Source:http://linkedlifedata.com/resource/pubmed/id/11012027
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
19
|
pubmed:dateCreated |
2001-1-3
|
pubmed:abstractText |
A series of benzimidazole-4,7-diones bearing at the 2-position the thiomethyl group or the 2-pyridyl moiety has been synthesized and tested in vitro on three tumor cell lines. Two of them show a very good antiproliferative effect. Compounds 1 and 2d are more active or equiactive, respectively, than MMC against human lymphoblastic leukemia. Both compounds exhibit high activity on human non-Hodgkin lymphoma. Compound 1 is non toxic at all the concentrations used in the antiproliferative assay and 2d is toxic only at high concentration.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
0960-894X
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
2
|
pubmed:volume |
10
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
2193-5
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:11012027-Antibiotics, Antineoplastic,
pubmed-meshheading:11012027-Antineoplastic Agents,
pubmed-meshheading:11012027-Benzimidazoles,
pubmed-meshheading:11012027-Drug Screening Assays, Antitumor,
pubmed-meshheading:11012027-Humans,
pubmed-meshheading:11012027-Mitomycin,
pubmed-meshheading:11012027-Molecular Structure,
pubmed-meshheading:11012027-Tumor Cells, Cultured
|
pubmed:year |
2000
|
pubmed:articleTitle |
Synthesis and antiproliferative activity of some benzimidazole-4,7-dione derivatives.
|
pubmed:affiliation |
Department of Pharmaceutical Science, University of Bologna, Italy. mrobi@alma.unibo.it
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|