First 2-hydroxy-3-methylbut-3-enyl substituted xanthones isolated from plants: Structure elucidation, synthesis and antifungal activity

Natural Product Research

Volumn 17, Issue 3, 2003, Pages 195-199

  Oger, Jean Michel ^a   Morel, Cécile ^a   Helesbeux, Jean Jacques ^a   Litaudon, Marc ^b   Séraphin, Denis ^a   Dartiguelongue, Caroline ^a   Larcher, Gérald ^c   Richomme, Pascal ^a   Duval, Olivier ^a  

^a UNIVERSITÉ D'ANGERS   (France)

^b INSTITUT DE CHIMIE DES SUBSTANCES NATURELLES   (France)

^c ANGERS UNIVERSITY HOSPITAL   (France)

Author keywords

Antifungal activity; Clusiaceae; Photooxygenation; Xanthone

Indexed keywords

1,3,5 TRIHYDROXYXANTHONE; AMPHOTERICIN B; CALEDOL; DICALEDOL; DICHLOROMETHANE; PLANT EXTRACT; PYRANOXANTHONE; UNCLASSIFIED DRUG; XANTHONE DERIVATIVE;

ANALYTIC METHOD; ANTIFUNGAL ACTIVITY; ARTICLE; ASPERGILLUS FUMIGATUS; BIOMIMETICS; CONTROLLED STUDY; DRUG ISOLATION; DRUG STRUCTURE; DRUG SYNTHESIS; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PHOTOOXIDATION; PRENYLATION;

ASPERGILLUS FUMIGATUS; CALOPHYLLUM; MAGNETIC RESONANCE SPECTROSCOPY; MICROBIAL SENSITIVITY TESTS; XANTHONES;

ASPERGILLUS; ASPERGILLUS FUMIGATUS; CALOPHYLLUM; CLUSIACEAE;

EID: 0038054569     PISSN: 14786419     EISSN: None     Source Type: Journal    
DOI: 10.1080/1057563021000040808     Document Type: Article

References (18)

1. (a) C. Morel, C. Dartiguelongue, T. Youhana, J.-M. Oger, D. Séraphin, O. Duval, P. Richomme and J. Bruneton (1999). Heterocycles, 51, 2183-2191.
2. (b) C. Morel, D. Guilet, J.-J. Oger, D. Séraphin, T. Sévenet, C. Wiart, A.H.A. Hadi, P. Richomme and J. Bruneton (1999). Phytochemistry, 50, 1243-1247.
3. D. Guilet, C. Morel, N. Noyer, M. Cornec, D. Séraphin, C. Wiart, A.H.A. Hadi, T. Sévenet, P. Richomme and J. Bruneton (1999). Heterocycles, 51, 67-76.
4. C. Morel, D. Séraphin, A. Teyrouz, G. Larcher, J.-P. Bouchara, M. Litaudon, P. Richomme and J. Bruneton (2001). Planta Med., 67, 1-4.
5. C. Morel, D. Séraphin, J.-M. Oger, M. Litaudon, T. Sévenet, P. Richomme and J. Bruneton (2000). J. Nat. Prod., 63, 1471-1474.
6. D. Guilet, D. Séraphin, D. Rondeau, P. Richomme and J. Bruneton (2001). Phytochemistry, 48, 571-575.
7. (a) A.G. Vlietinck, T. De Bruyne, S. Apers and L.A. Pieters (1998). Planta Med., 64, 97-109.
8. (b) G. Rath, O. Potterat, S. Mavi and K. Hostettman (1996). Phytochemistry, 43, 513-520.
9. (c) M. Iinuma, H. Tosa, T. Tanaka, F. Asai, Y. Kobayashi, R. Shimano and K.I. Miyauchi (1996). J. Pharm. Pharmacol., 48, 861-865.
10. (d) M.J. Gonzalez, M.S.J. Nascimmento, H.M. Cidade, M.M.M. Pinto, A. Kijjoa, C. Anantachoke, A.M.S. Silva and W. Herz (1999). Planta Med., 65, 368-371.
11. J.-J. Helesbeux, D. Guilet, D. Seraphin, O. Duval, P. Richomme and J. Bruneton (2000). Tetrahedron Lett., 41, 4559-4562.
12. (a) S.P. Gunasekera, G.S. Jayatilake, S.S. Selliah and M.U.S. Sultanbawa (1977). J. Chem. Soc. Perkin Trans. I, 1505-1511.
13. (b) T.R. Govindachari, P.S. Kalyanaraman, N. Muthukumaraswamy and B.R. Pai (1971). Tetrahedron, 27, 3919-3926.
14. V. Gujraj and S.R. Gupta (1979). Bull. Chem. Soc. Jap., 52, 3679-3681.
15. (a) A.J. Quillinan and F. Scheinmann (1973). J. Chem. Soc. Perkin Trans. I, 1329-1337.
16. (b) C.N. Lin, S.-S. Liou, F.-N. Ko and C.-M. Teng (1992). J. Pharm. Sci., 81, 1109-1113.
17. S.M. Anand and A.C. Jain (1972). Tetrahedron, 28, 987-990.
18. 80).