摘要:
The invention relates to compounds of formula (I), wherein the symbols have the meanings indicated in the specification. The inventive compounds exhibit dramatic antiarrhythmic proprieties and contain a cardioprotective compound. They can preventively inhibit or strongly reduce pathophysiologic processes upon occurrence of ischemic injuries, especially ischemic cardiac arrhythmia. Said compounds also exhibit a strong inhibiting effect on cellular proliferation.
摘要:
The invention relates to compounds represented by formula (I), wherein the symbols have the meanings indicated in the description, which exhibit outstanding antiarrhythmic properties and comprise a cardioprotective component. The inventive compounds can preventively inhibit or strongly reduce pathophysiological processes upon occurrence of ischemic injuries, especially ischemic cardiac arrhythmia. Said compounds also exhibit a strong inhibiting effect on cellular proliferation.
摘要:
The invention relates to anthranilic acids of formula (I) wherein the substituents R1-R3 have the designations cited in the claims. Said acids have no unwanted and detrimental salidiuretic properties, but rather very good cardioprotective properties, for example in terms of oxygen deficiency phenomena. Due to their pharmacological properties, said acids are highly suitable as cardioprotective pharmaceuticals for the prophylaxis and treatment of infarction, as well as the treatment of angina pectoris, also preventively inhibiting or strongly reducing the pathophysiological processes in the case of disorders caused by ischaemia. The protective action of the inventive compounds of formula (I) against pathological, hypoxic and ischaemic situations, and the inhibition of the cellular Na+/HCO3 cotransporter (NBC), enables said compounds to be used as pharmaceuticals for treating all acute or chronic disorders caused by ischaemia, or diseases induced in a primary or secondary manner by said disorders.
摘要:
The invention relates to benzoylguanidines of formula (I), wherein R2 stands for -Y-p-(C6H4)-R11, -Y-m-(C6-H4)-R11 or -Y-o-(C6H4)-R11; R11 represents (C1-C9)-heteroaryl, which is bonded by C or N and is substituted or unsubstituted with 1 to 3 substituents selected from the group consisting of F, Cl, CF3, CH3, methoxy, hydroxy, amino, methylamino, dimethylamino and benzyl; Y represents oxygen, -S- or NR12; R12 represents H or (C1-C4)-alkyl; R4 F, Cl, Br, I or C1-C4-alkyl; R1 and R3 are defined as per the claims. Said benzoylguanidines are suitable for use as anti-arrhythmic medicaments containing cardioprotective components for the prophylaxis and treatment of infarcts and for the treatment of angina pectoris. They also preventively inhibit the pathophysiological processes associated with the origination of defects caused by ischaemia, in particular during the triggering of ischaemically induced cardiac arrhythmia.
摘要:
The invention relates to heterocyclically substituted benzoylguanidine of formula (I), wherein the substituents R(1) to R(4) have the meanings given in the claims. These compounds (I) are suitable for use as anti-arrhythmic medicaments containing a cardio-protective component for infarct prophylaxis and infarct treatment and for the treatment of angina pectoris. The benyozlguanadines also preventively inhibit the pathophysiological processes arising from ischaemically induced traumas, in particular during the triggering of ischaemically induced cardiac arrhythmia.
摘要:
The invention relates to compounds of formula (I) in which the symbols have the meanings given in the claims. Said compounds are inhibitors of the sodium-dependent bicarbonate/chloride ion exchanger which can be used as medicines for the prophylaxis or treatment of a wide range of diseases, for example the treatment and/or prophylaxis of myocardial infarction, angina pectoris, diseases caused by ischaemia, impaired respiration, cardiac ischaemia, ischaemia of the peripheral and central nervous system and stroke, ischaemia of the peripheral organs and limbs and diseases in which cell proliferation is a primary or secondary cause, in the treatment of shock, during surgical interventions and organ transplants or for preserving and storing transplants to be used in surgical interventions.
摘要:
The invention relates to compounds of formula (I) in which the symbols have the meanings given in the description. The compounds have excellent antiarrhythmic properties and comprise a cardioprotective component. The inventive compounds can preventively inhibit or strongly reduce the pathophysiological processes when ischaemic induced damages arise, especially during the onset of ischaemic induced cardiac arrhythmias. In addition, the inventive compounds have a strong inhibiting effect on the proliferation of cells.
摘要:
The invention relates to the use of 2-amino-3,4-dihydro-quinazolines of formula (I) and to their pharmaceutically compatible salts for producing a medicament for treating and preventing ischaemic conditions. R1, R2 and R3 have the meanings given in the claims.
摘要:
The invention relates to compounds of formula (I) in which the symbols have the meanings given in the description. The compounds have excellent antiarrhythmic properties and comprise a cardioprotective component. The inventive compounds can preventively inhibit or strongly reduce the pathophysiological processes when ischaemic induced damages arise, especially during the onset of ischaemic induced cardiac arrhythmias. In addition, the inventive compounds have a strong inhibiting effect on the proliferation of cells.
摘要:
The invention relates to substituted phenyl alkenoyl guanidines, the pharmaceutically acceptable salts thereof, and physiolgically functional derivatives. Compounds of formula (I) are disclosed, wherein the radicals have the meanings thus cited. Also disclosed are the physiologically acceptable salts thereof, physiologically functional derivatives and methods for the production thereof. The inventive compounds are, for instance, suitable for use as medicaments for the prophylaxis or treatment of gall stones.