摘要:
The invention concerns compounds of Formula (I) (Formula (I)) or pharmaceutically-acceptable salts thereof, wherein R 1 and R 2 have any of the meanings defined herein before in the description; processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of cell proliferative disorders.
摘要:
The invention concerns pyridine a nd pyrazine derivatives of Formula (I) or a pharmaceutically-acceptable salt thereof, wherein each of W, G1, G 2, G3, G4, J, Ring A, n and R 3 has any of the meanings defined hereinbefo re in the description; processes for their preparation, pharmaceutical compositions containi ng them and their use in the manufacture of a medicament for use in the treatment of cell proliferative disorders.
摘要:
The invention concerns pyridine a nd pyrazine derivatives of Formula (I) or a pharmaceutically-acceptable salt thereof, wherein each of W, G1, G 2, G3, G4, J, Ring A, n and R 3 has any of the meanings defined hereinbefo re in the description; processes for their preparation, pharmaceutical compositions containi ng them and their use in the manufacture of a medicament for use in the treatment of cell proliferative disorders.
摘要:
The present invention relates to compounds that inhibit a5b1 function, processes for their preparation, pharmaceutical compositions containing them as the active ingredient, to their use as medicaments and to their use in the manufacture of medicaments for use in the treatment in warm blooded animals such as humans of diseases that have a significant angiogenesis or vascular component such as for treatment of solid tumours. The present invention also relates to compounds that inhibit a5b1, and also that exhibit appropriate selectivity profile(s) against other integrins.