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  • Novel compounds termed lipophosphonoxins were prepared using a simple and efficient synthetic approach. The general structure of lipophosphonoxins consists of four modules: (i) a nucleoside module, (ii) an iminosugar module, (iii) a hydrophobic module (lipophilic alkyl chain), and (iv) a phosphonate linker module that holds together modules i–iii. Lipophosphonoxins displayed significant antibacterial properties against a panel of Gram-positive species, including multiresistant strains. The minimum inhibitory concentration (MIC) values of the best inhibitors were in the 1–12 .mu.g/mL range, while their cytotoxic concentrations against human cell lines were significantly above this range. The modular nature of this artificial scaffold offers a large number of possibilities for further modifications/exploitation of these compounds.
  • Novel compounds termed lipophosphonoxins were prepared using a simple and efficient synthetic approach. The general structure of lipophosphonoxins consists of four modules: (i) a nucleoside module, (ii) an iminosugar module, (iii) a hydrophobic module (lipophilic alkyl chain), and (iv) a phosphonate linker module that holds together modules i–iii. Lipophosphonoxins displayed significant antibacterial properties against a panel of Gram-positive species, including multiresistant strains. The minimum inhibitory concentration (MIC) values of the best inhibitors were in the 1–12 .mu.g/mL range, while their cytotoxic concentrations against human cell lines were significantly above this range. The modular nature of this artificial scaffold offers a large number of possibilities for further modifications/exploitation of these compounds. (en)
Title
  • Lipophosphonoxins: New Modular Molecular Structures with Significant Antibacterial Properties
  • Lipophosphonoxins: New Modular Molecular Structures with Significant Antibacterial Properties (en)
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  • Lipophosphonoxins: New Modular Molecular Structures with Significant Antibacterial Properties
  • Lipophosphonoxins: New Modular Molecular Structures with Significant Antibacterial Properties (en)
skos:notation
  • RIV/68378050:_____/11:00367626!RIV12-AV0-68378050
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • I, P(2B06065), P(GA204/09/0583), P(GAP302/11/0855), P(LC06077), V, Z(AV0Z40550506), Z(AV0Z50200510), Z(AV0Z50520514)
http://linked.open...iv/cisloPeriodika
  • 22
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
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  • 209660
http://linked.open...ai/riv/idVysledku
  • RIV/68378050:_____/11:00367626
http://linked.open...riv/jazykVysledku
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  • lipofosfonoxin; antibacterial; nucleoside (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • US - Spojené státy americké
http://linked.open...ontrolniKodProRIV
  • [5CC7003A6A09]
http://linked.open...i/riv/nazevZdroje
  • Journal of Medicinal Chemistry
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http://linked.open...v/svazekPeriodika
  • 54
http://linked.open...iv/tvurceVysledku
  • Bartůněk, Petr
  • Krásný, Libor
  • Kolář, M.
  • Nyč, O.
  • Pohl, Radek
  • Zborníková, Eva
  • Šanderová, Hana
  • Bogdanová, K.
  • Kovačková, Soňa
  • Látal, T.
  • Pombinho, António R.
  • Rabatinová, Alžběta
  • Rejman, Dominik
http://linked.open...ain/vavai/riv/wos
  • 000297001600011
http://linked.open...n/vavai/riv/zamer
issn
  • 0022-2623
number of pages
http://bibframe.org/vocab/doi
  • 10.1021/jm2009343
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