Cargando…
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...
Autores principales: | , , , , |
---|---|
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 |
_version_ | 1783377064159608832 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6272023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT huizi synthesisandantiproliferativeeffectsofaminomodifiedperillylalcoholderivatives AT zhangmeihui synthesisandantiproliferativeeffectsofaminomodifiedperillylalcoholderivatives AT conglin synthesisandantiproliferativeeffectsofaminomodifiedperillylalcoholderivatives AT xiamingyu synthesisandantiproliferativeeffectsofaminomodifiedperillylalcoholderivatives AT dongjinhua synthesisandantiproliferativeeffectsofaminomodifiedperillylalcoholderivatives |