Synthesis and antiviral activity of 18α-glycyrrhizic acid and its esters

New esters (sulfate, nicotinates, and 4-methoxycinnamate) of 18α-glycyrrhizic acid (18α-GA) were synthesized; these were D/E-trans-isomers of natural 18β-GA (GA), which is the major triterpene glycoside in the roots of Spanish licorice and Urals licorice (Glycyrrhiza glabra L. and Gl. uralensis Fish...

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Veröffentlicht in:Pharmaceutical chemistry journal 2010, Vol.44 (6), p.299-302
Hauptverfasser: Baltina, L. A. Jr, Stolyarova, O. V, Baltina, L. A, Kondratenko, R. M, Plyasunova, O. A, Pokrovskii, A. G
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Sprache:eng
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Zusammenfassung:New esters (sulfate, nicotinates, and 4-methoxycinnamate) of 18α-glycyrrhizic acid (18α-GA) were synthesized; these were D/E-trans-isomers of natural 18β-GA (GA), which is the major triterpene glycoside in the roots of Spanish licorice and Urals licorice (Glycyrrhiza glabra L. and Gl. uralensis Fisher). Changes in the stereochemistry of the GA aglycone led to significant decreases in its anti-HIV-1 activity.
ISSN:0091-150X
1573-9031
DOI:10.1007/s11094-010-0454-1