z-logo
open-access-imgOpen Access
Isolation, Characterization and Antiproliferative Activity of Secondary Metabolites from Tanacetum alyssifolium (Bornm.) Grierson
Author(s) -
Ekrem Köksal,
Yakup ULUTAŞ,
Samed Şimşek,
aha Bayraktar,
Ahmet Altay,
Mustafa Çatır,
İbrahim Demirtaş,
Ali Rıza Tüfekçi,
Ali Kandemir,
Cemalettin Alp,
Mohammed B. Anwer Alemdar Alemdar,
Hüseyin Akşit
Publication year - 2020
Publication title -
records of natural products
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.43
H-Index - 31
ISSN - 1307-6167
DOI - 10.25135/rnp.201.20.07.1702
Subject(s) - chemistry , acetophenone , luteolin , stereochemistry , glucoside , sesquiterpene , rutin , cytotoxicity , in vitro , flavonoid , biochemistry , antioxidant , medicine , alternative medicine , pathology , catalysis
Secondary metabolites of Tanacetum alyssifolium (Bornm.) Grierson (Asteraceae) were investigated for the first time. Thirteen compounds including axillarin (1), Luteolin-7-O-β-glucoside (8) and rutin (13) as flavonoids, fraxetin (7), isofraxidin (9), isofraxidin-7-O-glucoside (11) and fraxidin (12) as coumarins, tatridin A (2), altissin (3), tamirin (4) and tanachin (5) as sesquiterpene lactones and 2,4-dihydroxy-6-methoxy acetophenone (6) and picein (10) as acetophenone derivatives were isolated from the methanol extract of the species. The structures of all isolated compounds were elucidated by 1D and 2D-NMR techniques and by comparing with the literature data. In addition, in vitro cytotoxic activity of all isolated compounds was evaluated against breast cancer MCF-7 cell line by XTT assay. Sesquiterpene lactones; tatridin A (2), tamirin (4) and tanachin (5) were found to be the most cytotoxic molecules against MCF-7 cell line.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom