Rosaleen Anderson, Paul Groundwater, Adam Todd, Alan Worsley

Antibacterial Agents

Chemistry, Mode of Action, Mechanisms of Resistance and Clinical Applications

• Broschiertes Buch

Produktbeschreibung

Antibacterial agents act against bacterial infection either by killing the bacterium or by arresting its growth. They do this by targeting bacterial DNA and its associated processes, attacking bacterial metabolic processes including protein synthesis, or interfering with bacterial cell wall synthesis and function.

Antibacterial Agents is an essential guide to this important class of chemotherapeutic drugs. Compounds are organised according to their target, which helps the reader understand the mechanism of action of these drugs and how resistance can arise. The book uses an integrated "lab-to-clinic" approach which covers drug discovery, source or synthesis, mode of action, mechanisms of resistance, clinical aspects (including links to current guidelines, significant drug interactions, cautions and contraindications), prodrugs and future improvements. Agents covered include:

agents targeting DNA - quinolone, rifamycin, and nitroimidazole antibacterial agents
agents targeting metabolic processes - sulfonamide antibacterial agents and trimethoprim
agents targeting protein synthesis - aminoglycoside, macrolide and tetracycline antibiotics, chloramphenicol, and oxazolidinones
agents targeting cell wall synthesis - ß-Lactam and glycopeptide antibiotics, cycloserine, isonaizid, and daptomycin

Antibacterial Agents will find a place on the bookshelves of students of pharmacy, pharmacology, pharmaceutical sciences, drug design/discovery, and medicinal chemistry, and as a bench reference for pharmacists and pharmaceutical researchers in academia and industry.

Produktdetails

• Verlag: Wiley & Sons
• 1. Auflage
• Seitenzahl: 378
• Erscheinungstermin: 23. Juli 2012
• Englisch
• Abmessung: 246mm x 189mm x 22mm
• Gewicht: 835g
• ISBN-13: 9780470972458
• ISBN-10: 0470972459
• Artikelnr.: 35057079

Autorenporträt

Professor Rosaleen Anderson, Professor of Pharmaceutical Chemistry, Sunderland Pharmacy School, University of Sunderland, UK Professor Paul Groundwater, Professor of Medicinal Chemistry, Faculty of Pharmacy, The University of Sydney, Australia Dr Adam Todd, Senior Lecturer in Pharmacy Practice, Sunderland Pharmacy School, University of Sunderland, UK Dr Alan Worsley, Principal Lecturer in Pharmacy Practice, Sunderland Pharmacy School, University of Sunderland, UK

Inhaltsangabe

Preface xiii SECTION 1 INTRODUCTION TO MICROORGANISMS AND ANTIBACTERIAL
CHEMOTHERAPY 1 1.1 Microorganisms 3 Key points 3 1.1.1 Classification 3
1.1.2 Structure 4 1.1.3 Antibacterial targets 6 1.1.4 Bacterial detection
and identification 17 1.1.5 Other than its mode of action, what factors
determine the antibacterial activity of a drug? 25 1.1.6 Bacterial
resistance 27 1.1.7 The 'post-antibiotic age'? 29 References 31 Questions
33 SECTION 2 AGENTS TARGETING DNA 35 2.1 Quinolone antibacterial agents 37
Key points 37 2.1.1 Discovery 37 2.1.2 Synthesis 39 2.1.3 Bioavailability
41 2.1.4 Mode of action and selectivity 44 2.1.5 Bacterial resistance 45
2.1.6 Clinical applications 47 2.1.7 Adverse drug reactions 50 2.1.8 Drug
interactions 55 2.1.9 Recent developments 56 References 60 2.2 Rifamycin
antibacterial agents 63 Key points 63 2.2.1 Discovery 63 2.2.2 Synthesis 65
2.2.3 Bioavailability 68 2.2.4 Mode of action and selectivity 69 2.2.5
Bacterial resistance 71 2.2.6 Clinical applications 71 2.2.7 Adverse drug
reactions 77 2.2.8 Drug interactions 78 2.2.9 Recent developments 81
References 81 2.3 Nitroimidazole antibacterial agents 85 Key points 85
2.3.1 Discovery 85 2.3.2 Synthesis 86 2.3.3 Bioavailability 86 2.3.4 Mode
of action and selectivity 87 2.3.5 Mechanisms of resistance 89 2.3.6
Clinical applications 90 2.3.7 Adverse drug reactions 94 2.3.8 Drug
interactions 95 2.3.9 Recent developments 96 References 97 Questions 101
SECTION 3 AGENTS TARGETING METABOLIC PROCESSES 103 3.1 Sulfonamide
antibacterial agents 105 Key points 105 3.1.1 Discovery 105 3.1.2 Synthesis
107 3.1.3 Bioavailability 108 3.1.4 Mode of action and selectivity 111
3.1.5 Bacterial resistance 114 3.1.6 Clinical applications 115 3.1.7
Adverse drug reactions 119 3.1.8 Drug interactions 121 3.1.9 Recent
developments 123 References 124 3.2 Trimethoprim 127 Key points 127 3.2.1
Discovery 127 3.2.2 Synthesis 128 3.2.3 Bioavailability 130 3.2.4 Mode of
action and selectivity 130 3.2.5 Bacterial resistance 136 3.2.6 Clinical
applications 136 3.2.7 Adverse drug reactions 138 3.2.8 Drug interactions
138 3.2.9 Recent developments 139 References 140 Questions 145 SECTION 4
AGENTS TARGETING PROTEIN SYNTHESIS 147 4.1 Aminoglycoside antibiotics 149
Key points 149 4.1.1 Discovery 149 4.1.2 Synthesis 152 4.1.3
Bioavailability 156 4.1.4 Mode of action and selectivity 158 4.1.5
Bacterial resistance 160 4.1.6 Clinical applications 161 4.1.7 Adverse drug
reactions 165 4.1.8 Drug interactions 167 4.1.9 Recent developments 168
References 168 4.2 Macrolide antibiotics 173 Key points 173 4.2.1 Discovery
173 4.2.2 Synthesis 175 4.2.3 Bioavailability 177 4.2.4 Mode of action and
selectivity 180 4.2.5 Bacterial resistance 181 4.2.6 Clinical applications
182 4.2.7 Adverse drug reactions 187 4.2.8 Drug interactions 189 4.2.9
Recent developments 191 References 193 4.3 Tetracycline antibiotics 197 Key
points 197 4.3.1 Discovery 197 4.3.2 Synthesis 200 4.3.3 Bioavailability
205 4.3.4 Mode of action and selectivity 210 4.3.5 Bacterial resistance 213
4.3.6 Clinical applications 217 4.3.7 Adverse drug reactions 223 4.3.8 Drug
interactions 224 4.3.9 Recent developments 224 References 225 4.4
Chloramphenicol 231 Key points 231 4.4.1 Discovery 231 4.4.2 Synthesis 231
4.4.3 Bioavailability 232 4.4.4 Mode of action and selectivity 235 4.4.5
Bacterial resistance 235 4.4.6 Clinical applications 236 4.4.7 Adverse drug
reactions 239 4.4.8 Drug interactions 239 4.4.9 Recent developments 240
References 241 4.5 Oxazolidinones 243 Key points 243 4.5.1 Discovery 243
4.5.2 Synthesis 245 4.5.3 Bioavailability 247 4.5.4 Mode of action and
selectivity 248 4.5.5 Bacterial resistance 249 4.5.6 Clinical applications
251 4.5.7 Adverse drug reactions 252 4.5.8 Drug interactions 253 4.5.9
Recent developments 254 References 254 Questions 259 SECTION 5 AGENTS
TARGETING CELL-WALL SYNTHESIS 261 5.1 b-Lactam antibiotics 263 Key points
263 5.1.1 Discovery 263 5.1.2 Synthesis 272 5.1.3 Bioavailability 277 5.1.4
Mode of action and selectivity 284 5.1.5 Bacterial resistance 285 5.1.6
Clinical applications 290 5.1.7 Adverse drug reactions 296 5.1.8 Drug
interactions 298 5.1.9 Recent developments 300 References 301 5.2
Glycopeptide antibiotics 305 Key points 305 5.2.1 Discovery 305 5.2.2
Synthesis 306 5.2.3 Bioavailability 307 5.2.4 Mode of action and
selectivity 308 5.2.5 Bacterial resistance 309 5.2.6 Clinical applications
313 5.2.7 Adverse drug reactions 314 5.2.8 Drug interactions 316 5.2.9
Recent developments 316 References 317 5.3 Cycloserine 319 Key points 319
5.3.1 Discovery 319 5.3.2 Synthesis 320 5.3.3 Bioavailability 320 5.3.4
Mode of action and selectivity 321 5.3.5 Bacterial resistance 323 5.3.6
Clinical applications 323 5.3.7 Adverse drug reactions 325 5.3.8 Drug
interactions 325 5.3.9 Recent developments 325 References 325 5.4 Isoniazid
327 Key points 327 5.4.1 Discovery 327 5.4.2 Synthesis 328 5.4.3
Bioavailability 329 5.4.4 Mode of action and selectivity 329 5.4.5
Bacterial resistance 330 5.4.6 Clinical applications 331 5.4.7 Adverse drug
reactions 333 5.4.8 Drug interactions 334 5.4.9 Recent developments 335
References 335 5.5 Daptomycin 339 Key points 339 5.5.1 Discovery 339 5.5.2
Synthesis 340 5.5.3 Bioavailability 341 5.5.4 Mode of action and
selectivity 341 5.5.5 Bacterial resistance 343 5.5.6 Clinical applications
343 5.5.7 Adverse drug reactions 344 5.5.8 Drug interactions 345 5.5.9
Recent developments 345 References 346 Questions 349 Index 351