Abstract:
Compounds represented by formula (I) or pharmaceutically acceptable salts and solvates thereof, wherein A, B, B', X, Y, R1, R1 ', R2, R2', R3, R3', R5, R5', R6, m, n, or p are as defined herein, are useful for treating flaviviridae viral infections.
Abstract:
The present invention relates to compounds useful as inhibitors of PI3K, particularly of PI3Kγ. The invention also provides pharmaceutically acceptable compositions comprising said compounds and methods of using the compositions in the treatment of various disease, conditions, or disorders.
Abstract:
The present invention relates to compounds useful as inhibitors of PI3K, particularly of PI3Kγ. The invention also provides pharmaceutically acceptable compositions comprising said compounds and methods of using the compositions in the treatment of various disease, conditions, or disorders.
Abstract:
Compuesto que presenta la fórmula: **(Ver fórmula)** o una sal farmacéuticamente aceptable del mismo, en la que: X1 es CH o N; R1 se selecciona entre un anillo fenilo o piridinilo, en el que el anillo fenilo o piridinilo está opcionalmente sustituido con 1 o 2 apariciones independientes de R1a; R1a es cloro, flúor, alifático C1-6, cicloalifático C3-6, -CN, -C(O)R1b, -C(O)N(R1b)2, -C(O)O(R1b) u -OR1b, en los que cada uno de dicho alifático o cicloalifático se sustituye opcionalmente con hasta 3 apariciones de JR; cada JR es independientemente flúor, oxo, -CN, -C(O)R1b, -C(O)N(R1b)2, -C(O)O(R1b), -N(R1b)2, -N(R1b)C(O)R1b, OR1b o un heteroarilo o heterociclilo de 5 miembros que tiene hasta 3 átomos seleccionados entre nitrógeno, oxígeno o azufre; cada R1b se selecciona, independientemente de entre hidrógeno, alifático C1-4 o cicloalifático C3-6; R2 es hidrógeno, F, Cl, CF3 o CH3; B es N; C es CRC, en donde Rc es hidrógeno, flúor, cloro, alifático C1-3, CF3, -OCF3 u -Oalifático C1-2 y D es CRD, en donde RD es flúor, cloro, alifático C1-3, CF3, -OCF3 u -Oalifático C1-2.
Abstract:
The present invention relates to compounds having the formula: (see formula I) useful as inhibitors of PI3K, particularly of PI3K.gamma.. The invention also provides pharmaceutically acceptable compositions comprising said compounds and methods of using the compositions in the treatment of various disease, conditions, or disorders.
Abstract:
The invention relates to triazole compounds of formula I and I' or pharmaceutically acceptable salts thereof, useful as modulators of demyelinating diseases: The invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention, methods of using the compositions and kits thereof in the treatment of various demyelinating and neurodegenerative diseases, including multiple sclerosis.
Abstract:
The present invention relates to compounds useful as inhibitors of PI3K, particularly of PI3Kγ. The invention also provides pharmaceutically acceptable compositions comprising said compounds and methods of using the compositions in the treatment of various disease, conditions, or disorders.
Abstract:
Compounds represented by formula (I) or pharmaceutically acceptable salts and solvates thereof, where A, B, B', X, Y, Rl', R2', R3', R5, R5', R6, m, n, or p are as defined herein, are useful for treating flaviviridae viral infections.
Abstract:
La invención se refiere a compuestos de triazol de la fórmula I y I' o sus sales farmacéuticamente aceptables, útiles como moduladores de enfermedades desmielinizantes:La invención también proporciona composiciones farmacéuticamente aceptables que comprende los compuestos de la invención, métodos de uso de las composiciones y sus kits en el tratamiento de diversas enfermedades desmielinizantes y neurodegenerativas, incluyendo esclerosis múltiple.
Abstract:
La presente invención se refiere a compuestos útiles como inhibidores de PI3K, particularmente de PI3Ky. La invención también proporciona composiciones farmacéuticamente aceptables que comprenden los compuestos y métodos para usar las composiciones en el tratamiento de diversas enfermedades, afecciones o trastornos.