Titlebook: New Neuromuscular Blocking Agents; Basic and Applied As Dimitry A. Kharkevich (Professor and Chairman of t Book 1986 Springer-Verlag Berlin

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书目名称New Neuromuscular Blocking Agents影响因子(影响力)




书目名称New Neuromuscular Blocking Agents影响因子(影响力)学科排名




书目名称New Neuromuscular Blocking Agents网络公开度




书目名称New Neuromuscular Blocking Agents网络公开度学科排名




书目名称New Neuromuscular Blocking Agents被引频次




书目名称New Neuromuscular Blocking Agents被引频次学科排名




书目名称New Neuromuscular Blocking Agents年度引用




书目名称New Neuromuscular Blocking Agents年度引用学科排名




书目名称New Neuromuscular Blocking Agents读者反馈




书目名称New Neuromuscular Blocking Agents读者反馈学科排名

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On the Principles of Postsynaptic Action of Neuromuscular Blocking Agentsrtainly be argued that the important facts about tubocurarine were all known long before the voltage clamp was invented, it could not be argued that the reasons for its behaviour were understood. The emphasis in this chapter will be on the fundamental molecular effects of the drugs, rather than on t

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On the Comparative Sensitivity of Acetylcholine Receptors of Various Groups of Skeletal Muscles to Nes. Thus, for instance, tubocurarine causes relaxation, first, of the cervical and facial muscles, then, of the muscles of the torso and limbs, and last, of respiratory muscles (intercostal and diaphragm). Often, this is considered to be true of other neuromuscular blocking agents, although the data

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The Interaction of Neuromuscular Blocking Agents With Human Cholinesterases and Their Binding to Plaof the ester type NMBA, e.g., succinylcholine chloride (suxamethonium; SCh), suxethonium bromide, are hydrolyzed by human plasma butyrylcholinesterase (EC 3.1.1.8; BuChE) (. and . 1953; . et al. 1956). Their hydrolysis rate in most other mammalian plasmas is much lower than in human plasma (. and .

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Biodegradation and Elimination of Neuromuscular Blocking Agentsns. Thus, although quaternary ammonium compounds can be degraded to tertiary amines, in general this requires treatment with caustic alkali, i.e. approximately pH 14, at temperatures of around 100 °C (. 1851). It is not surprising, therefore, that the tetraalkylammonium group is not normally subject

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