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Cytotoxic activity of abietane diterpenoids from roots of Salvia sahendica by HPLC-based activity profiling
Moradi-Afrapoli, Fahimeh; Shokrzadeh, Mohammad; Barzegar, Fatemeh; Gorji-Bahri, Gilar; Zadali, Reza; Nejad Ebrahimi, Samad.
  • Moradi-Afrapoli, Fahimeh; Mazandaran University of Medical Sciences. Faculty of Pharmacy. Department of Pharmacognosy. Sari. IR
  • Shokrzadeh, Mohammad; Mazandaran University of Medical Sciences. Faculty of Pharmacy. Department of Pharmacognosy. Sari. IR
  • Barzegar, Fatemeh; Mazandaran University of Medical Sciences. Faculty of Pharmacy. Department of Pharmacognosy. Sari. IR
  • Gorji-Bahri, Gilar; Mazandaran University of Medical Sciences. Faculty of Pharmacy. Department of Pharmacognosy. Sari. IR
  • Zadali, Reza; Mazandaran University of Medical Sciences. Faculty of Pharmacy. Department of Pharmacognosy. Sari. IR
  • Nejad Ebrahimi, Samad; Mazandaran University of Medical Sciences. Faculty of Pharmacy. Department of Pharmacognosy. Sari. IR
Rev. bras. farmacogn ; 28(1): 27-33, Jan.-Feb. 2018. tab, graf
Article in English | LILACS | ID: biblio-898736
ABSTRACT
ABSTRACT Screening of medicinal plants from Iranian flora against human cancer cell-lines have shown that an hexane extract from roots of Salvia sahendica Boiss. & Buhse, Lamiaceae, is active against human cervical cancer (HeLa) and colorectal adenocarcinoma (Caco-2) cell-lines at the test concentration of 100 µg/ml (100% inhibition). Cytotoxicity of the extract was localized with the aid of HPLC-time-based activity profiling adapted to the tetrazolium colorimetric bioassay. Four abietane-type diterpenoids in active time-windows were identified as cytotoxic compounds namely sahandone (1), sahandol (2), 12-deoxy-salvipisone (3) and sahandinone (4). Compound 1 showed the highest toxicity against HeLa cells (IC50 = 5.6 ± 0.1 µg/ml), which was comparable with betulinic acid (IC50 = 4.3 ± 1.2 µg/ml), the positive control. Compound 2 was active against the HeLa cells (IC50 = 8.9 ± 0.7 µg/ml) but not the Caco-2 cell-line. Compounds 1, 3 and 4 exhibited moderate activity (IC50 = 22.9-41.4 µg/ml) against the Caco-2 cells. This study reveals that the HeLa cells are more sensitive to all tested compounds than the Caco-2 cells. In silico molecular docking study showed a rigid binding of the compounds to tyrosine kinase pp60src, and proved their cytotoxic activity.


Full text: Available Index: LILACS (Americas) Language: English Journal: Rev. bras. farmacogn Journal subject: Pharmacy Year: 2018 Type: Article Affiliation country: Iran Institution/Affiliation country: Mazandaran University of Medical Sciences/IR

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Full text: Available Index: LILACS (Americas) Language: English Journal: Rev. bras. farmacogn Journal subject: Pharmacy Year: 2018 Type: Article Affiliation country: Iran Institution/Affiliation country: Mazandaran University of Medical Sciences/IR