摘要:
The invention relates to novel tiotropium salts, methods for the production thereof, pharmaceutical formulations containing the same, and the use thereof for producing a medicament that is used for the treatment of respiratory diseases, especially COPD (chronic obstructive pulmonary disease) and asthma.
摘要:
The invention relates to methods for increasing the titer of a protein of interest in a cell as well as enhancing production and purification of optimized biomolecules, the component of which is, inter alia, the CH3 domain. In biomolecules, the C-terminal amino acid(s), e.g. the C-terminal lysine, frequently separate(s). The mostly incomplete processing of, for example, the heavy chain of antibodies results in products being heterogeneous. In order to avoid said product heterogeneity, the respective codon of the C-terminal lysine of the heavy antibody chain is deleted using recombinant DNA technology. Said optimized antibodies result in an increased product titer than in the wild type. In addition, said optimized antibodies are advantageous in the purification process as a result of an improved elution behavior due to the reduced charge heterogeneity.
摘要:
Die vorliegende Erfindung betrifft in 6-Stellung substituierte Indolinone der allgemeinen Formel
in der R 1 bis R 5 und X wie im Anspruch 1 definiert sind, deren Isomere und deren Salze, insbesondere deren physiologisch verträgliche Salze, welche wertvolle pharmakologische Eigenschaften aufweisen, insbesondere eine inhibierende Wirkung auf verschiedene Rezeptor-Tyrosinkinasen und Cyclin/CDK-Komplexe sowie auf die Proliferation von Endothelzellen und verschiedener Tumorzellen, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Verfahren zu ihrer Herstellung.
摘要:
Compounds of the formula (I) wherein R1, R2, R3, R4, R5, R6, W, and Y are as described herein, or a tautomer, prodrug, solvate, or salt thereof. These compounds are useful as inhibitors of Urotensin II and are thus useful for treating a variety of diseases and disorders that are mediated or sustained through the interaction of Urotensin II with its receptor, including cardiovascular diseases. This invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds, and intermediates useful in these processes.
摘要:
Compounds of Formula (I) wherein R1, R2, R3, R4, R5, R6, X, R7, and R8 are as defined herein, or a tautomer, prodrug, solvate, or salt thereof; pharmaceutical compositions containing such compounds, and methods of modulating the glucocorticoid receptor function and methods of treating disease-states or conditions mediated by the glucocorticoid receptor function or characterized by inflammatory, allergic, or proliferative processes in a patient using these compounds.
摘要:
The invention relates to a crystalline form of 1-chloro-4-(β-D-glucopyranos-1-yl)-2-[4-((Sj-tetrahydrofuran-3-yloxy)-benzyl]-benzene, to a method for the preparation thereof, as well as to the use thereof for preparing medicaments.