20(S)-Ginsenoside Rh2 as aldose reductase inhibitor from Panax ginseng

  • Sri Fatmawati
  • , Taslim Ersam
  • , Hongshan Yu
  • , Chunzhi Zhang
  • , Fengxie Jin
  • , Kuniyoshi Shimizu*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

27 Citations (Scopus)

Abstract

The root of Panax ginseng C. A. Meyer (Araliaceae) is a well-known herbal medicine in East Asia. The major bioactive metabolites in this root are commonly identified as ginsenosides. A series of ginsenosides were determined for in vitro human recombinant aldose reductase. This Letter aims to clarify the structural requirement for aldose reductase inhibition. We discovered that only ginsenoside 20(S)-Rh2 showed potent against aldose reductase, with an IC50of 147.3 μM. These results implied that the stereochemistry of the hydroxyl group at C-20 may play an important role in aldose reductase inhibition. An understanding of these requirements is considered necessary in order to develop a new type of aldose reductase inhibitor. Furthermore, P. ginseng might be an important herbal medicine in preventing diabetic complications.

Original languageEnglish
Pages (from-to)4407-4409
Number of pages3
JournalBioorganic and Medicinal Chemistry Letters
Volume24
Issue number18
DOIs
Publication statusPublished - 15 Sept 2014

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Aldose reductase inhibitor
  • Ginsenoside
  • Panax ginseng
  • Structure-activity relationships

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