Source:http://linkedlifedata.com/resource/pubmed/id/19850476
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
23
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pubmed:dateCreated |
2009-11-5
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pubmed:abstractText |
A preliminary library of novel N(6),5'-bis-ureidoadenosine analogs and related derivatives was prepared and tested for activity against the NCI 60 panel of human cancers. A 2'-O-TBS group was found to be necessary, but not sufficient, for optimal antiproliferative activity. Neither the N(6)- nor 5'-ureido substituents were sufficient to achieve significant antiproliferative effects when present in the absence of the other. The 2'-O-TBS, and N(6),5'-bis-ureido substitution patterns were found to be necessary for optimal antiproliferative 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 |
1464-3405
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
1
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
6775-9
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pubmed:meshHeading |
pubmed-meshheading:19850476-Adenosine,
pubmed-meshheading:19850476-Antineoplastic Agents,
pubmed-meshheading:19850476-Cell Line, Tumor,
pubmed-meshheading:19850476-Cell Proliferation,
pubmed-meshheading:19850476-Drug Screening Assays, Antitumor,
pubmed-meshheading:19850476-Humans,
pubmed-meshheading:19850476-Methylurea Compounds,
pubmed-meshheading:19850476-Molecular Structure,
pubmed-meshheading:19850476-Stereoisomerism,
pubmed-meshheading:19850476-Structure-Activity Relationship
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pubmed:year |
2009
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pubmed:articleTitle |
Preliminary SAR analysis of novel antiproliferative N(6),5'-bis-ureidoadenosine derivatives.
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pubmed:affiliation |
Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT 84602, United States. matt_peterson@byu.edu
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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