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04947nam a2200733 4500 |
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ocn867001313 |
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OCoLC |
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20170124070005.1 |
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131230s2014 enk ob 001 0 eng |
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|a 2013051081
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|a DLC
|b eng
|e rda
|c DLC
|d YDX
|d N$T
|d YDXCP
|d DG1
|d IDEBK
|d CUS
|d CDX
|d COO
|d OCLCF
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|d EBLCP
|d OCLCQ
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|c (S
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|a 928632128
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|a 9781118683149 (ePub)
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|a 1118683145 (ePub)
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|a 9781118683842 (Adobe PDF)
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|a 1118683846 (Adobe PDF)
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|z 9781119950608 (hardback)
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|a 9781118683033
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|a 9781119950608
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|a DEBBG
|b BV043396448
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|a (OCoLC)867001313
|z (OCoLC)928632128
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|a pcc
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|a RS431.P38
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|a MED
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|2 bisacsh
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|a 615.1/9
|2 23
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|a SCI013050
|2 bisacsh
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|a MAIN
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|a Trabocchi, Andrea,
|e author.
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|a Peptidomimetics in organic and medicinal chemistry /
|c Dr. Andrea Trabocchi and Professor Antonio Guarna.
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|a Chichester, West Sussex, UK ;
|a Hoboken, NJ :
|b John Wiley & Sons Inc.,
|c 2014.
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300 |
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|a 1 online resource.
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336 |
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|a text
|2 rdacontent
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|a computer
|2 rdamedia
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|a online resource
|2 rdacarrier
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|a "A peptidomimetic is a small protein-like chain designed to mimic a peptide with adjusted molecular properties such as enhanced stability or biological activity. It is a very powerful approach for the generation of small-molecule-based drugs as enzyme inhibitors or receptor ligands.Peptidomimetics in Organic and Medicinal Chemistry outlines the concepts and synthetic strategies underlying the building of bioactive compounds of a peptidomimetic nature. Topics covered include the chemistry of unnatural amino acids, peptide- and scaffold-based peptidomimetics, amino acid-side chain isosteres, backbone isosteres, dipeptide isosteres, beta-turn peptidomimetics, proline-mimetics as turn inducers, cyclic scaffolds, amino acid surrogates, and scaffolds for combinatorial chemistry of peptidomimetics. Case studies in the hit-to-lead process, such as the development of integrin ligands and thrombin inhibitors, illustrate the successful application of peptidomimetics in drug discovery"--
|c Provided by publisher.
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|a "Peptidomimetics in Organic and Medicinal Chemistry outlines the concepts and synthetic strategies underlying the building of bioactive compounds of a peptidomimetic nature"--
|c Provided by publisher.
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|a Includes bibliographical references and index.
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|a Description based on print version record and CIP data provided by publisher.
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|a Title Page; Copyright; Dedication; Preface; Abbreviations; Part I: The Basics of Peptidomimetics; Chapter 1: The Basics of Peptidomimetics; 1.1 Introduction; 1.2 Definition and Classification; 1.3 Strategic Approaches to Peptidomimetic Design; 1.4 Successful Examples of Peptidomimetic Drugs; 1.5 Conclusion; References; Chapter 2: Synthetic Approaches towards Peptidomimetic Design; 2.1 Introduction; 2.2 Local Modifications; 2.3 Global Restrictions through Cyclic Peptidomimetics; 2.4 Peptidomimetic Scaffolds; 2.5 Conclusions; References; Part II: Synthetic Methods and Molecules
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|a Chapter 3: Peptidomimetic Bioisosteres3.1 Introduction; 3.2 Peptide Bond Isosteres; 3.3 Side-Chain Isosteres; 3.4 Dipeptide Isosteres; 3.5 Tripeptide Isosteres; 3.6 Conclusion; References; Chapter 4: Solid-Phase Synthesis and Combinatorial Approaches to Peptidomimetics; 4.1 Introduction; 4.2 Solid-Phase Synthesis of Peptidomimetics; 4.3 Conclusion; References; Chapter 5: Click Chemistry: The Triazole Ring as a Privileged Peptidomimetic Scaffold; 5.1 Introduction; 5.2 Triazole-Containing Peptidomimetics Elaborated through 'Click Chemistry'; 5.3 Relevant Applications in Drug Discovery
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|a Peptide drugs.
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650 |
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|a Proteins
|x Therapeutic use.
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650 |
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|a Drugs
|x Design.
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650 |
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7 |
|a SCIENCE / Chemistry / Physical & Theoretical.
|2 bisacsh
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650 |
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|a Drugs
|x Design.
|2 fast
|0 (OCoLC)fst00898790
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650 |
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7 |
|a Peptide drugs.
|2 fast
|0 (OCoLC)fst01057556
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650 |
|
7 |
|a Proteins
|x Therapeutic use.
|2 fast
|0 (OCoLC)fst01079767
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655 |
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4 |
|a Electronic books.
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655 |
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|a Electronic books.
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700 |
1 |
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|a Guarna, Antonio,
|e author.
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776 |
0 |
8 |
|i Print version:
|a Trabocchi, Andrea, author.
|t Peptidomimetics in organic and medicinal chemistry
|d Chichester, West Sussex ; Hoboken, NJ : John Wiley & Sons Inc., 2014
|z 9781119950608
|w (DLC) 2013048681
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856 |
4 |
0 |
|u https://doi.org/10.1002/9781118683033
|z Full Text via HEAL-Link
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|a 92
|b DG1
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