pubmed-article:20422266 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:20422266 | lifeskim:mentions | umls-concept:C0035647 | lld:lifeskim |
pubmed-article:20422266 | lifeskim:mentions | umls-concept:C0346647 | lld:lifeskim |
pubmed-article:20422266 | lifeskim:mentions | umls-concept:C0302350 | lld:lifeskim |
pubmed-article:20422266 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
pubmed-article:20422266 | lifeskim:mentions | umls-concept:C0243071 | lld:lifeskim |
pubmed-article:20422266 | lifeskim:mentions | umls-concept:C0076611 | lld:lifeskim |
pubmed-article:20422266 | pubmed:issue | 6 | lld:pubmed |
pubmed-article:20422266 | pubmed:dateCreated | 2010-5-18 | lld:pubmed |
pubmed-article:20422266 | pubmed:abstractText | Pancreatic cancer (PC) is one of the deadliest of all tumors. Previously, we were the first to show that Thymoquinone (TQ) derived from black seed (Nigella sativa) oil has anti-tumor activity against PC. However, the concentration of TQ required was considered to be high to show this efficacy. Therefore, novel analogs of TQ with lower IC(50) are highly desirable. | lld:pubmed |
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pubmed-article:20422266 | pubmed:language | eng | lld:pubmed |
pubmed-article:20422266 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20422266 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:20422266 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:20422266 | pubmed:month | Jun | lld:pubmed |
pubmed-article:20422266 | pubmed:issn | 1573-904X | lld:pubmed |
pubmed-article:20422266 | pubmed:author | pubmed-author:SarkarFazlul... | lld:pubmed |
pubmed-article:20422266 | pubmed:author | pubmed-author:PadhyeSubhash... | lld:pubmed |
pubmed-article:20422266 | pubmed:author | pubmed-author:MohammadRamzi... | lld:pubmed |
pubmed-article:20422266 | pubmed:author | pubmed-author:BanerjeeSanje... | lld:pubmed |
pubmed-article:20422266 | pubmed:author | pubmed-author:PhilipPhilip... | lld:pubmed |
pubmed-article:20422266 | pubmed:author | pubmed-author:BaruahJubaraj... | lld:pubmed |
pubmed-article:20422266 | pubmed:author | pubmed-author:AzmiAsfar SAS | lld:pubmed |
pubmed-article:20422266 | pubmed:author | pubmed-author:SinghMarjit... | lld:pubmed |
pubmed-article:20422266 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:20422266 | pubmed:volume | 27 | lld:pubmed |
pubmed-article:20422266 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:20422266 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:20422266 | pubmed:pagination | 1146-58 | lld:pubmed |
pubmed-article:20422266 | pubmed:dateRevised | 2011-9-26 | lld:pubmed |
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pubmed-article:20422266 | pubmed:year | 2010 | lld:pubmed |
pubmed-article:20422266 | pubmed:articleTitle | Structure-activity studies on therapeutic potential of Thymoquinone analogs in pancreatic cancer. | lld:pubmed |
pubmed-article:20422266 | pubmed:affiliation | Department of Pathology, Barbara Ann Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, Michigan 48201, USA. | lld:pubmed |
pubmed-article:20422266 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:20422266 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |