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Two New Cinnamyl Isovalerate Derivatives from Sabina gaussenii
Chemical investigation of the 90% acetone extract of the branches and leaves of Sabina gaussenii led to the isolation of two new cinnamyl isovalerate derivatives (1–2) and eighteen known compounds (3–20). Their structures were determined mainly by means of MS, 1D- and 2D-NMR data, and this is the fi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273497/ https://www.ncbi.nlm.nih.gov/pubmed/27136522 http://dx.doi.org/10.3390/molecules21050571 |
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author | Sun, Zhang-Hua Tan, Ning-Hua Zeng, Guang-Zhi Zhang, Yu-Mei |
author_facet | Sun, Zhang-Hua Tan, Ning-Hua Zeng, Guang-Zhi Zhang, Yu-Mei |
author_sort | Sun, Zhang-Hua |
collection | PubMed |
description | Chemical investigation of the 90% acetone extract of the branches and leaves of Sabina gaussenii led to the isolation of two new cinnamyl isovalerate derivatives (1–2) and eighteen known compounds (3–20). Their structures were determined mainly by means of MS, 1D- and 2D-NMR data, and this is the first time these compounds have been reported from this plant. The biological activity test results indicated that the 90% acetone extract showed cytotoxicity against the human lung adenocarcinoma (A549) cell line (IC(50) = 0.98 ± 0.1 μg/mL), compound 6 showed cytotoxicities against human cervical carcinoma (HeLa) (IC(50) = 0.4 ± 0.1 μM ) and human gastric carcinoma (BGC-823) (IC(50) = 0.9 ± 0.2 μM) cancer cell lines, and compound 19 showed cytotoxicities against HeLa (IC(50) = 1.5 ± 0.4 μM), BGC-823 (IC(50) = 7.0 ± 0.8 μM ), and A549 (IC(50) = 10.6 ± 1.5 μM ) cancer cell lines. |
format | Online Article Text |
id | pubmed-6273497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62734972018-12-28 Two New Cinnamyl Isovalerate Derivatives from Sabina gaussenii Sun, Zhang-Hua Tan, Ning-Hua Zeng, Guang-Zhi Zhang, Yu-Mei Molecules Article Chemical investigation of the 90% acetone extract of the branches and leaves of Sabina gaussenii led to the isolation of two new cinnamyl isovalerate derivatives (1–2) and eighteen known compounds (3–20). Their structures were determined mainly by means of MS, 1D- and 2D-NMR data, and this is the first time these compounds have been reported from this plant. The biological activity test results indicated that the 90% acetone extract showed cytotoxicity against the human lung adenocarcinoma (A549) cell line (IC(50) = 0.98 ± 0.1 μg/mL), compound 6 showed cytotoxicities against human cervical carcinoma (HeLa) (IC(50) = 0.4 ± 0.1 μM ) and human gastric carcinoma (BGC-823) (IC(50) = 0.9 ± 0.2 μM) cancer cell lines, and compound 19 showed cytotoxicities against HeLa (IC(50) = 1.5 ± 0.4 μM), BGC-823 (IC(50) = 7.0 ± 0.8 μM ), and A549 (IC(50) = 10.6 ± 1.5 μM ) cancer cell lines. MDPI 2016-04-29 /pmc/articles/PMC6273497/ /pubmed/27136522 http://dx.doi.org/10.3390/molecules21050571 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 Sun, Zhang-Hua Tan, Ning-Hua Zeng, Guang-Zhi Zhang, Yu-Mei Two New Cinnamyl Isovalerate Derivatives from Sabina gaussenii |
title | Two New Cinnamyl Isovalerate Derivatives from Sabina gaussenii |
title_full | Two New Cinnamyl Isovalerate Derivatives from Sabina gaussenii |
title_fullStr | Two New Cinnamyl Isovalerate Derivatives from Sabina gaussenii |
title_full_unstemmed | Two New Cinnamyl Isovalerate Derivatives from Sabina gaussenii |
title_short | Two New Cinnamyl Isovalerate Derivatives from Sabina gaussenii |
title_sort | two new cinnamyl isovalerate derivatives from sabina gaussenii |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273497/ https://www.ncbi.nlm.nih.gov/pubmed/27136522 http://dx.doi.org/10.3390/molecules21050571 |
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