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Structural elucidation and urease inhibitory activity of four compounds isolated from the Curcuma aromatica Salisb. rhizomes

Tho Huu Le 1, * ORCID logo
Ngoc Thi Hoang 2
Nga Thuy Thanh Le 2
Hai Xuan Nguyen 2
Truong Nhat Van Do 2
Mai Thanh Thi Nguyen 2
Nhan Trung Nguyen 2
  1. Faculty of Chemistry, University of Science, VNU-HCM, Research Lab for Drug Discovery and Development, University of Science, VNU-HCM
  2. Faculty of Chemistry, University of Science, Ho Chi Minh City, Vietnam
Correspondence to: Tho Huu Le, Faculty of Chemistry, University of Science, VNU-HCM, Research Lab for Drug Discovery and Development, University of Science, VNU-HCM. ORCID: https://orcid.org/0000-0001-9623-2858. Email: lhtho@hcmus.edu.vn.
Volume & Issue: Vol. 9 No. 1 (2025) | Page No.: 3248-3256 | DOI: 10.32508/stdjns.v9i1.1394
Published: 2025-03-31

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This article is published with open access by Viet Nam National University Ho Chi Minh City, Viet Nam. This article is distributed under the terms of the Creative Commons Attribution License (CC-BY 4.0) which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.

Abstract

White turmeric (Curcuma aromatica Salisb.) belonging to the ginger family (Zingiberaceae), is widely distributed in tropical and subtropical regions such as India, China, Japan, and Southeast Asian countries. In traditional Vietnamese medicine, white turmeric rhizomes are used to treat gastrointestinal disorders, skin infections, joint pain, and insect bites. This paper reports the isolation and structural elucidation of four compounds from the fraction NTC-F of the white turmeric rhizomes. The chemical structures of these compounds were elucidated by analyzing nuclear magnetic resonance (1D- and 2D-NMR) spectroscopic data, high-resolution electrospray ionization mass spectrometry (HRESI-MS) data, and comparison with references in the literature. The isolated compounds were meso-hannokinol (1), anti-3-acetoxy-5-hydroxy-1,7-bis(4-hydroxyphenyl)heptane (2), longpene A (3) and (12Z,14R)-labda-8(17),12-diene-14,15,16-triol (4). All four were evaluated for urease inhibitory activity, and compound (1) exhibited significant urease inhibitory activity with an IC50 value of 86.7 μM, compared to the positive control hydroxyurea (IC50 74.5 μM). This result could contribute the species Curcuma aromatica to the database of Vietnamese medicinal plants with the potential to treat Helicobacter pylori-induced gastric ulcers.

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