메뉴 건너뛰기




Volumn 55, Issue 1, 2015, Pages 16-31

Advance in Dietary Polyphenols as Aldose Reductases Inhibitors: Structure-Activity Relationship Aspect

Author keywords

aldose reductases inhibitors (ARIs); flavonoids; Polyphenols; structure activity relationship

Indexed keywords

ALKYLATION; ESTERIFICATION; GLYCOSYLATION; HYDROGENATION; HYDROXYLATION; METHYLATION; STRUCTURES (BUILT OBJECTS);

EID: 84905717277     PISSN: 10408398     EISSN: 15497852     Source Type: Journal    
DOI: 10.1080/10408398.2011.584252     Document Type: Article
Times cited : (67)

References (96)
  • 1
    • 77958476424 scopus 로고    scopus 로고
    • Inhibitory activities of cyanidin and its glycosides and synergistic effect with acarbose against intestinal α-glucosidase and pancreatic α-amylase
    • Akkarachiyasit, S., Charoenlertkul, P., Yibchok-anun, S. and Adisakwattana, S. (2010). Inhibitory activities of cyanidin and its glycosides and synergistic effect with acarbose against intestinal α-glucosidase and pancreatic α-amylase. Int. J. Mol. Sci. 11:3387-3396.
    • (2010) Int. J. Mol. Sci. , vol.11 , pp. 3387-3396
    • Akkarachiyasit, S.1    Charoenlertkul, P.2    Yibchok-anun, S.3    Adisakwattana, S.4
  • 4
    • 74349097440 scopus 로고    scopus 로고
    • Hypolipidemic effects of proanthocyanidins and their underlying biochemical and molecular mechanisms
    • Blade, C., Arola, L. and Salvado, M.J. (2010). Hypolipidemic effects of proanthocyanidins and their underlying biochemical and molecular mechanisms. Mol. Nutr. Food Res. 54:37-59.
    • (2010) Mol. Nutr. Food Res. , vol.54 , pp. 37-59
    • Blade, C.1    Arola, L.2    Salvado, M.J.3
  • 5
    • 77953708661 scopus 로고    scopus 로고
    • The effect of co-administered flavonoids on the metabolism of hesperetin and the disposition of its metabolites in Caco-2 cell monolayers
    • Brand, W., Padilla, B., van Bladeren, P.J., Williamson, G. and Rietjens, I.M. C. M. (2010). The effect of co-administered flavonoids on the metabolism of hesperetin and the disposition of its metabolites in Caco-2 cell monolayers. Mol. Nutr. Food Res. 54:851-860.
    • (2010) Mol. Nutr. Food Res. , vol.54 , pp. 851-860
    • Brand, W.1    Padilla, B.2    van Bladeren, P.J.3    Williamson, G.4    Rietjens, I.M.C.M.5
  • 6
    • 0035856980 scopus 로고    scopus 로고
    • Biochemistry and molecular cell biology of diabetic complications
    • Brownlee, M. (2001). Biochemistry and molecular cell biology of diabetic complications. Nature. 414:813-820.
    • (2001) Nature , vol.414 , pp. 813-820
    • Brownlee, M.1
  • 7
    • 78649503741 scopus 로고    scopus 로고
    • 3D-QSAR (CoMFA and CoMSIA) and pharmacophore (GALAHAD) studies on the differential inhibition of aldose reductase by flavonoid compounds
    • Caballero, J. (2010). 3D-QSAR (CoMFA and CoMSIA) and pharmacophore (GALAHAD) studies on the differential inhibition of aldose reductase by flavonoid compounds. J. Mol. Graph. Model. 29:363-371.
    • (2010) J. Mol. Graph. Model. , vol.29 , pp. 363-371
    • Caballero, J.1
  • 8
    • 55749083042 scopus 로고    scopus 로고
    • Inhibition of aldose reductase from cataracted eye lenses by finger millet (Eleusine coracana) polyphenols
    • Chethan, S., Dharmesh, S.M. and Malleshi, N.G. (2008). Inhibition of aldose reductase from cataracted eye lenses by finger millet (Eleusine coracana) polyphenols. Bioorg. Med. Chem. 16:10085-10090.
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 10085-10090
    • Chethan, S.1    Dharmesh, S.M.2    Malleshi, N.G.3
  • 9
    • 0003906557 scopus 로고
    • The influence of coffee bean maturity on the content of chlorogenic acids, caffeine and trigonelline
    • Clifford, M.N. and Kazi, T. (1987). The influence of coffee bean maturity on the content of chlorogenic acids, caffeine and trigonelline. Food Chem. 26:59-69.
    • (1987) Food Chem. , vol.26 , pp. 59-69
    • Clifford, M.N.1    Kazi, T.2
  • 10
    • 33645760745 scopus 로고    scopus 로고
    • Characterization by LC-MSn of four new classes of chlorogenic acid in green coffee beans: Dimethoxycinnamoylquinic acids, diferuloylquinic acids, and feruloyl-dimethoxycinnamoylquinic acids
    • Clifford, M.N., Knight, S., Surucu, B. and Kuhnert, N.T. (2006). Characterization by LC-MSn of four new classes of chlorogenic acid in green coffee beans: Dimethoxycinnamoylquinic acids, diferuloylquinic acids, and feruloyl-dimethoxycinnamoylquinic acids. J. Agric. Food Chem. 54:1957-1969.
    • (2006) J. Agric. Food Chem. , vol.54 , pp. 1957-1969
    • Clifford, M.N.1    Knight, S.2    Surucu, B.3    Kuhnert, N.T.4
  • 11
    • 77955368220 scopus 로고    scopus 로고
    • Plant metabolism and the environment: Implications for managing phenolics
    • Cohen, S.D. and Kennedy, J.A. (2010). Plant metabolism and the environment: Implications for managing phenolics. Crit. Rev. Food Sci. Nutr. 50:620-543.
    • (2010) Crit. Rev. Food Sci. Nutr. , vol.50 , pp. 543-620
    • Cohen, S.D.1    Kennedy, J.A.2
  • 15
  • 16
    • 77954468243 scopus 로고    scopus 로고
    • Inhibitory activity of caffeoylquinic acids from the aerial parts of Artemisia princeps on rat lens aldose reductase and on the formation of advanced glycation end products
    • Cui, C.B., Jeong, S.K., Lee, Y.S., Lee, S.O., Kang, I.J. and Lim, S.S. (2009). Inhibitory activity of caffeoylquinic acids from the aerial parts of Artemisia princeps on rat lens aldose reductase and on the formation of advanced glycation end products. J. Korean Soc. Appl. Biol. Chem. 52:655-662.
    • (2009) J. Korean Soc. Appl. Biol. Chem. , vol.52 , pp. 655-662
    • Cui, C.B.1    Jeong, S.K.2    Lee, Y.S.3    Lee, S.O.4    Kang, I.J.5    Lim, S.S.6
  • 17
    • 0032566518 scopus 로고    scopus 로고
    • Deglycosylation of favonoid and isofavonoid glycosides by human small intestine and liver L-glucosidase activity
    • Day, A.J., DuPont, M.S., Ridley, S., Rhodes, M., Rhodes, M.J. C. and Williamson, G. (1998). Deglycosylation of favonoid and isofavonoid glycosides by human small intestine and liver L-glucosidase activity. FEBS Lett. 436:71-75.
    • (1998) FEBS Lett. , vol.436 , pp. 71-75
    • Day, A.J.1    DuPont, M.S.2    Ridley, S.3    Rhodes, M.4    Rhodes, M.J.C.5    Williamson, G.6
  • 18
    • 0037392916 scopus 로고    scopus 로고
    • Aldose reductase inhibitors from natural sources
    • de la Fuente, J.Á. and Manzanaro, S. (2003). Aldose reductase inhibitors from natural sources. Nat. Prod. Rep. 20:243-251.
    • (2003) Nat. Prod. Rep. , vol.20 , pp. 243-251
    • de la Fuente, J.Á.1    Manzanaro, S.2
  • 19
    • 16644374803 scopus 로고    scopus 로고
    • Reductase (AR) and hematological activity, and on AR inhibitory activity of quercetin-3-O-methyl ether isolated from Cistus laurifolius L
    • Enomoto, S., Okada, Y., Güvenc, A., Erdurak, C.S., Coşkun, M. and Okuyama, T. (2004). Reductase (AR) and hematological activity, and on AR inhibitory activity of quercetin-3-O-methyl ether isolated from Cistus laurifolius L. Biol. Pharm. Bull. 27:1140-1143.
    • (2004) Biol. Pharm. Bull. , vol.27 , pp. 1140-1143
    • Enomoto, S.1    Okada, Y.2    Güvenc, A.3    Erdurak, C.S.4    Coşkun, M.5    Okuyama, T.6
  • 20
    • 33751271179 scopus 로고    scopus 로고
    • Progress in research of aldose reductase inhibitors in traditional medicinal herbs
    • Feng, C.G., Zhang, L.X. and Liu, X. (2005). Progress in research of aldose reductase inhibitors in traditional medicinal herbs. Chin. J. Chin. Mater. Med. 30:1496-1500.
    • (2005) Chin. J. Chin. Mater. Med. , vol.30 , pp. 1496-1500
    • Feng, C.G.1    Zhang, L.X.2    Liu, X.3
  • 21
    • 16244394858 scopus 로고    scopus 로고
    • Quantitative structure-activity relationship to predict differential inhibition of aldose reductase by flavonoid compounds
    • Fernandez, M., Caballero, J., Helguera, A.M., Castro, E.A. and Gonzalez, M.P. (2005). Quantitative structure-activity relationship to predict differential inhibition of aldose reductase by flavonoid compounds. Bioorg. Med. Chem. 13:3269-3277.
    • (2005) Bioorg. Med. Chem. , vol.13 , pp. 3269-3277
    • Fernandez, M.1    Caballero, J.2    Helguera, A.M.3    Castro, E.A.4    Gonzalez, M.P.5
  • 25
    • 69349102649 scopus 로고    scopus 로고
    • Investigations of anti-inflammatory, antinociceptive, antioxidant and aldose reductase inhibitory activities of phenolic compounds from Sideritis brevibracteata
    • Güvenç, A., Okada, Y., Akkol, EK.K., Duman, H., Okuyama, T. and Çaliş, I. (2010). Investigations of anti-inflammatory, antinociceptive, antioxidant and aldose reductase inhibitory activities of phenolic compounds from Sideritis brevibracteata. Food Chem. 118:686-692.
    • (2010) Food Chem. , vol.118 , pp. 686-692
    • Güvenç, A.1    Okada, Y.2    Akkol, E.K.3    Duman, H.4    Okuyama, T.5    Çaliş, I.6
  • 26
    • 0030005819 scopus 로고    scopus 로고
    • Effect of Polygonum hydropiper sulfated flavonoids on lens aldose reductase and related enzymes
    • Haraguchi, H., Ohmi, I., Sakai, S. and Fukuda, A. (1996). Effect of Polygonum hydropiper sulfated flavonoids on lens aldose reductase and related enzymes. J. Nat. Prod. 59:443-445
    • (1996) J. Nat. Prod. , vol.59 , pp. 443-445
    • Haraguchi, H.1    Ohmi, I.2    Sakai, S.3    Fukuda, A.4
  • 27
    • 28944447255 scopus 로고    scopus 로고
    • A neural networks-based drug discovery approachand its application for designing aldose reductase inhibitors
    • Hu, L., Chen, G. and Chau, R.M. (2006). A neural networks-based drug discovery approachand its application for designing aldose reductase inhibitors. J. Mol. Graph. Model. 24:244-253.
    • (2006) J. Mol. Graph. Model. , vol.24 , pp. 244-253
    • Hu, L.1    Chen, G.2    Chau, R.M.3
  • 28
    • 79957965555 scopus 로고    scopus 로고
    • α-Glucosidase and aldose reductase inhibitory activities from the fruiting body of Phellinus merrillii
    • Huang, G.J., Hsieh, W.T., Chang, H.Y., Huang, S.S., Lin, Y.C. and Kuo, Y.H. (2011). α-Glucosidase and aldose reductase inhibitory activities from the fruiting body of Phellinus merrillii. J. Agric. Food Chem. 59:2702-5706. doi: 10.1021/jf2003943.
    • (2011) J. Agric. Food Chem. , vol.59 , pp. 2702-5706
    • Huang, G.J.1    Hsieh, W.T.2    Chang, H.Y.3    Huang, S.S.4    Lin, Y.C.5    Kuo, Y.H.6
  • 29
    • 76049101556 scopus 로고    scopus 로고
    • 3,5-Di-O-caffeoyl-epi-quinic acid from the leaves and stems of erigeron annuus inhibits protein glycation, aldose reductase, and cataractogenesis
    • Jang, D.S., Yoo, N.H., Kim, N.H., Lee, Y.M., Kim, C.S., Kim, J.H., Kim, J.H. and Kim, J.S. (2010). 3,5-Di-O-caffeoyl-epi-quinic acid from the leaves and stems of erigeron annuus inhibits protein glycation, aldose reductase, and cataractogenesis. Biol. Pharm. Bull. 33:329-333.
    • (2010) Biol. Pharm. Bull. , vol.33 , pp. 329-333
    • Jang, D.S.1    Yoo, N.H.2    Kim, N.H.3    Lee, Y.M.4    Kim, C.S.5    Kim, J.H.6    Kim, J.H.7    Kim, J.S.8
  • 30
  • 31
    • 70350198024 scopus 로고    scopus 로고
    • Quantitative HPLC analysis of two key flavonoids and inhibitory activities against aldose reductase from different parts of the Korean thistle, Cirsium maackii
    • Jung, H.A., Kim, Y.S. and Choi, J.S. (2009). Quantitative HPLC analysis of two key flavonoids and inhibitory activities against aldose reductase from different parts of the Korean thistle, Cirsium maackii. Food Chem. Toxicol. 47:2790-2797.
    • (2009) Food Chem. Toxicol , vol.47 , pp. 2790-2797
    • Jung, H.A.1    Kim, Y.S.2    Choi, J.S.3
  • 32
    • 1542318408 scopus 로고    scopus 로고
    • Inhibitory effects of naturally occurring flavonoids on rat lens aldose reductase
    • Jung, S.H., Kang, S.S., Shin, K.H. and Kim, Y.S. (2004). Inhibitory effects of naturally occurring flavonoids on rat lens aldose reductase. Nat. Prod. Sci. 10:35-39.
    • (2004) Nat. Prod. Sci. , vol.10 , pp. 35-39
    • Jung, S.H.1    Kang, S.S.2    Shin, K.H.3    Kim, Y.S.4
  • 33
    • 34548041862 scopus 로고    scopus 로고
    • Aldose reductase and advanced glycation endproducts inhibitory effect of Phyllostachys nigra
    • Jung, S.H., Lee, J.M., Lee, H.J., Kim, C.Y., Lee, E.H. and Um, B.H. (2007). Aldose reductase and advanced glycation endproducts inhibitory effect of Phyllostachys nigra. Biol. Pharm. Bull. 30:1569-1572.
    • (2007) Biol. Pharm. Bull. , vol.30 , pp. 1569-1572
    • Jung, S.H.1    Lee, J.M.2    Lee, H.J.3    Kim, C.Y.4    Lee, E.H.5    Um, B.H.6
  • 34
    • 0023899991 scopus 로고
    • The role of aldose reductase in the development of diabetic complications
    • Kador, P.F. (1988). The role of aldose reductase in the development of diabetic complications. Med. Res. Rev. 8:325-352.
    • (1988) Med. Res. Rev , vol.8 , pp. 325-352
    • Kador, P.F.1
  • 35
    • 77951938261 scopus 로고    scopus 로고
    • In vitro inhibition of α-glucosidases and glycogen phosphorylase by catechin gallates in green tea
    • Kamiyama, O., Sanae, F., Ikeda, K., Higashi, Y., Minami, Y., Asano, N., Adachi, I. and Kato, A. (2010). In vitro inhibition of α-glucosidases and glycogen phosphorylase by catechin gallates in green tea. Food Chem. 122:1061-1066.
    • (2010) Food Chem. , vol.122 , pp. 1061-1066
    • Kamiyama, O.1    Sanae, F.2    Ikeda, K.3    Higashi, Y.4    Minami, Y.5    Asano, N.6    Adachi, I.7    Kato, A.8
  • 36
    • 78951486316 scopus 로고    scopus 로고
    • Inhibition of aldose reductase by phenylethanoid glycoside Isolated from the seeds of Paulownia coreana
    • Kim, J.K., Lee, Y.S., Kim, S.H., Bae, Y.S. and Lim, S.S. (2011). Inhibition of aldose reductase by phenylethanoid glycoside Isolated from the seeds of Paulownia coreana. Biol. Pharm. Bull. 34:160-163.
    • (2011) Biol. Pharm. Bull. , vol.34 , pp. 160-163
    • Kim, J.K.1    Lee, Y.S.2    Kim, S.H.3    Bae, Y.S.4    Lim, S.S.5
  • 37
    • 45849115105 scopus 로고    scopus 로고
    • The key importance of soy isoflavone bioavailability to understanding health benefits
    • Larkin, T., Price, W.E. and Astheimer, L. (2008). The key importance of soy isoflavone bioavailability to understanding health benefits. Crit. Rev. Food Sci. Nutr. 48:538-552.
    • (2008) Crit. Rev. Food Sci. Nutr. , vol.48 , pp. 538-552
    • Larkin, T.1    Price, W.E.2    Astheimer, L.3
  • 38
    • 48849111676 scopus 로고    scopus 로고
    • Inhibitory effect of the compounds isolated from Rhus verniciflua on aldose reductase and advanced glycation end products
    • Lee, E.H., Song, D.G., Lee, J.Y., Pan, C.H., Um, B.H. and Jung, S.H. (2008). Inhibitory effect of the compounds isolated from Rhus verniciflua on aldose reductase and advanced glycation end products. Biol. Pharm. Bull. 31, 1626-1630.
    • (2008) Biol. Pharm. Bull. , vol.31 , pp. 1626-1630
    • Lee, E.H.1    Song, D.G.2    Lee, J.Y.3    Pan, C.H.4    Um, B.H.5    Jung, S.H.6
  • 39
    • 84874929921 scopus 로고    scopus 로고
    • Flavonoids from the leaves of Thuja orientalis inhibit the aldose reductase and the formation of advanced glycation endproducts
    • Lee, E.H., Song, D.G., Lee, J.Y., Pan, C.H., Um, B.H. and Jung, S.H. (2009a). Flavonoids from the leaves of Thuja orientalis inhibit the aldose reductase and the formation of advanced glycation endproducts. J. Korean Soc. Appl. Biol. Chem. 52:448-455.
    • (2009) J. Korean Soc. Appl. Biol. Chem. , vol.52 , pp. 448-455
    • Lee, E.H.1    Song, D.G.2    Lee, J.Y.3    Pan, C.H.4    Um, B.H.5    Jung, S.H.6
  • 41
    • 79953324958 scopus 로고    scopus 로고
    • Inhibitory effect of glucodistylin from the bark of Quercus acutissima on human recombinant aldose reductase and sorbitol accumulation
    • Lee, Y.S., Kim, J.K., Bae, Y.S., Won, M.H., Kang, I.J. and Lim, S.S. (2011). Inhibitory effect of glucodistylin from the bark of Quercus acutissima on human recombinant aldose reductase and sorbitol accumulation. Arch. Pharm. Res. 34:211-215.
    • (2011) Arch. Pharm. Res , vol.34 , pp. 211-215
    • Lee, Y.S.1    Kim, J.K.2    Bae, Y.S.3    Won, M.H.4    Kang, I.J.5    Lim, S.S.6
  • 43
    • 0026124930 scopus 로고
    • Inhibition of rat lens aldose reductase by quercetagetin and patuletin
    • Li, S.Z., Mao, W., Cao, X.Y., Liang, S.W., Ding, Z. and Li, N.M. (1991). Inhibition of rat lens aldose reductase by quercetagetin and patuletin. Eye Sci. 7:29-33.
    • (1991) Eye Sci. , vol.7 , pp. 29-33
    • Li, S.Z.1    Mao, W.2    Cao, X.Y.3    Liang, S.W.4    Ding, Z.5    Li, N.M.6
  • 44
    • 33750211170 scopus 로고    scopus 로고
    • Rat lens aldose reductase inhibitory constituents of Nelumbo nucifera stamens
    • Lim, S.S., Jung, Y.J., Hyun, S.K., Lee, Y.S. and Choi, J.S. (2006). Rat lens aldose reductase inhibitory constituents of Nelumbo nucifera stamens. Phytother. Res. 20:825-830.
    • (2006) Phytother. Res , vol.20 , pp. 825-830
    • Lim, S.S.1    Jung, Y.J.2    Hyun, S.K.3    Lee, Y.S.4    Choi, J.S.5
  • 45
    • 0035006715 scopus 로고    scopus 로고
    • Synthesis of flavonoids and their effects on aldose reductase and sorbitol accumulation in streptozotocin-induced diabetic rat tissues
    • Lim, S.S., Jung, S.H., Ji, J., Shin, K.H. and Keum, S.R. (2001). Synthesis of flavonoids and their effects on aldose reductase and sorbitol accumulation in streptozotocin-induced diabetic rat tissues. J. Pharm. Pharmacol. 53:653-668.
    • (2001) J. Pharm. Pharmacol. , vol.53 , pp. 653-668
    • Lim, S.S.1    Jung, S.H.2    Ji, J.3    Shin, K.H.4    Keum, S.R.5
  • 46
    • 67349254122 scopus 로고    scopus 로고
    • CoMFA, CoMSIA analysis of 2,4-thiazolidinediones derivatives as aldose reductase inhibitors
    • Liu, H., Liu, S., Qin, L. and Mo, L. (2009). CoMFA, CoMSIA analysis of 2,4-thiazolidinediones derivatives as aldose reductase inhibitors. J. Mol. Model. 15:837-845.
    • (2009) J. Mol. Model. , vol.15 , pp. 837-845
    • Liu, H.1    Liu, S.2    Qin, L.3    Mo, L.4
  • 47
    • 70049109449 scopus 로고    scopus 로고
    • Flavonoids with aldose reductase inhibiting activity: Pharmacophore modeling and implications for mechanism
    • Liu, H.B., Wang, Z.L., Qiao, Y.X. and Zhou, J.J. (2007). Flavonoids with aldose reductase inhibiting activity: Pharmacophore modeling and implications for mechanism. Acta Phys. Chim. Sin. 23:1059-1064.
    • (2007) Acta Phys. Chim. Sin. , vol.23 , pp. 1059-1064
    • Liu, H.B.1    Wang, Z.L.2    Qiao, Y.X.3    Zhou, J.J.4
  • 48
    • 85006542607 scopus 로고    scopus 로고
    • Inhibition of aldose reductase from rat lens by tea polyphenol
    • Liu, Y.H., Xue, C.Y., Ou, Y.H., Zhang, R.X. and Zhang, Y. (2006). Inhibition of aldose reductase from rat lens by tea polyphenol. Pract. Prevent. Med. 13:1162-1164.
    • (2006) Pract. Prevent. Med. , vol.13 , pp. 1162-1164
    • Liu, Y.H.1    Xue, C.Y.2    Ou, Y.H.3    Zhang, R.X.4    Zhang, Y.5
  • 50
    • 0036594601 scopus 로고    scopus 로고
    • Structural requirements of flavonoids and related compounds for aldose reductase inhibitory activity
    • Matsuda, H., Morikawa, T., Toguchida, I. and Yoshikawa, M. (2002). Structural requirements of flavonoids and related compounds for aldose reductase inhibitory activity. Chem. Pharm. Bull. 50:788-795.
    • (2002) Chem. Pharm. Bull. , vol.50 , pp. 788-795
    • Matsuda, H.1    Morikawa, T.2    Toguchida, I.3    Yoshikawa, M.4
  • 51
    • 0344851580 scopus 로고    scopus 로고
    • Structural requirements of flavonoids for inhibition of protein glycation and radical scavenging activities
    • Matsuda, H., Wang, T., Managi, H. and Yoshikawa, M. (2003). Structural requirements of flavonoids for inhibition of protein glycation and radical scavenging activities. Bioorg. Med. Chem. 11:5317-5323.
    • (2003) Bioorg. Med. Chem. , vol.11 , pp. 5317-5323
    • Matsuda, H.1    Wang, T.2    Managi, H.3    Yoshikawa, M.4
  • 54
    • 2442516583 scopus 로고    scopus 로고
    • Molecular modeling and structure-based drug discovery studies of aldose reductase inhibitors
    • Miyamoto, S. (2002). Molecular modeling and structure-based drug discovery studies of aldose reductase inhibitors. Chem-Bio. Informatics J. 2(3):74-85.
    • (2002) Chem-Bio. Informatics J. , vol.2 , Issue.3 , pp. 74-85
    • Miyamoto, S.1
  • 56
    • 0042544329 scopus 로고
    • Aldose reductase inhibitors from green tea
    • Murata, M., Irie, J. and Homma, S. (1994). Aldose reductase inhibitors from green tea. LWT-Food Sci. Technol. 27:401-405.
    • (1994) LWT-Food Sci. Technol , vol.27 , pp. 401-405
    • Murata, M.1    Irie, J.2    Homma, S.3
  • 57
    • 77955845291 scopus 로고    scopus 로고
    • 4-Methylcoumarins as antioxidants: Scavenging of peroxyl radicals and inhibition of human low-density lipoprotein oxidation
    • Natella, F., Lorrain, B., Prasad, A.K., Parmar, V.S., Saso, L. and Scaccini, C. (2010). 4-Methylcoumarins as antioxidants: Scavenging of peroxyl radicals and inhibition of human low-density lipoprotein oxidation. Biochimie 92:1147-1152.
    • (2010) Biochimie , vol.92 , pp. 1147-1152
    • Natella, F.1    Lorrain, B.2    Prasad, A.K.3    Parmar, V.S.4    Saso, L.5    Scaccini, C.6
  • 58
    • 0031920049 scopus 로고    scopus 로고
    • Aldose reductase in glucose toxicity: A potential target for the prevention of diabetic complications
    • Nishimura-Yabe, C. (1998). Aldose reductase in glucose toxicity: A potential target for the prevention of diabetic complications. Pharmacol. Rev. 50:21-33.
    • (1998) Pharmacol. Rev. , vol.50 , pp. 21-33
    • Nishimura-Yabe, C.1
  • 59
    • 0020463117 scopus 로고
    • Inhibition of aldose reductases from rat and bovine lenses by flavonoids
    • Okuda, J., Miwa, I., Inagaki, K., Horie, T. and Nakayama, M. (1982). Inhibition of aldose reductases from rat and bovine lenses by flavonoids. Biochem. Pharmacol. 31:3807-3822.
    • (1982) Biochem. Pharmacol. , vol.31 , pp. 3807-3822
    • Okuda, J.1    Miwa, I.2    Inagaki, K.3    Horie, T.4    Nakayama, M.5
  • 63
    • 33947517492 scopus 로고    scopus 로고
    • Structure-activity relationships of components from the roots of Pueraria thunbergiana having aldose reductase inhibitory and antioxidative activity
    • Park, C.H., Lim, S.S. and Lee, D.U. (2007). Structure-activity relationships of components from the roots of Pueraria thunbergiana having aldose reductase inhibitory and antioxidative activity. Bull. Korean Chem. Soc. 28:493-495.
    • (2007) Bull. Korean Chem. Soc. , vol.28 , pp. 493-495
    • Park, C.H.1    Lim, S.S.2    Lee, D.U.3
  • 64
    • 70350022343 scopus 로고    scopus 로고
    • Artificial neural networks-based approach to design ARIs using QSAR for diabetes mellitus
    • Patra, J.C. and Singh, O. (2009). Artificial neural networks-based approach to design ARIs using QSAR for diabetes mellitus. J. Comput. Chem. 30:2494-2508.
    • (2009) J. Comput. Chem , vol.30 , pp. 2494-2508
    • Patra, J.C.1    Singh, O.2
  • 65
    • 33244477896 scopus 로고    scopus 로고
    • A high dimensional qsar study on the aldose reductase inhibitory activity of some flavones: Topological descriptors in modeling the activity
    • Prabhakar, Y.S., Gupta, M.K., Roy, N. and Venkateswarlu, Y. (2006). A high dimensional qsar study on the aldose reductase inhibitory activity of some flavones: Topological descriptors in modeling the activity. J. Chem. Inf. Model. 46:86-92.
    • (2006) J. Chem. Inf. Model. , vol.46 , pp. 86-92
    • Prabhakar, Y.S.1    Gupta, M.K.2    Roy, N.3    Venkateswarlu, Y.4
  • 67
    • 0028863169 scopus 로고
    • Isolation of aldose reductase inhibitors from the flowers of Chrysanthemum boreale
    • Shin, K.H., Kang, S.S., Seo, E.A. and Shin, S.W. (1995). Isolation of aldose reductase inhibitors from the flowers of Chrysanthemum boreale. Arch. Pharm. Res. 18:65-68.
    • (1995) Arch. Pharm. Res. , vol.18 , pp. 65-68
    • Shin, K.H.1    Kang, S.S.2    Seo, E.A.3    Shin, S.W.4
  • 69
    • 77950883461 scopus 로고    scopus 로고
    • 3D-QSAR studies on a series of 5-arylidine-2,4-thiazolidinediones as aldose reductase inhibitors: A selforganizing molecular field analysis approach
    • Thareja, S., Aggarwal, S., Bhardwaj, T.R. and Kumar, M. (2010). 3D-QSAR studies on a series of 5-arylidine-2,4-thiazolidinediones as aldose reductase inhibitors: A selforganizing molecular field analysis approach. Med. Chem. 6:30-36.
    • (2010) Med. Chem. , vol.6 , pp. 30-36
    • Thareja, S.1    Aggarwal, S.2    Bhardwaj, T.R.3    Kumar, M.4
  • 70
    • 0031570301 scopus 로고    scopus 로고
    • A 'specificity' pocket inferred from the crystal structures of the complexes of aldose reductase with the pharmaceutically important inhibitors tolrestat and sorbinil
    • Urzhumtsev, A., Tête-Favier, F., Mitschler, A., Barbanton, J., Barth, P., Urzhumtseva, L., Biellmann, J.F., Podjarny, A.D. and Moras, D.A. (1997). A 'specificity' pocket inferred from the crystal structures of the complexes of aldose reductase with the pharmaceutically important inhibitors tolrestat and sorbinil. Structure. 5:601-612.
    • (1997) Structure , vol.5 , pp. 601-612
    • Urzhumtsev, A.1    Tête-Favier, F.2    Mitschler, A.3    Barbanton, J.4    Barth, P.5    Urzhumtseva, L.6    Biellmann, J.F.7    Podjarny, A.D.8    Moras, D.A.9
  • 72
    • 44349167688 scopus 로고    scopus 로고
    • Flavonoids and their glycosides, including anthocyanins
    • Veitch, N.C. and Grayer, R.J. (2008). Flavonoids and their glycosides, including anthocyanins. Nat. Prod. Rep. 25:555-611.
    • (2008) Nat. Prod. Rep. , vol.25 , pp. 555-611
    • Veitch, N.C.1    Grayer, R.J.2
  • 73
    • 78049242972 scopus 로고    scopus 로고
    • The biological potential of flavones
    • Verma, A.K. and Pratap, R. (2010). The biological potential of flavones. Nat. Prod. Rep. 27:1571-1593.
    • (2010) Nat. Prod. Rep. , vol.27 , pp. 1571-1593
    • Verma, A.K.1    Pratap, R.2
  • 74
    • 1642528478 scopus 로고    scopus 로고
    • Absorption and metabolism of flavonoids
    • Walle, T. (2004). Absorption and metabolism of flavonoids. Free. Radical Bio. Med. 36:829-837.
    • (2004) Free. Radical Bio. Med. , vol.36 , pp. 829-837
    • Walle, T.1
  • 75
    • 37549024168 scopus 로고    scopus 로고
    • Methylation of dietary flavones greatly improves their hepatic metabolic stability and intestinal absorption
    • Walle, T. (2007a). Methylation of dietary flavones greatly improves their hepatic metabolic stability and intestinal absorption. Mol. Pharmaceut. 4:826-832.
    • (2007) Mol. Pharmaceut. , vol.4 , pp. 826-832
    • Walle, T.1
  • 76
    • 34548423695 scopus 로고    scopus 로고
    • Methoxylated flavones, a superior cancer chemopreventive flavonoid subclass?
    • Walle, T. (2007b). Methoxylated flavones, a superior cancer chemopreventive flavonoid subclass? Semin. Cancer Biol. 17:354-362.
    • (2007) Semin. Cancer Biol. , vol.17 , pp. 354-362
    • Walle, T.1
  • 77
    • 71649098481 scopus 로고    scopus 로고
    • Methylation of dietary flavones increases their metabolic stability and chemopreventive effects
    • Walle, T. (2009). Methylation of dietary flavones increases their metabolic stability and chemopreventive effects. Int. J. Mol. Sci. 10:5002-5019.
    • (2009) Int. J. Mol. Sci. , vol.10 , pp. 5002-5019
    • Walle, T.1
  • 78
    • 11844269306 scopus 로고    scopus 로고
    • Flavonoid glucosides are hydrolyzed and thus activated in the oral cavity in humans
    • Walle, T., Browning, A.M., Steed, L.L., Reed, S.G. and Walle, U.K. (2005). Flavonoid glucosides are hydrolyzed and thus activated in the oral cavity in humans. J. Nutr. 135:48-52.
    • (2005) J. Nutr. , vol.135 , pp. 48-52
    • Walle, T.1    Browning, A.M.2    Steed, L.L.3    Reed, S.G.4    Walle, U.K.5
  • 79
    • 80052967721 scopus 로고    scopus 로고
    • Advances in studies on aldose reductase inhibitors from plants
    • Wang, Q., Zhou, L.X. and Luo, X.D. (2005). Advances in studies on aldose reductase inhibitors from plants. Chin. Trad. Herb. Drugs 36:298-303.
    • (2005) Chin. Trad. Herb. Drugs , vol.36 , pp. 298-303
    • Wang, Q.1    Zhou, L.X.2    Luo, X.D.3
  • 80
    • 77649305163 scopus 로고    scopus 로고
    • Differential effects of resveratrol and its naturally occurring methylether analogs on cell cycle and apoptosis in human androgen-responsive LNCaP cancer cells
    • Wang, T.T. Y., Schoene, N.W., Kim, Y.S., Mizuno, C.S. and Rimando, A.M. (2010). Differential effects of resveratrol and its naturally occurring methylether analogs on cell cycle and apoptosis in human androgen-responsive LNCaP cancer cells. Mol. Nutr. Food Res. 54:335-344.
    • (2010) Mol. Nutr. Food Res. , vol.54 , pp. 335-344
    • Wang, T.T.Y.1    Schoene, N.W.2    Kim, Y.S.3    Mizuno, C.S.4    Rimando, A.M.5
  • 81
    • 33748916241 scopus 로고    scopus 로고
    • Methylated flavonoids have greatly improved intestinal absorption and metabolic stability
    • Wen, X. and Walle, T. (2006). Methylated flavonoids have greatly improved intestinal absorption and metabolic stability. Drug Metab. Dispos. 34:1786-1792.
    • (2006) Drug Metab. Dispos. , vol.34 , pp. 1786-1792
    • Wen, X.1    Walle, T.2
  • 82
    • 76749093711 scopus 로고    scopus 로고
    • Oral administration of resveratrol in suppression of pulmonary metastasis of BALB/c mice challenged with CT26 colorectal adenocarcinoma cells
    • Weng, Y.L., Liao, H.F., Li, A.F. Y., Chang, J.C. and Chiou, R.Y. Y. (2010). Oral administration of resveratrol in suppression of pulmonary metastasis of BALB/c mice challenged with CT26 colorectal adenocarcinoma cells. Mol. Nutr. Food Res. 54:259-267.
    • (2010) Mol. Nutr. Food Res. , vol.54 , pp. 259-267
    • Weng, Y.L.1    Liao, H.F.2    Li, A.F.Y.3    Chang, J.C.4    Chiou, R.Y.Y.5
  • 83
    • 0026719692 scopus 로고
    • An unlikely sugar substrate site in the 1.65 A structure of the human aldose reductase holoenzyme implicated in diabetic complications
    • Wilson, D.K., Bohren, K., Gabbay, K.H. and Quiocho, F.A. (1992). An unlikely sugar substrate site in the 1.65 A structure of the human aldose reductase holoenzyme implicated in diabetic complications. Science, 257:81-84.
    • (1992) Science , vol.257 , pp. 81-84
    • Wilson, D.K.1    Bohren, K.2    Gabbay, K.H.3    Quiocho, F.A.4
  • 84
    • 0027378377 scopus 로고
    • Refined 1.8 A structure of human aldose reductase complexed with the potent inhibitor zopolrestat
    • Wilson, D.K., Tarle, I., Petrash, J.M. and Quiocho, F.A. (1993). Refined 1.8 A structure of human aldose reductase complexed with the potent inhibitor zopolrestat. Proc. Natl. Acad. Sci. USA 90:9847-9851.
    • (1993) Proc. Natl. Acad. Sci. USA , vol.90 , pp. 9847-9851
    • Wilson, D.K.1    Tarle, I.2    Petrash, J.M.3    Quiocho, F.A.4
  • 85
    • 78650971978 scopus 로고    scopus 로고
    • Structure-affinity relationship of flavones on binding to serum albumins: Effect of hydroxyl groups on ring A
    • Xiao, J.B., Cao, H., Wang, Y.F., Yamamoto, K. and Wei, X.L. (2010). Structure-affinity relationship of flavones on binding to serum albumins: Effect of hydroxyl groups on ring A. Mol. Nutr. Food Res. 54:S253-S260.
    • (2010) Mol. Nutr. Food Res. , vol.54
    • Xiao, J.B.1    Cao, H.2    Wang, Y.F.3    Yamamoto, K.4    Wei, X.L.5
  • 86
    • 68249112377 scopus 로고    scopus 로고
    • Glycosylation of dietary flavonoids decreases the affinities for plasma protein
    • Xiao, J.B., Cao, H., Wang, Y.F., Zhao, J.Y. and Wei, X.L. (2009). Glycosylation of dietary flavonoids decreases the affinities for plasma protein. J. Agric. Food Chem. 57:6642-6648.
    • (2009) J. Agric. Food Chem. , vol.57 , pp. 6642-6648
    • Xiao, J.B.1    Cao, H.2    Wang, Y.F.3    Zhao, J.Y.4    Wei, X.L.5
  • 87
    • 78651333774 scopus 로고    scopus 로고
    • Molecular property-affinity relationship of flavanoids and flavonoids for human serum albumin in vitro
    • Xiao, J.B., Chen, T.T., Cao, H., Chen, L. and Yang, F. (2011a). Molecular property-affinity relationship of flavanoids and flavonoids for human serum albumin in vitro. Mol. Nutr. Food Res. 55:310-317.
    • (2011) Mol. Nutr. Food Res. , vol.55 , pp. 310-317
    • Xiao, J.B.1    Chen, T.T.2    Cao, H.3    Chen, L.4    Yang, F.5
  • 88
    • 79957832646 scopus 로고    scopus 로고
    • Molecular structure-affinity relationship of natural polyphenols for bovine γ-globulin
    • Xiao, J.B., Kai, G.Y., Yang, F., Liu, C.X., Xu, X.C. and Yamamoto, K. (2011b). Molecular structure-affinity relationship of natural polyphenols for bovine γ-globulin. Mol. Nutr. Food Res. 55:S86-S92.
    • (2011) Mol. Nutr. Food Res. , vol.55
    • Xiao, J.B.1    Kai, G.Y.2    Yang, F.3    Liu, C.X.4    Xu, X.C.5    Yamamoto, K.6
  • 89
    • 84873686356 scopus 로고    scopus 로고
    • A review on structure-activity relationship of dietary polyphenols inhibiting α-amylase
    • Xiao, J.B., Ni, X. L., Kai, G. Y., Chen, X. Q. (2013a). A review on structure-activity relationship of dietary polyphenols inhibiting α-amylase. Crit. Rev. Food Sci. Nut.r. 53:497-506.
    • (2013) Crit. Rev. Food Sci. Nut.r. , vol.53 , pp. 497-506
    • Xiao, J.B.1    Ni, X.L.2    Kai, G.Y.3    Chen, X.Q.4
  • 90
    • 84879533000 scopus 로고    scopus 로고
    • Advance in dietary polyphenols as α-glucosidases inhibitors: a review on structure-activity relationship aspect
    • Xiao, J.B., Kai, G. Y., Yamamoto, K., Chen, X. Q. (2013b). Advance in dietary polyphenols as α-glucosidases inhibitors: a review on structure-activity relationship aspect. Crit. Rev. Food Sci. Nutr. 53:818-836.
    • (2013) Crit. Rev. Food Sci. Nutr. , vol.53 , pp. 818-836
    • Xiao, J.B.1    Kai, G.Y.2    Yamamoto, K.3    Chen, X.Q.4
  • 91
    • 27744479680 scopus 로고    scopus 로고
    • Bioactive constituents from Chinese natural medicines. XV. Inhibitory effect on aldose reductase and structures of Saussureosides A and B from Saussurea medusa
    • Xie, H.H., Wang, T., Matsuda, H., Morikawa, T., Yoshikawa, M. and Tani, T. (2005). Bioactive constituents from Chinese natural medicines. XV. Inhibitory effect on aldose reductase and structures of Saussureosides A and B from Saussurea medusa. Chem. Pharm. Bull. 53:1416-1422.
    • (2005) Chem. Pharm. Bull. , vol.53 , pp. 1416-1422
    • Xie, H.H.1    Wang, T.2    Matsuda, H.3    Morikawa, T.4    Yoshikawa, M.5    Tani, T.6
  • 92
    • 33947322652 scopus 로고    scopus 로고
    • Identification of phenolic compounds isolated from pigmented rices and their aldose reductase inhibitory activities
    • Yawadio, R., Tanimori, S. and Morita, N. (2007). Identification of phenolic compounds isolated from pigmented rices and their aldose reductase inhibitory activities. Food Chem. 101:1616-1625.
    • (2007) Food Chem. , vol.101 , pp. 1616-1625
    • Yawadio, R.1    Tanimori, S.2    Morita, N.3
  • 93
    • 43249086213 scopus 로고    scopus 로고
    • Erigeroflavanone, a flavanone derivative from the flowers of Erigeron annuus with protein glycation and aldose reductase inhibitory activity
    • Yoo, N.H., Jang, D.S., Yoo, J.L., Lee, Y.M., Kim, Y.S., Cho, J.H. and Kim, J.S. (2008). Erigeroflavanone, a flavanone derivative from the flowers of Erigeron annuus with protein glycation and aldose reductase inhibitory activity. J. Nat. Prod. 71:713-715
    • (2008) J. Nat. Prod. , vol.71 , pp. 713-715
    • Yoo, N.H.1    Jang, D.S.2    Yoo, J.L.3    Lee, Y.M.4    Kim, Y.S.5    Cho, J.H.6    Kim, J.S.7
  • 94
    • 0032919388 scopus 로고    scopus 로고
    • Medicinal flowers. I. Aldose reductase inhibitors and three new eudesmane-type sesquiterpenes, kikkanols A, B, and C, from the flowers of Chrysanthemum indicum L
    • Yoshikawa, M., Morikawa, T., Murakami, T., Toguchida, I., Harima, S. and Matsuda, H. (1999). Medicinal flowers. I. Aldose reductase inhibitors and three new eudesmane-type sesquiterpenes, kikkanols A, B, and C, from the flowers of Chrysanthemum indicum L. Chem. Pharm. Bull. 47:340-345.
    • (1999) Chem. Pharm. Bull. , vol.47 , pp. 340-345
    • Yoshikawa, M.1    Morikawa, T.2    Murakami, T.3    Toguchida, I.4    Harima, S.5    Matsuda, H.6
  • 96
    • 77953868489 scopus 로고    scopus 로고
    • Aldose reductase inhibitors as potential drugs for diabetic complications
    • Zhu, C.J. (2009). Aldose reductase inhibitors as potential drugs for diabetic complications. Chin. J. New Drugs 18:302-306.
    • (2009) Chin. J. New Drugs , vol.18 , pp. 302-306
    • Zhu, C.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.