Structure-activity relationships of analogs of 3,4,5-trimethylfuran-2(5H)-one with germination inhibitory activities

Copyright © 2013 Elsevier GmbH. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Journal of plant physiology. - 1979. - 170(2013), 14 vom: 15. Sept., Seite 1235-42
1. Verfasser: Pošta, Martin (VerfasserIn)
Weitere Verfasser: Light, Marnie E, Papenfus, Heino B, Van Staden, Johannes, Kohout, Ladislav
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2013
Zugriff auf das übergeordnete Werk:Journal of plant physiology
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Butenolide KAR(1) Karrikinolide Lactuca sativa Seed germination Smoke karrikinolide (3-methyl-2H-furo[2,3-c]pyran-2-one) 3,4,5-trimethylfuran-2(5H)-one mehr... Furans Plant Growth Regulators Pyrans karrikinolide
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245 1 0 |a Structure-activity relationships of analogs of 3,4,5-trimethylfuran-2(5H)-one with germination inhibitory activities 
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520 |a Smoke-derived butenolide compounds have, in recent years, been shown to be important germination signaling molecules, which also affect seedling growth. The butenolide 3,4,5-trimethylfuran-2(5H)-one was previously isolated from plant-derived smoke and was found to significantly reduce the effect on germination by the highly active promotor karrikinolide (KAR1, 3-methyl-2H-furo[2,3-c]pyran-2-one), another smoke-derived compound. In this study, 11 analogs of 3,4,5-trimethylfuran-2(5H)-one were synthesized and their effect on the germination of light-sensitive 'Grand Rapids' lettuce seeds (Lactua sativa cv. 'Grand Rapids') were evaluated. A concentration series (1mM-1μM) of the analogs were tested alone, or in combination with 0.01μM KAR1. Only two compounds were found to reduce the germination promotory effect of 0.01μM KAR1 in a similar manner as observed with 3,4,5-trimethylfuran-2(5H)-one, with activity ranging from 1mM to 10μM. Four compounds were found to have inhibitory activity at 1mM and 100μM. The retention of activity by some of the analogs may be useful for designing novel compounds with improved activity. Furthermore, understanding the structure-activity relationships of these compounds may be helpful in synthesizing molecular probes that can be used to further investigate the mechanism of action of these compounds in regulating seed germination 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 4 |a Butenolide 
650 4 |a KAR(1) 
650 4 |a Karrikinolide 
650 4 |a Lactuca sativa 
650 4 |a Seed germination 
650 4 |a Smoke 
650 4 |a karrikinolide (3-methyl-2H-furo[2,3-c]pyran-2-one) 
650 7 |a 3,4,5-trimethylfuran-2(5H)-one  |2 NLM 
650 7 |a Furans  |2 NLM 
650 7 |a Plant Growth Regulators  |2 NLM 
650 7 |a Pyrans  |2 NLM 
650 7 |a Smoke  |2 NLM 
650 7 |a karrikinolide  |2 NLM 
700 1 |a Light, Marnie E  |e verfasserin  |4 aut 
700 1 |a Papenfus, Heino B  |e verfasserin  |4 aut 
700 1 |a Van Staden, Johannes  |e verfasserin  |4 aut 
700 1 |a Kohout, Ladislav  |e verfasserin  |4 aut 
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856 4 0 |u http://dx.doi.org/10.1016/j.jplph.2013.04.002  |3 Volltext 
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