| Literature DB >> 18590964 |
Maya Spasova1, Stefan Philipov, L Nikolaeva-Glomb, A S Galabov, Ts Milkova.
Abstract
The aporphine alkaloid glaucine has been converted into 3-aminomethylglaucine and its free amino group has been linked to cinnamic, ferulic, sinapic, o-, and p-coumaric acids. The antioxidative potential of the synthesized amides was studied against DPPH(*) test. All of the tested compounds demonstrated higher radical scavenging activity than glaucine and 3-aminomethylglaucine, and lower antioxidative effect than the free hydroxycinnamic acids. The newly synthesized compounds were tested in vitro for antiviral activity against viruses belonging to different taxonomic groups.Entities:
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Year: 2008 PMID: 18590964 DOI: 10.1016/j.bmc.2008.06.010
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641