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Synthesis and Biological Activity of 2′,3′-iso-Aryl-abscisic Acid Analogs
2′,3′-iso-Benzoabscisic acid (iso-PhABA), an excellent selective abscisic acid (ABA) analog, was developed in our previous work. In order to find its more structure-activity information, some structural modifications were completed in this paper, including the substitution of phenyl ring and replaci...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149786/ https://www.ncbi.nlm.nih.gov/pubmed/29244719 http://dx.doi.org/10.3390/molecules22122229 |
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author | Wan, Chuan Wang, Mingan Yang, Dongyan Han, Xiaoqiang Che, Chuanliang Ding, Shanshan Xiao, Yumei Qin, Zhaohai |
author_facet | Wan, Chuan Wang, Mingan Yang, Dongyan Han, Xiaoqiang Che, Chuanliang Ding, Shanshan Xiao, Yumei Qin, Zhaohai |
author_sort | Wan, Chuan |
collection | PubMed |
description | 2′,3′-iso-Benzoabscisic acid (iso-PhABA), an excellent selective abscisic acid (ABA) analog, was developed in our previous work. In order to find its more structure-activity information, some structural modifications were completed in this paper, including the substitution of phenyl ring and replacing the ring with heterocycles. Thus, 16 novel analogs of iso-PhABA were synthesized and screened with three bioassays, Arabidopsis and lettuce seed germination and rice seedling elongation. Some of them, i.e., 2′,3′-iso-pyridoabscisic acid (iso-PyABA) and 2′,3′-iso-franoabscisic acid (iso-FrABA), displayed good bioactivities that closed to iso-PhABA and natural (+)-ABA. Some others, for instance, substituted-iso-PhABA, exhibited certain selectivity to different physiological process when compared to iso-PhABA or (+)-ABA. These analogs not only provided new candidates of ABA-like synthetic plant growth regulators (PGRs) for practical application, but also new potential selective agonist/antagonist for probing the specific function of ABA receptors. |
format | Online Article Text |
id | pubmed-6149786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61497862018-11-13 Synthesis and Biological Activity of 2′,3′-iso-Aryl-abscisic Acid Analogs Wan, Chuan Wang, Mingan Yang, Dongyan Han, Xiaoqiang Che, Chuanliang Ding, Shanshan Xiao, Yumei Qin, Zhaohai Molecules Communication 2′,3′-iso-Benzoabscisic acid (iso-PhABA), an excellent selective abscisic acid (ABA) analog, was developed in our previous work. In order to find its more structure-activity information, some structural modifications were completed in this paper, including the substitution of phenyl ring and replacing the ring with heterocycles. Thus, 16 novel analogs of iso-PhABA were synthesized and screened with three bioassays, Arabidopsis and lettuce seed germination and rice seedling elongation. Some of them, i.e., 2′,3′-iso-pyridoabscisic acid (iso-PyABA) and 2′,3′-iso-franoabscisic acid (iso-FrABA), displayed good bioactivities that closed to iso-PhABA and natural (+)-ABA. Some others, for instance, substituted-iso-PhABA, exhibited certain selectivity to different physiological process when compared to iso-PhABA or (+)-ABA. These analogs not only provided new candidates of ABA-like synthetic plant growth regulators (PGRs) for practical application, but also new potential selective agonist/antagonist for probing the specific function of ABA receptors. MDPI 2017-12-15 /pmc/articles/PMC6149786/ /pubmed/29244719 http://dx.doi.org/10.3390/molecules22122229 Text en © 2017 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 | Communication Wan, Chuan Wang, Mingan Yang, Dongyan Han, Xiaoqiang Che, Chuanliang Ding, Shanshan Xiao, Yumei Qin, Zhaohai Synthesis and Biological Activity of 2′,3′-iso-Aryl-abscisic Acid Analogs |
title | Synthesis and Biological Activity of 2′,3′-iso-Aryl-abscisic Acid Analogs |
title_full | Synthesis and Biological Activity of 2′,3′-iso-Aryl-abscisic Acid Analogs |
title_fullStr | Synthesis and Biological Activity of 2′,3′-iso-Aryl-abscisic Acid Analogs |
title_full_unstemmed | Synthesis and Biological Activity of 2′,3′-iso-Aryl-abscisic Acid Analogs |
title_short | Synthesis and Biological Activity of 2′,3′-iso-Aryl-abscisic Acid Analogs |
title_sort | synthesis and biological activity of 2′,3′-iso-aryl-abscisic acid analogs |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149786/ https://www.ncbi.nlm.nih.gov/pubmed/29244719 http://dx.doi.org/10.3390/molecules22122229 |
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