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Eupatorine (French Wikipedia)

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

refsWebsite
Global rank French rank
14nih.gov
4th place
12th place
8doi.org
2nd place
3rd place
1sigmaaldrich.com
924th place
1,245th place
1qmul.ac.uk
1,735th place
168th place

doi.org

dx.doi.org

  • J. H. Adams, J. R. Lewis: Eupatorin, a constituent of Merrillia caloxylon. In: Planta medica. volume 32, numéro 1, août 1977, p.86–87, DOI 10.1055/s-0028-1097564, PMID 905420.
  • B. Csapi, Z. Hajdú, I. Zupkó, A. Berényi, P. Forgo, P. Szabó, J. Hohmann: Bioactivity-guided isolation of antiproliferative compounds from Centaurea arenaria. In: Phytotherapy research : PTR. volume 24, numéro 11, novembre 2010, p.1664–1669, DOI 10.1002/ptr.3187, PMID 21031625.
  • E. Verykokidou-Vitsaropoulou, C. Vajias: Methylated Flavones from Teucrium polium. In: Planta medica. numéro 5, Oktober 1986, p.401–402, DOI 10.1055/s-2007-969198, PMID 17345353.
  • A. R. Gohari, S. Saeidnia, M. Malmir, A. Hadjiakhoondi, Y. Ajani: Flavones and rosmarinic acid from Salvia limbata. In: Natural Product Research. volume 24, numéro 20, décembre 2010, p.1902–1906, DOI 10.1080/14786411003766912, PMID 21108116.
  • A. L. Salmela, J. Pouwels, A. Kukkonen-Macchi, S. Waris, P. Toivonen, K. Jaakkola, J. Mäki-Jouppila, L. Kallio, M. J. Kallio: The flavonoid eupatorin inactivates the mitotic checkpoint leading to polyploidy and apoptosis. In: Experimental cell research. volume 318, numéro 5, mars 2012, p.578–592, DOI 10.1016/j.yexcr.2011.12.014, PMID 22227008.
  • V. Androutsopoulos, R. R. Arroo, J. F. Hall, S. Surichan, G. A. Potter: Antiproliferative and cytostatic effects of the natural product eupatorin on MDA-MB-468 human breast cancer cells due to CYP1-mediated metabolism. In: Breast cancer research : BCR. volume 10, numéro 3, 2008, p.R39, DOI 10.1186/bcr2090, PMID 18454852, PMC 2481486.
  • V. P. Androutsopoulos, A. Papakyriakou, D. Vourloumis, D. A. Spandidos: Comparative CYP1A1 and CYP1B1 substrate and inhibitor profile of dietary flavonoids. In: Bioorganic & medicinal chemistry. volume 19, numéro 9, mai 2011, p.2842–2849, DOI 10.1016/j.bmc.2011.03.042, PMID 21482471.
  • M. Laavola, R. Nieminen, M. F. Yam, A. Sadikun, M. Z. Asmawi, R. Basir, J. Welling, H. Vapaatalo, R. Korhonen, E. Moilanen: Flavonoids eupatorin and sinensetin present in Orthosiphon stamineus leaves inhibit inflammatory gene expression and STAT1 activation. In: Planta medica. volume 78, numéro 8, mai 2012, p.779–786, DOI 10.1055/s-0031-1298458, PMID 22516932.

nih.gov

ncbi.nlm.nih.gov

  • S. M. Kupchan, J. R. Knox, M. S. Udayamurthy: Tumor inhibitors. 8. Eupatorin, new cytotoxic flavone from Eupatorium semiserratum. In: Journal of pharmaceutical sciences. volume 54, numéro 6, juin 1965, p.929–930, PMID 5847037.
  • J. H. Adams, J. R. Lewis: Eupatorin, a constituent of Merrillia caloxylon. In: Planta medica. volume 32, numéro 1, août 1977, p.86–87, DOI 10.1055/s-0028-1097564, PMID 905420.
  • D. G. Kingston, M. M. Rao, W. V. Zucker: Plant anticancer agents. IX. Constituents of Hyptis tomentosa. In: Journal of natural products. volume 42, numéro 5, 1979 Sep-Oct, p.496–499, PMID 521819.
  • T. Nagao, F. Abe, J. Kinjo, H. Okabe: Antiproliferative constituents in plants 10. Flavones from the leaves of Lantana montevidensis Briq. and consideration of structure-activity relationship. In: Biological & pharmaceutical bulletin. volume 25, numéro 7, juillet 2002, p.875–879, PMID 12132661.
  • B. Csapi, Z. Hajdú, I. Zupkó, A. Berényi, P. Forgo, P. Szabó, J. Hohmann: Bioactivity-guided isolation of antiproliferative compounds from Centaurea arenaria. In: Phytotherapy research : PTR. volume 24, numéro 11, novembre 2010, p.1664–1669, DOI 10.1002/ptr.3187, PMID 21031625.
  • M. Ono, H. Morinaga, C. Masuoka, T. Ikeda, M. Okawa, J. Kinjo, T. Nohara: New Bisabolane-Type Sesquiterpenes from the Aerial Parts of Lippia dulcis. In: Chemical & pharmaceutical bulletin. volume 53, numéro 9, septembre 2005, p.1175–1177, PMID 16141591.
  • E. Verykokidou-Vitsaropoulou, C. Vajias: Methylated Flavones from Teucrium polium. In: Planta medica. numéro 5, Oktober 1986, p.401–402, DOI 10.1055/s-2007-969198, PMID 17345353.
  • A. R. Gohari, S. Saeidnia, M. Malmir, A. Hadjiakhoondi, Y. Ajani: Flavones and rosmarinic acid from Salvia limbata. In: Natural Product Research. volume 24, numéro 20, décembre 2010, p.1902–1906, DOI 10.1080/14786411003766912, PMID 21108116.
  • G. R. Schinella, R. M. Giner, M. C. Recio, P. Mordujovich de Buschiazzo, J. L. Ríos, S. Máñez: Anti-inflammatory effects of South American Tanacetum vulgare. In: The Journal of pharmacy and pharmacology. volume 50, numéro 9, septembre 1998, p.1069–1074, PMID 9811170.
  • Y. Tezuka, P. Stampoulis, A. H. Banskota, S. Awale, K. Q. Tran, I. Saiki, S. Kadota: Constituents of the Vietnamese medicinal plant Orthosiphon stamineus. In: Chemical & pharmaceutical bulletin. volume 48, numéro 11, novembre 2000, p.1711–1719, PMID 11086900.
  • A. L. Salmela, J. Pouwels, A. Kukkonen-Macchi, S. Waris, P. Toivonen, K. Jaakkola, J. Mäki-Jouppila, L. Kallio, M. J. Kallio: The flavonoid eupatorin inactivates the mitotic checkpoint leading to polyploidy and apoptosis. In: Experimental cell research. volume 318, numéro 5, mars 2012, p.578–592, DOI 10.1016/j.yexcr.2011.12.014, PMID 22227008.
  • V. Androutsopoulos, R. R. Arroo, J. F. Hall, S. Surichan, G. A. Potter: Antiproliferative and cytostatic effects of the natural product eupatorin on MDA-MB-468 human breast cancer cells due to CYP1-mediated metabolism. In: Breast cancer research : BCR. volume 10, numéro 3, 2008, p.R39, DOI 10.1186/bcr2090, PMID 18454852, PMC 2481486.
  • V. P. Androutsopoulos, A. Papakyriakou, D. Vourloumis, D. A. Spandidos: Comparative CYP1A1 and CYP1B1 substrate and inhibitor profile of dietary flavonoids. In: Bioorganic & medicinal chemistry. volume 19, numéro 9, mai 2011, p.2842–2849, DOI 10.1016/j.bmc.2011.03.042, PMID 21482471.
  • M. Laavola, R. Nieminen, M. F. Yam, A. Sadikun, M. Z. Asmawi, R. Basir, J. Welling, H. Vapaatalo, R. Korhonen, E. Moilanen: Flavonoids eupatorin and sinensetin present in Orthosiphon stamineus leaves inhibit inflammatory gene expression and STAT1 activation. In: Planta medica. volume 78, numéro 8, mai 2012, p.779–786, DOI 10.1055/s-0031-1298458, PMID 22516932.

qmul.ac.uk

chem.qmul.ac.uk

sigmaaldrich.com