Anticancer activity of Indonesian Melia azedarach L.: Phyto-chemistry, in vitro and in silico studies

被引:0
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作者
Nugraha, Ari Satia [1 ]
Firli, Lilla Nur [1 ]
Hendra, Rudi [2 ]
Keller, Paul A. [3 ,4 ]
Purwoko, Reza Yuridian [5 ,6 ]
Idrus, Hasta Handayani [7 ]
Ritawidya, Rien [8 ,9 ]
Febrian, Muhamad B. [8 ]
Mahendra, Isa [8 ,9 ]
Kurniawan, Ahmad [8 ]
Forentin, Alfian M. [8 ]
Susilo, Veronika Y. [8 ]
Kusumaningrum, Crhisterra E. [8 ]
Setiadi, Yanuar [10 ]
Wongso, Hendris [8 ,9 ]
机构
[1] Univ Jember, Fac Pharm, Drug Utilisat & Discovery Res Grp, Jember 68121, Indonesia
[2] Univ Riau, Fac Math & Nat Sci, Dept Chem, Riau, Indonesia
[3] Univ Wollongong, Sch Chem & Mol Biosci & Mol Horizons, Wollongong, NSW 2522, Australia
[4] Illawarra Hlth & Med Res Inst, Wollongong, NSW 2522, Australia
[5] President Univ, Fac Med, Bekasi 17530, Indonesia
[6] Univ Indonesia, Master Program Biomed Sci, Specializat Stem Cells, Fac Med, Jakarta, Indonesia
[7] Natl Res & Innovat Agcy, Cibinong Sci Ctr, Res Org Hlth, Ctr Biomed Res, Jalan Raya Jakarta Bogor KM 46, Bogor 16911, Jawa Bara, Indonesia
[8] Natl Res & Innovat Agcy, Res Org Nucl Energy, Res Ctr Radioisotope Radiopharmaceut & Biodosimetr, Puspiptek 15314, Banten, Indonesia
[9] Natl Res & Innovat Agcy, Res Collaborat Ctr Theranost Radiopharmaceut, Jl Ir Soekarno KM 21, Jatinangor 45363, Indonesia
[10] Natl Res & Innovat Agcy, Res Org Life Sci & Environm, Res Ctr Environm & Clean Technol, Puspiptek 15314, Banten, Indonesia
关键词
Melia azedarach L; kaempferol; resorcinol; phytochemistry; anticancer; LIMONOIDS;
D O I
10.1080/22311866.2023.2172079
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This study describes the isolation of bioactive compounds and their in vitro anticancer activities from Melia azedarach L leaves from Karanglor, Karangan, Karanganom Klaten, Central Java-Indonesia. Isolated and characterised were the phenolics, kaempferol 7-O-rutinoside 1 and 4-methoxyresorcinol 3, The anticancer activity of the crude methanol extract of M. azedarach against a number cell lines (LNCaP, MDA-MB-231, and MCF-7) was found to be moderate; kaempferol derivatives were notable for their antiproliferative activities. Computational analysis, including molecular docking simulations and molecular dynamic studies, were used to investigate the feasibility of radiolabelled versions of 1 and 3 as theranostic agents targeting tyrosine kinase-type cell surface receptor HER2 in cancer - the iodinated derivatives 2 and 4, respectively, were used in this investigation as surrogates. The corresponding radioiodinated 2 and 4 were found to have high binding affinities of 10.1 and 5.7 kcal/mol, respectively, and have a good stability on the receptor.
引用
收藏
页码:12 / 26
页数:15
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