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藥物化學(xué)(英中雙語(yǔ)注解版 第2版)

藥物化學(xué)(英中雙語(yǔ)注解版 第2版)

定 價(jià):¥90.00

作 者: 李紹順,周虎臣 主編
出版社: 科學(xué)出版社
叢編項(xiàng):
標(biāo) 簽: 藥學(xué)理論

ISBN: 9787030354969 出版時(shí)間: 2009-07-01 包裝: 平裝
開本: 16開 頁(yè)數(shù): 493 字?jǐn)?shù):  

內(nèi)容簡(jiǎn)介

  李紹順、周虎臣主編的《藥物化學(xué)(第2版英中雙語(yǔ)注解版)》是藥物化學(xué)專業(yè)唯一一本英中雙語(yǔ)教材。以英文編寫,加以中文注釋?!端幬锘瘜W(xué)(第2版英中雙語(yǔ)注解版)》分為17章,前6章為總論部分,主要闡述藥物研發(fā)的基本理論和基本方法,內(nèi)容包括新藥研究中先導(dǎo)化合物的發(fā)現(xiàn)和結(jié)構(gòu)優(yōu)化、藥物與受體相互作用、酶及其抑制劑的基礎(chǔ)理論和應(yīng)用、藥物代謝的基本概念、前藥的設(shè)計(jì)及計(jì)算機(jī)輔助藥物設(shè)計(jì)的基礎(chǔ)知識(shí)。第7~17章為各論,按目前新藥研究的重點(diǎn)領(lǐng)域分類,主要內(nèi)容包括神經(jīng)系統(tǒng)藥物、鎮(zhèn)痛及麻醉藥、代謝綜合征治療藥、胃腸道系統(tǒng)藥物、心血管系統(tǒng)藥物、抗腫瘤、抗病毒、抗真菌、抗感染及免疫抗炎藥,重點(diǎn)講解各類藥物治療現(xiàn)狀、作用機(jī)制、結(jié)構(gòu)與活性關(guān)系,代表性藥物的合成路線設(shè)計(jì)、臨床應(yīng)用及藥物代謝的相關(guān)知識(shí)。

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暫缺《藥物化學(xué)(英中雙語(yǔ)注解版 第2版)》作者簡(jiǎn)介

圖書目錄

第二版前言
第一版前言
1 Drug Discovery, Design and Development
1.1 Drug Discovery
1.1.1 A Drug Discovery without a Lead
1.1.2 Lead Discovery
1.2 Lead Modification
1.2.1 Identification of the Active Part: The Pharmacophore
1.2.2 Structure Modifications to Increase Potency and the Therapeutic Index
1.3 New Drug Development
1.3.1 General Process of New Drug Development
1.3.2 Precliblinical Development and Investigational New Drug Application
1.4 Problems
本章重點(diǎn)內(nèi)容
2 Receptors
2.1 Drug-Receptor Interactions
2.1.1 Interactions(Forces) Involved in the Drug-Receptor Complex
2.2 Theories for Drug-Receptor Interactions
2.2.1 Induced-Fit Theory
2.2.2 The Two-State(Multistate)Model of Receptor Activation
2.3 Topographical and Stereochemical Considerations
2.3.1 Spatial Arrangement of Atoms
2.3.2 Drug and Receptor Chirality
2.3.3 Geometric Isomers(Diastereomers)
2.3.4 Conformational Isomers
2.3.5 Ring Topology
2.4 Problems
本章重點(diǎn)內(nèi)容
3 Enzymes and Enzyme Inhibition
3.1 Enzymes
3.1.1 Enzymes as Catalysts
3.1.2 Mechanism of Enzyme Catalysis
3.1.3 Coenzyme Catalysis
3.2 Enzyme Inhibition
3.2.1 Enzyme Inhibitors in Medicine
3.2.2 Design of Enzyme Inhibitors
3.3 Reversible Enzyme Inhibitors
3.3.1 Mechanism of Reversible Inhibition
3.3.2 Selected Examples of Competitive Reversible Inhibitor Drugs
3.3.3 Transition State Analogs
3.3.4 Slow, Tight-Binding Inhibitors
3.4 Irreversible Enzyme Inhibitors
3.4.1 Affinity Labeling Agents
3.4.2 Mechanism-Based Enzyme Inactivators
3.5 Problems
References
本章重點(diǎn)內(nèi)容
4 Drug Metabolism
4.1 Introduction
4.2 Phase I Transformations
4.2.1 Oxidative Reactions
4.2.2 Reductive Reactions
4.2.3 Carboxylation Reaction
4.2.4 Hydrolytic Reactions
4.3 Phase II Transformations: Conjugation Reactions
4.3.1 Introduction
4.3.2 Glucuronic Acid Conjugation
4.3.3 Sulfate Conjugation
4.3.4 Amino Acid Conjugation
4.3.5 Glutathione Conjugation
4.3.6 Acetyl Conjugation
4.4 Problems
本章重點(diǎn)內(nèi)容
5 Prodrugs and Drug Delivery System
5.1 Introduction
5.1.1 Utility of Prodrugs
5.1.2 Types of Prodrugs
5.2 Mechanism of Drug Activation
5.2.1 Carrier-Linked Prodrugs
……
6 Computer Aided Drug Design
7 Central Nervous System Drugs
8 Analgesics and Anesthetics
9 Drugs for Metabolic Syndrome Treatment
10 Agents for Gastrointestinal Diseases
11 Cardiovascular Agents
12 Anticancer Agents
13 Antivlral Agents
14 Antifungal Agents
15 Antibacterials
16 Antiparasitic
17 Inflammatory Diseases and Nonsteroidal Anti-inflammatory Drugs(NSAIDs)

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