Bromomyrothenone B and botrytinone, cyclopentenone derivatives from a marine isolate of the fungus Botrytis

Journal of Natural Products

Volumn 70, Issue 2, 2007, Pages 307-309

  Li, Xifeng ^a,f   Zhang, Dahai ^a,b   Lee, Uk ^a   Li, Xianguo ^b   Cheng, Jiagao ^c   Zhu, Weiliang ^c   Jung, Jee H ^d   Hong, Dae Choi ^e   Byeng, Wha Son ^a  

^a Pukyong National University   (South Korea)

^b OCEAN UNIVERSITY OF CHINA   (China)

^c SHANGHAI INSTITUTE OF MATERIA MEDICA   (China)

^d Pusan National University   (South Korea)

^e Dong Eui University   (South Korea)

^f YANBIAN UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

(5) 3 AMINO 2 BROMO 5 ETHENYL 5 HYDROXY 2 CYCLOPENTEN 1 ONE; 4,5 DIHYDROXY 3 (1 HYDROXYETHYL) 2 CYCLOPENTEN 1 ONE; BOTRYTINONE; BROMOMYROTHENONE B; CYCLONERODIOL; CYCLOPENTENONE DERIVATIVE; MYROTHENONE B; UNCLASSIFIED DRUG;

ARTICLE; BOTRYTIS; CIRCULAR DICHROISM; DRUG ISOLATION; DRUG STRUCTURE; PHYSICAL CHEMISTRY; QUANTUM CHEMISTRY; X RAY ANALYSIS;

BOTRYTIS; CIRCULAR DICHROISM; CRYSTALLOGRAPHY, X-RAY; CYCLOPENTANES; KOREA; MARINE BIOLOGY; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE;

BOTRYTIS; FUNGI;

EID: 33947400111     PISSN: 01633864     EISSN: None     Source Type: Journal    
DOI: 10.1021/np0600548     Document Type: Article

References (15)

1. Blunt, J. W.; Copp, B. R.; Munro, M. H. G.; Northcote, P. T.; Prinsep, M. R. Nat. Prod. Rep. 2005, 22, 15-61.
2. Li, X.; Kim, M. K.; Lee, U.; Kim, S.-K.; Kang, J. S.; Choi, H. D.; Son, B. W. Chem. Pharm. Bull. 2005, 53, 453-455.
3. Hanson, J. R.; Hitchcock, P. B.; Nyfeler, R. J. Chem. Soc., Perkin Trans. 1 1975, 1586-1590.
4. 13C-NMR Spectroscopy of Organic Compounds. In Carbon-13 NMR Spectroscopy; Breitmaier, E., Voelter, W., Eds.; VCH: Weinheim, Germany, 1990; pp 238-240.
5. Mikolajczyk, M.; Mikina, M.; Wieczorek, M. W.; Blaszczyk, J. Angew. Chem., Int. Ed. Engl. 1996, 35, 1560-1562.
6. Ghisalberti, E. L.; Narbey, M. J.; Rowland, C. Y. J. Nat. Prod. 1990, 53, 520-522.
7. Malmstrom, J.; Christophersen, C.; Barrero, A. F.; Oltra, J. E.; Justicia, J.; Rosales, A. J. Nat. Prod. 2002, 65, 364-367.
8. A full list of crystallographic data and parameters is deposited at the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK (deposition number CCDC 615055).
9. Koreeda, M.; Harada, N.; Nakanishi, K. J. Am. Chem. Soc. 1974, 96, 266-268.
10. Mitre, G. B.; Kamiya, N.; Bardon, A.; Asakawa, Y. J. Nat. Prod. 2004, 67, 31-36.
11. Takahashi, M.; Fuchino, H.; Sekita, S.; Satake, M. Phytother. Res. 2004, 18, 573-578.
12. Sassa, T.; Ooi, T.; Kinoshita, H. Biosci. Biotechnol. Biochem. 2004, 68, 2633-2636.
13. Vertesy, L.; Burger, H.-J.; Kenja, J.; Knauf, M.; Kogler, H.; Paulus, E. F.; Ramakrishna, N. V. S.; Swamy, K. H. S.; Vijayakumar, E. K. S.; Hammann, P. J. Antibiot. 2000, 53, 677-686.
14. Lee, S.; Kim, W.-G.; Kim, E.; Ryoo, I.-J.; Lee, H. K.; Kim, J. N.; Jung, S.-H.; Yoo, I.-D. Bioorg. Med. Chem. Lett. 2005, 15, 471-473.
15. Tang, Y.-Q.; Sattler, I.; Thiericke, R.; Grabley, S.; Feng, X.-Z. Eur. J. Org. Chem. 2000, 2401-2406.