摘要:
The invention concerns novel amino acid derivatives of general formula (I) and their pharmaceutically acceptable salts, in which the R2 group is (II) and R1, A, G, Y, Z and m have the meanings given in the description, and their production and use. The novel compounds are valuable neurokinin (tachykinin) antagonists.
摘要:
The invention concerns the use of the salts of the L-(-)-enantiomer of (endo, syn)-(-)-3-(3-hydroxy-1-oxo-2-phenylpropoxy)-8-methyl-8-(methylethyl)-8-azoniabicyclo[3.2.1] octane as active substances for medicaments administered by inhalation for treatment of the respiratory tract. These salts are suitable for such treatment owing to their unexpectedly intense and prolonged effect.
摘要:
The invention relates to novel aryl glycinamide derivatives of formula (I) and their pharmaceutically acceptable salts, in which R?1 and R2¿ together with the N to which they are bound form a ring of one of the formulae (a), (b), (c) or (d), in which R?3, R4, R5, Ar, R6, R7, R8, R9, R10, R11¿, r, s and t have the meanings indicated in the description. Also disclosed are the production and use of these compounds. The novel compounds are valuable neurokinin (tachykinin) antagonists.
标题翻译:PIPERIDINSUBSTITUIERTE ARYLGLYCINAMIDE ALS NEUROKININANTAGONISTEN,VERFAHREN ZU IHRER HERSTELLUNG UND DIESE VERBINDUNGEN ENTHALTENDE PHARMAZEUTISCHE ZUSAMMENSETZUNGEN
摘要:
The invention relates to novel compounds of formula (I) or the pharmaceutically acceptable salts thereof, wherein R1 represents 3-hydroxypropyl, 1,3-dihydroxyprop-2-yl or C¿3?-C6 cycloalkylmethyl, and R?2, R3, R4¿ and Ar have the designations cited in the description. The invention also relates to the production and use of said compounds. The inventive novel compounds are valuable neurokinin (tachykinin) antagonists.
摘要:
The invention relates to substituted benzimidazol derivatives of the general formula (I) wherein the radicals R?1, R2, R3 and R4¿ have the significance cited in the Claims and a method for the production of said derivatives and use of substituted benzimidazol derivatives as a medicament, in particular as a medicament with tryptase-inhibiting activity.
摘要:
The invention relates to novel aryl glycinamide derivatives of formula (I) and their pharmaceutically acceptable salts, in which R?1 and R2¿ together with the N to which they are bound form a ring of one of the formulae (a), (b), (c) or (d), in which R?3, R4, R5, Ar, R6, R7, R8, R9, R10, R11¿, r, s and t have the meanings indicated in the description. Also disclosed are the production and use of these compounds. The novel compounds are valuable neurokinin (tachykinin) antagonists.
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 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.