Cytotoxic compounds from the leaves and stems of the endemic Thai plant Mitrephora sirikitiae

被引:10
作者
Anantachoke, Natthinee [1 ]
Lovacharaporn, Duangporn [1 ]
Reutrakul, Vichai [2 ,3 ]
Michel, Sylvie [4 ]
Gaslonde, Thomas [4 ]
Piyachaturawat, Pawinee [5 ]
Suksen, Kanoknetr [5 ]
Prabpai, Samran [6 ]
Nuntasaen, Narong [7 ]
机构
[1] Mahidol Univ, Fac Pharm, Dept Pharmacognosy, Bangkok 10400, Thailand
[2] Mahidol Univ, Fac Sci, Dept Chem, Bangkok, Thailand
[3] Mahidol Univ, Fac Sci, Ctr Excellence Innovat Chem, Bangkok, Thailand
[4] Univ Paris 05, Fac Pharm Paris, UMR 8038 CITCOM, Prod Nat Anal & Synth,Univ Paris,CNRS, Paris, France
[5] Mahidol Univ, Fac Sci, Dept Physiol, Bangkok, Thailand
[6] CP FOODLAB Co Ltd, Sci Pk, Pathum Thani, Thailand
[7] Minist Nat Resources & Environm, Forest Herbarium, Dept Natl Pk Wildlife & Plant Conservat, Bangkok, Thailand
关键词
Annonaceae; plant metabolite; alkaloid; lignan; diterpenoid; cytotoxicity; anticancer agent; CELL-CYCLE ARREST; ENT-TRACHYLOBANE DITERPENOIDS; DIHYDROBENZOFURAN LIGNAN; CANCER CELLS; FLOWER BUDS; CONSTITUENTS; SESQUITERPENOIDS; LIRIODENINE; INHIBITION; INDUCTION;
D O I
10.1080/13880209.2020.1765813
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Context: Mitrephora sirikitiae Weeras., Chalermglin & R.M.K. Saunders (Annonaceae) is a plant endemic to Thailand. Its constituents and their biological activities are unknown. Objective: Isolation and identification of the compounds in the leaves and stems of M. sirikitiae and determination of their cytotoxicity. Materials and methods: Methanol extracts of the leaves and stems of M. sirikitiae were separated by chromatography, and spectroscopic methods were used to determine the structures of the components. The cytotoxicity of the extracts and pure compounds was evaluated using the sulforhodamine B assay with several cell lines. The cells were treated with the compounds at concentrations of 0.16-20 mu g/mL for 48 or 72 h. Results: The investigation of the extracts of M. sirikitiae leaves and stems resulted in the isolation of a new lignan, mitrephoran, and 15 known compounds. Among these compounds, 2-(3,4-dimethoxyphenyl)-6-(3,5-dimethoxyphenyl)-3,7-dioxabicyclo[3.3.0]octane, ciliaric acid, 6-methoxymarcanine A, and stepharanine were isolated from this genus for the first time. The alkaloids liriodenine and oxoputerine exhibited strong cytotoxicity against all tested cells (IC50 values of 6.59-11.02 mu M). In contrast, magnone A, 3 ',4-O-dimethylcedrusin, and 6-methoxymarcanine A inhibited the growth of some of the tested cells (IC50 values of 2.03-19.73 mu M). Magnone A and 6-methoxymarcanine A showed low toxicity for Hek 293 cells (IC50 >20 mu M). Discussion and conclusions: M. sirikitiae is a source of cytotoxic lignans and alkaloids. Among the cytotoxic compounds, magnone A and 6-methoxymarcanine A are potentially useful lead compounds for the further development of anticancer agents because of their selective inhibitory effects on cancer cell lines.
引用
收藏
页码:490 / 497
页数:8
相关论文
共 59 条
[1]   Two highly oxygenated eudesmanes and 10 lignans from Achillea holosericea [J].
Ahmed, AA ;
Mahmoud, AA ;
Ali, ET ;
Tzakou, O ;
Couladis, M ;
Mabry, TJ ;
Gáti, T ;
Tóth, G .
PHYTOCHEMISTRY, 2002, 59 (08) :851-856
[2]  
[Anonymous], J PHARM SOC NIPPON
[3]  
Ardalani H, 2017, AVICENNA J PHYTOMEDI, V7, P285
[4]   Natural Compounds as Modulators of Cell Cycle Arrest: Application for Anticancer Chemotherapies [J].
Bailon-Moscoso, Natalia ;
Cevallos-Solorzano, Gabriela ;
Carlos Romero-Benavides, Juan ;
Ramirez Orellana, Maria Isabel .
CURRENT GENOMICS, 2017, 18 (02) :106-131
[5]   Synthesis and trypanocidal activity of ent-kaurane glycosides [J].
Batista, Ronan ;
Humberto, Jorge Luiz ;
Chiari, Egler ;
de Oliveira, Alaide Braga .
BIOORGANIC & MEDICINAL CHEMISTRY, 2007, 15 (01) :381-391
[6]  
Bray F, 2018, CA-CANCER J CLIN, V68, P394, DOI [10.3322/caac.21492, 10.3322/caac.21609]
[7]   Liriodenine induces G1/S cell cycle arrest in human colon cancer cells via nitric oxide- and p53-mediated pathway [J].
Chen, Chung-Yi ;
Chen, Sing-Ying ;
Chen, Ching-Hsein .
PROCESS BIOCHEMISTRY, 2012, 47 (10) :1460-1468
[8]   Bio-Functional Constituents from the Stems of Liriodendron tulipifera [J].
Chiu, Chien-Chih ;
Chou, Han-Lin ;
Wu, Pei-Fang ;
Chen, Hsin-Liang ;
Wang, Hui-Min ;
Chen, Chung-Yi .
MOLECULES, 2012, 17 (04) :4357-4372
[9]   Chemical constituents of Mitrephora maingayi [J].
Deepralard, Khanittha ;
Pengsuparp, Thitima ;
Moriyasu, Masataka ;
Kawanishi, Kazuko ;
Suttisri, Rutt .
BIOCHEMICAL SYSTEMATICS AND ECOLOGY, 2007, 35 (10) :696-699
[10]   OLEX2: a complete structure solution, refinement and analysis program [J].
Dolomanov, Oleg V. ;
Bourhis, Luc J. ;
Gildea, Richard J. ;
Howard, Judith A. K. ;
Puschmann, Horst .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 2009, 42 :339-341