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dianoside/dianthus superbus
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5 results
Structures of Dianosides A and B, Analgesic Principles of Dianthus superbus var. longicalycinus Herbs1.
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Novel triterpenoid saponins, dianosides A and B, showing analgesic activity, have been isolated from DIANTHUS SUPERBUS var. LONGICALYCINUS herbs. Degradative and spectroscopic studies have established their structures as shown in formulas 1 and 2.
Structure of Dianosides C, D, E and F, Triterpenoid Saponins of Dianthus superbus var. longicalycinus Herb1.
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On the basis of chemical and spectroscopic evidence, the structures of four triterpenoid saponins, dianosides C, D, E and F, from DIANTHUS SUPERBUS var. LONGICALYCINUS herb, have been elucidated as shown in formulas 1, 2, 3 and 4, respectively.
Structures of Dianosides G, H and I, Triterpenoid Saponins of Dianthus superbus var. longicalycinus Herbs1.
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Three novel triterpenoid saponins, dianosides G, H and I, together with the known saponin, azukisaponin IV, have been isolated from DIANTHUS SUPERBUS var. LONGICALYCINUS. The structures of the new saponins have been assigned as indicated in formulas 1,2 and 3, respectively, by spectral and chemical
Analgesic and antihepatotoxic actions of dianosides, triterpenoid saponins of Dianthus superbus var. longicalycinus herbs.
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Longicalycinin A, a new cytotoxic cyclic peptide from Dianthus superbus var. longicalycinus (MAXIM.) WILL.
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A new cyclic peptide, longicalycinin A (1), and six known compounds, vaccaroside A, dianoside A, dianoside G, 3-(4-hydroxy-3-methoxy-phenyl)propionic acid methyl ester, p-hydroxybenzoic acid, and p-hydroxybenzaldehyde were isolated from the MeOH extract of Dianthus superbus var. longicalycinus. The
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