LEADER 05312nam 2200661Ia 450 001 9910830512703321 005 20170814175001.0 010 $a3-527-65574-3 010 $a1-283-60402-7 010 $a9786613916471 010 $a3-527-65576-X 010 $a3-527-65577-8 035 $a(CKB)2670000000253894 035 $a(EBL)1023284 035 $a(SSID)ssj0000741733 035 $a(PQKBManifestationID)11486002 035 $a(PQKBTitleCode)TC0000741733 035 $a(PQKBWorkID)10742950 035 $a(PQKB)11591595 035 $a(MiAaPQ)EBC1023284 035 $a(PPN)178891037 035 $a(OCoLC)811060211 035 $a(EXLCZ)992670000000253894 100 $a20111102d2012 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aReactive drug metabolites$b[electronic resource] /$fAmit S. Kalgutkar ...[et. al.] 210 $aWeinheim $cWiley-VCH$d2012 215 $a1 online resource (403 p.) 225 0 $aMethods and principles in medicinal chemistry 300 $aDescription based upon print version of record. 311 $a3-527-33085-2 320 $aIncludes bibliographical references and index. 327 $aReactive Drug Metabolites; Contents; Preface; A Personal Foreword; 1 Origin and Historical Perspective on Reactive Metabolites; Abbreviations; 1.1 Mutagenesis and Carcinogenesis; 1.2 Detection of Reactive Metabolites; 1.3 Induction and Inhibition: Early Probes for Reactive Metabolites and Hepatotoxicants; 1.4 Covalent Binding and Oxidative Stress: Possible Mechanisms of Reactive Metabolite Cytotoxicity; 1.5 Activation and Deactivation: Intoxication and Detoxification; 1.6 Genetic Influences on Reactive Metabolite Formation 327 $a1.7 Halothane: the Role of Reactive Metabolites in Immune-Mediated Toxicity1.8 Formation of Reactive Metabolites, Amount Formed, and Removal of Liability; 1.9 Antibodies: Possible Clues but Inconclusive; 1.10 Parent Drug and Not Reactive Metabolites, Complications in Immune-Mediated Toxicity; 1.11 Reversible Pharmacology Should not be Ignored as a Primary Cause of Side Effects; 1.12 Conclusions: Key Points in the Introduction; References; 2 Role of Reactive Metabolites in Genotoxicity; Abbreviations; 2.1 Introduction; 2.2 Carcinogenicity of Aromatic and Heteroaromatic Amines 327 $a2.3 Carcinogenicity of Nitrosamines2.4 Carcinogenicity of Quinones and Related Compounds; 2.5 Carcinogenicity of Furan; 2.6 Carcinogenicity of Vinyl Halides; 2.7 Carcinogenicity of Ethyl Carbamate; 2.8 Carcinogenicity of Dihaloalkanes; 2.9 Assays to Detect Metabolism-Dependent Genotoxicity in Drug Discovery; 2.10 Case Studies in Eliminating Metabolism-Based Mutagenicity in Drug Discovery Programs; References; 3 Bioactivation and Inactivation of Cytochrome P450 and Other Drug-Metabolizing Enzymes; Abbreviations; 3.1 Introduction 327 $a3.2 Pharmacokinetic and Enzyme Kinetic Principles Underlying Mechanism-Based Inactivation and Drug-Drug Interactions3.2.1 Enzyme Kinetic Principles of Mechanism-Based Inactivation; 3.2.2 Pharmacokinetic Principles Underlying DDIs Caused by Mechanism-Based Inactivation; 3.3 Mechanisms of Inactivation of Cytochrome P450 Enzymes; 3.3.1 Quasi-Irreversible Inactivation; 3.3.2 Heme Adducts; 3.3.3 Protein Adducts; 3.4 Examples of Drugs and Other Compounds that are Mechanism-Based Inactivators of Cytochrome P450 Enzymes; 3.4.1 Amines; 3.4.2 Methylenedioxyphenyl Compounds 327 $a3.4.3 Quinones, Quinone Imines, and Quinone Methides3.4.4 Thiophenes; 3.4.5 Furans; 3.4.6 Alkynes; 3.4.7 2-Alkylimidazoles; 3.4.8 Other Noteworthy Cytochrome P450 Inactivators; 3.5 Mechanism-Based Inactivation of Other Drug-Metabolizing Enzymes; 3.5.1 Aldehyde Oxidase; 3.5.2 Monoamine Oxidases; 3.6 Concluding Remarks; References; 4 Role of Reactive Metabolites in Drug-Induced Toxicity - The Tale of Acetaminophen, Halothane, Hydralazine, and Tienilic Acid; Abbreviations; 4.1 Introduction; 4.2 Acetaminophen; 4.2.1 Metabolism of Acetaminophen; 4.2.2 Metabolic Activation of Acetaminophen 327 $a4.3 Halothane 330 $aClosing a gap in the scientifi c literature, this first comprehensive introduction to the topic is based on current best practice in one of the largestpharmaceutical companies worldwide. The first chapters trace the development of our understanding of drug metabolite toxicity, covering basic concepts and techniques in the process, while the second part details chemical toxicophores that are prone to reactive metabolite formation. This section also reviews the various drug-metabolizing enzymes that can participate in catalyzing reactive metabolite formation, including a discussion of the st 410 0$aMethods and Principles in Medicinal Chemistry 606 $aFree radicals (Chemistry)$xPhysiological effect 606 $aDrugs$xMetabolism 615 0$aFree radicals (Chemistry)$xPhysiological effect. 615 0$aDrugs$xMetabolism. 676 $a615.19 700 $aKalgutkar$b Amit S.$f1965-$01628722 701 $aKalgutkar$b Amit S.$f1965-$01628722 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830512703321 996 $aReactive drug metabolites$93966002 997 $aUNINA LEADER 01965nam0 2200421 i 450 001 RMG0016417 005 20251003044335.0 010 $a8814050929 020 $aIT$b95-7787 100 $a20170731d1995 ||||0itac50 ba 101 | $aita 102 $ait 181 1$6z01$ai $bxxxe 182 1$6z01$an 183 1$6z01$anc$2RDAcarrier 200 1 $aStudi di diritto processuale canonico$fMario F. Pompedda 210 $aMilano$cGiuffrè$d1995 215 $aXIII, 289 p.$d22 cm. 225 | $aMonografie giuridiche$fAteneo romano della Santa Croce$g[poi] Pontificio Ateneo della Santa Croce$g[poi] Pontificia università della Santa Croce$v9 410 0$1001CFI0171343$12001 $aMonografie giuridiche$fAteneo romano della Santa Croce$g[poi] Pontificio Ateneo della Santa Croce$g[poi] Pontificia università della Santa Croce$v9$171202$aAteneo romano della Santa Croce$3CFIV124730 606 $aProcesso canonico$2FIR$3CFIC049587$9E 606 $aDiritto processuale canonico$2FIR$3CFIC077781$9E 676 $a262.9$9ECCLESIOLOGIA. DIRITTO E DISCIPLINA DELLA CHIESA$v12 676 $a262.94$9DIRITTO E DISCIPLINA DELLA CHIESA. 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