Search Results - "BOM, Anton"
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Preclinical pharmacology of sugammadex
Published in Journal of critical care (01-03-2009)“…Abstract Since the introduction of nondepolarizing neuromuscular blocking agents, acetylcholinesterase inhibitors have been used to increase the speed of…”
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Cyclodextrin-Derived Host Molecules as Reversal Agents for the Neuromuscular Blocker Rocuronium Bromide: Synthesis and Structure−Activity Relationships
Published in Journal of medicinal chemistry (25-04-2002)“…A series of mono- and per-6-substituted cyclodextrin derivatives were synthesized as synthetic receptors (or host molecules) of rocuronium bromide, the most…”
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Reversal of rocuronium-induced neuromuscular block by sugammadex is independent of renal perfusion in anesthetized cats
Published in Journal of anesthesia (01-04-2011)“…Purpose Sugammadex is a selective relaxant binding agent designed to encapsulate the aminosteroidal neuromuscular blocking agent rocuronium, thereby reversing…”
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Sugammadex reverses neuromuscular block induced by 3-desacetyl-vecuronium, an active metabolite of vecuronium, in the anaesthetised rhesus monkey
Published in European journal of anaesthesiology (01-04-2011)“…BACKGROUND AND OBJECTIVE3-Desacetyl-vecuronium is an active metabolite of the neuromuscular blocking agent (NMBA) vecuronium, which might lead to residual…”
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Reversal of neuromuscular blockade and simultaneous increase in plasma Rocuronium concentration after the intravenous infusion of the novel reversal agent Org 25969
Published in Anesthesiology (Philadelphia) (01-09-2003)“…The purpose of this study was to determine the changes in the plasma concentration of rocuronium and the reversal of its neuromuscular blockade after the…”
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A Novel Concept of Reversing Neuromuscular Block: Chemical Encapsulation of Rocuronium Bromide by a Cyclodextrin-Based Synthetic Host
Published in Angewandte Chemie International Edition (18-01-2002)“…Superior to current clinically used reversal agents in terms of efficacy and side effects: The formation of a high‐affinity host–guest binary complex…”
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A Novel Concept of Reversing Neuromuscular Block: Chemical Encapsulation of Rocuronium Bromide by a Cyclodextrin-Based Synthetic Host
Published in Angewandte Chemie (18-01-2002)“…Stark wirksam bei geringen Nebenwirkungen: In der Anästhesie dienen Muskelrelaxantien zum Einstellen guter Intubationsbedingungen über eine tiefe…”
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Selective relaxant binding agents for reversal of neuromuscular blockade
Published in Current opinion in pharmacology (01-06-2007)“…Traditionally, reversal of neuromuscular blockade during anaesthesia was achieved by increasing the acetylcholine concentration in the neuromuscular junction…”
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Reversal of profound rocuronium neuromuscular blockade by sugammadex in anesthetized rhesus monkeys
Published in Anesthesiology (Philadelphia) (01-04-2006)“…Reversal of neuromuscular blockade can be accomplished by chemical encapsulation of rocuronium by sugammadex, a synthetic gamma-cyclodextrin derivative. The…”
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Org 25969 Causes Rapid Reversal of Rocuronium-Induced Neuromuscular Block, Independent of Acid-Base Status: 2002[A-1009
Published in Anesthesiology (Philadelphia) (01-09-2002)Get full text
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Synthesis and evaluation of N-3 substituted phenoxypropyl piperidine benzimidazol-2-one analogues as NOP receptor agonists with analgesic and sedative properties
Published in Bioorganic & medicinal chemistry (15-02-2007)“…A series of N-3 substituted phenoxypropyl piperidine benzimidazol-2-one analogues were prepared and evaluated as NOP agonists. The selective NOP agonist (+)-…”
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Effects of 5-hydroxytryptamine on capillary and arteriovenous anastomotic blood flow in the human hand and forearm and in the pig hind leg
Published in Journal of cardiovascular pharmacology (01-02-1991)“…The effects of intraarterially infused serotonin (5-HT) on capillary and arteriovenous anastomotic (AVA) blood flow were investigated in the hand and forearm…”
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2- O-Substituted Cyclodextrins as Reversal Agents for the Neuromuscular Blocker Rocuronium Bromide
Published in Bioorganic & medicinal chemistry (01-06-2002)“…A series of secondary face modified cyclodextrins (CDs) were synthesised with the aim of constructing host molecules capable of forming host–guest complexes…”
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Parallel solid-phase synthesis of zatebradine analogues as potential If channel blockers
Published in Bioorganic & medicinal chemistry letters (03-09-2001)Get full text
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Parallel solid-Phase synthesis of zatebradine analogues as potential I f channel blockers
Published in Bioorganic & medicinal chemistry letters (03-09-2001)“…The first solid-phase synthesis of zatebradine 1 and its analogues is reported. This has resulted in the preparation of compounds with increased ability to…”
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A Novel Concept of Reversing Neuromuscular Block: Chemical Encapsulation of Rocuronium Bromide by a Cyclodextrin-Based Synthetic Host The discovery of Org 25969 is the result of teamwork with contributions from a number of scientists both inside Organon and outside the company. We would like in particular to acknowledge the following scientists for their invaluable contributions: E. Hutchinson, D. Stevenson, R. Roy, and J. Pick for scaling-up the synthesis; F. Hope, S. Miller, and R. Mason for v
Published in Angewandte Chemie International Edition (18-01-2002)Get full text
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Carotid haemodynamics in pigs during infusions of 8‐O‐DPAT: reduction in arteriovenous shunting is mediated by 5‐HT1‐like receptors
Published in British journal of pharmacology (01-01-1989)“…1 The effects of intracarotid infusions of 8‐hydroxy‐2‐[di‐n‐propyl‐amino]‐tetralin (8‐OH‐DPAT) on heart rate, blood pressure and carotid blood flow and its…”
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