2010
DOI: 10.1016/j.phytochem.2010.01.018
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Cytokinin receptor antagonists derived from 6-benzylaminopurine

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Cited by 54 publications
(51 citation statements)
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“…The subcellular localisation of CK receptors that was recently discoverd calls for the revision of the CK signalling model and promises new exciting plots within the CK story. Structural insights into how CK bindis to the CRE1/AHK4 receptor (Hothorn et al 2011) should accelerate the search for CK receptor antagonists that might have interesting applications in agriculture Nisler et al 2010) as root-growth promoting substances (Arata et al 2010). Similarly, due to the finding that CKX activity is a determinant of generative organ development and yield (Ashikari et al 2005;Bartrina et al 2011), great potential lies ahead for the practical use of deregulation of CK degradation by transgenic approaches or by chemical inhibition of CKX activity.…”
Section: Discussionmentioning
confidence: 99%
“…The subcellular localisation of CK receptors that was recently discoverd calls for the revision of the CK signalling model and promises new exciting plots within the CK story. Structural insights into how CK bindis to the CRE1/AHK4 receptor (Hothorn et al 2011) should accelerate the search for CK receptor antagonists that might have interesting applications in agriculture Nisler et al 2010) as root-growth promoting substances (Arata et al 2010). Similarly, due to the finding that CKX activity is a determinant of generative organ development and yield (Ashikari et al 2005;Bartrina et al 2011), great potential lies ahead for the practical use of deregulation of CK degradation by transgenic approaches or by chemical inhibition of CKX activity.…”
Section: Discussionmentioning
confidence: 99%
“…LVS when used at 1 mM or at a lower concentration is known to act in blocking specifically the synthesis of the CK precursor from the mevalonate pathway (Alberts, 1988;Crowell and Salaz, 1992;Hartig and Beck, 2005). PI-55 and LGR-991 are inhibitors of CK perception, acting, respectively, as competitors of the CK receptors Arabidopsis His kinase AHK4 and AHK3/4 (Spíchal et al, 2009;Nisler et al, 2010). PI-55 and LGR-991 up to a concentration of 5 mM were shown to be active in tomato (Solanum lycopersicum) seedlings with no toxic effect (Bergougnoux et al, 2012).…”
Section: Exogenous Applications Of Chemicals and Growth Measurementsmentioning
confidence: 99%
“…As an indication of reduced CK perceptions, positive effects on rooting parameters have been demonstrated [21]. Together with other newly discovered CK antagonists such as (2,5-dihydroxybenzylamino)purine (LRG-991) [45] and 6-(benzyloxymethyl)adenosine (BOMA) [46], PI-55 may serve as a valuable chemical for better understanding of plant response during micropropagation. In addition, these compounds may be helpful for the manipulation and regulation of micropropagation protocols as well as elucidation of the physiological basis for the in vitro-induced physiological disorders.…”
Section: Role Of Incyde Pi-55 and Plant Growth Regulators On In Vitrmentioning
confidence: 99%