A novel sulfur-containing diterpenoid from Fritillaria anhuiensis

Tetrahedron Letters

Volumn 50, Issue 28, 2009, Pages 4185-4187

  Shou, Qing Yao ^a   Tan, Qing ^a   Shen, Zheng Wu ^a,b  

^a SHANGHAI UNIVERSITY OF TRADITIONAL CHINESE MEDICINE   (China)

^b Basilea Pharmaceutica China Ltd   (China)

Author keywords

Fritillaria anhuiensis; Kaurane type diterpenoid; Sulfur containing diterpenoid

Indexed keywords

DITERPENOID; GAMMA INTERFERON; NITRIC OXIDE; SULFUR;

ARTICLE; DRUG ACTIVITY; DRUG ISOLATION; DRUG STRUCTURE; FRITILLARIA; HUMAN; HUMAN CELL; INFRARED RADIATION; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE; X RAY DIFFRACTION;

FRITILLARIA ANHUIENSIS;

EID: 66049134519     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.05.002     Document Type: Article

References (12)

1. Li A.-R. Chin. Tradit. Herb. Drugs 26 (1995) 218-221
2. Li Q.-H., and Wu Z.-H. Acta Pharm. Sinica 21 (1986) 767-771
3. Li Q.-H., Zhang L.-L., and Wu Z.-H. Zhongguo Zhongyao Zazhi 15 (1990) 42-43
4. Kang L., Zhou J.-X., and Shen Z.-W. Acta Pharm. Sinica 42 (2007) 58-60
5. w were 0.0626 and 0.1328, respectively, with goodness-of-fit of 0.991. Crystallographic data for the structure reported in this paper have been deposited with the Cambridge Crystallographic Data Center, deposit No. CCDC 713572. Copies of the data can be obtained, free of charge, on application to the Director, CCDC, 12 Union Road, Cambridge CB21EZ, UK [fax: +44-(0)-1223-336033 or e-mail: deposit@ccdc.cam.ac.uk].
6. 3) δ 40.7, C-1; 21.6, C-2; 39.9, C-3; 45.7, C-4; 59.7, C-5; 28.1, C-6; 40.4, C-7; 150.8, C-8; 53.7, C-9; 41.7, C-10; 32.0, C-11; 76.4, C-12; 143.0, C-13; 125.2, C-14; 59.7, C-15; 14.0, C-16; 107.5, C-17; 28.1, C-18; 181.8, C-19; 12.6, C-20.
7. Markus W., and Michel D. Photosynth. Res. 86 (2005) 345-362
8. Yuan H.-L., and Wu J.-Z. Chin. Tradit. Herb. Drugs 30 (1999) 404-407
9. Garthwaite J. Trends Neurosci. 18 (1995) 51-52
10. Nathan C., and Xie Q.-W. Cell 78 (1994) 915-918
11. Zhou R., Zheng S.-X., Tang W., He P.-L., Li X.-Y., Yang Y.-F., Li Y.-C., Geng J.-G., and Zuo J.-P. J. Pharmacol. Exp. Ther. 316 (2006) 121-128
12. 2 standard curve.