6-Hydroxy-4-en-3-one sterols from the marine sponge Iotrochoto birotulata

Journal of Asian Natural Products Research

Volumn 7, Issue 2, 2005, Pages 115-120

  Li, Li Ya ^a   Deng, Zhi Wei ^b   Fu, Hong Zheng ^a   Li, Jun ^a   Lin, Wen Han ^a   Proksch, Peter ^c  

^a PEKING UNIVERSITY   (China)

^b BEIJING NORMAL UNIVERSITY   (China)

^c HEINRICH HEINE UNIVERSITY   (Germany)

Author keywords

Ergosta 6 hydroxy 4, 22 E dien 3 one; Ergosta 6 hydroxy 4,24(28) dien 3 one; Ergosta 6 hydroxy 4,24(28) dien 3 one; Iotrochoto birotulata; Marine sponge

Indexed keywords

CHOLESTA 6BETA HYDROXY 4 EN 3 ONE; ERGOSTA 28 METHYL 6BETA HYDROXY 4,24(28) DIEN 3 ONE; ERGOSTA 6ALPHA HYDROXY 4,22 DIEN 3 ONE; ERGOSTA 6ALPHA HYDROXY 4,24(28) DIEN 3 ONE; ERGOSTA 6BETA HYDROXY 4,24(28) DIEN 3 ONE; STEROL DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHINA; COELENTERATE; COLUMN CHROMATOGRAPHY; DRUG ISOLATION; DRUG STRUCTURE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; INFRARED SPECTROSCOPY; IOTROCHOTO BIROTULATA; MASS SPECTROMETRY; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ANALYSIS;

ANIMALS; CHROMATOGRAPHY, GEL; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PORIFERA; SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION; SPECTROPHOTOMETRY, INFRARED; SPECTROPHOTOMETRY, ULTRAVIOLET; STEROLS;

COELENTERATA;

EID: 12344291207     PISSN: 10286020     EISSN: None     Source Type: Journal    
DOI: 10.1080/10286020310001617200     Document Type: Article

References (15)

1. T. Rasmussen, J. Jensen, U. Anthoni, C. Christophersen, P.H. Nielsen. J. Nat. Prod., 56, 1553-1557 (1993).
2. G. Dellar, P. Djura, M.V. Sargent. J. Chem. Soc., Perkin Trans. 1, 1679-1682 (1981).
3. I. Carletti, B. Banaigs, P. Amade. J. Nat. Prod., 63, 981-983 (2000).
4. J.V. Martin, M.L. Koenig, W.O. McClure. Toxicon, 30, 1001-1010 (1992).
5. V. Costantino, E. Fattorusso, A. Mangoni. J. Nat. Prod. 57, 1552-1556 (1994).
6. V. Costantino, C. Dell' Aversano, E. Fattorusso, A. Mangoni. Steroids, 65, 138-142 (2000).
7. G.W. Chan, T. Francis, D.R. Thureen, P.H. Offen, N.J. Pierce, J.W. Westley, R.K. Johnson, D.J. Faulkner. J. Org. Chem., 58, 2544-2546 (1993).
8. T.A. Berkhout, L.M. Havekes, N.J. Pearce, P.H.E. Groot. Biochem. J., 272, 181-186 (1990).
9. J.H. Sheu, S.Y. Huang, G.H. Wang, C.Y. Duh. J. Nat. Prod., 60, 900-903 (1997).
10. L.F. Fiester, J. Am. Chem. Soc., 75, 4377-4385 (1953).
11. J.H. Sheu, G.H. Wang, P.J. Sung, C.Y. Duh. J. Nat. Prod., 62, 224-227 (1999).
12. M.D. Greca, P. Monaco, L. Previtera. J. Nat. Prod., 53, 1430-1435 (1990).
13. N.S. Bgacca, D.H. Williams. Application of NMR Spectroscopy in Organic Chemistry, pp. 19-21, Holden-Day, San Francisco (1964).
14. J.H. Sheu, C.C. Liaw, C.Y. Duh. J. Nat. Prod., 58, 1521-1526 (1995).
15. Y.M. Sheikh, C. Djerassi. Tetrahedron, 30, 4095-4103 (1974).