Source:http://linkedlifedata.com/resource/pubmed/id/15571864
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2004-12-1
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pubmed:abstractText |
The synthesis of several acridine thioethers is described. These compounds were oxidized to give new sulfoxides and sulfones. Among 23 compounds prepared, 19 were tested in vitro against the human cancer cell lines panel of NCI screening. Activity is increased 5-10 times from sulfides to sulfoxides. Among substituted groups in the side chain, sulfur mustard, epoxy sulfide and sulfoxide displayed the most interesting activity.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0223-5234
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
39
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1029-38
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15571864-Antineoplastic Agents,
pubmed-meshheading:15571864-Cell Line, Tumor,
pubmed-meshheading:15571864-Cell Proliferation,
pubmed-meshheading:15571864-DNA Damage,
pubmed-meshheading:15571864-Drug Screening Assays, Antitumor,
pubmed-meshheading:15571864-Humans,
pubmed-meshheading:15571864-Molecular Structure,
pubmed-meshheading:15571864-Saccharomyces cerevisiae,
pubmed-meshheading:15571864-Structure-Activity Relationship,
pubmed-meshheading:15571864-Sulfides,
pubmed-meshheading:15571864-Sulfones,
pubmed-meshheading:15571864-Sulfoxides
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pubmed:year |
2004
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pubmed:articleTitle |
Synthesis of 9-acridinyl sulfur derivatives: sulfides, sulfoxides and sulfones. Comparison of their activity on tumour cells.
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pubmed:affiliation |
GERCTOP-UMR CNRS 6009, faculté de pharmacie, université de la Méditerranée, 27, boulevard Jean Moulin, 13385 Marseille 5, France. christiane.santelli@pharmacie.univ-mrs.fr
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pubmed:publicationType |
Journal Article,
Comparative Study
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