摘要:
Die vorliegende Anmeldung betrifft positiv allosterische Modulatoren des muskarinergen M2 Rezeptors, insbesondere solche, die gegenüber den verschiedenen muskarinergen Acetylcholin-Rezeptoren eine Subtyp-Selektivität für den M2-Rezeptor hinsichtlich der positiv-allosterischen Wirkung aufweisen, weiterhin deren Verwendung zur Behandlung und/oder Prävention von Krankheiten sowie ihre Verwendung zur Herstellung von Arzneimitteln zur Behandlung und/oder Prävention von Krankheiten, insbesondere zur Behandlung und/oder Prävention von kardiovaskulären Erkrankungen und/oder Nierenerkrankungen.
摘要:
The present invention relates to chemical compounds that selectively inhibit glucose transporter 1 (GLUT1), to methods of preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds, to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, as well as to intermediate compounds useful in the preparation of said compounds.
摘要:
The present invention relates to chemical compounds that selectively inhibit glucose transporter 1 (GLUT1), to methods of preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds, to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, as well as to intermediate compounds useful in the preparation of said compounds.
摘要:
The invention relates to novel (2-phenylimidazo[1,2-a]pyridin-3-yl)methyl-substituted perhydropyrrolo[3,4-c]pyrrole derivatives, to methods for producing same, to the use thereof alone or in combination for the treatment and/or prevention of diseases, and to the use thereof for producing drugs for the treatment and/or prevention of diseases, especially for the treatment and/or prevention of breathing disorders including sleep-related breathing disorders such as obstructive and central sleep apnea and snoring.
摘要:
The present application relates to positive allosteric modulators of the muscarinic M2 receptor, in particular novel 7-substituted 1-aryl-naphthyridin-3-carboxylic acid amides, to processes for the preparation thereof, to the use thereof alone or in combinations for the treatment and/or prevention of diseases, and to the use thereof for the production of medicaments for the treatment and/or prevention of diseases, particular for the treatment and/or prevention of cardiovascular disorders and/or renal diseases.