Source:http://linkedlifedata.com/resource/pubmed/id/19683442
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
18
|
| pubmed:dateCreated |
2009-8-26
|
| 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.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Sep
|
| pubmed:issn |
1464-3405
|
| pubmed:author | |
| pubmed:issnType |
Electronic
|
| pubmed:day |
15
|
| pubmed:volume |
19
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
5325-8
|
| pubmed:meshHeading |
pubmed-meshheading:19683442-Antineoplastic Agents,
pubmed-meshheading:19683442-Apoptosis,
pubmed-meshheading:19683442-Autophagy,
pubmed-meshheading:19683442-Carcinoma,
pubmed-meshheading:19683442-Cell Line, Tumor,
pubmed-meshheading:19683442-Cell Proliferation,
pubmed-meshheading:19683442-Humans,
pubmed-meshheading:19683442-Lung Neoplasms,
pubmed-meshheading:19683442-Pyrazoles,
pubmed-meshheading:19683442-Structure-Activity Relationship
|
| pubmed:year |
2009
|
| pubmed:articleTitle |
Synthesis of novel pyrazole carboxamide derivatives and discovery of modulators for apoptosis or autophagy in A549 lung cancer cells.
|
| pubmed:affiliation |
Institute of Organic Chemistry, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, PR China.
|
| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|