About: 1,1-Dimethylvanadocene -amino acid complexes: synthesis, characterization and antimicrobial behavior toward Escherichia coli B     Goto   Sponge   NotDistinct   Permalink

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  • Eight water-soluble 1,1-dimethylvanadocene amino acid complexes have been prepared via the reaction of (MeCp)2VCl2 (2) with one equivalent of amino acid (aa) in water affording [(MeCp)2V(aa)]Cl, where aa is glycine (3), L-alanine (4), L-valine (5), L-leucine (6), L-isoleucine (7), L-phenylalanine (8), L-histidine (9) and L-tryptophane (10). All prepared complexes have been characterized by EPR, IR and Raman spectroscopy, elemental analysis and mass spectrometry. Molecular structures of [(MeCp)2V(ala)]BPh4*CH3OH (11), [(MeCp)2V(leu)]PF6 (12) and [(MeCp)2V(ile)]PF6 (13) were determined by X-ray diffraction analysis. Cytotoxic properties of complexes 2-10 were investigated toward Escherichia coli B and compared with analogical unsubstituted vanadocene compounds (1, 14-21). The results showed that 1,1-dimethylvanadocene amino acid complexes have identical or slightly higher antiproliferative activity then their unsubstituted analogs.
  • Eight water-soluble 1,1-dimethylvanadocene amino acid complexes have been prepared via the reaction of (MeCp)2VCl2 (2) with one equivalent of amino acid (aa) in water affording [(MeCp)2V(aa)]Cl, where aa is glycine (3), L-alanine (4), L-valine (5), L-leucine (6), L-isoleucine (7), L-phenylalanine (8), L-histidine (9) and L-tryptophane (10). All prepared complexes have been characterized by EPR, IR and Raman spectroscopy, elemental analysis and mass spectrometry. Molecular structures of [(MeCp)2V(ala)]BPh4*CH3OH (11), [(MeCp)2V(leu)]PF6 (12) and [(MeCp)2V(ile)]PF6 (13) were determined by X-ray diffraction analysis. Cytotoxic properties of complexes 2-10 were investigated toward Escherichia coli B and compared with analogical unsubstituted vanadocene compounds (1, 14-21). The results showed that 1,1-dimethylvanadocene amino acid complexes have identical or slightly higher antiproliferative activity then their unsubstituted analogs. (en)
  • Eight water-soluble 1,1-dimethylvanadocene amino acid complexes have been prepared via the reaction of (MeCp)2VCl2 (2) with one equivalent of amino acid (aa) in water affording [(MeCp)2V(aa)]Cl, where aa is glycine (3), L-alanine (4), L-valine (5), L-leucine (6), L-isoleucine (7), L-phenylalanine (8), L-histidine (9) and L-tryptophane (10). All prepared complexes have been characterized by EPR, IR and Raman spectroscopy, elemental analysis and mass spectrometry. Molecular structures of [(MeCp)2V(ala)]BPh4*CH3OH (11), [(MeCp)2V(leu)]PF6 (12) and [(MeCp)2V(ile)]PF6 (13) were determined by X-ray diffraction analysis. Cytotoxic properties of complexes 2-10 were investigated toward Escherichia coli B and compared with analogical unsubstituted vanadocene compounds (1, 14-21). The results showed that 1,1-dimethylvanadocene amino acid complexes have identical or slightly higher antiproliferative activity then their unsubstituted analogs. (cs)
Title
  • 1,1-Dimethylvanadocene -amino acid complexes: synthesis, characterization and antimicrobial behavior toward Escherichia coli B
  • 1,1-Dimethylvanadocene -amino acid complexes: synthesis, characterization and antimicrobial behavior toward Escherichia coli B (en)
  • 1,1-Dimethylvanadocene -amino acid complexes: synthesis, characterization and antimicrobial behavior toward Escherichia coli B (cs)
skos:prefLabel
  • 1,1-Dimethylvanadocene -amino acid complexes: synthesis, characterization and antimicrobial behavior toward Escherichia coli B
  • 1,1-Dimethylvanadocene -amino acid complexes: synthesis, characterization and antimicrobial behavior toward Escherichia coli B (en)
  • 1,1-Dimethylvanadocene -amino acid complexes: synthesis, characterization and antimicrobial behavior toward Escherichia coli B (cs)
skos:notation
  • RIV/00216275:25310/06:00004373!RIV07-MSM-25310___
http://linked.open.../vavai/riv/strany
  • 603-609
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • Z(MSM0021627501)
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
  • 510547
http://linked.open...ai/riv/idVysledku
  • RIV/00216275:25310/06:00004373
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • bent metallocene; antitumor agents; 1; 1-dimethylvanadocene dichloride; X-ray structural analysis; EPR spectroscopy; Escherichia coli (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [0C210CAAF4EE]
http://linked.open...i/riv/nazevZdroje
  • Applied Organometallic Chemistry
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...UplatneniVysledku
http://linked.open...iv/tvurceVysledku
  • Císařová, Ivana
  • Erben, Milan
  • Frumarová, Božena
  • Holubová, Jana
  • Vinklárek, Jaromír
  • Paláčková, Hana
http://linked.open...n/vavai/riv/zamer
issn
  • 0268-2605
number of pages
http://localhost/t...ganizacniJednotka
  • 25310
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