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1

1962-, Thakore Jogin H., and Leonard B. E, eds. Metabolic effects of psychotropic drugs. Karger, 2009.

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2

H, Jeffery Elizabeth, ed. Human drug metabolism: From molecular biology to man. CRC Press, 1993.

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3

C, Kauffman Frederick, and Bock K. W. 1935-, eds. Conjugation-deconjugation reactions in drug metabolism and toxicity. Springer-Verlag, 1994.

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4

Peter, Eyer, ed. Metabolic aspects of cell toxicity. Wissenschaftsverlag, 1994.

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5

Goudot-Perrot, Andrée. Metabolic inhibitors: Antibiotics - antimitotics - psychotropics. Schwer Verlag, 1992.

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6

Emel, Arinç, Schenkman John B, and Hodgson Ernest 1932-, eds. Molecular and applied aspects of oxidative drug metabolizing enzymes. Plenum Press, 1999.

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7

J, Mulder Gerard, ed. Conjugation reactions in drug metabolism: An integrated approach : substrates, co-substrates, enzymes and their interactions in vivo and in vitro. Taylor & Francis, 1990.

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8

Lau, Grace S. N. Metabolic activation of drugs and other xenobiotics in hepatocellular carcinoma. Chinese University Press, 1997.

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9

1955-, Mrsny Randall J., and Daugherty Ann L. 1954-, eds. Proteins and peptides: Pharmacokinetic, pharmacodynamic, and metabolic outcomes. Informa Healthcare, 2010.

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10

Predrag, Cudic. Peptide modifications to increase metabolic stability and activity. Humana Press, 2013.

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11

S, Rapaka Rao, Chiang C. Nora, Martin Billy R, and National Institute on Drug Abuse, eds. Pharmacokinetics, metabolism, and pharmaceutics of drugs of abuse. U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, National Institute on Drug Abuse, 1997.

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12

Center for Substance Abuse Treatment (U.S.), ed. Detoxification from alcohol and other drugs. U.S. Dept of Health and Human Services, Public Health Service, Substance Abuse and Mental Health Services Administration, Center for Substance Abuse Treatment, 1995.

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13

Beard, Jonathan C. Illicit drug use: Acute and chronic pharmacological intervention. Quay Books, 1995.

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14

Kenʼichi, Kitani, ed. Liver and aging, 1986: Liver and brain : proceedings of the Third Symposium on Liver and Aging--Liver and Brain, held in Tokyo, Japan on August 20-22, 1986. Elsevier Science Publishers, 1986.

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15

D, Hayes J., Pickett C. B, Mantle T. J, University of Edinburgh. Dept. of Clinical Chemistry., and International GST Conference (3rd : 1989 : Royal College of Physicians of Edinburgh), eds. Glutathione S-transferases and drug resistance. Taylor & Francis, 1990.

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16

Michenfelder, John D. Anesthesia and the brain: Clinical, functional, metabolic, and vascular correlates. Churchill Livingstone, 1988.

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17

Berger, W., R. Flückiger, H. G. Köppe, et al. Metabolic Control in Diabetes Mellitus Beta Adrenoceptor Blocking Drugs NMR Analysis of Cancer Cells Immunoassay in the Clinical Laboratory Cyclosporine. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-70998-2.

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18

W, Berger, ed. Metabolic control in diabetes mellitus ; Beta adrenoceptor blocking drugs ; NMR analysis of cancer cells ; Immunoassay in the clinical laboratory ; Cyclosporine. Springer-Verlag, 1986.

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19

Garth, Powis, ed. Anticancer drugs: Reactive metabolism and drug interactions. Pergamon Press, 1994.

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20

1949-, Gibson G. Gordon, ed. Progress in drug metabolism. John Wiley, 1988.

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21

1938-, Bieck Peter R., ed. Colonic drug absorption and metabolism. M. Dekker, 1993.

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22

Lyubimov, Alexander V. Encyclopedia of drug metabolism and interactions. Wiley, 2012.

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23

Barthel, Andreas, and Michael Bauer. Psychotropic drugs and metabolic risk. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198789284.003.0011.

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Increased appetite and weight gain represent a significant problem related with particular antipsychotic drugs, antidepressants, mood stabilizers, and—to a lesser extent—anxiolytic drugs. Psychotropic drug-induced weight gain may contribute to obesity-related metabolic changes and pathological conditions such as dyslipidaemia, type-2-diabetes and hypertension—summarized as the metabolic syndrome—with an increased risk for cardiovascular morbidity and mortality. Interestingly, psychotropic drugs are also used for the treatment of diabetes-related complications. For example, antidepressants are
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24

Thakore, J., and B. E. Leonard, eds. Metabolic Effects of Psychotropic Drugs. S. Karger AG, 2009. http://dx.doi.org/10.1159/isbn.978-3-8055-9002-0.

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25

Kritchevky, David. Lipids, Lipoproteins, and Drugs. Springer London, Limited, 2012.

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26

Li, Jie Jack. Top Drugs. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780199362585.001.0001.

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Drugs like Lipitor, Plavix, Taxol, and Zoloft are integral in today's medicinal world. These widely used products save lives and improve the quality of lives, playing a crucial role in everything from cholesterol management to cancer treatment. These advances in medicine were brought into existence after nuanced process of creation, featuring a wide range of chemical and pharmacological experimentation and discovery. Top Drugs: Their History, Pharmacology, and Synthesis provides an in-depth study on ten prominent drugs, outlining the chemistry behind each one's creation. Jie Jack Li, a medicin
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27

Burchell, B., Frederick C. Kauffman, K. W. Bock, and M. Chiba. Conjugation--Deconjugation Reactions in Drug Metabolism and Toxicity. Springer London, Limited, 2012.

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28

Burchell, B., Frederick C. Kauffman, K. W. Bock, and M. Chiba. Conjugation-Deconjugation Reactions in Drug Metabolism and Toxicity. Springer London, Limited, 2011.

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29

Meyler's Side Effects of Endocrine and Metabolic Drugs. Elsevier Science & Technology Books, 2009.

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30

Kritchevky, David. Lipids, Lipoproteins, and Drugs. Springer, 2012.

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31

Ng, Linda Fung-yee. Metabolic Activation of Drugs (Young Scholars Dissertation Awards). Columbia University Press, 1997.

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32

Aronson, Jeffrey K. Meyler's Side Effects of Endocrine and Metabolic Drugs. Elsevier Science & Technology Books, 2009.

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33

Lazarus, J. H. Endocrine and Metabolic Effects of Lithium. Springer London, Limited, 2013.

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34

Lazarus, J. H. Endocrine and Metabolic Effects of Lithium. Springer, 2013.

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35

Mulder, Gerard J. Conjugation Reactions in Drug Metabolism: An Integrated Approach, Substrates, Co-Substrates, Enzymes and Their Interactions in Vivo and in Vitro. Taylor & Francis Group, 1990.

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36

Mulder, Gerard J. Conjugation Reactions in Drug Metabolism: An Integrated Approach. Taylor & Francis Group, 1990.

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37

Cudic, Predrag. Peptide Modifications to Increase Metabolic Stability and Activity. Humana Press, 2016.

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38

Ioannides, Costas. Enzyme Systems that Metabolise Drugs and Other Xenobiotics (Current Toxicology). Wiley, 2002.

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39

Proteins and peptides: Pharmacokinetic, pharmacodynamic, and metabolic outcomes. Informa Healthcare, 2009.

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40

Mulder, Gerard J. Conjugation Reactions in Drug Metabolism: An Integrated Approach. Taylor & Francis Group, 1990.

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41

Mulder, Gerard J. Conjugation Reactions in Drug Metabolism: An Integrated Approach. Taylor & Francis Group, 1990.

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42

Mulder, Gerard J. Conjugation Reactions in Drug Metabolism: An Integrated Approach. Taylor & Francis Group, 1990.

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43

Metz, Thomas O. Metabolic Profiling: Methods and Protocols. Humana Press, 2016.

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44

Mrsny, Randall J., and Ann Daugherty. Proteins and Peptides: Pharmacokinetic, Pharmacodynamic, and Metabolic Outcomes. Taylor & Francis Group, 2009.

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45

Mrsny, Randall J., and Ann Daugherty. Proteins and Peptides: Pharmacokinetic, Pharmacodynamic, and Metabolic Outcomes. Taylor & Francis Group, 2009.

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46

Iversen, Les. 2. How drugs work. Oxford University Press, 2016. http://dx.doi.org/10.1093/actrade/9780198745792.003.0002.

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‘How drugs work’ outlines the basic mechanisms of pharmacology. Drugs are chemicals that can be naturally occurring or man-made, and which can be administered in a variety of ways. They can act on receptors—often highly specific proteins in cells which can up-regulate or down-regulate processes—or on other targets, such as DNA or enzymes. The molecular action of drugs can be investigated in a lab, but the effects on the whole organism are more important. Effective doses need to be determined, taking into account metabolic rates, drug interactions, and side effects. Prolonged drug use can cause
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47

Sutter, Johan De, Miguel Mendes, and Oscar H. Franco. Cardioprotective drugs. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656653.003.0019.

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Cardioprotective drugs are important in the treatment of patients at risk for or with documented cardiovascular disease. Beta-blockers are indicated after acute coronary syndromes, stable coronary artery disease, heart failure, and arrhythmias. Angiotensin-converting enzyme inhibitors (ACEi) are important in congestive heart failure, stable angina, post-acute myocardial infarction, and secondary prevention after any event or revascularization. Angiotensin receptor blockers are mainly alternative drugs for the same indications in case of intolerance to ACEi. Calcium channel blockers are first l
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48

Sutter, Johan De, Miguel Mendes, and Oscar H. Franco. Cardioprotective drugs. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199656653.003.0019_update_001.

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Cardioprotective drugs are important in the treatment of patients at risk for or with documented cardiovascular disease. Beta-blockers are indicated after acute coronary syndromes, stable coronary artery disease, heart failure, and arrhythmias. Angiotensin-converting enzyme inhibitors (ACEi) are important in congestive heart failure, stable angina, post-acute myocardial infarction, and secondary prevention after any event or revascularization. Angiotensin receptor blockers are mainly alternative drugs for the same indications in case of intolerance to ACEi. Calcium channel blockers are first l
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49

Mendelson, Scott D. Metabolic Syndrome and Psychiatric Illness: Interactions, Pathophysiology, Assessment and Treatment. Elsevier Science & Technology Books, 2007.

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50

Beard, Jonathan C. Illicit Drug Use. Quay Books,a division of Mark Allen Publishing Ltd, 1995.

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