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Identification of auxins by a chemical genomics approach

Thirteen auxenic compounds were discovered in a screen of 10 000 compounds for auxin-like activity in Arabidopsis roots. One of the most potent substances was 2-(4-chloro-2-methylphenoxy)-N-(4-H-1,2,4-triazol-3-yl)acetamide (WH7) which shares similar structure to the known auxenic herbicide 2,4-dich...

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Detalles Bibliográficos
Autores principales: Christian, May, Hannah, William B., Lüthen, Hartwig, Jones, Alan M.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2486469/
https://www.ncbi.nlm.nih.gov/pubmed/18515827
http://dx.doi.org/10.1093/jxb/ern133
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author Christian, May
Hannah, William B.
Lüthen, Hartwig
Jones, Alan M.
author_facet Christian, May
Hannah, William B.
Lüthen, Hartwig
Jones, Alan M.
author_sort Christian, May
collection PubMed
description Thirteen auxenic compounds were discovered in a screen of 10 000 compounds for auxin-like activity in Arabidopsis roots. One of the most potent substances was 2-(4-chloro-2-methylphenoxy)-N-(4-H-1,2,4-triazol-3-yl)acetamide (WH7) which shares similar structure to the known auxenic herbicide 2,4-dichlorophenoxyacetic acid (2,4-D). A selected set of 20 analogues of WH7 was used to provide detailed information about the structure–activity relationship based on their efficacy at inhibiting and stimulating root and shoot growth, respectively, and at induction of gene expression. It was shown that WH7 acts in a genetically defined auxin pathway. These small molecules will extend the arsenal of substances that can be used to define auxin perception site(s) and to dissect subsequent signalling events.
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spelling pubmed-24864692009-02-25 Identification of auxins by a chemical genomics approach Christian, May Hannah, William B. Lüthen, Hartwig Jones, Alan M. J Exp Bot Research Papers Thirteen auxenic compounds were discovered in a screen of 10 000 compounds for auxin-like activity in Arabidopsis roots. One of the most potent substances was 2-(4-chloro-2-methylphenoxy)-N-(4-H-1,2,4-triazol-3-yl)acetamide (WH7) which shares similar structure to the known auxenic herbicide 2,4-dichlorophenoxyacetic acid (2,4-D). A selected set of 20 analogues of WH7 was used to provide detailed information about the structure–activity relationship based on their efficacy at inhibiting and stimulating root and shoot growth, respectively, and at induction of gene expression. It was shown that WH7 acts in a genetically defined auxin pathway. These small molecules will extend the arsenal of substances that can be used to define auxin perception site(s) and to dissect subsequent signalling events. Oxford University Press 2008-07 2008-05-31 /pmc/articles/PMC2486469/ /pubmed/18515827 http://dx.doi.org/10.1093/jxb/ern133 Text en © 2008 The Author(s). This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. This paper is available online free of all access charges (see http://jxb.oxfordjournals.org/open_access.html for further details)
spellingShingle Research Papers
Christian, May
Hannah, William B.
Lüthen, Hartwig
Jones, Alan M.
Identification of auxins by a chemical genomics approach
title Identification of auxins by a chemical genomics approach
title_full Identification of auxins by a chemical genomics approach
title_fullStr Identification of auxins by a chemical genomics approach
title_full_unstemmed Identification of auxins by a chemical genomics approach
title_short Identification of auxins by a chemical genomics approach
title_sort identification of auxins by a chemical genomics approach
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2486469/
https://www.ncbi.nlm.nih.gov/pubmed/18515827
http://dx.doi.org/10.1093/jxb/ern133
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