| pubmed-article:19683442 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:19683442 | lifeskim:mentions | umls-concept:C0684249 | lld:lifeskim |
| pubmed-article:19683442 | lifeskim:mentions | umls-concept:C0162638 | lld:lifeskim |
| pubmed-article:19683442 | lifeskim:mentions | umls-concept:C0004391 | lld:lifeskim |
| pubmed-article:19683442 | lifeskim:mentions | umls-concept:C0334227 | lld:lifeskim |
| pubmed-article:19683442 | lifeskim:mentions | umls-concept:C0072662 | lld:lifeskim |
| pubmed-article:19683442 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:19683442 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:19683442 | lifeskim:mentions | umls-concept:C1709060 | lld:lifeskim |
| pubmed-article:19683442 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:19683442 | lifeskim:mentions | umls-concept:C1880355 | lld:lifeskim |
| pubmed-article:19683442 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:19683442 | lifeskim:mentions | umls-concept:C0243072 | lld:lifeskim |
| pubmed-article:19683442 | pubmed:issue | 18 | lld:pubmed |
| pubmed-article:19683442 | pubmed:dateCreated | 2009-8-26 | lld:pubmed |
| pubmed-article:19683442 | pubmed:abstractText | A series of novel 3-aryl-1-arylmethyl-1H-pyrazole-5-carboxamide derivatives 3a-l, were synthesized by the reaction of 3-aryl-1-arylmethyl-1H-pyrazole-5-carbonyl chloride with substituted amine in excellent yields. The compounds 3e-h could suppress A549 lung cancer cell growth. More interestingly, compounds 3e and 3f might inhibit the A549 cell growth by inducing apoptosis; whereas compounds 3g and 3h with fluorine group might inhibit the A549 cell growth by inducing autophagy. | lld:pubmed |
| pubmed-article:19683442 | pubmed:language | eng | lld:pubmed |
| pubmed-article:19683442 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19683442 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:19683442 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19683442 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19683442 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19683442 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:19683442 | pubmed:issn | 1464-3405 | lld:pubmed |
| pubmed-article:19683442 | pubmed:author | pubmed-author:MiaoJun-YingJ... | lld:pubmed |
| pubmed-article:19683442 | pubmed:author | pubmed-author:ZhaoBao-Xiang... | lld:pubmed |
| pubmed-article:19683442 | pubmed:author | pubmed-author:ZhangHai-YanH... | lld:pubmed |
| pubmed-article:19683442 | pubmed:author | pubmed-author:LeiQiQ | lld:pubmed |
| pubmed-article:19683442 | pubmed:author | pubmed-author:DingXiao-Ling... | lld:pubmed |
| pubmed-article:19683442 | pubmed:author | pubmed-author:LianSongS | lld:pubmed |
| pubmed-article:19683442 | pubmed:author | pubmed-author:LvHong-ShuiHS | lld:pubmed |
| pubmed-article:19683442 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:19683442 | pubmed:day | 15 | lld:pubmed |
| pubmed-article:19683442 | pubmed:volume | 19 | lld:pubmed |
| pubmed-article:19683442 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19683442 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19683442 | pubmed:pagination | 5325-8 | lld:pubmed |
| pubmed-article:19683442 | pubmed:meshHeading | pubmed-meshheading:19683442... | lld:pubmed |
| pubmed-article:19683442 | pubmed:meshHeading | pubmed-meshheading:19683442... | lld:pubmed |
| pubmed-article:19683442 | pubmed:meshHeading | pubmed-meshheading:19683442... | lld:pubmed |
| pubmed-article:19683442 | pubmed:meshHeading | pubmed-meshheading:19683442... | lld:pubmed |
| pubmed-article:19683442 | pubmed:meshHeading | pubmed-meshheading:19683442... | lld:pubmed |
| pubmed-article:19683442 | pubmed:meshHeading | pubmed-meshheading:19683442... | lld:pubmed |
| pubmed-article:19683442 | pubmed:meshHeading | pubmed-meshheading:19683442... | lld:pubmed |
| pubmed-article:19683442 | pubmed:meshHeading | pubmed-meshheading:19683442... | lld:pubmed |
| pubmed-article:19683442 | pubmed:meshHeading | pubmed-meshheading:19683442... | lld:pubmed |
| pubmed-article:19683442 | pubmed:meshHeading | pubmed-meshheading:19683442... | lld:pubmed |
| pubmed-article:19683442 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:19683442 | pubmed:articleTitle | Synthesis of novel pyrazole carboxamide derivatives and discovery of modulators for apoptosis or autophagy in A549 lung cancer cells. | lld:pubmed |
| pubmed-article:19683442 | pubmed:affiliation | Institute of Organic Chemistry, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, PR China. | lld:pubmed |
| pubmed-article:19683442 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:19683442 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| http://linkedlifedata.com/r... | http://linkedlifedata.com/r... | pubmed-article:19683442 | lld:chembl |
