4.5 Article

Acasiane A and B and Farnesirane A and B, Diterpene Derivatives From the Roots of Acacia farnesiana

Journal

PLANTA MEDICA
Volume 75, Issue 3, Pages 256-261

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0028-1112201

Keywords

Mimosoideae; Acacia farnesiana; cassane diterpene; betulinic acid; cytotoxicity; anti-inflammatory

Funding

  1. National Science Council
  2. National Science Technology Program/Biotechnology and Pharmaceuticals, Taiwan [KMUEM-97-21]
  3. Center of Excellence for Environmental Medicine, Kaohsiung Medical University

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Four new diterpenes, acasiane A (1), acasiane B (2), farnesirane A (3), and farnesirane B (4), along with three known diterpenes (5-7), two triterpenes (8 and 9), and eight flavonoids (10-17) were isolated from the roots of Acacia farnesiana. The structures and relative configurations of these compounds were determined by various spectroscopic and x-ray analyses. All isolated compounds were evaluated for their in vitro cytotoxic activities against six human cancer cell lines (Hep G2, Hep 313, MIDA-MB-231, MCF-7, A549, and Ca9-22) with the MTT method. Betulinic acid (8) displayed moderate cytotoxicity (1.70-5.74 mu g/mL) towards five human cancer cell lines and the flavonoids had slight effects. In addition, 8, diosmetin (13), and 3',4',5-trihydroxy-7-methoxyflavone (15) slightly inhibited superoxide anion generation or elastase release by human neutrophils, indicating moderate anti-inflammatory activities.

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