Abstract: The present application relates to novel 2,5-disubstituted 6-(trifluoromethyl)pyrimidin-4(3H)-one derivatives, to processes for their preparation, to their use alone or in combinations for the treatment and/or prevention of diseases, and to their use for preparing medicaments for the treatment and/or prevention of diseases, in particular for treatment and/or prevention of cardiovascular, renal, inflammatory and fibrotic diseases.

Abstract: This invention relates to novel substituted 5-(1-benzothiophen-2-yl)pyrrolo[2,1-f][1,2,4]triazin-4-amine derivatives having protein tyrosine kinase inhibitory activities, to processes for the preparation of such compounds, to pharmaceutical compositions containing such compounds, and to the use of such compounds or compositions for treating proliferative disorders, in particular cancer and tumor diseases.

Abstract: This invention relates to novel substituted 5-(1-benzothiophen-2-yl)pyrrolo[2,1-fJ[1,2,4]triazin-4-amine derivatives having protein tyrosine kinase inhibitory activities, to processes for the preparation of such compounds, to pharmaceutical compositions containing such compounds, and to the use of such compounds or compositions for treating proliferative disorders, in particular cancer and tumor diseases.

Abstract: This invention relates to novel substituted 5-(1-benzothiophen-2-yl)pyrrolo[2,1-f][1,2,4]triazin-4-amine derivatives having protein tyrosine kinase inhibitory activities, to processes for the preparation of such compounds, to pharmaceutical compositions containing such compounds, and to the use of such compounds or compositions for treating proliferative disorders, in particular cancer and tumor diseases.

Abstract: This invention relates to novel substituted 5-(1-benzothiophen-2-yl)pyrrolo[2,1-f][1,2,4]triazin-4-amine derivatives of formula (I) wherein R1 is hydrogen, chloro, methyl or methoxy, R2 is hydrogen or methoxy, with the proviso that at least one of R1 and R2 is other than hydrogen, G1 represents chloro, (C1-C4)-alkyl, (C1-C4)-alkoxycarbonyl, 5-membered aza-heteroaryl, or the group —CH2—OR3, —CH2—NR4R5 or —C(?O)—NR4R6, and G2 represents chloro, cyano, (C1-C4)-alkyl, or the group —CR8AR8B—OH, —CH2—NR2R10, —C(?O)—NR11R12 or —CH2—OR15, having protein tyrosine kinase inhibitory activities, to processes for the preparation of such compounds, to pharmaceutical compositions containing such compounds, and to the use of such compounds or compositions for treating proliferative disorders, in particular cancer and tumor diseases.

Abstract: Needle-shaped solid crystallites of specific LaCeTb phosphates, well suited for the production of green phosphors therefrom, are essentially pure white in color after calcination at 900.degree. C. and have the formula (I):La.sub.x Ce.sub.y Tb.sub.(1-x-y) PO.sub.4 (I)in which x and y are numbers, with x ranging from 0.4 to 0.6 and x+y being greater than 0.8.

Abstract: Novel cerium/lanthanum/terbium (LaCeTb) mixed phosphates, especially useful in luminescence for the production of green phosphors, have the formula (I):La.sub.x Ce.sub.y Tb.sub.1-x-y PO.sub.4in which X ranges from 0.4 to 0.6 and x+y is greater than 0.8, display a lightness (L.sup.*) of greater than 98% after calcination at a temperature above 700.degree. C. in air, and the cerium (IV) and/or terbium (IV) contents of which are very low, even after calcination in air at a temperature above 500.degree. C.

Abstract: Novel cerium/lanthanum/terbium (LaCeTb) mixed phosphates, especially useful in luminescence for the production of green phosphors, have the formula (I):La.sub.x Ce.sub.y Tb.sub.1-x-y PO.sub.4in which x ranges from 0.4 to 0.6 and x+y is greater than 0.8, display a lightness (L*) of greater than 98% after calcination at a temperature above 700.degree. C. in air, and the cerium (IV) and/or terbium (IV) contents of which are very low, even after calcination in air at a temperature above 500.degree. C.

Abstract: Needle-shaped solid crystallites of specific LaCeTb phosphates, well suited for the production of green phosphors therefrom, are essentially pure white in color after calcination at 900.degree. C. and have the formula (I):La.sub.x Ce.sub.y Tb.sub.(1-x-y) PO.sub.4 (I)in which x and y are numbers, with x ranging from 0.4 to 0.6 and x+y being greater than 0.8.