Anserinones A and B: new antifungal and antibacterial benzoquinones from the coprophilous fungus Podospora anserina.J Nat Prod. 1997 Jun; 60(6):629-31.JN
Abstract
Two new benzoquinones with antifungal, antibacterial, and cytotoxic activities have been isolated from liquid cultures of the coprophilous fungus Podospora anserina. The structures of anserinones A (1) and B (2) were assigned on the basis of MS and NMR results, and the absolute stereochemistry of 2 was deduced by analysis of 1H-NMR data for its (R)- and (S)-2-phenylbutyryl ester derivatives.
MeSH
Pub Type(s)
Journal Article
Research Support, U.S. Gov't, P.H.S.
Language
eng
PubMed ID
9214737
Citation
Wang, H, et al. "Anserinones a and B: New Antifungal and Antibacterial Benzoquinones From the Coprophilous Fungus Podospora Anserina." Journal of Natural Products, vol. 60, no. 6, 1997, pp. 629-31.
Wang H, Gloer KB, Gloer JB, et al. Anserinones A and B: new antifungal and antibacterial benzoquinones from the coprophilous fungus Podospora anserina. J Nat Prod. 1997;60(6):629-31.
Wang, H., Gloer, K. B., Gloer, J. B., Scott, J. A., & Malloch, D. (1997). Anserinones A and B: new antifungal and antibacterial benzoquinones from the coprophilous fungus Podospora anserina. Journal of Natural Products, 60(6), 629-31.
Wang H, et al. Anserinones a and B: New Antifungal and Antibacterial Benzoquinones From the Coprophilous Fungus Podospora Anserina. J Nat Prod. 1997;60(6):629-31. PubMed PMID: 9214737.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Anserinones A and B: new antifungal and antibacterial benzoquinones from the coprophilous fungus Podospora anserina.
AU - Wang,H,
AU - Gloer,K B,
AU - Gloer,J B,
AU - Scott,J A,
AU - Malloch,D,
PY - 1997/6/1/pubmed
PY - 1997/6/1/medline
PY - 1997/6/1/entrez
SP - 629
EP - 31
JF - Journal of natural products
JO - J Nat Prod
VL - 60
IS - 6
N2 - Two new benzoquinones with antifungal, antibacterial, and cytotoxic activities have been isolated from liquid cultures of the coprophilous fungus Podospora anserina. The structures of anserinones A (1) and B (2) were assigned on the basis of MS and NMR results, and the absolute stereochemistry of 2 was deduced by analysis of 1H-NMR data for its (R)- and (S)-2-phenylbutyryl ester derivatives.
SN - 0163-3864
UR - https://www.unboundmedicine.com/medline/citation/9214737/Anserinones_A_and_B:_new_antifungal_and_antibacterial_benzoquinones_from_the_coprophilous_fungus_Podospora_anserina_
L2 - https://doi.org/10.1021/np970071k
DB - PRIME
DP - Unbound Medicine
ER -