Abstract: (R/S)-(?/+)-2-[5-(4-fluorophenyl)-3-pyridylmethylaminomethyl]-chromane or a physiologically acceptable salt thereof and/or (S)-(+)-2-[5-(4-fluorophenyl)-3-pyridylmethylaminomethyl]-chromane or a physiologically acceptable salt thereof are used for the manufacture of a medicament for the treatment of extrapyramidal movement disorders and/or adverse effects in extrapyramidal movement disorders.
Type:
Grant
Filed:
July 10, 2002
Date of Patent:
January 18, 2011
Assignee:
Merck Patent GmbH
Inventors:
Gerd Bartoszyk, Herman Russ, Christoph Seyfried, Frank Weber
Abstract: The present invention relates to novel compounds of general formula (I) and uses thereof. The present invention relates to novel compounds of general formula (I) for use as glucokinase activators in the treatment of diabetes and obesity.
Type:
Application
Filed:
February 5, 2009
Publication date:
January 13, 2011
Applicant:
Merck Patent Gesellschaft
Inventors:
Christoph Saal, Lars Burgdorf, Ulrich Emde, Norbert Beier, Johannes Gleitz, Christine Charon
Abstract: The invention relates to an expression vector comprising the promoter of the mCMV-IE2 gene, or a functional expression promoting fragment thereof, and/or an enhancer of the mCMV-IE2 gene, or a functional expression enhancing fragment thereof, wherein the expression vector does not contain any complete gene of the mCMV.
Abstract: The invention relates to a process for preparing a formulation comprising an organic semiconductor (OSC) and one or more organic solvents, to novel formulations obtained by this process, to their use as coating or printing inks for the preparation of organic electronic (OE) devices, especially organic field effect transistors (OFET) and organic photovoltaic (OPV) cells, to a process for preparing OE devices using the novel formulations, and to OE devices prepared from such a process or from the novel formulations.
Type:
Application
Filed:
February 6, 2009
Publication date:
January 13, 2011
Applicant:
Merck Patent Gesellschaft Mit Beschrankter Haftung
Abstract: Novel heterocyclic compounds of the formula I wherein D is wherein R1, R2, E?, E?, E??, Y?, Y?, G?, G?, G?? and G?? have the meaning of claim 1, are activators of glucokinase and can be used for the prevention and/or treatment of Diabetes Typ 1 and 2, obesity, neuropathy and/or nephropathy.
Type:
Application
Filed:
February 3, 2009
Publication date:
January 13, 2011
Applicant:
MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG
Inventors:
Lars Thore Burgdorf, Stefan Bender, Christoph Saal, Christine Charon, Norbert Beier
Abstract: The present invention relates to pyridopyrazinone derivatives of formula (I), wherein X, Y, Z, W, A and R1 are as defined in claim 1, as insulin secretion stimulators. The invention also relates to the preparation and use of these pyridopyrazinone derivatives for the prophylaxis and/or treatment of diabetes and pathologies associated.
Type:
Application
Filed:
February 27, 2009
Publication date:
January 13, 2011
Applicant:
Merck Patent Gesellschaft Mit Beschrankter Haftung
Abstract: The invention relates to a process of preparing an alignment film for the alignment of liquid crystals (LCs) or reactive mesogens (RMs), by a direct particle beam deposition process, to an alignment film obtainable by said process, to the use of said alignment film for the alignment of LCs or RMs, especially in the form of thin layers, to a multilayer comprising said alignment film and one or more LC and/or RM layers, and to the use of the alignment film and multilayer in optical, electronic and electrooptical applications.
Type:
Application
Filed:
February 3, 2009
Publication date:
January 13, 2011
Applicant:
MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG
Abstract: The invention relates to a method for the thermal control of at least one temperature-dependent enzymatic reaction in the presence of magnetic particles, particularly nanoparticles, or magnetic beads in vitro by means of the heating of the magnetic beads or magnetic particles to at least one certain target temperature by means of alternating magnetic fields. The enzymatic reaction which can be controlled with the method according to the invention is preferably a PCR reaction or another reaction for the elongation or amplification of nucleic acids, including DNA, RNA or hybrids or derivatives thereof, which takes place directly on the functionalized magnetic beads. Further aspects of the invention relate to a reactor for carrying out the method and the use of the method or the reactor in analytics and diagnostics.
Type:
Application
Filed:
March 19, 2009
Publication date:
January 13, 2011
Applicants:
Fraunhofer-Gesellschaft zur Foederung der angewandten Forschung e.V., Merck Patent GmbH
Inventors:
Christian Zilch, Wilhelm Gerdes, Johann Bauer, Karl Holschuh
Abstract: The present invention is related to N-hydroxyamide derivatives of Formula (I): and use thereof in particular for the treatment and/or prophylaxis of autoimmune disorders, inflammatory diseases, cardiovascular diseases, neurodegenerative diseases, cancer, respiratory diseases and fibrosis, including multiple sclerosis, arthritis, emphysema, chronic obstructive pulmonary disease, liver and pulmonary fibrosis.
Abstract: The invention relates to novel compositions, in particular cosmetic and/or pharmaceutical compositions or food supplements, comprising at least one oxidized flavonoid derivative of the formula I, to novel oxidized flavonoid derivatives, and to novel uses of the oxidized flavonoid derivatives.
Abstract: Compounds of the formula I, in which W, R, R1, R2, R3, R4, R5, R6 and R7 have the meanings indicated in Claim 1, can be employed, inter alia, for the treatment of tumours
Type:
Grant
Filed:
December 14, 2004
Date of Patent:
January 11, 2011
Assignee:
Merck Patent GmbH
Inventors:
Kai Schiemann, Ulrich Emde, Dirk Finsinger, Johannes Gleitz, Helmut Reubold, Frank Zenke
Abstract: The invention relates to a liquid-crystalline medium comprising one or more compounds of the formula I in which R0, X0 and L1-6 have the meanings indicated in Claim 1, and to the use thereof in electro-optical liquid-crystal displays.
Type:
Application
Filed:
February 18, 2009
Publication date:
January 6, 2011
Applicant:
Merck Patent Gesellschaft
Inventors:
Michael Wittek, Brigitte Schuler, Volker Reiffenrath, Mark Goebel, Markus Czanta
Abstract: The invention provides substituted pyrazolidinone compounds, and methods of treatment and pharmaceutical compositions that utilize or comprise one or more such compounds. Compounds of the invention are useful for a variety of therapies, including treating or preventing preterm labor, dysmenorrhea, asthma, hypertension, infertility or fertility disorder, undesired blood clotting, preeclampsia or eclampsia, an eosinophil disorder, sexual dysfunction, osteoporosis and other destructive bone disease or disorder, and other diseases and disorders associated with the prostaglandin EP2 and/or EP4 receptors.
Type:
Grant
Filed:
May 14, 2008
Date of Patent:
January 4, 2011
Assignee:
Merck Serono SA
Inventors:
Gian Luca Araldi, Yihua Liao, Adulla P. Reddy, Zhong Zhao
Abstract: The present invention relates to G-CSF polypeptides and their uses, particularly for therapeutic or prophylactic treatment in human subjects. The invention also relates to nucleic acids encoding said polypeptides, vectors comprising such nucleic acids and recombinant cells containing the same. The invention further discloses methods of producing such polypeptides, as well as methods and tools for detecting or dosing these polypeptides in any sample.
Type:
Grant
Filed:
June 26, 2009
Date of Patent:
January 4, 2011
Assignee:
Merck Serono SA
Inventors:
Catherine Gonthier, Philippe Millasseau
Abstract: The present invention relates to G-CSF polypeptides and their uses, particularly for therapeutic or prophylactic treatment in human subjects. The invention also relates to nucleic acids encoding said polypeptides, vectors comprising such nucleic acids and recombinant cells containing the same. The invention further discloses methods of producing such polypeptides, as well as methods and tools for detecting or dosing these polypeptides in any sample.
Type:
Grant
Filed:
June 26, 2009
Date of Patent:
January 4, 2011
Assignee:
Merck Serono S.A.
Inventors:
Catherine Gonthier, Philippe Millasseau
Abstract: An ionic liquid according to the invention is substantially halogen-free, has a low viscosity and is stable to hydrolytic degradation under test conditions. The ionic liquid is a compound of the formula (cation) (R?—O—SO3), (cation) (R?—SO3), or a mixture of the two compounds. It can be used in processes for the chemical conversion and separation of materials by employing the ionic liquid as a solvent, solvent additive, extraction agent or phase-transfer catalyst. It can also be used in a heat exchange device wherein the ionic liquid serves as a heat carrier or heat carrier additive.
Type:
Grant
Filed:
August 31, 2004
Date of Patent:
January 4, 2011
Assignee:
Merck Patent GmbH
Inventors:
Peter Wasserscheid, Andreas Bösmann, Roy Van Hal
Abstract: The present invention relates to novel enfumafungin derivatives of formula I and pharmaceutically acceptable salts thereof, their synthesis, and their use as inhibitors of (1,3)-?-D-glucan synthase. The present compounds and pharmaceutically acceptable salts thereof, as well as pharmaceutical compositions comprising the present compounds and pharmaceutically acceptable salts thereof, are useful for treating or preventing antifungal infections and associated diseases and conditions.
Type:
Grant
Filed:
March 29, 2007
Date of Patent:
January 4, 2011
Assignees:
Merck Sharp & Dohme Corp., Scynexis, Inc.
Inventors:
James M. Balkovec, Frances Aileen Bouffard, Bruno Tse, James Dropinski, Dongfang Meng, Mark L. Greenlee, Michael Peel, Weiming Fan, Ahmed Mamai, Hao Liu, Keqaing Li
Abstract: The invention relates to compounds of the formula (I) or (II), to compositions which comprise such compounds, to corresponding processes for the preparation of the compounds or the compositions comprising same, and to the use thereof as light-protection filters.
Type:
Grant
Filed:
July 27, 2005
Date of Patent:
January 4, 2011
Assignee:
Merck Patent GmbH
Inventors:
Christophe Carola, Frank Pfluecker, Herwig Buchholz, Hansjürgen Driller, Hans Neunhoeffer, Evgeniy V. Blyumin
Abstract: Compounds of the formula (1) in which R1, R2, X, Y and Z are as defined in the description, the processes for the preparation of these compounds, the uses thereof for the treatment of dyslipidaemia, atherosclerosis and diabetes, and the pharmaceutical compositions comprising them.
Type:
Grant
Filed:
December 22, 2005
Date of Patent:
January 4, 2011
Assignee:
Merck Patent GmbH
Inventors:
Michel Brunet, Nathalie Adje, Valérie Guyard-Dangremont, Francis Contard