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A new eudesmane sesquiterpene glucoside from Liriope muscari fibrous roots.
- Source :
-
Molecules (Basel, Switzerland) [Molecules] 2011 Oct 26; Vol. 16 (11), pp. 9017-24. Date of Electronic Publication: 2011 Oct 26. - Publication Year :
- 2011
-
Abstract
- The screening of several Chinese medicinal herbs for nematocidal properties showed that the ethanol extract of Liriope muscari fibrous roots possessed significant nematocidal activity against the pine wood nematode (Bursaphelenchus xylophilus). From the ethanol extract, a new constituent (1,4-epoxy-cis-eudesm-6-O-β-D-glucopyranoside) and three known glycosides [1β,6α-dihydroxy-cis-eudesm-3-ene-6-O-β-D-glucopyranoside (liriopeoside A), 1β,6β-dihydroxy-cis-eudesm-3-ene-6-O-β-D-glucopyranoside, and 1α,6β-dihydroxy-5,10-bis-epi-eudesm-4(15)-ene-6-O-β D-glucopyranoside] were isolated by bioassay-guided fractionation. The structures were elucidated by 1D and 2D NMR and MS techniques. 1,4-Epoxy-cis-eudesm-6-O-β-D-glucopyranoside possessed moderate nemato-cidal activity against B. xylophilus with a LC(50 )value of 339.76 μg/mL, while liriopeoside A (LC(50) = 82.84 μg/mL) and 1β,6β-dihydroxy-cis-eudesm-3-ene-6-O-β-D-glucopyranoside (LC(50) = 153.39 μg/mL) also exhibited nematocidal activity against B. xylophilus. The crude extract of L. muscari fibrous roots exhibited nematocidal activity against the pine wood nematode with a LC(50) value of 182.56 μg/mL.
- Subjects :
- Animals
Antinematodal Agents chemistry
Antinematodal Agents isolation & purification
Antinematodal Agents pharmacology
Glucosides chemistry
Glucosides pharmacology
Liriope Plant anatomy & histology
Medicine, Chinese Traditional
Molecular Structure
Nematoda drug effects
Pinus parasitology
Sesquiterpenes, Eudesmane chemistry
Sesquiterpenes, Eudesmane pharmacology
Glucosides isolation & purification
Liriope Plant chemistry
Plant Roots chemistry
Sesquiterpenes, Eudesmane isolation & purification
Subjects
Details
- Language :
- English
- ISSN :
- 1420-3049
- Volume :
- 16
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Molecules (Basel, Switzerland)
- Publication Type :
- Academic Journal
- Accession number :
- 22031065
- Full Text :
- https://doi.org/10.3390/molecules16119017