Abstract: Novel compounds which are di-t-butylphenyl alkyl or benzyl ethers which alkyl or benzyl group is substituted by an acidic group are useful an antiallergic agents. Synthetic intermediates for making such compounds are also disclosed.
Abstract: Novel compounds which are 2,6-di-t-butylphenols substituted in the 4 position by an alkoxy or benzyloxy group or a benzylthio group, which alkoxy or benzyloxy group is directly substituted by a tetrazole ring, and which benzylthio group is directly substituted by carboxy or tetrazolyl are useful as inhibitors of leukotriene biosynthesis and as antiallergic agents. Synthetic intermediates for preparing such compounds are also described.
Abstract: Certain 2,5-disubstituted N-(2-piperidylmethyl)benzamides, wherein one substituent is 2,2,2-trifluoroethyoxy, and pharmaceutically acceptable acid-addition salts thereof, are active as antiarrhythmic agents.
Abstract: Controlled release pharmaceutical formulations containing flecainide acetate and methods of suppressing arrhythmia using the formulations are described.
Abstract: Novel 1-substituted 1H-imidazo-[4,5-c]quinolin-4-amines are disclosed. These compounds function as antiviral agents, and they are potential synthetic intermediates in the preparation of known antiviral agents and labeled known antiviral agents. This invention also provides intermediates for preparing such compounds, pharmaceutical compositions containing such compounds, and pharmacological methods of using such compounds.
Type:
Grant
Filed:
March 23, 1989
Date of Patent:
May 29, 1990
Assignee:
Minnesota Mining and Manufacturing Company
Abstract: An ear tip for use with a stethoscope, audio headset or like device, the ear tip being of a construction and design that provides substantial deformation of the ear tip under normal stethoscope pressures such that in use the ear tip is seated comfortably and conformably against the ear canal opening.
Type:
Grant
Filed:
May 30, 1989
Date of Patent:
April 3, 1990
Assignee:
Minnesota Mining and Manufacturing Company
Abstract: A process for preparing 6,7-dihydro-9-fluoro-5,8-dimethyl-1-oxo-1H,5H-benzo[i,j]quinolizine-2-carb oxylic acid, an antimicrobial, using 6-fluoro-2-methylquinoline as a starting material. A synthetic intermediate is also disclosed.
Type:
Grant
Filed:
November 4, 1988
Date of Patent:
February 6, 1990
Assignee:
Minnesota Mining and Manufacturing Company
Abstract: Organic fluoride sources comprising a tetrafluoroborate salt and capable of releasing fluoride ions into dentition in order to provide inhibition and/or prevention of dental caries are disclosed. A method of releasing fluoride ion into dental tissue is also disclosed.
Type:
Grant
Filed:
October 3, 1988
Date of Patent:
October 3, 1989
Assignee:
Minnesota Mining and Manufacturing Company
Inventors:
Steven M. Aasen, Joel D. Oxman, F. Andrew Ubel, III
Abstract: An ear tip for use with a stethoscope, audio headset or like device, the ear tip being of a construction and design that provides substantial deformation of the ear tip under normal stethoscope pressures such that in use the ear tip is seated comfortably and conformably against the ear canal opening.
Type:
Grant
Filed:
September 30, 1988
Date of Patent:
August 1, 1989
Assignee:
Minnesota Mining and Manufacturing Company
Abstract: The invention is a dispenser for use with aerosol formulations for inhalation therapy. The dispenser is small, conveniently carried, and features means to prevent unintended actuation of the aerosol canister and means to prevent dust and dirt from entering the dispenser during storage.
Type:
Grant
Filed:
May 12, 1988
Date of Patent:
May 30, 1989
Assignee:
Minnesota Mining and Manufacturing Company
Inventors:
David C. Byram, Gerald W. Teiken, Ralph D. Whaley
Abstract: Trifluoromethanesulfonamide and salts thereof are active as antiglaucoma agent and may be administered topically to the eye. Pharmaceutical formulations of such compounds are also described.
Abstract: Certain substituted pyridine compounds are useful synthetic intermediates for preparing compounds of pharmaceutical interest. A synthetic process for using these intermediates is also described.
Abstract: Certain substituted cyclopentanone ethylene ketal compounds, and ketones and amides derived therefrom are useful synthetic intermediates for compounds of pharmaceutical interest. A synthetic process for using the intermediates is also described.
Type:
Grant
Filed:
May 3, 1988
Date of Patent:
April 18, 1989
Assignee:
Minnesota Mining and Manufacturing Company
Abstract: Complete dissolution of a wide range of drugs in chlorofluorocarbon aerosol propellents is achieved by the presence of glycerol phosphatides, preferably phosphatidylcholine.
Type:
Grant
Filed:
November 10, 1986
Date of Patent:
March 21, 1989
Assignee:
Riker Laboratories, Inc.
Inventors:
Philip A. Jinks, Alexander Bell, Franz X. Fischer
Abstract: A method for preparing a stable aerosol formulation of beclomethasone dipropionate in which the steroid is contacted with an alcohol containing 1 to 5 carbon atoms to form a crystalline solvate therewith, the crystalline material so formed being reduced to a particle size below 10 microns and thereafter dispersed in a composition comprising chlorofluorocarbon propellents.
Abstract: A pressure-sensitive adhesive tape for delivering nitroglycerin to skin, the tape comprising a backing with a layer of inert pressure-sensitive adhesive attached thereto, said pressure-sensitive adhesive layer comprising a pressure-sensitive adhesive polymer, skin penetration-enhancing ingredients and a relatively high concentration of nitroglycerin. The tape is useful for systemic treatment of angina pectoris, control of hypertension and treatment of congestive heart failure.
Abstract: Substituted 1,2,4-triazolo[1,5-a]triazines as bronchodilators are disclosed. Pharmaceutical formulations comprising such compounds and pharmacological methods of using such compounds are also described.
Abstract: Novel compounds which are 2,6-di-t-butylphenols substituted on the 4 position by an anilino group, which anilino group is substituted by a group which includes carboxyl, tetrazolyl or N-methyltetrazolyl are useful as inhibitors of leukotriene synthesis and as antiallergic agents. Pharmaceutical compositions containing such compounds and pharmacological methods for use of such compounds are also disclosed.
Abstract: Novel antiallergic agents are described which are carboxy-substituted 3,5-di(tertiary-butyl)-4-hydroxybenzophenones. Pharmaceutical compositions containing and pharmacological methods for using such compounds are also described, as are synthetic intermediates for preparing such compounds.