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Description
  • The synthesis of a new group of 2-X-6-anilinopurines, including compounds with potential cytokinin-like activities, with various substitutions (X = H, halogen, amino, methylthio or nitro) on the phenyl ring is described. The prepared compounds have been characterized using standard physico-chemical methods, and the influence of individual substituents on biological activity has been compared in three different bioassays, based on the stimulation of tobacco callus growth, retention of chlorophyll in excised wheat leaves and the dark induction of betacyanin synthesis in Amaranthus cotyledons. The biological activity of the prepared compounds was also assessed in receptor assays, in which the ability of the compounds to activate the cytokinin receptors AHK3 and AHK4/CRE1 was studied. Finally, the interactions of the compounds with the Arabidopsis cytokinin oxidase/dehydrogenase AtCKX2 (heterologously expressed) were investigated. Systematic testing led to the identification of two very potent inhibitors
  • The synthesis of a new group of 2-X-6-anilinopurines, including compounds with potential cytokinin-like activities, with various substitutions (X = H, halogen, amino, methylthio or nitro) on the phenyl ring is described. The prepared compounds have been characterized using standard physico-chemical methods, and the influence of individual substituents on biological activity has been compared in three different bioassays, based on the stimulation of tobacco callus growth, retention of chlorophyll in excised wheat leaves and the dark induction of betacyanin synthesis in Amaranthus cotyledons. The biological activity of the prepared compounds was also assessed in receptor assays, in which the ability of the compounds to activate the cytokinin receptors AHK3 and AHK4/CRE1 was studied. Finally, the interactions of the compounds with the Arabidopsis cytokinin oxidase/dehydrogenase AtCKX2 (heterologously expressed) were investigated. Systematic testing led to the identification of two very potent inhibitors (en)
Title
  • Novel potent inhibitors of A. thaliana cytokinin oxidase/dehydrogenase
  • Novel potent inhibitors of A. thaliana cytokinin oxidase/dehydrogenase (en)
skos:prefLabel
  • Novel potent inhibitors of A. thaliana cytokinin oxidase/dehydrogenase
  • Novel potent inhibitors of A. thaliana cytokinin oxidase/dehydrogenase (en)
skos:notation
  • RIV/61989592:15310/08:00010328!RIV10-MSM-15310___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(1M06030), P(GA206/07/0570), P(GA522/06/0108), P(LC06034), Z(AV0Z50380511), Z(MSM6198959216)
http://linked.open...iv/cisloPeriodika
  • 20
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 383281
http://linked.open...ai/riv/idVysledku
  • RIV/61989592:15310/08:00010328
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • cytokinins; 6-anilinopurines; cytokinin oxidase/dehydrogenase (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [FA4E79F36DB2]
http://linked.open...i/riv/nazevZdroje
  • Bioorganic & Medicinal Chemistry
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
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http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 16
http://linked.open...iv/tvurceVysledku
  • Doležal, Karel
  • Havlíček, Libor
  • Strnad, Miroslav
  • Spíchal, Lukáš
  • Zatloukal, Marek
  • Gemrotová, Markéta
http://linked.open...n/vavai/riv/zamer
issn
  • 0968-0896
number of pages
http://localhost/t...ganizacniJednotka
  • 15310
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