An anti-herpes simplex virus-type 1 agent from Xylaria mellisii (BCC 1005)

Tetrahedron Letters

Volumn 46, Issue 8, 2005, Pages 1341-1344

  Pittayakhajonwut, Pattama ^a   Suvannakad, Rapheephat ^a   Thienhirun, Surang ^b   Prabpai, Samran ^c   Kongsaeree, Palangpon ^c   Tanticharoen, Morakot ^a  

^a NATIONAL SCIENCE AND TECHNOLOGY DEVELOPMENT AGENCY   (Thailand)

^b ROYAL FOREST DEPARTMENT   (Thailand)

^c MAHIDOL UNIVERSITY   (Thailand)

Author keywords

1,8 Dihydroxynaphthol 1 O glucopyranoside; Anti HSV 1; Mellisol; Xylaria mellisii

Indexed keywords

1,8 DIHYDROXYNAPHTHOL 1 O ALPHA GLUCOPYRANOSIDE; ANTIVIRUS AGENT; MELLISOL; UNCLASSIFIED DRUG;

ANIMAL CELL; ANTIVIRAL ACTIVITY; ARTICLE; CONCENTRATION RESPONSE; CYTOTOXICITY; DRUG ISOLATION; DRUG STRUCTURE; FUNGUS; HERPES SIMPLEX VIRUS 1; NONHUMAN; VERO CELL; X RAY CRYSTALLOGRAPHY;

FUNGI; HUMAN HERPESVIRUS 1; SIMPLEXVIRUS; XYLARIA;

EID: 13244268386     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.12.110     Document Type: Article

References (20)

1. G. Schneider, H. Anke, and O. Sterner Nat. Prod. Lett. 7 1995 309 316
2. G. Schneider, H. Anke, and O. Sterner Z. Naturforsch. 51c 1996 802 806
3. S. Boonphong, P. Kittakoop, D. Pittayakhajonwut, M. Tatichareon, and Y. Thebtaranonth J. Nat. Prod. 64 2001 965 967
4. Y. Lin, X. Wu, S. Feng, G. Jiang, J. Luo, S. Zhou, L.L.P. Vrijmoed, E.B.G. Jones, K. Krohn, K. Steingrover, and F. Zsila J. Org. Chem. 66 2001 6252 6256
5. R.L. Edwards, D.J. Maitland, and A.J.S. Whalley J. Chem. Soc., Perkin Trans. 1 1991 1411 1417
6. E. Dagne, A.A.L. Gunatilaka, S. Asmellash, D. Abate, D.G.I. Kingston, G.A. Hofmann, and R.K. Johnson Tetrahedron 50 1994 5615 5620
7. R.L. Edwards, D.J. Maitland, P. Pittayakhajonwut, and A.J.S. Whalley J. Chem. Soc., Perkin Trans. 1 2001 1296 1299
8. M. Isaka, A. Jaturapat, W. Kladwang, J. Punya, Y. Lertwerawat, M. Tanticharoen, and Y. Thebtaranonth Planta Med. 66 2000 473 475
9. M. Chinworrungsee, P. Kittakoop, M. Isaka, A. Rungrod, M. Tanticharoen, and Y. Thebtaranonth Bioorg. Med. Chem. Lett. 11 2001 1965 1970
10. J.R. Anderson, R.L. Edwards, and A.J.S. Whalley J. Chem. Soc., Perkin Trans. 1 1983 2185 2192
11. N. Claydon, J.F. Grove, and M. Pople Phytochemistry 24 1985 937 943
12. T. Okuno, S. Oikawa, T. Goto, K. Sawai, H. Shirahama, and T. Matsumoto Agric. Biol. Chem. 50 1986 997 1001
13. E. Merifield, and E.J. Thomas J. Chem. Soc., Perkin Trans. 1 1999 3269 3283
14. 3 colourless crystal. Atomic coordinates, bond lengths, bond angles and thermal parameters have been deposited with the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, England (CCDC 251036)
15. 7Na (M+Na): 347.1107; found 347.1114
16. 7 (M-H): 321.0983; found 321.0984
17. D.W. Cameron, and J.C.A. Craik J. Chem. Soc. (C) 1968 3068 3072
18. A.N. Starratt, L.M. Ross, and G. Lazarovits Can. J. Microbiol. 48 2002 320 325
19. M. Abou-Karam, and W.T. Shier J. Nat. Prod. 53 1990 340 344
20. P. Skehan, R. Storeng, D. Scudiero, A. Monks, J. McMahon, D. Vistica, J.T. Warren, H. Bokesch, S. Kenney, and M.R. Boyd J. Natl. Cancer Inst. 82 1990 1107 1112