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Antiviral spirooliganones A and B with unprecedented skeletons from the roots of Illicium oligandrum.
- Source :
-
Organic letters [Org Lett] 2013 Sep 06; Vol. 15 (17), pp. 4450-3. Date of Electronic Publication: 2013 Aug 12. - Publication Year :
- 2013
-
Abstract
- Two novel spirooliganones A (1) and (2), a pair of spiro carbon epimers, with a rare dioxaspiro skeleton were isolated from the roots of Illicium oligandrum. The structures were fully determined by spectroscopic analysis and chemical methods, especially modified Mosher's method, and X-ray diffraction analysis. Spirooliganone B was found to exhibit more potent activities against coxsackie virus B3 and influenza virus A (H3N2) (IC50 3.70-5.05 μM) than spirooliganone A. The biosynthetic pathway involving a hetero-Diels-Alder reaction of the epimers was proposed.
- Subjects :
- Antiviral Agents chemistry
Cycloaddition Reaction
Enterovirus B, Human drug effects
Influenza A Virus, H3N2 Subtype drug effects
Molecular Structure
Plant Roots chemistry
Spiro Compounds chemistry
Stereoisomerism
Antiviral Agents isolation & purification
Antiviral Agents pharmacology
Illicium chemistry
Spiro Compounds isolation & purification
Spiro Compounds pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1523-7052
- Volume :
- 15
- Issue :
- 17
- Database :
- MEDLINE
- Journal :
- Organic letters
- Publication Type :
- Academic Journal
- Accession number :
- 23937631
- Full Text :
- https://doi.org/10.1021/ol401992s