ArticleViewAbstractPharmacognosy Journal,2020,12,6s,1641-1652.DOI:10.5530/pj.2020.12.224Published:November 2020Type:Research ArticleIsolation and Identification of Chemical Compounds from Garcinia fruticosa Lauterb Stem Bark ExtractNovia Delita, Berna Elya, and Muhammad Hanafi Novia Delita1,2, Berna Elya3*, Muhammad Hanafi4,5 1Graduate Programme of Biology Pharmacy, Faculty of Pharmacy, Universitas Indonesia, Depok, INDONESIA. 2Department of Pharmacognosy- Phytochemistry, Faculty of Pharmacy and Science, Universitas Muhammadiyah Prof. Dr. Hamka, 1340 Jakarta, INDONESIA. 3Department of Pharmacognosy- Phytochemistry, Faculty of Pharmacy, Universitas Indonesia, Depok, INDONESIA. 4Research Center for Chemistry, Indonesian Institute of Sciences, Serpong, INDONESIA. 5Faculty of Pharmacy, Universitas Pancasila, Jakarta, INDONESIA. Abstract:Background: Garcinia is a tropical plant that grows in Indonesia. Garcinia has many health benefits for the body. Garcinia contains many phenolic compounds and their derivatives, such as xanthon, flavonoids, benzophenone, lactone, and phenolic acids. Garcinia fruticosa Lauterb. comes from the family Clusiaceae. The results of the phytochemical examination showed that G. fruticosa bark extract contained alkaloids, flavonoids, glycosides, tannins, and saponins. Objective: This study aims to isolate and identify chemical compounds from the ethyl acetate extract of G. fruticosa Lauterb stem bark. Method: G. fruticosa Lauterb bark. dried, milled, and extracted with Step Gradient Polarity/SGP maceration using n-hexane, ethyl acetate, and methanol. Isolation was done by column chromatography and identified by thin layer chromatography and IR spectroscopy, LC-MS/MS, 1H-NMR, 13C-NMR, 2D-NMR (HSQC, HMBC). Results: Compound D7a has a molecular weight 168.0496. The IR spectrum shows the presence of a group –OH appears on 3483 cm-1, aromatic presence in 1609 cm-1. The H-NMR spectrum shows the presence of aromatic signals on 6.96 (d, 8 Hz), 6.96 (d, 2 Hz) and 7.70 (dd, 8; 2 Hz). The C-NMR spectrum shows the presence of a carboxylic-COOH group appearing at 166.57 ppm, the presence of 2 x C-OH appearing at 147.18 and 151.18. In the HMBC spectrum, the -OCH3 position is located at C-3 with a correlation between the 3.79 (s) signal and the C signal at the chemical shift 147.18. Conclusions: Structural elucidation shows that compound D7a is a 4-hydroxy-3-methoxy benzoate acid (Vanylic Acid) and isolate I-1 is an impure compound namely β-Sitosterol and Stigmasterol. Keywords:4-hydroxy-3-methoxy benzoic acid, Garcinia fruticosa, Isolation, Stigmasterol, Structural elucidation, β-sitosterolView:PDF (1.8 MB) PDF Images Pattern of chromatogram of compounds I-1 ‹ Hepatoprotective Effect of Bioactive Fraction of Lagerstroemia speciosa (L.) Pers. Bark Against Monosodium Glutamate-Induced Liver Toxicity up Pharmacological Screening of Anti Lice and Antidandruff Activity of Ethanolic Extract of Leaves of Datura metel ›