51. Two new glycosides from the fruits of Forsythia suspense.
- Author
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Yan XJ, Bai XY, Liu QB, Liu S, Gao PY, Li LZ, and Song SJ
- Subjects
- Antineoplastic Agents, Phytogenic chemistry, Antineoplastic Agents, Phytogenic pharmacology, Caffeic Acids, Drug Screening Assays, Antitumor, Drugs, Chinese Herbal chemistry, Drugs, Chinese Herbal pharmacology, Fruit chemistry, Glucosides, Glycosides chemistry, Glycosides pharmacology, HL-60 Cells, Humans, KB Cells, Molecular Structure, Nuclear Magnetic Resonance, Biomolecular, Antineoplastic Agents, Phytogenic isolation & purification, Drugs, Chinese Herbal isolation & purification, Forsythia chemistry, Glycosides isolation & purification
- Abstract
Two new glycosides suspensaside C (1) and 2,3,5,6-tetrahydro-jacaranone-4-O-β-D-glucopyranoside (2), together with four known compounds suspensaside A (3), rengynic acid-1'-O-β-D-glucopyranoside (4), forsythoside A (5), and rengynic acid (6), were isolated from the fruits of Forsythia suspense (Thunb.) Vahl. The structures of 1 and 2 were elucidated on the basis of chemical and spectral analysis, including 1D, 2D NMR analyses and HR-ESI-MS. All isolates were tested for their cytotoxicities against five human cancer cell lines (A549, Colo-205, Hep-3B, HL60, and KB). Compound 3 exhibited cytotoxicity against HL-60, Hep-3B, and A549 cancer cell lines.
- Published
- 2014
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