Triterpenoid saponins from the roots of Pulsatilla koreana

• Published in: Journal of natural products (Washington, D.C.) Vol. 68; no. 2; pp. 268 - 272
• Main Authors: Bang, S.C, Kim, Y, Lee, J.H, Ahn, B.Z
• Format: Journal Article
• Language: English
• Published: Washington, DC American Chemical Society 01-02-2005; Glendale, AZ American Society of Pharmacognosy
• Subjects: Anemone; Anemone cernua; anticarcinogenic activity; Antineoplastic Agents, Phytogenic - chemistry; Antineoplastic Agents, Phytogenic - isolation & purification; Antineoplastic Agents, Phytogenic - pharmacology; Biological and medical sciences; cell lines; chemical structure; cytotoxicity; Drug Screening Assays, Antitumor; General pharmacology; Humans; Korea; lupanes; Medical sciences; medicinal plants; Molecular Structure; oleanane; Pharmacognosy. Homeopathy. Health food; Pharmacology. Drug treatments; phytochemicals; plant extracts; Plant Roots - chemistry; Plants, Medicinal - chemistry; Pulsatilla koreana; roots; Saponins - chemistry; Saponins - isolation & purification; Saponins - pharmacology; spectral analysis; stereochemistry; Triterpenes - chemistry; Triterpenes - isolation & purification; Triterpenes - pharmacology; triterpenoid saponins; Tumor Cells, Cultured; Korea; Carcinoma; Lung; Cytotoxicity; NMR spectrometry; Saponin; Hydrogen 1; Dicotyledones; Angiospermae; Glycoside; Carbon 13; Tumor cell; Below ground plant part; Human; Terpenoid; Root; Ranunculaceae; Malignant tumor; In vitro; Biological activity; Oleanane derivatives; Cell line; Hydroxyacid; Plant origin; Triterpene; Isolation; Spermatophyta; Tetrasaccharide; Structural analysis
• ISSN: 0163-3864; 1520-6025
• DOI: 10.1021/np049813h

Six new saponins, five lupanes (1-5) and one oleanane (6), along with 11 known saponins, were isolated from the roots of Pulsatilla koreana. The structures of the new saponins were found to be 23-hydroxy-3beta-[(O-alpha-L-rhamnopyranosyl-(1-->2)-O-[O-beta-D-glucopyranosyl-(1-->4)]-alpha-L-arabinopyranosyl)oxy]lup-20(29)-en-28-oic acid (1), 23-hydroxy-3beta-[(O-beta-D-glucopyranosyl-(1-->3)-O-alpha-L-rhamnopyranosyl-(1-->2)-alpha-L-arabinopyranosyl)oxy]lup-20(29)-en-28-oic acid (2), 3beta-[(O-alpha-L-rhamnopyranosyl-(1-->2)-O-[O-beta-D-glucopyranosyl-(1-->4)]-alpha-L-arabinopyranosyl)oxy]lup-20(29)-en-28-oic acid (3), 3beta-[(O-beta-D-glucopyranosyl-(1-->3)-O-alpha-L-rhamnopyranosyl-(1-->2)-alpha-L-arabinopyranosyl)oxy]lup-20(29)-en-28-oic acid (4), 23-hydroxy-3beta-[(O-beta-D-glucopyranosyl-(1-->4)-alpha-L-arabinopyranosyl)oxy]lup-20(29)-en-28-oic acid (5), and hederagenin 3-O-beta-D-glucopyranosyl-(1-->4)-beta-D-glucopyranosyl-(1-->3)-alpha-L-rhamnopyranosyl-(1-->2)-alpha-L-arabinopyranoside (6). Their structures were determined on the basis of 1D and 2D NMR ((13)C NMR, (1)H NMR, (1)H-(1)H COSY, HMQC, and HMBC) methods, FABMS, and hydrolysis. All isolated compounds were evaluated for their cytotoxic activity against A-549 human lung carcinoma cells.