Abstract | OBJECTIVES:
Quillaic acid is the major aglycone of the widely studied saponins of the Chilean indigenous tree Quillaja saponaria Mol. The industrial availability of quillaja saponins and the extensive functionalization of this triterpenoid provide unique opportunities for structural modification and pose a challenge from the standpoint of selectivity in regard to one or the other secondary alcohol group, the aldehyde, and the carboxylic acid functions. The anti-inflammatory activity of this sapogenin has not been studied previously and it has never been used to obtain potential anti-inflammatory derivatives. METHODS: KEY FINDINGS:
Quillaic acid exhibited strong topical anti-inflammatory activity in both models. Most of its derivatives were less potent, but the hydrazone 8 showed similar potency to quillaic acid in the TPA assay. CONCLUSIONS: The structural modifications performed and the biological results suggest that the aldehyde and carboxyl groups are relevant to the anti-inflammatory activity in these models.
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Authors | Maité Rodríguez-Díaz, Carla Delporte, Carlos Cartagena, Bruce K Cassels, Patricia González, Ximena Silva, Fredy León, Ludger A Wessjohann |
Journal | The Journal of pharmacy and pharmacology
(J Pharm Pharmacol)
Vol. 63
Issue 5
Pg. 718-24
(May 2011)
ISSN: 2042-7158 [Electronic] England |
PMID | 21492174
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2011 The Authors. JPP © 2011 Royal Pharmaceutical Society. |
Chemical References |
- Anti-Inflammatory Agents
- Phorbol Esters
- Plant Extracts
- Arachidonic Acid
- quillaic acid
- Oleanolic Acid
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Topics |
- Administration, Topical
- Animals
- Anti-Inflammatory Agents
(administration & dosage, pharmacology)
- Arachidonic Acid
- Inflammation
(chemically induced, drug therapy)
- Male
- Mice
- Mice, Inbred Strains
- Oleanolic Acid
(administration & dosage, analogs & derivatives, pharmacology)
- Phorbol Esters
- Phytotherapy
- Plant Extracts
(administration & dosage, pharmacology)
- Quillaja
(chemistry)
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