Rubesanolides A and B: Diterpenoids from Isodon rubescens

Organic Letters

Volumn 13, Issue 6, 2011, Pages 1406-1409

  Zou, Juan ^a,b   Pan, Lutai ^a   Li, Qiji ^a   Zhao, Junhua ^a   Pu, Jianxin ^b   Yao, Ping ^c   Gong, Ningbo ^d   Lu, Yang ^d   Kondratyuk, Tamara P ^e   Pezzuto, John M ^e   Fong, Harry H S ^c   Zhang, Hongjie ^c   Sun, Handong ^b  

^a GUIYANG COLLEGE OF TRADITIONAL CHINESE MEDICINE   (China)

^b KUNMING INSTITUTE OF BOTANY   (China)

^c UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

^d INSTITUTE OF MATERIA MEDICA   (China)

^e UNIVERSITY OF HAWAII AT HILO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; DITERPENE; LACTONE; RUBESANOLIDE A; RUBESANOLIDE B;

ARTICLE; CELL STRAIN K 562; CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; DRUG SCREENING; HELA CELL; HUMAN; ISODON; ISOLATION AND PURIFICATION; MEDICINAL PLANT; NUCLEAR MAGNETIC RESONANCE; PLANT LEAF; X RAY CRYSTALLOGRAPHY;

ANTINEOPLASTIC AGENTS, PHYTOGENIC; CRYSTALLOGRAPHY, X-RAY; DITERPENES; DRUG SCREENING ASSAYS, ANTITUMOR; HELA CELLS; HUMANS; ISODON; K562 CELLS; LACTONES; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PLANT LEAVES; PLANTS, MEDICINAL;

EID: 79952576817     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol200086k     Document Type: Article

References (17)

1. Sun, H. D.; Xu, Y. L.; Jiang, B. Diterpenoids from Isodon Species; Science Press: Beijing, 2001.
2. Sun, H. D.; Huang, S. X.; Han, Q. B. Nat. Prod. Rep 2006, 23, 673-698
3. In the Pharmacopoecia of People's Repulic of China; People's Health Press: Beijing, 1977; p 186.
4. 4Na).
5. Wang, X. N.; Shao, P. L.; Lv, H.; Ye, S. Org. Lett. 2009, 11, 4029-4031
6. 2), s = 1.016. Crystallographic data for the structure of 1 have been deposited in the Cambridge Crystallographic Data Centre (Deposition No. CCDC798778). Copies of these data can be obtained, free of charge, on application to the CCDC via the Internet at www.ccdc.com.ac.uk/conts/retrieving. html (or 12 Union Road, Cambridge CB2 1EZ, UK, fax: +44 1223 336033, e-mail: deposit@ccdc.cam.ac.uk).
7. Flack, H. D.; Bernardinelli, G. Chirality 2008, 20, 681-690
8. Flack, H. D. Act Crystallogr. 1983, A39, 876-881
9. 4Na).
10. Dewick, P. M. In Medicinal Natural Products: A Biosynthetic Approach, 2 nd ed.; John Wiley & Sons, Ltd., The Atrium, Southern Gate, Chichester, West Sussex, U.K., 2002.
11. Wang, Z. Q.; Xu, F. M.; Dong, H. Z.; Node, M.; Fuji, K. Tianran Chanwu Yanjiu Yu Kaifa 1995, 7, 24-28
12. Jiang, B.; Lu, Z. Q.; Zhang, H. J.; Zhao, Q. S.; Sun, H. D. Fitoterapia 2000, 71, 360-364
13. Niu, X. M.; Li, M. L.; Zhao, Q. S.; Mei, S. X.; Na, Z.; Wang, S. J.; Lin, Z. W.; Sun, H. D. Planta Med. 2002, 68, 528-533
14. Monks, A.; Scuduero, D.; Skehan, P.; Shoemaker, R.; Paull, K.; Vistica, D.; Hose, C.; Langley, J.; Cronise, P.; Vaigro-Wolff, A. J. Natl. Cancer Inst. 1991, 83, 757-766
15. Jutiviboonsuk, A.; Zhang, H. J.; Tan, G. T.; Ma, C. Y.; Hung, N. V.; Cuong, N. M.; Bunyapraphatsara, N.; Soejarto, D. D.; Fong, H. H. S. Phytochemistry 2005, 66, 2745-2751
16. Homhual, S.; Zhang, H. J.; Bunyapraphatsara, N.; Kondratyuk, T.; Santarsiero, B. D.; Mesecar, A. D.; Herunsalee, A.; Chaukul, W.; Pezzuto, J. M.; Fong, H. H. S. Planta Med. 2006, 72, 255-260
17. Yang, J. H.; Kondratyuk, T. P.; Marler, L. E.; Qiu, X.; Choi, Y. S.; Cao, H. M.; Sturdy, M.; Pegan, S.; Liu, Y; Wang, L. Q.; Mesecar, A. D.; van Breemen, R. B.; Pezzuto, J, M.; Fong, H. H. S.; Chen, Y. G.; Zhang, H. J. Phytochemistry 2010, 71, 641-647