New polyacetylene glucosides from the florets of Carthamus tinctorius and their weak anti-inflammatory activities

Carbohydrate Research

Volumn 346, Issue 13, 2011, Pages 1903-1908

  He, Jun ^a   Shen, Yi ^a   Jiang, Jian Shuang ^a   Yang, Ya Nan ^a   Feng, Zi Ming ^a   Zhang, Pei Cheng ^a   Yuan, Shao Peng ^a   Hou, Qi ^a  

^a INSTITUTE OF MATERIA MEDICA   (China)

Author keywords

Anti inflammatory activity; Carthamus tinctorius; Polyacetylene glucosides; Structure elucidation

Indexed keywords

DICHROISM; RHODIUM COMPOUNDS; SPECTROSCOPIC ANALYSIS;

ABSOLUTE CONFIGURATION; ANTI-INFLAMMATORY ACTIVITY; CARTHAMUS TINCTORIUS; CHEMICAL EVIDENCES; INDUCED CIRCULAR DICHROISM; INHIBITORY ACTIVITY; SPECTROSCOPIC METHOD; STRUCTURE ELUCIDATION;

CARBOHYDRATES;

CARBOHYDRATE DERIVATIVE; DEXAMETHASONE; LIPOPOLYSACCHARIDE; NITRIC OXIDE; POLYACETYLENE GLUCOSIDE; TRIFLUOROACETIC ACID; UNCLASSIFIED DRUG;

ANIMAL CELL; ANTIINFLAMMATORY ACTIVITY; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CIRCULAR DICHROISM; CONCENTRATION RESPONSE; CONTROLLED STUDY; DRUG ISOLATION; FLORET; MACROPHAGE; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; SAFFLOWER; STRUCTURE ACTIVITY RELATION;

CARTHAMUS TINCTORIUS; MURINAE;

EID: 80053567153     PISSN: 00086215     EISSN: 1873426X     Source Type: Journal    
DOI: 10.1016/j.carres.2011.06.015     Document Type: Article

References (17)

1. Zheng, H. Z.; Dong, Z. H.; She, J. In Modern Study of Traditional Chinese Medicine; Xue Yuan Press: Beijing, 1998; Vol. 3, p2057.
2. Kazuma, K.; Takahashi, T.; Sato, K.; Takeuchi, H.; Matsumoto, T.; Okuno, T. Biosci. Biotech. Bioch. 2000, 64, 1588-1599
3. Jiang, J. S.; Lü, L.; Yang, Y. J.; Zhang, J. L.; Zhang, P. C. J. Asian Nat. Prod. Res. 2008, 10, 447-451
4. Nagatsu, A.; Zhang, H. L.; Watanabe, T.; Taniguchi, N.; Hatano, K.; Mizukami, H.; Sakakibara, J. Chem. Pharm. Bull. 1998, 46, 1044-1047
5. Jiang, J. S.; He, J.; Feng, Z. M.; Zhang, P. C. Org. Lett. 2010, 12, 1196-1199
6. Zhou, Y. Z.; Ma, H. Y.; Chen, H.; Qiao, L.; Yao, Y.; Cao, J. Q.; Pei, Y. H. Chem. Pharm. Bull. 2006, 54, 1455-1456
7. Wang, N. L.; Yao, X. S.; Ishii, R.; Kitanaka, S. Chem. Pharm. Bull. 2001, 49, 938-942.
8. Li, S.; Kuang, H. X.; Okada, Y.; Okuyama, T. Chem. Pharm. Bull. 2004, 52, 439-440.
9. Jente, R.; Bohlmann, F.; Schoneweiss, S. Phytochemistry 1979, 18, 829-837
10. Gerards, M.; Snatzke, G. Tetrahedron: Asymmetry 1990, 1, 221-236
11. Frelek, J.; Szczepek, W. J. Tetrahedron: Asymmetry 1999, 10, 1507-1520
12. Frelek, J.; Jagodzinski, J.; Figge, H. M.; Sheldrick, W. S.; Wieteska, E.; Szczepek, W. J. Chirality 2001, 13, 313-321
13. Wang, C. Z.; Yu, D. Q. Phytochemistry 1998, 48, 711-717
14. Calixto, J. B.; Otuki, M. F.; Santos, A. R. S. Planta Med. 2003, 69, 973-983
15. Li, S. M.; Long, C. L.; Liu, F. Y.; Lee, S. W.; Guo, Q.; Li, R.; Liu, Y. H. J. Ethnophamacol. 2006, 108, 59-67
16. Xia, P. F.; Feng, Z. M.; Yang, Y. Y.; Zhang, P. C. J. Asian Nat. Prod. Res. 2009, 11, 766-771
17. Li, J.; Zhao, F.; Li, M. Z.; Chen, L. X.; Qiu, F. J. Nat. Prod. 2010, 73, 1667-1671.