-
1
-
-
38649132291
-
Resveratrol and its analogs: Defense against cancer, coronary disease and neurodegenerative maladies or just a fad?
-
Saiko, P.; Szakmary, A.; Jaeger, W.; Szekeres, T. Resveratrol and its analogs: Defense against cancer, coronary disease and neurodegenerative maladies or just a fad? Mutat. Res. 2008, 658, 68-94
-
(2008)
Mutat. Res.
, vol.658
, pp. 68-94
-
-
Saiko, P.1
Szakmary, A.2
Jaeger, W.3
Szekeres, T.4
-
2
-
-
0037108201
-
Vascular dysfunction and free radicals. Redox signaling in vascular angiogenesis
-
Maulik, N.; Das, D. K. Vascular dysfunction and free radicals. Redox signaling in vascular angiogenesis Free Radical Biol. Med. 2002, 33, 1047-1060
-
(2002)
Free Radical Biol. Med.
, vol.33
, pp. 1047-1060
-
-
Maulik, N.1
Das, D.K.2
-
3
-
-
22544475022
-
Antioxidants and endothelium protection
-
Praticò, D. Antioxidants and endothelium protection Atherosclerosis 2005, 181, 215-224
-
(2005)
Atherosclerosis
, vol.181
, pp. 215-224
-
-
Praticò, D.1
-
4
-
-
55549134620
-
The role of arterial smooth muscle in vasorelaxation
-
Buchwalow, I. B.; Cacanyiova, S.; Neumann, J.; Samoilova, V. E.; Boecker, W.; Kristek, F. The role of arterial smooth muscle in vasorelaxation Biochem. Biophys. Res. Commun. 2008, 377, 504-507
-
(2008)
Biochem. Biophys. Res. Commun.
, vol.377
, pp. 504-507
-
-
Buchwalow, I.B.1
Cacanyiova, S.2
Neumann, J.3
Samoilova, V.E.4
Boecker, W.5
Kristek, F.6
-
5
-
-
0036872336
-
Nitric oxide formation and corresponding relaxation of porcine coronary arteries induced by plant phenols: Essential structural features
-
Taubert, D.; Berkels, R.; Klaus, W.; Roesen, R. Nitric oxide formation and corresponding relaxation of porcine coronary arteries induced by plant phenols: essential structural features J. Cardiovasc. Pharmacol. 2002, 40, 701-713
-
(2002)
J. Cardiovasc. Pharmacol.
, vol.40
, pp. 701-713
-
-
Taubert, D.1
Berkels, R.2
Klaus, W.3
Roesen, R.4
-
6
-
-
69049109766
-
Resveratrol and chemoprevention
-
Goswami, S. K.; Das, D. K. Resveratrol and chemoprevention Cancer Lett. 2009, 284, 1-6
-
(2009)
Cancer Lett.
, vol.284
, pp. 1-6
-
-
Goswami, S.K.1
Das, D.K.2
-
7
-
-
0038623968
-
Dihydrochalcones: Evaluation as novel radical scavenging antioxidants
-
Nakamura, Y.; Watanabe, S.; Miyake, N.; Kohno, H.; Osawa, T. Dihydrochalcones: evaluation as novel radical scavenging antioxidants J. Agric. Food Chem. 2003, 51, 3309-3312
-
(2003)
J. Agric. Food Chem.
, vol.51
, pp. 3309-3312
-
-
Nakamura, Y.1
Watanabe, S.2
Miyake, N.3
Kohno, H.4
Osawa, T.5
-
8
-
-
0034074880
-
Plant-derived estrogens relax coronary arteries in vitro by a calcium antagonistic mechanism
-
Figtree, G. A.; Griffiths, H.; Lu, Y.-Q.; Webb, C. M.; MacLeod, K.; Collins, P. Plant-derived estrogens relax coronary arteries in vitro by a calcium antagonistic mechanism J. Am. Coll. Cardiol. 2000, 35, 1977-1985
-
(2000)
J. Am. Coll. Cardiol.
, vol.35
, pp. 1977-1985
-
-
Figtree, G.A.1
Griffiths, H.2
Lu, Y.-Q.3
Webb, C.M.4
MacLeod, K.5
Collins, P.6
-
9
-
-
34249720541
-
Chronic resveratrol enhances endothelium-dependent relaxation but does not alter eNOS levels in aorta of spontaneously hypertensive rats
-
Rush, J. W. E.; Quadrilatero, J.; Levy, A. S.; Ford, R. J. Chronic resveratrol enhances endothelium-dependent relaxation but does not alter eNOS levels in aorta of spontaneously hypertensive rats Exp. Biol. Med. 2007, 232, 814-822
-
(2007)
Exp. Biol. Med.
, vol.232
, pp. 814-822
-
-
Rush, J.W.E.1
Quadrilatero, J.2
Levy, A.S.3
Ford, R.J.4
-
10
-
-
50949093304
-
The effect of long-term resveratrol treatment on relaxation to estrogen in aortae from male and female rats: Role of nitric oxide and superoxide
-
Soylemez, S.; Gurdal, H.; Sepici, A.; Akar, F. The effect of long-term resveratrol treatment on relaxation to estrogen in aortae from male and female rats: role of nitric oxide and superoxide Vasc. Pharmacol. 2008, 49, 97-105
-
(2008)
Vasc. Pharmacol.
, vol.49
, pp. 97-105
-
-
Soylemez, S.1
Gurdal, H.2
Sepici, A.3
Akar, F.4
-
11
-
-
33644814524
-
Resveratrol decreases calcium sensitivity of vascular smooth muscle and enhances cytosolic calcium increase in endothelium
-
Buluc, M.; Demirel-Yilmaz, E. Resveratrol decreases calcium sensitivity of vascular smooth muscle and enhances cytosolic calcium increase in endothelium Vasc. Pharmacol. 2006, 44, 231-237
-
(2006)
Vasc. Pharmacol.
, vol.44
, pp. 231-237
-
-
Buluc, M.1
Demirel-Yilmaz, E.2
-
12
-
-
0036280760
-
Resveratrol activates membrane-bound guanylyl cyclase in coronary arterial smooth muscle: A novel signaling mechanism in support of coronary protection
-
El-Mowafy, A. M. Resveratrol activates membrane-bound guanylyl cyclase in coronary arterial smooth muscle: a novel signaling mechanism in support of coronary protection Biochem. Biophys. Res. Commun. 2002, 291, 1218-1214
-
(2002)
Biochem. Biophys. Res. Commun.
, vol.291
, pp. 1218-1214
-
-
El-Mowafy, A.M.1
-
13
-
-
0029981730
-
Vasorelaxing activity of resveratrol and quercetin in isolated rat aorta
-
Chen, C. K.; Pace-Asciak, C. R. Vasorelaxing activity of resveratrol and quercetin in isolated rat aorta Gen. Pharmacol. 1996, 27, 363-366
-
(1996)
Gen. Pharmacol.
, vol.27
, pp. 363-366
-
-
Chen, C.K.1
Pace-Asciak, C.R.2
-
14
-
-
66449128912
-
Potential antioxidants and tyrosinase inhibitors from synthetic polyphenolic deoxybenzoins
-
Ng, L. T.; Ko, H. H.; Lu, T. M. Potential antioxidants and tyrosinase inhibitors from synthetic polyphenolic deoxybenzoins Bioorg. Med. Chem. 2009, 17, 4360-4366
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 4360-4366
-
-
Ng, L.T.1
Ko, H.H.2
Lu, T.M.3
-
15
-
-
6444224110
-
A new class of phytoestrogens: Evaluation of the estrogenic activity of deoxybenzoins
-
Fokialakis, N.; Lambrinidis, G.; Mitsiou, D. Z.; Aligiannis, N.; Mitakou, S.; Skaltsounis, A.-L.; Pratsinis, H.; Mikros, E.; Alexis, M. N. A new class of phytoestrogens: evaluation of the estrogenic activity of deoxybenzoins Chem. Biol. 2004, 11, 397-406
-
(2004)
Chem. Biol.
, vol.11
, pp. 397-406
-
-
Fokialakis, N.1
Lambrinidis, G.2
Mitsiou, D.Z.3
Aligiannis, N.4
Mitakou, S.5
Skaltsounis, A.-L.6
Pratsinis, H.7
Mikros, E.8
Alexis, M.N.9
-
16
-
-
77956643867
-
Tyrosine kinase inhibitor 2,4,6-trihydroxy-α p- methoxyphenylacetophenone (compound D-58) is a potent inhibitor of allergic and inflammatory reactions
-
(1, Part 2), Abstr. 1061
-
Uckun, F.; Malaviya, R.; Jan, S.-T.; Zhu, D.-M.; Malaviya, R. Tyrosine kinase inhibitor 2,4,6-trihydroxy-α p-methoxyphenylacetophenone (compound D-58) is a potent inhibitor of allergic and inflammatory reactions. J. Allergy Clin. Immunol. 2000, 105 (1, Part 2), Abstr. 1061.
-
(2000)
J. Allergy Clin. Immunol.
, vol.105
-
-
Uckun, F.1
Malaviya, R.2
Jan, S.-T.3
Zhu, D.-M.4
Malaviya, R.5
-
17
-
-
58849133370
-
Discovery of novel 2′,3′,4′-trihydroxy-2- phenylacetophenone derivatives as anti-Gram-positive antibacterial agents
-
Goto, H.; Kumada, Y.; Ashida, H.; Yoshida, K. Discovery of novel 2′,3′,4′-trihydroxy-2-phenylacetophenone derivatives as anti-Gram-positive antibacterial agents Biosci., Biotechnol., Biochem. 2009, 73, 124-128
-
(2009)
Biosci., Biotechnol., Biochem.
, vol.73
, pp. 124-128
-
-
Goto, H.1
Kumada, Y.2
Ashida, H.3
Yoshida, K.4
-
18
-
-
40049084450
-
Synthesis, crystal structure and antimicrobial activity of deoxybenzoin derivatives from genistein
-
Li, H,-Q.; Xue, J.-Y.; Shi, L.; Gui, S.-Y.; Zhu, H.-L. Synthesis, crystal structure and antimicrobial activity of deoxybenzoin derivatives from genistein Eur. J. Med. Chem. 2008, 43, 662-667
-
(2008)
Eur. J. Med. Chem.
, vol.43
, pp. 662-667
-
-
Li, H.-Q.1
Xue, J.-Y.2
Shi, L.3
Gui, S.-Y.4
Zhu, H.-L.5
-
19
-
-
34247481934
-
Polyphenols based on isoflavones as inhibitors of Helicobacter pylori urease
-
Xiao, Z.-P.; Shi, D.-H.; Li, H,-Q.; Zhang, L.-N.; Xu, C.; Zhu, H.-L. Polyphenols based on isoflavones as inhibitors of Helicobacter pylori urease Bioorg. Med. Chem. 2007, 15, 3703-3710
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 3703-3710
-
-
Xiao, Z.-P.1
Shi, D.-H.2
Li, H.-Q.3
Zhang, L.-N.4
Xu, C.5
Zhu, H.-L.6
-
21
-
-
0033968996
-
An efficient "one pot" synthesis of isoflavone
-
Balasubramanian, S.; Nair, M. G. An efficient "one pot" synthesis of isoflavone Synth. Commun. 2000, 30, 469-484
-
(2000)
Synth. Commun.
, vol.30
, pp. 469-484
-
-
Balasubramanian, S.1
Nair, M.G.2
-
22
-
-
85047676779
-
The first isolation and crystal structure of a boron difluoro complex (isoflavone yellow). Biologically active intermediates produced during isoflavone synthesis
-
Balasubramanian, S.; Ward, D. L.; Nair, M. G. The first isolation and crystal structure of a boron difluoro complex (isoflavone yellow). Biologically active intermediates produced during isoflavone synthesis J. Chem. Soc., Perkin Trans. 1 2000, 567-569
-
(2000)
J. Chem. Soc., Perkin Trans. 1
, pp. 567-569
-
-
Balasubramanian, S.1
Ward, D.L.2
Nair, M.G.3
-
23
-
-
28444492700
-
Synthetic model of a new deoxybenzoin derivative from Deguelia hatschbachii A.M.G. Azevedo
-
Magalhães, A. F.; Magalhães, E. G.; Trazzi, G.; Moraes, V. R. de S. Synthetic model of a new deoxybenzoin derivative from Deguelia hatschbachii A.M.G. Azevedo Ecletica Quim. 2005, 30, 43-49
-
(2005)
Ecletica Quim.
, vol.30
, pp. 43-49
-
-
Magalhães, A.F.1
Magalhães, E.G.2
Trazzi, G.3
Moraes, V.R.D.S.4
-
24
-
-
0035341550
-
Prenylated flavonoids from Deguelia hatschbachii and their systematic significance in Deguelia
-
Magalhães, A. F.; Tozzi, A. M.; Magalhães, E. G.; Moraes, V. R. de S. Prenylated flavonoids from Deguelia hatschbachii and their systematic significance in Deguelia Phytochemistry 2001, 57, 77-89
-
(2001)
Phytochemistry
, vol.57
, pp. 77-89
-
-
Magalhães, A.F.1
Tozzi, A.M.2
Magalhães, E.G.3
Moraes, V.R.D.S.4
-
25
-
-
33645529006
-
New prenylated metabolites from Degulia longeracemosa and evaluation of their antimicrobial potential
-
Magalhães, A. F.; Tozzi, A. M.; Magalhães, E. G.; Souza-Neta, L. C. New prenylated metabolites from Degulia longeracemosa and evaluation of their antimicrobial potential Planta Med. 2006, 72, 358-363
-
(2006)
Planta Med.
, vol.72
, pp. 358-363
-
-
Magalhães, A.F.1
Tozzi, A.M.2
Magalhães, E.G.3
Souza-Neta, L.C.4
-
26
-
-
17444423248
-
Phenolic constituents of the rhizomes of the Thai medicinal plant Belamcanda chinensis with proliferative activity for two breast cancer cell lines
-
Monthakantirat, O.; De-Eknamkul, W.; Umehara, K.; Yoshinaga, Y.; Miyase, T.; Warashina, T.; Noguchi, H. Phenolic constituents of the rhizomes of the Thai medicinal plant Belamcanda chinensis with proliferative activity for two breast cancer cell lines J. Nat. Prod. 2005, 68, 361-364
-
(2005)
J. Nat. Prod.
, vol.68
, pp. 361-364
-
-
Monthakantirat, O.1
De-Eknamkul, W.2
Umehara, K.3
Yoshinaga, Y.4
Miyase, T.5
Warashina, T.6
Noguchi, H.7
-
27
-
-
0010708052
-
The isoflavonoids
-
In, 1 st ed.;, Eds.; Academic: New York
-
Wong, E. The isoflavonoids. In The Flavonoids, 1 st ed.; Harborne, J. B.; Mabry, T. J.; Mabry, H., Eds.; Academic: New York, 1975; p 750.
-
(1975)
The Flavonoids
, pp. 750
-
-
Wong, E.1
Harborne, J.B.2
Mabry, T.J.3
Mabry, H.4
-
28
-
-
34547485050
-
Metabolism of dietary soy isoflavones to equol by human intestinal microflora-implications for health
-
Yuan, J.-P.; Wang, J.-H.; Liu, X. Metabolism of dietary soy isoflavones to equol by human intestinal microflora-implications for health Mol. Nutr. Food Res. 2007, 51, 765-781
-
(2007)
Mol. Nutr. Food Res.
, vol.51
, pp. 765-781
-
-
Yuan, J.-P.1
Wang, J.-H.2
Liu, X.3
-
29
-
-
33947449876
-
Some isoflavones derived from genistein
-
Whalley, W. B. Some isoflavones derived from genistein J. Am. Chem. Soc. 1953, 75, 1059-1065
-
(1953)
J. Am. Chem. Soc.
, vol.75
, pp. 1059-1065
-
-
Whalley, W.B.1
-
30
-
-
65349140959
-
Carbon-13 NMR shifts and C-H coupling constants of deoxybenzoins and related acetophenones
-
Jha, H. C.; Zilliken, F.; Offermann, W.; Breitmaier, E. Carbon-13 NMR shifts and C-H coupling constants of deoxybenzoins and related acetophenones Can. J. Chem. 1981, 59, 2266-2282
-
(1981)
Can. J. Chem.
, vol.59
, pp. 2266-2282
-
-
Jha, H.C.1
Zilliken, F.2
Offermann, W.3
Breitmaier, E.4
-
31
-
-
40949091876
-
Synthesis and evaluation of derrubone and selected analogs
-
Hastings, J. M.; Hadden, M. K.; Blagg, B. S. J. Synthesis and evaluation of derrubone and selected analogs J. Org. Chem. 2008, 73, 369-373
-
(2008)
J. Org. Chem.
, vol.73
, pp. 369-373
-
-
Hastings, J.M.1
Hadden, M.K.2
Blagg, B.S.J.3
-
32
-
-
0035671803
-
Synthesis and vasorelaxing evaluation of α-methylidene-γ- butyrolactone bearing quinolin-2(1 H)-one and 3,4-dihydroquinolin-2(1 H)-one derivatives
-
Wang, T. C.; Zhao, Y. L.; Kuo, D. H. Synthesis and vasorelaxing evaluation of α-methylidene-γ-butyrolactone bearing quinolin-2(1 H)-one and 3,4-dihydroquinolin-2(1 H)-one derivatives Eur. J. Med. Chem. 2001, 36, 909-914
-
(2001)
Eur. J. Med. Chem.
, vol.36
, pp. 909-914
-
-
Wang, T.C.1
Zhao, Y.L.2
Kuo, D.H.3
-
33
-
-
34249277041
-
The relaxant effect of curcumin on porcine coronary arterial ring segments
-
Xu, P.-H.; Long, Y.; Dai, F.; Liu, Z.-L. The relaxant effect of curcumin on porcine coronary arterial ring segments Vasc. Pharmacol. 2007, 47, 25-30
-
(2007)
Vasc. Pharmacol.
, vol.47
, pp. 25-30
-
-
Xu, P.-H.1
Long, Y.2
Dai, F.3
Liu, Z.-L.4
-
34
-
-
34047130348
-
Structure-activity relationships of flavonoids for vascular relaxation in porcine coronary artery
-
Xu, Y. C.; Leung, S. W. S.; Yeung, D. K. Y.; Hu, L. H.; Chen, G. H.; Che, C. M.; Man, R. Y. K. Structure-activity relationships of flavonoids for vascular relaxation in porcine coronary artery Phytochemistry 2007, 68, 1179-1188
-
(2007)
Phytochemistry
, vol.68
, pp. 1179-1188
-
-
Xu, Y.C.1
Leung, S.W.S.2
Yeung, D.K.Y.3
Hu, L.H.4
Chen, G.H.5
Che, C.M.6
Man, R.Y.K.7
-
35
-
-
2342567855
-
The relation between the chemical structure of flavonoids and their estrogen-like activities
-
Vaya, J.; Tamir, S. The relation between the chemical structure of flavonoids and their estrogen-like activities Curr. Med. Chem. 2004, 11, 1333-1343
-
(2004)
Curr. Med. Chem.
, vol.11
, pp. 1333-1343
-
-
Vaya, J.1
Tamir, S.2
-
36
-
-
0006813144
-
Metabolism of toxicants: Phase i reactions and pharmacogenetics
-
In, 3 rd ed.;, Eds.; Wiley-Interscience: New York
-
Hodgson, E.; Goldstein, J. A. Metabolism of toxicants: phase I reactions and pharmacogenetics. In Introduction to Biochemical Toxicology, 3 rd ed.; Hodgson, E.; Smart, R. C., Eds.; Wiley-Interscience: New York, 2001; pp 77-79.
-
(2001)
Introduction to Biochemical Toxicology
, pp. 77-79
-
-
Hodgson, E.1
Goldstein, J.A.2
Hodgson, E.3
Smart, R.C.4
-
37
-
-
0037636423
-
Identification of CYP1A2 as the main isoform for the phase i hydroxylated metabolism of genistein and a prodrug converting enzyme of methylated isoflavones
-
Hu, M.; Krausz, K.; Chen, J.; Ge, X.; Li, J.; Gelboin, H. L.; Gonzalez, F. J. Identification of CYP1A2 as the main isoform for the phase I hydroxylated metabolism of genistein and a prodrug converting enzyme of methylated isoflavones Drug Metab. Dispos. 2003, 31, 924-931
-
(2003)
Drug Metab. Dispos.
, vol.31
, pp. 924-931
-
-
Hu, M.1
Krausz, K.2
Chen, J.3
Ge, X.4
Li, J.5
Gelboin, H.L.6
Gonzalez, F.J.7
-
38
-
-
0037077406
-
Metabolism of biochanin A and formononetin by human liver microsomes in vitro
-
Tolleson, W. H.; Doerge, D. R.; Churchwell, M. I.; Marques, M.; Roberts, D. W. Metabolism of biochanin A and formononetin by human liver microsomes in vitro J. Agric. Food Chem. 2002, 50, 4783-4790
-
(2002)
J. Agric. Food Chem.
, vol.50
, pp. 4783-4790
-
-
Tolleson, W.H.1
Doerge, D.R.2
Churchwell, M.I.3
Marques, M.4
Roberts, D.W.5
|