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020 _a9780123820303
028 _aGlobal Information Systems Technology Pvt Ltd
_b877, Udhyog Vihar, Phase-V, Gurgaon
082 _a615.1 SIL
100 _aSilverman, Richard B.,
245 _aThe organic chemistry of drug design and drug action.
_bThird edition /
260 _aAmsterdam ;
_bAcademic Press, an imprint of Elsevier,
_c©2014
300 _axviii, 517 pages :
_billustrations ;
_c24 cm.
505 _aChapter 1 - Introduction, In The Organic Chemistry of Drug Design and Drug Action
_uhttp://www.sciencedirect.com/science/article/pii/B9780123820303000015
505 _aChapter 2 - Lead Discovery and Lead Modification,
_uhttp://www.sciencedirect.com/science/article/pii/B9780123820303000027
505 _aChapter 3 - Receptors, In The Organic Chemistry of Drug Design and Drug Action
_uhttp://www.sciencedirect.com/science/article/pii/B9780123820303000039
505 _aChapter 4 - Enzymes, In The Organic Chemistry of Drug Design and Drug Action
_uhttp://www.sciencedirect.com/science/article/pii/B9780123820303000040
505 _aChapter 5 - Enzyme Inhibition and Inactivation,
_uhttp://www.sciencedirect.com/science/article/pii/B9780123820303000052
505 _aChapter 6 - DNA-Interactive Agents,
_uhttp://www.sciencedirect.com/science/article/pii/B9780123820303000064
505 _aChapter 7 - Drug Resistance and Drug Synergism,
_uhttp://www.sciencedirect.com/science/article/pii/B9780123820303000076
505 _aChapter 8 - Drug Metabolism,
_uhttp://www.sciencedirect.com/science/article/pii/B9780123820303000088
505 _aChapter 9 - Prodrugs and Drug Delivery Systems,
_uhttp://www.sciencedirect.com/science/article/pii/B978012382030300009X
520 _aAbstract : Provides a basis and overall context for concepts introduced and discussed in more detail in subsequent chapters in this book. An historical context is given to the topic of drug discovery, followed by a high level overview of modern approaches to rational drug design. The approaches and steps typically encountered in modern rational drug design, including target identification, lead discovery, and lead modification, are introduced, and an overview of the subsequent steps required for drug development prior to regulatory approval, such as pharmacokinetics, preclinical studies, clinical trials, and intellectual property issues, are summarized.
_uhttp://www.sciencedirect.com/science/book/9780124186910
650 _aBioorganic chemistry.
_2
650 _aPharmaceutical chemistry.
650 _aMolecular pharmacology.
650 _aDrugs
650 _aDesign.
650 _aE-Books
700 _aHolladay, Mark W.,
856 _3E-Book
_uhttp://www.sciencedirect.com/science/book/9780123820303
942 _2ddc
_cER
999 _c46931
_d46931