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Synthesis and Antiproliferative Effects of Amino-Modified Perillyl Alcohol Derivatives

Two series of amino-modified derivatives of (S)-perillyl alcohol were designed and synthesized using (S)-perillaldehyde as the starting material. These derivatives showed increased antiproliferative activity in human lung cancer A549 cells, human melanoma A375-S2 cells and human fibrosarcoma HT-1080...

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Autores principales: Hui, Zi, Zhang, Meihui, Cong, Lin, Xia, Mingyu, Dong, Jinhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272023/
https://www.ncbi.nlm.nih.gov/pubmed/24858099
http://dx.doi.org/10.3390/molecules19056671
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author Hui, Zi
Zhang, Meihui
Cong, Lin
Xia, Mingyu
Dong, Jinhua
author_facet Hui, Zi
Zhang, Meihui
Cong, Lin
Xia, Mingyu
Dong, Jinhua
author_sort Hui, Zi
collection PubMed
description Two series of amino-modified derivatives of (S)-perillyl alcohol were designed and synthesized using (S)-perillaldehyde as the starting material. These derivatives showed increased antiproliferative activity in human lung cancer A549 cells, human melanoma A375-S2 cells and human fibrosarcoma HT-1080 cells comparing with that of (S)-perillyl alcohol. Among these derivatives, compounds VI(5) and VI(7) were the most potent agents, with the IC(50)s below 100 μM. It was demonstrated that the antiproliferative effect of VI(5) was mediated through the induction of apoptosis in A549 cells.
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spelling pubmed-62720232018-12-21 Synthesis and Antiproliferative Effects of Amino-Modified Perillyl Alcohol Derivatives Hui, Zi Zhang, Meihui Cong, Lin Xia, Mingyu Dong, Jinhua Molecules Article Two series of amino-modified derivatives of (S)-perillyl alcohol were designed and synthesized using (S)-perillaldehyde as the starting material. These derivatives showed increased antiproliferative activity in human lung cancer A549 cells, human melanoma A375-S2 cells and human fibrosarcoma HT-1080 cells comparing with that of (S)-perillyl alcohol. Among these derivatives, compounds VI(5) and VI(7) were the most potent agents, with the IC(50)s below 100 μM. It was demonstrated that the antiproliferative effect of VI(5) was mediated through the induction of apoptosis in A549 cells. MDPI 2014-05-22 /pmc/articles/PMC6272023/ /pubmed/24858099 http://dx.doi.org/10.3390/molecules19056671 Text en © 2014 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 license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Hui, Zi
Zhang, Meihui
Cong, Lin
Xia, Mingyu
Dong, Jinhua
Synthesis and Antiproliferative Effects of Amino-Modified Perillyl Alcohol Derivatives
title Synthesis and Antiproliferative Effects of Amino-Modified Perillyl Alcohol Derivatives
title_full Synthesis and Antiproliferative Effects of Amino-Modified Perillyl Alcohol Derivatives
title_fullStr Synthesis and Antiproliferative Effects of Amino-Modified Perillyl Alcohol Derivatives
title_full_unstemmed Synthesis and Antiproliferative Effects of Amino-Modified Perillyl Alcohol Derivatives
title_short Synthesis and Antiproliferative Effects of Amino-Modified Perillyl Alcohol Derivatives
title_sort synthesis and antiproliferative effects of amino-modified perillyl alcohol derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272023/
https://www.ncbi.nlm.nih.gov/pubmed/24858099
http://dx.doi.org/10.3390/molecules19056671
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