Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10594347 | Bioorganic & Medicinal Chemistry Letters | 2012 | 5 Pages |
Abstract
The primary amino function of teicoplanin pseudoaglycon has been transformed into arylthioisoindole or benzoisoindole and glycosylthioisoindole derivatives, in a reaction with o-phthalaldehyde or naphtalene-2,3-dicarbaldehyde and various thiols. All of the obtained semisynthetic antibiotics exhibited potent antibacterial activities against Gram-positive bacteria in the ng per ml concentration range. A few of them showed antiviral activity, in particular against influenza virus.
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Authors
Attila Sipos, Zsolt Török, Erzsébet RÅth, Attila Kiss-Szikszai, Gyula Batta, Ilona Bereczki, Zsolt Fejes, Anikó Borbás, Eszter Ostorházi, Ferenc Rozgonyi, Lieve Naesens, Pál Herczegh,