Egis Gyogyszergyar

Egis Gyogyszergyar Rt.

Basf Aktiengesellschaft

Other

Knorr-Bremse Systeme Fuer Nutzfahrzeuge Gmbh

Egyt Gyogyszervegyeszeti Gyar

Egis Pharmaceutical

Egis Cyogyszergvar

Egis Gyogyszergyat

Marton Fekete

Lujza E Petocz

Gabor Gigler

Frigyes Gorgenyi

Istvan Gacsalyi

Istvan Gyertyan

Zoltan Budai

Eniko Szirt Nee Kiszelly

Jozsef Reiter

Katalin Szemeredi

Gyula Simig

Tibor Mezei

Attila Mandi

Gabor Blasko

Klara Reiter Nee Esses

Maria Szecsey Nee Hegedus

Istvan Simonyi

Jozsef Barkoczy

Andras Egyed

Laszlo Pongo

Gizella Zsila

Laszlo Kapolnai

Jozsef Knoll

Gyula Sebestyen

Ivan Beck

Pal Vago

Berta Knoll

Andras Dietz

Marta Kovacs

Elemer Jakfalvi

Endre Rivo

Judit Bajnogel

Enik Szirt Nee Kiszelly

Istvan Seres

Valeria Hoffmann

Maria Szeli

Gabriella Zsilla

Laszlo Jaszlits

Janos Egri

Peter Matyus

Eva Schmidt

Gyula Hornyak

Peter Tompe

Gyorgy Rabloczky

Ilona Bodi

Karoly Lempert

Jozsef Fetter

Edit Berenyi Nee Poldermann

Andras Varro

Laszlo Rozsa

Margit Csorgo

Eniko Kiszelly

Laszlo Gaal

Gabor Makara

Agnes Papp

Katalin Zukovics Nee Sumeg

Erzsebet Zara

Eva J Tajthy Nee Juhasz

Miklos Tanczos

Erzsebet Barczay

Katalin Budai Nee Simonyi

Gizella Miholics

Jozsef Kenderfi

Ildiko Varga

Klara Czako

Maria Hegedus

Szilveszter E Vizi

Klara Kazo Nee Daroczi

Klara Gado

Gyula Deak

Margit Doda

Lajos Gyorgy

Tibor Lang

Bela Kanyicska

Sandor Erdos

Maria Krisztian

Laszlo Nagy

Antal Feller

Szabolcs Sovago

Eniko Sziri Nee Kiszelly

Josef Reiter

Daniel Bujdoso

Josef Barkoczy

Lujza Pet Cz

Gabor Berecz

Maria Szecsey Nee Heged S

Ludmila Rohacs Nee Zamkovaja

Margit Csorg

Luiza Petocz

Klara Reiter Nee Eszes

Ludmilla Rohacas Nee Zamkovaja

Andrea Jednakovics

Aniko Miklos

Gvorgy Schmidt

Luca Levay

Erika Karaffa

Kalara Reiter Nee Esses

Eniko Szirt Nee Kislelly

Eniko Sziri neKiszelly

Aranka Hegedus Nee Szima

A noise damper for a compressed-air system, for a brake system of a utility vehicle, including: a housing having an inlet channel for a compressed-air stream and with a chamber for accommodating sound-damping material, in which the inlet channel and the chamber are separated, perpendicularly with respect to the compressed-air stream, by a separating plate which is closed in a central region and which, in an outer peripheral region of the compressed-air stream, has multiple openings for introducing the compressed air directly into the chamber. Also described are a related pneumatic brake system and method.

Noise damper for compressed air systems and a method for the production of same

Acid amide derivatives and process for the preparation thereof

The invention refers to pharmaceutical compositions for the prevention and/or treatment of gastrointestinal diseases connected with infections caused by Helicobacter pylori and a method for the treatment of such diseases. The pharmaceutical composition of the invention comprises as active ingredient a cyclic ketone derivative of the formula I ##STR1## wherein and R.sup.1 mean independently hydrogen or halo;

Pharmaceutical compositions for the prevention and/or treatment a

The invention relates to novel, pharmaceutically active trisubstituted cycloalkane derivatives, a process for the preparation thereof and pharmaceutical compositions comprising the same. The invention also encompasses the use of the said cycloalkane derivatives for the treatment of diseases and for the preparation of pharmaceutical compositions suitable for the treatment of diseases. The compounds according to the invention are characterized by the general formula (I), ##STR1## wherein R represents hydrogen, C.sub.1-4 alkyl or hydroxyl,

Trisubstituted cycloalkane derivatives and process for the preparation

Novel basic ether of general formula (I), ##STR1## wherein R.sup.1 and R.sup.2 are independently hydrogen, halogen or C.sub.1-4 alkoxy, or together they represent a 3,4-methylenedioxy group,

Basic ethers and process for the preparation thereof

The disclosed compounds have the formula ##STR1## wherein Q is a 6-membered saturated heterocyclic group or a group S(O)pR.sup.3, wherein

5-(substituted amino)-1,2,4-triazolo (1,5-A) pyrimidine derivatives

The invention relates to novel, pharmaceutically active benz[e]indene derivatives, a process for the preparation thereof, pharmaceutical compositions comprising the same, further to the use of the said benz[e]indene derivatives in the treatment of certain diseases and in the preparation of pharmaceutical compositions suitable for the treatment of said diseases. The new benz[e]indene derivatives according to the invention correspond to the general formula ##STR1## wherein A represents a group of the formula alk-NR.sup.1 R.sup.2, wherein alk represents a C.sub.2-7 alkylene group optionally carrying a hydroxy substituent,

Benz[e]indene derivatives

Racemic or optically active new 3(2H)-pyridazinone derivatives, a process for the preparation thereof, pharmaceutical compositions comprising the same, to the use of the said 3(2H)-pyridazinone derivatives for the treatment of diseases and for the preparation of pharmaceutical compositions suitable for the treatment of diseases. The new 3(2H)-pyridazinone derivatives according to the invention correspond to the general formula (I), ##STR1##

3(2H)-pyridazinone derivatives and process for the preparation thereof

The invention relates to novel triazolyl thioamides of the general formula (I), ##STR1## wherein Q represents hydrogen or a heterocyclic group optionally bearing one or more C.sub.1-4 alkyl substituent(s), or a group of the formula SR.sup.1, wherein

Triazolyl thioamide derivates

The invention relates to new 2-(substituted imino)-thiazolidines, a process for the preparation thereof, pharmaceutical compositions comprising the same, the use of the said 2-(substituted imino)thiazolidines for the treatment of diseases and for the preparation of pharmaceutical compositions suitable for the treatment of diseases. The new 2-(substituted imino)-thiazolidine derivatives provided by the present invention correspond to the general formula (I), ##STR1## wherein R.sup.1 and R.sup.2 each represent halogen, nitro, C.sub.1-4 alkoxy or C.sub.1-4 alkyl, which latter may optionally carry one or more halogen substituent(s),

2-(substituted imino)-thiazolidines and process for the preparation

The invention relates to novel racemic or optically active aminopropanol derivatives of formula I ##STR1## wherein R and R.sup.1 are independently hydrogen atom, halogen atom, lower alkoxy, or together represent a methylene dioxy group,

Aminopropanol derivatives, process for their preparation and

This invention relates to novel triazolyl hydrazide derivatives and a process for the preparation thereof. The new triazolyl hydrazide derivatives of the general formula (I). ##STR1## wherein Q represents hydrogen or a heterocyclic group optionally substituted by a C.sub.1-4 alkyl group; or a group of general formula SR.sup.1, wherein

Triazolyl hydrazide derivatives

This invention relates to novel triazolo derivatives, a process for the preparation thereof, pharmaceutical compositions comprising the same, to the use of the said triazolo derivatives for the treatment of diseases and also for the preparation of pharmaceutical compositions suitable for the treatment of the said diseases. The new triazolo derivatives of the general formulae (Ia) and (Ib), ##STR1## wherein Q represents hydrogen or a heterocyclic group optionally bearing one or more C.sub.1-4 alkyl substituent(s); or a group of the formula SR.sup.1, wherein

Triazolo derivatives and process for their preparation

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Budapest, Hungary

Marton Fekete