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Bioorg Med Chem Lett ; 16(16): 4223-7, 2006 Aug 15.
Article in English | MEDLINE | ID: mdl-16765045

ABSTRACT

A large series of alkyl C-glycosides was synthesized from D-glucal or D-galactal. These compounds were screened against the human promyelocytic leukemia cell line (HL60), showing significant activity and apoptosis. Up to 13 C-glucopyranosides, but no C-galacto- or C-mannopyranosides, exhibited inhibitory concentrations (IC(50) values) below 20 microM, five of them in the range 4-8 microM. Preliminary structure-activity relationships were established.


Subject(s)
Antineoplastic Agents/pharmacology , Glycosides/chemistry , Leukemia/drug therapy , Leukemia/metabolism , Leukemia/pathology , Apoptosis , Cell Line, Tumor , Cell Proliferation , Drug Screening Assays, Antitumor , HL-60 Cells , Humans , Inhibitory Concentration 50 , Ketones , Models, Chemical , Structure-Activity Relationship
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