Abstract: The present invention relates to oral compositions and methods for inhibiting bone resoprtion in a mammal while counteracting the occurrence of potentially adverse gastrointestinal effects. The compositions useful herein comprise the combination of a pharmaceutically effective amount of a nitrogen-containing bisphosphonate or a pharmaceutically-acceptable salt thereof and a pharmaceutically effective amount of a caspase inhibitor.
Abstract: The invention encompasses the novel class of compounds represented by formula I, which are caspase-3 inhibitors.
The invention also encompasses certain pharmaceutical compositions for treatment of caspase-3 mediated diseases comprising compounds of formula I.
Type:
Grant
Filed:
December 2, 1999
Date of Patent:
April 22, 2003
Assignee:
Merck Frosst Canada & Co.
Inventors:
Erich L. Grimm, Johanne Renaud, Renee Aspiotis, Christopher I. Bayly, Robert Zamboni, Shawn Black
Abstract: The present invention relates to a pigment preparation comprising BiOCl pigments, one or more luster pigments and spherical particles, and to the use thereof in printing inks, security printing inks, surface coatings, paints, plastics and in cosmetic formulations.
Abstract: The present invention relates to a process for the preparation of cyclopropaneacetylene by reacting a ketophosphonate with a diazo-transfer reagent in the presence of non-nucleophilic base in an aprotic solvent to generate a reaction mixture containing a ketodiazophosphonate compound and then reacting the reaction mixture with cyclopropanecarboxaldehyde in a non-nucleophilic base and a protic solvent to yield cyclopropaneacetylene.
Abstract: A solution for cleaning silicon semiconductors or silicon oxides comprising H2O2, NH4OH and at least one component A selected from the group consisting of fluoro-containing compounds and other ammonium salts than NH4OH, wherein the weight ratio of H2O2 to H2O is between 1:5 and 1:50, the weight ratio of NH4OH to H2O is between 1:5 and 1:50, and the molar ratio of component A to NH4OH is between 1:10 and 1:5000 is disclosed. The solution can achieve the efficacy equivalent to that of the conventional RCA two-step cleaning solution within a shorter time by one step and effectively remove contaminants such as organics, dust and metals from the surfaces of silicon semiconductors and silicon oxides without using strong acids such as HCl and H2SO4.
Abstract: The present invention relates to benzimidazolinylpiperidine derivatives useful as ligands for CGRP (Calcitonin Gene-Related Peptide) receptors, their use in therapy, pharmaceutical compositions comprising them and methods of treatment using them.
Type:
Grant
Filed:
May 30, 2001
Date of Patent:
April 22, 2003
Assignees:
Merck Sharpe & Dohme Ltd., Merck & Co, Inc.
Inventors:
Arthur A. Patchett, Raymond George Hill, Lihu Yang
Abstract: Continuous separation methods, in partricular using SMB methods, are disclosed, in which the analytes are separated by size exclusion chromatography (gel permeation chromatography).
Type:
Grant
Filed:
June 13, 2001
Date of Patent:
April 22, 2003
Assignee:
Merck Patent Gesellschaft mit beschrankter Haftung
Inventors:
Lothar Britsch, Michael Schulte, Jochen Strube
Abstract: The present invention is directed to the improved synthesis of compounds of formula I:
which may be useful in the treatment of prostate cancer. Such compounds are synthesized in the presence of a carboxyl activating agent, an additive and a base for the preparation of a PSA conjugate which comprises an anthracycline antibiotic and an oligopeptide.
Type:
Grant
Filed:
October 18, 2000
Date of Patent:
April 22, 2003
Assignee:
Merck & Co., Inc.
Inventors:
Joseph E. Lynch, Michael A. Robbins, Yao-Jun Shi, David R. Lieberman
Abstract: The invention relates to cyclohexane derivatives of the formula I
in which n, m, p, R1, X1, X2, Z1, Z2, Z3, A1 A2 and Y are as defined above.
Type:
Grant
Filed:
June 28, 2001
Date of Patent:
April 22, 2003
Assignee:
Merck Patent Gesellschaft Mit
Inventors:
Peer Kirsch, Joachim Krause, Michael Heckmeier
Abstract: Described are chiral liquid crystalline polymer materials and polymerizable compounds used for preparing them. The polymer materials can serve as a carrier material or are coated onto a carrier material. Also described are methods of making such materials and using them to make pigment flakes used in paints, printing inks, spray paints, cosmetic products, colored plastics, optical elements and security applications.
Type:
Grant
Filed:
July 3, 2001
Date of Patent:
April 22, 2003
Assignee:
Merck Patent Gesellschaft mit beschränkter
Haftung
Inventors:
Eike Poetsch, Gerhard Pfaff, Matthias Kuntz, Stephan Derow, David Coates
Abstract: Liquid-crystalline mediums based on a mixture of polar compounds of negative dielectric anisotropy, comprising one or more compounds of the general formula I, 1
Abstract: A class of substituted or 6,7-ring fused 1,2,3-triazolo[4,5-b]pyridine derivatives, possessing an optionally substituted cycloalkyl, phenyl or heteroaryl substituent at the 3-position and a substituted alkoxy moiety at the 5-position, are selective ligands for GABAA receptors, in particular having high affinity for the &agr;2 and/or &agr;3 subunit thereof, and are accordingly of benefit in the treatment and/or prevention of disorders of the central nervous system, including anxiety and convulsions.
Type:
Application
Filed:
November 8, 2002
Publication date:
April 17, 2003
Applicant:
Merck & Co., Inc.
Inventors:
Howard Barff Broughton, Jose Luis Castro Pineiro, Ian James Collins, Leslie Joseph Street
Abstract: Piperidine derivatives of the formula I
and their physiologically acceptable salts
in which X, Y, Z, R1, R2, R3 and R4 are as defined in claim 1
can be as excitatory amino acid antagonists for combating neurodegenerative disorders including cerebrovascular diseases, epilepsy, schizophrenia, Alzheimer's disease, Parkinson's disease and Huntington's disease, cerebral ischaemias, infarcts and psychosis.
Type:
Grant
Filed:
September 14, 2000
Date of Patent:
April 15, 2003
Assignee:
Merck Patent GmbH
Inventors:
Helmut Prücher, Joachim Leibrock, Andrew Barber, Gerd Bartoszyk
Abstract: The invention relates to a method of isolating plasmid DNA from microorganism cultures with the aid of solid-phase bodies. The solid-phase bodies can be silica gels, silicates, or glass-like materials and the solid-phase bodies can have magnetic properties. The solid-phase bodies are used for isolating the microorganisms and for isolating the plasmid DNA.
Abstract: The invention relates to a non-dusting, homogeneous pigment preparation, comprising
≧40% by weight of one or more effect pigments,
0.5-60% by weight of a polyalkylene glycol and/or one or more polyalkylene glycol derivatives,
0-10% by weight of a redispersing auxiliary,
0-40% by weight of water or an organic solvent or solvent mixture,
0-40% by weight of at least one further hydroxyl-rich resin,
and to its use as a precursor for printing inks.
Type:
Grant
Filed:
December 13, 2000
Date of Patent:
April 15, 2003
Assignee:
Merck Patent Gesellschaft mit beschränkter
Haftung
Abstract: Described is a process for preparing a powder coating material, in which a mixture comprising binders, pigments and also, where appropriate, fillers, additives and cross linkers is extruded and then ground. The pigment fraction of this mixture at least in part comprises surface-modified effect pigment that has been coated with a low molecular mass polyethylene or polypropylene. Also, described is a powder coating material prepared by this process and the use of effect pigments coated with low molecular mass polyethylene or polypropylene to prepare powder coating materials.
Abstract: This invention relates to the use of potent potassium channel blockers or a formulation thereof in the treatment of glaucoma and other conditions related to elevated intraoccular pressure in the eye of a patient. This invention also relates to the use of such compounds to provide a neuroprotective effect to the eye of a mammalian species, particularly humans.
Type:
Grant
Filed:
January 17, 2001
Date of Patent:
April 15, 2003
Assignee:
Merck & Co., Inc.
Inventors:
Maria L. Garcia, Gregory J. Kaczorowski, Owen B. McManus
Abstract: A novel process for preparing a stabilized, lyophilized carbapenem, antibiotic formulation suitable for intravenous administration to patients in need thereof, wherein the active ingredient is of formula II:
The process entails compounding a unstable, monosodium salt carbapenem with a sodium bicarbonate solution at a temperature range of from about 0° to about 5° C. while maintaining a pH between about 7.0 and about 8.0, filtering the resultant solution, bottling under sterile conditions, and lyophilizing to produce the formulation.
Type:
Grant
Filed:
October 27, 2000
Date of Patent:
April 15, 2003
Assignee:
Merck & Co., Inc.
Inventors:
Anthony Al-Dehneh, William A. Hunke, Kathleen J. Illig, Anand Kanike, Hiren Patel, Scott D. Reynolds, Stelios C. Tsinontides