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Design, synthesis, in silico, and in vitro evaluation of pyrrol-2-yl-phenyl allylidene hydrazine carboximidamide derivatives as AChE/BACE 1 dual inhibitors. [PDF]
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The effect of high-intensity interval training on type 2 diabetic muscle: A metabolomics-based study. [PDF]
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Turbidimetric detection of decamethonium
Experientia, 1959Si descrive un metodo per la determinazione del decametonio in piccole concentrazioni (2–20 γ/ml) impiegando il reattivo di Nessler.
B, GIOVANELLA, C, MANNI, G, MORICCA
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Estimation of decamethonium in biological fluids
Experientia, 1961Les auteurs ont modifie la methode de dosage de sels de methonium, proposee dans leur travail precedent, pour rendre possible son application a la recherche du C10 dans les serums et les urines. Cette methode est rigoureusement specifique pour la determination du decamethonium dans le serum entre 100 e 500γ/ml mais moins specifique pour les urines.
G, MORICCA +3 more
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2007
Decamethonium (C 10) is a bisquaternary methonium compound with selectivity for blockade of the muscle nicotinic acetylcholine receptor. It produces a depolarizing type of neuromuscular blockade and does not affect ganglionic nicotinic receptors. Its actions are similar to those of succinylcholine.
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Decamethonium (C 10) is a bisquaternary methonium compound with selectivity for blockade of the muscle nicotinic acetylcholine receptor. It produces a depolarizing type of neuromuscular blockade and does not affect ganglionic nicotinic receptors. Its actions are similar to those of succinylcholine.
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Autoradiography of Decamethonium in Rat Muscle
Nature, 1967DECAMETHONIUM and other depolarizing drugs have a pharmacological effect at the endplate and adjacent regions of muscle fibres. Various modes of action have been proposed for these compounds; some are based on attachment to surface receptors while others require penetration into the fibres.
R, Creese, J, Maclagan
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Decamethonium and the conditioned avoidance response
Psychopharmacologia, 1967The inhibition of performance of a conditioned avoidance response (CAR) by drugs has been a subject of much prominence in psychopharmacological research. This type of learned behavior is well known to be susceptible to selective suppression by diverse agents, especially the phenothiazine-type and reserpine-type tranquilizers, morphinelike analgesics ...
W M, Davis, M, Babbini
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Potentiation and Antagonism of Vecuronium by Decamethonium
Anesthesia & Analgesia, 1993Enhancement of a vecuronium neuromuscular blockade by prior administration of succinylcholine has been attributed to both pharmacokinetic and pharmacodynamic mechanisms. This study was performed to elucidate the mechanism of this interaction using decamethonium as the agonist drug.
S, Feldman, N, Fauvel
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