Biflavonoids from Daphne feddei and their inhibitory activities against nitric oxide production

Chemical and Pharmaceutical Bulletin

Volumn 56, Issue 12, 2008, Pages 1729-1731

  Liang, Shuang ^a   Tang, Jian ^a   Shen, Yun Heng ^b   Jin, Hui Zi ^a   Tian, Jun Mian ^b   Wu, Zhi Jun ^b   Zhang, Wei Dong ^a,b   Yan, Shi Kai ^a  

^a SHANGHAI JIAO TONG UNIVERSITY   (China)

^b SECOND MILITARY MEDICAL UNIVERSITY   (China)

Author keywords

Biflavonoid; Daphne feddei; Nitric oxide; RAW 264.7 macrophages

Indexed keywords

2'' METHOXY 2 EPIDAPHNODORIN C; 2'' METHOXYDAPHNODORIN C; BIFLAVONOID; DAPHNODORIN A; DAPHNODORIN B; DAPHNODORIN C; DAPHNODORIN I; DAPHNODORIN J; DAPHNODORIN M; DAPHNODORIN N; DIHYDRODAPHNODORIN B; GENKWANOL B; GENKWANOL C; ISONEOCHAMAEJASMIN A; NEOCHAMAEJASMIN B; NITRIC OXIDE; PLANT EXTRACT; UNCLASSIFIED DRUG; WIKSTROL A; WIKSTROL B;

ANIMAL CELL; ANTIINFLAMMATORY ACTIVITY; ARTICLE; BARK; BIOSYNTHESIS; CONCENTRATION RESPONSE; CONTROLLED STUDY; DAPHNE; DAPHNE FEDDEI; DRUG ISOLATION; DRUG MECHANISM; DRUG STRUCTURE; FRACTIONATION; MACROPHAGE; MOUSE; NONHUMAN; STRUCTURE ANALYSIS; X RAY CRYSTALLOGRAPHY;

ANIMALS; BIFLAVONOIDS; CRYSTALLOGRAPHY, X-RAY; DAPHNE; FLAVONOIDS; LIPOPOLYSACCHARIDES; MACROPHAGES; MAGNETIC RESONANCE SPECTROSCOPY; MICE; MODELS, MOLECULAR; MOLECULAR CONFORMATION; NITRIC OXIDE; PLANT BARK; PLANT STEMS; SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 57349172025     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.56.1729     Document Type: Article

References (21)

1. Li P. T., Jiang Y., "Flora of China," Vol. 52, Science Press, Beijing, 1979, p. 378.
2. Wu D. G., Sorg B., Adolf W., Seip E. H., Hecher E., Phytother. Res., 5, 163-168 (1991).
3. Wei Z., Weidong Z., Tingzhao L., Fitoterapia, 75, 799-800 (2004).
4. Weidong Z., Qirong S., Yunheng S., Haisheng C., Fitoterapia, 78, 596-597 (2007).
5. Juan S., Zhijun W., Runhui L., Yunheng S., Chuan Z., Huiliang L., Wei Z., Weidong Z., Chin. Chem. Lett., 18, 835-836 (2007).
6. Baba K., Takeuchi K., Doi M., Masatoshi T., Inoue M., Kozawa M., Chem. Pharm. Bull., 34, 1540-1545 (1986).
7. Baba K., Takeuchi K., Hamasaki F., Kozawa M., Chem. Pharm. Bull., 33, 416-419 (1985).
8. Baba K., Takeuchi K., Doi M., Kozawa M., Chem. Pharm. Bull., 34, 2680-2683 (1985).
9. Taniguchi M., Baba K., Phytochemistry, 42, 1447-1453 (1996).
10. Taniguchi M., Fujiwara A., Baba K., Phytochemistry, 45, 183-188 (1997).
11. Taniguchi M., Fujiwara A., Baba K., Wang N., Phytochemistry, 49, 863-867 (1998).
12. Baba K., Taniguchi M., Kozawa M., Phytochemistry, 37, 879-883 (1994).
13. Baba K., Taniguchi M., Kozawa M., Phytochemistry, 31, 975-980 (1992).
14. Baba K., Taniguchi M., Kozawa M., Phytochemistry, 33, 913-916 (1991).
15. Zhou L., Yuan C., Qin B., Miao F., Liu L., Acta Bot. Borea-Occid Sin., 24, 2346-2349 (2004).
16. Feng B. M., Pei Y. H., Zhang H. I., Hua H. M., Wang Y. Q., Chin. Tradit. Herb. Drugs, 35, 12-14 (2004).
17. 3. Crystal size; 0.20x0.15x0.10 mm. CCDC 694965 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/data_request/cif.
18. Moncada S., Palmer R. M., Higgss E. A., Pharmacol. Rev., 43, 109-142 (1991).
19. Anggard E., Lancet, 343, 1199-1206 (1994).
20. Su-Mei L., Xian-Wen Y., Yun-Heng S., Lin F., Yue-Hu W., Hua-Wu Z., Xiao-Hua L., Jun-Mian T., Ya-Na S., Chun-Lin L., Wei-Dong Z., Phytochemistry, 69, 2200-2204 (2008).
21. Xian-Wen Y., Su-Mei L., Lin F. C., Yun-Heng S., Jun-Mian T., Xiao-Hua L., Hua-Wu Z., Chuan Z., Wei-Dong Z., Tetrahedron, 64, 4354-4362 (2008).