Xanthones from stems of Hypericum chinense

Chemical and Pharmaceutical Bulletin

Volumn 55, Issue 1, 2007, Pages 19-21

  Tanaka, Naonobu ^a   Takaishi, Yoshihisa ^a  

^a UNIVERSITY OF TOKUSHIMA   (Japan)

Author keywords

Clusiaceae; Hypericum chinense; Xanthone

Indexed keywords

1,5 DIHYDROXY 3 DIMETHOXYXANTHONE; 1,5,6 TRIHYDROXY 3 DIMETHOXYXANTHONE; 2,6 DIHYDROXY 3,4 DIMETHOXYXANTHONE; 3 HYDROXY 2 METHOXYXANTHONE; 3,4 DIHYDROXY 2 METHOXYXANTHONE; 3,6 DIHYDROXY 1,2 DIMETHOXYXANTHONE; 3,7 DIHYDROXY 2,4 DIMETHOXYXANTHONE; 4,6 DIHYDROXY 2,3 DIMETHOXYXANTHONE; 4,7 DIHYDROXY 2,3 DIMETHOXYXANTHONE; 6 HYDROXY 2,3,4 TRIMETHOXYXANTHONE; HYPERICUM EXTRACT; UNCLASSIFIED DRUG; XANTHONE DERIVATIVE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CONTROLLED STUDY; DRUG IDENTIFICATION; DRUG ISOLATION; DRUG STRUCTURE; HYPERICUM; NONHUMAN; PLANT STEM; PROTON NUCLEAR MAGNETIC RESONANCE; SPECTROSCOPY;

CHROMATOGRAPHY, HIGH PRESSURE LIQUID; HYPERICUM; MAGNETIC RESONANCE SPECTROSCOPY; PLANT STEMS; SPECTROPHOTOMETRY, INFRARED; XANTHONES;

EID: 33846061329     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.55.19     Document Type: Article

References (18)

1. Sultanbawa M. U. S., Tetrahedron, 36, 1465-1506 (1980).
2. Bennett G. J., Lee H.-K., Phytochemistry, 28, 967-998 (1989).
3. Rukachaisirikul V., Kamkaew M., Sukavisit D., Phongpaichit S., Sawangchote P., Taylor W., J. Nat. Prod., 66, 1531-1535 (2003).
4. Rukachaisirikul V., Tadpetch K., Watthanaphanit A., Saengsanae N., Phongpaichit S., J. Nat. Prod., 68, 1218-1221 (2005).
5. Sukpondma Y., Rukachaisirikul V., Phongpaichit S., J. Nat. Prod., 68, 1010-1017 (2005).
6. Sakagami Y., Iinuma M., Piyasena K. G. N. P., Dharmaratne H. R. W., Phytomedicine, 12, 203-208 (2005).
7. Ignatushchenko M. V., Winter R. W., Riscoe M., Am. J. Trop. Med. Hygiene, 62, 77-81 (2000).
8. Ito C., Itoigawa M., Takakura T., Ruangrungsi N., Enjo F., Tokuda H., Nishino H., Furukawa H., J. Nat. Prod., 66, 200-205 (2003).
9. Zou J., Jin D., Chen W., Wang J., Liu Q., Zhu X., Zhao W., J. Nat. Prod., 68, 1514-1518 (2005).
10. Oku H., Ueda Y., Iinuma M., Ishiguro K., Planta Med., 71, 90-92 (2005).
11. Tanaka N., Okasaka M., Ishimaru Y., Takaishi Y., Sato M., Okamoto M., Oshikawa T., Ahmed S. U., Consentino L. M., Lee K.-H., Organic Lett., 7, 2997-2999 (2005).
12. Nagai M., Tada M., Chemistry Lett., 16, 1337-1340 (1987).
13. Tada M., Nagai M., Chemistry Lett., 18, 683-686 (1989).
14. Aramaki Y., Chiba K., Tada M., Phytochemistry, 38, 1419-1421 (1995).
15. Habib A. M., Reddy K. S., Mccloud T. G., Chang C.-J., Cassady J. M., J. Nat. Prod., 50, 141-145 (1987).
16. Wolfender J.-L., Hamburger M., Msonthi J. D., Hostettmann K., Phytochemistry, 30, 3625-3629 (1991).
17. Gottlieb O. R., Taveira Magalhães M., Camey M., Lins Mesquita A. A., de Barros Corrêa D., Tetrahedron, 22, 1777-1784 (1966).
18. Terreaux C., Maillard M., Gupta M. P., Hostettmann K., Phytochemistry, 40, 1791-1795 (1995).