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RESEARCH PRODUCT
The Structure and the Stereochemistry of Atractyliretin
Conrado PascualLeopoldo CerauloLorenzo CamardaVincenzo SprioMirella Ferrugiasubject
PharmacologyStereochemistryChemistryOrganic ChemistryPharmaceutical ScienceToxic substanceAnalytical Chemistrychemistry.chemical_compoundComplementary and alternative medicineDrug DiscoveryMolecular MedicineMoleculeAcid hydrolysisAtractylosideDiterpeneChemical decompositionAtractylis gummiferadescription
The nor-kaurane diterpene Atractyliretin was obtained by acid hydrolysis of Atractyloside, a toxic substance isolated from ATRACTYLIS GUMMIFERA L (Compositae). On the basis of spectral (IR, (1)H-NMR, (13)C-NMR and MS) analysis and chemical degradation its structure and stereochemistry was identified as 4.
year | journal | country | edition | language |
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1986-10-01 | Planta Medica |