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J Med Chem ; 27(4): 548-50, 1984 Apr.
Article in English | MEDLINE | ID: mdl-6708058

ABSTRACT

Several aromatic seleno lactones have been synthesized and shown to possess significant inhibitory activity against human colon tumor-8r cells in culture at concentrations lower than 1 mM. Although all of the compounds tested were found to be active, 5-hydroxy-3-[(phenylseleno)methyl]hydrocoumarinoctanoate (3d) and 5-hydroxy-3-[(phenylseleno)methyl]hydrocoumarindecanoate (3e) were found to be the most effective in inhibiting cell growth. In situ formation of the corresponding alpha-methylene lactones is postulated to account for the cytotoxic activity in this class of compounds.


Subject(s)
Antineoplastic Agents/chemical synthesis , Coumarins/chemical synthesis , Selenium/chemical synthesis , Cell Line , Cell Survival/drug effects , Colonic Neoplasms , Coumarins/toxicity , Humans , Indicators and Reagents , Magnetic Resonance Spectroscopy , Selenium/toxicity , Structure-Activity Relationship
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