COMPUESTOS HETEROCICLICOS SATURADOS PDF

Taumi Compounds of Comluestos 0and stereoisomers and pharmaceutically acceptable salts thereof, as well as methods of use as Interleukin-1 Receptor Associated Kinase IRAK4 inhibitors are described herein. Carbocyclic carboxylic acid amides and esters of azabicyclic compounds as gastric prokinetic, antiemetic, anxiolytic and antiarrhythmic agents. Resultados de Country of ref document: Acetamide and urea derivatives, process for their preparation and their use in the treatment of cns disorders. Meso-azacyclic amides of imidazopyridine carboxylic acids and analogs thereof as pharmaceuticals. New meso-azacyclic aromatic acid amides and esters as novel serotonergic agents.

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Kile The invention relates to novel indole and indazole compounds characterized in that the compound has general formula Iin which the chemical groupings, substituents, variables and indices are as defined in the description, and to their use as medicaments, in particular as medicaments for the treatment of conditions and diseases that can be treated by inhibition of the PDE4 enzyme.

Satyrados carboxylic acid amides and esters of azabicyclic compounds as gastric prokinetic, antiemetic, anxiolytic and antiarrhythmic agents.

Resultados de Fused bicyclic-n-bridged-heteroaromatic carboxamides for the treatment of disease. The present invention relates to cyclopropyl compounds of formula I wherein the variables have the meanings as defined in the specification, to compositions comprising them, to active aaturados combinations comprising them, and to their use for protecting growing plants and animals from attack or infestation by invertebrate pests, furthermore, to seed comprising such compounds.

The present invention concerns a saturaeos composition C1 that can be crosslinked by exposure to radiation with a wavelength of between and nm, comprising: Un procedimiento para la preparacion de nuevos derivados delacido 6- dacilamidofenilacetamido penicilanico. Procedimiento para la preparacion de 1- 3-trifluorometilfe- nil 2-benzoiloxietilamino -propano.

N- azabicyclo moieties -substituted hetero-bicyclic aromatic compounds for the treatment of disease. Compounds of Formula 0and stereoisomers and pharmaceutically acceptable salts thereof, as well as methods of use as Interleukin-1 Receptor Associated Kinase IRAK4 inhibitors are described herein.

Procedimiento para preparar nuevos acidos 3- 5-aminopentil -aminobenzazepinonaalcanoico. A process for preparing oxycodone hydrochloride, said process comprising hydrogenating hydroxycodeinone in an alcoholic solvent and hydrochloric acid to form oxycodone hydrochloride, wherein a the heterociclkcos is carried out in the presence of a heterogeneous platinum group metal PGM catalyst and hydrogen gas, b the hydrogenation is carried out at one or more temperatures greater than ambient temperature in the presence of a hydrogenation catalyst and hydrogen gas, wherein the solution of hydroxycodeinone and hydrochloric acid is heated to temperature before it is exposed to the hydrogen gas, hetsrociclicos the oxycodone hydrochloride comprises 6a-oxycodol in an amount.

The present invention concerns type II photoinitiators for the free-radical crosslinking of silicone compositions, in particular acrylic silicone compositions. The heterpciclicos invention also concerns the provision of a silicone composition that can be polymerised or crosslinked by free-radical process comprising a type II photoinitiator system suitable for crosslinking silicone compositions, in particular by exposure to radiation, and absorbing light radiation with a wavelength greater than nm.

Meso-azacyclic amides of imidazopyridine carboxylic acids and analogs thereof as pharmaceuticals. Heterocyclic carboxylic acid amides and esters of azabicyclic compounds as gastric prokinetic, antiemetic, anxiolytic and antiarrhythmic agents. WIPO translate Wipo internal translation tool.

Acetamide and urea derivatives, process for their preparation and their use in the treatment of cns disorders. Nombre de la persona solicitante. According to the invention, the organic molecule has -a first chemical moiety with a structure of formula I and -two second chemical moieties, each with a structure of formula II wherein the first chemical moiety is linked to each of the two second chemical moieties via a single bond; wherein T, V is independently from another the binding site of a single bond linking the first chemical moiety to one of the two second chemical moieties or is hydrogen; W, X, Y is independently from another the binding site of a single bond linking the first chemical moiety to one of the two second chemical moieties or is selected from the group consisting of hydrogen, CN,and CF3; wherein exactly one substituent selected of the group consisting of W, X, and Y is CN or CF3, and exactly two substituents selected of the group consisting of T, V, W, X and Y represent the binding sites of a single bond linking the first chemical moiety to one of the two second chemical moieties.

The present invention relates to compounds of the formula 1 which are suitable for use in electronic devices, in particular organic electroluminescent devices, and to electronic devices which comprise these compounds. Fecha de la solicitud, orden descendente. Nombre de la persona inventora. Azabicyclische verbindungen, verfahren zu ihrer herstellung und ihre pharmazeutische verwendung. The invention relates to zaturados organic molecule, in particular for use in organic optoelectronic devices.

The invention relates to novel 3-indole and 3-indazole compounds characterized in that the compound has general formula I in which the chemical groupings, substituents. Substituted phenylcarbamates and phenylureas, their preparation and their use as 5-ht antagonists. TOP Related Posts.

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Faugor New meso-azacyclic aromatic acid amides and esters as novel serotonergic agents. Compounds of Formula 0and stereoisomers and pharmaceutically acceptable salts thereof, as well as methods of use as Interleukin-1 Receptor Associated Kinase IRAK4 inhibitors are described herein. Heterocyclic carboxylic acid amides and esters of azabicyclic compounds as gastric prokinetic, antiemetic, anxiolytic and antiarrhythmic agents. Substituted phenylcarbamates and phenylureas, their preparation and their use as 5-ht antagonists.

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