-
1
-
-
0023913225
-
The involvement of aldose reductase in diabetic complications
-
Kinoshita, J. H.; Nishimura, C. The Involvement of Aldose Reductase in Diabetic Complications. Diabetes Metab. Rev. 1988, 4, 323-337.
-
(1988)
Diabetes Metab. Rev.
, vol.4
, pp. 323-337
-
-
Kinoshita, J.H.1
Nishimura, C.2
-
2
-
-
0022381194
-
Synthesis, absolute configuration, and conformation of the aldose reductase inhibitor sorbinil
-
Sarges, R.; Bordner, J.; Dominy, B. W.; Peterson, M. J.; Whipple, E. B. Synthesis, Absolute Configuration, and Conformation of the Aldose Reductase Inhibitor Sorbinil. J. Med. Chem. 1985, 28, 1716-1720.
-
(1985)
J. Med. Chem.
, vol.28
, pp. 1716-1720
-
-
Sarges, R.1
Bordner, J.2
Dominy, B.W.3
Peterson, M.J.4
Whipple, E.B.5
-
3
-
-
0025119897
-
Profile of a new aldose reductase inhibitor, (2S,4S)-6-fluoro-2′,5′-dioxospiro[chroman4,4′-imidazolidine]- 2-carboxamide
-
(a) Mizuno, K.; Yamaguchi, T.; Inoue, A.; Tomiya, N.; Unno, R.; Miura, K.; Usui, T.; Matsumoto, Y.; Kondo, Y.; Yoshina, S.; Kondo, Y.; Sato, M.; Matsubara, A.; Kato, N.; Nakano, K.; Shirai, M.; Inoue, T.; Awaya, J.; Asaeda, N.; Hayasaka, I.; Koide, M.; Hibi, C.; Ban, M.; Sawai, K.; Kurono, M. Profile of a new aldose reductase inhibitor, (2S,4S)-6-fluoro-2′,5′-dioxospiro[chroman4,4′-imidazolidine]- 2-carboxamide. Excerpta Med. 1990, 913, 89-96.
-
(1990)
Excerpta Med.
, vol.913
, pp. 89-96
-
-
Mizuno, K.1
Yamaguchi, T.2
Inoue, A.3
Tomiya, N.4
Unno, R.5
Miura, K.6
Usui, T.7
Matsumoto, Y.8
Kondo, Y.9
Yoshina, S.10
Kondo, Y.11
Sato, M.12
Matsubara, A.13
Kato, N.14
Nakano, K.15
Shirai, M.16
Inoue, T.17
Awaya, J.18
Asaeda, N.19
Hayasaka, I.20
Koide, M.21
Hibi, C.22
Ban, M.23
Sawai, K.24
Kurono, M.25
more..
-
4
-
-
0028344047
-
Synthesis and aldose reductase inhibitory activity of 2-Substituted-6-Fluoro-2,3-dihydrospiro[4H-1-benzopyran-4,4′- imidazolidine]-2′,5′-diones
-
(b) Yamaguchi, T.; Miura, K.; Usui, T.; Unno, R.; Matsumoto, Y.; Fukushima, M.; Mizuno, K.; Kondo, Y.; Baba, Y.; Kurono, M. Synthesis and Aldose Reductase Inhibitory Activity of 2-Substituted-6-Fluoro-2,3-dihydrospiro[4H-1-benzopyran-4,4′- imidazolidine]-2′,5′-diones. Arzneim.-Forsch./Drug Res. 1994, 44, 344-348.
-
(1994)
Arzneim.-Forsch./Drug Res.
, vol.44
, pp. 344-348
-
-
Yamaguchi, T.1
Miura, K.2
Usui, T.3
Unno, R.4
Matsumoto, Y.5
Fukushima, M.6
Mizuno, K.7
Kondo, Y.8
Baba, Y.9
Kurono, M.10
-
5
-
-
0025967888
-
Novel, potent aldose reductase inhibitors: 3,4-Dihydro-4-oxo-3-[[5-(trifluoromethyl)-2-benzothiazoly]methyl]-1- phthalazineacetic acid (Zopolrestat) and congeners
-
Mylari, B. L.; Larson, E. R.; Beyer, T. A.; Zembrowski, W. J.; Aldinger, C. E.; Dee, M. F.; Siegel, T. W.; Singleton, D. H. Novel, Potent Aldose Reductase Inhibitors: 3,4-Dihydro-4-oxo-3-[[5-(trifluoromethyl)-2-benzothiazoly]methyl]-1- phthalazineacetic Acid (Zopolrestat) and Congeners. J. Med. Chem. 1991, 34, 108-122.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 108-122
-
-
Mylari, B.L.1
Larson, E.R.2
Beyer, T.A.3
Zembrowski, W.J.4
Aldinger, C.E.5
Dee, M.F.6
Siegel, T.W.7
Singleton, D.H.8
-
6
-
-
0021323690
-
N-[[5-(Trifluoromethyl)-6-methoxy-1-naphthalenyl]]thioxomethyl|-N- methylglycine (Tolrestat), a potent, orally active aldose reductase inhibitor
-
Sestanj, K.; Bellini, F.; Fung, S.; Abraham, N.; Treasurywala, A.; Humber, L.; Simard-Duquesne, N.; Dvornik, D. N-[[5-(Trifluoromethyl)-6-methoxy-1-naphthalenyl]]thioxomethyl|-N-methylglycine (Tolrestat), a Potent, Orally Active Aldose Reductase Inhibitor. J. Med. Chem. 1984, 27, 255-256.
-
(1984)
J. Med. Chem.
, vol.27
, pp. 255-256
-
-
Sestanj, K.1
Bellini, F.2
Fung, S.3
Abraham, N.4
Treasurywala, A.5
Humber, L.6
Simard-Duquesne, N.7
Dvornik, D.8
-
7
-
-
0015887637
-
Polyol accumulation in galactosemic and diabetic rats: Control by an aldose reductase inhibitor
-
Dvornik, D.; Simard-Duquesne, N.; Krami, M.; Sestanj, K.; Gabbay, K. H.; Kinoshita, J. H.; Varma, S. D.; Merola, L. O. Polyol Accumulation in Galactosemic and Diabetic Rats: Control by an Aldose Reductase Inhibitor. Science 1973, 182, 1146-1148.
-
(1973)
Science
, vol.182
, pp. 1146-1148
-
-
Dvornik, D.1
Simard-Duquesne, N.2
Krami, M.3
Sestanj, K.4
Gabbay, K.H.5
Kinoshita, J.H.6
Varma, S.D.7
Merola, L.O.8
-
8
-
-
0020526445
-
Effect of a new aldose reductase inhibitor, (E)-3-Carboxymethyl-5-(2E)-Methyl-3-Phenylpropenylidene|rhadanine (ONO2235), on peripheral nerve disorders in streptozotocin-diabetic rats
-
Kikkawa, R.; Hatanaka, I.; Yasuda, H.; Kobayashi, N.; Shigeta, Y.; Terashima, H.; Morimura, T.; Tsuboshima, M. Effect of A New Aldose Reductase Inhibitor, (E)-3-Carboxymethyl-5-[(2E)-Methyl-3-Phenylpropenylidene|Rhadanine (ONO2235), on Peripheral Nerve Disorders in Streptozotocin-Diabetic Rats. Diabetologia 1983, 24, 290-292.
-
(1983)
Diabetologia
, vol.24
, pp. 290-292
-
-
Kikkawa, R.1
Hatanaka, I.2
Yasuda, H.3
Kobayashi, N.4
Shigeta, Y.5
Terashima, H.6
Morimura, T.7
Tsuboshima, M.8
-
9
-
-
0025956755
-
Characterization of a novel aldose reductase inhibitor, FR74366, and its effects on diabetic cataract and neuropathy in the rats
-
Ao, S.; Shingu, Y.; Kikuchi, C.; Takano, Y.; Nomura, K.; Fujiwara, T.; Ohkubo, Y.; Notsu, Y.; Yamaguchi, I. Characterization of a Novel Aldose Reductase Inhibitor, FR74366, and its Effects on Diabetic Cataract and Neuropathy in the Rats. Metabolism 1991, 40, 77-87.
-
(1991)
Metabolism
, vol.40
, pp. 77-87
-
-
Ao, S.1
Shingu, Y.2
Kikuchi, C.3
Takano, Y.4
Nomura, K.5
Fujiwara, T.6
Ohkubo, Y.7
Notsu, Y.8
Yamaguchi, I.9
-
10
-
-
0026719692
-
An unlikely sugar substrate site in the 1.65 å structure of the human aldose reductase holoenzyme implicated in diabetic complications
-
Wilson, D. K.; Bohren, K. M.; Gabbay, K. H.;,Quiocho, F. A. An Unlikely Sugar Substrate Site in the 1.65 Å Structure of the Human Aldose Reductase Holoenzyme Implicated in Diabetic Complications. Science 1992, 257, 81-84.
-
(1992)
Science
, vol.257
, pp. 81-84
-
-
Wilson, D.K.1
Bohren, K.M.2
Gabbay, K.H.3
Quiocho, F.A.4
-
11
-
-
0026443085
-
The crystal structure of the aldose reductase·NADPH binary complex
-
Borhani, D. W.; Harter, T. M.; Petrash, J. M. The Crystal Structure of the Aldose Reductase·NADPH Binary Complex. J. Biol. Chem. 1992, 267, 24841-24847.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 24841-24847
-
-
Borhani, D.W.1
Harter, T.M.2
Petrash, J.M.3
-
12
-
-
0026531024
-
Novel NADPH-binding domain revealed by the crystal structure of aldose reductase
-
Rondeau, J.-M.; Tête-Favier, F.; Podjarny, A.; Reymann, J.-M.; Barth, P.; Biellmann, J.-F.; Moras, D. Novel NADPH-binding domain revealed by the crystal structure of aldose reductase. Nature 1992, 355, 469-472.
-
(1992)
Nature
, vol.355
, pp. 469-472
-
-
Rondeau, J.-M.1
Tête-Favier, F.2
Podjarny, A.3
Reymann, J.-M.4
Barth, P.5
Biellmann, J.-F.6
Moras, D.7
-
13
-
-
0028331867
-
An anion binding site in human aldose reductase: Mechanistic implications for the binding of citrate, cacodylate, and glucose 6-Phosphate
-
Harrison, D. H.; Bohren, K. M.; Ringe, D.; Petsko, G. A.; Gabbay, K. H. An Anion Binding Site in Human Aldose Reductase: Mechanistic Implications for the Binding of Citrate, Cacodylate, and Glucose 6-Phosphate. Biochemistry 1994, 33, 2011-2020.
-
(1994)
Biochemistry
, vol.33
, pp. 2011-2020
-
-
Harrison, D.H.1
Bohren, K.M.2
Ringe, D.3
Petsko, G.A.4
Gabbay, K.H.5
-
14
-
-
0027378377
-
Refined 1.8 å structure of human aldose reductase complexed with the potent inhibitor zopolrestat
-
Wilson, D. K.; Tarle, I.; Petrash, J. M.; Quiocho, F. A. Refined 1.8 Å structure of human aldose reductase complexed with the potent inhibitor zopolrestat. Proc. Natl. Acad. Sci. U.S.A. 1993, 90, 9847-9851.
-
(1993)
Proc. Natl. Acad. Sci. U.S.A.
, vol.90
, pp. 9847-9851
-
-
Wilson, D.K.1
Tarle, I.2
Petrash, J.M.3
Quiocho, F.A.4
-
15
-
-
0031424157
-
The alrestatin double-decker: Binding of two inhibitor molecules to human aldose reductase reveals a new specificity determinant
-
Harrison, D. H. T.; Bohren, K. M.; Petsko, G. A.; Ringe, D.; Gabbay, K. H. The Alrestatin Double-Decker: Binding of Two Inhibitor Molecules to Human Aldose Reductase Reveals a New Specificity Determinant. Biochemistry 1997, 36, 16134-16140.
-
(1997)
Biochemistry
, vol.36
, pp. 16134-16140
-
-
Harrison, D.H.T.1
Bohren, K.M.2
Petsko, G.A.3
Ringe, D.4
Gabbay, K.H.5
-
16
-
-
0031570301
-
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, AD.; Moras, D. A 'specificity' pocket inferred from the crystal structures of the complexes of aldose reductase with the pharmaceutically important inhibitors tolrestat and sorbinil. Structure 1997, 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.9
-
17
-
-
0024420222
-
Cloning and sequence determination of human placental aldose reductase gene
-
Chung, S.; LaMendola, J. Cloning and Sequence Determination of Human Placental Aldose Reductase Gene. J. Biol. Chem. 1989, 264, 14775-14777.
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 14775-14777
-
-
Chung, S.1
LaMendola, J.2
-
18
-
-
0024333867
-
The aldo-keto reductase superfamily
-
Bohren, K. M.; Bullock, B.; Wermuth, B.; Gabbay, K. H. The Aldo-Keto Reductase Superfamily. J. Biol. Chem. 1989, 264, 9547-9551.
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 9547-9551
-
-
Bohren, K.M.1
Bullock, B.2
Wermuth, B.3
Gabbay, K.H.4
-
19
-
-
0028155824
-
Structures of human and porcine aldehyde reductase: An enzyme implicated in diabetic complications
-
El-Kabbani, O.; Green, N. C.; Lin, G.; Carson, M.; Narayana, S. V. L.; Moore, K. M.; Flynn, T. G.; DeLucas, L. J. Structures of Human and Porcine Aldehyde Reductase: an Enzyme Implicated in Diabetic Complications. Acta Crystallogr. 1994, D50, 859-868.
-
(1994)
Acta Crystallogr.
, vol.D50
, pp. 859-868
-
-
El-Kabbani, O.1
Green, N.C.2
Lin, G.3
Carson, M.4
Narayana, S.V.L.5
Moore, K.M.6
Flynn, T.G.7
DeLucas, L.J.8
-
20
-
-
0029130137
-
Structure of porcine aldehyde reductase holoenzyme
-
El-Kabbani, O.; Judge, K.; Ginell, S. L.; Myles, D. A. A.; DeLucas, L. J.; Flynn, T. G. Structure of porcine aldehyde reductase holoenzyme. Nature Struct. Biol. 1995, 2, 687-692.
-
(1995)
Nature Struct. Biol.
, vol.2
, pp. 687-692
-
-
El-Kabbani, O.1
Judge, K.2
Ginell, S.L.3
Myles, D.A.A.4
DeLucas, L.J.5
Flynn, T.G.6
-
21
-
-
0030982582
-
Studies on the inhibitor-binding site of porcine aldehyde reductase: Crystal structure of the holoenzyme-inhibitor ternary complex
-
El-Kabbani, O.; Carper, D. A.; McGowan, M. H.; Devedjiev, Y.; Rees-Milton, K. J.; Flynn, T. G. Studies on the Inhibitor-Binding Site of Porcine Aldehyde Reductase: Crystal Structure of the Holoenzyme-Inhibitor Ternary Complex. Proteins: Struct., Funct., Genet. 1997, 29, 186-192.
-
(1997)
Proteins: Struct., Funct., Genet.
, vol.29
, pp. 186-192
-
-
El-Kabbani, O.1
Carper, D.A.2
McGowan, M.H.3
Devedjiev, Y.4
Rees-Milton, K.J.5
Flynn, T.G.6
-
22
-
-
0032578366
-
Structural features of the aldose reductase and aldehyde reductase inhibitor-binding sites
-
El-Kabbani, O.; Wilson, D. K.; Petrash, J. M.; Quiocho, F. A. Structural Features of the Aldose Reductase and Aldehyde Reductase Inhibitor-Binding Sites. Mol. Vision 1998, 4, 19-25.
-
(1998)
Mol. Vision
, vol.4
, pp. 19-25
-
-
El-Kabbani, O.1
Wilson, D.K.2
Petrash, J.M.3
Quiocho, F.A.4
-
23
-
-
0029103124
-
Mechanism of human aldehyde reductase: Characterization of the active site pocket
-
Barski, O. A.; Gabbay, K. H.; Grimshaw, C. E.; Bohren, K. M. Mechanism of Human Aldehyde Reductase: Characterization of the Active Site Pocket. Biochemistry 1995, 34, 11264-11275.
-
(1995)
Biochemistry
, vol.34
, pp. 11264-11275
-
-
Barski, O.A.1
Gabbay, K.H.2
Grimshaw, C.E.3
Bohren, K.M.4
-
25
-
-
85069119717
-
-
Max-Planck-Institute for Biochemistry
-
Steigemann, W. PROTEIN, revision 5; Max-Planck-Institute for Biochemistry, 1993.
-
(1993)
PROTEIN, Revision 5
-
-
Steigemann, W.1
-
28
-
-
0001099937
-
Traitement statistique des erreurs dans la determination des structures cristallines
-
Luzzati, P. V. Traitement Statistique des Erreurs dans la Determination des Structures Cristallines. Acta Crystallogr. 1952, 5, 802-810.
-
(1952)
Acta Crystallogr.
, vol.5
, pp. 802-810
-
-
Luzzati, P.V.1
-
29
-
-
85069109304
-
-
QUANTA/CHARMm was developed by Molecular Simulations Inc.
-
QUANTA/CHARMm was developed by Molecular Simulations Inc.
-
-
-
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