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Triterpenoids from Aglaia shawiana with their Cytotoxicity against MDA-MB468 and MCF-7 Cancer Cell Lines

Molekul: Jurnal Ilmiah Kimia · Vol. 21 No. 2 (2026) · hlm. 297–305

DOI
10.20884/1.jm.2026.21.2.18839
ISSN
2503-0310, 1907-9761
Terbit
2026-07-20
Penerbit
Universitas Jenderal Soedirman
Bahasa
eng

Abstrak

Triterpenoids are secondary metabolite compounds that are predominantly found in plants of the genus Aglaia. Since the 1960s, various triterpenoid structures from Aglaia species have been successfully isolated, and many are known to have interesting biological activities. This study aims to find triterpenoid compounds from Aglaia shawiana, which will then be tested for their activity against two breast cancer cell lines, MCF-7 and MDA MB 468. This research is expected to be used as a basis for further study in the development of cancer drug substances from Aglaia triterpenoids. Two triterpenoids were isolated from n-hexane extract of Aglaia shawiana leaves and twigs which is, namely cycloartan-3β,29-diol-24-ones (1), and 3-epi-cabraleahydroxylactone (2). Their chemical structures were determined based on spectroscopic data using infrared, high-resolution mass spectrometry, and including one and two-dimensional NMR techniques. Comparative data analysis was also carried out with appropriate reference journals and through a biosynthesis approach of the triterpene compounds. Both compounds were evaluated for their cytotoxic effects on MCF-7 and MDA MB-468 breast cancer cells. Compound 1 showed cytotoxicity with IC50 values of 118,2668 and 3,6505 µg/ml, meanwhile compound 2 values of 115,1065 μg/ml and 14,5274µg/ml, respectively. Doxorubicin used as a positive control with IC50 values of 3,2724 and 0,0303 µg/ml, respectively.

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  • Padjadjaran University
  • National Research and Innovation Agency
  • Indonesian Institute of Sciences
  • Universitas Nusa Bangsa
  • IPB University
  • Yamagata University
  • Maranatha Christian University
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Rekan penulisOrganisasiArtikel bersama
Unang SupratmanPadjadjaran University15
Desi HarnetiPadjadjaran University9
Yoshihito ShionoYamagata University9
Ace Tatang HidayatPadjadjaran University8
Tri MayantiPadjadjaran University7
Al Arofatus NainiPadjadjaran University7
Muhammad Eka PrastyaNational Research and Innovation Agency7
Kindi FarabiPadjadjaran University6
Nurlelasari NurlelasariPadjadjaran University5
Khalijah AwangUniversity of Malaya5
Wahyu WidowatiMaranatha Christian University4
Erina HilmayantiPadjadjaran University3
Dewa Gede KatjaSam Ratulangi University3
Mohamad Nurul AzmiUniversiti Sains Malaysia3
Rani MaharaniPadjadjaran University3
Vera PermatasariNational Research and Innovation Agency3
Akhmad DarmawanIndonesian Institute of Sciences3
Ervi AfifahAfiliasi tidak diketahui2
Rizal RizalUniversity of Indonesia2
Jepri Agung PriyantoIPB University2
Ahmad RandyNational Research and Innovation Agency2
Chandra RisdianIndonesian Institute of Sciences2
Ferry SandraUniversitas Trisakti2
Tati NurhayatiIPB University2
Gian PrimahanaAfiliasi tidak diketahui2
‪Tati NurhayatiIPB University2
Darwati DarwatiPadjadjaran University2
Harizon HarizonUniversitas Jambi2
Ferry Ferdiansyah SofianPadjadjaran University2
Indri YatiNational Research and Innovation Agency2
Erma SuryantiSumatera Institute of Technology2
Indah Dwiatmi DewijantiIndonesian Institute of Sciences2
Novita ArianiNational Research and Innovation Agency2

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Sumber metadata: OAI-PMH (metadata jurnal) https://jos.unsoed.ac.id/index.php/jm/oai, pertama di-harvest 9 Nov 2026, terakhir terlihat 9 Nov 2026.
Metadata asli (oai_dc)
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	<dc:title xml:lang="en-US"> Triterpenoids from Aglaia shawiana with their Cytotoxicity against MDA-MB468 and MCF-7 Cancer Cell Lines</dc:title>
	<dc:creator>Hutagaol, Ricson Pemimpin</dc:creator>
	<dc:creator>Mozef, Tjandrawati</dc:creator>
	<dc:creator>Primahana, Gian</dc:creator>
	<dc:creator>Fajriah, Sofa</dc:creator>
	<dc:creator>Nuralih, Nuralih</dc:creator>
	<dc:creator>Aini, Fitri Nur</dc:creator>
	<dc:creator>Setyaningsih, Desy</dc:creator>
	<dc:description xml:lang="en-US">Triterpenoids are secondary metabolite compounds that are predominantly found in plants of the genus Aglaia. Since the 1960s, various triterpenoid structures from Aglaia species have been successfully isolated, and many are known to have interesting biological activities. This study aims to find triterpenoid compounds from Aglaia shawiana, which will then be tested for their activity against two breast cancer cell lines, MCF-7 and MDA MB 468. This research is expected to be used as a basis for further study in the development of cancer drug substances from Aglaia triterpenoids. Two triterpenoids were isolated from n-hexane extract of Aglaia shawiana leaves and twigs which is, namely cycloartan-3β,29-diol-24-ones (1), and 3-epi-cabraleahydroxylactone (2). Their chemical structures were determined based on spectroscopic data using infrared, high-resolution mass spectrometry, and including one and two-dimensional NMR techniques. Comparative data analysis was also carried out with appropriate reference journals and through a biosynthesis approach of the triterpene compounds. Both compounds were evaluated for their cytotoxic effects on MCF-7 and MDA MB-468 breast cancer cells. &amp;nbsp;Compound 1 showed cytotoxicity with IC50 values of 118,2668 and 3,6505 µg/ml, meanwhile compound 2 values of 115,1065 μg/ml and 14,5274µg/ml, respectively. Doxorubicin used as a positive control with IC50 values of 3,2724 and 0,0303 µg/ml, respectively.</dc:description>
	<dc:publisher xml:lang="en-US">Universitas Jenderal Soedirman</dc:publisher>
	<dc:date>2026-07-20</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:type xml:lang="en-US">Peer-reviewed Article</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://jos.unsoed.ac.id/index.php/jm/article/view/18839</dc:identifier>
	<dc:identifier>10.20884/1.jm.2026.21.2.18839</dc:identifier>
	<dc:source xml:lang="en-US">Molekul; Vol 21 No 2 (2026); 297-305</dc:source>
	<dc:source>2503-0310</dc:source>
	<dc:source>1907-9761</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://jos.unsoed.ac.id/index.php/jm/article/view/18839/8752</dc:relation>
	<dc:relation>https://jos.unsoed.ac.id/index.php/jm/article/view/18839/8753</dc:relation>
</oai_dc:dc>