Journal of Asian Natural Products Research · 2015 · 16 citations · 14 references
PharmacyChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistryStructure-activity RelationshipsAntiviral AgentsAntiviral PharmacologyMedicinal PlantsStructure-activity Relationship AnalysisTerpenoid BiosynthesisAntiviral Structure-activity RelationshipsMedicinal Aromatic PlantsMonoterpene BiosynthesisSesquiterpene BiosynthesisTerpene CompoundsX-ray Diffraction Analysis
Two new sesquiterpenes, oligandrin (1) and oligandric acid (2), together with three analogues, tashironin A (3), tashironin (4), and oplodiol (5), were isolated from the roots of Illicium oligandrum. The structures of new compounds were determined based on 1D and 2D NMR experiments and X-ray diffraction. Compound 1 represents a presumed biosynthetic precursor of seco-prezizaane sesquiterpenes which consists of a novel 6/6/5 tricarbocyclic skeleton. Compound 2 is the first example of chamipinene-type sesquiterpene possessing a 6/4/6 tricyclic system from the genus Illicium. Compounds 1-5 were evaluated in vitro for their activity against coxsackie virus B3 (CVB3), influenza virus A/Hanfang/359/95 (H3N2), and influenza virus A/FM/1/47 (H1N1). Compound 1 showed selective antiviral activity against CVB3 with IC50 value of 11.11 μM.
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Two New Compounds and Anti-HIV Active Constituents from <i>Illicium verum</i>
Wen-Yong Song, Yun‐Bao Ma, Xuemei Zhang et al. · Planta Medica · 2007 · 61 citations
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Sesquiterpenes from Cupressus macrocarpa foliage
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