Antifungal flavanones and prenylated hydroquinones from Piper crassinervium Kunth.Phytochemistry. 2003 Sep; 64(2):555-9.P
Abstract
Bioactivity-guided fractionation of the EtOAc extract from leaves of Piper crassinervium yielded three prenylated hydroquinones together with two known flavanones naringenin and sakuranetin. Their structures were determined by means of spectroscopic analysis (NMR, IR, UV and MS) including two-dimensional NMR spectroscopy experiments (1H-1H COSY, HMQC, HMBC and NOESY). The antifungal activity was determined by direct bioautography against Cladosporium cladosporioides and C. sphaerospermum.
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
12943774
Citation
Danelutte, Ana Paula, et al. "Antifungal Flavanones and Prenylated Hydroquinones From Piper Crassinervium Kunth." Phytochemistry, vol. 64, no. 2, 2003, pp. 555-9.
Danelutte AP, Lago JH, Young MC, et al. Antifungal flavanones and prenylated hydroquinones from Piper crassinervium Kunth. Phytochemistry. 2003;64(2):555-9.
Danelutte, A. P., Lago, J. H., Young, M. C., & Kato, M. J. (2003). Antifungal flavanones and prenylated hydroquinones from Piper crassinervium Kunth. Phytochemistry, 64(2), 555-9.
Danelutte AP, et al. Antifungal Flavanones and Prenylated Hydroquinones From Piper Crassinervium Kunth. Phytochemistry. 2003;64(2):555-9. PubMed PMID: 12943774.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Antifungal flavanones and prenylated hydroquinones from Piper crassinervium Kunth.
AU - Danelutte,Ana Paula,
AU - Lago,João Henrique G,
AU - Young,Maria Claudia M,
AU - Kato,Massuo J,
PY - 2003/8/29/pubmed
PY - 2004/1/17/medline
PY - 2003/8/29/entrez
SP - 555
EP - 9
JF - Phytochemistry
JO - Phytochemistry
VL - 64
IS - 2
N2 - Bioactivity-guided fractionation of the EtOAc extract from leaves of Piper crassinervium yielded three prenylated hydroquinones together with two known flavanones naringenin and sakuranetin. Their structures were determined by means of spectroscopic analysis (NMR, IR, UV and MS) including two-dimensional NMR spectroscopy experiments (1H-1H COSY, HMQC, HMBC and NOESY). The antifungal activity was determined by direct bioautography against Cladosporium cladosporioides and C. sphaerospermum.
SN - 0031-9422
UR - https://www.unboundmedicine.com/medline/citation/12943774/Antifungal_flavanones_and_prenylated_hydroquinones_from_Piper_crassinervium_Kunth_
DB - PRIME
DP - Unbound Medicine
ER -