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020 _a0128010762
020 _a9780128010761
035 _a(OCoLC)990756593
040 _aLIP
_beng
_cLIP
_dOCLCQ
_dESU
_dOCLCQ
_dOCLCL
_dOCLCQ
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082 0 4 _a615/.19
_qOCoLC
_222/eng/20230216
100 1 _aDi, Li.
245 1 0 _aDrug-Like Properties :
_bConcepts, Structure Design and Methods from ADME to Toxicity Optimization.
246 3 _aDrug-Like Properties - Concepts, Structure, Design, and Methods from ADME to Toxicity Optimization
250 _a2nd ed.
260 _aSaint Louis :
_bElsevier Science,
_c2015.
300 _a1 online resource (582 pages)
336 _atext
_btxt
337 _acomputer
_bc
338 _aonline resource
_bcr
500 _a7.1. Introduction.
505 0 _aFront Cover; Drug-Like Properties: Concepts, Structure, Design, and Methods from ADME to Toxicity Optimization; Copyright; Dedication; Contents; Preface; Preface to Second Edition; Preface to First Edition; Chapter 1: Introduction; 1.1. Drug-like Properties in Drug Discovery; 1.2. Purpose of This Book; Problems; References; Chapter 2: Benefits of Property Assessment and Good Drug-Like Properties; 2.1. Introduction; 2.2. Discovery Scientists Optimize Many Properties; 2.3. Introduction to the Drug Discovery and Development Process; 2.4. Benefits of Good Drug-like Properties.
505 8 _a2.4.1. Reduced Development Attrition2.4.2. More Efficient Drug Discovery; 2.4.3. More Efficient Drug Development; 2.4.4. Higher Patient Compliance; 2.4.5. Improved Biological Research in Drug Discovery; 2.4.6. Enabled Partnerships for Drug Development; 2.4.7. Human Modeling and Clinical Planning; 2.4.8. Balance of Properties and Activity; 2.5. Property Profiling in Drug Discovery; 2.6. Drug-like Property Optimization in Drug Discovery; Problems; References; Chapter 3: In Vivo Environments Affect Drug Exposure; 3.1. Introduction; 3.2. Drug Dosing; 3.3. Stomach.
505 8 _a3.3.1. Gastric Acidic Degradation3.4. Intestinal Environment; 3.4.1. Dissolution Rate; 3.4.2. Solubility; 3.4.3. Permeability; 3.4.4. Intestinal Metabolism; 3.4.5. Intestinal Enzymatic Hydrolysis; 3.4.6. Absorption Enhancement in the Intestine; 3.5. Bloodstream; 3.5.1. Plasma Enzyme Hydrolysis; 3.5.2. Plasma Protein Binding; 3.5.3. Red Blood Cell Binding; 3.6. Liver; 3.6.1. Permeation into and out of Hepatocytes; 3.6.2. Hepatic Metabolism; 3.6.3. Biliary Extraction; 3.7. Kidney; 3.8. Blood-Tissue Barriers; 3.9. Tissue Distribution; 3.9.1. Nonspecific Binding in Tissue.
505 8 _a3.10. Consequences of Chirality3.11. Overview of in vivo Challenges to Drug Exposure; Problems; References; Chapter 4: Prediction Rules for Rapid Property Profiling from Structure; 4.1. Introduction; 4.2. General Concepts for Prediction Rules; 4.3. Rule of 5; 4.4. Veber Rules; 4.5. Waring Rules; 4.6. Golden Triangle; 4.7. Other Predictive Rules; 4.8. Application of Rules for Compound Assessment; 4.9. Applications of Predictive Rules; Problems; References; Chapter 5: Lipophilicity; 5.1. Lipophilicity Fundamentals; 5.2. Lipophilicity Effects.
505 8 _a5.3. Lipophilicity Case Studies and Structure Modification5.3.1. Lipophilicity Modification for Biological Activity; 5.3.2. Lipophilicity Modification for Pharmacokinetics; 5.3.3. Lipophilicity Modification for Toxicity; Problems; References; Chapter 6: pKa; 6.1. pKa Fundamentals; 6.2. pKa Effects; 6.2.1. pKa Affects Efficacy; 6.2.2. pKa Affects Pharmacokinetics; 6.2.3. pKa Affects Toxicity; 6.3. pKa Case Studies; 6.3.1. pKa and Activity Examples; 6.3.2. pKa and Pharmacokinetics Examples; 6.4. Structure Modification Strategies for pKa; Problems; References; Chapter 7: Solubility.
546 _aEnglish.
588 0 _aPrint version record.
650 4 _aPharmacy, Therapeutics, & Pharmacology.
650 4 _aHealth & Biological Sciences.
650 7 _aPharmacy, Therapeutics, & Pharmacology.
_2hilcc
650 7 _aHealth & Biological Sciences.
_2hilcc
700 1 _aKerns, Edward H.
758 _ihas work:
_aDrug-like properties (Text)
_1https://id.oclc.org/worldcat/entity/E39PCGK43gt4xT4bqrrprbkX7d
_4https://id.oclc.org/worldcat/ontology/hasWork
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