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Nitric oxide radical scavenging activity of compounds isolated from Plantago major

Tho Huu Le 1, * ORCID logo
Vi Phuong Trinh 2, 3
Anh Phuong Nguyen Vu 2, 3
Hai Xuan Nguyen 2, 3, 4
Truong Nhat Van Do 2, 3, 4
Khang Minh Le 5, 3
Quang That Ton 2, 3
Mai Thanh Thi Nguyen 2, 3, 4
  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
  3. Vietnam National University, Ho Chi Minh City, Vietnam
  4. Research Lab for Drug Discovery and Development, University of Science, Ho Chi Minh City, Vietnam
  5. Central Laboratory for Analysis, 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. 10 No. 1 (2026) | Page No.: 3556-3563 | DOI: 10.32508/stdjns.v10i1.1409
Published: 2026-03-27

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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

Plantago major, a perennial herbaceous plant found across various provinces in Vietnam, is known for its short stem, growing 15-45 cm tall, with fibrous roots forming clusters. A study investigating the nitric oxide (NO) radical scavenging activity of several Vietnamese medicinal plants revealed that the methanol extract of P. major exhibited significant inhibitory activity with an IC50 value of 75,8 μg/mL. Utilizing column chromatography combined with preparative thin-layer chromatography on both normal and reverse phases, fractions PMA and PMC of this species led to the isolation of eight compounds. These include two iridoids: 3β-methoxyartselawnin C (1) and iridolactone (2); three alkaloids: uridine (3), caffeine (4), and paraxanthine (5); and three phenolics: 4-hydroxybenzoic acid (6), vanillin (7), and 3,5-dihydroxyfuran-2(5H)-one (8). Their structures were identified by analyzing nuclear magnetic resonance (1D- and 2D-NMR) data, high-resolution mass spectrometry (HRMS) data, and comparing them with literature references. Compounds 1-5 and 8 are reported for the first time in this species. NO radical scavenging activity assays indicated that compounds 2, 3, and 7 displayed IC50 values of 99,6, 77,9, and 34,2 µM, respectively, while the remaining compounds exhibited weak biological activity.

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