Sesquiterpenoids from <i>Dysoxylum amooroides</i> Stem Bark: Isolation, Structure Determination, and Cytotoxicity Against MCF-7 Breast Cancer Cells

Three sesquiterpenoids, guaianediol (1), alismol (2), and spathulenol (3), were isolated from the n-hexane and ethyl acetate extracts of the stem bark of Dysoxylum amooroides. The three compounds were found in D. amooroides species for the first time. The structures of the isolated compounds were id...

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Main Authors: Latifah Gunawan, Hidayat Nurul Mustofa, Al Arofatus Naini, Desi Harneti, Ace Tatang Hidayat, Nurlelasari Nurlelasari, Rani Maharani, Tri Mayanti, Sofa Fajriah, Khalijah Awang, Mohamad Nurul Azmi, Unang Supratman
Format: Article
Language:English
Published: Department of Chemistry, Universitas Gadjah Mada 2025-01-01
Series:Indonesian Journal of Chemistry
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Online Access:https://jurnal.ugm.ac.id/ijc/article/view/99121
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author Latifah Gunawan
Hidayat Nurul Mustofa
Al Arofatus Naini
Desi Harneti
Ace Tatang Hidayat
Nurlelasari Nurlelasari
Rani Maharani
Tri Mayanti
Sofa Fajriah
Khalijah Awang
Mohamad Nurul Azmi
Unang Supratman
author_facet Latifah Gunawan
Hidayat Nurul Mustofa
Al Arofatus Naini
Desi Harneti
Ace Tatang Hidayat
Nurlelasari Nurlelasari
Rani Maharani
Tri Mayanti
Sofa Fajriah
Khalijah Awang
Mohamad Nurul Azmi
Unang Supratman
author_sort Latifah Gunawan
collection DOAJ
description Three sesquiterpenoids, guaianediol (1), alismol (2), and spathulenol (3), were isolated from the n-hexane and ethyl acetate extracts of the stem bark of Dysoxylum amooroides. The three compounds were found in D. amooroides species for the first time. The structures of the isolated compounds were identified and established based on an extensive spectroscopic analysis involving HR-TOF-ESI-MS, IR, and NMR data, as well as a comparison with the previously reported works of literature. Compounds 1-3 were further assessed for cytotoxic effects against MCF-7 breast cancer cells. Guaianediol (1) showed inactive activity with IC50 > 100 µM, alismol (2) showed weak activity with IC50 value of 82.1 µM and spathulenol (3) showed considerable activity with an IC50 value of 15.2 µM. A brief structure-activity relationship and comparison with the previous works were also discussed to understand better the role of guaiane- and aromadendrane-type sesquiterpenoids in the biological activity perspective.
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institution Kabale University
issn 1411-9420
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language English
publishDate 2025-01-01
publisher Department of Chemistry, Universitas Gadjah Mada
record_format Article
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spelling doaj-art-af68bfcf8b1840a6a1f3da645cad854a2025-02-03T04:32:43ZengDepartment of Chemistry, Universitas Gadjah MadaIndonesian Journal of Chemistry1411-94202460-15782025-01-0125115716810.22146/ijc.9912136770Sesquiterpenoids from <i>Dysoxylum amooroides</i> Stem Bark: Isolation, Structure Determination, and Cytotoxicity Against MCF-7 Breast Cancer CellsLatifah Gunawan0Hidayat Nurul Mustofa1Al Arofatus Naini2Desi Harneti3Ace Tatang Hidayat4Nurlelasari Nurlelasari5Rani Maharani6Tri Mayanti7Sofa Fajriah8Khalijah Awang9Mohamad Nurul Azmi10Unang Supratman11Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Padjadjaran, Jl. Raya Bandung-Sumedang Km. 21, Jatinangor, Sumedang 45363, IndonesiaDepartment of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Padjadjaran, Jl. Raya Bandung-Sumedang Km. 21, Jatinangor, Sumedang 45363, IndonesiaResearch Center for Chemistry, National Research and Innovation Agency (BRIN), Jl. Kw. Puspiptek, Muncul, Kawasan PUSPIPTEK Serpong, Tangerang Selatan 15314, IndonesiaDepartment of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Padjadjaran, Jl. Raya Bandung-Sumedang Km. 21, Jatinangor, Sumedang 45363, IndonesiaDepartment of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Padjadjaran, Jl. Raya Bandung-Sumedang Km. 21, Jatinangor, Sumedang 45363, IndonesiaDepartment of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Padjadjaran, Jl. Raya Bandung-Sumedang Km. 21, Jatinangor, Sumedang 45363, IndonesiaDepartment of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Padjadjaran, Jl. Raya Bandung-Sumedang Km. 21, Jatinangor, Sumedang 45363, Indonesia; Central Laboratory of Universitas Padjadjaran, Jl. Raya Bandung-Sumedang Km. 21, Jatinangor, Sumedang 45363, IndonesiaDepartment of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Padjadjaran, Jl. Raya Bandung-Sumedang Km. 21, Jatinangor, Sumedang 45363, IndonesiaResearch Center for Chemistry, National Research and Innovation Agency (BRIN), Jl. Kw. Puspiptek, Muncul, Kawasan PUSPIPTEK Serpong, Tangerang Selatan 15314, IndonesiaDepartment of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur 50603, MalaysiaSchool of Chemical Sciences, Universiti Sains Malaysia, Minden, Penang 11800, MalaysiaDepartment of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Padjadjaran, Jl. Raya Bandung-Sumedang Km. 21, Jatinangor, Sumedang 45363, Indonesia; Central Laboratory of Universitas Padjadjaran, Jl. Raya Bandung-Sumedang Km. 21, Jatinangor, Sumedang 45363, IndonesiaThree sesquiterpenoids, guaianediol (1), alismol (2), and spathulenol (3), were isolated from the n-hexane and ethyl acetate extracts of the stem bark of Dysoxylum amooroides. The three compounds were found in D. amooroides species for the first time. The structures of the isolated compounds were identified and established based on an extensive spectroscopic analysis involving HR-TOF-ESI-MS, IR, and NMR data, as well as a comparison with the previously reported works of literature. Compounds 1-3 were further assessed for cytotoxic effects against MCF-7 breast cancer cells. Guaianediol (1) showed inactive activity with IC50 > 100 µM, alismol (2) showed weak activity with IC50 value of 82.1 µM and spathulenol (3) showed considerable activity with an IC50 value of 15.2 µM. A brief structure-activity relationship and comparison with the previous works were also discussed to understand better the role of guaiane- and aromadendrane-type sesquiterpenoids in the biological activity perspective.https://jurnal.ugm.ac.id/ijc/article/view/99121cytotoxic activitydysoxylum amooroidesmcf-7sesquiterpenoids
spellingShingle Latifah Gunawan
Hidayat Nurul Mustofa
Al Arofatus Naini
Desi Harneti
Ace Tatang Hidayat
Nurlelasari Nurlelasari
Rani Maharani
Tri Mayanti
Sofa Fajriah
Khalijah Awang
Mohamad Nurul Azmi
Unang Supratman
Sesquiterpenoids from <i>Dysoxylum amooroides</i> Stem Bark: Isolation, Structure Determination, and Cytotoxicity Against MCF-7 Breast Cancer Cells
Indonesian Journal of Chemistry
cytotoxic activity
dysoxylum amooroides
mcf-7
sesquiterpenoids
title Sesquiterpenoids from <i>Dysoxylum amooroides</i> Stem Bark: Isolation, Structure Determination, and Cytotoxicity Against MCF-7 Breast Cancer Cells
title_full Sesquiterpenoids from <i>Dysoxylum amooroides</i> Stem Bark: Isolation, Structure Determination, and Cytotoxicity Against MCF-7 Breast Cancer Cells
title_fullStr Sesquiterpenoids from <i>Dysoxylum amooroides</i> Stem Bark: Isolation, Structure Determination, and Cytotoxicity Against MCF-7 Breast Cancer Cells
title_full_unstemmed Sesquiterpenoids from <i>Dysoxylum amooroides</i> Stem Bark: Isolation, Structure Determination, and Cytotoxicity Against MCF-7 Breast Cancer Cells
title_short Sesquiterpenoids from <i>Dysoxylum amooroides</i> Stem Bark: Isolation, Structure Determination, and Cytotoxicity Against MCF-7 Breast Cancer Cells
title_sort sesquiterpenoids from i dysoxylum amooroides i stem bark isolation structure determination and cytotoxicity against mcf 7 breast cancer cells
topic cytotoxic activity
dysoxylum amooroides
mcf-7
sesquiterpenoids
url https://jurnal.ugm.ac.id/ijc/article/view/99121
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