Source:http://linkedlifedata.com/resource/pubmed/id/10733610
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2000-6-19
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pubmed:abstractText |
New nitrosoureido derivatives of di- or tri-deoxy-sugars have been synthesized. Very potent antitumour activity against L1210 leukaemia was exhibited by the compounds derived from methyl 3-amino-3, 4-dideoxy-beta- and alpha- and 4-amino-2,4-dideoxy-beta- and alpha-D-arabino-hexopyranosides, 24, 26, 28 and 29, respectively. In further evaluation against B16 melanocarcinoma bearing mice, only compounds 24 and 26 displayed significant activity. Owing to its lower acute toxicity, methyl 3-[3-(2-chloroethyl)-3-nitrosoureido]-3, 4-dideoxy-beta-D-arabino-hexopyranoside 24 appeared as the best candidate for preclinical studies.
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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 |
Jan
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pubmed:issn |
0223-5234
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
35
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
137-46
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10733610-Animals,
pubmed-meshheading:10733610-Antineoplastic Agents,
pubmed-meshheading:10733610-Carmustine,
pubmed-meshheading:10733610-Glucosides,
pubmed-meshheading:10733610-Leukemia L1210,
pubmed-meshheading:10733610-Melanoma, Experimental,
pubmed-meshheading:10733610-Mice,
pubmed-meshheading:10733610-Mice, Inbred C57BL,
pubmed-meshheading:10733610-Molecular Structure,
pubmed-meshheading:10733610-Nitrosourea Compounds,
pubmed-meshheading:10733610-Structure-Activity Relationship
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pubmed:year |
2000
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pubmed:articleTitle |
Synthesis and antitumour activity of a new series of nitrosoureido sugars.
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pubmed:affiliation |
Laboratoire de pharmacochimie, unité mixte 176 CNRS/ Institut Curie, 26, rue d'Ulm, F-75248, Paris, France. Claude.Monneret@curie.fr
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pubmed:publicationType |
Journal Article,
Comparative Study
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