Triterpenoid saponins from the seeds of Celosia argentea and their anti-inflammatory and antitumor activities

Chemical and Pharmaceutical Bulletin

Volumn 59, Issue 5, 2011, Pages 666-671

  Wu, Qingbin ^a   Wang, Yan ^a   Guo, Meili ^a  

^a SECOND MILITARY MEDICAL UNIVERSITY   (China)

Author keywords

Amaranthaceae; Anti inflammatory; Antitumor; Celosia argentea; Triterpenoid saponin

Indexed keywords

ANTIINFLAMMATORY AGENT; ANTINEOPLASTIC AGENT; CELOSIN E; CELOSIN F; CELOSIN G; CRISTATAIN; SAPONIN DERIVATIVE; TRITERPENOID; UNCLASSIFIED DRUG;

ANTIINFLAMMATORY ACTIVITY; ANTINEOPLASTIC ACTIVITY; ARTICLE; CELOSIA; CELOSIA ARGENTEA; DRUG STRUCTURE; HUMAN; HUMAN CELL; IN VITRO STUDY; MASS SPECTROMETRY; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; PLANT SEED;

ANTI-INFLAMMATORY AGENTS; ANTINEOPLASTIC AGENTS, PHYTOGENIC; CELL LINE, TUMOR; CELOSIA; HUMANS; INHIBITORY CONCENTRATION 50; MAGNETIC RESONANCE SPECTROSCOPY; MASS SPECTROMETRY; SAPONINS; SEEDS; TRITERPENES;

EID: 79955616338     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.59.666     Document Type: Article

References (17)

1. Chinese Academy of Sciences in China Plant Volunteer Editors Committee, "Flora Reipublicae Popularis Sinicae," 1st ed., Vol. 25, Science Press, Beijing, 1979, p. 200.
2. Institute of Materia Medica Chinese Academy of Medical Sciences, "Chi Traditional Chinese Medicine," 2nd ed., Vol. 3, People's Health Publishing House, Beijing, 1984, p. 441.
3. Hase K., Kadota S., Basnet P., Planta Med., 63, 216-219 (1997).
4. Xue Q., Guo M. L., Zhang G., Pharm. Care Res., 6, 345-347 (2006).
5. Xue Q., Guo M. L., Sun Z. L., Wang Y., Zhang G., Wang X. K., Nat. Prod. Res., 2009, doi:10.1080/14786410902833948
6. Sun Z. L., Wang Y., Li Y. X., Guo M. L., Fitoterapia, 81, 375-380 (2010).
7. C2hi X., Guo M. L., Song H., Chen Y. D., J. Jilin Agric. Univ., 32, 657-660 (2010).
8. Wang Y., Lou Z. Y., Wu Q. B., Guo M. L., Fitoterapia, 81, 1246-1252 (2010).
9. Wanas A. S., Matsunami K., Otsuka H., Desoukey S. Y., Fouad M. A., Kamel M. S., Chem. Pharm. Bull., 58, 1596-1601 (2010).
10. Reynolds W. F., McLean S., Poplawski J., Enriquez R. G., Escobar L. I., Leon I., Tetrahedron, 42, 3419-3428 (1986).
11. Inoue M., Ohtani K., Kasai R., Okukubo M., Andriantsiferana M., Yamasaki K., Koike T., Phytochemistry, 70, 1195-1202 (2009).
12. Luo J. G., Ma L., Kong L. Y., Bioor. Med. Chem., 16, 2912-2920 (2008).
13. Kuo P. C., Schroeder R. A., Ann. Surg., 221, 220-226 (1995).
14. Pacher P., Joseph S., Beckman J. S., Liaudet L., Physiol. Rev., 87, 315-424 (2007).
15. Chen Q., Luo J. G., Kong L. Y., Chem. Pharm. Bull., 58 412-414 (2010).
16. Liu Y. J., Zeng C. H., Liang Z. H., Yao J. H., Huang H. L., Li Z. Z., Wu F. H., Eur. J. Med. Chem., 45, 3087-3095 (2010).
17. Zheng C. J., Huang B. K., Han T., Zhang Q. Y., Zhang H., Rahman K., Qin L. P., J. Nat. Prod., 72, 1627-1630 (2009).