Rhodiolosides A - E, monoterpene glycosides from Rhodiola rosea

Chemical and Pharmaceutical Bulletin

Volumn 54, Issue 8, 2006, Pages 1229-1233

  Ma, Guizhi ^a   Li, Wei ^b   Dou, Deqiang ^c   Chang, Xiaolong ^b   Bai, Hong ^b   Satou, Tadaaki ^b   Li, Jun ^a   Sun, Dianjia ^a   Kang, Tingguo ^c   Nikaido, Tamotsu ^b   Koike, Kazuo ^b  

^a XINJIANG MEDICAL UNIVERSITY   (China)

^b TOHO UNIVERSITY   (Japan)

^c LIAONING UNIVERSITY OF TRADITIONAL CHINESE MEDICINE   (China)

Author keywords

Crassulaceae; Glycoside; Monoterpene; Rhodiola rosea; Rhodioloside

Indexed keywords

4 HYDROXY 3,7 DIMETHY 2,6 OCTADIENYL BETA DEXTRO GLUCOPYRANOSYL (1-3) BETA DEXTRO GLUCOPYRANOSIDE; 4,7 DIHYDROXY 3,7 DIMETHYL 2 OCTENYL BETA DEXTRO GLUCOPYRANOSIDE; 4,8 DIHYDROXY 3,7 DIMETHYL 2,6 OCTADIENYL BETA DEXTRO GLUCOPYRANOSIDE; 7 HYDROXY 3,7 DIMETHYL 2 OCTENYL ALPHA LEVO ARABINOPYRANOSYL (1-6) BETA DEXTRO GLUCOPYRANOSIDE; GLYCOSIDE; RHODIOLOSIDE A; RHODIOLOSIDE B; RHODIOLOSIDE C; RHODIOLOSIDE D; RHODIOLOSIDE E; TERPENE; UNCLASSIFIED DRUG;

ARTICLE; CRASSULACEAE; DRUG ISOLATION; DRUG STRUCTURE; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PLANT ROOT; RHODIOLA;

CARBOHYDRATE SEQUENCE; CELL LINE, TUMOR; CELL PROLIFERATION; DRUG SCREENING ASSAYS, ANTITUMOR; GLUCOSIDES; GLYCOSIDES; HUMANS; MOLECULAR SEQUENCE DATA; MOLECULAR STRUCTURE; MONOTERPENES; PHENOLS; PLANT ROOTS; RHODIOLA;

EID: 33746696652     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.54.1229     Document Type: Article

References (17)

1. Richard P. B., Patricia L. G., Zakir P., Herbal Gram, 56, 40-52 (2002).
2. Khanum F., Bawa A. S., Singh B., Comprehensive Reviews in Food Science and Food Safety, 4, 55-62 (2005).
3. Ganzera M., Yayla Y., Khan I. A., Chem. Pharm. Bull., 49, 465-467 (2001).
4. Rohloff J., Phytochemistry, 59, 655-661 (2002).
5. Akgul Y., Ferreira D., Abourashed E. A., Khan I. A., Fitoterapia, 75, 612-614 (2004).
6. Yoshikawa M., Shimada H., Horikawa S., Murakami T., Shimoda H., Yamahara J., Matsuda H., Chem. Pharm. Bull., 45, 1498-1503 (1997).
7. Fan W., Tezuka Y., Ni M. K., Kodota S., Chem. Pharm. Bull., 49, 396-401 (2001).
8. Kurkin V. A., Zapesochnaya G. G., Shchavlinskii A. N., Khimiya Prirodnykh Soedinenii, 5, 632-636 (1985)
9. [Chem. Abstr., 104, 165302].
10. Bai H., Li W., Koike K., Satou T., Chen Y., Nikaido T., Tetrahedron, 61, 5797-5811 (2005).
11. Wei K., Li W., Koike K., Chen Y., Nikaido T., J. Org. Chem., 70, 1164-1176 (2005).
12. Koike K., Li W., Liu L., Hata E., Nikaido T., Chem. Pharm. Bull., 53, 225-228 (2005).
13. Fu H., Koike K., Li W., Nikaido T., Lin W., Guo D., J. Nat. Prod., 68, 754-758 (2005).
14. Hara S., Okabe H., Mihashi K., Chem. Pharm. Bull., 35, 501-506 (1987).
15. Ohtani I., Kusumi T., Kashman Y., Kakisawa H., J. Am. Chem. Soc., 113, 4092-4096 (1991).
16. Hong B. C., Hong J. H., Tsai Y. C., Angew. Chem. Int. Ed., 37, 458-470 (1998).
17. Liu L., Sato T., Koike K., Li W., Nikaido T., Natural Medicines, 58, 226-229 (2004).