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повний	інформаційний	короткий

Пошуковий запит: (<.>K=національні підручники<.>)

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   577.1
   Б 63


    Biological and Bioorganic Chemistry. In 2 books : national textbook. Book 1. Bioorganic Chemistry / B. S. Zimenkovsky, V. A. Muzychenko, I. V. Nizhenkovska, Q. O. Syrova ; ed. B. S. Zimenkovsky, I. V. Nizhenkovska. - 3rd ed. - K. : Medicine Publishing, 2020. - 287 p. - На англ. мові. - Бібліогр.: с. 272. - Index: с. 273-287. - ISBN 978-617-505-791-9 : 260.00 грн.
Переклад назви: Біологічна і біоорганічна хімія. В 2-х кн. Кн. 1: Біоорганічна хімія: підручник / Б. С. Зіменковський, В. А. Музиченко, І. В. Ніженковська, Г. О. Сирова

УДК

577.1(075.8)

Рубрики: БІОХІМІЯ(англ)--Підручник

Кл.слова (ненормовані):
підручники(англ) -- національні підручники -- national textbook
Анотація: The textbook contains the information about the structure, chemical properties and biological role of organic compounds which take part in human metabolic processes: low-molecular bioregulators (vitamins, hormones, other natural and synthetic biologically active compounds, including certain medications and toxic compounds) and biopolymers (carbohydrates, proteins and nucleic acids). This textbook is recommended for students and teachers of higher medical education establishments. PART І. THEORETICAL BASIS OF ORGANIC AND BIOORGANIC CHEMISTRY. THE STRUCTURE OF ORGANIC AND BIOORGANIC COMPOUNDS Сhapter 1. Classification and Nomenclature of Organic Compounds 1.1. Classification of Organic Compounds 1.1.1. Classification Based on the Carbon Chain Structure 1.1.2. Classification Based on the Nature of the Functional Group 1.2. Nomenclature of Organic Compounds Сhapter 2. The Structure of Organic Compounds 2.1. Representation of the Structure of Organic Compounds 2.2. Isomerism of Organic Compounds 2.2.1. Structural Isomerism 2.2.2. Stereoisomerism Сhapter 3. Electronic Conceptions in Organic Chemistry 3.1. Chemical Bonds in Bioorganic Molecules 3.1.1. The Structure of Covalent Bonds 3.1.2. Сharacteristics of Covalent Bonds 3.2. Electronic Effects, the Mutual Effect of Atoms in Molecules 3.2.1. The Inductive Effect 3.2.2. The Mesomeric Effect 3.3. Classification of Chemical Reactions and Reagents. the Mechanism of Chemical Reactions 3.3.1. Classification of Chemical Reactions Based on Their Mechanisms 3.3.2. Classification of Chemical Reactions Based on the Bond Cleavage 3.3.3. The Mechanisms of Chemical Reactions 3.4. The Acid and Base Properties of Organic Compounds 3.4.1. The Theory of Bronsted 3.4.2. The Theory of Lewis PART ІI. HYDROCARBONS AND THEIR DERIVATIVES Сhapter 4. Acyclic Hydrocarbons 4.1. Alkanes 4.1.1. The Structure, Homology, Nomenclature, and Isomerism 4.1.2. Chemical Properties 4.1.3. Industrial and Biomedical Significance 4.2. Alkenes 4.2.1. The Structure, Nomenclature and Isomerism 4.2.2. Chemical Properties 4.3. Alkynes 4.4. Alkadienes Сhapter 5. Carbocyclic Hydrocarbons 5.1. Alicyclic Hydrocarbons 5.1.1. Classification and Nomenclature 5.1.2. Chemical Properties 5.1.3. Biomedical Significance 5.2. Arenes 5.2.1. Classification, Aromaticity 5.2.2. Nomenclature and Isomerism of Mononuclear Arenes 5.2.3. Chemical Properties of Mononuclear Arenes 5.2.4. Polynuclear Arenes Сhapter 6. Halogen Derivatives of Hydrocarbons 6.1. Chemical Properties 6.1.1. Reactions of Nucleophilic Substitution 6.1.2. Reactions of Elimination 6.2. Biomedical Significance Сhapter 7. Hydroxyl Derivatives of Nydrocarbons. Thiols 7.1. Monoatomic Alcohols 7.1.1. Structure, Nomenclature and Isomerism 7.1.2. Chemical Properties 7.1.3. Individual Representatives 7.2. DI- and Polyatomic Alcohols 7.2.1. Structure, Nomenclature and Isomerism 7.2.2. Chemical Properties 7.2.3. Individual Representatives 7.3. Thiols and Thio Ethers 7.3.1. Structure and Nomenclature 7.3.2. Chemical Properties 7.4. Phenols 7.4.1. Structure, Classification and Nomenclature 7.4.2. Chemical Properties 7.4.3. Medical Application Сhapter 8. Amines 8.1. Classification and Nomenclature 8.2. Chemical Properties 8.3. Biological Activity and Toxicity Сhapter 9. Biologically Important Carbonyl Compounds 9.1. Structure and Nomenclature 9.2. Chemical Properties 9.2.1. Oxidation and Reduction Reactions 9.2.2. Reactions of Nucleophilic Addition 9.2.3. Reactions of the Addition-Elimination 9.2.4. Condensation Reactions 9.2.5. α-Carbon Atom Reactions 9.2.6. Polymerization Reactions 9.3. Biomedical Significance Сhapter 10. Carboxylic Acids and Their Functional Derivatives 10.1. Aliphatic and Aromatic Monocarboxylic Acids 10.1.1. Nomenclature 10.1.2. Chemical Properties 10.2. Carbonic Acid Derivatives 10.3. Aliphatic and Aromatic Dicarboxylic Acids 10.3.1. Classification and Nomenclature 10.3.2. Chemical Properties Сhapter 11. Biologically Important Heterofunctional Compounds 11.1. Hydroxy Derivatives of Amines 11.1.1. Amino Alcohols 11.1.2. Aminophenols 11.2. Hydroxy Acids 11.2.1. Aliphatic Hydroxy Acids 11.2.2. Aromatic Hydroxy Acids 11.3. Oxoacids 11.3.1. Some Representatives of Oxoacids 11.3.2. Biosynthesis of Higher Fatty Acids 11.4. Amino Acids 11.4.1. Structure of Amino Acids 11.4.2. Nomenclature and Isomerism of Amino Acids 11.4.3. Chemical Properties 11.5. Derivatives of Para-Amino Benzoic and Sulfanilic Acids PART ІII. BIOLOGICALLY ACTIVE HETEROCYCLIC COMPOUNDS Сhapter 12. Three-, Four- and Five-Membered Heterocyclic Compounds 12.1. Three- and Four-Membered Heterocyclic Compounds 12.2. Five-Membered Heterocycles Containing One Heteroatom 12.2.1. Chemical Properties 12.2.2. Some Representatives Having Biomedical Significance 12.3. Five-Membered Heterocycles Containing Two Heteroatoms 12.3.1. Oxazole and Isooxazole 12.3.2. Thiazole 12.3.3. Pyrazole 12.3.4. The Most Important Derivatives of Pyrazole 12.3.5. Imidazole 12.3.6. The Most Important Derivatives of Imidazole Сhapter 13. Six- and Seven-Membered Heterocyclic Compounds 13.1. Six-Membered Heterocycles Containing One Heteroatom 13.1.1. Six-Membered Heterocycles With Nitrogen Heteroatom 13.1.2. Six-Membered Heterocycles With Oxygen Heteroatom 13.2. Six-Membered Heterocycles Containing Two Heteroatoms 13.2.1. Six-Membered Heterocycles With Two Nitrogen Heteroatoms 13.2.2. Six-Membered Heterocycles With Nitrogen and Sulfur Heteroatoms 13.3. Seven-Membered Heterocycles Сhapter 14. Biologically Important Condensed Heterocyclic Systems, Alkaloids 14.1. Purine Derivatives 14.1.1. Hydroxy Derivatives of Purine 14.1.2. Amino Derivatives of Purine 14.2. Pteridine Derivatives 14.3. Alkaloids 14.3.3. Pyridine and Piperidine Alkaloids 14.3.2. Quinoline Alkaloids 14.3.3. Isoquinoline and Phenanthrene Isoquinoline Alkaloids 14.3.4. Tropane Alkaloids PART ІV. BIOPOLYMERS AND BIOREGULATORS Сhapter 15. Carbohydrates or Saccharides (Sugars) 15.1. Monosaccharides (Monoses) 15.1.1. Isomerism 15.1.2. Tautomerism 15.1.3. Chemical Properties 15.1.4. Individual Representatives 15.1.5. Derivatives of Monosaccharides 15.2. Disaccharides 15.2.1. Reducing Disaccharides 15.2.2. Non-Rreducing Disaccharides 15.3. Higher Polysaccharides 15.3.1. Homopolysaccharides 15.3.2. Heteropolysaccharides Сhapter 16. Proteinogenic Amino Acids, Peptides and Proteins 16.1. Proteinogenic Amino Acids and Their Properties 16.1.1. Isomerism and Structure 16.1.2. Chemical Properties 16.2. Peptides and Proteins 16.2.1. Amino Acid Composition and Amino Acid Sequence 16.2.2. Structural Organization of Proteins 16.2.3. Electrophoresis of Amino Acids and Proteins 16.2.4. Classification of Proteins 16.2.5. Qualitative Reactions on Proteins Сhapter 17. Nucleic Acids. Coenzymes 17.1. Nucleosides 17.2. Nucleotides 17.3. The Structure of Nucleic Acids 17.3.1. The Primary Structure 17.3.2. The Secondary Structure of DNA 17.3.3. The Structure and Functions of RNA 17.4. Nucleotide Coenzymes Сhapter 18. Lipids 18.1. Saponifiable Lipids 18.1.1. Simple Saponifiable Lipids 18.1.2. Complex Saponifiable Lipids 18.2. Nonsaponifiable Lipids 18.2.1. Terpenes 18.2.2. Carotenoids 18.2.3. Steroids 18.2.4. Prostaglandins Answer on the Test for Self Control Recommended Literature List Index
Дод.точки доступу:
Zimenkovsky, Boris Semenovich
Зіменковський Борис Семенович
Muzychenko, Volodymyr Afanasiiovych
Музиченко Володимир Опанасович
Nizhenkovska, Iryna Volodymyrivna
Ніженковська Ірина Володимирівна
Syrova, Ganna Olegivna
Сирова Ганна Олегівна
Zimenkovsky, Boris Semenovich \ред.\
Nizhenkovska, Iryna Volodymyrivna \ред.\

Примірників всього: 14
Наук.Аб. (3), Уч.Аб. (5), ННА (6)
Вільні: Наук.Аб. (3), Уч.Аб. (5), ННА (6)

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