About: Synthesis of Various 5-Alkoxymethyluracil Analogues and Structure-Cytotoxic Activity Relationship Study     Goto   Sponge   NotDistinct   Permalink

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  • A number of 5-alkoxymethyluracil analogues were synthesized in order to evaluate their cytotoxic activity. 5-Alkoxymethyluracil derivatives 1 were prepared via known nucleophilic substitution of 5-chloromethyluracil 5 and subsequently transformed to their corresponding nucleosides 2. All prepared compounds were submitted to cytotoxic activity testing against drug sensitive and drug resistant leukemia cells and solid tumor derived cell lines. In addition to this, the cytotoxic activity of 5-alkoxymethyluracil analogues 1,2 was compared with the previously published 5-[alkoxy(4-nitrophenyl)methyl]uracil analogues 3,4. Extensive structure-cytotoxic activity relationship studies are reported.
  • A number of 5-alkoxymethyluracil analogues were synthesized in order to evaluate their cytotoxic activity. 5-Alkoxymethyluracil derivatives 1 were prepared via known nucleophilic substitution of 5-chloromethyluracil 5 and subsequently transformed to their corresponding nucleosides 2. All prepared compounds were submitted to cytotoxic activity testing against drug sensitive and drug resistant leukemia cells and solid tumor derived cell lines. In addition to this, the cytotoxic activity of 5-alkoxymethyluracil analogues 1,2 was compared with the previously published 5-[alkoxy(4-nitrophenyl)methyl]uracil analogues 3,4. Extensive structure-cytotoxic activity relationship studies are reported. (en)
Title
  • Synthesis of Various 5-Alkoxymethyluracil Analogues and Structure-Cytotoxic Activity Relationship Study
  • Synthesis of Various 5-Alkoxymethyluracil Analogues and Structure-Cytotoxic Activity Relationship Study (en)
skos:prefLabel
  • Synthesis of Various 5-Alkoxymethyluracil Analogues and Structure-Cytotoxic Activity Relationship Study
  • Synthesis of Various 5-Alkoxymethyluracil Analogues and Structure-Cytotoxic Activity Relationship Study (en)
skos:notation
  • RIV/61989592:15310/11:33118318!RIV12-MSM-15310___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(ED0030/01/01), Z(MSM6198959216), Z(MSM6198959223)
http://linked.open...iv/cisloPeriodika
  • 14
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
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  • 233924
http://linked.open...ai/riv/idVysledku
  • RIV/61989592:15310/11:33118318
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • Nucleosides, Alkoxymethyluracils, Alkoxymethyluridines, Cytotoxic activity (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [84BCDFDC6798]
http://linked.open...i/riv/nazevZdroje
  • Carbohydrate Research
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
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http://linked.open...vavai/riv/projekt
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http://linked.open...v/svazekPeriodika
  • 346
http://linked.open...iv/tvurceVysledku
  • Džubák, Petr
  • Hajdúch, Marián
  • Hlaváč, Jan
  • Brulíková, Lucie
http://linked.open...ain/vavai/riv/wos
  • 000295754100011
http://linked.open...n/vavai/riv/zamer
issn
  • 0008-6215
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.carres.2011.07.026
http://localhost/t...ganizacniJednotka
  • 15310
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