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Research Articles

Vol. 13 No. 3 (2026)

Phytochemical composition and antioxidant activity of four naturally growing Aquilaria species from North Padang Lawas, Indonesia

DOI
https://doi.org/10.14719/pst.13656
Submitted
13 January 2026
Published
30-09-2026 — Updated on 01-10-2026
Versions

Abstract

Agarwood-producing species of the genus Aquilaria occur naturally in Sumatra, including North Padang Lawas Regency, Indonesia. Leaves of Aquilaria are increasingly explored as raw material for herbal tea due to their bioactive compounds. This research aims to assess the phytochemical composition, tannin levels and antioxidant potential of four agarwood species that grow naturally in North Padang Lawas, Indonesia. Fresh agarwood leaves were powdered and extracted using a 96 % ethanol solution for further testing. The phytochemical analysis indicated the presence of various bioactive compounds such as flavonoids, alkaloids, tannins, saponins and triterpenoids, which are recognized for their biological functions. The evaluation of antioxidant capacity was conducted using the DPPH radical scavenging assay. In addition, gas chromatography-mass spectrometry (GC-MS) analysis detected a variety of chemical compounds, including phenolic compounds and particular fatty acids, which may be linked to the antioxidant effects noted. Both dried leaf material and ethanol extracts contained similar classes of secondary metabolites, although the presence of specific compounds varied among species. All four species were classified in the “very strong” category of antioxidant activity with IC50 values below 40 μg/mL. GC-MS analysis revealed dominant compounds in each species, including Nortopsentin B in A. microcarpa (13.46 %), Propanamide in A. beccariana (14.66 %), Acetaldehyde in A. malaccensis (26.39 %) and 2′-oxa-3′-adeninylyl-4′,5′-dihydroxycyclopentyl in A. hirta (14.43 %). Overall, the findings support the traditional use of agarwood leaves as a healthful tea and warrant further development as an alternative raw material for functional food or pharmaceutical applications.

References

  1. 1. Santoso E, Subiakto A, Turjaman M. Silviculture and cultivation techniques for agarwood-producing plants. 5th ed. Bogor: Conservation and Rehabilitation Research and Development Center; 2011.
  2. 2. Lloren R. Inoculation strategies for agarwood-producing species in Asia: a systematic review. IOP Conf Ser Earth Environ Sci. 2023;1277(1):012032. https://doi.org/10.1088/1755-1315/1277/1/012032
  3. 3. Adam AZ, Lee SY, Mohamed R. Pharmacological properties of agarwood tea derived from Aquilaria (Thymelaeaceae) leaves: an emerging contemporary herbal drink. J Herb Med. 2017;10:37–44. https://doi.org/10.1016/j.hermed.2017.06.002
  4. 4. Batubara R, Surjanto M, Purba M. Safety of agarwood tea (Aquilaria malaccensis Lamk.) from induced trees against oral toxics. Wahana Foresta. 2018;13(1):1–11. https://doi.org/10.31849/forestra.v13i1.1399
  5. 5. Batubara R, Surjanto M, Sihombing TM, Ginting H. Safety of gaharu tea (Aquilaria malaccensis) from induction trees through a 90-day oral subchronic toxicity test. Biofarmasi. 2017;14(2):69–76. https://doi.org/10.13057/biofar/f140205
  6. 6. Indonesia. Directorate General of POM. Indonesian Materia Medika. Vol. 6. Jakarta: Republic of Indonesia Ministry of Health; 1979.
  7. 7. Lestari U, Muhaimin M, Chaerunnisaa AY, Sujarwo W. Antioxidant activities and phytochemical screening of ethanol extract from surian leaves (Toona sinensis). Int J Appl Pharm. 2023;15(2):37–43. https://doi.org/10.22159/ijap.2023.v15s2.07
  8. 8. Baliyan S, Mukherjee R, Priyadarshini A, Vibhuti A, Gupta A, Pandey RP, et al. Determination of antioxidants by DPPH radical scavenging activity and quantitative phytochemical analysis of Ficus religiosa. Molecules. 2022;27(4):1326–45. https://doi.org/10.3390/molecules27041326
  9. 9. Batubara R, Wirjosentono B, Siregar AH, Harahap U, Tamrin. Chemical compounds and antioxidant potential in hot water extract of cultivated agarwood (Aquilaria malaccensis) Lamk. leaves. IOP Conf Ser Earth Environ Sci. 2021;830:012070. https://doi.org/10.1088/1755-1315/830/1/012070
  10. 10. Batubara R, Hanum TI, Affandi O, Wahyuni HS. Chemical compounds contained in young and mature leaves of agarwood species Wikstroemia tenuiramis and its antioxidant properties. Biodiversitas. 2020;21(10):4616–22. https://doi.org/10.13057/biodiv/d211020
  11. 11. Sari R, Muhani M, Fajriaty I. Test of the antibacterial activity of ethanol extract of agarwood leaves (Aquilaria microcarpa Baill.) against Staphylococcus aureus and Proteus mirabilis. Pharm Sci Res. 2017;4(3):143–54. https://doi.org/10.7454/psr.v4i3.3756
  12. 12. Eissa MA, Hashim YZHY, El-Kersh DM, Azziz SSSA, Salleh HM, Isa MLM, et al. Metabolite profiling of Aquilaria malaccensis leaf extract using liquid chromatography-Q-TOF-mass spectrometry and investigation of its potential antilipoxygenase activity in vitro. Processes. 2020;8(2):1–22. https://doi.org/10.3390/pr8020202
  13. 13. Mousavi SM, Hashemi SA, Ghahramani Y, Azhdari R, Yousefi K, Gholami A, et al. Antiproliferative and apoptotic effects of graphene oxide @AlFu MOF based saponin natural product on OSCC line. Pharmaceuticals. 2022;15(9):1–22. https://doi.org/10.3390/ph15091137
  14. 14. Batubara R, Hanum TI, Surjanto M. Phytochemical and tannin content in two species of agarwood leaves from Mandailing Natal Regency, North Sumatra Province. In: Proceedings of the 3rd International Seminar on Chemistry; 2018; Surabaya, Indonesia. https://doi.org/10.1063/1.5082510
  15. 15. Siqueira CFDQ, Cabral DLV, Sobrinho TJDSP, Amorin ELCD, Melo JGD, Araujo TADS, et al. Levels of tannins and flavonoids in medicinal plants: evaluating bioprospecting strategies. Evid Based Complement Alternat Med. 2012:1–7. https://doi.org/10.1155/2012/434782
  16. 16. Adnan M, Alu S, Sheikh K, Amber R. Review on antibacterial activity of Himalayan medicinal plants traditionally used to treat pneumonia and tuberculosis. J Pharm Pharmacol. 2019;71(11):1599–625. https://doi.org/10.1111/jphp.13156
  17. 17. Rohdiana D. Capture activities of radical polyphenol in tea leaves. Bandung: Tea and Quinine Research Center; 2001.
  18. 18. Shih YE, Lin YC, Chung T, Liu MC, Cheng GH, Wu CC, et al. In vitro assay to estimate tea astringency via observing flotation of artificial oil bodies sheltered by caleosin fused with histatin 3. J Food Drug Anal. 2017;25(4):828–36. https://doi.org/10.1016/j.jfda.2016.08.008
  19. 19. Abdulhussein AA, Dakheel MM, Quijada J. Potential and challenge assessment of tannin extracts from black tea in male rabbits fed contaminated diet by mycotoxins. Acta Zool Bulg. 2022;25(2):107–18. https://doi.org/10.2478/azibna-2022-0018
  20. 20. Wangiyana IGAS, Triandini IGAAH. Forest herbal tea should be promoted in Indonesia. J Silva Samalas. 2023;6(2):8–14. https://doi.org/10.33394/jss.v6i2.10223
  21. 21. Mabruroh AI. Test of the antioxidant activity of tannin extract from bamboo grass (Lopatherum gracile Brongn.) leaves and its identification [thesis]. Malang: Maulana Malik Ibrahim State Islamic University; 2015.
  22. 22. Dakheel MM, Alkandari FA, Mueller-Harvey I, Woodward MJ, Rymer C. Antimicrobial in vitro activities of condensed tannin extracts on avian pathogenic Escherichia coli. Lett Appl Microbiol. 2020;70(3):165–72. https://doi.org/10.1111/lam.13253
  23. 23. Ortiz LV, Garcia DC, Rodriguez MB, Yucailla VA, Orozco RL, Rodriguez EM, et al. Rumen function and in vitro gas production of diets influenced by two levels of tannin-rich forage. Fermentation. 2022;8(11):1–11. https://doi.org/10.3390/fermentation8110607
  24. 24. Permadi A, Aziz A, Ramadani N, Mayudi M. Evaluation and comparison of anti-aging facial serum from algae extract. Chemica. 2023;10(3):144–50. https://doi.org/10.26555/chemica.v10i3.27898
  25. 25. Warsito W, Alief MF, Azzahra VO, Rahman MF, Retnowati R. Screening of aroma compounds in commercial tea (Camellia sinensis) from Indonesia and testing their activity as antioxidants. J Trop Pharm Chem. 2024;8(2):116–22.
  26. 26. Batubara R, Hanum TI, Risnasari I, Ginting H, Lubis LA. Antioxidant activity and preferences test of agarwood leaves tea (Aquilaria malaccensis Lamk.) based on leaves drying methods. In: BROMO Conference-Symposium on Natural Products and Biodiversity; 2018; Surabaya, Indonesia. https://doi.org/10.5220/0009843700002406
  27. 27. Sudaryat YM, Kusmiati CR, Pelangi A, Rustamsyah, Rohdiana D. Antioxidant activity of ten grades of Indonesian black tea (Camellia sinensis (L.) O. Kuntze) liquor. J Tea Quinine Res. 2015;18(2):95–100. https://doi.org/10.22302/pptk.jur.jptk.v18i2.70
  28. 28. Zargoosh Z, Ghavam M, Bacchetta G, Tavili A. Effects of ecological factors on the antioxidant potential and total phenol content of Scrophularia striata Boiss. Sci Rep. 2019;9(1):1–15. https://doi.org/10.1038/s41598-019-52605-8
  29. 29. Hossain MA, Ahmad NU, Alam M, Hossain MM, Sarkar A. Screening of different extraction methods for maximum production of total flavonoids, tannins, and antioxidants from Centella asiatica. Food Res. 2022;8(1):44–51. https://doi.org/10.26656/fr.2017.8(1).057
  30. 30. Hendra H, Moeljopawiro S, Nuringtyas TR. Antioxidant and antibacterial activities of agarwood (Aquilaria malaccensis Lamk.) leaves. In: Proceedings of the 1st International Conference on Science and Technology; 2016; Yogyakarta, Indonesia. https://doi.org/10.1063/1.4958565
  31. 31. Sari DI, Rahmawanty D, Apriana D, Amelia R. Antioxidant activity of gel preparations containing ethanol extract and ethyl acetate fraction of Aquilaria microcarpa leaves. In: Proceedings of the National Seminar on Wetland Environment; 2018; Banjarmasin, Indonesia.
  32. 32. Batubara R, Wirjosentono B, Siregar AH, Harahap U, Tamrin. Phytochemical screening and PY-GC-MS analysis of agarwood leaves (Aquilaria malaccensis Lamk.) cultivated in Bahorok, Langkat Regency, North Sumatra. Rasayan J Chem. 2021;14(2):751–9. https://doi.org/10.31788/RJC.2021.1426021
  33. 33. Cartus AT, Lachenmeier DW, Guth S, Roth A, Baum M, Diel P, et al. Acetaldehyde as a food flavoring substance: aspects of risk assessment. Mol Nutr Food Res. 2023;67(23):1–29. https://doi.org/10.1002/mnfr.202200661
  34. 34. Ghfil ZAHA, Aboalhur FJ, Mshachal A, Alobaidi AAA. Antioxidant and antifungal activities of n-hexadecanoic acid extracted from algae. South Asian Res J Pharm Sci. 2025;7(4):125–7. https://doi.org/10.36346/sarjps.2025.v07i04.003
  35. 35. Chen B, Su J, Hu Y, Liu S, Ouyang X, Cai R, et al. Antioxidant mechanisms and products of four 4′,5,7-trihydroxyflavonoids with different structural types. RSC Med Chem. 2023;14(1):173–82. https://doi.org/10.1039/D2MD00333C
  36. 36. Nasution AA, Siregar UJ, Miftahudin, Turjaman M. Identification of chemical compounds in agarwood-producing species Aquilaria malaccensis and Gyrinops versteegii. J For Res. 2020;31(4):1371–80. https://doi.org/10.1007/s11676-018-00875-9
  37. 37. Syed I, Lee J, Vieira PMM, Donalds CJ, Sontheimer A, Aryal P, et al. Palmitic acid hydroxy stearic acids activate GPR40 which is involved in their beneficial effects on glucose homeostasis. Cell Metab. 2018;27(2):419–27. https://doi.org/10.1016/j.cmet.2018.01.001
  38. 38. Vieira PMM, Saghatelian A, Khan BB. GLUT4 expression in adipocytes regulates de novo lipogenesis and levels of a novel class of lipids with antidiabetic and anti-inflammatory effects. Diabetes. 2016;65(7):1808–15. https://doi.org/10.2337/db16-0221
  39. 39. An N, Wang Y, He DX, Mei PC, Zhu QF, Feng YQ. A dataset of branched fatty acid esters of hydroxy fatty acids diversity in foods. Sci Data. 2023;10:790. https://doi.org/10.1038/s41597-023-02712-z

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