摘要:
The active substances identified as inhibitors of the cellular Na+/H+ exchanger (NHE) are used to prepare a medicament for normalizing serum lipids. They are used in the preparation of a medicament which reduces lipid levels in the blood and can be administered for treating diseases caused by lipid levels which are too high, and for alleviating the endothelial dysfunctional syndrome and for treating diseases caused thereby.
摘要:
The invention relates to aryl-substituted propanolamine derivatives and their pharmaceutically acceptable salts and functional derivatives. The invention relates to compounds of formula (I), wherein the radicals have the defined meanings, to their physiologically acceptable salts, physiologically functional derivatives and to methods for their production. The compounds are suitable as, e.g. hypolipidemic agents.
摘要:
The invention relates to substituted 1,4-benzothiazepine-1,1-dioxide derivatives and to the acid addition salts thereof. The invention discloses 1,4-benzothiazepine-1,1-dioxide derivatives of formula (I), wherein R?1, R2, R3¿ and Z have the cited descriptions, the physiologically compatible salts thereof and physiologically functional derivatives, as well as methods for producing the same. The compounds are suited for use, e.g. as hypolipidemic agents.
摘要:
The invention relates to aryl-substituted propanolamine derivatives and their pharmaceutically acceptable salts and functional derivatives. The invention relates to compounds of formula (I), wherein the radicals have the defined meanings, to their physiologically acceptable salts, physiologically functional derivatives and to methods for their production. The compounds are suitable as, e.g. hypolipidemic agents.
摘要:
The invention relates to substituted 1,4-benzothiazepine-1,1-dioxide derivatives and to the acid addition salts thereof. The invention discloses 1,4-benzothiazepine-1,1-dioxide derivatives of formula (I), wherein R?1, R2, R3¿ and Z have the cited descriptions, the physiologically compatible salts thereof and physiologically functional derivatives, as well as methods for producing the same. The compounds are suited for use, e.g. as hypolipidemic agents.