Four new sesquiterpenoids from Ligularia cymbulifera.J Asian Nat Prod Res. 2012; 14(12):1130-6.JA
Abstract
Four new highly oxygenated bisabolane sesquiterpenoids were obtained from the EtOH extract from Ligularia cymbulifera, and their structures were elucidated by interpretation of spectroscopic data. Their relative configurations were clarified by a detailed analysis of ¹H NMR coupling constants, nuclear overhauser effect (NOE) experiments and two-dimensional NMR spectra. These four new compounds were assayed for their antimicrobial activities against four Gram-positive and Gram-negative bacteria, as well as against one human pathogenic fungus.
Links
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
23088569
Citation
Wu, Yu-Xue, et al. "Four New Sesquiterpenoids From Ligularia Cymbulifera." Journal of Asian Natural Products Research, vol. 14, no. 12, 2012, pp. 1130-6.
Wu YX, Chen YJ, Liu CM, et al. Four new sesquiterpenoids from Ligularia cymbulifera. J Asian Nat Prod Res. 2012;14(12):1130-6.
Wu, Y. X., Chen, Y. J., Liu, C. M., & Gao, K. (2012). Four new sesquiterpenoids from Ligularia cymbulifera. Journal of Asian Natural Products Research, 14(12), 1130-6. https://doi.org/10.1080/10286020.2012.733002
Wu YX, et al. Four New Sesquiterpenoids From Ligularia Cymbulifera. J Asian Nat Prod Res. 2012;14(12):1130-6. PubMed PMID: 23088569.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Four new sesquiterpenoids from Ligularia cymbulifera.
AU - Wu,Yu-Xue,
AU - Chen,Yan-Jun,
AU - Liu,Chun-Mei,
AU - Gao,Kun,
Y1 - 2012/10/23/
PY - 2012/10/24/entrez
PY - 2012/10/24/pubmed
PY - 2013/2/14/medline
SP - 1130
EP - 6
JF - Journal of Asian natural products research
JO - J Asian Nat Prod Res
VL - 14
IS - 12
N2 - Four new highly oxygenated bisabolane sesquiterpenoids were obtained from the EtOH extract from Ligularia cymbulifera, and their structures were elucidated by interpretation of spectroscopic data. Their relative configurations were clarified by a detailed analysis of ¹H NMR coupling constants, nuclear overhauser effect (NOE) experiments and two-dimensional NMR spectra. These four new compounds were assayed for their antimicrobial activities against four Gram-positive and Gram-negative bacteria, as well as against one human pathogenic fungus.
SN - 1477-2213
UR - https://www.unboundmedicine.com/medline/citation/23088569/Four_new_sesquiterpenoids_from_Ligularia_cymbulifera_
L2 - https://www.tandfonline.com/doi/full/10.1080/10286020.2012.733002
DB - PRIME
DP - Unbound Medicine
ER -