Biflavonoid

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Biflavonoids are a type of flavonoids with the general formula scheme (C6-C3-C6)2.

Examples[edit]

References[edit]

  1. ^ Pegnyemb, Dieudonné Emmanuel; Mbing, Josephine Ngo; de Théodore Atchadé, Alex; Tih, Raphael Ghogomu; Sondengam, Beiban Lucas; Blond, Alain; Bodo, Bernard (July 2005). "Antimicrobial biflavonoids from the aerial parts of Ouratea sulcata". Phytochemistry. 66 (16): 1922–1926. doi:10.1016/j.phytochem.2005.06.017. 
  2. ^ Lin, Y. M.; Chen, F. C.; Lee, K. H. (April 1989). "Hinokiflavone, a cytotoxic principle from Rhus succedanea and the cytotoxicity of the related biflavonoids". Planta Med. 55 (2): 166–168. doi:10.1055/s-2006-961914. PMID 2526343. 
  3. ^ Suganya P., Rathi; Kalva, Sukesh; Saleena, Lilly M. (May 2011). "Hinokiflavone from Juniperus as therapeutic lead against osteoarthritis by inhibiting ADAMTS-5". International Journal of Bioscience, Biochemistry and Bioinformatics. 1 (1): 16–20. doi:10.7763/IJBBB.2011.V1.3. 
  4. ^ Krauze-Baranowska, M.; Pobłocka, L.; El-Hela, A. A. (September–October 2005). "Biflavones from Chamaecyparis obtusa". Z. Naturforsch. C. 60 (9-10): 679–685. PMID 16320608. 
  5. ^ Moawad, Abeer; Hetta, Mona; Zjawiony, Jordan K.; Jacob, Melissa R.; Hifnawy, Mohamed; Marais, Jannie P. J.; Ferreira, Daneel (2010). "Phytochemical investigation of Cycas circinalis and Cycas revoluta leaflets: Moderately active antibacterial biflavonoids". Planta Med. 76 (8): 796–802. doi:10.1055/s-0029-1240743. PMC 3711132Freely accessible. 
  6. ^ Chirumbolo S, Bjørklund G (March 2018). "Agathisflavone and GABAAreceptors in the biflavone-mediated action on rat primary cortical neurons". Neurotoxicology. doi:10.1016/j.neuro.2018.03.002. PMID 29530473. 
  7. ^ Dos Santos Souza C, Grangeiro MS, Lima Pereira EP, Dos Santos CC, da Silva AB, Sampaio GP, Ribeiro Figueiredo DD, David JM, David JP, da Silva VD, Butt AM, Lima Costa S (February 2018). "Agathisflavone, a flavonoid derived from Poincianella pyramidalis (Tul.), enhances neuronal population and protects against glutamate excitotoxicity". Neurotoxicology. 65: 85–97. doi:10.1016/j.neuro.2018.02.001. PMID 29425760. 
  8. ^ http://www.mdpi.net/molecules/papers/80800614.pdf