4.6 Article

Phenanthrene derivatives from roots and rhizomes of Asarum heterotropoides var. mandshuricum

Journal

FITOTERAPIA
Volume 117, Issue -, Pages 101-108

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.fitote.2017.01.008

Keywords

Asarum heterotropoides var. mandshuricum; Phenanthrene derivatives; Aristolochic acid; Aristololactam; Nephrotoxicity

Funding

  1. National Natural Science Foundation of China [81274073, 81173494]
  2. 985 Project of Peking University
  3. National Eleventh Five-year Key Technologies R&D Program of China [2006BAI14B01]

Ask authors/readers for more resources

Five new phenanthrene derivatives: 9-ethoxy-7-methoxy-aristololactam IV (1), norcepharadione A N-beta-D-glucopyranoside (2), aristololactamoside I (3), aristololactamoside II (4) and aristothiolactoside (5) together with eleven known phenanthrene derivatives (6-16) were isolated from the ethanol extract of the roots and rhizomes of Asarum heterotropoides var. mandshuricum. The aristololactams with substitution of ethoxy at C-9 position (1, 9, and 10) and the sulfur-containing phenanthrene derivative (5) were reported in the genus Asarum for the first time. Furthermore, six phenanthrene glucoside derivatives (2-5, 13 and 14) were also found in this genus for the first time and compounds 7 and 9-15 were isolated from the genus Asarum for the first time. Six of them (1, 2, 9, 10, 13 and 14) were submitted to cytotoxicity test against human renal proximal tubular epithelial cell lines (HK-2) using mu and LDH assays. Compounds 1 and 10 showed significant cytotoxic activity against HK-2 cell lines with IC50 values of 18.18 and 20.44 mu mol/L in MIT assay and 8436 and 35.06 mu mol/L in LDH assay, respectively. Compound 9 showed moderate cytotoxicity in MIT assay with IC50 values of 95.60 mu mol/L, but no cytotoxicity in LDH assay. Compounds 2, 13 and 14 showed cytotoxic effect in neither MIT assay nor LDH assay. Considering the other nephrotoxic phenanthrene derivatives (6, 8, 12, 15 and 16) previously tested, the results implied the potency of renal toxicity of this herb used as a medicine. (C) 2017 Published by Elsevier B.V.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available