Structures of new beta-carboline-type alkaloids with antiallergic effects from Stellaria dichotoma(1,2).

Abstract

The aqueous ethanolic extract from the roots of Stellaria dichotoma showed an antiallergic effect on ear passive cutaneous anaphylaxis (PCA) reaction in mice (in vivo) and inhibitory activity on the release of beta-hexosaminidase in RBL-2H3 cells (in vitro). From the aqueous ethanolic extract, new beta-carboline-type alkaloids, dichotomines A (1), B (2), C (3), and D (4) and dichotomides I (5) and II (6), were isolated. The structures of the new constituents (1-6) were determined on the basis of chemical and physicochemical evidence, including the application of the modified Mosher's method. The effects of the isolated constituents on the release of beta-hexosaminidase in RBL-2H3 cells were examined, and 3 was found to show inhibitory activity (IC(50) = 62 microM). Moreover, 3 also inhibited the releases of antigen-IgE-mediated TNF-alpha and IL-4 (19 and 15 microM, respectively) in RBL-2H3 cells, both of which participate in the late phase of type I allergic reactions.

• Authors: Bohang Sun, Toshio Morikawa, Hisashi Matsuda, Supinya Tewtrakul, Li Jun Wu, Shoichi Harima, Masayuki Yoshikawa
• Journal: Journal of natural products (J Nat Prod) Vol. 67 Issue 9 Pg. 1464-9 (Sep 2004) ISSN: 0163-3864 [Print] United States
• PMID: 15387643 (Publication Type: Journal Article)

Chemical References

• Alkaloids
• Anti-Allergic Agents
• Carbolines
• Tumor Necrosis Factor-alpha
• Hexosaminidases

Topics

• Alkaloids (chemistry, isolation & purification, pharmacology)
• Animals
• Anti-Allergic Agents (chemistry, isolation & purification, pharmacology)
• Carbolines (chemistry, isolation & purification, pharmacology)
• China
• Hexosaminidases (antagonists & inhibitors)
• Inhibitory Concentration 50
• Male
• Mice
• Molecular Structure
• Nuclear Magnetic Resonance, Biomolecular
• Passive Cutaneous Anaphylaxis
• Plant Roots (chemistry)
• Plants, Medicinal (chemistry)
• Stellaria (chemistry)
• Tumor Necrosis Factor-alpha (antagonists & inhibitors)