Xestospongienols A-L, brominated acetylenic acids from the Chinese marine sponge Xestospongia testudinaria

Helvetica Chimica Acta

Volumn 94, Issue 9, 2011, Pages 1600-1607

  Liu, Dong ^a   Xu, Jing ^a   Jiang, Wei ^a   Deng, Zhiwei ^b   De Voogd, Nicole J ^c   Proksch, Peter ^d   Lin, Wenhan ^a  

^a PEKING UNIVERSITY   (China)

^b BEIJING NORMAL UNIVERSITY   (China)

^c NATURALIS BIODIVERSITY CENTER   (Netherlands)

^d HEINRICH HEINE UNIVERSITY   (Germany)

Author keywords

Acetylenic acids, brominated; Marine sponges; Xestospongia testudinaria; Xestospongienols A L

Indexed keywords

ACETYLENIC ACIDS, BROMINATED; ALKYL CHAIN; CHEMICAL EXAMINATION; CHINESE MARINES; ISOLATION AND CHARACTERIZATION; MARINE SPONGE; MOSHER METHOD; STRUCTURAL PATTERN; XESTOSPONGIA TESTUDINARIA; XESTOSPONGIENOLS A - L;

ACETYLENE;

BROMINATED ACETYLENIC ACID; NATURAL PRODUCT; POLYUNSATURATED FATTY ACID; UNCLASSIFIED DRUG; XESTOSPONGIENOL A; XESTOSPONGIENOL B; XESTOSPONGIENOL C; XESTOSPONGIENOL D; XESTOSPONGIENOL E; XESTOSPONGIENOL F; XESTOSPONGIENOL G; XESTOSPONGIENOL H; XESTOSPONGIENOL I; XESTOSPONGIENOL J; XESTOSPONGIENOL K; XESTOSPONGIENOL L;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL COMPOSITION; DRUG ISOLATION; DRUG STRUCTURE; ELECTROSPRAY MASS SPECTROMETRY; ENANTIOMER; HETERONUCLEAR MULTIPLE BOND CORRELATION; HETERONUCLEAR MULTIPLE QUANTUM COHERENCE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; INFRARED SPECTROSCOPY; MASS SPECTROMETRY; NONHUMAN; PRIORITY JOURNAL; SPONGE (PORIFERA); XESTOSPONGIA TESTUDINARIA;

EID: 80052849321     PISSN: 0018019X     EISSN: 15222675     Source Type: Journal    
DOI: 10.1002/hlca.201100015     Document Type: Article

References (17)

1. N. M. Carballeira, F. Shalabi, J. Nat. Prod. 1993, 56, 739.
2. N. Fusetani, H.-Y. Li, K. Tamura, S. Matsunaga, Tetrahedron 1993, 49, 1203.
3. T. Ichiba, P. J. Scheuer, M. Kelly-Borges, Helv. Chim. Acta 1993, 76, 2814.
4. R. J. Quinn, D. J. Tucker, Tetrahedron Lett. 1985, 26, 1671.
5. M. L. Bourguet-Kondracki, M. T. Rakotoarisoa, M. T. Martin, M. Guyot, Tetrahedron Lett. 1992, 33, 225.
6. S. Hirsh, S. Carmely, Y. Kashman, Tetrahedron 1987, 42, 3257.
7. A. D. Patil, W. C. Kokke, S. Cochran, T. A. Francis, T. Tomszek, J. W. Westley, J. Nat. Prod. 1992, 55, 1170.
8. R. J. Quinn, D. J. Tucker, J. Nat. Prod. 1991, 54, 290.
9. W. Jiang, D. Liu, Z. Deng, N. J. de Voogd, P. Proksch, W. Lin, Tetrahedron 2011, 67, 58.
10. F. J. Schmitz, Y. Gopichand, Tetrahedron Lett. 1978, 39, 3637.
11. D. J. Vanderah, F. J. Schmitz, J. Org. Chem. 1976, 41, 3480.
12. F. J. McDonald, D. C. Campbell, D. J. Vanderah, F. J. Schmitz, D. M. Washecheck, J. E. Burks, D. Van der Helm, J. Org. Chem. 1975, 40, 665.
13. J. M. Seco, M. Martino, E. Quiñoá, R. Riguera, Org. Lett. 2000, 2, 3261.
14. S. G. Batrakov, A. G. Panosyan, I. V. Konova, L. D. Bergelson, Biochim. Biophys. Acta 1974, 337, 29.
15. K.-H. van Pée, S. Unversucht, Chemosphere 2003, 52, 299.
16. W. K. Lam, S. Hahn, E. Ayanoglu, C. Djerassi, J. Org. Chem. 1989, 54, 3428.
17. M. Blumenberg, W. Michaelis, Mar. Biol. 2007, 150, 1153.