3-Hydroxymethylglutaryl flavonol glycosides from a mongolian and tibetan medicine, Oxytropis racemosa

Chemical and Pharmaceutical Bulletin

Volumn 58, Issue 12, 2010, Pages 1587-1590

  Song, Shuang ^b   Zheng, Xiuping ^c   Liu, Weidong ^c   Du, Ruifang ^c   Bi, Lifu ^a   Zhang, Peicheng ^b  

^a INNER MONGOLIA MEDICAL COLLEGE   (China)

^b INSTITUTE OF MATERIA MEDICA   (China)

^c Inner Mongolia Yongye Biotechnology Co Ltd   (China)

Author keywords

3 hydroxy 3 methylglutaroyl; Cytotoxic activity; Fabaceae; Flavonol glycoside; Oxytropis racemosa

Indexed keywords

3 (4,5 DIMETHYL 2 THIAZOLYL) 2,5 DIPHENYLTETRAZOLIUM BROMIDE; 3 HYDROXYMETHYLGLUTARYLFLAVONOL GLYCOSIDE DERIVATIVE; DIMETHYL SULFOXIDE; FLAVONOID GLYCOSIDE; ISORHAMNETIN 3 O [3 HYDROXY 3 METHYLGLUTAROYL(1-6)] LEVO RHAMNOPYRANOSYL(1-2) BETA DEXTRO GLUCOPYRANOSIDE; PLANT EXTRACT; RHAMNETIN 3 O [3 HYDROXY 3 METHYL GLUTAROYL(1-6)] BETA DEXTRO GLUCOPYRANOSIDE; RHAMNOCITRIN 3 O [3 HYDROXY 3 METHYL GLUTAROYL(1-6)] BETA DEXTRO GLUCOPYRANOSIDE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CYTOTOXICITY; DRUG ISOLATION; DRUG STRUCTURE; HUMAN; HUMAN CELL; OXYTROPIS; OXYTROPIS RACEMOSA; PROTON NUCLEAR MAGNETIC RESONANCE;

CELL LINE, TUMOR; FLAVONOLS; GLYCOSIDES; HUMANS; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR CONFORMATION; MONGOLIA; OXYTROPIS; PLANTS, MEDICINAL; TIBET;

EID: 78649867110     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.58.1587     Document Type: Article

References (21)

1. Li Y. L., Liao Z. X., Du Y. Z., Suo Y. R., Nat. Prod. Res. Dev., 14, 75-79 (2002).
2. Liu B., Chin. Wild Plant Resour., 16, 15-18 (1997).
3. Lu P., Zhao M. L., Han G. D., Cao Z., Chen X., Wang Z. N., J. Inner Mongolia Univ., 38, 160-165 (2007).
4. Ma Y. Q., "Flora Intramongolica," 2nd ed., Vol. 3, Inner Mongolia People's Press, Huhhot, 1989, pp. 309-310.
5. Bergot B. J., Baker F. C., Lee E., Schooley D. A., J. Am. Chem. Soc., 101, 7432-7434 (1979).
6. Hattori Y., Horikawa K., Makabe H., Hirai N., Hirota M., Kamo T., Tetrahedron: Asymmetr., 18, 1183-1186 (2007).
7. Liu J., Yu Z. B., Ye Y. H., Zhou Y. W., Nat. Prod. Res. Dev., 19, 398-399 (2007).
8. Xie B. B., Xu F. Q., Li L. B., Chen C. X., Acta Bot. Yunnan, 27, 232-234 (2005).
9. Berardini N., Fezer R., Conrad J., Beifuss U., Carle R., Schieber A., J. Agric. Food Chem., 53, 1563-1570 (2005).
10. Ma Y. L., Tian Z. K., Yuan C. S., Meng R., J. Shenyang Coll. Pharm., 8, 121-123 (1991).
11. Zuo L., Li J. B., Xu J., Yang J. Z., Zhang D. M., Tong Y. L., China J. Chin. Mat. Med., 32, 688-691 (2007).
12. Markham R. K., Ternal B., Mabry J. T., Tetrahedron, 34, 1389-1397 (1973).
13. Wang Y., Zhang Y. J., Gao W. Y., Yan, L. L., China J. Chin. Mat. Med., 32, 1425-1428 (2007).
14. Watanabe K., Kinjo J., Nohara T., Chem. Pharm. Bull., 41, 394-396 (1993).
15. Irena M., Maria S., Acta Pol. Pharm., 56, 69-71 (1999).
16. Park J. C., Lee J. H., Choi J. S., Phytochemistry, 39, 261-262 (1995).
17. Tang Y. P., Wang Y., Lou F. C., Li Y. F., Wang J. H., Acta Pharm. Sin., 35, 363-366 (2000).
18. Victoire C., Berrurier M. H., Guth A. L., Balz J. P., Anton R., Planta Med., 54, 245-247 (1988).
19. Chaurasia N., Wichtl M., Planta Med., 53, 432-434 (1987).
20. Mosumann T., J. Immunol. Methods, 65, 55-63 (1983).
21. Carmichael J., DeGraff W. G., Gazdar A. F., Minna J. D., Mitchell J. B., Cancer Res., 47, 936-942 (1987).