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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...

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Autores principales: Sun, Zhang-Hua, Tan, Ning-Hua, Zeng, Guang-Zhi, Zhang, Yu-Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
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.
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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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