Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/66953
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Type: Journal article
Title: In vivo activity of benzoyl ester clerodane diterpenoid derivatives from Dodonaea polyandra
Author: Simpson, B.
Claudie, D.
Gerber, J.
Pyke, S.
Wang, J.
McKinnon, R.
Semple, S.
Citation: Journal of Natural Products, 2011; 74(4):650-657
Publisher: Amer Chemical Soc
Issue Date: 2011
ISSN: 0163-3864
1520-6025
Statement of
Responsibility: 
Bradley S. Simpson, David J. Claudie, Jacobus P. Gerber, Simon M. Pyke, Jiping Wang, Ross A. McKinnon and Susan J. Semple
Abstract: Four new benzoyl ester clerodane diterpenoids, 15,16-epoxy-8α-(benzoyloxy)methylcleroda-3,13(16),14-trien-18-oic acid (1), 15,16-epoxy-8α-(benzoyloxy)methyl-2α-hydroxycleroda-3,13(16),14-trien-18-oic acid (2), 15,16-epoxy-8α-(benzoyloxy)methyl-2-oxocleroda-3,13(16),14-trien-18-oic acid (3), and 15,16-epoxy-2α-benzoyloxycleroda-3,13(16),14-trien-18-oic acid (4), have been isolated from the leaves and stems of Dodonaea polyandra. The anti-inflammatory activities of compounds 1, 2, and 4 were evaluated by means of 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced mouse ear edema. Compounds 2 and 4 exhibited maximum inhibition of inflammation (70-76%) at doses of 0.22 and 0.9 μmol/ear, respectively. Modest activity (~45% inhibition) was maintained at nanomole/ear doses.
Keywords: Ear
Animals
Mice
Sapindaceae
Plant Leaves
Plant Stems
Disease Models, Animal
Edema
Diterpenes, Clerodane
Tetradecanoylphorbol Acetate
Anti-Inflammatory Agents, Non-Steroidal
Molecular Structure
Australia
Rights: Copyright © 2011 The American Chemical Society and American Society of Pharmacognosy
DOI: 10.1021/np100701s
Grant ID: ARC
Published version: http://dx.doi.org/10.1021/np100701s
Appears in Collections:Aurora harvest 5
Chemistry and Physics publications

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