New sesquiterpenes from the roots of Coriaria nepalensis

Tetrahedron

Volumn 68, Issue 31, 2012, Pages 6204-6210

  Zhao, Fen ^a   Liu, Yun Bao ^a   Ma, Shuang Gang ^a   Qu, Jing ^a   Yu, Shi Shan ^a   Fang, Zhen Feng ^a   Li, Li ^a   Si, Yi Kang ^a   Zhang, Jian Jun ^a  

^a INSTITUTE OF MATERIA MEDICA   (China)

Author keywords

Anti convulsant activity; Coriaria nepalensis; Sesquiterpene

Indexed keywords

CORIALACTONE A; CORIALACTONE B; CORIALACTONE C; CORIALACTONE D; CORIAMYRTIN; CORIANIN; CORIANLACTONE; CORIANOL; CORIANTONE; CORIATIN; CORIATONE; DIHYDROCORIAMYRTIN; DIHYDROTUTIN; HYDROXYCORIATIN; SESQUITERPENE; TUTIN; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANTICONVULSANT ACTIVITY; ARTICLE; CORIARIA NEPALENSIS; CRYSTAL STRUCTURE; ELECTRIC SHOCK; MEDICINAL PLANT; MOUSE; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PLANT ROOT; PRIORITY JOURNAL; X RAY CRYSTALLOGRAPHY;

CORIARIA NEPALENSIS;

EID: 84862664113     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.05.067     Document Type: Article

References (19)

1. Jiangsu New Medical College. Dictionary of Traditional Chinese Medicine; Shanghai Science & Technology: Shanghai, 1977, pp 294.
2. Okuda, T.; Yoshida, T. Chem. Pharm. Bull. 1967, 15, 1955-1965.
3. Wei, H.; Zeng, F. J.; Lu, M. Y.; Tang, R. J. Acta Pharm. Sin. 1998, 33, 688-692.
4. Koike, K.; Suzuki, Y.; Ohmoto, T. Phytochemistry 1994, 35, 701-704.
5. Okuda, T.; Yoshida, T. Tetrahedron Lett. 1971, 47, 4499-4502.
6. Shen, Y. H.; Li, S. H.; Li, R. T.; Han, Q. B.; Zhao, Q. S.; Li, L.; Sun, H. D.; Lu, Y.; Cao, P.; Zheng, Q. T. Org. Lett. 2004, 6, 1593-1595.
7. Takeshi, K.; Nao, I.; Maho, H.; Yutaka, A.; Yukio, H.; Koichi, T. Chem. Pharm. Bull. 2005, 53, 1040-1042.
8. Okuda, T.; Yoshida, T.; Chen, X. M.; Xie, J. X.; Fukushima, M. Chem. Pharm. Bull. 1987, 35, 182-187.
9. Chen, X. M. Zhong Cao Yao Tong Xun 1977, 11, 34-37 (in Chinese).
10. Yuan, D. J. Zhonghua Shenjingjingshenke Zazhi 1979, 12, 196-199 (in Chinese).
11. Minkin, V. I.; Legrand, M.; Rougier, M. J. Stereochemistry. Determination of Configurations by Dipole Moments, CD or ORD; Georg Thieme: Stuttgart, 1977; Vol. 2, pp 135-136.
12. Frelek, J.; Szczepek, W. J. Tetrahedron: Asymmetry 1999, 10, 1507-1520.
13. Minkin, V. I.; Legrand, M.; Rougier, M. J. Stereochemistry. Determination of Configurations by Dipole Moments, CD or ORD; Georg Thieme: Stuttgart, 1977; Vol. 2, pp 105-106.
14. Bari, L. D.; Pescitelli, G.; Pratelli, C.; Pini, D.; Salvadori, P. J. Org. Chem. 2001, 66, 4819-4825.
15. Politi, M.; Tommasi, N. D.; Pescitelli, G.; Bari, L. D.; Morelli, I.; Braca, A. J. Nat. Prod. 2002, 65, 1742-1745.
16. Liu, J.; Liu, Y. B.; Si, Y. K.; Yu, S. S.; Qu, J.; Xu, S.; Hu, Y. C.; Ma, S. G. Steroids 2009, 74, 51-61.
17. Kitano, Y.; Usui, C.; Takasuna, K.; Hirohashi, M.; Nomura, M. J. Pharmacol. Toxicol. Methods 1996, 35, 25-29.
18. Alley, M. C.; Scudiero, D. A.; Monks, A.; Hursey, M. L.; Czerwinski, M. J.; Fine, D. L.; Abbott, B. J.; Mayo, J. G.; Shoemaker, R. H.; Boyd, M. R. Cancer Res. 1988, 48, 589-601.
19. Crystallagraphic data (excluding structure factors) for the compound 3 has been deposited with the Cambridge Crystallographic Data Centre (deposition number: CCDC 864899). Copies of the data can be obtained, free of charge, on application to the director, CCDC, 12 Union Rd., Cambridge CB21EZ, UK (fax: +44 1223 336033 or e-mail: deposit@ccdc.cam.ac.uk).