2,5-diketopiperazines from the marine-derived fungus Aspergillus fumigatus YK-7

Chemistry and Biodiversity

Volumn 9, Issue 2, 2012, Pages 385-393

  Wang, Yu ^a   Li, Zhan Lin ^a   Bai, Jiao ^a   Zhang, Li Min ^a   Wu, Xin ^a   Zhang, Lin ^a   Pei, Yue Hu ^a   Jing, Yong Kui ^b   Hua, Hui Ming ^a  

^a SHENYANG PHARMACEUTICAL UNIVERSITY   (China)

^b MOUNT SINAI SCHOOL OF MEDICINE   (United States)

Author keywords

Antiproliferative activity; Aspergillus fumigatus; Fungi; Marine natural products; Piperazine 2,5 diones

Indexed keywords

2,5 DIKETOPIPERAZINE DERIVATIVE; 20 HYDROXYCYCLOTRYPROSTATIN B; 6 HYDROXYTRYPROSTATIN B; 9 HYDROXYFUMITREMORGIN; ANTINEOPLASTIC AGENT; DOXORUBICIN; PIPERAZINE DERIVATIVE; PRENYLCYCLOTRYPROSTATIN B; SPIROGLIOTOXIN; UNCLASSIFIED DRUG;

ANTIPROLIFERATIVE ACTIVITY; ARTICLE; ASPERGILLUS FUMIGATUS; CANCER CELL CULTURE; CANCER INHIBITION; CONTROLLED STUDY; DRUG ISOLATION; DRUG STRUCTURE; HUMAN; HUMAN CELL; IC 50; LEUKEMIA CELL; MALE; PROSTATE CANCER; SPECTROSCOPY;

ANTINEOPLASTIC AGENTS; ASPERGILLUS FUMIGATUS; DIKETOPIPERAZINES; HUMANS; MAGNETIC RESONANCE SPECTROSCOPY; MALE; MARINE BIOLOGY; MOLECULAR STRUCTURE; PROSTATIC NEOPLASMS; U937 CELLS;

EID: 84863144291     PISSN: 16121872     EISSN: 16121880     Source Type: Journal    
DOI: 10.1002/cbdv.201100061     Document Type: Article

References (26)

1. B. Haefner, Drug Discovery Today 2003, 8, 536.
2. J. C. Frisvad, C. Rank, K. F. Nielsen, T. O. Larsen, Med. Mycol. 2008, S1.
3. H. W. Lu, C. R. Chong, X. Hu, J. O. Liu, J. Med. Chem. 2006, 49, 5645.
4. S. Kim, K. LaMontagne, M. Sabio, S. Sharma, R. W. Versace, N. Yusuff, P. E. Phillips, Cancer Res. 2004, 64, 2984.
5. H. W. Lee, C. S. Cho, S. K. Kang, Y. S. Yoo, J. S. Shin, S. K. Ahn, Chem. Pharm. Bull. 2007, 55, 1024.
6. E. A. Kruger, W. D. Figg, Expert Opin. Invest. Drugs 2000, 9, 1383.
7. H. S. Lee, W. K. Choi, H. J. Son, S. S. Lee, J. K. Kim, S. K. Ahn, C. I. Hong, H.-K. Min, M. Kim, S.-W. Myung, Arch. Pharm. Res. 2004, 27, 265.
8. Y. M. Kim, J. J. An, Y.-J. Jin, Y. Rhee, B. S. Cha, H. C. Lee, S.-K. Lim, J. Mol. Endocrinol. 2007, 38, 455.
9. C. B. Cui, H. Kakeya, H. Osada, Tetrahedron 1997, 53, 59.
10. M. Yamazaki, K. Sasago, K. Miyaki, J. Chem. Soc., Chem. Commun. 1974, 408.
11. M. Yamazaki, H. Fujimoto, T. Akiyama, U. Sankawa, Y. Litaka, Tetrahedron Lett. 1975, 16, 27.
12. S.-i. Kodato, M. Nakagawa, M. Hongu, T. Kawate, T. Hino, Tetrahedron 1988, 44, 359.
13. C. B. Cui, H. Kakeya, H. Osada, J. Antibiot. 1996, 49, 534.
14. P. H. H. Hermkens, R. Plate, H. C. J. Ottenheijm, Tetrahedron 1988, 44, 1991.
15. W.-R. Abraham, H.-A. Arfmann, Phytochemistry 1990, 29, 1025.
16. J. Fayos, D. Lokensgard, J. Clardy, R. J. Cole, J. W. Kirksey, J. Am. Chem. Soc. 1974, 96, 6785.
17. M. Kaouadji, R. Steiman, F. Seigle-Murandi, S. Krivobok, L. Sage, J. Nat. Prod. 1990, 53, 717.
18. G. W. Kirby, G. V. Rao, D. J. Robins, J. Chem. Soc., Perkin Trans. 1 1988, 301.
19. G. W. Kirby, D. J. Robins, M. A. Sefton, R. R. Talekar, J. Chem. Soc., Perkin Trans. 1 1980, 119.
20. S.-M. Li, Nat. Prod. Rep. 2010, 27, 57.
21. P. H. H. Hermkens, R. Plate, C. G. Kruse, H. W. Scheeren, H. C. J. Ottenheijm, J. Org. Chem. 1992, 57, 3881.
22. T. Kato, S. Yonezawa, H. Imanaka, Jpn. Pat. 226,377, 2001.
23. X. X. Han, X. Y. Xu, C. B. Cui, Q. Q. Gu, Chin. J. Med. Chem. 2007, 17, 155.
24. T. Henry, P. C. Iwen, S. H. Hinrichs, J. Clin. Microbiol. 2000, 38, 1510.
25. F. Wang, H. M. Hua, Y. H. Pei, D. Chen, Y. K. Jing, J. Nat. Prod. 2006, 69, 807.
26. T. Mosmann, J. Immunol. Methods 1983, 65, 55.