AMIDATE label
ثبت نشده
چکیده
CLINICAL PHARMACOLOGY Etomidate is a general anesthetic without analgesic activity. Intravenous injection of etomidate produces anesthesia characterized by a rapid onset of action, usually within one minute. Duration of anesthesia is dose dependent but relatively brief, usually three to five minutes when an average dose of 0.3 mg/kg is employed. Immediate recovery from anesthesia (as assessed by awakening time, time needed to follow simple commands and time to perform simple tests after anesthesia as well as they were performed before anesthesia), based upon data derived from short operative procedures where intravenous etomidate was used for both induction and maintenance of anesthesia, is about as rapid as, or slightly faster than, immediate recovery after similar use of thiopental. These same data revealed that the immediate recovery period will usually be shortened in adult patients by the intravenous administration of approximately 0.1 mg of intravenous fentanyl, one or two minutes before induction of anesthesia, probably because less etomidate is generally required under these circumstances (consult the package insert for fentanyl before using).
منابع مشابه
Oxygen extrusion from amidate ligands to generate terminal Ta=O units under reducing conditions. How to successfully use amidate ligands in dinitrogen coordination chemistry.
A series of mixed Cp* amidate tantalum complexes Cp*Ta(RNC(O)R')X(3) (where R = Me(2)C(6)H(3), (i)Pr, R' = (t)Bu, Ph, X = Cl, Me) have been prepared via salt metathesis and their fundamental reactivities under reducing conditions have been explored. Reaction of the tantalum chloro precursors with potassium graphite under N(2) or Ar leads to the stereoselective formation of the terminal tantalum...
متن کاملSynthesis, structure, and reactivity of tris(amidate) mono(amido) and tetrakis(amidate) complexes of group 4 transition metals.
The syntheses of a series of tris(amidate) mono(amido) titanium and zirconium complexes are reported. The binding motif of the amidate ligand has been determined to depend on the size of the metal centre for these sterically demanding N,O-chelating ligands; the larger zirconium metal centre supports three κ(2)-(N,O) bound amidate ligands while the titanium analogue has one ligand bound in a κ(1...
متن کاملYttrium Amidate Complexes: Fundamental Reactivity and Applications in Catalysis and Polymerization
Rare-earth complexes are attractive catalyst systems due to their low cost, low toxicity and high reactivity. Modular ligand sets are ideal for complex formation since the steric and electronic properties of the resultant metal complexes can be easily varied. This thesis explores the structure and reactivity of new yttrium amidate complexes, which combine the highly reactive metal with the modu...
متن کاملStructure, bonding, and reactivity of Ti and Zr amidate complexes: DFT and X-ray crystallographic studies.
Easily prepared and highly modular organic amide proligands have been used to synthesize a series of new bis(amidate)-bis(amido) Ti and Zr complexes via protonolysis. These complexes have been structurally characterized by NMR spectroscopy and X-ray crystallography. The solid-state molecular structures of these complexes indicate that the amidate ligands bind to the metal centers in an exclusiv...
متن کاملSynthesis, Crystal Structure, and Magnetic Properties of Amidate and Carboxylate Dimers of Ruthenium
Solvothermal and microwave-assisted methods have been used to prepare several amidate and carboxylate complexes of the type [Ru2X(μ-NHOCC6H3-3,5-(OMe)2)4]n [X = Cl (1), Br (2), I (3)] and [Ru2X(μ-O2CC6H3-3,5-(OMe)2)4]n [X = Cl (4), Br (5), I (6)]. Complexes 4–6 have also been obtained by conventional synthesis which is ineffective to prepare the amidate compounds. However, single crystals of co...
متن کاملAmidate prodrugs of 9-[2-(phosphonomethoxy)ethyl]adenine as inhibitors of adenylate cyclase toxin from Bordetella pertussis.
Adenylate cyclase toxin (ACT) is the key virulence factor of Bordetella pertussis that facilitates its invasion into the mammalian body. 9-[2-(Phosphonomethoxy)ethyl]adenine diphosphate (PMEApp), the active metabolite of the antiviral drug bis(POM)PMEA (adefovir dipivoxil), has been shown to inhibit ACT. The objective of this study was to evaluate six novel amidate prodrugs of PMEA, both phenyl...
متن کامل