Abstract:
A fumarate salt and a maleate salt of compound (I) represented by the following structural formula, as well as their corresponding pharmaceutical compositions, are disclosed. Particular single crystalline forms of 1:1 compound (I) fumarate and 1:1 compound (I) maleate are characterized by a variety of properties and physical measurements. Methods of preparing specific crystalline forms of 1:1 compound (I) fumarate and 1:1 compound (I) maleate are also disclosed. The present invention also provides methods of treating a subject with a cancer. Compound (I)
Abstract:
The present teachings provide a compound represented by structural formula (1-0), or a pharmaceutically acceptable salt thereof. Also described are pharmaceutical compositions and methods of use thereof.
Abstract:
The invention is directed to a compound represented by the following structural formula and pharmaceutically acceptable salts thereof: Compounds represented by this structural formula are kinase inhibitors and are therefore disclosed herein for the treatment of cancer. Definitions for the variables in the structural formula are provided herein.
Abstract:
La presente invencion se refiere a un novedoso co-cristal del compuesto de formula (I): (Formula (I)) en donde la molecula co-formadora es hemihidrato de bifosfato, a procesos para la preparacion del co-cristal, a composiciones farmaceuticas que contienen el co-cristal, al uso de tal co-cristal en la manufactura de un medicamento para uso en el tratamiento de cancer y a métodos para tratar tales enfermedades en el cuerpo humano o animal por administracion de una cantidad terapeuticamente efectiva de tal co-cristal.
Abstract:
Abstract The present invention relates to a hydrobromide salt of the compound of formula (1), to process for the preparation of the hydrobromide salt, to pharmaceutical compositions containing the hydrobromide salt, to the use of such a hydrobromide salt in the manufacture of a medicament for use in the treatment of cancer and to methods of treating such diseases in the human or animal body by administering a therapeutically effective amount of such a hydrobromide salt. H $ NH 0 H (I)
Abstract:
Sunt descrişi compuşii tienopiridinonici cu Formula (I) şi sărurile acceptabile farmaceutic ale acestora. În aceşti compuşi, unul dintre X1; X2 şi X3 sunt S şi celelalte două sunt fiecare independent CR, în care R şi toate celelalte variabile sunt definite aici. Se arată că compuşii inhibă activitatea kinazei HPK1 şi au activitate antitumorală in vivo. Compuşii pot fi combinaţi eficient cu purtători acceptabili farmaceutic şi, de asemenea, cu alte abordări imunomodulatoare, cum ar fi inhibarea punctului de control sau inhibitorii oxidării triptofanului. Formula (I).
Abstract:
Fumarate and maleate salts of compound (I), a PLK-4 inhibitor, are disclosed wherein the molar ratio is 1:1. These salts form crystalline solids which are suitable for pharmaceutical development and preparing pharmaceutical compositions. These fumarate and maleate crystalline forms have good oral bioavailability. Particular single crystalline forms of 1:1 compound (I) fumarate and 1:1 compound (I) maleate are characterized by a variety of properties and physical measurements. Methods of preparing specific crystalline forms of 1:1 compound (I) fumarate and 1:1 compound (I) maleate are disclosed along with the use of the fumarate and maleate salts of compound (I) for the treatment of cancers.
Abstract:
A fumarate salt and a maleate salt of compound (I) represented by the following structural formula, as well as their corresponding pharmaceutical compositions, are disclosed. Particular single crystalline forms of 1:1 compound (I) fumarate and 1:1 compound (I) maleate are characterized by a variety of properties and physical measurements. Methods of preparing specific crystalline forms of 1:1 compound (I) fumarate and 1:1 compound (I) maleate are also disclosed. The present invention also provides methods of treating a subject with a cancer. Compound (I)