yujie
Liu, Lei
Hong, Yin
Xiang, Honglin
Ma, Ming
Zou, Hui
Kuang, Junwei
Three New Benzophenone Derivatives from Selaginella tamariscina
title Three New Benzophenone Derivatives from Selaginella tamariscina
title_full Three New Benzophenone Derivatives from Selaginella tamariscina
title_fullStr Three New Benzophenone Derivatives from Selaginella tamariscina
title_full_unstemmed Three New Benzophenone Derivatives from Selaginella tamariscina
title_short Three New Benzophenone Derivatives from Selaginella tamariscina
title_sort three new benzophenone derivatives from selaginella tamariscina
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10304954/
https://www.ncbi.nlm.nih.gov/pubmed/37375139
http://dx.doi.org/10.3390/molecules28124582
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