Two new pregnane glycosides from Dioscorea futschauensis R. Kunth

Chemical and Pharmaceutical Bulletin

Volumn 51, Issue 9, 2003, Pages 1089-1091

  Liu, Hongwei ^a   Xiong, Zhili ^a   Li, Famei ^a   Qu, Gexia ^a   Kobayashi, Hisayoshi ^b   Yao, Xinsheng ^a  

^a SHENYANG PHARMACEUTICAL UNIVERSITY   (China)

^b UNIVERSITY OF TOKYO   (Japan)

Author keywords

Anti fungal activity; Dioscorea futschauensis; Osteoblastic proliferation stimulatory activity; Pregnane glycoside; UMR106 cell line

Indexed keywords

16ALPHA METHOXY 3BETA [[O ALPHA LEVO RHAMNOPYRANOSYL (1-2) O (ALPHA LEVO RHAMNOPYRANOSYL (1-4)) BETA DEXTRO GLUCOPYRANOSYL]OXY]PREGN 5 EN 20 ONE; 21 METHOXY 3BETA [[O ALPHA LEVO RHAMNOPYRANOSYL (1-2) O (ALPHA LEVO RHAMNOPYRANOSYL (1-4)) BETA DEXTRO GLUCOPYRANOSYL]OXY]PREGN 5,16 EN 20 ONE; DIOSCIN; GLYCOSIDE; GRACILLIN; METHYLPROTOGRACILLIN; PROSAPOGENIN A; PROSAPOGENIN B; PROTODIOSCIN; PSEUDOPROTODIOSCIN; PSEUDOPROTOGRACILLIN; SAPONIN DERIVATIVE; UNCLASSIFIED DRUG; FUNGICIDE; PREGNANE DERIVATIVE;

ANIMAL CELL; ARTICLE; CELL LINE; CELL PROLIFERATION; DRUG ACTIVITY; DRUG ISOLATION; FUNGUS; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OSTEOBLAST; RAT; YAM; ASCOMYCETES; CELL DIVISION; CHEMISTRY; DRUG EFFECT; FAST ATOM BOMBARDMENT MASS SPECTROMETRY; HUMAN; INFRARED SPECTROPHOTOMETRY; ISOLATION AND PURIFICATION; MASS FRAGMENTOGRAPHY; MICROBIOLOGICAL EXAMINATION; PLANT ROOT;

ASCOMYCOTA; CELL DIVISION; CELL LINE; DIOSCOREA; FUNGICIDES, INDUSTRIAL; GAS CHROMATOGRAPHY-MASS SPECTROMETRY; GLYCOSIDES; HUMANS; MAGNETIC RESONANCE SPECTROSCOPY; MICROBIAL SENSITIVITY TESTS; OSTEOBLASTS; PLANT ROOTS; PREGNANES; SPECTROMETRY, MASS, FAST ATOM BOMBARDMENT; SPECTROPHOTOMETRY, INFRARED;

EID: 2142857792     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.51.1089     Document Type: Article

References (15)

1. Shen P., Wang S. L., Liu X. K., Yang C. R., Cai B., Yao X. S., J. Asian Nat. Prod. Res., 4, 211-215 (2002).
2. Hu K., Dong A. J., Yao X. S., Kobayashi H., Iwasaki S., Planta Med., 62, 573-575 (1996).
3. Hu K., Dong A. J., Yao X. S., Kobayashi H., Iwasaki S., Planta Med., 63, 161-165 (1997).
4. Hu K., Dong A. J., Yao X. S., Kobayashi H., Iwasaki S., Phytochemistry, 44, 1339-1342 (1997).
5. Hu K., Dong A. J., Kobayashi H., Jing Y. K., Iwasaki S., Yao X. S., J. Nat. Prod., 62, 299-301 (1999).
6. Hu K., Yao X. S., Anticancer Drugs, 12, 541-547 (2001).
7. Hu K., Yao X. S., Anticancer Res., 22, 1001-1005 (2002).
8. Liu H. W., Kobayashi H., Qu G. X., Yao X. S., Chin. Chem. Lett., 12, 613-616 (2001).
9. Liu H. W., Kobayashi H., Qu G. X., Yao X. S., Chin. Chem. Lett., 13, 241-244 (2002).
10. Liu H. W., Wang S. L., Cai B., Qu G. X., Yang X. J., Kobayashi H., Yao X. S., J. Asian Nat. Prod. Res., (2003), in press.
11. Dong M., Feng X. Z., Wu L. J., Wang B. X., Ikejima T., Planta Med., 67, 853-857 (2001).
12. Agrawal P. K., Phytochemistry, 31, 3307-3330 (1992).
13. Terada S., Hayashi K., Mitsuhoshi H., Tetrahedron Lett., 23, 1995-1998 (1978).
14. Hu K., Dong A. J., Liu H. W., Feng H. S., Yao X. S., Pharm. Bio., 37, 225-330 (1999).
15. Wang D. W., Li F. M., Jiang Z. H., Planta Med., 67, 748-749 (2002).