Abstract: The present invention relates to substituted indolinones of general formula
wherein
R1 to R6 and X are defined as in claim 1, the isomers and the salts thereof, in particular the physiologically acceptable salts thereof which have valuable pharmacological properties, especially an inhibitory effect on various receptor-tyrosine kinases, and cycline/CDK complexes as well as on the proliferation of endothelial cells and various tumor cells, pharmaceutical compositions containing these compounds, their use and processes for preparing them.
Type:
Grant
Filed:
July 22, 2002
Date of Patent:
September 21, 2004
Assignee:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Gerald Juergen Roth, Armin Heckel, Rainer Walter, Ulrike Tontsch-Grunt, Walter Spevak, Jacobus C. A. Van Meel
Abstract: The present invention relates to the compound 3-Z-[1-(4-(N-((4-methyl-piperazin-1-yl)-methylcarbonyl)-N-methyl-amino)-anilino)-1-phenyl-methylene]-6-methoxycarbonyl-2-indolinone-monoethanesulphonate of formula I and the use thereof as a pharmaceutical composition.
Type:
Application
Filed:
July 21, 2003
Publication date:
September 9, 2004
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Gerald J. Roth, Guenter Linz, Peter Sieger, Werner Rall, Frank Hilberg, Thomas Bock
Abstract: The present invention relates to a new crystalline modification of the compound 4-hydroxy-2-methyl-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazin-3-carboxamide-1,1-dioxide in the form of an acetic acid solvate of formula I as well as the use thereof as a pharmaceutical composition.
Type:
Application
Filed:
September 22, 2003
Publication date:
September 2, 2004
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Guenter Trummlitz, Rainer Soyka, Peter Sieger, Ulrike Werthmann, Peter Luger
Abstract: The present invention relates to atomizers for administering preservative-free liquids to the cornea or conjunctiva of the eye, with special eye adapters for atomizers and the use of atomizers for ophthalmological administration. The atomizers according to the invention are free from propellant gas.
Type:
Application
Filed:
December 18, 2003
Publication date:
August 26, 2004
Applicant:
Boehringer Ingelheim Pharma GmbH & Co., KG
Inventors:
Michael Diestelhorst, Isolde Martin, Bernd Zierenberg, Dieter Hochrainer
Abstract: Compounds of which the following are exemplary:
These have tryptase-inhibiting activity and are useful for the treatment of inflammatory and allergic disease conditions.
Type:
Grant
Filed:
October 30, 2000
Date of Patent:
August 24, 2004
Assignee:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Ralf Anderskewitz, Christine Braun, Rainer Hamm, Bernd Disse, Hans Michael Jennewein, Georg Speck
Abstract: The invention relates to a new industrially useable process for preparing tropenol, optionally in the form of the acid addition salts thereof.
Type:
Application
Filed:
January 26, 2004
Publication date:
August 12, 2004
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Rolf Banholzer, Gisela Bodenbach, Andreas Mathes, Helmut Meissner, Peter Specht
Abstract: The present invention relates to amide compounds of general formula I 1
Type:
Application
Filed:
October 31, 2003
Publication date:
August 5, 2004
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Dirk Stenkamp, Stephan Georg Mueller, Gerald Juergen Roth, Philipp Lustenberger, Klaus Rudolf, Thorsten Lehmann-Lintz, Kirsten Arndt, Ralf Lotz, Martin Lenter, Heike-Andrea Wieland
Abstract: The invention relates to a powder inhaler operating on the Bernoulli principle with replaceable cylindrical disposable capsules as the active substance reservoir. The powder inhaler consists essentially of a preferably cylindrical capsule chamber provided with means for laterally opening the capsule, an air inlet opening in the capsule chamber and an air outlet opening and a mouthpiece mounted downstream of the air outlet opening. The capsule chamber is constructed so that after insertion the reservoir capsule can essentially only move in the longitudinal direction when a sufficiently powerful air stream passes through the capsule chamber, guided substantially parallel to the longitudinal axis of the capsule. According to the invention, the inner wall of the capsule chamber is uneven in order to achieve a better emptying of the capsule than is obtained with a smooth inner surface.
Type:
Application
Filed:
December 4, 2003
Publication date:
August 5, 2004
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Abstract: The invention relates to powdered preparations for inhalation containing a tiotropium salt and salmeterol xinafoate, processes for preparing them and their use in the preparation of a pharmaceutical composition for treating respiratory diseases, particularly for treating COPD (chronic obstructive pulmonary disease) and asthma.
Type:
Application
Filed:
December 15, 2003
Publication date:
August 5, 2004
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Mareke Hartig, Michael Trunk, Rainer Soyka, Peter Sieger, Hagen Graebner, Michael Walz
Abstract: Disclosed is a process which can be used on an industrial scale for preparing and purifying 1,7′-dimethyl-2′-propyl-2,5′-bi-1H-benzimidazole in which the crude product is subjected to charcoal treatment.
Type:
Grant
Filed:
January 16, 2003
Date of Patent:
August 3, 2004
Assignee:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Werner Belzer, Rolf Dach, Volker Fachinger, Markus Heitzmann, Hartmut Schmidt
Abstract: A pharmaceutical composition comprising a compound of formula 1 1
Type:
Application
Filed:
November 10, 2003
Publication date:
July 29, 2004
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Ingo Konetzki, Kurt Schromm, Hermann Schollenberger, Sabine Pestel, Andreas Schnapp, Thierry Bouyssou, Frank Buettner, Claudia Heine, Philipp Lustenberger, Christoph Hoenke, Klaus Rudolf
Abstract: An expression vector for eukaryotic cells comprising a gene which codes for a protein of interest, functionally linked to a hamster-ubiquitin/S27a-promoter and a gene which codes for a fluorescent protein. Preferably the expression vector also contains an amplifiable selectable marker gene.
Type:
Application
Filed:
November 26, 2003
Publication date:
July 29, 2004
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Barbara Enenkel, Juergen Fieder, Ralf Otto, Stefanos Grammatikos
Abstract: Disclosed are improved processes for the preparation of a polymorph of 1-[tert-butyl-1-p-tolyl-1H-pyrazol-5-yl]-3-[4-(2-morpolinin-4-yl-ethoxy)naphthalen-1-yl]-urea (1) by crystallization from an alcohol, wherein the improvement is that crude (1) is treated with ethanol.
Type:
Application
Filed:
December 3, 2003
Publication date:
July 15, 2004
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Abstract: Disclosed are oral pharmaceutical compositions, kits and methods of treating and preventing Hepatitis C Viral (HCV) infections wherein the following Compound (1), a potent inhibitor of HCV serine protease, or a pharmaceutically acceptable salt thereof, is administered in a selected dosage range: 1
Abstract: The invention relates to powdered preparations containing tiotropium for inhalation, processes for preparing them as well as their use in preparing a pharmaceutical composition for the treatment of respiratory complaints, particularly for the treatment of COPD (chronic obstructive pulmonary disease) and asthma.
Type:
Application
Filed:
November 20, 2003
Publication date:
July 15, 2004
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Mareke Hartig, Michael Trunk, Michael Walz