Drimane sesquiterpenoids from the mangrove-derived fungus Aspergillus ustus

Chemical and Pharmaceutical Bulletin

Volumn 59, Issue 6, 2011, Pages 762-766

  Zhou, Huinan ^a   Zhu, Tianjiao ^a   Cai, Shengxin ^a   Gu, Qianqun ^a   Li, Dehai ^a  

^a OCEAN UNIVERSITY OF CHINA   (China)

Author keywords

Aspergillus ustus; Drimane sesquiterpene; Mangrove derived fungus

Indexed keywords

6 (1' CARBOXYOCTA 2',4',6' TRIENE) 11,12 EPOXY 9 HYDROXY 11 METHOXY DRIM 7 ENE; 6 STROBILACTONE B; 9ALPHA HYDROXYL 9 FORMYL 5ALPHA DRIM 7 EN 6 ONE; ANTINEOPLASTIC AGENT; DRIM 8 EN 6BETA,7ALPHA 11 TRIOL; O METHYLALBRASSITRIOL; SESQUITERPENE DERIVATIVE; SULFORHODAMINE B; UNCLASSIFIED DRUG;

ANTINEOPLASTIC ACTIVITY; ARTICLE; ASPERGILLUS USTUS; CARBON NUCLEAR MAGNETIC RESONANCE; DRUG ISOLATION; DRUG STRUCTURE; ELECTROSPRAY MASS SPECTROMETRY; HETERONUCLEAR MULTIPLE BOND CORRELATION; HUMAN; HUMAN CELL; LIVER CELL CARCINOMA; MANGROVE; NONHUMAN; NUCLEAR OVERHAUSER EFFECT; PROMYELOCYTIC LEUKEMIA; PROTON NUCLEAR MAGNETIC RESONANCE;

ANTINEOPLASTIC AGENTS; ASPERGILLUS; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR CONFORMATION; SESQUITERPENES;

EID: 79957840817     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.59.762     Document Type: Article

References (18)

1. Lu Z. Y., Wang Y., Miao C. D., Liu P. P., Hong K., Zhu W. M., J. Nat. Prod., 72, 1761-1767 (2009).
2. Lin Y. C., Wu X. Y., Feng S., Jiang G. C., Luo J. H., Zhou S. N., Vrijmoed L. L. P., Jones E. B. G., Krohn K., Steingröver K., Zsila F., J. Org. Chem., 62, 6252-6256 (2001).
3. Xu M. J., Gessner G., Groth I., Lange C., Christner A., Bruhn T., Deng Z. W., Li X., Heinemann S. H., Grabley S., Bringmann G., Sattler I., Lin W. H., Tetrahedron, 63, 435-444 (2007).
4. Lu Z. Y., Lin Z. J., Wang W. L., Du L., Zhu T. J., Fang Y. C., Gu Q. Q., Zhu W. M., J. Nat. Prod., 71, 543-546 (2008).
5. Wang W. L., Lu Z. Y., Tao H. W., Zhu T. J., Fang Y. C., Gu Q. Q., Zhu W. M., J. Nat. Prod., 70, 1558-1564 (2007).
6. Du L., Zhu T. J., Fang Y. C., Gu Q. Q., Zhu W. M., J. Nat. Prod., 71, 1343-1351 (2008).
7. Liu H. B., Edrada-Ebel R., Ebel R., Wang Y., Schulz B., Draeger S., Müller W. E. G., Wray V., Lin W. H., Proksch P., J. Nat. Prod., 72, 1585-1588 (2009).
8. Uosaki Y., Yoshida M., Ogawa T., Saitoh Y., J. Antibiot., 49, 6-12 (1996).
9. Hayes M. A., Wrigley S. K., Chetland I., Reynolds E. E., Ainsworth A. M., Renno D. V., Latif M. A., Cheng X. M., Hupe D. J., Charlton P., Doherty A. M., J. Antibiot., 49, 505-512 (1996).
10. Bernardi M. D., Mellerio G., Vidari G., Vita-Finzi P., J. Chem. Soc., Perkin Trans. 1, 1983, 2739-2743 (1983).
11. Garlaschelli L., Vidari G., Tetrahedron, 45, 7371-7378 (1989).
12. Urones J. G., Díez D., Gómez P. M., Marcos I. S., Basabe P., Moro R. F., J. Chem. Soc., Perkin Trans. 1, 1997, 1815-1818 (1997).
13. William A. A., Luis M. P., J. Nat. Prod., 50, 408-417 (1987).
14. Cai S. X., Li D. H., Zhu T. J., Wang F. P., Xiao X., Gu Q. Q., Helv. Chim. Acta, 93, 791-795 (2010).
15. Rifai Y., Arai M. A., Koyano T., Kowithayakorn T., Ishibashi M., J. Nat. Prod., 73, 995-997 (2010).
16. Toyota M., Ooiso Y., Kusuyama T., Asakawa Y., Phytochemistry, 35, 1263-1265 (1994).
17. Weyerstahl P., Marschall H., Weirauch M., Thefeld K., Surburg H., Flavour Fragrance J., 13, 295-318 (1998).
18. Jansen B. J. M., de Groot A., Nat. Prod. Rep., 21, 449-477 (2004).