Melola Discovery

← Melola Discovery

Journal SINTA 1

Azadirone-Type Limonoids from the Fruit of Chisocheton lasiocarpus and Their Cytotoxic Activity Against MCF-7 Breast Cancer Lines

Molekul: Jurnal Ilmiah Kimia · Vol. 17 No. 1 (2022) · pp. 60–67

DOI
10.20884/1.jm.2022.17.1.5593
ISSN
2503-0310, 1907-9761
Published
2022-03-13
Publisher
Universitas Jenderal Soedirman
Language
eng

Abstract

Limonoid is derivatives of triterpenoid compound that have a wide variety of structures due to various ring-opening, rearrangements, and high-degree of oxidation. Limonoid is known as compounds that have wide-range of biological activities, including anticancer activity. This research was aimed to determine the chemical structure and cytotoxic activity of limonoid in the n-hexane extract of Chisocheton lasiocarpus fruit. Dried powder of C. lasiocarpus fruit was extracted using methanol followed by fractionated using n-hexane, ethyl acetate, and n-butanol. Five azadirone-type limonoids, 6α-(acetoxy)-14β,15β-epoxyazadirone (1), dysobinin (2), 7α-acetylneotricilenone (3), 6α-O-acetyl-7-deacetylnimocinol (4), and 7α-hyroxyneotricilenone (5), were isolated from the n-hexane extract of Chisocheton lasiocarpus fruit. The chemical structure of all compounds was identified by spectroscopic analysis, including 1D, 2D-NMR, IR, UV and HR-TOF MS as well as by comparison with previous reported spectra data. Compounds 1-5 were investigated from this plant for first time. The cytotoxic activity of the isolated compounds against MCF-7 breast cancer line were examined and the results showed that 7α-hyroxyneotricilenone (5) showed the moderate activity with IC50 values of 53 μM

Collaboration network of the authors

40 authors · 267 co-authorship links · showing the 40 most connected

Hover or tap a name to highlight its co-authors. Double-click to open the author's page.

  • University of Malaya
  • University of Brawijaya
  • Affiliation unknown
  • Different organisations
  • Same organisation
  • Affiliation unknown
  • Thicker line = more joint articles · bigger circle = more articles
Show as table
Co-authorOrganisationJoint articles
Kindi FarabiAffiliation unknown49
Desi HarnetiAffiliation unknown47
Tri MayantiAffiliation unknown46
Rani MaharaniAffiliation unknown41
Al Arofatus NainiAffiliation unknown33
Darwati DarwatiAffiliation unknown19
Tati HerlinaAffiliation unknown9
Khalijah AwangUniversity of Malaya9
Ricson Pemimpin HutagaolAffiliation unknown9
Wahyu SafriansyahAffiliation unknown8
Fajar Fauzi AbdullahAffiliation unknown8
Hadi KuncoroAffiliation unknown7
Gian PrimahanaAffiliation unknown7
Risyandi AnwarAffiliation unknown7
Tjandrawati MozefAffiliation unknown6
Harizon HarizonAffiliation unknown6
Sandra Amalia RiyadiAffiliation unknown6
Euis JulaehaAffiliation unknown5
Ronny LesmanaAffiliation unknown5
Aprilia Permata SariAffiliation unknown5
Dudi RunadiAffiliation unknown4
Purnama PurnamaAffiliation unknown4
Agus SafariAffiliation unknown4
Muhammad HanafiAffiliation unknown4
Laode RijaiAffiliation unknown3
Susianti SusiantiAffiliation unknown3
Raihan Fathurrahman HasbillaAffiliation unknown3
Marissa AngelinaAffiliation unknown2
Sofna Dewita Sari BanjarnahorAffiliation unknown2
Sari PurbayaAffiliation unknown2
Sri HandayaniUniversity of Brawijaya2

Affiliations come from OpenAlex; journal OAI-PMH metadata carries none. Authors without an OpenAlex ID are matched by name, which can merge or split people.

Metadata source: OAI-PMH (metadata jurnal) https://jos.unsoed.ac.id/index.php/jm/oai, first harvested 9 Nov 2026, last seen 9 Nov 2026.
Original metadata (oai_dc)
<oai_dc:dc xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/  http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
	<dc:title xml:lang="en-US"> Azadirone-Type Limonoids from the Fruit of Chisocheton lasiocarpus and Their Cytotoxic Activity Against MCF-7 Breast Cancer Lines</dc:title>
	<dc:creator>Hilmayanti, Erina</dc:creator>
	<dc:creator>Nurlelasari, Nurlelasari</dc:creator>
	<dc:creator>Katja, Dewa Gede</dc:creator>
	<dc:creator>Hidayat, Ace Tatang</dc:creator>
	<dc:creator>Fajriah, Sofa</dc:creator>
	<dc:creator>Darmawan, Akhmad</dc:creator>
	<dc:creator>Supratman, Unang</dc:creator>
	<dc:creator>Azmi, Mohamad Nurul</dc:creator>
	<dc:creator>Shiono, Yoshihito</dc:creator>
	<dc:description xml:lang="en-US">Limonoid is derivatives of triterpenoid compound that have a wide variety of structures due to various ring-opening, rearrangements, and high-degree of oxidation. Limonoid is known as compounds that have wide-range of biological activities, including anticancer activity. This research was aimed to determine the chemical structure and cytotoxic activity of limonoid in the n-hexane extract of Chisocheton lasiocarpus fruit. Dried powder of C. lasiocarpus fruit was extracted using methanol followed by fractionated using n-hexane, ethyl acetate, and n-butanol. Five azadirone-type limonoids, 6α-(acetoxy)-14β,15β-epoxyazadirone (1), dysobinin (2), 7α-acetylneotricilenone (3), 6α-O-acetyl-7-deacetylnimocinol (4), and 7α-hyroxyneotricilenone (5), were isolated from the n-hexane extract of Chisocheton lasiocarpus fruit. The chemical structure of all compounds was identified by spectroscopic analysis, including 1D, 2D-NMR, IR, UV and HR-TOF MS as well as by comparison with previous reported spectra data. Compounds 1-5 were investigated from this plant for first time. The cytotoxic activity of the isolated compounds against MCF-7 breast cancer line were examined and the results showed that 7α-hyroxyneotricilenone (5) showed the moderate activity with IC50 values of 53 μM</dc:description>
	<dc:publisher xml:lang="en-US">Universitas Jenderal Soedirman</dc:publisher>
	<dc:date>2022-03-13</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://jos.unsoed.ac.id/index.php/jm/article/view/5593</dc:identifier>
	<dc:identifier>10.20884/1.jm.2022.17.1.5593</dc:identifier>
	<dc:source xml:lang="en-US">Molekul; Vol 17 No 1 (2022); 60-67</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/5593/2817</dc:relation>
	<dc:rights xml:lang="en-US">Copyright (c) 2022 Molekul</dc:rights>
	<dc:rights xml:lang="en-US">http://jos.unsoed.ac.id/index.php/jm/index</dc:rights>
</oai_dc:dc>