The inhibitory activity of aldose reductase of flavonoid compounds: Combining DFT and QSAR calculationsFootnote

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References

• Z.KyselovaM.StefekV.BauerPharmacological prevention of diabetic cataractJ. Diabetes Complicat.182004129140
   PubMed Web of Science ®Google Scholar
• Y.HamadaJ.NakamuraClinical potential of aldose reductase inhibitors in diabetic neuropathyTreat. Endocrinol.32004245255
   PubMedGoogle Scholar
• J.M.ForbesM.T.CoughlanM.E.CooperOxidative stress as a major culprit in kidney disease in diabetesDiabetes57200814461454
   PubMed Web of Science ®Google Scholar
• S.MiyamotoRecent advances in aldose reductase inhibitors: potential agents for the treatment of diabetic complicationsExpert Opin. Ther. Patents122002621631
   Web of Science ®Google Scholar
• P.E.KadorN.E.SharplessStructure–activity studies of aldose reductase inhibitors containing the 4-oxo-4H-chromen ring systemBiophys. Chem.819788185
   PubMed Web of Science ®Google Scholar
• P.E.KadorJ.H.KinoshitaN.E.SharplessAldose reductase inhibitors: a potential new class of agents for the pharmacological control of certain diabetic complicationsJ. Med. Chem.281985841849
   PubMed Web of Science ®Google Scholar
• J.R.PfisterW.E.WymannJ.M.MahoneyL.D.WaterburySynthesis and aldose reductase inhibitory activity of 7-sulfamoylxanthone-2-carboxylic acidsJ. Med. Chem.23198012641267
   Web of Science ®Google Scholar
• M.S.MalamasJ.MillenQuinazoline acetic acids and related analogues as aldose reductase inhibitorsJ. Med. Chem.34199114921503
   PubMed Web of Science ®Google Scholar
• Y.S.PrabhakarM.K.GuptaN.RoyY.VenkateswarluA high dimensional QSAR study on the aldose reductase inhibitory activity of some flavones: topological descriptors in modeling the activityJ. Chem. Inf. Model.4620068692
   PubMed Web of Science ®Google Scholar
• A.G.MercaderP.R.DuchowiczF.M.FernandezE.A.CastroD.O.BennardiJ.C.Autinoet al.QSAR prediction of inhibition of aldose reductase for flavonoidsJ. Bioorg. Med. Chem.16200874707476
   PubMed Web of Science ®Google Scholar
• H.LiuS.LiuL.QinL.MoCoMFA, CoMSIA analysis of 2,4-thiazolidinediones derivatives as aldose reductase inhibitorsJ. Mol. Model.152009837845
   PubMed Web of Science ®Google Scholar
• S.TharejaS.AggarwalT.R.BhardwajM.Kumar3D-QSAR studies on a series of 5-arylidine-2,4-thiazolidinediones as aldose reductase inhibitors: a self-organizing molecular field analysis approachMed. Chem.620103036
   PubMed Web of Science ®Google Scholar
• G.D.CarloN.MascoloA.A.IzzoF.CapassoFlavonoid: old and new aspects of a class of natural therapeutic drugsLife Sci.651999337353
   PubMed Web of Science ®Google Scholar
• P.C.H.HaollmanI.C.W.ArtsFlavonols, flavones and flavanols – nature, occurrence and dietary burdenJ. Sci. Food Agric.80200010811093
   Web of Science ®Google Scholar
• S.A.AherneN.M.O’BrienDietary flavonols: chemistry, food content, and metabolismNutrition1820027581
   PubMed Web of Science ®Google Scholar
• O.P.AgarwalThe anti-inflammatory action of nepitrin, a flavonoidAgents Actions121982298302
   PubMedGoogle Scholar
• M.K.ChurchCromoglycate-like anti-allergic drugs: a reviewDrugs Today141978281341
   Google Scholar
• B.F.RasulevN.D.AbdullaevV.N.SyrovJ.LeszczynskiA quantitative structure–activity relationship (QSAR) study of the antioxidant activity of flavonoidsQSAR Comb. Sci.24200510561065
   Google Scholar
• H.KubinyiQSAR: Hansch analysis and related approachesR.MannholdP.Krokgsgaard-LarsenH.TimmermanMethods and Principles in Medicinal Chemistry1993VCHWeinheim
   Google Scholar
• A.Stefanic-PetekA.KrbavcicT.SolmajerQSAR of flavonoids. 4. Differential inhibition of aldose reductase and p56lck protein tyrosine kinaseCroat. Chem. Acta752002517529
   Web of Science ®Google Scholar
• M.J.FrischGaussian 03 Revision B.012003Gaussian, Inc.Pittsburgh, PA
   Google Scholar
• U.SakarR.ParthasarathiV.SubramanianP.K.ChattarajiToxicity analysis of polychlorinated dibenzofurans through globalJ. Mol. Des. IECMD2004124
   Google Scholar
• Advanced Chemistry Development, Inc., Toronto, Canada, 2009 (www.acdlabs.com/resources/freeware/chemsketch/).
   Google Scholar
• M.LarifA.AdadR.HmammouchiA.I.TaghkiA.SoulaymaniA.ElmidaouiM.BouachrineT.LakhlifiBiological activities of triazine derivatives combining DFT and QSAR resultsArab. J. Chem.201610.1016/j.arabjc.2012.12.033 (in press)
   Web of Science ®Google Scholar
• XLSTAT. software2013XLSTAT Companyhttp://www.xlstat.com
   Google Scholar
• S.ChtitaM.LarifM.GhamaliM.BouachrineT.LakhlifiDFT-based QSAR studies of MK801 derivatives for non competitive antagonists of NMDA using electronic and topological descriptorsJ. Taibah Univ. Chem.922014143154
   Google Scholar
• A.AdadM.LarifR.HmamouchiM.BouachrineT.LakhlifiJ. Comp. Methods Mol. Des.4320147283
   Google Scholar
• R.HmamouchiM.LarifA.AdadM.BouachrineT.LakhlifiJ. Comp. Methods Mol. Des.4320146171
   Google Scholar
• D.CherqaouiD.VilleminJ. Chem. Soc. Faraday Trans.90199497102
   Google Scholar
• J.A.FreemanD.M.SkapuraNeural Networks, Algorithms, Applications and Programming Techniques1991Addison-Wesley Publishing CompanyReading, MA
   Google Scholar
• A.GolbraikhA.TropshaBeware of q2!J. Mol. Graph. Model.202002269276
   PubMed Web of Science ®Google Scholar
• Software STATITCF1987Technical Institute of Cereals and FodderParis, France
   Google Scholar
• A.OusaaB.ElidrissiM.GhamaliS.ChtitaM.BouachrineT.LakhlifiJ. Comp. Methods Mol. Des.4320141018
   Google Scholar