Cytotoxic prenylated xanthones from Calophyllum inophyllum

Journal of Asian Natural Products Research

Volumn 10, Issue 10, 2008, Pages 993-997

  Xiao, Qi ^a   Zeng, Yan Bo ^a   Mei, Wen Li ^a   Zhao, You Xing ^b   Deng, Yuan Yuan ^a   Dai, Hao Fu ^a  

^a INSTITUTE OF TROPICAL BIOSCIENCE AND BIOTECHNOLOGY   (China)

^b KUNMING INSTITUTE OF BOTANY   (China)

Author keywords

Calophyllum inophyllum; Caloxanthone N; Cytotoxic activity; Prenylated xanthone

Indexed keywords

2 HYDROXYXANTHONE; ANTINEOPLASTIC AGENT; CALOXANTHONE N; GERONTOXANTHONE C; UNCLASSIFIED DRUG;

ANTINEOPLASTIC ACTIVITY; ARTICLE; CALOPHYLLUM; CALOPHYLLUM INOPHYLLUM; CANCER CELL CULTURE; CHRONIC MYELOID LEUKEMIA; DRUG STRUCTURE; HUMAN; HUMAN CELL; IC 50; NUCLEAR MAGNETIC RESONANCE;

ANTINEOPLASTIC AGENTS, PHYTOGENIC; CALOPHYLLUM; MOLECULAR STRUCTURE; XANTHONES;

CALOPHYLLUM INOPHYLLUM;

EID: 55949086318     PISSN: 10286020     EISSN: 14772213     Source Type: Journal    
DOI: 10.1080/10519990802240387     Document Type: Article

References (15)

1. H.Y. Chen, Flora of Hainanica, Vol. 2, (Science Press, Beijing, 1965), p. 56.
2. H.F. Dai and W.L. Mei, Modern Research on Medicinal Plants in Hainan, (China Science and Technology Press, Beijing, 2007), p. 31.
3. A.D. Patil, A.J. Freyer, D.S. Eggleston, R.C. Haltiwanger, M.F. Bean, P.B. Taylor, M.J. Caranfa, A.L. Breen, H.R. Bartus, R.K. Johnson, R.P. Hertzberg, and J.W. Westley, J. Med. Chem. 36, 4132 (1993).
4. M. Iinuma, H. Tosa, T. Tanaka, and S. Yonemori, Phytochemistry 35, 527 (1994).
5. M. Iinuma, H. Tosa, T. Tanaka, and S. Yonemori, Phytochemistry 38, 725 (1995).
6. C. Spino, M. Dodier, and S. Sotheeswaran, Bioorg. Med. Chem. Lett. 8, 3475 (1998).
7. M. Itoigawa, C. Ito, H.T-W. Tan, M. Kuchide, H. Tokuda, H. Nishino, and H. Furukawa, Cancer Lett. 169, 15 (2001).
8. Y. Wu, P.C. Zhang, R.Y. Chen, D.Q. Yu, and X.T. Liang, Acta Chimica. Sinica 61, 1047 (2003).
9. M.C. Yimdjo, A.G. Azebaze, A.E. Nkengfack, A.M. Meyre, B. Bodo, and Z.T. Fomum, Phytochemistry 65, 2789 (2004).
10. T.R. Govindachari, N. Viswanathan, B.R. Pai, U.R. Rao, and M. Srinivasan, Tetrahedron 23, 1901 (1967).
11. Y.Z. Li, L.Z. li, H.M. Hua, Z.G. Li, and M.S. Liu, J. Chin. Materia Medica 32, 692 (2007).
12. M. Iinuma, T. Ito, R. Miyake, H. Tosa, T. Tanaka, and V. Chelladurai, Phytochemistry 47, 1169 (1998).
13. C.H. Chang, C.C. Lin, H. Masao, and N. Tsuneo, Phytochemistry 28, 595 (1989).
14. C. Gnerre, U. Thull, P. Gaillard, P.A. Carrupt, B. Testa, E. Fernandes, F. Silva, M. Pinto, M.M.M. Pinto, J.L. Wolfender, K. Hostettmann, and G. Cruciani, Helv. Chim. Acta 84, 552 (2001).
15. T. Mosmann, J. Immunol. Methods 65, 55 (1983).