Abstract:
A series of 3-pyrrolidinyloxy-3'-pyridyl ether compounds, a method for selectively controlling neurotransmitter release in mammals using these compounds, and pharmaceutical compositions including these compounds. Preferred compounds are 3-pyrrolidinylmethoxy-3'-(5'-and/or 6'-substituted) pyridyl ethers.
Abstract:
The present invention is directed to a series of substituted pyridine compounds, a method for selectively controlling neurotransmitter release in mammals using these compounds, and pharmaceutical compositions containing these compounds. Preferred compounds are 3'-(5'- and/or 6'-substituted) pyridyl ethers.
Abstract:
Un compuesto seleccionado del grupo que se compone de (a) un compuesto de la estructura o una sal del mismo farmacéuticamente admisible, en donde R1 es hidrógeno o metilo; R2 es hidrógeno; R5 es F, Cl o Br; y R6 es metilo, F, Cl o Br; (b) un compuesto de la estructura o una sal del mismo farmacéuticamente admisible, en donde R1 es hidrógeno o metilo; R2 es metilo; R5 es F, Cl o Br; y R6 es metilo, F, Cl o Br; (c) 5-[(S)-2-amino-1-propiloxi]-2-cloropiridina o una sal del mismo farmacéuticamente admisible; (d) ácido 5-[(R)-2-metilamino-1-propiloxi]-2-cloropiridina p-toluensulfónico; (e) 5-[(S)-2-amino-1-propiloxi]-2-fluoropiridina o una sal del mismo farmacéuticamente admisible; (f) ácido 5-[(R)-2-amino-1-propiloxi]-2-fluoropiridina p-toluensulfónico; (g) ácido 5-[(R)-2-metilamino-1-propiloxi]-2-fluoropiridina p-toluensulfónico; (h) ácido 5-[(R)-2-dimetilamino-1-propiloxi]-2-cloro-3-bromopiridina p-toluensulfónico; (i) ácido 5-[(S)-2-dimetilamino-1-propiloxi]-2-cloro-3-metilpiridina p-toluensulfónico; y (j) ácido 5-[(R)-2-dimetilamino-1-propiloxi]-2-cloro-3-metilpiridina p-toluensulfónico.
Abstract:
The present invention is directed to a series of substituted pyridine compounds, a method for selectively controlling neurotransmitter release in mammals using these compounds, and pharmaceutical compositions containing these compounds. Preferred compounds are 3'-(5'- and/or 6'-substituted) pyridyl ethers.
Abstract:
The present invention is directed to a series of substituted pyridine compounds (I), a method for selectively controlling neurotransmitter release in mammals using these compounds, and pharmaceutical compositions containing these compounds. Preferred compounds are 3'-(5'- and/or 6'-substituted) pyridyl ethers. n = 1-4, R1-R6 as in the claims.
Abstract:
La presente invencion esta dirigida a una serie de compuestos de piridina substituida (1), un metodo para controlar selectivamente la liberacion de neurotransmisor en mamiferos utilizando estos compuestos, y composiciones farmaceuticas que contienen estos compuestos. Los compuestos preferidos son piridil eteres 3'-(5'-y/o 6'- substituidos). El valor de n es 1-4, R1-R6 son como se presenta en las reivindicaciones.
Abstract:
A series of 3-pyrrolidinyloxy-3'-pyridyl ether compounds, a method for selectively controlling neurotransmitter release in mammals using these compounds, and pharmaceutical compositions including these compounds. Preferred compounds are 3-pyrrolidinylmethoxy-3'-(5'-and/or 6'-substituted) pyridyl ethers.
Abstract:
The present invention is directed to a series of substituted pyridine compounds, a method for selectively controlling neurotransmitter release in mammals using these compounds, and pharmaceutical compositions containing these compounds. Preferred compounds are 3'-(5'- and/or 6'-substituted) pyridyl ethers.
Abstract:
The present invention is directed to a series of substituted pyridine compounds (I), a method for selectively controlling neurotransmitter release in mammals using these compounds, and pharmaceutical compositions containing these compounds. Preferred compounds are 3'-(5'- and/or 6'-substituted) pyridyl ethers. n = 1-4, R1-R6 as in the claims.