Sesquiterpenoids from the endophytic fungus Trichoderma sp. PR-35 of paeonia delavayi

Chemistry and Biodiversity

Volumn 8, Issue 9, 2011, Pages 1717-1723

  Wu, Shao Hua ^a   Zhao, Li Xing ^a   Chen, You Wei ^a   Huang, Rong ^a   Miao, Cui Ping ^a   Wang, Jiao ^a  

^a YUNNAN UNIVERSITY   (China)

Author keywords

Antimicrobial activity; Fungi; Paeonia delavayi; Sesquiterpenes; Trichoacorenol, 2 hydroxy ; Trichoderic acid; Trichoderma species

Indexed keywords

2BETA HYDROXYTRICHOACORENOL; ANTIBIOTIC AGENT; ANTIFUNGAL AGENT; CYCLONERODIOL; CYCLONERODIOL OXIDE; NYSTATIN; PENICILLIN G; PLANT EXTRACT; SESQUITERPENE; SORBICILLIN; TRICHODERIC ACID; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ANTIFUNGAL ACTIVITY; ARTICLE; BOTRYTIS CINEREA; CONTROLLED STUDY; DRUG ISOLATION; DRUG STRUCTURE; ESCHERICHIA COLI; FUNGUS; FUNGUS CULTURE; FUSARIUM; FUSARIUM AVENACEUM; FUSARIUM MONILIFORME; HORMODENDRUM DERMATITIDIS; MINIMUM INHIBITORY CONCENTRATION; NONHUMAN; NUCLEOTIDE SEQUENCE; PAEONIA; PAEONIA DELAVAYI; PYRICULARIA ORYZAE; SHIGELLA SONNEI; STAPHYLOCOCCUS ALBUS; TRICHODERMA;

ANTI-BACTERIAL AGENTS; ANTIFUNGAL AGENTS; BACTERIA; FUNGI; MAGNETIC RESONANCE SPECTROSCOPY; MASS SPECTROMETRY; MICROBIAL SENSITIVITY TESTS; MOLECULAR CONFORMATION; PAEONIA; SESQUITERPENES; SPECTROPHOTOMETRY, INFRARED; TRICHODERMA;

FUNGI; PAEONIA DELAVAYI; TRICHODERMA;

EID: 80052906039     PISSN: 16121872     EISSN: 16121880     Source Type: Journal    
DOI: 10.1002/cbdv.201000236     Document Type: Article

References (17)

1. H. W. Zhang, Y. C. Song, R. X. Tan, Nat. Prod. Rep. 2006, 23, 753.
2. B. Schulz, C. Boyle, S. Draeger, A.-K. Römmert, K. Krohn, Mycolog. Res. 2002, 106, 996.
3. A. A. L. Gunatilaka, J. Nat. Prod. 2006, 69, 509.
4. H.-C. Lin, H.-Y. Ding, T.-S. Wu, P.-L. Wu, Phytochemistry 1996, 41, 237.
5. S. S. Kang, K. H. Shin, H.-J. Chi, Arch. Pharm. Res. 1991, 14, 52.
6. M. Kubo, T. Tani, H. Kosoto, Y. Kimura, S. Arichi, Shoyakugaku Zasshi 1979, 33, 155.
7. S.-H. Wu, D.-G. Wu, Y.-W. Chen, Chem. Biodiversity 2010, 7, 90.
8. S.-H. Wu, Y.-W. Chen, S.-C. Shao, L.-D. Wang, Y. Yu, Z.-Y. Li, L.-Y. Yang, S.-L. Li, R. Huang, Chem. Biodiversity 2009, 6, 79.
9. S.-H. Wu, Y.-W. Chen, S.-C. Shao, L.-D. Wang, Z.-Y. Li, L.-Y. Yang, S.-L. Li, R. Huang, J. Nat. Prod. 2008, 71, 731.
10. M. Stadler, H. Anke, O. Sterner, Tetrahedron 1994, 50, 12649.
11. M. Stadler, H. Anke, O. Sterner, J. Antibiot. 1994, 47, 1284.
12. W. R. Abraham, H. P. Hanssen, I. Urbasch, Z. Naturforsch., C 1991, 46, 169.
13. Q. Huang, Y. Tezuka, Y. Hatanaka, T. Kikuchi, A. Nishi, K. Tubaki, Chem. Pharm. Bull. 1995, 43, 1035.
14. H. G. Cutler, J. M. Jacyno, R. S. Phillips, R. L. Vontersch, P. D. Cole, N. Montemurro, Agric. Biol. Chem. 1991, 55, 243.
15. T. Fujita, Y. Takaishi, Y. Takeda, T. Fujiyama, T. Nishi, Chem. Pharm. Bull. 1984, 32, 4419.
16. N. Abe, T. Murata, A. Hirota, Biosci. Biotechnol. Biochem. 1998, 62, 2120.
17. A. L. Barry, M. B. Coyle, C. Thornsberry, E. H. Gerlach, R. W. Howkinson, J. Clin. Microbiol. 1979, 10, 885.