INTERACTIONS OF XANTHONE COMPOUNDS FROM THE MANGOSTEEN (GARCINIA MANGOSTANA L) PERICARPS AGAINST INOS, COX-1, AND COX-2 ENZYME RECEPTORS AS ANTI-INFLAMMATORY

Authors

  • DWINTHA LESTARI Department of Pharmacy, Universitas Muhammadiyah Bandung, Indonesia
  • RISKA PERMATA SARI Department of Pharmacy, Universitas Muhammadiyah Bandung, Indonesia https://orcid.org/0000-0001-6047-4927
  • IDA MUSFIROH Department of Pharmaceutical Analysis Pharmacy and Medicinal Chemistry, Faculty of Pharmacy, Universitas Padjadjaran, Indonesia https://orcid.org/0000-0002-2569-8914
  • SANDRA MEGANTARA Department of Pharmaceutical Analysis Pharmacy and Medicinal Chemistry, Faculty of Pharmacy, Universitas Padjadjaran, Indonesia https://orcid.org/0000-0003-4951-7740
  • MEILINDA SETYA PRACEKA Department of Pharmacy, Universitas Halim Sanusi, Bandung, Indonesia https://orcid.org/0000-0002-2632-8958
  • NUR KUSAIRA KHAIRUL IKRAM Institute of Biological Sciences, Faculty of Science, University of Malaya, Kuala Lumpur, Malaysia
  • MUCHTARIDI Department of Pharmaceutical Analysis Pharmacy and Medicinal Chemistry, Faculty of Pharmacy, Universitas Padjadjaran, Indonesia https://orcid.org/0000-0002-6156-8025

DOI:

https://doi.org/10.22159/ijap.2023v15i1.45861

Keywords:

Anti-inflammator, iNOS, COX-1, and COX-2, Pharmacophore, Ligandscout, Molecular docking, α-mangosteen, and γ-mangosteen

Abstract

Objective: Mangosteen is a plant that is very effective for inflammation. Besides that, the skin of the mangosteen plant in Indonesia continues to be developed because it is an antioxidant and suppresses the production of cytokines.

Methods: Screening pharmacophores and molecular docking simulations by molecular modeling computation to predict the activity of the Mangosteen plant in silico and to determine potential drug candidates from mangosteen for inflammation to the iNOS, COX-1, and COX-2.

Results: Pharmacophore Screening, γ-mangosteen has the highest pharmacophore fit score of 33.32 and 33.64 on COX-1 and COX-2 and is selective to iNOS target. Molecular docking of α-mangosteen and γ-mangosteen test compounds to the active site of used, COX-1, and COX-2 enzymes showed free energy binding (ΔG °) values of,-5.09,-5.00,-6.15; and-6.76,-5.30,-7.81 Kcal/mol respectively. Meanwhile, hydrogen bonds and good ΔG ° values ​​were formed between γ-mangosteen and COX-2, where the Hydroxyl group on γ-mangosteen interacted with the amino acids His75, Ser339, and Ala513 with ΔG ° of-7.81 Kcal/mol.

Conclusion: It can be said that α-mangosteen and γ-mangosteen have molecular interactions with COX-1 and COX-2 active sites with the highest affinity for COX-2 compared to COX-1, and iNOS.

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Published

07-01-2023

How to Cite

LESTARI, D., SARI, R. P., MUSFIROH, I., MEGANTARA, S., PRACEKA, M. S., KHAIRUL IKRAM, N. K., & MUCHTARIDI. (2023). INTERACTIONS OF XANTHONE COMPOUNDS FROM THE MANGOSTEEN (GARCINIA MANGOSTANA L) PERICARPS AGAINST INOS, COX-1, AND COX-2 ENZYME RECEPTORS AS ANTI-INFLAMMATORY. International Journal of Applied Pharmaceutics, 15(1), 186–194. https://doi.org/10.22159/ijap.2023v15i1.45861

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