Anticomplement triterpenoids from the roots of Ilex asprella

Bioorg Med Chem Lett. 2017 Feb 15;27(4):880-886. doi: 10.1016/j.bmcl.2017.01.007. Epub 2017 Jan 6.

Abstract

Five new (1-5) and twenty-eight known (6-33) triterpenoids were isolated from the roots of Ilex asprella. The structures of the new compounds were elucidated by the detailed spectral analysis. The ursane and oleanane triterpenoids were found to show anticomplement activity with some structure-activity relationships. Several triterpenoids (1-3, 6-7) exhibited potent anticomplement activity with the CH50 and AP50 values of 0.058-0.131mg/mL and 0.080-0.444mg/mL, respectively. It was found that caffeoyl group could enhance activity remarkably, followed by coumaroyl and feruloyl group. The 28-carboxyl group was also important to anticomplement activity for the triterpenoids. However, the triterpenoids with lactone ring (4, 9-14) exhibited weak activity and triterpenoid glycosides (5, 23-33) showed no inhibition. The targets of several bioactive triterpenoids in complement activation cascade were identified as well.

Keywords: Anticomplement; Ilex asprella; Oleanane-type; Triterpenoids; Ursane-type.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Complement Inactivator Proteins / chemistry*
  • Complement Inactivator Proteins / isolation & purification
  • Complement Inactivator Proteins / pharmacology
  • Erythrocytes / cytology
  • Erythrocytes / drug effects
  • Erythrocytes / metabolism
  • Hemolysis / drug effects
  • Ilex / chemistry*
  • Ilex / metabolism
  • Magnetic Resonance Spectroscopy
  • Molecular Conformation
  • Oleanolic Acid / analogs & derivatives
  • Oleanolic Acid / chemistry
  • Plant Roots / chemistry
  • Plant Roots / metabolism
  • Sheep
  • Structure-Activity Relationship
  • Triterpenes / chemistry*
  • Triterpenes / isolation & purification
  • Triterpenes / pharmacology

Substances

  • Complement Inactivator Proteins
  • Triterpenes
  • anticomplement
  • oleanane
  • ursane
  • Oleanolic Acid