Caulerprenylols A and B, two rare antifungal prenylated para-xylenes from the green alga Caulerpa racemosa

Bioorganic and Medicinal Chemistry Letters

Volumn 23, Issue 9, 2013, Pages 2491-2494

  Liu, Ai Hong ^a   Liu, Ding Quan ^a   Liang, Tong Jun ^b   Yu, Xiao Qing ^a   Feng, Mei Tang ^a   Yao, Li Gong ^c   Fang, Yi ^a   Wang, Bin ^a   Feng, Li Hua ^a   Zhang, Min Xian ^a   Mao, Shui Chun ^a  

^a NANCHANG UNIVERSITY   (China)

^b INSTITUTE OF GEOLOGY AND GEOPHYSICS   (China)

^c SHANGHAI INSTITUTE OF MATERIA MEDICA   (China)

Author keywords

Antifungal activity; Caulerpa racemosa; Caulerprenylols A and B; Green alga; Prenylated xylenes

Indexed keywords

AMPHOTERICIN B; ANTIFUNGAL AGENT; CAULERPRENYLOL A; CAULERPRENYLOL B; NATURAL PRODUCT; PARA XYLENE; UNCLASSIFIED DRUG;

ANTIFUNGAL ACTIVITY; ARTICLE; CANDIDA GLABRATA; CARBON NUCLEAR MAGNETIC RESONANCE; CARCINOMA CELL; CAULERPA; CAULERPA RACEMOSA; CONTROLLED STUDY; CRYPTOCOCCUS NEOFORMANS; DRUG STRUCTURE; HELA CELL; HETERONUCLEAR MULTIPLE BOND CORRELATION; HETERONUCLEAR MULTIPLE QUANTUM COHERENCE; HUMAN; HUMAN CELL; MINIMUM INHIBITORY CONCENTRATION; NONHUMAN; PRENYLATION; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ANALYSIS; TRICHOPHYTON RUBRUM;

ANTIFUNGAL AGENTS; CANDIDA GLABRATA; CAULERPA; CELL LINE, TUMOR; CELL PROLIFERATION; CRYPTOCOCCUS NEOFORMANS; HL-60 CELLS; HUMANS; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR CONFORMATION; TRICHOPHYTON; XYLENES;

ALGAE; CANDIDA GLABRATA; CAULERPA RACEMOSA; CHLOROPHYTA; FILOBASIDIELLA NEOFORMANS; TRICHOPHYTON RUBRUM;

EID: 84876105951     PISSN: 0960894X     EISSN: 14643405     Source Type: Journal    
DOI: 10.1016/j.bmcl.2013.03.038     Document Type: Article

References (22)

1. K. Yazaki, K. Sasaki, and Y. Tsurumaru Phytochemistry 70 2009 1739
2. S.N. Sunassee, and M.T. Davies-Coleman Nat. Prod. Rep. 29 2012 513
3. S.P.B. Ovenden, J.L. Nielson, C.H. Liptrot, R.H. Willis, A.D. Wright, C.A. Motti, and D.M. Tapiolas J. Nat. Prod. 74 2011 739
4. S. Tsukamoto, H. Umaoka, K. Yoshikawa, T. Ikeda, and H. Hirota J. Nat. Prod. 73 2010 1438
5. S. Tsukamoto, H. Kato, T.J. Greshock, H. Hirota, T. Ohta, and R.M. Williams J. Am. Chem. Soc. 131 2009 3834
6. R. Raju, A.M. Piggott, X.-C. Huang, and R.J. Capon Org. Lett. 13 2011 2770
7. A.R. Carroll, G.A. Fechner, J. Smith, G.P. Guymer, and R.J. Quinn J. Nat. Prod. 71 2008 1479
8. O.I. Zhuravleva, S.S. Afiyatullov, V.A. Denisenko, S.P. Ermakova, N.N. Slinkina, P.S. Dmitrenok, and N.Y. Kim Phytochemistry 80 2012 123
9. O. Ohno, T. Chiba, S. Todoroki, H. Yoshimura, N. Maru, K. Maekawa, H. Imagawa, K. Yamada, A. Wakamiya, K. Suenaga, and D. Uemura Chem. Commun. 47 2011 12453
10. Y. Li, X. Li, J.S. Kang, H.D. Choi, and B.W. Son J. Antibiot. 57 2004 337
11. B. Simone, G. Winklet, H. George, T.T.-R. Jeremy, and D. Rupika Org. Med. Chem. Lett. 2 2012 21
12. S.-C. Mao, E. Manzo, Y.-W. Guo, M. Gavagnin, E. Mollo, M.L. Ciavatta, R. van Soest, and G. Cimino Tetrahedron 63 2007 11108
13. S.-C. Mao, Y. Liu, J.B. Morgan, M.B. Jekabsons, Y.-D. Zhou, and D.G. Nagle J. Nat. Prod. 72 2009 1927
14. D.-Q. Liu, S.-C. Mao, X.-Q. Yu, L.-H. Feng, and X.-P. Lai Heterocycles 85 2012 661
15. U.V. Solmssen, and E. Wenis J. Am. Chem. Soc. 70 1948 4197
16. M. Fukuoka, M. Kuroyanagi, M. Toyama, K. Yoshihira, and S. Natori Chem. Pharm. Bull. 20 1972 2282
17. S.-C. Mao, Y.-W. Guo, and X. Shen Bioorg. Med. Chem. Lett. 16 2006 2947
18. T.W. Lyons, D. Guironnet, M. Findlater, and M.J. Brookhart J. Am. Chem. Soc. 134 2012 15708
19. N. Katsui, A. Matsunaga, K. Imaizumi, T. Masamune, and K. Tomiyama Bull. Chem. Soc. Jpn. 45 1972 2871
20. N. Katsui, A. Matsunaga, K. Imaizumi, T. Masamune, and K. Tomiyama Tetrahedron Lett. 1971 83
21. Y. Hirose, and T. Nakatsuka Bull. Agric. Chem. Soc. Jpn. 23 1959 143
22. A. Bruns, D. Berg, and A. Werner-Busse J. Chromatogr. 450 1988 111