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Crude Drugs from Aquatic Plants. V. On the Constituents of Alismatis Rhizoma. (3). Stereostructures of Water-Soluble Bioactive Sesquiterpenes, Sulfoorientalols a,b,c, and d, from Chinese Alismatis Rhizoma.
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1994
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Chinese Alismatis RhizomaSecondary MetabolitePharmaceutical ChemistryMedicinal ChemistryBiochemistryBioassay-guided IsolationAlismatis RhizomaCrude DrugsPharmacologyNatural Product SynthesisSulfoorientalol CongenersSynthetic CongenersAquatic PlantsNatural SciencesPhysiologyMicrobiologyPhytochemistryMedicineDrug Discovery
From the water-soluble portion of Chinese Alismatis Rhizoma, four bioactive sesquiterpenes, sulfoorientalols a, b, c, and d, were isolated and their structures having a sulfonic acid function were established on the basis of chemical and physicochemical evidence. In addition, two sulfoorientalol congeners were derived from alismol by sulfonation of the exo-methylene moiety. Sulfoorientalols and the synthetic congeners were found to inhibit the carbachol-induced contraction of isolated bladder smooth muscle of guinea pig.