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0031026509
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Comparison of the effects of inhibitors of aldose reductase and sorbitol dehydrogenase on neurovascular function, nerve conduction and tissue polyol pathway metabolites in streptozotocin-diabetic rats
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Cameron, N. E.; Cotter, M. A.; Basso, M.; Hohman, T. C. Comparison of the Effects of Inhibitors of Aldose Reductase and Sorbitol Dehydrogenase on Neurovascular Function, Nerve Conduction and Tissue Polyol Pathway Metabolites in Streptozotocin-Diabetic Rats. Diabetalogia 1997, 40, 271-281.
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Novel spirosuecinimide aldose reductase inhibitors derived from isoquinoline-1,3-diones: 2-[(4-Bromo-2-fluorophenyl)methyl]-6-fluorospiro- [isoquinoline-4(11H),3′-pyrrolidine]-1,2′,3,5′(2H)-tetrone and Congeners. 1
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note
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Experimental procedures for phenyl substituted compounds can be found in Patents EP 1236720 and CAN 137:216953.
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16
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0021814782
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Properties of ICI 128,436, a novel aldose reductase inhibitor, and its effects on diabetic complications in the rat
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Stribling, D.; Mirrlees, D. J.; Harrison, H. E.; Earl, D. C. Properties of ICI 128,436, a Novel Aldose Reductase Inhibitor, and Its Effects on Diabetic Complications in the Rat. Metabolism 1985, 34 (4), 336-344.
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Stribling, D.1
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17
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0025967888
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Novel, potent aldose reductase inhibitors: 3,4-Dihydro-4-oxo-3-[[5-(trifluoromethyl)-2- benzothiazolyl]methyl]-1-phthalazineacetic acid (zopolrestat) and congeners
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(a) 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- benzothiazolyl]methyl]-1-phthalazineacetic Acid (Zopolrestat) and Congeners. J. Med. Chem. 1991, 34, 108-122.
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18
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0026551050
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Potent, orally active aldose reductase inhibitors related to zopolrestat: Surrogates for benzothiazole side chain
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(b) Mylari, B. L.; Beyer, T. A.; Scott, P. J.; Aldinger, C. E.; Dee, M. F.; Siegel, T. W.; Zembrowski, W. J. Potent, Orally Active Aldose Reductase Inhibitors Related to Zopolrestat: Surrogates for Benzothiazole Side Chain. J. Med. Chem. 1992, 35, 457-465.
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19
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0027378377
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Refined 1.8 Å structure of human aldose reductase complexed with the potent inhibitor zopolrestat
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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.
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20
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0025737815
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Properties of novel aldose reductase inhibitors, M16209 and M16287, in comparison with known inhibitors. ONO-2235 and sorbinil
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Kato, K.; Nakayama, K.; Mizota, M.; Miwa, I.; Okuda, J. Properties of Novel Aldose Reductase Inhibitors, M16209 and M16287, in Comparison with Known Inhibitors. ONO-2235 and Sorbinil. Chem. Pharm. Bull. (Tokyo) 1991, 39, 540-545.
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Okuda, J.5
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21
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12444261773
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note
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Experimental procedures for heterocyclic substituted pyridazinones can be found in Patents U.S. 2,002,143,017 and CAN 137: 279206.
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22
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12444309394
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note
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Indole analogue 20 was more conveniently prepared starting from 2-mercaptoindole and following Scheme 1.
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23
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0026492673
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Pharmacological profile of GR117289 in vitro: A novel, potent and specific non-peptide angiotensin AT1 receptor antagonist
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Robertson, M. J.; Barnes, J. C.; Drew, G. M.; Clark, K. L.; Marshall, F. H.; Michel, A.; Middlemiss, D.; Ross, B. C.; Scopes, D.; Dowle, M. D. Pharmacological Profile of GR117289 in Vitro: A Novel, Potent and Specific Non-Peptide Angiotensin AT1 Receptor Antagonist. Br. J. Pharmacol. 1992, 107, 1173-1180.
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Marshall, F.H.5
Michel, A.6
Middlemiss, D.7
Ross, B.C.8
Scopes, D.9
Dowle, M.D.10
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