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Updated: Jul 15, 2026

Analytical Techniques for Assaying Nitric Oxide Bioactivity
Published on: June 18, 2012
Structural modification of (‒)-xanthorrhizol isolated from Curcuma aromatica rhizomes to analogs with potent nitric
Wachirachai Pabuprapap1, Waraluck Chaichompoo2, Porawan Pratumwan3
1Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Ramkhamhaeng University, Bangkok, 10240, Thailand.
Abstract:
(‒)-Xanthorrhizol (1), a natural sesquiterpenoid isolated from Curcuma aromatica rhizomes, exhibits notable anti-inflammatory activity by inhibiting nitric oxide (NO) production. To enhance its NO inhibitory activity, a series of 22 analogs were synthesized through chemical modifications, including alkylation, esterification, hydrogenation, oxidation, and oximination. The NO inhibitory activities of these analogs were evaluated in LPS-stimulated RAW264.7 macrophage cells using the Griess method, while cytotoxicity was assessed with the MTT assay. Among the tested compounds, the oxime analog 23 demonstrated the strongest NO inhibitory activity (IC50 = 9.4 µM, SI = 13.2), significantly outperforming the reference drug aminoguanidine (IC50 = 29.5 µM, SI > 5.4). Structure-activity relationship (SAR) analysis revealed that electron-donating substituents and increased molecular rigidity generally decreased NO inhibition potency. However, some modifications also increased cytotoxicity against RAW264.7 cells. In addition, the oximation of xanthorrhizol enhanced NO inhibitory activity approximately 5-fold compared with the parent compound, while maintaining similarly low toxicity. These SAR findings underscore the critical influence of the oxime substructure in modulating NO inhibitory activity. Notably, the oxime analog 23 emerges as a promising lead candidate for the development of anti-inflammatory agents targeting NO-mediated pathways.
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