Flavonoïdes prénylés et perméabilité membranaire

Acta Botanica Gallica

Volumn 143, Issue 6, 1996, Pages 509-520

  Barron, Denis ^a   Balland, Christine ^b   Possety, Françoise ^b   Ravanel, Patrick ^c   Desfougères, Aline ^c  

^a UNIVERSITÉ LYON 1   (France)

^b Laboratoire de Physiologie Cellulaire Vegetale Grenoble   (France)

^c UFR de Pharmacie   (France)

Author keywords

Biological membranes; Mitochondria; Natural distribution; Prenyl flavonoids; Synthesis

Indexed keywords

EID: 0040752338     PISSN: 12538078     EISSN: None     Source Type: Journal    
DOI: 10.1080/12538078.1996.10515348     Document Type: Article

References (17)

1. Barron, D., and Mariotte, A. M., 1994. Syntheses of 8-C-(1,1—dimethylallyl) flavones and 3-methyl flavonols. Nat. Prod. Lett., 4:21–28.
2. Barron, D., and Ibrahim, R. K., 1996. Isoprenylated flavonoids, a survey. Phytochemistry, 43:921–982.
3. Barron, D., Jolivet, S., Crouzet, J. M., and Mariotte, A. M., 1992. Synthesis of 6-C-(3,3-dimethyl-2-propen-1-yl) norwogonin. Tetrahedron Lett., 33:7137–7140.
4. 13C Nuclear magnetic resonance analysis of two prenyl flavonols from Platan us acerifolia buds
5. Creuzet, S., Ravanel, P., Tissut, M., and Kaouadji, M., 1988. Uncoupling properties of three flavonols from plane-tree buds. Phytochemistry, 27:3093–3099.
6. Fomum, Z. T., Ayafor, J. F., Mbafor, J. T., and Mbi, C. M., 1986. “ Erythrina studies. Part 2. Structures of three novel prenylated antibacterial flavanones, sigmoidins A-C, from Erythrina sigmoldea Hua. ”. In J. Chem. Soc. Perkin Trans. I 33–37.
7. Fukui, H., Goto, K., and Tabata, M., 1988. Two antimicrobial flavanones from the leaves of. Glycyrrhiza glabra. Chem. Pharm. Bull., 36:4174–4176.
8. Lincoln, D. E., 1980. Leaf resin flavonoids of. Diplacus aurantiacus. Biochem. Syst. Ecol., 8:397–400.
9. Lincoln, D. E., and Walla, M. D., 1986. Flavonoids from Diplacus aurantiacus leaf resin. Biochem. Syst. Ecol., 14:195–198.
10. Maillard, M., Hamburger, M., Gupta, M. P., and Hostettmann, K., 1989. An antifungal isoflavanone and a structure revision of a flavanone from. Erythrina berteroana. Planta Med., 55:281–282.
11. Noungoué-Tchamo, D., Barron, D., and Mariotte, A. M., 1995. Synthesis of 5′-(3,3-dimethylallyl)-4′methoxyethoxymethyl resacetophenone and improved preparation of broussochalcones A and B. Nat. Prod. Lett., 7:73–80.
12. Raguenet, H., Barron, D., and Mariotte, A. M., 1996. Total synthesis of 8-(1,1-dimethylallyl)-apigenin. Heterocycles, 43:277–285.
13. Ravanel, P., Tissut, M., and Douce, R., 1986. Platanetin:a potent natural uncoupler and inhibitor of the exogenous NADH deshydrogenase in intact plant mitochondria. Plant Physiol., 80:500–504.
14. Ravanel, P., Creuzet, S., and Tissut, M., 1990. Inhibitory effect of hydroxyflavones on the exogenous NADH deshydrogenase of plant mitochondrial inner membranes. Phytochemistry, 29:441–445.
15. Roussis, V., Ampofo, S. A., and Wiemer, D. F., 1987. Flavanones from. Lonchocarpus minimiflorus. Phytochemistry, 26:2371–2375.
16. Tahara, S., Ingham, J. L., Nakahara, S., Mizutani, J., and Harborne, J. B., 1984. Fungitoxic dihydrofuranoisoflavones and related compounds in white lupin. Lupinus albus. Phytochemistry, 23:1889–1900.
17. Tahara, S., Katagiri, Y., Ingham, J. L., and Mizutani, J., 1994. Prenylated flavonoids in the roots of yellow lupin. Phytochemistry, 36:1261 1271