Schoepfiajasmins A-H: C-glycosyl dihydrochalcones, dihydrochalcone glycoside, C-glucosyl flavanones, flavanone glycoside and flavone glycoside from the branches of schoepfia jasminodora

Chemical and Pharmaceutical Bulletin

Volumn 61, Issue 11, 2013, Pages 1136-1142

  Ukida, Kouki ^a   Doi, Takashi ^a   Sugimoto, Sachiko ^a   Matsunami, Katsuyoshi ^a   Otsuka, Hideaki ^a,b   Takeda, Yoshio ^b  

^a HIROSHIMA UNIVERSITY   (Japan)

^b YASUDA WOMEN'S UNIVERSITY   (Japan)

Author keywords

Chalcone; Flavanone; Flavone; Olacaceae; Schoepfia jasminodora

Indexed keywords

C GLYCOSYL DIHYDROCHALCONE DERIVATIVE; DIHYDROCHALCONE GLYCOSIDE; FLAVANONE DERIVATIVE; FLAVANONE GLYCOSIDE; FLAVONE GLYCOSIDE; GLYCOSIDE; SCHOEPFIAJASMIN A; SCHOEPFIAJASMIN B; SCHOEPFIAJASMIN C; SCHOEPFIAJASMIN D; SCHOEPFIAJASMIN E; SCHOEPFIAJASMIN F; SCHOEPFIAJASMIN G; SCHOEPFIAJASMIN H; UNCLASSIFIED DRUG;

ARTICLE; DRUG ISOLATION; DRUG STRUCTURE; OLACACEAE; SCHOEPFIA JASMINODORA;

CHALCONES; FLAVANONES; GLYCOSIDES; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR CONFORMATION; OLACACEAE; PLANT STEMS;

EID: 84888862351     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.c13-00466     Document Type: Article

References (19)

1. Tsuboi Y., Doi T., Matsunami K., Otsuka H., Shinzato T., Takeda Y., J. Nat. Med., 65, 617-622 (2010).
2. Tang W., Hioki H., Harada K., Kubo M., Fukuyama Y., J. Nat. Prod., 71, 1760-1763 (2008).
3. Buskas T., Söderberg E., Konradsson P., Fraser-Reid B., J. Org. Chem., 65, 958-963 (2000).
4. Miyaichi Y., Tomimori T., Nat. Med., 49, 350-353 (1995).
5. Okamura N., Yagi A., Nishioka I., Chem. Pharm. Bull., 29, 3507-3514 (1981).
6. Ono M., Ito Y., Ishikawa T., Kitajima J., Tanaka Y., Niiho Y., Nohara T., Chem. Pharm. Bull., 44, 337-342 (1996).
7. Kanho H., Yaoya S., Kawahara N., Nakane T., Takase Y., Masuda K., Kuroyanagi M., Chem. Pharm. Bull., 53, 361-365 (2005).
8. Sakai S., Kawaguchi K., Kamakura H., Kawahara N., Goda Y., Jpn. J. Food Chem., 14, 56-62 (2007).
9. Yoshizawa F., Deyama T., Takizawa N., Usmanghani K., Ahmad M., Chem. Pharm. Bull., 38, 1927-1930 (1990).
10. Shahat A. A., Abdel-Azim N. S., Pieters L., Vlietinck A. J., Fitoterapia, 75, 771-773 (2004).
11. Huang C. F., Gan X. W., Bai H. Y., Ma L., Hu L. H., Nat. Prod. Res., 22, 623-627 (2008).
12. Ohashi H., Goto M., Imamura H., Phytochemistry, 16, 1106-1107 (1977).
13. Hammami S., Jannet H. B., Bergaoui A., Ciavatta L., Cimino G., Mighri Z., Molecule, 9, 602-608 (2004).
14. Ersöz T., Harput Ü. S., Saracoǧlu I., Çaliş I., Ogihara Y., Turk. J. Chem., 26, 581-588 (2002).
15. El Antri A., Messouri I., Tlemçani R. C., Bouktaib M., El Alami R., El Bali B., Lachkar M., Molecules, 9, 568-573 (2004).
16. Mustafa K. A., Kjaergaard H. G., Perry N. B., Weavers R. T., Tetrahedron, 59, 6113-6120 (2003).
17. Slade D., Ferreira D., Marais J. P. J., Phytochemistry, 66, 2177-2215 (2005).
18. Gaffield W., Tetrahedron, 26, 4093-4108 (1970).
19. Werner S. R., Chen H., Jiang H., Morgan J. A., Enzymatic, 66, 257-263 (2010). Technology Technology