Structural revision of aspernigrin A, reisolated from Cladosporium herbarum IFB-E002.J Nat Prod. 2005 Jul; 68(7):1106-8.JN
Abstract
Aspernigrin A was reisolated as a secondary metabolite of the Cynodon dactylon-associated endophytic fungus Cladosporium herbarum IFB-E002 coproducing rubrofusarin B, fonsecinone A, 7-hydroxy-4-methoxy-5-methylcoumarin, orlandin, kotanin, and 3beta,5alpha,6beta-trihydroxyergosta-7,22-diene. The structure of aspernigrin A, previously elucidated to be 4-benzyl-6-oxo-1,6-dihydropyridine-3-carboxamide (1), was revised as 6-benzyl-4-oxo-1,4-dihydropyridine-3-carboxamide (2) on the basis of its additional NMR spectroscopic data and the X-ray crystallographic analysis.
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
16038560
Citation
Ye, Yong H., et al. "Structural Revision of Aspernigrin A, Reisolated From Cladosporium Herbarum IFB-E002." Journal of Natural Products, vol. 68, no. 7, 2005, pp. 1106-8.
Ye YH, Zhu HL, Song YC, et al. Structural revision of aspernigrin A, reisolated from Cladosporium herbarum IFB-E002. J Nat Prod. 2005;68(7):1106-8.
Ye, Y. H., Zhu, H. L., Song, Y. C., Liu, J. Y., & Tan, R. X. (2005). Structural revision of aspernigrin A, reisolated from Cladosporium herbarum IFB-E002. Journal of Natural Products, 68(7), 1106-8.
Ye YH, et al. Structural Revision of Aspernigrin A, Reisolated From Cladosporium Herbarum IFB-E002. J Nat Prod. 2005;68(7):1106-8. PubMed PMID: 16038560.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Structural revision of aspernigrin A, reisolated from Cladosporium herbarum IFB-E002.
AU - Ye,Yong H,
AU - Zhu,Hai L,
AU - Song,Yong C,
AU - Liu,Jun Y,
AU - Tan,Ren X,
PY - 2005/7/26/pubmed
PY - 2005/8/27/medline
PY - 2005/7/26/entrez
SP - 1106
EP - 8
JF - Journal of natural products
JO - J Nat Prod
VL - 68
IS - 7
N2 - Aspernigrin A was reisolated as a secondary metabolite of the Cynodon dactylon-associated endophytic fungus Cladosporium herbarum IFB-E002 coproducing rubrofusarin B, fonsecinone A, 7-hydroxy-4-methoxy-5-methylcoumarin, orlandin, kotanin, and 3beta,5alpha,6beta-trihydroxyergosta-7,22-diene. The structure of aspernigrin A, previously elucidated to be 4-benzyl-6-oxo-1,6-dihydropyridine-3-carboxamide (1), was revised as 6-benzyl-4-oxo-1,4-dihydropyridine-3-carboxamide (2) on the basis of its additional NMR spectroscopic data and the X-ray crystallographic analysis.
SN - 0163-3864
UR - https://www.unboundmedicine.com/medline/citation/16038560/Structural_revision_of_aspernigrin_A_reisolated_from_Cladosporium_herbarum_IFB_E002_
DB - PRIME
DP - Unbound Medicine
ER -