Structure-activity relationship of karrikin germination stimulants
Karrikins (2H-furo[2,3-c]pyran-2-ones) are potent smoke-derived germination promoters for a diverse range of plant species but, to date, their mode of action remains unknown. This paper reports the structure-activity relationship of numerous karrikin analogues to increase understanding of the key st...
| Main Authors: | , , , , , , , , , |
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| Format: | Journal Article |
| Published: |
American Chemical Society
2010
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| Online Access: | http://hdl.handle.net/20.500.11937/43926 |
| _version_ | 1848756849633918976 |
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| author | Flematti, G. Scaffidi, A. Goddard-Borger, E. Heath, C. Nelson, D. Commander, L. Stick, R. Dixon, Kingsley Smith, S. Ghisalberti, E. |
| author_facet | Flematti, G. Scaffidi, A. Goddard-Borger, E. Heath, C. Nelson, D. Commander, L. Stick, R. Dixon, Kingsley Smith, S. Ghisalberti, E. |
| author_sort | Flematti, G. |
| building | Curtin Institutional Repository |
| collection | Online Access |
| description | Karrikins (2H-furo[2,3-c]pyran-2-ones) are potent smoke-derived germination promoters for a diverse range of plant species but, to date, their mode of action remains unknown. This paper reports the structure-activity relationship of numerous karrikin analogues to increase understanding of the key structural features of the molecule that are required for biological activity. The results demonstrate that modification at the C5 position is preferred over modification at the C3, C4, or C7 positions for retaining the highest bioactivity. © 2010 American Chemical Society. |
| first_indexed | 2025-11-14T09:18:44Z |
| format | Journal Article |
| id | curtin-20.500.11937-43926 |
| institution | Curtin University Malaysia |
| institution_category | Local University |
| last_indexed | 2025-11-14T09:18:44Z |
| publishDate | 2010 |
| publisher | American Chemical Society |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | curtin-20.500.11937-439262017-09-13T13:42:27Z Structure-activity relationship of karrikin germination stimulants Flematti, G. Scaffidi, A. Goddard-Borger, E. Heath, C. Nelson, D. Commander, L. Stick, R. Dixon, Kingsley Smith, S. Ghisalberti, E. Karrikins (2H-furo[2,3-c]pyran-2-ones) are potent smoke-derived germination promoters for a diverse range of plant species but, to date, their mode of action remains unknown. This paper reports the structure-activity relationship of numerous karrikin analogues to increase understanding of the key structural features of the molecule that are required for biological activity. The results demonstrate that modification at the C5 position is preferred over modification at the C3, C4, or C7 positions for retaining the highest bioactivity. © 2010 American Chemical Society. 2010 Journal Article http://hdl.handle.net/20.500.11937/43926 10.1021/jf101690a American Chemical Society restricted |
| spellingShingle | Flematti, G. Scaffidi, A. Goddard-Borger, E. Heath, C. Nelson, D. Commander, L. Stick, R. Dixon, Kingsley Smith, S. Ghisalberti, E. Structure-activity relationship of karrikin germination stimulants |
| title | Structure-activity relationship of karrikin germination stimulants |
| title_full | Structure-activity relationship of karrikin germination stimulants |
| title_fullStr | Structure-activity relationship of karrikin germination stimulants |
| title_full_unstemmed | Structure-activity relationship of karrikin germination stimulants |
| title_short | Structure-activity relationship of karrikin germination stimulants |
| title_sort | structure-activity relationship of karrikin germination stimulants |
| url | http://hdl.handle.net/20.500.11937/43926 |