NMR-Based Chemical Profiling, Isolation and Evaluation of the Cytotoxic Potential of the Diterpenoid Siderol from Cultivated Sideritis euboea Heldr.

被引:20
作者
Tomou, Ekaterina-Michaela [1 ]
Chatziathanasiadou, Maria V. [2 ]
Chatzopoulou, Paschalina [3 ]
Tzakos, Andreas G. [2 ]
Skaltsa, Helen [1 ]
机构
[1] Natl & Kapodistrian Univ Athens, Sch Pharm, Dept Pharmacognosy & Chem Nat Prod, Athens 15771, Greece
[2] Univ Ioannina, Sect Organ Chem & Biochem, Dept Chem, Ioannina 45110, Greece
[3] Hellen Agr Org DEMETER, Inst Breeding & Plant Genet Resources, IBPGR, Dept Med & Aromat Plants, Thessaloniki 57001, Greece
关键词
cultivated Sideritis euboea; siderol; MTT assay; cancer cell lines; NMR; ENT-KAURANE DITERPENOIDS; CONSTITUENTS; ANTIOXIDANT; PACLITAXEL; AGENTS;
D O I
10.3390/molecules25102382
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Diterpenes are characteristic compounds from the genus Sideritis L., possessing an array of biological activities. Siderol is the main constituent of the ent-kaurene diterpenes in Sideritis species. In order to isolate the specific compound and evaluate for the first time its cytotoxic activity, we explored the dichloromethane extract of cultivated Sideritis euboea Heldr. To track the specific natural bioactive agent, we applied NMR spectroscopy to the crude plant extract, since NMR can serve as a powerful and rapid tool both to navigate the targeted isolation process of bioactive constituents, and to also reveal the identity of bioactive components. Along these lines, from the rapid 1D H-1 NMR spectrum of the total crude plant extract, we were able to determine the characteristic proton NMR signals of siderol. Furthermore, with the same NMR spectrum, we were able to categorize several secondary metabolites into chemical groups as a control of the isolation process. Therefore, this non-polar extract was explored, for the first time, revealing eleven compounds-one fatty acid ester; 2-(p-hydroxyphenyl)ethylstearate (1), three phytosterols; beta -sitosterol (2), stigmasterol (3), and campesterol (4); one triterpenoid; ursolic acid (5), four diterpenoids; siderol (6), eubol (7), eubotriol (8), 7-epicandicandiol (9) and two flavonoids; xanthomicrol (10) and penduletin (11). The main isolated constituent was siderol. The antiproliferative potential of siderol was evaluated, using the MTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide) assay, on three human cancer cell lines DLD1, HeLa, and A549, where the IC50 values were estimated at 26.4 +/- 3.7, 44.7 +/- 7.2, and 46.0 +/- 4.9 mu Mu, respectively. The most potent activity was recorded in the human colon cancer cell line DLD1, where siderol exhibited the lowest IC50. Our study unveiled the beneficial potential of siderol as a remarkable cytotoxic agent and the significant contribution of NMR spectroscopy towards the isolation and identification of this potent anticancer agent.
引用
收藏
页数:11
相关论文
共 36 条
[1]   Genus Sideritis, section Empedoclia in southeastern Europe and Turkey - studies in ethnopharmacology and recent progress of biological activities [J].
Aneva, Ina ;
Zhelev, Peter ;
Kozuharova, Ekaterina ;
Danova, Kalina ;
Nabavi, Seyed Fazel ;
Behzad, Sahar .
DARU-JOURNAL OF PHARMACEUTICAL SCIENCES, 2019, 27 (01) :407-421
[2]   BRUSELAS: HPC Generic and Customizable Software Architecture for 3D Ligand-Based Virtual Screening of Large Molecular Databases [J].
Banegas-Luna, Antonio J. ;
Ceron-Carrasco, Jose P. ;
Puertas-Martin, Savins ;
Perez-Sanchez, Horacio .
JOURNAL OF CHEMICAL INFORMATION AND MODELING, 2019, 59 (06) :2805-2817
[3]   Anti-HIV agents derived from the ent-kaurane diterpenoid linearol [J].
Bruno, M ;
Rosselli, S ;
Pibiri, I ;
Kilgore, N ;
Lee, KH .
JOURNAL OF NATURAL PRODUCTS, 2002, 65 (11) :1594-1597
[4]  
Çarikçi S, 2012, REC NAT PROD, V6, P101
[5]  
Chaturvedula V. S., 2012, INT CURR PHARM J, V1, P239, DOI [10.3329/icpj.v1i9.11613, DOI 10.3329/ICPJ.V1I9.11613]
[6]   Penetration of paclitaxel and 5-fluorouracil in multicellular layers of human colorectal cancer cells [J].
Choi, Mi-Sun ;
Kim, Soo-Hyun ;
Kuh, Hyo-Jeong .
ONCOLOGY REPORTS, 2011, 25 (03) :863-870
[7]  
Committee on Herbal Medicinal Products (HMPC), ASS REP SID SCARD GR
[8]   Antioxidant and Anticholinesterase Activity Evaluation of ent-Kaurane Diterpenoids from Sideritis arguta [J].
Ertas, Abduelselam ;
Ozturk, Mehmet ;
Boga, Mehmet ;
Topcu, Guelacti .
JOURNAL OF NATURAL PRODUCTS, 2009, 72 (03) :500-502
[9]   Diterpenes and phenolic compounds from Sideritis pullulans [J].
Faiella, Laura ;
Dal Piaz, Fabrizio ;
Bader, Ammar ;
Braca, Alessandra .
PHYTOCHEMISTRY, 2014, 106 :164-170
[10]   Phytochemistry and chemotaxonomy of Sideritis species from the Mediterranean region [J].
Fraga, Braulio M. .
PHYTOCHEMISTRY, 2012, 76 :7-24