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Herbicidal and Cytotoxic Constituents from Aralia armata (Wall.) Seem
- Source :
- Chemistrybiodiversity. 13(4)
- Publication Year :
- 2015
-
Abstract
- Two new triterpenoids, 3β-hydroxyoleana-11,13(18)-diene-28,30-dioic acid (1) and 3-oxooleana-11,13(18)-diene-28,30-dioic acid (2), one novel triterpenoid glycoside, 3β-O-(6'-O-methyl-β-D-glucuronopyranosyl)oleana-11,13(18)-dien-28-oic acid (3) along with six known compounds (4 - 9) were isolated from the stem bark of Aralia armata (Wall.) Seem. Their structures were elucidated through extensive spectroscopic methods. The herbicidal activities of these compounds against Bidens pilosa L., an invasive weed in P. R. China, were evaluated. Compounds 3, 5, and 6 exhibited more significant herbicidal activities on B. pilosa than the positive-control pendimethalin. Their possible use as herbicidal chemicals or model compounds deserved more attention. The effects of compounds 1 - 9 on Spodoptera litura cultured cell line Sl-1 cell proliferation and its morphology were also evaluated. The results indicated that compounds 1 - 5 affected Sl-1 cell proliferation. Compound 3 showed more obvious proliferation inhibition activities on Sl-1 cell than the positive-control rotenone. With regard to the effect on morphology, compound 2 significantly changed Sl-1 cell, resulting in cell blebbing and vacuole forming. Triterpenoids aremedicinally and agriculturally important, and cytotoxicity of the three new compounds 1 - 3 deserved further studies.
- Subjects :
- Stereochemistry
Cell
Spodoptera litura
Bioengineering
Spodoptera
01 natural sciences
Biochemistry
Cell Line
chemistry.chemical_compound
medicine
Animals
Cytotoxicity
Molecular Biology
chemistry.chemical_classification
biology
010405 organic chemistry
Cell growth
Herbicides
Glycoside
General Chemistry
General Medicine
Rotenone
Aralia
biology.organism_classification
Antineoplastic Agents, Phytogenic
0104 chemical sciences
010404 medicinal & biomolecular chemistry
medicine.anatomical_structure
chemistry
Bidens pilosa
Molecular Medicine
Subjects
Details
- ISSN :
- 16121880
- Volume :
- 13
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- Chemistrybiodiversity
- Accession number :
- edsair.doi.dedup.....7468a8c28261ba28b52c91abfd8cb67e