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Authors

Megawati Megawati, Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency of Indonesia (BRIN), KST BJ Habibie, Puspiptek, South Tangerang, IndonesiaFollow
Akhmad Darmawan, Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency of Indonesia (BRIN), KST BJ Habibie, Puspiptek, South Tangerang, Indonesia
Agus Budiawan Naro Putra, Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency of Indonesia (BRIN), KST BJ Habibie, Puspiptek, South Tangerang, Indonesia
Kartika Dyah Palupi, Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency of Indonesia (BRIN), KST BJ Habibie, Puspiptek, South Tangerang, Indonesia
Marissa Angelina, Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency of Indonesia (BRIN), KST BJ Habibie, Puspiptek, South Tangerang, Indonesia
Ahmad Randy, Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency of Indonesia (BRIN), KST BJ Habibie, Puspiptek, South Tangerang, Indonesia
Siska Andrina Kusumastuti, Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency of Indonesia (BRIN), KST BJ Habibie, Puspiptek, South Tangerang, Indonesia
Faris Hermawan, Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency of Indonesia (BRIN), KST BJ Habibie, Puspiptek, South Tangerang, Indonesia
Sumi Hudiyono, Department of Chemistry, Faculty of Mathematics and Natural Sciences (FMIPA), University of Indonesia, Depok, Indonesia

Abstract

This study investigated the phytochemical constituents and biological activities of Horsfieldia macrothyrsa leaves to identify their bioactive compounds. Methanol extracts were fractionated using n-hexane and ethyl acetate, followed by silica gel column chromatography with a stepwise polarity gradient. From 100 g of powdered leaves, three major    compounds were successfully isolated from the ethyl acetate fraction: 1-(2,4,6-trihydroxyphenyl)dodecan-1-one (1), sesamin (2), and β-sitosterol (3). Their chemical structures were confirmed using UV, IR, LC–MS/MS, and NMR  spectroscopy. Biological activities of the fractions and isolates were evaluated through DPPH antioxidant assays, α-glucosidase inhibition for antidiabetic activity, MTT assays on MCF-7 and T47D breast cancer cell lines for             cytotoxicity, and antibacterial tests (MIC and MBC) against Escherichia coli, Bacillus subtilis, Staphylococcus aureus, and Pseudomonas aeruginosa. The ethyl acetate fraction showed the strongest DPPH and α-glucosidase inhibitory  activities, with IC₅₀ values of 12.72 ± 0.12 and 6.69 ± 0.44 μg/mL, respectively. Isolate 1 exhibited the highest  antioxidant potential and mild antibacterial effects against B. subtilis, P. aeruginosa, and E. coli. β-sitosterol (3) demonstrated significant cytotoxicity toward MCF-7 (IC₅₀ = 20.71 μg/mL) and T47D (IC₅₀ = 18.19 μg/mL), while  sesamin (2) showed moderate cytotoxicity on MCF-7 cells. Molecular docking against EGFR (PDB ID: 4HJO)            indicated strong binding affinities for all three isolate: -7.41 kcal/mol (1), -9.99 kcal/mol (2), and -9.15 kcal/mol (3). These results suggest that sesamin and β-sitosterol form stable interactions with EGFR. Overall, the methanol and ethyl acetate fractions of H. macrothyrsa represent promising natural sources of antioxidants, while isolate 1-3 exhibit potential antibacterial and anticancer activities.

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This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License.

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