SYNTHESIS OF ACETYL AND BENZOYL ESTERS OF XANTHORRHIZOL AND ITS OXIDATION PRODUCTS AND EVALUATION OF THEIR INHIBITORY ACTIVITY AGAINST NITRIC OXIDE PRODUCTION

  • MAYA DAMAYANTI RAHAYU Center of Pharmaceutical and Medical Technology, Agency for the Assessment and Application of Technology (BPPT), Jakarta, Indonesia
  • SUSI KUSUMANINGRUM Center of Pharmaceutical and Medical Technology, Agency for the Assessment and Application of Technology (BPPT), Jakarta, Indonesia.
  • HAYUN HAYUN Laboratory of Pharmaceutical and Medicinal Chemistry, Faculty of Pharmacy, Universitas Indonesia, Depok, West Java, Indonesia

Abstract

Objective: Xanthorrhizol is known to have anti-inflammatory activity. However, new xanthorrhizol derivatives with improved anti-inflammatory
activity and reduced toxicity are needed.
Methods: In this study, the derivatives of xanthorrhizol were synthesized and spectroscopically characterized, and their inhibitory activities against
nitric oxide (NO) production were evaluated in RAW 264.7 macrophage cells.
Results: The first stage of synthesis produced compounds 2a and 2b in 58.49% and 63.26% yields, respectively. Compounds 2a and 2b were oxidized
using potassium permanganate, giving compounds 3a and 3b in yields of 51.92% and 43.78%, respectively. Compounds 1, 2a, 3a, and 3b along
with diclofenac sodium (the positive control) exhibited IC50 values for NO production of 31.82, 73.85, 354.05, 97.19, and 78.43 μM, respectively. In
contrast, compound 2b did not show any inhibitory activity. Based on cytotoxicity assay, compounds 1, 2a, 2b, 3a, 3b, and diclofenac sodium had LD50
values of 30.97, 65.15, 31.15, 117.86, 53.40, and 51.67 μM, respectively. The NO inhibitory activities of compounds 2a, 3a, and 3b were lower than that
of xanthorrhizol (compound 1). However, cytotoxicity tests showed that compounds 2a, 3a, and 3b had reduced toxicities compared to xanthorrhizol.
Conclusion: The modification of xanthorrhizol through esterification and oxidation produced derivative compounds with weaker anti-inflammatory
activity but reduced cytotoxicity.

Keywords: Xanthorrhizol, Oxidation, Potassium permanganate, Nitric oxide, RAW 264.7 cells

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RAHAYU, M. D., KUSUMANINGRUM, S., & HAYUN, H. (2020). SYNTHESIS OF ACETYL AND BENZOYL ESTERS OF XANTHORRHIZOL AND ITS OXIDATION PRODUCTS AND EVALUATION OF THEIR INHIBITORY ACTIVITY AGAINST NITRIC OXIDE PRODUCTION. International Journal of Applied Pharmaceutics, 12(1), 135-138. https://doi.org/10.22159/ijap.2020.v12s1.FF030
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