Selective synthesis and biological evaluation of sulfate-conjugated resveratrol metabolites.
Selective synthesis and biological evaluation of sulfate-conjugated resveratrol metabolites.
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DOI:
10.1021/jm100274c
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发表时间:
2010-07-08
影响因子:
7.3
通讯作者:
Cushman M
中科院分区:
文献类型:
--
作者:
Hoshino J;Park EJ;Kondratyuk TP;Marler L;Pezzuto JM;van Breemen RB;Mo S;Li Y;Cushman M
Five resveratrol sulfate metabolites were synthesized and assessed for activities known to be mediated by resveratrol: inhibition of tumor necrosis factor (TNF)-α-induced NFκB activity, cylcooxygenases (COX-1 and COX-2), aromatase, nitric oxide production in endotoxin-stimulated macrophages, and proliferation of KB or MCF7 cells, induction of quinone reductase 1 (QR1), accumulation in the sub-G1 phase of the cell cycle, and quenching of 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical. Two metabolites showed activity in these assays; the 3-sulfate exhibited QR1 induction, DPPH free radical scavenging, and COX-1 and COX-2 inhibitory activities, and the 4′-sulfate inhibited NFκB induction, as well as COX-1 and COX-2 activities. Resveratrol, as well as its 3′-sulfate and 4-sulfate, inhibit NO production by NO scavenging and down-regulation of iNOS expression in RAW 264.7 cells. Resveratrol sulfates displayed low antiproliferative activity and negligible uptake in MCF7 cells.
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影响因子:
1.8
作者:
De Santi, C;Pietrabissa, A;Pacifici, GM
通讯作者:
Pacifici, GM
影响因子:
6.1
作者:
Kennelly, EJ;Gerhauser, C;Kinghorn, AD
通讯作者:
Kinghorn, AD
影响因子:
6.1
作者:
Dudley, Jocelyn I.;Lekli, Istvan;Das, Dipak K.
通讯作者:
Das, Dipak K.
影响因子:
1.8
作者:
De Santi, C;Pietrabissa, A;Pacifici, GM
通讯作者:
Pacifici, GM
DOI:
10.1006/bbrc.1998.9916
发表时间:
1999-01-27
影响因子:
3.1
作者:
Carbó, N;Costelli, P;Argilés, JM
通讯作者:
Argilés, JM