Novel Cytotoxic Sesquiterpene Ester Derivatives from the Roots of Ferula mervynii

被引:2
|
作者
Yazici Bektas, Nurdan [1 ,2 ]
Altiparmak Ulbegi, Gulsum [3 ]
Aksoy Sagirli, Pinar [3 ]
Miski, Mahmut [1 ]
机构
[1] Istanbul Univ, Fac Pharm, Dept Pharmacognosy, TR-34116 Istanbul, Turkiye
[2] Karadeniz Tech Univ, Fac Pharm, Dept Pharmacognosy, Trabzon, Turkiye
[3] Istanbul Univ, Fac Pharm, Dept Biochem, Istanbul, Turkiye
关键词
Apiaceae; cytotoxicity; Ferula mervynii; nor-ketoelemane type sesquiterpene; putative biosynthetic pathway; quantum chemistry calculation; sesquiterpene; ANTITUMOR-ACTIVITY; DAUCANE ESTERS; ARYL ESTERS; ANTIOXIDANT; COMMUNIS; APIACEAE; CELLS; RESIN;
D O I
10.1002/cbdv.202201058
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
This study is the first chemical investigation of Ferula mervynii M. Sagiroglu & H. Duman, an endemic species to Eastern Anatolia. The isolations of nine compounds including six previously undescribed sesquiterpene esters, 8-trans-cinnamoyltovarol (1), 8-trans-cinnamoylantakyatriol (3), 6-acetyl-8-trans-cinnamoyl-3-epi-antakyatriol (5), 6-acetyl-8-trans-cinnamoylshiromodiol (6), 6-acetyl-8-trans-cinnamoylfermedurone (7), and 6-acetyl-8-trans-cinnamoyl-(1S),2-epoxyfermedurone (8), were described along with three known sesquiterpene esters, 6-acetyl-8-benzoyltovarol (2), 6-acetyl-8-trans-cinnamoylantakyatriol (4), and ferutinin (9). The structures of novel compounds were elucidated through extensive spectroscopic analyses and quantum chemistry calculations. The putative biosynthetic pathways for compounds 7 and 8 were discussed. The extracts and isolated compounds were tested for cytotoxic activity against the COLO 205, K-562, MCF-7 cancer cell lines, and Human Umbilical Vein Endothelial Cell (HUVEC) lines using MTT assay. Compound 4 showed the highest activity against the MCF-7 cell lines with an IC50 value of 16.74 +/- 0.21 mu M.
引用
收藏
页数:12
相关论文
共 50 条
  • [31] An unusual sesquiterpene derivative from Ferula kuhistanica
    Tamemoto, K
    Takaishi, Y
    Kawazoe, K
    Honda, G
    Ito, M
    Kiuchi, F
    Takeda, Y
    Kodzhimatov, OK
    Ashurmetov, O
    Shimizu, K
    Nagasawa, H
    Uto, Y
    Hori, H
    JOURNAL OF NATURAL PRODUCTS, 2002, 65 (09): : 1323 - 1324
  • [32] CAROTANE SESQUITERPENE FROM FERULA-SINAICA
    ELSAYED, NH
    PHARMAZIE, 1990, 45 (07): : 538 - 538
  • [33] Sesquiterpene coumarins and sesquiterpenes from Ferula sinaica
    Ahmed, AA
    PHYTOCHEMISTRY, 1999, 50 (01) : 109 - 112
  • [34] Bioactive Sesquiterpene Coumarins from Ferula pseudalliacea
    Dastan, Dara
    Salehi, Peyman
    Gohari, Ahmad Reza
    Ebrahimi, Samad Nejad
    Aliahmadi, Atousa
    Hamburger, Matthias
    PLANTA MEDICA, 2014, 80 (13) : 1118 - 1123
  • [35] SESQUITERPENE LACTONES FROM FERULA-LITVINOWIANA
    BAGIROV, VY
    SHEICHENKO, VI
    MIRBABAYEV, NF
    PIMENOV, MG
    KHIMIYA PRIRODNYKH SOEDINENII, 1984, (01): : 114 - 114
  • [36] Histone deacetylase inhibitory and cytotoxic activities of the constituents from the roots of three species of Ferula
    Soltani, Saba
    Amin, Gholamreza
    Salehi-Sourmaghi, Mohammad Hossein
    Iranshahi, Mehrdad
    IRANIAN JOURNAL OF BASIC MEDICAL SCIENCES, 2019, 22 (01) : 93 - 98
  • [37] New sesquiterpene esters and a saponin from Ferula elaeochytris and their cytotoxic evaluation against leukemia cell lines
    Al Khatib, R.
    Hennebelle, T.
    Joha, S.
    Idziorek, T.
    Preudhomme, C.
    Quesnel, B.
    Sahpaz, S.
    Bailleul, F.
    PLANTA MEDICA, 2008, 74 (09) : 1030 - 1031
  • [38] Sesquiterpene coumarins from seeds of Ferula sinkiangensis
    Li, Guangzhi
    Li, Xiaojin
    Cao, Li
    Zhang, Lijing
    Shen, Liangang
    Zhu, Jun
    Wang, Junchi
    Si, Jianyong
    FITOTERAPIA, 2015, 103 : 222 - 226
  • [39] Sesquiterpene coumarins from the fruits of Ferula badrakema
    Iranshahi, M.
    Rezaee, R.
    Sahebkar, A.
    Bassarello, C.
    Piacente, S.
    Pizza, C.
    PHARMACEUTICAL BIOLOGY, 2009, 47 (04) : 344 - 347
  • [40] Three new tetrahydrobenzofuran derivatives from Ferula sinkiangensis KMShen and their cytotoxic activities
    Yi, Xianguo
    Li, Zhili
    Zheng, Quanfang
    Sang, Ruijuan
    Li, Haili
    Gao, Ge
    Qin, Qingming
    Zhu, Nailiang
    NATURAL PRODUCT RESEARCH, 2023, 37 (20) : 3369 - 3373