Cytotoxicity of New Ferulic-Acid Derivatives on Human Colon Carcinoma (HCT116) Cells

Chi tiết về thư mục
Parent link:Pharmaceutical Chemistry Journal
Vol. 53, iss. 6.— 2019.— [P. 516-520]
Tác giả của công ty: Национальный исследовательский Томский политехнический университет Инженерная школа новых производственных технологий Научно-образовательный центр Н. М. Кижнера
Tác giả khác: Bakholdina L. A. Lyubov Alekseevna, Markova A. A. Alyona Aleksandrovna, Khlebnikov A. I. Andrey Ivanovich, Sevodin V. P. Valery Pavlovich
Tóm tắt:Title screen
A series of esters of ferulic acid and alcohols were synthesized and characterized structurally. All tested synthetic compounds were more cytotoxic against HCT116 cell line (human colon carcinoma) than ferulic acid. Benzyl and phenylethyl esters of ferulic acid were the most active compounds (IC50 = 0.0077 and 0.0065 g/L, respectively). Feruloylated wheat-bran oligosaccharides were less active than free ferulic acid against HCT116 tumor cells.
Режим доступа: по договору с организацией-держателем ресурса
Được phát hành: 2019
Những chủ đề:
Truy cập trực tuyến:https://doi.org/10.1007/s11094-019-02030-y
Định dạng: Điện tử Chương của sách
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=661890
Miêu tả
Tóm tắt:Title screen
A series of esters of ferulic acid and alcohols were synthesized and characterized structurally. All tested synthetic compounds were more cytotoxic against HCT116 cell line (human colon carcinoma) than ferulic acid. Benzyl and phenylethyl esters of ferulic acid were the most active compounds (IC50 = 0.0077 and 0.0065 g/L, respectively). Feruloylated wheat-bran oligosaccharides were less active than free ferulic acid against HCT116 tumor cells.
Режим доступа: по договору с организацией-держателем ресурса
DOI:10.1007/s11094-019-02030-y