[Structure modification on sesquiterpene lactones from Elephantopus scaber].Yao Xue Xue Bao. 2007 Nov; 42(11):1159-61.YX
Abstract
In order to look for lower toxic and strongly active compounds, the structure of sesquiterpene lactones from Elephantopus scaber was modified. Deoxyelephantopin and scabertopin were isolated from the whole plant of Elephantopus scaber and hydrogenated and epoxidated. Five sesquiterpenoide derivatives were prepared and their structures were identified by IR, NMR and MS spectra analysis. Four sesquiterpenoides are new compounds. Part of the compounds show definite antitumor activity.
MeSH
Pub Type(s)
English Abstract
Journal Article
Language
chi
PubMed ID
18300472
Citation
Liang, Qiao-li, and Zhi-da Min. "[Structure Modification On Sesquiterpene Lactones From Elephantopus Scaber]." Yao Xue Xue Bao = Acta Pharmaceutica Sinica, vol. 42, no. 11, 2007, pp. 1159-61.
Liang QL, Min ZD. [Structure modification on sesquiterpene lactones from Elephantopus scaber]. Yao Xue Xue Bao. 2007;42(11):1159-61.
Liang, Q. L., & Min, Z. D. (2007). [Structure modification on sesquiterpene lactones from Elephantopus scaber]. Yao Xue Xue Bao = Acta Pharmaceutica Sinica, 42(11), 1159-61.
Liang QL, Min ZD. [Structure Modification On Sesquiterpene Lactones From Elephantopus Scaber]. Yao Xue Xue Bao. 2007;42(11):1159-61. PubMed PMID: 18300472.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - [Structure modification on sesquiterpene lactones from Elephantopus scaber].
AU - Liang,Qiao-li,
AU - Min,Zhi-da,
PY - 2008/2/28/pubmed
PY - 2009/8/7/medline
PY - 2008/2/28/entrez
SP - 1159
EP - 61
JF - Yao xue xue bao = Acta pharmaceutica Sinica
JO - Yao Xue Xue Bao
VL - 42
IS - 11
N2 - In order to look for lower toxic and strongly active compounds, the structure of sesquiterpene lactones from Elephantopus scaber was modified. Deoxyelephantopin and scabertopin were isolated from the whole plant of Elephantopus scaber and hydrogenated and epoxidated. Five sesquiterpenoide derivatives were prepared and their structures were identified by IR, NMR and MS spectra analysis. Four sesquiterpenoides are new compounds. Part of the compounds show definite antitumor activity.
SN - 0513-4870
UR - https://www.unboundmedicine.com/medline/citation/18300472/[Structure_modification_on_sesquiterpene_lactones_from_Elephantopus_scaber]_
DB - PRIME
DP - Unbound Medicine
ER -