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Eur J Med Chem ; 45(1): 203-9, 2010 Jan.
Article in English | MEDLINE | ID: mdl-19853328

ABSTRACT

A series of novel phosphorylated derivatives of galanthamine 6-11 and 12-17 were synthesized in two step process with high yields. In the first step galanthamine 1 was reacted with bis (2-chloroethyl) phosphoramidic dichloride 2/4-nitrophenyl phosphorodichloridate 3 in presence of triethylamine (TEA) in dry tetrahydrofuran (THF) yielded the intermediates 4/5. They were further reacted with various compounds like 2-aminoethanol, ethyleneglycol, ethylenediamine, 2-aminoethanethiol, 2-hydroxyethanethiol, monopotassium dihydrogenphosphate to obtain the title compounds 6-11 and 12-17. The title compounds showed promising antimicrobial, antioxidant activities and was greatly influenced by the presence of different bioactive groups.


Subject(s)
Anti-Bacterial Agents/chemical synthesis , Anti-Bacterial Agents/pharmacology , Antioxidants/chemical synthesis , Antioxidants/pharmacology , Galantamine/chemical synthesis , Galantamine/pharmacology , Animals , Anti-Bacterial Agents/chemistry , Antioxidants/chemistry , Bacteria/drug effects , Catalase/metabolism , Galantamine/analogs & derivatives , Galantamine/chemistry , Glutathione/metabolism , Lipid Peroxidation/drug effects , Magnetic Resonance Spectroscopy , Microbial Sensitivity Tests , Phosphorylation , Rats , Rats, Wistar , Superoxide Dismutase/metabolism
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