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  • Produktbild: Transition Metal Complexes as Drugs and Chemotherapeutic Agents
  • Produktbild: Transition Metal Complexes as Drugs and Chemotherapeutic Agents
Band 11

Transition Metal Complexes as Drugs and Chemotherapeutic Agents

Aus der Reihe Catalysis by Metal Complexes

Fr. 72.90

inkl. gesetzl. MwSt., Versandkostenfrei

Beschreibung

Produktdetails

Einband

Taschenbuch

Erscheinungsdatum

15.03.2012

Verlag

Springer Netherland

Seitenzahl

304

Maße (L/B/H)

22.9/15.2/1.7 cm

Gewicht

443 g

Auflage

Softcover reprint of the original 1st ed. 1989

Sprache

Englisch

ISBN

978-94-011-7570-8

Beschreibung

Rezension

`
The book is well written, thoroughly documented and presents useful information to both scientists and clinicians.
'

Oncology, 48:2

`
The book is very readable, well referenced and there is a useful glossary for those baffled by pharmacological terms. The discovery of truly novel drugs in the future may well hinge on the application of the principles in inorganic chemistry - both metals and non-metals - to pharmacology. This book should therefore be welcome on all library shelves.
'

Chemistry in Britain, 1990

Produktdetails

Einband

Taschenbuch

Erscheinungsdatum

15.03.2012

Verlag

Springer Netherland

Seitenzahl

304

Maße (L/B/H)

22.9/15.2/1.7 cm

Gewicht

443 g

Auflage

Softcover reprint of the original 1st ed. 1989

Sprache

Englisch

ISBN

978-94-011-7570-8

Herstelleradresse

Springer-Verlag KG
Sachsenplatz 4-6
1201 Wien
AT

Email: ProductSafety@springernature.com

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  • Produktbild: Transition Metal Complexes as Drugs and Chemotherapeutic Agents
  • Produktbild: Transition Metal Complexes as Drugs and Chemotherapeutic Agents
  • Metals in Medicine.- Chemotherapeutic Agents and Drugs.- Mechanisms of Toxicity.- Metal Accumulation and Activation.- Biochemical Targets for Metal Complexes.- Summary.- References.- 1. Interaction of Metal Complexes with DNA.- 1.1. DNA and Conformation.- 1.1.1. Nucleases and DNA.- 1.2. Experimental Methods for the Study of Conformational Changes.- 1.2.1. Uvltraviolet Spectroscopy.- 1.2.2. Circular Dichroism and Optical Dispersion.- 1.2.3. Nuclear Magnetic Resonance.- 1.2.4. Hydrodynamic and Light Scattering Properties.- 1.3. Binding of Metal Complexes to DNA.- 1.3.1. Intercalation.- 1.3.1.1. Platinum—Terpyridine Complexes.- 1.3.1.2. Metal—(1, 10-Phenanthroline) Complexes.- 1.3.1.3. Porphyrins and Metalloporphyrins.- 1.3.1.4. Intercalators as Drugs.- 1.3.1.5. Redox Activity of Metallointercalators.- 1.3.2. Outer Sphere Binding.- 1.3.2.1. Metal—Amine Complexes.- 1.3.3. Inner Sphere (Covalent) Binding.- 1.3.3.1. Binding of Platinum—Amine Complexes.- 1.3.3.2. Platinum—Amine Complexes and Intercalators.- 1.3.3.3. Restriction Enzymes and Platinum Complexes.- 1.3.4. Strand Breakage.- 1.3.4.1. Copper—(1, 10-phenanthroline) Complexes.- 1.3.4.2. Cobalt—(1, 10-phenanthroline) Complexes.- 1.3.4.3. Iron—EDTA—(DNA-binder) Complexes.- 1.4. Summary.- References.- 2. Platinum—Amine Complexes as Anticancer Agents.- 2.1. The Discovery of Cisplatin as an Antitumour Agent.- 2.2. Clinical Properties of Cisplatin.- 2.3. Development of Cisplatin Analogues.- 2.3.1. Clinical trials of Cisplatin Analogues.- 2.4. Biochemical Mechanism of Action of Platinum Complexes.- 2.4.1. Biological Effects Implying DNA as Target.- 2.4.2. Biological Effects not Involving DNA.- 2.5. Summary.- References.- 3. Structure—Activity Relationships of Platinum— Amine Complexes.- 3.1. The Requirement for Neutrality.- 3.2. Complexes of Pt(IV).- 3.3. Nature of the Leaving Group.- 3.3.1. Bisplatinum Complexes Containing Bridging Dicarboxylates.- 3.3.2. Sulfoxides as Leaving groups.- 3.4. Nature of the Nonleaving Group.- 3.4.1. Stereospecific Effects in Amine Complexes.- 3.5. Novel and Targeted Approaches to [PtX2(am)2] Complexes.- 3.5.1. Ternary Complexes.- 3.5.2. Amines as Carrier Ligands.- 3.6. Quantitative Structure—Activity Relationships.- 3.7. Chemistry of Platinum—Amine Complexes.- 3.7.1. Reactions with Biomolecules Other Than DNA.- 3.8. Summary.- References.- 4. Interactions of Platinum Complexes with DNA Components.- 4.1. Structural Aspects of Metal—Nucleobase Binding.- 4.1.1. Binding in Solution.- 4.1.1.1. Basicity and pH.- 4.1.1.2. Hard—Soft Relationship of Donor Atom and Metal Ion.- 4.1.1.3. Steric Effects Including Hydrogen Bonding.- 4.1.1.4. Base Stacking and Chelation.- 4.1.2. Binding of Platinum Complexes in Solution.- 4.2. Reactivity of Platinum Metal—Base Complexes.- 4.2.1. Effect of Metallation on Acidity of Noncoordinated Atoms.- 4.2.1.1. The Platinum—N7, O6 Chelate.- 4.2.2. Effect of Metallation on C—H Exchange.- 4.2.3. Susceptibility to Oxidation of Metal—Base Complexes.- 4.2.4. Reactivity of Nucleoside and Nucleotide Linkages.- 4.2.5. Reactivity of Metal—Base Complexes toward Nucleophiles.- 4.2.6. Linkage Isomerization.- 4.2.7. Rotation around Metal—Purine Bonds.- 4.3. Solid State Structural Studies.- 4.4. Structural Studies on Di- and Oligonucleotide Complexes.- 4.4.1. Studies on Dinucleotide Complexes.- 4.4.2. Studies on Trinucleotides.- 4.4.3. Studies on Oligonucleotides.- 4.4.3.1. Structural Studies on Oligonucleotides.- 4.5. Platinum Adducts from DNA Degradation.- 4.6. On the Molecular Mechanism of Antitumour Action of Cisplatin.- 4.7. Summary.- References.- 5. The Platinum—Pyrimidine Blues.- 5.1. Properties of the Platinum—Pyrimidine Blues.- 5.2. Platinum Blues not Derived from Pyrimidines.- 5.3. X-Ray Structure of Platinum—Pyrimidine and ?-Pyridone Blues.- 5.4. Formation of Platinum—Pyrimidine and ?-Pyridone Blues.- 5.4.1. Monomeric Complexes.- 5.4.2. Dimeric Complexes.- 5.4.3. Complexes of Pt(III).- 5.5. Studies of Crystalline Blues.- 5.6. Biological Studies on Platinum—Pyrimidine Blue Precursors.- 5.7. Summary.- References.- 6. Antitumour Activity of Metal Complexes.- 6.1. Platinum Group Metal Complexes.- 6.1.1. Palladium Complexes.- 6.1.2. Rhodium Complexes.- 6.1.2.1. Studies on Rhodium Carboxylates.- 6.1.3. Ruthenium Complexes.- 6.1.3.1. Studies on Ruthenium—Amine Complexes.- 6.2. Copper Complexes.- 6.2.1. Bis(Thiosemicarbazone) Complexes.- 6.2.2. Thiosemicarbazone Complexes.- 6.2.3. Nitrogen Chelates.- 6.2.4. Copper Salicylates.- 6.3. Silver and Gold.- 6.4. Organometallic Complexes.- 6.5. Summary.- References.- 7. Metal-Mediated Antibiotic Action.- 7.1. Discovery and Pharmacology of Bleomycin.- 7.2. Structure of Bleomycin and Analogues.- 7.3. Metal Complexes of Bleomycin.- 7.3.1. Copper Bleomycin.- 7.3.2. Cobalt Bleomycin.- 7.3.3. Manganese Bleomycin.- 7.4. Mechanism of Action of Bleomycin.- 7.4.1. DNA—Bleomycin Interactions.- 7.4.2. Iron and Iron—Oxygen Adducts.- 7.5. Other Metal Binding Antibiotics.- 7.5.1. Anthracyclines.- 7.5.1.1. Biochemical Aspects of Metal—Anthracyclines.- 7.5.2. Streptonigrin.- 7.6. Summary.- References.- 8. Metals, Metal Complexes, and Radiation.- 8.1. Interaction of Radiation and Biological Tissue.- 8.2. Chemical Modification of Radiation Damage.- 8.2.1. Oxygen Mimics and Electron Affinity.- 8.3. Metal Complexes as Radiation Sensitizers.- 8.3.1. Radiosensitization by Metal Salts.- 8.3.2. Cobalt—Amine Complexes.- 8.3.3. Radiosensitization by Electron Affinity.- 8.3.3.1. Metal—Radiosensitizer Complexes.- 8.3.3.2. Metal Chelates.- 8.3.4. Potentiation of Radiation Damage by Platinum—Amines. Differential Repair Processes.- 8.3.4.1. Mechanism of Action of Platinum—Amine Complexes.- 8.3.5. Radiosensitization by Thiol Depletion.- 8.4. Metal Complexes and Radioprotection.- 8.4.1. Metal Complexes as Radioprotectors.- 8.5. Activation of Metal Complexes.- 8.6. Summary.- References.- 9. Antibacterial Effects of Metal Complexes.- 9.1. Mercury and Silver Salts as Antibacterial Agents.- 9.1.1. Mercury.- 9.1.2. Silver.- 9.2. Antibacterial Activity of Chelating Agents and Metal Chelates.- 9.3. Antibacterial Activity of Metal—Amine Complexes.- 9.4. Redox Activity and Antibacterial Activity.- 9.5. Summary.- References.- 10. Antiviral and Antiparasitic Effects of Metal Complexes.- 10.1. Antiviral Therapy.- 10.2. Chelating Agents and Metal Complexes as Antiviral Agents.- 10.2.1. Chelating Agents.- 10.2.2. Metal—(1, 10-Phenanthroline) Complexes.- 10.2.3. Platinum— and Palladium—Amine Complexes.- 10.2.4. Zinc Complexes.- 10.2.5. Other Metal Complexes.- 10.3 Metal Complexes as Antiprotozoal Agents.- 10.3.1. Metal Complexes in Trypanosomiasis.- 10.3.2. Platinum—Amine Complexes as Trypanocides.- 10.3.3. Other Metal Complexes.- 10.3.4. Porphyrins and Metalloporphyrins as Trypanocides. Metal Sequestration.- 10.3.5. Metal Complexes with Trypanocidal Drugs. Dual-Function Agents.- 10.3.6. Metal Complexes in American Trypanosomiasis.- 10.4. Summary.- References.- 11 Metal Complexes in Arthritis.- 11.1. Gold Complexes in the Treatment of Rheumatoid Arthritis.- 11.1.1. Activity and Toxicity of Gold Drugs.- 11.1.2. Structures of Gold Complexes.- 11.1.3. Chemistry and Biochemistry of Gold Drugs.- 11.1.4. Mechanism of Action of Gold Drugs.- 11.2. Copper in Arthritis.- 11.2.1. Copper Complexes in Arthritis.- 11.2.2. Copper Bracelets.- 11.2.3. Copper and D-Penicillamine.- 11.2.4. Mechanism of Action of Copper Complexes.- 11.3. Other Metals.- 11.4. Summary.- References.- 12. Miscellaneous Uses of Metal Complexes.- 12.1. Mercurial Diuretics.- 12.2. Neuromuscular Effects of Metal Complexes.- 12.3. Nitroprusside as Vasodilator.- 12.3.1. Activity and Toxicity of Nitroprusside.- 12.3.2. Mechanism of Action of Nitroprusside.- 12.4. Summary.- References.- Names and Abbreviations.- Glossary of Terms and Definitions.- Appendix 1.- Appendix 2.- Index of Subjects.