pubmed-article:16681032 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:16681032 | lifeskim:mentions | umls-concept:C0025914 | lld:lifeskim |
pubmed-article:16681032 | lifeskim:mentions | umls-concept:C0026809 | lld:lifeskim |
pubmed-article:16681032 | lifeskim:mentions | umls-concept:C0262950 | lld:lifeskim |
pubmed-article:16681032 | lifeskim:mentions | umls-concept:C0024880 | lld:lifeskim |
pubmed-article:16681032 | lifeskim:mentions | umls-concept:C0003693 | lld:lifeskim |
pubmed-article:16681032 | lifeskim:mentions | umls-concept:C0291982 | lld:lifeskim |
pubmed-article:16681032 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:16681032 | pubmed:dateCreated | 2006-5-9 | lld:pubmed |
pubmed-article:16681032 | pubmed:abstractText | Ochnaflavone is a medicinal herbal product isolated from Lonicera japonica that inhibits cyclooxygenase-2 (COX-2) dependent phases of prostaglandin D2 (PGD2) generation in bone marrow-derived mast cells (BMMC) in a concentration-dependent manner with IC50 values of 0.6 microM. Western blotting probed with specific anti-COX-2 antibodies showed that the decrease in quantity of the PGD2 product was accompanied by a decrease in the COX-2 protein level. In addition, this compound consistently inhibited the production of leukotriene C4 (LTC4) in a dose dependent manner, with an IC50 value of 6.56 microM. These results demonstrate that ochnaflavone has a dual cyclooxygenase-2/5-lipoxygenase inhibitory activity. Furthermore, this compound strongly inhibited degranulation reaction in a dose dependent manner, with an IC50 value of 3.01 microM. Therefore, this compound might provide a basis for novel anti-inflammatory drugs. | lld:pubmed |
pubmed-article:16681032 | pubmed:language | eng | lld:pubmed |
pubmed-article:16681032 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16681032 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:16681032 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16681032 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16681032 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16681032 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16681032 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16681032 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16681032 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16681032 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16681032 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16681032 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:16681032 | pubmed:month | Apr | lld:pubmed |
pubmed-article:16681032 | pubmed:issn | 0253-6269 | lld:pubmed |
pubmed-article:16681032 | pubmed:author | pubmed-author:KimHyun PyoHP | lld:pubmed |
pubmed-article:16681032 | pubmed:author | pubmed-author:SonKun HoKH | lld:pubmed |
pubmed-article:16681032 | pubmed:author | pubmed-author:ChangHyeun... | lld:pubmed |
pubmed-article:16681032 | pubmed:author | pubmed-author:KangSam SikSS | lld:pubmed |
pubmed-article:16681032 | pubmed:author | pubmed-author:LeeEun... | lld:pubmed |
pubmed-article:16681032 | pubmed:author | pubmed-author:MoonTae... | lld:pubmed |
pubmed-article:16681032 | pubmed:author | pubmed-author:LeeSeung HoSH | lld:pubmed |
pubmed-article:16681032 | pubmed:author | pubmed-author:SonJong... | lld:pubmed |
pubmed-article:16681032 | pubmed:author | pubmed-author:SonMin JungMJ | lld:pubmed |
pubmed-article:16681032 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:16681032 | pubmed:volume | 29 | lld:pubmed |
pubmed-article:16681032 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:16681032 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:16681032 | pubmed:pagination | 282-6 | lld:pubmed |
pubmed-article:16681032 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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pubmed-article:16681032 | pubmed:year | 2006 | lld:pubmed |
pubmed-article:16681032 | pubmed:articleTitle | Naturally occurring biflavonoid, ochnaflavone, inhibits cyclooxygenases-2 and 5-lipoxygenase in mouse bone marrow-derived mast cells. | lld:pubmed |
pubmed-article:16681032 | pubmed:affiliation | Skeletal Diseases Genome Research Center, Kyungpook National University, Daegu 702-701, Korea. | lld:pubmed |
pubmed-article:16681032 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:16681032 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:16681032 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:16681032 | lld:pubmed |