Angiotensin-I-Converting Enzyme Inhibitory Activity of Coumarins from Angelica decursiva

  • Md Yousof Ali
  • , Su Hui Seong
  • , Hyun Ah Jung*
  • , Jae Sue Choi
  • *Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

Abstract

The bioactivity of ten traditional Korean Angelica species were screened by angiotensin-converting enzyme (ACE) assay in vitro. Among the crude extracts, the methanol extract of Angelica decursiva whole plants exhibited potent inhibitory effects against ACE. In addition, the ACE inhibitory activity of coumarins 1–5, 8–18 was evaluated, along with two phenolic acids (6, 7) obtained from A. decursiva. Among profound coumarins, 11–18 were determined to manifest marked inhibitory activity against ACE with IC50 values of 4.68–20.04 µM. Compounds 12, 13, and 15 displayed competitive inhibition against ACE. Molecular docking studies confirmed that coumarins inhibited ACE via many hydrogen bond and hydrophobic interactions with catalytic residues and zinc ion of C- and N-domain ACE that blocked the catalytic activity of ACE. The results derived from these computational and in vitro experiments give additional scientific support to the anecdotal use of A. decursiva in traditional medicine to treat cardiovascular diseases such as hypertension.

Original languageEnglish
Article number3937
JournalMolecules
Volume24
Issue number21
DOIs
StatePublished - 2019

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

  • Angelica decursiva
  • Angiotensin-I-converting enzyme
  • Antihypertension
  • Coumarins
  • Molecular docking

Quacquarelli Symonds(QS) Subject Topics

  • Medicine
  • Engineering - Petroleum
  • Pharmacy & Pharmacology
  • Chemistry

Fingerprint

Dive into the research topics of 'Angiotensin-I-Converting Enzyme Inhibitory Activity of Coumarins from Angelica decursiva'. Together they form a unique fingerprint.

Cite this