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Książki na temat „Chemist activity”

Autor: Grafiati

Data publikacji: 12 października 2024

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1

Pitaud, Henri. Paysan et militant: Mes chemins sauvages : souvenirs 1921-1940. Beauvoir-sur-Mer: Etrave, 2001.

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2

Paxton, Robert O. Le temps des chemises vertes: Révoltes paysannes et fascisme rural, 1929-1939. Paris: Editions du Seuil, 1996.

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3

Pillon, Lilianna Z. Surface activity of petroleum derived lubricants. Boca Raton: Taylor & Francis, 2010.

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4

Pillon, Lilianna Z. Surface activity of petroleum derived lubricants. Boca Raton [Fla.]: Taylor & Francis, 2011.

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5

Sylvio, Canuto, red. Solvation effects on molecules and biomolecules: Computational methods and applications. [Dordrecht]: Springer, 2008.

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6

Cairns, Donald. Essentials of pharmaceutical chemistry. Wyd. 3. London: Pharmaceutical Press, 2008.

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7

Delehedde, Maryse, i Hugues Lortat-Jacob. New developments in therapeutic glycomics. Trivandrum, Kerala, India: Research Signpost, 2006.

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8

Casy, Alan F. The steric factor in medicinal chemistry: Dissymmetric probesof pharmacological receptors. New York: Plenum Press, 1993.

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9

H, Dewar George, red. The steric factor in medicinal chemistry: Dissymmetric probes of pharmacological receptors. New York: Plenum Press, 1993.

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10

Tsujii, Kaoru. Surface activity: Principles, phenomena, and applications. San Diego: Academic Press, 1998.

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11

International Workshop on Quantitative Structure-Activity Relationships in Environmental Sciences (7th 1996 Elsinore, Denmark). Quantitative structure-activity relationships in environmental sciences, VII. Pensacola, Fla: SETAC Press, 1997.

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12

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

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13

Mager, Peter P. Multivariate chemometrics in QSAR (quantitative structure-activity relationships): A dialogue. Letchworth, Hertfordshire, England: Research Studies Press, 1988.

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14

1947-, Abe Masahiko, i Scamehorn John F. 1953-, red. Mixed surfactant systems. Wyd. 2. New York: Marcel Dekker, 2005.

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15

C, Srivastava R. Surface activity in drug action. Amsterdam: Elsevier, 2005.

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16

J, Stezowski John, Huang Jin-Ling, Shao Mei-Cheng i International Union of Crystallography, red. Molecular structure: Chemical reactivity and biological activity. Oxford OX: Oxford University Press, 1988.

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17

International Symposium on the Properties of Water (10th 2007 Bangkok, Thailand). Water properties in food, health, pharmaceutical and biological systems: ISOPOW 10. Ames, Iowa: Wiley-Blackwell, 2009.

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18

European, Symposium on Quantitative Structure-Activity Relationships (6th 1986 Portoroz Slovenia). QSAR in drug design and toxicology: Proceedings of the Sixth European Symposium on Quantitative St[r]ucture-Activity Relationships, Portorož - Portorose (Yugoslavia), 22-26 September 1986. Amsterdam: Elsevier, 1987.

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19

Royal Society of Chemistry (Great Britain), red. Polymeric materials with antimicrobial activity: From synthesis to applications. Cambridge: RSC Publishing, 2014.

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20

ACS Satellite Television Seminar (1997). New techniques for drug discovery: Better ways to find the needle in the haystack! : ACS Satellite Television Seminar, March 27, 1997. Washington, DC: American Chemical Society, 1997.

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21

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 medicinal chemist and an expert on drug discovery, offers a thorough analysis of the landscape of current drug development. The comprehensive text is divided by health issues, including cardiovascular, cancer, metabolic diseases, and infectious diseases. Each section features individual chapters on significant drugs, outlining the chemistry and history of the drug's discovery. Li begins each chapter with the product's history, providing necessary context. Li then proceeds to describe the mechanism of action, structure-activity relationship (SAR), bioavailability, metabolism, toxicology, the discovery route, and the process route. Top Drugs: Their History, Pharmacology, and Synthesis will acclimate students, scientists, and interested laypersons to the world of chemistry and drug discovery.

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22

Atta-ur-Rahman i M. Iqbal Choudhary, red. Frontiers in Cardiovascular Drug Discovery: Volume 4. BENTHAM SCIENCE PUBLISHERS, 2019. http://dx.doi.org/10.2174/97816810839951180401.

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Frontiers in Cardiovascular Drug Discovery is an eBook series devoted to publishing the latest advances in cardiovascular drug design and discovery. Each volume brings reviews on the biochemistry, in-silico drug design, combinatorial chemistry, high-throughput screening, drug targets, recent important patents, and structure-activity relationships of molecules used in cardiovascular therapy. The eBook series should prove to be of great interest to all medicinal chemists and pharmaceutical scientists involved in preclinical and clinical research in cardiology. The fourth volume of the series covers the following topics: -Aspirin administration -Adenosine receptor targeting for cardiovascular therapy -Drug treatment of patients with coronary stenting -Immunosuppressive drugs in heart transplantation -PCSK9 inhibition for lowering LDL-C levels.

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23

Singh, Rajesh Kumar, red. Key Heterocyclic Cores for Smart Anticancer Drug–Design Part I. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/97898150400741220101.

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This book provides an update on heterocyclic compounds that serve as key components of anti-cancer agents administered in pre-clinical settings. Many of the compounds highlighted in the book are being actively investigated for the bioactive properties against a range of cancer cell lines. There is potential for heterocyclic compounds to design agents that can target specific molecules to treat different types of cancers. Chapters are contributed by experts in pharmaceutical chemistry and are written to give a general overview of the topic to readers involved in all levels of research and decision-making in pharmaceutical chemistry and anti-cancer drug design. Part 1 of the book set covers these topics: - Heterocyclic anticancer compounds derived from natural sources with their mechanism of action - The role of terpenoids as anticancer compounds: an insight into prevention and treatment - Recent advances in synthesis and anticancer activity of benzothiazole hybrids as anticancer agents - Structure-activity relationship studies of novel hybrid quinoline and quinolone derivatives as anticancer agents - Tetrazoles: structure and activity relationship as anticancer agents - Progress in nitrogen and oxygen-based heterocyclic compounds for their anticancer activity: an update (2017-2020)

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24

Srivastava, R. C. C., i A. N. N. Nagappa. Surface Activity in Drug Action. Elsevier Science & Technology Books, 2005.

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25

Gang, David R. The Biological Activity of Phytochemicals. Springer, 2012.

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26

Burgot, Jean-Louis. The Notion of Activity in Chemistry. Springer, 2016.

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27

Burgot, Jean-Louis. The Notion of Activity in Chemistry. Springer, 2018.

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28

Sieber, Stephan A. Activity-Based Protein Profiling. Springer Berlin / Heidelberg, 2014.

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29

Hulme, Philippa Gardom, i Andrew Chandler-Grevatt. Activate Chemistry. Oxford University Press, 2014.

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30

Jetter, Reinhard. Formation, Structure and Activity of Phytochemicals. Springer International Publishing AG, 2016.

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31

Jetter, Reinhard. Formation, Structure and Activity of Phytochemicals. Springer, 2015.

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32

Les chemins de l'Etat. 3, Propos sur la démocratie. Interfaces, 1994.

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33

Duke, James A. Database of Biologically Active Phytochemicals & Their Activity. CRC, 1992.

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34

Jetter, Reinhard. The Formation, Structure and Activity of Phytochemicals. Springer, 2015.

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35

Naray-Szabo, G. Naray. Steric Aspects of Biomolecular Interactions. Taylor & Francis Group, 2018.

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36

Naray-Szabo, G. Naray. Steric Aspects of Biomolecular Interactions. Taylor & Francis Group, 2018.

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37

Steric Aspects of Biomolecular Interactions. Taylor & Francis Group, 2017.

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38

Pillon, Lilianna. Surface Activity of Petroleum Derived Lubricants. Taylor & Francis Group, 2011.

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39

QSAR: Quantitative structure-activity relationships in drug design : Proceedings of the 7th European Symposium on QSAR, held in Interlaken, Switzerland, ... in clinical and biological research). Liss, 1989.

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40

Copeland, Robert A. Evaluation of Enzyme Inhibitors in Drug Discovery: A Guide for Medicinal Chemists and Pharmacologists. Wiley & Sons, Incorporated, John, 2013.

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41

Bionanodesign: Following nature's touch. Cambridge: RSC Publishing, 2009.

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42

Ryadnov, Maxim. Bionanodesign: Old Forms for New Functions. Royal Society of Chemistry, The, 2021.

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43

Ryadnov, Maxim. Bionanodesign: Old Forms for New Functions. Royal Society of Chemistry, The, 2020.

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44

Bionanodesign: Following Nature's Touch. Royal Society of Chemistry, The, 2009.

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45

Tro, Nivaldo J., i Michael Everest. Student's Guided Activity Workbook for Introductory Chemistry. Pearson Education, Limited, 2014.

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46

Totally Gross Chemistry-the Creative Activity Kit. Publications International, 2000.

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47

Gang, David R. Biological Activity of Phytochemicals. Springer, 2010.

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48

Copeland, Robert A. Evaluation of Enzyme Inhibitors in Drug Discovery: A Guide for Medicinal Chemists and Pharmacologists. Wiley & Sons, Incorporated, John, 2007.

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49

Copeland, Robert A. Evaluation of Enzyme Inhibitors in Drug Discovery: A Guide for Medicinal Chemists and Pharmacologists. Wiley-Interscience, 2005.

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50

Copeland, Robert A. Evaluation of Enzyme Inhibitors in Drug Discovery: A Guide for Medicinal Chemists and Pharmacologists. Wiley & Sons, Limited, John, 2013.

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