Eremophilane-type sesquiterpene derivatives from the roots of Ligularia lapathifolia.J Nat Prod. 2007 Feb; 70(2):241-5.JN
Abstract
Six new highly oxygenated eremophilane-type sesquiterpene derivatives (1-6), including a norbisesquiterpene, were isolated from an extract of the roots of Ligularia lapathifolia, and their structures were elucidated by spectroscopic methods. The structure of 1 was confirmed by single-crystal X-ray crystallography. In addition, the cytotoxicity of compounds 1, 2, 3, 5, and 6 was evaluated against selected cancer cell lines, including human stomach carcinoma (MGC-803), human hepatoma (HEP-G2), and murine sarcoma (S-180) cell lines.
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
17284071
Citation
Fei, Dong-Qing, et al. "Eremophilane-type Sesquiterpene Derivatives From the Roots of Ligularia Lapathifolia." Journal of Natural Products, vol. 70, no. 2, 2007, pp. 241-5.
Fei DQ, Li SG, Liu CM, et al. Eremophilane-type sesquiterpene derivatives from the roots of Ligularia lapathifolia. J Nat Prod. 2007;70(2):241-5.
Fei, D. Q., Li, S. G., Liu, C. M., Wu, G., & Gao, K. (2007). Eremophilane-type sesquiterpene derivatives from the roots of Ligularia lapathifolia. Journal of Natural Products, 70(2), 241-5.
Fei DQ, et al. Eremophilane-type Sesquiterpene Derivatives From the Roots of Ligularia Lapathifolia. J Nat Prod. 2007;70(2):241-5. PubMed PMID: 17284071.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Eremophilane-type sesquiterpene derivatives from the roots of Ligularia lapathifolia.
AU - Fei,Dong-Qing,
AU - Li,Shi-Gang,
AU - Liu,Chun-Mei,
AU - Wu,Gang,
AU - Gao,Kun,
Y1 - 2007/02/07/
PY - 2007/2/8/pubmed
PY - 2007/4/5/medline
PY - 2007/2/8/entrez
SP - 241
EP - 5
JF - Journal of natural products
JO - J Nat Prod
VL - 70
IS - 2
N2 - Six new highly oxygenated eremophilane-type sesquiterpene derivatives (1-6), including a norbisesquiterpene, were isolated from an extract of the roots of Ligularia lapathifolia, and their structures were elucidated by spectroscopic methods. The structure of 1 was confirmed by single-crystal X-ray crystallography. In addition, the cytotoxicity of compounds 1, 2, 3, 5, and 6 was evaluated against selected cancer cell lines, including human stomach carcinoma (MGC-803), human hepatoma (HEP-G2), and murine sarcoma (S-180) cell lines.
SN - 0163-3864
UR - https://www.unboundmedicine.com/medline/citation/17284071/Eremophilane_type_sesquiterpene_derivatives_from_the_roots_of_Ligularia_lapathifolia_
L2 - https://doi.org/10.1021/np060304k
DB - PRIME
DP - Unbound Medicine
ER -