Ceramicines E-I, new limonoids from Chisocheton ceramicus

Chemical and Pharmaceutical Bulletin

Volumn 59, Issue 3, 2011, Pages 407-411

  Wong, Chin Piow ^a   Shimada, Misae ^a   Nagakura, Yuta ^a   Nugroho, Alfarius Eko ^a   Hirasawa, Yusuke ^a   Kaneda, Toshio ^a   Awang, Khalijah ^b   Hadi, A Hamid A ^b   Mohamad, Khalit ^b   Shiro, Motoo ^c   Morita, Hiroshi ^a  

^a HOSHI UNIVERSITY   (Japan)

^b UNIVERSITY OF MALAYA   (Malaysia)

^c RIGAKU CORPORATION   (Japan)

Author keywords

Ceramicine; Chisocheton ceramicus; Cytotoxic activity; Limonoid

Indexed keywords

CERAMICINE B; CERAMICINE E; CERAMICINE F; CERAMICINE G; CERAMICINE H; CERAMICINE I; LIMONOID; UNCLASSIFIED DRUG;

ARTICLE; BARK; CARBON NUCLEAR MAGNETIC RESONANCE; CHISOCHETON CERAMICUS; CIRCULAR DICHROISM; CYTOTOXICITY; DRUG ISOLATION; DRUG STRUCTURE; HUMAN; HUMAN CELL; MELIACEAE; PROTON NUCLEAR MAGNETIC RESONANCE; X RAY CRYSTALLOGRAPHY;

CELL LINE, TUMOR; CIRCULAR DICHROISM; CRYSTALLOGRAPHY, X-RAY; HUMANS; LIMONINS; MAGNETIC RESONANCE SPECTROSCOPY; MELIACEAE; MOLECULAR CONFORMATION; PLANT BARK;

EID: 79952419202     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.59.407     Document Type: Article

References (12)

1. Roy A., Saraf S., Biol. Pharm. Bull., 29, 191-201 (2006).
2. Zhang H., Wang X., Chen F., Androulakis X. M., Wargovich M. J., Phytotherapy Res., 21, 731-734 (2007).
3. Carpinella M. C., Defago M. T., Valladares G., Palacios S. M., J. Agric. Food Chem., 51, 369-374 (2003).
4. Bray D. H., Warhurst D. C., Connolly J. D., O'Neill M. J., Philipson J. D., Phytotherapy Res., 4, 29-35 (1990).
5. Koul O., Singh G., Singh R., Singh J., Danielwski W. M., Berlozecki S., J. Biosci., 29, 409-416 (2004).
6. Mohamad K., Hirasawa Y., Lim C. S., Awang K., Hadi A. H. A., Takeya K., Morita H., Tetrahedron Lett., 49, 4276-4278 (2008).
7. Mohamad K., Hirasawa Y., Litaudon M., Awang K., Hadi A. H. A., Takeya K., Ekasari W., Widyawaruyanti A., Zaini N. C., Morita H., Bioorg. Med. Chem., 17, 727-730 (2009).
8. Turner C., Tempesta M., Taylor R., Zagorski M., Termini J., Schroeder D., Nakanishi K., Tetrahedron, 43, 2789-2803 (1987).
9. Baba H., Yaoita Y., Kikuchi M., Helv. Chim. Acta, 90, 1028-1037 (2007).
10. Subhadhirasakul S., Takayama H., Miyabe Y., Aimi N., Ponglux D., Sakai S., Chem. Pharm. Bull., 42, 2645-2646 (1994).
11. Flack H. D., Acta Cryst., A39, 876-881 (1983).
12. Reddy L., Odhav B., Bhoola K. D., Pharmacol. Ther., 99, 1-13 (2003).