Acridone (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "Acridone" in French language version.

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doi.org

dx.doi.org

  • C. F. H. Allen, G. H. W. McKee, « Acridone », Org. Synth., vol. 2,‎ , p. 6 (DOI 10.15227/orgsyn.019.0006)
  • Maier W, Baumert A, Schumann B, Furukawa H, Groger D, « Synthesis of 1,3-dihydroxy-N-methylacridone and its conversion to rutacridone by cell-free extracts of Ruta-graveolens cell cultures », Phytochemistry, vol. 32, no 3,‎ , p. 691–698 (DOI 10.1016/S0031-9422(00)95155-0)
  • J. A. Smith, R. M. West, M. Allen: Acridones and Quinacridones: Novel Fluorophores for Fluorescence Lifetime Studies, in: Journal of Fluorescence 2004, 14, S. 151–171; DOI 10.1023/B:JOFL.0000016287.56322.eb.
  • S. H. Mihindukulasuriya, T. K. Morcone, L. B. McGown: Characterization of acridone dyes for use in four-decay detection in DNA sequencing, in: Electrophoresis 2003, 24, S. 20–25; DOI 10.1002/elps.200390017.
  • Thomas Faller, Kathryn Hutton, George Okafo, Andy Gribble, Patrick Camilleri et David E. Games, « A novel acridone derivative for the fluorescence tagging and mass spectrometric sequencing of peptides », Chemical Communications, vol. 16,‎ , p. 1529-1530 (DOI 10.1039/A701787A)
  • S. Fukuzumi, K. Ohkubo: Fluorescence Maxima of 10-Methylacridone-Metal Ion Salt Complexes: A Convenient and Quantitative Measure of Lewis Acidity of Metal Ion Salts, in: J. Am. Chem. Soc. 2002, 124, S. 10270–10271; DOI 10.1021/ja026613o.
  • HISASHI FUJIOKA, YUKIHIRO NISHIYAMA, HIROSHI FURUKAWA et NOBUO KUMADA, « In Vitro and In Vivo Activities of Atalaphillinine and Related Acridone Alkaloids against Rodent Malaria », Antimicrobial Agents and Chemotherapy, vol. 33, no 1,‎ , p. 6–9 (PMID 2653215, PMCID 171411, DOI 10.1128/aac.33.1.6)
  • Kelly, Jane X., Smilkstein, Martin J., Brun, Reto, Wittlin, Sergio, Cooper, Roland A., Lane, Kristin D., Janowsky, Aaron, Johnson, Robert A., Dodean, Rozalia A., Winter, Rolf, Hinrichs, David J. et Riscoe, Michael K., « Discovery of dual function acridones as a new antimalarial chemotype », Nature, vol. 459, no 7244,‎ , p. 270–273 (PMID 19357645, DOI 10.1038/nature07937)

nih.gov

ncbi.nlm.nih.gov

  • HISASHI FUJIOKA, YUKIHIRO NISHIYAMA, HIROSHI FURUKAWA et NOBUO KUMADA, « In Vitro and In Vivo Activities of Atalaphillinine and Related Acridone Alkaloids against Rodent Malaria », Antimicrobial Agents and Chemotherapy, vol. 33, no 1,‎ , p. 6–9 (PMID 2653215, PMCID 171411, DOI 10.1128/aac.33.1.6)
  • Kelly, Jane X., Smilkstein, Martin J., Brun, Reto, Wittlin, Sergio, Cooper, Roland A., Lane, Kristin D., Janowsky, Aaron, Johnson, Robert A., Dodean, Rozalia A., Winter, Rolf, Hinrichs, David J. et Riscoe, Michael K., « Discovery of dual function acridones as a new antimalarial chemotype », Nature, vol. 459, no 7244,‎ , p. 270–273 (PMID 19357645, DOI 10.1038/nature07937)

orgsyn.org

qmul.ac.uk

chem.qmul.ac.uk

sigmaaldrich.com