Secondary metabolites from the leaves of Meliosma rhoifolia and evaluation of their cytotoxic activity

被引:0
作者
Cheng, Ming-Jen [1 ]
Chen, Jih-Jung [2 ,3 ]
Wu, Ming-Der [4 ]
Wei, Yu-Hui [4 ]
Kuo, Yang Cheng [4 ]
Weng, Jing-Ru [5 ,6 ]
机构
[1] Fu Jen Catholic Univ, Dept Life Sci, New Taipei City 24205, Taiwan
[2] Natl Yang Ming Chiao Tung Univ NYCU, Sch Pharmaceut Sci, Dept Pharm, Taipei 112304, Taiwan
[3] China Med Univ, China Med Univ Hosp, Dept Med Res, Taichung 404333, Taiwan
[4] Food Ind Res & Dev Inst, Bioresource Collect & Res Ctr, Hsinchu 300193, Taiwan
[5] Natl Sun Yat sen Univ, Dept Marine Biotechnol & Resources, Kaohsiung 80424, Taiwan
[6] Natl Sun Yat sen Univ, Doctoral Degree Program Marine Biotechnol, Kaohsiung 80424, Taiwan
关键词
Meliosma rhoifolia; Sabiaceae; Diterpenoid; Anti-tumor; Secondary metabolites;
D O I
10.1016/j.molstruc.2023.135346
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
One previously undescribed labdane diterpenoid, meliosmarhoifol (1), together with four known ones, 12R,15-dihydroxylabda-8(17),13E-dien-19-oic acid (2), 18-norlabda-8(17),14-diene-4 alpha,13 beta-diol (3), 5 alpha,6 alpha-epoxy-(22E,24R)-ergosta-8(14),22-diene-3 beta,7 alpha-diol (4), 5 alpha,6 alpha-epoxy-(22E,24R)-ergosta-8,22-diene-3 beta,7 alpha-diol (5), were isolated from the leaves of Meliosma rhoifolia. The structures of all isolates were elucidated on the basis of extensive analyses of spectroscopic data and comparison with literature data. In addition, the cytotoxicity of the isolates was evaluated on the MCF-7, NCI-H460 and SF-268 cell lines. Among them, compounds 2-5 were found to have moderate cytotoxic effects against these three cell lines in vitro. Four constituents, compounds 1, 2, 4 and 5 showed different sensitivities in inhibiting the growth of MCF-7 breast cancer cells, with IC50 values ranging from 4.21 to 25.70 mu M, while compound 3 did not show obvious effects. Amount these isolates, meliosmarhoifol (1) showed as the most actively compound against the MCF-7, NCI-H460 and SF-268 cell lines with IC50 values of 4.21, 4.76, and 8.32 mu M, respectively.
引用
收藏
页数:5
相关论文
共 50 条
  • [31] Evaluation of in vitro alpha-glucosidase inhibitory, antimicrobial, and cytotoxic activities of secondary metabolites from the endophytic fungus, Nigrospora sphaerica, isolated from Helianthus annuus
    Preuttiporn Supaphon
    Sita Preedanon
    Annals of Microbiology, 2019, 69 : 1397 - 1406
  • [32] Evaluation of in vitro alpha-glucosidase inhibitory, antimicrobial, and cytotoxic activities of secondary metabolites from the endophytic fungus, Nigrospora sphaerica, isolated from Helianthus annuus
    Supaphon, Preuttiporn
    Preedanon, Sita
    ANNALS OF MICROBIOLOGY, 2019, 69 (13) : 1397 - 1406
  • [33] Screening Evaluation of Antiproliferative, Antimicrobial and Antioxidant Activity of Lichen Extracts and Secondary Metabolites In Vitro
    Kello, Martin
    Goga, Michal
    Kotorova, Klaudia
    Sebova, Dominika
    Frenak, Richard
    Tkacikova, Ludmila
    Mojzis, Jan
    PLANTS-BASEL, 2023, 12 (03):
  • [34] Penicillium spp.: prolific producer for harnessing cytotoxic secondary metabolites
    Koul, Mytre
    Singh, Shashank
    ANTI-CANCER DRUGS, 2017, 28 (01) : 11 - 30
  • [35] Antimicrobial and Cytotoxic Activities of the Secondary Metabolites of Endophytic Fungi Isolated from the Medicinal Plant Hyssopus officinalis
    Eshboev, Farkhod
    Karakozova, Marina
    Abdurakhmanov, Jaloliddin
    Bobakulov, Khayrulla
    Dolimov, Khayotjon
    Abdurashidov, Akhror
    Baymirzaev, Asadali
    Makhnyov, Artyom
    Terenteva, Ekaterina
    Sasmakov, Sobirdjan
    Piyakina, Galina
    Egamberdieva, Dilfuza
    Nazarov, Pavel A.
    Azimova, Shakhnoz
    ANTIBIOTICS-BASEL, 2023, 12 (07):
  • [36] Secondary Metabolites from Ophiorrhiza
    Johnson, Anil J.
    Rajan, Renjith
    Baby, Sabulal
    NATURAL PRODUCTS JOURNAL, 2018, 8 (04) : 248 - 267
  • [37] Secondary Metabolites of Pteridium revolutum and Their Immunosuppressive Activity
    Zhou, Man-Qing
    Wu, Qiu-Yan
    Han, Yu-Ting
    Wang, Kui-Wu
    CHEMISTRY OF NATURAL COMPOUNDS, 2016, 52 (06) : 1147 - 1150
  • [38] Cytotoxic Flavonoids from the Leaves of Cryptocarya chinensis
    Chou, Tsung-Hsien
    Chen, Jih-Jung
    Lee, Shiow-Ju
    Chiang, Michael Y.
    Yang, Cheng-Wei
    Chen, Ih-Sheng
    JOURNAL OF NATURAL PRODUCTS, 2010, 73 (09): : 1470 - 1475
  • [39] Secondary Metabolites Production by Actinomycetes and their Antifungal Activity
    Dewi, Tirta Kumala
    Agustiani, Dwi
    Antonius, Sarjiya
    4TH INTERNATIONAL CONFERENCE ON BIOLOGICAL SCIENCE (2015), 2017, : 256 - 264
  • [40] The antifungal activity of Moroccan plants and the mechanism of action of secondary metabolites from plants
    Lagrouh, F.
    Dakka, N.
    Bakri, Y.
    JOURNAL DE MYCOLOGIE MEDICALE, 2017, 27 (03): : 303 - 311