Jozsef
Jozsef Aszodi, Tucson, AZ US
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20090215747 | HETEROCYCLIC COMPOUNDS AS INHIBITORS OF BETA-LACTAMASES - This invention discloses and claims methods for inhibiting bacterial β-lactamases and treating bacterial infections by inhibiting bacterial β-lactamases in man or an animal comprising administering a therapeutically effective amount to said man or said animal of a compound, or pharmaceutically acceptable salt thereof, of formula (I) either alone or in combination with a β-lactamine antibiotic wherein said combination can be administered separately, together or spaced out over time. Pharmaceutical compositions comprising a compound of formula (I), or a combination of a compound of formula (I) and a therapeutically effective amount of a β-lactamine antibiotic, and a pharmaceutically acceptable carrier are also disclosed and claimed. | 08-27-2009 |
20100048528 | HETEROCYCLIC COMPOUNDS AS INHIBITORS OF BETA-LACTAMASES - This invention discloses and claims methods for inhibiting bacterial β-lactamases and treating bacterial infections by inhibiting bacterial β-lactamases in man or an animal comprising administering a therapeutically effective amount to said man or said animal of a compound, or pharmaceutically acceptable salt thereof, of formula (I) either alone or in combination with a β-lactamine antibiotic wherein said combination can be administered separately, together or spaced out over time. Pharmaceutical compositions comprising a compound of formula (I), or a combination of a compound of formula (I) and a therapeutically effective amount of a β-lactamine antibiotic, and a pharmaceutically acceptable carrier are also disclosed and claimed. | 02-25-2010 |
20110021772 | New heterocyclic compounds, their preparation and their use as medicaments, in particular as anti-bacterial agents - The invention relates to new heterocyclic compounds of general formula (I), and their salts with a base or an acid: | 01-27-2011 |
20110213147 | New heterocyclic compounds, their preparation and their use as medicaments, in particular as anti-bacterial agents - The invention relates to new heterocyclic compounds of general formula (I), and their salts with a base or an acid: | 09-01-2011 |
20110245254 | HETEROCYCLIC COMPOUNDS AS INHIBITORS OF BETA-LACTAMASES - This invention discloses and claims methods for inhibiting bacterial β-lactamases and treating bacterial infections by inhibiting bacterial β-lactamases in man or an animal comprising administering a therapeutically effective amount to said man or said animal of a compound, or pharmaceutically acceptable salt thereof, of formula (I) either alone or in combination with a β-lactamine antibiotic wherein said combination can be administered separately, together or spaced out over time. Pharmaceutical compositions comprising a compound of formula (I), or a combination of a compound of formula (I) and a therapeutically effective amount of a β-lactamine antibiotic, and a pharmaceutically acceptable carrier are also disclosed and claimed. | 10-06-2011 |
Jozsef Bereznai, Budapest HU
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20090094789 | UNIVERSAL IMPACT-HINDER DEVICE - Universal impact-hinder device, comprising a body ( | 04-16-2009 |
20090166575 | Control Valve With Profiled Packing Element - Control valve with profiled packing element for making bidirectional flow-through with asymmetric intensity possible in a flow area. The packing element ( | 07-02-2009 |
20110053136 | TURNTABLE FOR SUPPORT OF LOADED SURFACES - A turntable for vertical support of substantially horizontal loaded surfaces, which has an upper and a lower half, between that it includes a vertical rotatable guiding element. A braking element ( | 03-03-2011 |
20110058796 | WATER HEATER ARRANGEMENT - A water heater arrangement comprising a gas-operated water heater device ( | 03-10-2011 |
20110297859 | PUSHBUTTON MECHANISM FOR MULTI-MEASURE CONTROLLING A FEEDER VALVE - The pushbutton mechanism comprises a lower part ( | 12-08-2011 |
20130131789 | DEVICE AND METHOD FOR BLOCKING PIPELINES, ESPECIALLY UNDER THE SEA - Transcorporal delivery system and method for valve replacement surgery that is minimally invasive. | 05-23-2013 |
20140284507 | AUXILIARY VALVE CONTROLLED SELF-CLEANING MAIN VALVE - Auxiliary valve controlled self-cleaning main valve with mechanical operating means. The valve body ( | 09-25-2014 |
20150211655 | VALVE ARRANGEMENT - Valve arrangement for ensuring different amount of medium flow-through comprising at least two chambers ( | 07-30-2015 |
Jozsef Borovszki, Budapest HU
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20150347802 | SYSTEMS AND METHODS FOR SORTING IMAGE ACQUISITION SETTINGS FOR PATTERN STITCHING AND DECODING USING MULTIPLE CAPTURED IMAGES - Systems and methods are described for acquiring and decoding a plurality of images. First images are acquired and then processed to attempt to decode a symbol. Contributions of the first images to the decoding attempt are identified. An updated acquisition-settings order is determined based at least partly upon the contributions of the first images to the decoding attempt. Second images are acquired or processed based at least partly upon the updated acquisition-settings order. | 12-03-2015 |
Jozsef Czege, Highland, MD US
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20090033938 | Process and apparatus for measurements of Mueller matrix parameters of polarized light scattering - A method and apparatus for measuring Mueller matrix parameters from scattered light. The apparatus is advantageous for use in countering bioterrorism by detecting information concerning airborne pathogens, particularly microorganism in aerosol form. The system provided is portable, more efficient, and less sensitive to wavelength changes. The method uses variation in retardation over wavelength as opposed to variation in retardation with time. | 02-05-2009 |
Jozsef Debreczeni, Budapest HU
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20120330018 | PROCESS FOR PREPARING PHARMACEUTICAL COMPOUNDS AND INTERMEDIATE COMPOUNDS - The object of the present invention is a process for preparing the 2-acetoxy-5-(2-fluor-α-cyclopropyl-carbonyl-benzyl)-4,5,6,7-tetrahydro-4H-tieno[3,2-c]pyridine (prasugrel) of the formula (I). The process starts form crystalline 5-trityl-4,5,6,7-tetrahydro-tieno[3,2-c]pyridine of the formula (VI). Further objects of the present invention are two novel crystalline forms of 5-trityl-4,5,6,7-tetrahydro-tieno[3,2-c]pyridine of the formula (VI) and the use thereof for preparing the compound of the formula (V) and process preparing thereof. | 12-27-2012 |
20130005790 | INORGANIC SALT COMPLEXES OF VILDAGLIPTIN - The present invention relates to the use of novel vildagliptin complexes for the manufacture of high purity vildagliptin of Formula I and/or pharmaceutical acceptable salts thereof. Further objects of the present invention are pharmaceutically acceptable complexes of vildagliptin and/or amorphous and crystalline forms, anhydrous forms, amorphous and crystalline hydrates, amorphous and crystalline solvates of the complexes and a process for the preparation thereof. Another object of the present invention is the high purity vildagliptin and pharmaceutically acceptable salts thereof prepared form the vildagliptin complexes of the present invention, a process for the preparation thereof and pharmaceutical compositions containing vildagliptin base, pharmaceutically acceptable salts and/or complexes and use thereof for the treatment of type 2 diabetes (NIDDM). The present invention provides pharmaceutically advantageous high purity vildagliptin complexes. | 01-03-2013 |
20130030183 | PROCESS FOR PREPARING A PHARMACEUTICAL COMPOUND - The object of the present invention is a one-pot process for preparing the 2-acetoxy-5-(2-fluoro-α-cyclopropyl-carbonyl-benzyl)-4,5,6,7-tetrahydro-4H-tieno[3,2-c]-pyridine (prasugrel) of the formula (I) by reacting the 5,6,7,7a-tetrahydro-4H-tieno[3,2-c]-pyridine-2-on of the formula (II) with 2-bromo-1-cyclopropyl-2-(2-fluorophenyl)-etanone of the formula (III) or with 2-chloro-1-cyclopropyl-2-(2-fluorphenyl)-etanone of the formula (IIIa) and acetylating of the formed compound of the formula (IV), wherein the reaction is carried out in the presence of an organic base with an acetylation agent without isolating the compound of the formula (IV). The coupling and acetylation are carried out in the presence of the same organic base such as triethylamine, N,N-diisopropyl-ethylamine or pyridine. At the end of the process the prasugrel of the formula (I) is purified by recrystallization from an organic solvent or a mixture of solvents. | 01-31-2013 |
20130281694 | METHOD FOR PREPARING ROSUVASTATIN SALTS - The present invention is related to methods for the preparation of pharmaceutically acceptable salts of (+)-7-[4-(4-fluorophenyl)-6-isopropyl-2-(methanesulfonyl-methyl-amino)-pyrimidin-5-yl]-(3R,5S,6E)-dihydroxy-hept-6-enoic acid, intermediates thereof and methods for producing said intermediates. | 10-24-2013 |
Jozsef Dombi, Szeged HU
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20120129505 | GENERATING RELATIONAL INDICATORS BASED ON ANALYSIS OF TELECOMMUNICATIONS EVENTS - A system for generating a relational indicator based on analysis of at least one telecommunications event between a first party and a second party, comprises: a relation management engine which is configured to process first content characteristics extracted from a plurality of telecommunications events to produce a first relation parameter and to process second content characteristics extracted from the plurality of telecommunications events to produce a second relation parameter; a terminal device configured to use the first and second relation parameters to generate the relational indicator. | 05-24-2012 |
Jozsef Felfoldi, Debrecen HU
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20080197141 | Drinking Straw - The invention relates to a drinking straw which is sealed and/or re-sealable at the ends and which can serve as a supply container for a dry food product or which can comprise multiple parts, and to its use. | 08-21-2008 |
Jozsef Fetter, Goedoelloe HU
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20120252784 | 2,3,4-BENZOTHIADIAZEPINE-2,2-DIOXIDE DERIVATIVES - Novel 2,3,4-benzothiadiazepines-2,2-dioxides and processes for the preparation thereof are disclosed. The compounds influence the central nervous system and may be used to treat or prevent Alzheimer's disease, Parkinson's disease or Huntington's disease, senile dementia not of the Alzheimer's type, vascular dementia, post-stroke dementia, Korsakoff's syndrome, Down's syndrome, schizophrenia, panic disorder, post-traumatic stress disorder, anxiety or depression. | 10-04-2012 |
Jozsef Gallai, Budapest HU
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20120170297 | REFLECTOR LAMP USED AS DAYTIME RUNNING LAMP - An automotive daytime running lamp assembly includes an incandescent light source received within a reflector member. The reflector member is formed as a surface of revolution about a longitudinal axis and has an enlarged, first end, and a narrowed, second end with an opening that receives at least a portion of a light source therethrough along the longitudinal axis. A sleeve is received over a portion of the light source and at least partially extends through the reflector member opening. A cap received over the second end of the reflector member about the opening is fixedly secured to a disk, preferably by fusing or welding the components together. Likewise, the disk and metal sleeve are fixedly secured or fused/welded together so that the light source is fixed relative to the reflector member. A mounting member is provided for secure optical positioning of the assembly in a fixture of the associated automotive vehicle. | 07-05-2012 |
20130051058 | OPTICALLY ADJUSTABLE LIGHT MODULE - An optically adjustable light module, such as a daytime running lamp of a motor vehicle, includes a light source (e.g., including an LED) which is rotatable about a rotational axis and has an optical axis. An arm is connected to the light source such that movement of the arm enables rotation of the light source and adjustment of the optical axis. | 02-28-2013 |
20130155707 | ANISOTROPIC INCANDESCENT LIGHT SOURCE - An improved incandescent light source as may be used in a vehicle headlamp for providing forward illumination. The illuminating system includes a filament coil and an anisotropic reflector assembly. The filament coil is constructed from a coil of wire that is electrically conductive and has a high melting point and the primary axis of the coil of wire is substantially aligned with a principal axis of the reflector system. The light flux emitted by the filament coil toward the reflector system is rotationally anisotropic. | 06-20-2013 |
Jozsef Imrek, Debrecen HU
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20090281810 | SYSTEM AND METHOD FOR VISUALLY PRESENTING AUDIO SIGNALS - A method of visually presenting audio signals includes receiving an audio signal to be presented; generating a predetermined number of discrete frequency components from the audio signal; assigning a graphical object to each of the frequency components, each of the graphical objects being specified by a geometrical shape, a position information and a size information; and all of the graphical objects associated with all of the frequency components are displayed simultaneously on a graphic display. The system includes a microphone for generating audio signals; an audio interface unit for sampling the audio signals and transforming them into digital signals; a processing unit for translating digital signals into a predetermined number of discrete frequency components and for assigning a graphical object to each of the discrete frequency components; a video interface unit for generating a video signal; and a graphic display for displaying a sonogram based on the video signal. | 11-12-2009 |
Jozsef Karman, Bridgewater, NJ US
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20140348832 | INHIBITORS OF T-CELL ACTIVATION - The present invention provides a bispecific biologic comprising a ligand specific for CTLA-4 and a ligand specific for a pMHC complex. | 11-27-2014 |
Jozsef Kiraly, Toszeg HU
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20090126821 | HIGH-PRESSURE RUBBER HOSE AND METHOD AND APPARATUS FOR PRODUCING THE SAME - The object of the invention is a high-pressure rubber hose comprising a liner ( | 05-21-2009 |
Jozsef Kis-Benedek, Budapest HU
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20110136663 | METHOD AND APPARATUS FOR SORBENT PRODUCTION, PRIMARILY FOR REMOVING ARSENIC FROM DRINKING WATER - The object of the invention is method and apparatus for sorbent production. The method comprises the steps of saturating a moisture-absorbent, wettable organic support material with the aqueous solution of a water-soluble ferric salt, then filtering it and drying it to constant weight; saturating the support material with a stoichiometric quantity (computed relative to the iron content of the support material) of oxalic acid and/or water-soluble salt of oxalic acid, then filtering it and drying it to constant weight, while converting the iron ions to insoluble ferric oxalate; converting the saturated support material to activated carbon by anaerobic heating, then subjecting said saturated support material to anaerobic cooling, while the ferric oxalate is decomposed into iron and carbon dioxide; preoxidizing iron particles of the activated carbon by a water-soluble peroxide compound, filtering the activated carbon, and rinsing it to completely remove salt therefrom, then filtering it again and drying it; converting the iron hydroxide formed on the surface of the iron particles into magnetite by anaerobic heating of the activated carbon, and subsequently cooling in an anaerobic manner the thus produced sorbent to room temperature. | 06-09-2011 |
Jozsef Kovecses, Saint-Bruno CA
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20150127091 | DEVICE FOR SOFT TISSUE SUPPORT AND METHOD FOR ANCHORING - A device for supporting soft tissue comprises a tubular body and is constituted of a sequence of compliant portions and anchoring portions. The anchoring portions each comprise anchor members adapted to penetrate into soft tissue. The compliant portions each comprise deformable members extending between ends of the compliant portion, at least one of a distance and orientation between said ends being adjustable by application of a force on the tubular body. The tubular body comprises a ring-like shape reached at least by deformation of the compliant portions, the ring-like shape having the anchor members of the anchoring portions protruding circumferentially along a direction defined by a vector having a component being at least tangential to the curve of the ring-like shape, for the retaining members to penetrate the soft tissue. A method for anchoring the device to soft tissue is also provided. | 05-07-2015 |
Jozsef Mandzsu, Jr., Fot HU
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20120225200 | METHODS FOR MAKING FASTENERS - Methods of forming fasteners are disclosed. One method comprises dispersing polymer particles into a contact release surface, transforming the polymer particles into an at least semiliquid state of a suitable viscosity for a time sufficient to transform into preform projections having contact edges, contacting and fixing a front surface of the base with the terminal ends of at least some of the preform projections, removing the base, thereby separating the preform projections, from the release surface, and forming engaging projections projecting from the front surface of the base. | 09-06-2012 |
Jozsef Mandzsu, Sr., Budapest HU
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20120225200 | METHODS FOR MAKING FASTENERS - Methods of forming fasteners are disclosed. One method comprises dispersing polymer particles into a contact release surface, transforming the polymer particles into an at least semiliquid state of a suitable viscosity for a time sufficient to transform into preform projections having contact edges, contacting and fixing a front surface of the base with the terminal ends of at least some of the preform projections, removing the base, thereby separating the preform projections, from the release surface, and forming engaging projections projecting from the front surface of the base. | 09-06-2012 |
Jozsef Margitfalvi, Budapest HU
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20140336411 | CATALYST FOR THE OXIDATION OF HYDROCARBONS CONSISTING OF MOLYBDENUM, VANADIUM, NIOBIUM, TELLURIUM, MANGANESE AND COBALT - A catalyst material for the oxidation and/or oxidative dehydrogenation of hydrocarbons, in particular for the selective oxidation of propane to acrylic acid, comprising a) molybdenum (Mo), b) vanadium (V), c) niobium (Nb), d) tellurium (Te), e) manganese (Mn) and cobalt, in which the molar ratio of at least one element, which is selected from manganese and cobalt, to molybdenum lies in the range 0.01 to 0.2. Furthermore, a catalyst for the oxidation and/or oxidative dehydrogenation of hydrocarbons, a use of the catalyst material or of the catalyst, a method for producing a catalyst material for the oxidation and/or oxidative dehydrogenation of hydrocarbons, and a method for the selective oxidation of propane to acrylic acid. | 11-13-2014 |
20150148563 | Catalyst Material for the Oxidation of Hydrocarbons - A catalyst material for the oxidation and/or oxidative dehydrogenation of hydrocarbons, in particular for the selective oxidation of propane to acrylic acid, is specified, comprising a) molybdenum (Mo), b) vanadium (V), c) niobium (Nb), d) tellurium (Te), e) nickel (Ni), f) tungsten (W) and g) manganese (Mn), in which the molar ratio of at least one element, which is selected from nickel, tungsten and manganese, to molybdenum lies in the range 0.01 to 0.2, more preferably 0.05 to 0.15 and particularly preferably from 0.0025:1 to 0.3:1. Furthermore, a catalyst for the oxidation and/or oxidative dehydrogenation of hydrocarbons, a use of the catalyst material or of the catalyst, a method for producing a catalyst material for the oxidation and/or oxidative dehydrogenation of hydrocarbons and a method for the selective oxidation of propane to acrylic acid is specified. | 05-28-2015 |
Jozsef Miklosi, Budapest HU
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20080262648 | DEMAND-DRIVEN SALES MODEL CAPITALIZING ON THE POWER OF ONLINE COMMUNITY - The business method according to the present invention concerns with spatially distributed configurable vending machines and their network, especially those which produce FMCG products, like beverages, hot drinks, cocktails, soups, soaps, perfumes, etc. The configurable vending machine can produce products in different phase, proportion, appearance, look and feel, etc. regarding its configuration set up. The different configurations are generally called recipe, formula which are stored in files in Internet servers. These files can be accessed by authorized persons, who can modify, delete, create new and share with other authorized users via an Internet based online community portal. The invention describes how the configurable vending machines and its network can be managed and the communication among consumers, resellers and franchise owner. The IT back office system automatically organizes product development, market survey, marketing communication, and logistics processes and serve information about actual trends, consumption, stock status in real-time. Variety of advantages are obtained by using the method invented, like a higher integration among B2C, B2B and C2C domains (processes) yielding shorter product development cycles, lower sales and development costs, and better market knowledge. | 10-23-2008 |
20130123084 | EQUIPMENT FOR IMPROVING PHYSICAL FITNESS - The invention discloses an equipment for improving physical fitness, whose primary aspect is muscle strengthening. Another objective of the invention, besides maximizing muscle development, is to minimize the risk of injury during and after practices. The invention has a comfortable, tailor-made design shell ( | 05-16-2013 |
Jozsef Nyarady, Pecs HU
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20080312545 | METHOD AND DEVICE FOR MEASURING BLOOD FLOW IN THE BONE AFTER A FRACTURE - A method and device for measuring blood flow in the bone after a fracture, wherein a hole is drilled into the bone. The method includes the steps of inserting the metal sleeve of an osteoscope into the hole; inserting the optics of an osteoscope into the metal sleeve and focused on the cavity created by the drill; filling the device and the cavity with a physiological solution such that the pressure of the solution is above the systolic blood pressure; decreasing the pressure of the solution while observing the cavity through the osteoscope, and recording the pressure in the system at the commencement of bleeding. | 12-18-2008 |
Jozsef Patvarczki, Framingham, MA US
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20120005483 | Method for Image-Based Authentication - A method for authenticating user access to a restricted resource that presents a login screen with an image separated into sections. To login, the user triggers sections in a preset sequence that is set up at account creation. At account creation, a cryptographic hash function is applied to a chosen sequence of sections to generate the user's account code. Optionally, elements of the image and/or the user name are included. The user invokes the login screen when access to a restricted resource is desired. The user must change login settings if any parameters, such as a particular image, are elements of the account code. The user triggers the sections in the appropriate order. The cryptographic hash function is applied to the section sequence and any optional elements to generate the login code, which is compared to the stored account codes to either grant or deny access to the restricted resource. | 01-05-2012 |
20130073865 | Identifying peers by their interpersonal relationships - According to this disclosure, a user is identified (and selectively granted access to protected resources) by using information that describes the user's interpersonal relationships. This information typically is stored in a datastore, such as a digital address book, an online profile page, or the like. The user's digital address book carries an “acquaintance pattern” that changes dynamically in time. This pattern comprises the information in the user's contact list entries. In this approach, the entropy inherent in this information is distilled into a unique acquaintance digest (or “fingerprint”) by normalizing the contact list data, and then applying a cryptographic function to the result. | 03-21-2013 |
Jozsef Patvarczki, San Bruno, CA US
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20140013446 | Method and System for Providing Presence Information - A system and method for a user to send presence information to authorized contacts in her device's address book and to receive the presence information of those contacts in her device's address book that have authorized her. A user can authorize any contact in her address book. Optionally, a user can only authorize a contact and be authorized by a contact if she is in that contact's address book. A local application on the device interacts with and displays the device's address book, manages the authorization of contacts, updates the user's presence, and receives and displays the presence of contacts. The local application updates the user's presence manually, semi-automatically, or automatically. Semi-automatic updates involve synchronizing with the device's calendar. Automatic updates may involve the use of location data, the device's built-in sensors, and augmented reality. | 01-09-2014 |
Jozsef Patvarczki, Sunnyvale, CA US
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20140089412 | Method and System for Connecting People in a Social Network - A system and method for connecting people in a social network using information from a user's digital address book. A social network member can unilaterally friend any contact in her address book. Optionally, a member can only friend a contact and be friended by a contact if she is in that contact's address book. An central server keeps track of friended members of the social network and contacts. | 03-27-2014 |
20150046999 | Identifying peers by their interpersonal relationships - According to this disclosure, a user is identified (and selectively granted access to protected resources) by using information that describes the user's interpersonal relationships. This information typically is stored in a datastore, such as a digital address book, an online profile page, or the like. The user's digital address book carries an “acquaintance pattern” that changes dynamically in time. This pattern comprises the information in the user's contact list entries. In this approach, the entropy inherent in this information is distilled into a unique acquaintance digest (or “fingerprint”) by normalizing the contact list data, and then applying a cryptographic function to the result. | 02-12-2015 |
20150120850 | Method and System for Providing Presence Information - A system and method for a user to send presence information to authorized contacts in her device's address book and to receive the presence information of those contacts in her device's address book that have authorized her. A user can authorize any contact in her address book. Optionally, a user can only authorize a contact and be authorized by a contact if she is in that contact's address book. A local application on the device interacts with and displays the device's address book, manages the authorization of contacts, updates the user's presence, and receives and displays the presence of contacts. The local application updates the user's presence manually, semi-automatically, or automatically. Semi-automatic updates involve synchronizing with the device's calendar. Automatic updates may involve the use of location data, the device's built-in sensors, and augmented reality. | 04-30-2015 |
Jozsef Petrovics, Leonberg DE
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20160052553 | STIFFENING ARRANGEMENT FOR A FORWARD STRUCTURE OF A MOTOR VEHICLE - A stiffening arrangement ( | 02-25-2016 |
Jozsef Repasi, Budapest HU
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20080293761 | Pyrrolopyridine-2-Carboxylic Acid Amide Derivative Useful as Inhibitor of Glycogen Phosphorylase - The present invention is directed to a novel form of a pyrrolopyridine-2-carboxylic acid amide of formula (I), which is an inhibitor of glycogen phosphorylase, compositions containing it and their use in therapy. The invention is also directed to processes for production of the novel form, novel intermediates used in said processes and processes for the production of said intermediates. | 11-27-2008 |
20100267988 | PROCESSES FOR PREPARING INTERMEDIATE COMPOUNDS USEFUL FOR THE PREPARATION OF CINACALCET - The invention relates, in general, to an improved process for preparing compounds (e.g., 3-(3-trifluoromethylphenyl)propanal (Compound III, below)), which are key intermediates for the synthesis of cinacalcet, its salts and/or solvates thereof, as well as the use of such compounds prepared by such process for the preparation of cinacalcet and/or its salts or solvates. | 10-21-2010 |
20110295037 | PROCESSES FOR PREPARING CINACALCET HYDROCHLORIDE AND POLYMORPHIC FORMS THEREOF - The invention relates to cinacalcet hydrochloride, new polymorphic crystalline forms of cinacalcet hydrochloride, amorphous cinacalcet hydrochloride and synthetic processes for their preparation. | 12-01-2011 |
Jozsef Samu, Budapest HU
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20140347868 | PIVOTING HEAT SINK FOR LED LUMINAIRE - An LED luminaire assembly which allows for the easy and safe removal and replacement of the PSU and other internal components wherein the heat sink can be folded or pivoted aside to allow access to and removal of the PSU. | 11-27-2014 |
Jozsef Simulak, Hajdusamson-Samsonkert HU
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20090082386 | Ascomycin and pimecrolimus having reduced levels of desmethylascomycin and 32-deoxy-32-epichloro-desmethylascomycin respectively, and methods for preparation thereof - Provided is ascomycin that has a low level of an FK523 impurity, and pimecrolimus that has a low level of a 32-deoxy-32-epichloro-FK523 impurity, methods of preparing them, and the use of such pimecrolimus for preparing a pharmaceutical composition. | 03-26-2009 |
Jozsef Sternbach, Scardale, NY US
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20110208235 | Pedi-Massaggio - This invention, Pedi-Massaggio , enables anyone to benefit from the stimulating effects of a walk on a pebble beach in the comfort of their home (shower) via the stimulating effects of the sole of the feet. | 08-25-2011 |
Jozsef Sternbach, Scarsdale, NY US
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20110214360 | GUTTER CLAW - This invention, ‘The Gutter Claw’, enables a typical do-it-yourself home or business property owner to more easily maintain and upkeep a rooftop gutter run-off system. By adding ‘The Gutter Claw’ to all down pipes/leader pipes (drainage down pipes that typically get clogged below ground due to seasonal debris accumulation), removal of debris from within the down pipe can be done more easily and conveniently. There an many advantages to the application of this invention, including where it can be located on any given down pipe at eye level, which works well with the easy remove and replace features on the molded parts' design. | 09-08-2011 |
20110222985 | Wing Wall Anchor - Essentially this invention the Wing Wall Anchor is unique because the wings are opened parallel to the wall by the spring which is riveted between the by the nut/rivet connector. The spring opens the wings even when they are adjacent to a stud a corner wall. Also because of the size, length, width, gauge, they are able to hold more securely and require substantially less backspace and a 50% shorter bolt than similar anchors. | 09-15-2011 |
20110226798 | Vita-Spence - Essentially this invention, the Vita-Spence will aid the consumer in tracking the consumption of vitamins or pills each day for one or two week intervals. It will also eliminate the daily drudge of opening and closing of two to ten jars daily as well as the aforementioned benefits to large number vitamin and pill takers, especially among the elderly people with slightly diminished capabilities. | 09-22-2011 |
Jozsef Szejtli, Budapest HU
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20080287553 | PHARMACEUTICAL COMPOSITIONS COMPRISING PERANHYDROCYCLODEXTRIN - The present invention relates to a pharmaceutical composition comprising a peranhydrocyclodextrin, a drug and a carrier, to the use of a peranhydrocyclodextrin as a drug transport enhancer (e.g. permeation enhancer), and to the use of a peranhydrocyclodextrin in the preparation of a pharmaceutical composition as a synergistic adjunctive system. | 11-20-2008 |
20080299166 | NOVEL BIOMATERIALS, THEIR PREPARATION AND USE - The present invention relates to novel materials, particularly biomaterials, in form of a precipitate, comprising at least an anionic polymeric component which is as such soluble in water and an amphiphilic ammonium-type component, which precipitate is obtainable by a process including the following steps: | 12-04-2008 |
20090110734 | QUATERNISED AMMONIUM CYCLODEXTRIN COMPOUNDS - Use of a compound of formula (I): | 04-30-2009 |
20100056476 | PHARMACEUTICAL COMPOSITIONS COMPRISING PERANHYDROCYCLODEXTRIN - The present invention relates to a pharmaceutical composition comprising a peranhydrocyclodextrin, a drug and a carrier, to the use of a peranhydrocyclodextrin as a drug transport enhancer (e.g. permeation enhancer), and to the use of a peranhydrocyclodextrin in the preparation of a pharmaceutical composition as a synergistic adjunctive system. | 03-04-2010 |
20120004158 | Quaternised Ammonium Cyclodextrin Compounds - Use of a compound of formula (I): | 01-05-2012 |
20120040901 | NOVEL BIOMATERIALS, THEIR PREPARATION AND USE - The present invention relates to novel materials, particularly biomaterials, in form of a precipitate, comprising at least an anionic polymeric component which is as such soluble in water and an amphiphilic ammonium-type component, which precipitate is obtainable by a process including the following steps: | 02-16-2012 |
20130137657 | QUATERNISED AMMONIUM CYCLODEXTRIN COMPOUNDS - Use of a compound of formula (I): | 05-30-2013 |
Jozsef Szelei, Mont-Saint-Hilaire CA
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20140017223 | Pharmaceutical Compositions Comprising A Pancreatic Enzyme Preparation With Viral Infectivity Reduced Below A Significant Level And Methods Of Preparing And Using The Same - The present invention provides for pharmaceutical compositions comprising pancreatic enzyme preparations (PEPs) with viral infectivity reduced below significant levels and having high enzymatic activity. The PEPs can comprise lipases, proteases, amylases, non-enveloped viruses (e.g., porcine parvovirus (PPV), porcine circovirus type 2 (PCV-2), porcine encephalomyocarditis virus (EMCV)), and enveloped viruses (e.g., vesicular stomatitis virus (VSV), and influenza A (IFA)). The present invention also includes methods of treating pancreatic insufficiency by administering these pharmaceutical compositions and methods of making the same by treating the PEP with beta-propiolactone (BPL) to reduce viral infectivity. | 01-16-2014 |
Jozsef Szelei, Laval CA
Jozsef Torley, Budapest HU
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20090111988 | NOVEL PROCESS FOR PRODUCTION OF 5--6-CHLORO-1,3-DIHYDRO-2H-INDOL-2-ONE (ZIPRASIDONE) - The present invention provides a novel, industrially easily realisable and economically preferable process for production of pure 5-{2-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]-ethyl}-6-chloro-1,3-dihydro-2H-indol-2-one i.e., ziprasidone hydrochloride shown in the reaction scheme (II), (III), (IV), (V) and (VI). According to the invention the intermediate compound 5-(2-bromoethyl)-6-chloro-1,3-dihydro-2H-indol-2-one of Formula (III) is produced from 5-(2-bromoacethyl)-6-chloro-1,3-dihydro-2H-indole-2-one of Formula (IV). The highly pure ziprasidone base of Formula (II) is obtained in the reaction of 3-piperazinyl-1,2-benzisothiazol of Formula (VI) with 5-(2-bromoethyl)-6-chloro-1,3-dihydro-2H-indol-2-one of Formula (III) in an organic solvent or organic solvent mixture. | 04-30-2009 |
Jozsef Vacity, Alkotmany U. HU
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20080245833 | Clothes Hanging Device For Transporting Clothes in a Passenger Vehicle - A clothes hanging for the comfortable transportation of articles of clothing within the interior of a passenger vehicle behind the back and head rests of the seat, includes of a clothes hanger body mounted in fixed fashion to a clothes hanger supporting rod, the lower end of the clothes hanger supporting rod is inserted into a matching fitting. The matching fitting is a pipe-like body of rectangular cross-section with an open upper end, which is built directly, in fixed fashion, into the back rest, at the middle part of the upper end of the back rest of the seat, into which the lower end of the clothes hanger supporting rod, also of rectangular cross-section is inserted with a direct contact, a hook to accommodate the placement of further conventional clothes hangers is mounted to the upper end of the clothes hanger supporting rod that projects beyond the clothes hanger body. | 10-09-2008 |
Jozsef Vizkeleti, Szolnok HU
József BÁlint, Berlin DE
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20120202810 | SUBSTITUTED 4-AMINOCYCLOHEXANE DERIVATIVES - The invention relates to compounds that have an affinity to the μ-opioid receptor and the ORL 1-receptor, methods for their production, medications containing these compounds and the use of these compounds for the treatment of pain and other conditions. | 08-09-2012 |
József Barcoczy, Budapest HU
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20100075975 | MEDICAMENT FOR THE ENHANCEMENT OF COGNITIVE FUNCTION AND NEUROPROTECTION - The invention relates the use of 4-chloro-5-{2-[4-(6-fluoro-1,2-benz[d]isoxazole-3-yl)piperidin-1-yl]ethyl-amino}-2-methyl-3-(2H) pyridazinone of the Formula (I) | 03-25-2010 |
József Barcoczy, Budapest HU
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20100075975 | MEDICAMENT FOR THE ENHANCEMENT OF COGNITIVE FUNCTION AND NEUROPROTECTION - The invention relates the use of 4-chloro-5-{2-[4-(6-fluoro-1,2-benz[d]isoxazole-3-yl)piperidin-1-yl]ethyl-amino}-2-methyl-3-(2H) pyridazinone of the Formula (I) | 03-25-2010 |
József Barkóczy, Budapest HU
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20090281137 | INDOL-2-ONE DERIVATIVES FOR THE TREATMENT OF CENTRAL NERVOUS DISORDERS, GASTROINTESTINAL DISORDERS AND CARDIOVASCULAR DISORDERS - The present invention is related to new 3,3-disubstituted indol-2-one derivatives of the general Formula (I) | 11-12-2009 |
20090306144 | PYRIDINE DERIVATIVES OF ALKYL OXINDOLES AS 5-HT7 RECEPTOR ACTIVE AGENTS - New 3,3-disubstituted indol-2-one derivatives of the general formula (I) | 12-10-2009 |
20110040093 | PROCESS FOR THE PREPARATION OF PHARMACEUTICAL INTERMEDIATE - The invention relates to a process for the preparation of compounds of general formula (III), wherein R represents fluorine or chlorine atom and X represents chlorine or bromine atom, by halogenation of cyclopropyl benzyl ketone of general formula (II), wherein R represents fluorine or chlorine atom and the halogenation is carried out in the mixture of aqueous hydrogen halide and aqueous hydrogen peroxide in the presence of a water miscible solvent or in the presence of a phase transfer catalyst; or the halogenation is carried out in the mixture of sulfuric acid and an alkali metal salt of aqueous hydrogen halide. The process can be applied preferably on industrial scale. | 02-17-2011 |
20120232065 | DIHYDRO-OXAZOLOBENZODIAZEPINONE COMPOUNDS, A PROCESS FOR THERE PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM - Compounds of formula (I): | 09-13-2012 |
20120330018 | PROCESS FOR PREPARING PHARMACEUTICAL COMPOUNDS AND INTERMEDIATE COMPOUNDS - The object of the present invention is a process for preparing the 2-acetoxy-5-(2-fluor-α-cyclopropyl-carbonyl-benzyl)-4,5,6,7-tetrahydro-4H-tieno[3,2-c]pyridine (prasugrel) of the formula (I). The process starts form crystalline 5-trityl-4,5,6,7-tetrahydro-tieno[3,2-c]pyridine of the formula (VI). Further objects of the present invention are two novel crystalline forms of 5-trityl-4,5,6,7-tetrahydro-tieno[3,2-c]pyridine of the formula (VI) and the use thereof for preparing the compound of the formula (V) and process preparing thereof. | 12-27-2012 |
20130030183 | PROCESS FOR PREPARING A PHARMACEUTICAL COMPOUND - The object of the present invention is a one-pot process for preparing the 2-acetoxy-5-(2-fluoro-α-cyclopropyl-carbonyl-benzyl)-4,5,6,7-tetrahydro-4H-tieno[3,2-c]-pyridine (prasugrel) of the formula (I) by reacting the 5,6,7,7a-tetrahydro-4H-tieno[3,2-c]-pyridine-2-on of the formula (II) with 2-bromo-1-cyclopropyl-2-(2-fluorophenyl)-etanone of the formula (III) or with 2-chloro-1-cyclopropyl-2-(2-fluorphenyl)-etanone of the formula (IIIa) and acetylating of the formed compound of the formula (IV), wherein the reaction is carried out in the presence of an organic base with an acetylation agent without isolating the compound of the formula (IV). The coupling and acetylation are carried out in the presence of the same organic base such as triethylamine, N,N-diisopropyl-ethylamine or pyridine. At the end of the process the prasugrel of the formula (I) is purified by recrystallization from an organic solvent or a mixture of solvents. | 01-31-2013 |
József Barkóczy, Budagpest HU
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20120108607 | OPTICALLY ACTIVE 3-[(PHENYLPIPERAZIN-1-YL)ALKYL]-3- ALKYL-OXINDOLE DERIVATIVES HAVING CNS ACTIVITY - The present invention relates to the enantiomers of 5,7-dichloro-3-{4-[4-(4-chlorophenyl)-piperazin-1-yl]butyl}-3-ethyl-1,3-dihydro-2H-indol-2-one of the Formula (II) pharmaceutically acceptable salts thereof, process for the preparation thereof, medicinal products containing said enantiomers and the use thereof and their pharmaceutically acceptable salts in the treatment of the disorders of the central nervous system. | 05-03-2012 |
József Bereznai, Budapest HU
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20120233756 | GRAVITY OPERATED MECHANICAL FLUSHING APPARATUS - The invention relates to a gravity operated mechanical flushing apparatus, which is operated without any external power source. A weight sensing element ( | 09-20-2012 |
20130131789 | DEVICE AND METHOD FOR BLOCKING PIPELINES, ESPECIALLY UNDER THE SEA - Transcorporal delivery system and method for valve replacement surgery that is minimally invasive. | 05-23-2013 |
József Bódi, Budapest HU
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20080200668 | Industrial Process for the Preparation of 17-Hydroxy-6Beta, 7Beta; 15Beta, 16Beta-Bismethylene-3-Oxo-17Alpha-Pregn-4-Ene-21-Carboxylic Acid Y-Lactone and Key Intermediates for this Process - The invention relates to an industrial process for the preparation of 17-hydroxy-6β,7β;15β,16β-bismethylene-3-oxo-17α-pregn-4-ene-21-carboxylic acid γ-lactone of formula (I), and to the key-intermediates for this process. | 08-21-2008 |
20090216009 | PROCESS FOR THE PRODUCTION OF EZETIMIBE AND INTERMEDIATES USED IN THIS PROCESS - An industrially easily realizable and economical process comprising only few steps, and built on new intermediates for the production of 1-(4-3(R)-[3(S)-(4-fluorophenyl)-3-hydroxypropyl]-4(S)-(4-hydroxyphenyl)-2-azetidinone (ezetimibe) according to the reaction scheme described herein. | 08-27-2009 |
20100137622 | INDUSTRIAL METHOD FOR THE SYNTHESIS OF 17-ACETOXY-11beta-[4-(DIMETHYLAMINO)-PHENYL]-21-METHOXY-19-NORPREGNA-4,9-- DIEN-3,20-DIONE AND THE KEY INTERMEDIATES OF THE PROCESS - The present invention relates to a process for the synthesis of the known 17-acetoxy-11-β-[4-(dimethyl amino)-phenyl]-21-methoxy-19-norpregna-4,9-dien-3,20-dione (further on CDB-4124) of formula (I) from 3,3-[1,2-ethandiyl-bis(oxy)]-oestr-5(10),9(11)-dien-17-one of formula (II). Compound CDB-4124 belongs to the group of anti-hormones. The process has the following steps: i) formation of an epoxide; ii) addition of hydrogen cyanide; iii) silylation of a hydroxyl group; iv) reaction with 4-(dimethylamino)-phenyl magnesium bromide Grignard reagent in the presence of CuCl (Teutsch reaction); v) silylation of a hydroxyl group with trimethyl chlorosilane; vi) reaction with diisobutyl aluminum hydride and after addition of acid to the reaction mixture; vii) methoxy-methylation with methoxy-methyl Grignard reagent formed in situ, while hydrolyzing the trimethylsilyl protective groups; viii) oxidation of a hydroxyl group with dicyclohexyl carbodiimide in the presence of dimethyl sulfoxide and a strong organic acid (Swern oxidation), and in given case after purification by chromatography; ix) acetylation of a hydroxyl group with acetic anhydride in the presence of perchloric acid, and in given case, purification by chromatography. The invention also relates to new intermediates of the process. | 06-03-2010 |
József Bódi, Budapest HU
Patent application number | Description | Published |
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20100137622 | INDUSTRIAL METHOD FOR THE SYNTHESIS OF 17-ACETOXY-11beta-[4-(DIMETHYLAMINO)-PHENYL]-21-METHOXY-19-NORPREGNA-4,9-- DIEN-3,20-DIONE AND THE KEY INTERMEDIATES OF THE PROCESS - The present invention relates to a process for the synthesis of the known 17-acetoxy-11-β-[4-(dimethyl amino)-phenyl]-21-methoxy-19-norpregna-4,9-dien-3,20-dione (further on CDB-4124) of formula (I) from 3,3-[1,2-ethandiyl-bis(oxy)]-oestr-5(10),9(11)-dien-17-one of formula (II). Compound CDB-4124 belongs to the group of anti-hormones. The process has the following steps: i) formation of an epoxide; ii) addition of hydrogen cyanide; iii) silylation of a hydroxyl group; iv) reaction with 4-(dimethylamino)-phenyl magnesium bromide Grignard reagent in the presence of CuCl (Teutsch reaction); v) silylation of a hydroxyl group with trimethyl chlorosilane; vi) reaction with diisobutyl aluminum hydride and after addition of acid to the reaction mixture; vii) methoxy-methylation with methoxy-methyl Grignard reagent formed in situ, while hydrolyzing the trimethylsilyl protective groups; viii) oxidation of a hydroxyl group with dicyclohexyl carbodiimide in the presence of dimethyl sulfoxide and a strong organic acid (Swern oxidation), and in given case after purification by chromatography; ix) acetylation of a hydroxyl group with acetic anhydride in the presence of perchloric acid, and in given case, purification by chromatography. The invention also relates to new intermediates of the process. | 06-03-2010 |
József Debreczeni, Budapest HU
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20120330018 | PROCESS FOR PREPARING PHARMACEUTICAL COMPOUNDS AND INTERMEDIATE COMPOUNDS - The object of the present invention is a process for preparing the 2-acetoxy-5-(2-fluor-α-cyclopropyl-carbonyl-benzyl)-4,5,6,7-tetrahydro-4H-tieno[3,2-c]pyridine (prasugrel) of the formula (I). The process starts form crystalline 5-trityl-4,5,6,7-tetrahydro-tieno[3,2-c]pyridine of the formula (VI). Further objects of the present invention are two novel crystalline forms of 5-trityl-4,5,6,7-tetrahydro-tieno[3,2-c]pyridine of the formula (VI) and the use thereof for preparing the compound of the formula (V) and process preparing thereof. | 12-27-2012 |
20130030183 | PROCESS FOR PREPARING A PHARMACEUTICAL COMPOUND - The object of the present invention is a one-pot process for preparing the 2-acetoxy-5-(2-fluoro-α-cyclopropyl-carbonyl-benzyl)-4,5,6,7-tetrahydro-4H-tieno[3,2-c]-pyridine (prasugrel) of the formula (I) by reacting the 5,6,7,7a-tetrahydro-4H-tieno[3,2-c]-pyridine-2-on of the formula (II) with 2-bromo-1-cyclopropyl-2-(2-fluorophenyl)-etanone of the formula (III) or with 2-chloro-1-cyclopropyl-2-(2-fluorphenyl)-etanone of the formula (IIIa) and acetylating of the formed compound of the formula (IV), wherein the reaction is carried out in the presence of an organic base with an acetylation agent without isolating the compound of the formula (IV). The coupling and acetylation are carried out in the presence of the same organic base such as triethylamine, N,N-diisopropyl-ethylamine or pyridine. At the end of the process the prasugrel of the formula (I) is purified by recrystallization from an organic solvent or a mixture of solvents. | 01-31-2013 |
József Fülöp, Pecs HU
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20130259437 | PULSE EXCITED THZ WAVEGUIDE SOURCE BASED ON OPTICAL RECTIFICATION - The invention is a THz waveguide source ( | 10-03-2013 |
József Fülöp, Budapest HU
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20080278057 | BULB-SHAPED OUTER ENVELOPE FOR LAMPS, METHOD FOR MANUFACTURE THEREOF, AND COMPACT FLUORESCENT LAMP THEREWITH - A bulb-shaped outer envelope for accommodating at least one lamp including a light-emitting body and a control gear is disclosed. The envelope has a substantially spherical section for receiving the light-emitting body, and an elongated end section for receiving at least a part of the control gear components. The elongated end section is provided with a neck section. A substantially tubular neck-extension portion connects to an inner surface portion of and protruding from the neck section. The neck-extension portion is suitable for accommodating a remaining part of the control gear components. In a method for the manufacture of a glass outer envelope, a flare that is normally used in the manufacture of incandescent lamps is turned around by 180°, put into a skirted bulbous envelope, melted into the envelope while the skirt is detached and the flare is formed into a neck-extension portion. A self-ballasted compact fluorescent lamp with the bulb-shaped outer envelope is also disclosed. A part of the ballast components are disposed in the neck-extension portion of the outer envelope. | 11-13-2008 |
20090167184 | COMPACT FLUORESCENT LAMP WITH MECHANICAL SUPPORT MEANS AND STARTING AID - The compact fluorescent lamp comprises a bulb shaped outer envelope enclosing a discharge tube having a coiled configuration and a ballast unit for controlling the current in the tube. The lamp further comprises at least one joint mechanical support and starting aid means for positioning the discharge tube and the ballast unit and reducing a breakdown voltage path of the discharge tube. The at least one mechanical support and starting aid means is made of an electrically conducting material and connected electrically to at least one of the electrodes. The neck portion has a retaining member, and the mechanical support and starting aid means is supported by the retaining member and clamped on the discharge tube at least at a location in a vicinity of a middle section of the arc path. The mechanical support means further comprises at least one support section to provide support against an apex of the outer envelope, and at least one fixing section for fixing of the discharge tube. | 07-02-2009 |
20100026162 | FIXING MECHANISM FOR AN INNER ASSEMBLY TO OUTER BULB - A lamp assembly includes an inner assembly that has a CFL source, an electronics board, and a holder that interconnects the CFL source and electronics board. An outer, light transmissive envelope surrounds the inner assembly and various fixing arrangements are disclosed for securing the inner assembly to the outer envelope. Three primary mechanisms are a ratchet mechanism, a spring mechanism, or using adhesive to secure the inner assembly to the outer envelope under a predetermined tension. | 02-04-2010 |
20100026182 | ELECTRIC LAMP WITH INNER ASSEMBLY AND OUTER BULB AND METHOD FOR MANUFACTURING - An electric lamp comprises an inner assembly including a light source and a control gear circuit. An outer envelope encloses the light source and at least a part of the control gear and has a predetermined wall thickness and an end portion. The outer envelope is comprised of two parts separated along a circumferential line. The two parts of the envelope are connectable and sealable to form a uniform outer envelope with a seal region. The seal region has a wall thickness and is merged in a surface portion of the two parts of the envelope so that the surface unevenness of the seal region is not greater than 0.5 millimeters, and the maximum difference of the wall thickness of the seal region with respect to the wall thickness of the outer envelope is not greater than 0.3 millimeters. | 02-04-2010 |
20100181911 | HOLDER FOR INTEGRAL COMPACT FLUORESCENT LAMP WITH OUTER BULB - A lamp assembly having a CFL light source includes an outer envelope received around the light source. The outer envelope includes a first enlarged portion dimensioned for receipt about the light source and a second narrowed portion adapted for connection with a lamp base. A platform receives a first end of the CFL light source and supports the CFL within the envelope, the platform including a tapered perimeter portion dimensioned for abutting engagement with an interior surface of the envelope. | 07-22-2010 |
20110012509 | COMPACT FLUORESCENT LAMP AND METHOD FOR MANUFACTURING - This compact fluorescent lamp comprises a discharge tube arrangement with at least one discharge tube. The tube is formed of glass, encloses a discharge volume filled with a discharge gas and has a fluorescent phosphor coating disposed on the inner surface of the tube. The tube forms a continuous arc path and the tube is provided with electrodes disposed at each end of the arc path. The lamp also comprises a ballast circuit connected to the electrodes for controlling the current in the tube and a lamp base for connecting said lamp to a power supply through a socket. The lamp is enclosed in an outer envelope comprising a substantially spherical portion enclosing the tube arrangement and an elongated end portion enclosing the ballast circuit. The end portion of the outer envelope is closed and sealed by a sealing means of the same material as the material of the outer envelope. The sealing means is connected to the envelope in a hermetically sealing way. | 01-20-2011 |
20110234094 | FAST WARM-UP AND INSTANT LIGHT ENERGY SAVING LAMP ASSEMBLY - A lamp assembly provides both instant light through use of an incandescent/halogen lamp source and an energy saving type light provided by a compact fluorescent lamp source. Both light sources are enclosed within a common envelope or outer bulb. The sensor member monitors a temperature of the cathode and mercury reservoir of the compact fluorescent lamp source in order to determine when to terminate power to the incandescent lamp source. | 09-29-2011 |
20110298356 | POSITIONING OF AUXILIARY AMALGAM - A compact fluorescent lamp includes a discharge tube having cathodes disposed adjacent opposite ends. A fill gas which includes mercury is disposed within the discharge tube. The lamp further includes an amalgam located in the discharge tube and dispersed in the arc to be heated thereby for emitting mercury vapor during at least a starting period. | 12-08-2011 |
20120007486 | LED LIGHT SOURCE IN INCANDESCENT SHAPED LIGHT BULB - An LED light bulb that includes a base providing an electrical connector and a substantially hollow envelope extending from the base. The light bulb further includes a metal space separator having a top side, bottom side and side wall that has a plurality of holes connected by at least one channel that extends through the interior of the separator, such that air can pass through the separator. At least one LED is mounted on the separator in electrical connection with the base connector. | 01-12-2012 |
20120019136 | COMPACT FLUORESCENT LAMP WITH IMPROVED THERMAL MANAGEMENT - A compact fluorescent lamp includes an inverted compact fluorescent light source housed within an outer envelope. Locating the first and second ends of the coiled CFL source positions the electrodes within a substantially spherical outer envelope at a location remotely spaced from the ballast compartment. In this manner, only small diameter first and second lead wires that mechanically and electrically engage the electrodes pass through small dimensioned passages in a separation member in the outer envelope cavity. This substantially reduces the thermal stress on the components. | 01-26-2012 |
20120104948 | COMPACT FLUORESCENT LAMP WITH IMPROVED PERFORMANCE AND SIZE - A compact fluorescent lamp includes a discharge tube forming a continuous arc path with electrodes disposed at each end of the path. The lamp includes a fill gas disposed within the discharge tube. The lamp further includes a ballast circuit for controlling current in the discharge tube and operatively connected to the electrodes. The discharge tube is spirally wound around the longitudinal axis of the lamp to form a partially closed cavity and in a preferred arrangement the ballast is positioned within cavity formed by the spirally wound discharge tube. A gap between adjacent turns of the spirally wound discharge tube is less than about 0.5 mm, and preferably about 0.0009 mm. | 05-03-2012 |
20120206030 | HYBRID COMPACT FLUORESCENT LAMP FIXING METHOD - A lamp assembly provides both instantlight through use of an incandescent/halogen lamp source and an energy saving type light provided by a compact fluorescent lamp source. Both light sources are fixed within the assembly by a fixing mechanism that spaces the lights sources from each other such that heat from one source does not negatively affect the second light source or any other portion of the assembly. | 08-16-2012 |
20140240992 | DEVICE AND METHOD FOR COUPLING A LIGHT SOURCE TO A PRINTED CIRCUIT BOARD IN LAMPS - A lamp includes a collar with internal and outer surfaces, where two or more connection pins extend from the internal surface of the collar. At least two connection pins have a head portion distal from the collar internal surface. The head portions include a slot. The lamp includes a light source with at least two external lead-in wires. The lead-in wires are located within respective slots and are mechanically coupled to respective surfaces of the slots in a press-fit manner which may be free of wrapping, winding, twisting, or soldering. A PCB disposed inside the lamp has two opposing surfaces and a rim between the two opposing surfaces. There are conductive surfaces disposed on at least one of the rim and one of the opposing surfaces at positions corresponding to connection pin slots. The PCB is located between connection pins with the conductive surfaces in electrical communication with the lead-in wires. | 08-28-2014 |
20160099140 | ADHESIVE-LESS ASSEMBLY FOR ELECTRONIC COMPACT FLUORESCENT LAMPS - A collar includes two sections that join together in an adhesive-less manner to form an aperture, an arm with a distally-located pawl extending from a base of each section, a frame on the other section at a position corresponding to the arm, a lower clamp located on the sections, an upper clamp including a distally-located projection extending from the base surface, first and second flexible clamps located at opposing ends of the aperture. A gas discharge tube lighting assembly includes a discharge tube collar, a discharge tube having a stem assembly with a first portion fitting within the discharge tube and a second portion having a seal ring with a diameter greater than the discharge tube outer diameter, the collar and tube connected by adhesive-less mechanical forces exerted on the upper, lower, and first and second flexible clamps with the discharge tube located partially in the aperture. | 04-07-2016 |
József Fülöp, Budapest HU
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20110012509 | COMPACT FLUORESCENT LAMP AND METHOD FOR MANUFACTURING - This compact fluorescent lamp comprises a discharge tube arrangement with at least one discharge tube. The tube is formed of glass, encloses a discharge volume filled with a discharge gas and has a fluorescent phosphor coating disposed on the inner surface of the tube. The tube forms a continuous arc path and the tube is provided with electrodes disposed at each end of the arc path. The lamp also comprises a ballast circuit connected to the electrodes for controlling the current in the tube and a lamp base for connecting said lamp to a power supply through a socket. The lamp is enclosed in an outer envelope comprising a substantially spherical portion enclosing the tube arrangement and an elongated end portion enclosing the ballast circuit. The end portion of the outer envelope is closed and sealed by a sealing means of the same material as the material of the outer envelope. The sealing means is connected to the envelope in a hermetically sealing way. | 01-20-2011 |
20110115372 | ELECTRIC LAMP WITH PIN CONNECTORS AND METHOD OF MANUFACTURE - An electric lamp comprises a bulb-shaped outer envelope made of a glass material with a substantially spherical portion for receiving at least a part of at least one light source and an elongated end portion for receiving at least a part of an electronic control gear for energizing the light sources. A base portion attached to the bulb-shaped envelope comprises connecting means for connecting the electronic control gear to an associated power supply. The base portion is provided with a base plate for closing the base portion and the connecting means are pin connectors embedded in the base plate of the base portion. A method of manufacturing a lamp with pin connectors is also disclosed. In this method, an outer envelope made of a glass material is connected to a base portion that has a base plate with embedded pin connectors. A lamp that comprises a bulb-shaped outer envelope made of a plastic material and has a base portion with pin connectors is also provided. | 05-19-2011 |
József Fülöp, Pecs HU
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20130259437 | PULSE EXCITED THZ WAVEGUIDE SOURCE BASED ON OPTICAL RECTIFICATION - The invention is a THz waveguide source ( | 10-03-2013 |
József Gaál, Budapest HU
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20100178329 | LIPOSOME COMPOSITION - The invention relates to a liposomal composition, containing a citrus type (Aurantioideae) essential oil of pharmaceutical grade 0.5-5.0 part by weight; lavender oil of pharmaceutical grade 0.5-5.0 part by weight; vitamin E 0.1-1.5 part by weight; vitamin A 0.1-1.5 part by weight; castor oil ethoxylated 1.0-6.0 part by weight; a phospholipid 0.1-1.0 part by weight; distilled water 15-30 part by weight; ethanol 96% 65-75 part by weight. The composition can be used for treatment of wounded, burned, frozen, infected skin surfaces. | 07-15-2010 |
József Gaál, Budapest HU
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20100178329 | LIPOSOME COMPOSITION - The invention relates to a liposomal composition, containing a citrus type (Aurantioideae) essential oil of pharmaceutical grade 0.5-5.0 part by weight; lavender oil of pharmaceutical grade 0.5-5.0 part by weight; vitamin E 0.1-1.5 part by weight; vitamin A 0.1-1.5 part by weight; castor oil ethoxylated 1.0-6.0 part by weight; a phospholipid 0.1-1.0 part by weight; distilled water 15-30 part by weight; ethanol 96% 65-75 part by weight. The composition can be used for treatment of wounded, burned, frozen, infected skin surfaces. | 07-15-2010 |
József Gábeli, Szodliget HU
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20120161623 | MERCURY-FREE CERAMIC METAL HALIDE LAMP WITH IMPROVED LUMEN RUN-UP - Disclosed herein are mercury free ceramic metal halide high intensity discharge lamps of specified arc tube geometry and composition of ionizable fill. Embodiments herein generally employ a discharge vessel formed of a ceramic material having an aspect ratio satisfied by 106-28-2012 | |
József Gungl, Sopron HU
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20090326219 | PROCESS FOR MANUFACTURING EXTREMELY PURE BENZAZEPINE DERIVATIVES - A process for the production of extremely pure galanthamine or extremely pure galanthamine derivatives, a start is made from racemic bromine narwedine, which is debrominated under palladium catalysis. In this case, the working-up of the reaction mixture, which is carried out in the presence of oxygen or peroxides so that the palladium catalyst in an insoluble form is converted into an easily separable form, is essential. The further reaction is carried out by reduction of enantiomer-pure narwedine to form enantiomer-pure galanthamine, whereby it is then alkylated or dealkylated so that a corresponding substitution on the ring-nitrogen atom is achieved. By further purification, such as recrystallization, residual portions of palladium of below 5 ppm are achieved, so that direct use as a pharmaceutical raw material is made possible. | 12-31-2009 |
20100249423 | TOLPERISONE CONTROLLED RELEASE TABLET - A GRDDS (Gastro Retentive Drug Delivery System) containing tolperisone and having a 2-methyl-1-(4-methylphenyl)-propenone (4-MMPPO) fraction of less than 1.5 ppm for the extended release of the active substance tolperisone while avoiding the formation of 4-MMPPO in the gastrointestinal tract. | 09-30-2010 |
20100324090 | COMPOSITIONS OF TOLPERISONE - The present disclosure is directed to methods for providing tolperisone having extremely low levels of 4-MMPPO (2-methyl-1-(4-methylphenyl)-propenone), as well as related compositions. The invention further relates to methods of treating a subject with tolperisone under conditions that limit exposure of the subject to tolerable levels of 4-MMPPO, among other features. | 12-23-2010 |
József Gungl, Sopron HU
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20090253743 | COMPOSITIONS OF TOLPERISONE - The present disclosure is directed to methods for providing tolperisone having extremely low levels of 4-MMPPO (2-methyl-1-(4-methylphenyl)-propenone), as well as related compositions. The invention further relates to methods of treating a subject with tolperisone under conditions that limit exposure of the subject to tolerable levels of 4-MMPPO, among other features. | 10-08-2009 |
20090326219 | PROCESS FOR MANUFACTURING EXTREMELY PURE BENZAZEPINE DERIVATIVES - A process for the production of extremely pure galanthamine or extremely pure galanthamine derivatives, a start is made from racemic bromine narwedine, which is debrominated under palladium catalysis. In this case, the working-up of the reaction mixture, which is carried out in the presence of oxygen or peroxides so that the palladium catalyst in an insoluble form is converted into an easily separable form, is essential. The further reaction is carried out by reduction of enantiomer-pure narwedine to form enantiomer-pure galanthamine, whereby it is then alkylated or dealkylated so that a corresponding substitution on the ring-nitrogen atom is achieved. By further purification, such as recrystallization, residual portions of palladium of below 5 ppm are achieved, so that direct use as a pharmaceutical raw material is made possible. | 12-31-2009 |
20100150995 | PROCESS FOR THE PRODUCTION OF HIGH-PURITY 2,4'-DIMETHYL-3-PIPERIDINO-PROPIOPHENONE (TOLPERISONE), PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THE LATTER, AS WELL AS ACTIVE INGREDIENT FORMULATIONS THAT CONTAIN TOLPERISONE - The invention relates to a method for producing highly pure 2,4′-dimethyl-3-piperidino-propiophenone (tolperisone) (formula I) and the pharmaceutically acceptable salts, hydrochlorides, and hydrates thereof. The method allows the content of the undesired byproduct 2-methyl-1-(4-methylphenyl) propenone (4-MMPPO) to be kept significantly lower than in previously known methods. The invention further relates to active substance formulations which contain tolperisone and are suitable, among other things, for producing combination preparations used for treating patients suffering from Alzheimer's disease. The invention also relates to topical formulations, controlled release (CR) formulations, and transdermal therapeutic systems, such as active substance patches, which contain less than 50 ppm, preferably less than 10 ppm, more preferably less than 7 ppm, and most preferably less than 3 ppm or 0 ppm (i.e. less than the detectable amount) of the undesired byproduct 2-methyl-1-(4-methylphenyl) propenone (4-MMPPO) in relation to 100 percent by weight of active substance. | 06-17-2010 |
20100249423 | TOLPERISONE CONTROLLED RELEASE TABLET - A GRDDS (Gastro Retentive Drug Delivery System) containing tolperisone and having a 2-methyl-1-(4-methylphenyl)-propenone (4-MMPPO) fraction of less than 1.5 ppm for the extended release of the active substance tolperisone while avoiding the formation of 4-MMPPO in the gastrointestinal tract. | 09-30-2010 |
20100324090 | COMPOSITIONS OF TOLPERISONE - The present disclosure is directed to methods for providing tolperisone having extremely low levels of 4-MMPPO (2-methyl-1-(4-methylphenyl)-propenone), as well as related compositions. The invention further relates to methods of treating a subject with tolperisone under conditions that limit exposure of the subject to tolerable levels of 4-MMPPO, among other features. | 12-23-2010 |
József Kis-Benedek, Decs HU
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20120067739 | COLLOID DECOMPOSITION METHOD AND APPARATUS FOR ELECTROCHEMICALLY RESOLVING EMULSIONS - Decomposition is performed with the application of the method and apparatus by separating solid contaminants from the emulsion, absorbing CO | 03-22-2012 |
József Kolossa US
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20150377023 | ECCENTRIC MOTOR - The eccentric motor has a motor housing with an internal cylinder space. A main shaft is concentrically aligned with a central axis of the cylindrical space. A rotary blade is rigidly fixed, and arranged radially with respect, to the main shaft. A rotor is eccentrically arranged inside the motor housing, wherein the rotational axis of the rotor is spaced at a predetermined distance of eccentricity from the central axis of the main sheath surface of the motor housing. The rotary blade and the rotor are coupled to each other through a coupling member to establish a forced mechanical connection therebetween. The coupling member is adapted to move relative to the rotary blade in a direction parallel to the longitudinal axis thereof, and also relative to the rotor in a direction perpendicular to the longitudinal axis of the rotary blade. | 12-31-2015 |
József Kolossa, Agárd HU
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20150377023 | ECCENTRIC MOTOR - The eccentric motor has a motor housing with an internal cylinder space. A main shaft is concentrically aligned with a central axis of the cylindrical space. A rotary blade is rigidly fixed, and arranged radially with respect, to the main shaft. A rotor is eccentrically arranged inside the motor housing, wherein the rotational axis of the rotor is spaced at a predetermined distance of eccentricity from the central axis of the main sheath surface of the motor housing. The rotary blade and the rotor are coupled to each other through a coupling member to establish a forced mechanical connection therebetween. The coupling member is adapted to move relative to the rotary blade in a direction parallel to the longitudinal axis thereof, and also relative to the rotor in a direction perpendicular to the longitudinal axis of the rotary blade. | 12-31-2015 |
József Kozma, Budapest HU
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20090312299 | Isolated Isomers of Norelgestromin and Methods of Making and Using the Same - The invention is directed to a process of preparing substantially pure d-(17α)-13-ethyl-17-hydroxy-18,19-dinorpregn-4-ene-20-yn-3-one-3E- and -3Z-oxime isomers, as well as a process for the synthesis of the mixture of isomers and the pure isomers. The invention also relates to substantially pure d-(17α)-13-ethyl-17-hydroxy-18,19-dinorpregn-4-ene20-yn-3-one-3E-oxime and substantially pure d-(17α)-13-ethyl-17-hydroxy-18,19-dinorpregn-4-ene-20-yn-3-one-3Z-oxime isomer. Further aspects of the invention include a composition comprising substantially pure d-(17α)-13-ethyl-17-hydroxy-18,19-dinorpregn-4-ene20-yn-3-one-3E-oxime or substantially pure d-(17α)-13-ethyl-17-hydroxy-18,19-dinorpregn-4-ene-20-yn-3-one-3Z-oxime isomer, and methods of treatment using said compositions. | 12-17-2009 |
20150044721 | METHOD FOR THE PRODUCTION OF POLYPEPTIDES - New methods for the production of recombinant polypeptides from inclusion bodies are disclosed. Modulation of the cell culture conditions positively affects the yield of the recombinant polypeptide in active form. In one aspect, the methods comprise (a) cultivating a host cell at a first temperature, the host cell comprising a nucleic acid encoding a recombinant polypeptide, (b) lowering the cultivation temperature from the first temperature to a second temperature, and (c) cultivating the host cell at the second temperature. | 02-12-2015 |
József Kozma, Budapest HU
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20090312299 | Isolated Isomers of Norelgestromin and Methods of Making and Using the Same - The invention is directed to a process of preparing substantially pure d-(17α)-13-ethyl-17-hydroxy-18,19-dinorpregn-4-ene-20-yn-3-one-3E- and -3Z-oxime isomers, as well as a process for the synthesis of the mixture of isomers and the pure isomers. The invention also relates to substantially pure d-(17α)-13-ethyl-17-hydroxy-18,19-dinorpregn-4-ene20-yn-3-one-3E-oxime and substantially pure d-(17α)-13-ethyl-17-hydroxy-18,19-dinorpregn-4-ene-20-yn-3-one-3Z-oxime isomer. Further aspects of the invention include a composition comprising substantially pure d-(17α)-13-ethyl-17-hydroxy-18,19-dinorpregn-4-ene20-yn-3-one-3E-oxime or substantially pure d-(17α)-13-ethyl-17-hydroxy-18,19-dinorpregn-4-ene-20-yn-3-one-3Z-oxime isomer, and methods of treatment using said compositions. | 12-17-2009 |
József Kutasi, God HU
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20150157594 | ANTIBACTERIAL MICROELEMENT CHELATES AND THE USE THEREOF IN ANIMAL FEEDS - The present invention relates to a microelement organic O-chelate or N-chelate complex compound, for the inhibition of facultative pathogenic bacteria. The present invention further relates to a composition, feed additive or feed comprising the compounds, as well as methods for the preparation thereof, and for the use thereof in animal stock farming. | 06-11-2015 |
József Mandzsu, Jr., Fot HU
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20120261278 | PACKAGING CONTAINER WITH OVERPRESSURE RELIEF, PACKING METHOD AND SYSTEM - The invention relates to packaging container, packaging method and system. | 10-18-2012 |
József Mandzsu, Sr., Budapest HU
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20120261278 | PACKAGING CONTAINER WITH OVERPRESSURE RELIEF, PACKING METHOD AND SYSTEM - The invention relates to packaging container, packaging method and system. | 10-18-2012 |
József Marinka-Tóth, Budapest HU
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20090309553 | Battery current charger - The object of the invention is a method for charging a rechargeable battery having non-liquid electrolyte, which battery has an internal resonance frequency. The charging process contains at least one charging interval performed with current pulses, the frequency of said current pulses is essentially identical with the internal resonance frequency of the battery to be charged. Following the charging interval consists of periodic current pulses optionally a second relaxation interval is inserted, in which no charging current is applied to the rechargeable battery, within which optionally a second discharging interval is applied. After the second relaxation interval the charging is performed in an interval consists of a continuous charging current, whereafter an optional first relaxation interval is inserted, within which optionally a second discharging interval is applied. This sequence of the above steps can be varied and applied repeatedly until the full charge of the battery is attained. | 12-17-2009 |
József Marinka-Tóth, Budapest HU
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20090309553 | Battery current charger - The object of the invention is a method for charging a rechargeable battery having non-liquid electrolyte, which battery has an internal resonance frequency. The charging process contains at least one charging interval performed with current pulses, the frequency of said current pulses is essentially identical with the internal resonance frequency of the battery to be charged. Following the charging interval consists of periodic current pulses optionally a second relaxation interval is inserted, in which no charging current is applied to the rechargeable battery, within which optionally a second discharging interval is applied. After the second relaxation interval the charging is performed in an interval consists of a continuous charging current, whereafter an optional first relaxation interval is inserted, within which optionally a second discharging interval is applied. This sequence of the above steps can be varied and applied repeatedly until the full charge of the battery is attained. | 12-17-2009 |
József MÉszÁros, Debrecen HU
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20140170233 | Natural feed mixture for breeding domesticated water birds - The invention relates to a natural feed mixture for breeding domesticated water birds, comprising a high carbohydrate containing basic component poor in methyl-donors, a component rich in carbohydrates, having hepatic insulin-sensitizing properties, hypothalamic appetite-stimulating plant parts, natural substances blocking cholesterol synthesis in the liver, and an additive for protecting the formation of non-cholesterol- mevalonate products. | 06-19-2014 |
József Miklósi, Budapest HU
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20130123084 | EQUIPMENT FOR IMPROVING PHYSICAL FITNESS - The invention discloses an equipment for improving physical fitness, whose primary aspect is muscle strengthening. Another objective of the invention, besides maximizing muscle development, is to minimize the risk of injury during and after practices. The invention has a comfortable, tailor-made design shell ( | 05-16-2013 |
József Mozsár, Osca HU
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20100229261 | NOVEL BRASSICA PLANTS - The present invention relates to novel brassica plants, in particular to novel cauliflower plants. In one embodiment, the novel cauliflower plants provided herein comprise a long stem and are suitable for mechanical harvesting. The application also further discloses seeds the cauliflower plants of the present invention and parts thereof, for example pollen, ovules and curds. The application also further discloses methods of using a plant of instant invention, such as methods of producing a cauliflower curd of the instant invention, and methods of harvesting the curds of plants of the instant invention. | 09-09-2010 |
20140157460 | NOVEL BRASSICA PLANTS - The present invention relates to novel | 06-05-2014 |
József Mozsár, Osca HU
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20100229261 | NOVEL BRASSICA PLANTS - The present invention relates to novel brassica plants, in particular to novel cauliflower plants. In one embodiment, the novel cauliflower plants provided herein comprise a long stem and are suitable for mechanical harvesting. The application also further discloses seeds the cauliflower plants of the present invention and parts thereof, for example pollen, ovules and curds. The application also further discloses methods of using a plant of instant invention, such as methods of producing a cauliflower curd of the instant invention, and methods of harvesting the curds of plants of the instant invention. | 09-09-2010 |
József Neu, Budapest HU
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20100081668 | POLYMORPHS OF 5--6-CHLORO-1,3-DIHYDRO-2H-INDOL-2-ONE HYDROBROMIDE AND PROCESSES FOR PREPARATION THEREOF - The present invention provides pharmaceutically applicable compounds and polymorphs belonging to the ziprasidone hydrobromide compound group with antipsychotic effect. The present invention provides hydrobromide polymorphs of 5-{-2-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]-ethyl}-6-chloro-1,3-dihydro-2H-indol-2-one, ziprasidone of Formula (I) having neuroleptic activity. | 04-01-2010 |
József Pandur, Erd HU
József Prechl, Fot HU
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20100075864 | MEASUREMENT OF COMPLEMENT ACTIVATION PRODUCTS ON ANTIGEN ARRAYS - The basis of the present invention is that antigens on an antigen array can initiate complement activation both by antibody-dependent or -independent way. The systems and methods disclosed herein can be used in methods of diagnosing and monitoring particular autoimmune disorders and infections. The invention relates to a new diagnostic method, utilizing an antigen array for simultaneously identifying different antigens capable of activating the complement system, in a quantitative fashion; to multiplex immunoassays utilizing antigen arrays, and more particularly to systems, methods and kits for qualitative and quantitative detection of antigens activating complement in a biological sample, via the measurement of complement components deposited on antigen arrays. The invention employs the functional complement system in the biological sample tested, thereby the information gained relates to antigen recognition properties and functional consequences in the organism from which the sample was taken and relies on the ability of antigen recognition molecules, primarily antibodies to activate the complement system in the sample tested, upon binding to elements of an antigen array. | 03-25-2010 |
József Prechl, Fot HU
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20100075864 | MEASUREMENT OF COMPLEMENT ACTIVATION PRODUCTS ON ANTIGEN ARRAYS - The basis of the present invention is that antigens on an antigen array can initiate complement activation both by antibody-dependent or -independent way. The systems and methods disclosed herein can be used in methods of diagnosing and monitoring particular autoimmune disorders and infections. The invention relates to a new diagnostic method, utilizing an antigen array for simultaneously identifying different antigens capable of activating the complement system, in a quantitative fashion; to multiplex immunoassays utilizing antigen arrays, and more particularly to systems, methods and kits for qualitative and quantitative detection of antigens activating complement in a biological sample, via the measurement of complement components deposited on antigen arrays. The invention employs the functional complement system in the biological sample tested, thereby the information gained relates to antigen recognition properties and functional consequences in the organism from which the sample was taken and relies on the ability of antigen recognition molecules, primarily antibodies to activate the complement system in the sample tested, upon binding to elements of an antigen array. | 03-25-2010 |
József Prokisch, Debrecen HU
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20100189634 | PROCESS FOR PRODUCING ELEMENTAL SELENIUM NANOSPHERES - The invention relates to microbiological processes using non-selenium-respiring bacteria for the production of elemental selenium nanospheres having a size in the 50-500 nm range and compositions comprising said nanospheres. The invention further concerns grey elemental selenium nanospheres directly obtainable by the processes of the invention. The compositions and materials of the invention are useful, in particular, as food additives and for use as raw material in the microelectronic and optical industries. | 07-29-2010 |
József Prokisch, Debrecen HU
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20100189634 | PROCESS FOR PRODUCING ELEMENTAL SELENIUM NANOSPHERES - The invention relates to microbiological processes using non-selenium-respiring bacteria for the production of elemental selenium nanospheres having a size in the 50-500 nm range and compositions comprising said nanospheres. The invention further concerns grey elemental selenium nanospheres directly obtainable by the processes of the invention. The compositions and materials of the invention are useful, in particular, as food additives and for use as raw material in the microelectronic and optical industries. | 07-29-2010 |
József Tímár, Budapest HU
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20090305329 | INTRACELLULAR TARGETING OF MOLECULES - The present invention provides methods for intracellular and/or nuclear targeting of an agent capable of specifically binding to syndecan-4. The present invention further provides methods for the modification of the intracellular and/or nuclear targeting of said agent, as well methods for identifying compounds capable of modifying the syndecan-4 delivery pathway. The present invention further provides experimental kits to perform the methods according to the invention. | 12-10-2009 |
József Tímár, Budapest HU
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20090305329 | INTRACELLULAR TARGETING OF MOLECULES - The present invention provides methods for intracellular and/or nuclear targeting of an agent capable of specifically binding to syndecan-4. The present invention further provides methods for the modification of the intracellular and/or nuclear targeting of said agent, as well methods for identifying compounds capable of modifying the syndecan-4 delivery pathway. The present invention further provides experimental kits to perform the methods according to the invention. | 12-10-2009 |
20110124572 | SYNDECAN-4 IS A REGULATOR OF RAC1-GTP - The present invention provides a method for modulating the activity of Rac1, comprising modifying the phosphorylation state of Ser179 in syndecan-4 through influencing the interaction between syndecan-4 and the guanin nucleotide exchange factor of Rac1 (RacGEF) named Tiam1 in a GTP-dependent manner. In particular, methods are provided for enhancing the epithelial phenotype of a cell and for initiating the polarization of a cell by increasing the de-phosphorylation of said Ser179 of syndecan-4, and for enhancing the migratory phenotype of a cell and for initiating the neuronal differentiation of a cell by increasing the phosphorylation of said Ser179 of syndecan-4. Polypeptides for use in modulating the activity of the small GTPase Rac are also provided, as well as a method for identifying an agent capable of indirectly modulating the activity of the small GTPase Rac 1. | 05-26-2011 |
József Tökés, Erdokertes HU
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20110115372 | ELECTRIC LAMP WITH PIN CONNECTORS AND METHOD OF MANUFACTURE - An electric lamp comprises a bulb-shaped outer envelope made of a glass material with a substantially spherical portion for receiving at least a part of at least one light source and an elongated end portion for receiving at least a part of an electronic control gear for energizing the light sources. A base portion attached to the bulb-shaped envelope comprises connecting means for connecting the electronic control gear to an associated power supply. The base portion is provided with a base plate for closing the base portion and the connecting means are pin connectors embedded in the base plate of the base portion. A method of manufacturing a lamp with pin connectors is also disclosed. In this method, an outer envelope made of a glass material is connected to a base portion that has a base plate with embedded pin connectors. A lamp that comprises a bulb-shaped outer envelope made of a plastic material and has a base portion with pin connectors is also provided. | 05-19-2011 |
József Toldi, Szeged HU
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20130172346 | USE OF KYNURENIC ACID AMIDE DERIVATIVES FOR THE TREATMENT OF HUNTINGTON'S DISEASE - The invention is directed to kynurenic acid analogues and pharmaceutically acceptable salts thereof and pharmaceutical compositions containing said compounds for treating the symptoms of Huntington's disease and preventing the development of the symptoms. | 07-04-2013 |
József Toldi, Szeged HU
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20130172346 | USE OF KYNURENIC ACID AMIDE DERIVATIVES FOR THE TREATMENT OF HUNTINGTON'S DISEASE - The invention is directed to kynurenic acid analogues and pharmaceutically acceptable salts thereof and pharmaceutical compositions containing said compounds for treating the symptoms of Huntington's disease and preventing the development of the symptoms. | 07-04-2013 |
József Tomcsik, Budapest HU
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20140341840 | RODENT CONTROL DEVICE - The present invention relates to a device for controlling rodents. More specifically, the present invention relates to a device consisting of a combination of a solid and a pulpy bait (commonly known as ‘fresh bait’ or ‘pasta bait’ in rodent control practice), wherein the solid part is a shaped paraffinized rodenticide bait with a rodenticide concentration which is lower than or equal to the rodenticide concentration of the combination and contains the pulpy rodenticide bait with a rodenticide concentration which is higher than or equal to the rodenticide concentration of the combination. The rodent control device according to the invention has an enhanced acceptance by the rodents and can preferably be fixed by a hole formed in the solid part preventing the rodents to take it away. Furthermore, the present invention relates to the preparation and use of such rodent control device. | 11-20-2014 |
20150147289 | Consumable Aqueous gel for use in Pest Control, A Pest control device Comprising an Aqueous Gel, And The Use Of An Aqueous Gel In A Pest Control Device And In A Method Of Controlling Pests - A consumable aqueous gel is provided for use in pest control. The gel sates the thirst of pests and increases the consumption of bait by pests. The gel is substantially free of biocides. The gel may be provided as a combination for use in a pest control device. The combination comprises an aqueous gel which is substantially free of biocides and a bait. A pest control device comprises a container having a first compartment containing an aqueous gel which is substantially free of biocides. A method of controlling pests comprises the step of deploying any of the aforementioned aqueous gel, combination according or pest control device. An aqueous gel which is substantially free of biocides may be used with or in a pest control device. | 05-28-2015 |
József Tözsér, Debrecen HU
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20110028397 | Use of Urokinase Type Plasminogen Activator Inhibitors for the Treatment of Corneal Disorders - The invention concerns the use of inhibitors of the urokinase type of plasminogen activator (uPA) appearing in the anterior segment of the eye, for the treatment and prevention of corneal ulcers and other disorders. The invention further concerns pharmaceutical compositions, comprising inhibitors of uPA, preferably eye drops and eye ointments. The pharmaceutical compositions according to the invention preferably comprise PAI-2 protein or a derivative thereof retaining uPA-inhibiting capacity, or a tripeptide aldehyde inhibitor, preferably the D-Phe-Pro-Arg-aldehyde (Ald-1). The PAI-2 protein, used according to the invention, is preferably produced through bacterial expression, as a fusion protein. | 02-03-2011 |
József Tözsér, Debrecen HU
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20100068745 | PROCESS AND KIT FOR MEASURING THE CONDITION OF THE FIBRINOLITIC SYSTEM - The invention relates to an assay and a kit for the determination of the status of the fibrinolytic system. In particular the invention relates to a method for the determination of the status of the fibrinolytic system from tear fluid samples. Additionally the invention relates to a sterilized, calibrated capillary equipped with a plastic balloon, suitable for tear fluid sampling, and a kit for the assessment of the status of the fibrinolytic system, or for the determination of its balance, comprising a sampling capillary, reaction sheets, color scale to help the evaluation, and reagents | 03-18-2010 |
20110028397 | Use of Urokinase Type Plasminogen Activator Inhibitors for the Treatment of Corneal Disorders - The invention concerns the use of inhibitors of the urokinase type of plasminogen activator (uPA) appearing in the anterior segment of the eye, for the treatment and prevention of corneal ulcers and other disorders. The invention further concerns pharmaceutical compositions, comprising inhibitors of uPA, preferably eye drops and eye ointments. The pharmaceutical compositions according to the invention preferably comprise PAI-2 protein or a derivative thereof retaining uPA-inhibiting capacity, or a tripeptide aldehyde inhibitor, preferably the D-Phe-Pro-Arg-aldehyde (Ald-1). The PAI-2 protein, used according to the invention, is preferably produced through bacterial expression, as a fusion protein. | 02-03-2011 |