摘要:
The invention relates to novel pyranoside derivatives of general formula (I), to methods for the production thereof, and to their use as medicaments.
摘要:
The invention relates to aminocarbonyl-substituted benzimidazole derivatives of general formula (I), wherein the radicals R?1, R2, R3 and R4¿ can have the meanings given in the claims or in the description. The invention also relates to the prodrugs thereof, a method for producing the same and the use of benzimidazole derivatives as medicaments, especially medicaments with tryptase-inhibiting action.
摘要:
The current invention relates to new benzamidine derivatives, a process for the manufacture and the use thereof as medicaments. The new benzamidine derivatives have the general formula (1).
摘要:
The invention relates to arylsulfonamide substituted benzimidazole derivatives of general formula (I), wherein the radicals R?1, R2, R3 and R4¿ are as cited in the claims and in the description, a method for the production thereof and the use of arylsulfonamide substituted benzimidazol derivatives as medicaments in particular as medicaments with tryptase-inhibiting activity.
摘要:
The present invention relates to novel pyranoside derivatives having general formula (I), process for the manufacture thereof and their use as medicaments.
摘要:
The invention relates to novel sulfoxybenzamides of formula (I), wherein: Z0 represents a group selected among formulas -X1-(CH2)r-X2- and -CR?4R5-; A1 and A2¿, independent of one another, represent a 1,4-phenylene group or 1,3-phenylene group optionally substituted by one or more halogen atoms, C¿1?-C8 alkyl groups, C2-C8 alkenyl groups, C1-C8 alkyl halide groups or by C1-C8 alkoxy groups; Z?1 and Z2¿, independent of one another, represent a group of formula -X3-(CH2)8-X4- or a single bond; m and n, independent of one another, represent 0 or 1, and; radicals R?1, R2, R3, R4, R5, X1, X2, X3, X4¿, r and s have the meanings cited in the description. The invention also relates to a method for producing these novel compounds and to their use as medicaments, especially as leukotriene B¿4?(LTB4) antagonists.
摘要:
The invention relates to a method for producing compounds of formula (I) wherein the radicals R?1 and R2¿ have the meanings given in the description and in the claims, which can be used on a large scale.