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Bioactive selaginellins from Selaginella tamariscina (Beauv.) Spring
A new selaginellin named selaginellin O (1), along with three other known selaginellins (2–4) were isolated from Selaginella tamariscina (Beauv.) Spring. On the basis of spectroscopic analysis, the structure of selaginellin O was demonstrated to be 4-[(4’-hydroxy-4-formyl-3-((4-hydroxyphenyl)ethynyl...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511026/ https://www.ncbi.nlm.nih.gov/pubmed/23209526 http://dx.doi.org/10.3762/bjoc.8.217 |
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author | Yang, Chao Shao, Yutian Li, Kang Xia, Wujiong |
author_facet | Yang, Chao Shao, Yutian Li, Kang Xia, Wujiong |
author_sort | Yang, Chao |
collection | PubMed |
description | A new selaginellin named selaginellin O (1), along with three other known selaginellins (2–4) were isolated from Selaginella tamariscina (Beauv.) Spring. On the basis of spectroscopic analysis, the structure of selaginellin O was demonstrated to be 4-[(4’-hydroxy-4-formyl-3-((4-hydroxyphenyl)ethynyl)biphenyl-2-yl)(4-hydroxyphenyl)methylene]cyclohexa-2,5-dien-1-one. Compound 1, 2 and 3 exhibited appreciable cytotoxic activity against cultured HeLa cells (human cervical carcinoma cells), as well as significant antioxidant activity. |
format | Online Article Text |
id | pubmed-3511026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-35110262012-12-03 Bioactive selaginellins from Selaginella tamariscina (Beauv.) Spring Yang, Chao Shao, Yutian Li, Kang Xia, Wujiong Beilstein J Org Chem Letter A new selaginellin named selaginellin O (1), along with three other known selaginellins (2–4) were isolated from Selaginella tamariscina (Beauv.) Spring. On the basis of spectroscopic analysis, the structure of selaginellin O was demonstrated to be 4-[(4’-hydroxy-4-formyl-3-((4-hydroxyphenyl)ethynyl)biphenyl-2-yl)(4-hydroxyphenyl)methylene]cyclohexa-2,5-dien-1-one. Compound 1, 2 and 3 exhibited appreciable cytotoxic activity against cultured HeLa cells (human cervical carcinoma cells), as well as significant antioxidant activity. Beilstein-Institut 2012-11-05 /pmc/articles/PMC3511026/ /pubmed/23209526 http://dx.doi.org/10.3762/bjoc.8.217 Text en Copyright © 2012, Yang et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Letter Yang, Chao Shao, Yutian Li, Kang Xia, Wujiong Bioactive selaginellins from Selaginella tamariscina (Beauv.) Spring |
title | Bioactive selaginellins from Selaginella tamariscina (Beauv.) Spring |
title_full | Bioactive selaginellins from Selaginella tamariscina (Beauv.) Spring |
title_fullStr | Bioactive selaginellins from Selaginella tamariscina (Beauv.) Spring |
title_full_unstemmed | Bioactive selaginellins from Selaginella tamariscina (Beauv.) Spring |
title_short | Bioactive selaginellins from Selaginella tamariscina (Beauv.) Spring |
title_sort | bioactive selaginellins from selaginella tamariscina (beauv.) spring |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511026/ https://www.ncbi.nlm.nih.gov/pubmed/23209526 http://dx.doi.org/10.3762/bjoc.8.217 |
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