31129-94-9Relevant academic research and scientific papers
Inhibitory activity of catechin metabolites produced by intestinal microbiota on proliferation of heLa cells
Hara-Terawaki, Aya,Takagaki, Akiko,Kobayashi, Hirotsugu,Nanjo, Fumio
, p. 1331 - 1335 (2017/08/09)
Eleven kinds of catechin metabolites produced from (?)-epigallocatechin (EGC) and (?)-epigallocatechin gallate (EGCg) by intestinal microbiota were evaluated for inhibitory activity on the proliferation of HeLa cells, which are human cervical cancer cells
Concise synthesis of ring-fission metabolites of epicatechin: 5-(3,4-dihydroxybenzyl)dihydrofuran-2(3H)-one M6
Chang, Xiaowei,Peng, Weimin,Yao, Yin-Fang,Koek, Jan
experimental part, p. 3346 - 3352 (2011/01/04)
The ring-fission metabolites of epicatechin, 5-(3,4-dihydroxybenzyl) dihydrofuran-2(3H)-one M6 and 3-methylated M6, were prepared from 3,4-dihydroxybenzaldehyde and furan-2(5H)-one using two new concise methods in excellent yields (three or two steps in 4
Biotransformation of (-)-epicatechin 3-O-gallate by human intestinal bacteria
Meselhy, Meselhy R.,Nakamura, Norio,Hattori, Masao
, p. 888 - 893 (2007/10/03)
The biotransformation of (-)-epicatechin 3-O-gallate (1) and related compounds was undertaken using a human fecal suspension. Of fifteen metabolites isolated, four compounds were new, namely, two epimers of 1-(3'- hydroxyphenyl)-3-(2'',4'',6''-trihydroxyphenyl)propan-2-ols (6, 19); 2'',3''- dihydroxyphenoxyl 3-(3',4'-dihydroxyphenyl)propionate (14) and 1-(3',4'- dihydroxyphenyl)-3-(2'',4'',6''-trihydroxyphenyl)propan-2-ol (18). (-)- Epicatechin (2), (-)-epigallocatechin (16) and their 3-O-gallates (1, 17) were extensively metabolized by a human fecal suspension after incubation for 24 h, whereas the gallates (1, 17) resisted any degradation by a rat fecal suspension, even after a prolonged incubation time (48 h), suggesting a difference in metabolic ability between two intestinal bacterial mixtures from different species.
