pubmed-article:11407809 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:11407809 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
pubmed-article:11407809 | lifeskim:mentions | umls-concept:C0439810 | lld:lifeskim |
pubmed-article:11407809 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
pubmed-article:11407809 | lifeskim:mentions | umls-concept:C0055651 | lld:lifeskim |
pubmed-article:11407809 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:11407809 | pubmed:dateCreated | 2001-6-15 | lld:pubmed |
pubmed-article:11407809 | pubmed:abstractText | Chrysanthemol (1), a trans-eudesmane type sesquiterpene from Chrysanthemum indicum L., possesses certain anti-inflammatory activity. Its total synthesis was approached from two alternative routes and finally accomplished in ten steps from R-(+)-carvone via alpha-eudesmol (10) as the key intermediate. The overall yield is 2.4% and the spectral data of the synthetic target compound were identical with that of natural chrysanthemol (1). Seven intermediary compounds were tested for inhibitory effects on the carragenan-induced swelling of mouse paw but demonstrated no obvious activities. | lld:pubmed |
pubmed-article:11407809 | pubmed:language | eng | lld:pubmed |
pubmed-article:11407809 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11407809 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:11407809 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11407809 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11407809 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11407809 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11407809 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11407809 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11407809 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11407809 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11407809 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:11407809 | pubmed:issn | 1028-6020 | lld:pubmed |
pubmed-article:11407809 | pubmed:author | pubmed-author:LinZ YZY | lld:pubmed |
pubmed-article:11407809 | pubmed:author | pubmed-author:LiangX TXT | lld:pubmed |
pubmed-article:11407809 | pubmed:author | pubmed-author:ZhuL YLY | lld:pubmed |
pubmed-article:11407809 | pubmed:author | pubmed-author:PazR MRM | lld:pubmed |
pubmed-article:11407809 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:11407809 | pubmed:volume | 3 | lld:pubmed |
pubmed-article:11407809 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:11407809 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:11407809 | pubmed:pagination | 103-16 | lld:pubmed |
pubmed-article:11407809 | pubmed:dateRevised | 2009-7-21 | lld:pubmed |
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pubmed-article:11407809 | pubmed:year | 2001 | lld:pubmed |
pubmed-article:11407809 | pubmed:articleTitle | Stereoselective total synthesis of chrysanthemol. | lld:pubmed |
pubmed-article:11407809 | pubmed:affiliation | Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing. | lld:pubmed |
pubmed-article:11407809 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:11407809 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |