rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
8
|
pubmed:dateCreated |
1998-9-29
|
pubmed:abstractText |
The structure of a new triterpene derivative isolated from Poria cocos was determined to be 3 beta-p-hydroxybenzoyldehydrotumulosic acid by spectral and chemical methods. 3 beta-p-hydroxybenzoyldehydrotumulosic acid showed marked inhibitory activity against 12-O-tetradecanoylphorbol-13-acetate (TPA)- and arachidonic acid (AA)-induced ear inflammation in mice. The 50% inhibitory doses of 3 beta-p-hydroxybenzoyldehydrotumulosic acid were 0.27 and 1.25 mg per ear on TPA- and AA-induced inflammation, respectively.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0031-9422
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
48
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1357-60
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:9720314-Animals,
pubmed-meshheading:9720314-Anti-Inflammatory Agents, Non-Steroidal,
pubmed-meshheading:9720314-Arachidonic Acid,
pubmed-meshheading:9720314-Female,
pubmed-meshheading:9720314-Inflammation,
pubmed-meshheading:9720314-Japan,
pubmed-meshheading:9720314-Medicine, Chinese Traditional,
pubmed-meshheading:9720314-Mice,
pubmed-meshheading:9720314-Mice, Inbred ICR,
pubmed-meshheading:9720314-Molecular Structure,
pubmed-meshheading:9720314-Nuclear Magnetic Resonance, Biomolecular,
pubmed-meshheading:9720314-Plants, Medicinal,
pubmed-meshheading:9720314-Tetradecanoylphorbol Acetate,
pubmed-meshheading:9720314-Triterpenes
|
pubmed:year |
1998
|
pubmed:articleTitle |
3 beta-p-hydroxybenzoyldehydrotumulosic acid from Poria cocos, and its anti-inflammatory effect.
|
pubmed:affiliation |
College of Pharmacy, Nihon University, Chiba, Japan.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|