Abstract: In an aerosol inhaler it is proposed that a thermal sensor 5 be arranged in the region of the atomization nozzle 4, which sensor, following the actuation of an actuating element and the triggering of an inhalation process, undergoes cooling as a result of the expansion of the propellant which then occurs. The actuation and cooling are electronically detected in an electronic module 3. Technical and therapeutic data can be derived from the signal, which data are communicated to the user via the display unit and/or alarm devices and influence the therapy in the desired manner. See FIG. 1.
Abstract: The invention relates to new arylglycinamide derivatives of general formula I
and the pharmaceutically acceptable salts thereof, wherein
R1 and R2 together with the N to which they are bound form a ring of the formula
wherein
is 2 or 3 and
X denotes oxygen, N(CH2)nR6 or CR7R8,
and R34 R5 R6 R7, R8, Ar and n have the meanings given in the specification, and the preparation and use thereof. The new compounds are valuable neurokinin (tachykinin)-antagonists.
Type:
Grant
Filed:
January 3, 2001
Date of Patent:
October 16, 2001
Assignee:
Boehringer Ingelheim KG
Inventors:
Gerd Schnorrenberg, Horst Dollinger, Franz Esser, Hans Briem, Birgit Jung, Georg Speck
Abstract: On account of the surprisingly powerful and long-lasting effect thereof, the salts of the L-(−)-enantiomer of (endo, syn)-(−)-3-(3-hydroxy-1-oxo-2-phenylpropoxy)-8-methyl-8-(methylethyl)-8-azoniabicyclo [3,2,1]octane are suitable as active substances for drugs administered by inhalation for respiratory tract therapy.
Type:
Grant
Filed:
August 6, 1999
Date of Patent:
October 9, 2001
Assignee:
Boehringer Ingelheim KG
Inventors:
Rolf Banholzer, Richard Reichl, Bernd Disse, Georg Speck
Abstract: The invention relates to new arylglycinamide derivatives of general formula I
and the pharmaceutically acceptable salts thereof, wherein
R1 and R2 together with the N to which they are bound form a ring of the formula
wherein
p is 2 or 3 and
X denotes oxygen, N(CH2)nR6 or CR7R8,
and R3, R4, R5, R6, R7, R8, Ar and n have the meanings given in the specification, and the preparation and use thereof. The new compounds are valuable neurokinin (tachykinin)-antagonists.
Type:
Grant
Filed:
February 18, 2000
Date of Patent:
September 25, 2001
Assignee:
Boehringer Ingelheim KG
Inventors:
Gerd Schnorrenberg, Horst Dollinger, Franz Esser, Hans Briem, Birgit Jung, Georg Speck
Abstract: The invention relates to oxadiazole derivatives of general formula (I)
wherein X, Y, Z and R1 are defined as described in the specification and claims, processes for preparing them and their use as pharmaceutical compositions.
Type:
Grant
Filed:
July 26, 1999
Date of Patent:
August 21, 2001
Assignee:
Boehringer Ingelheim KG
Inventors:
Michael Brenner, Roland Maier, Marion Wienrich, Thomas Weiser, Rainer Palluk, Wolf-Dietrich Bechtel, Angelo Sagrada, Helmut Ensinger, Uwe Pschorn, Raffaele Cesana
Abstract: The invention relates to new arylglycinamide derivatives of general formula I
and the pharmaceutically acceptable salts thereof, wherein
R1 and R2 together with the N to which they are bound form a ring of the formula
wherein
p is 2 or 3 and
X denotes oxygen, N(CH2)nR6 or CR7R8,
and R3, R4, R5, R6, R7, R8, Ar and n have the meanings given in the specification, and the preparation and use thereof. The new compounds are valuable neurokinin (tachykinin)-antagonists.
Type:
Grant
Filed:
February 18, 2000
Date of Patent:
June 26, 2001
Assignee:
Boehringer Ingelheim KG
Inventors:
Gerd Schnorrenberg, Horst Dollinger, Franz Esser, Hans Briem, Birgit Jung, Georg Speck
Abstract: The invention relates to new compounds of general formula I
and the pharmaceutically acceptable salts thereof, wherein A, B, Z, R1, R2, R3 and m are defined as in the specification, processes for preparing them and pharmaceutical compositions containing these compounds. The compounds are valuable neurokinin (tachykinin) antagonists.
Type:
Grant
Filed:
February 16, 1999
Date of Patent:
May 22, 2001
Assignee:
Boehringer Ingelheim KG
Inventors:
Horst Dollinger, Gerd Schnorrenberg, Hans Briem, Birgit Jung, Georg Speck
Abstract: Disclosed are compounds which are neurokinin (tachykinin)-antagonists, useful for the treatment or prevention of inflammatory and allergic disease.
Type:
Grant
Filed:
December 1, 1999
Date of Patent:
May 15, 2001
Assignee:
Boehringer Ingelheim KG
Inventors:
Franz Esser, Gerd Schnorrenberg, Hans-Peter Ignatow, Günther Giesler, Birgit Jung, Georg Speck
Abstract: Pyranoside derivatives of the formula I
wherein 1, m and n independently of one another denote an integer chosen from 0, 1, 2, 3 and 4 and 1+m+n≦4. These are are LTB4-antagonists. Also disclosed are processes for making these compounds.
Type:
Grant
Filed:
March 8, 1999
Date of Patent:
March 6, 2001
Assignee:
Boehringer Ingelheim KG
Inventors:
Ralf Anderskewitz, Kurt Schromm, Ernst-Otto Renth, Franz Birke, Hans M. Jennewein, Christopher J. M. Meade, Andreas Ding
Abstract: The invention relates to new compounds of general formula
and the pharmaceutically acceptable salts thereof, wherein A, B, Z, R1, R2, R3 and m are defined as in the specification, processes for preparing them and pharmaceutical compositions containing these compounds. The compounds are valuable neurokinin (tachykinin) antagonists.
Type:
Grant
Filed:
February 8, 2000
Date of Patent:
February 20, 2001
Assignee:
Boehringer Ingelheim KG
Inventors:
Horst Dollinger, Gerd Schnorrenberg, Hans Briem, Birgit Jung, Georg Speck
Abstract: The invention relates to new amino acid derivatives of general formula I and the pharmaceutically acceptable salts thereof, wherein group B is --A.sup.2 --NR.sup.2 R.sup.3 or R.sup.5, wherein group R.sup.5 is ##STR1## and R.sup.1, A.sup.1, A.sup.2, R.sup.2, R.sup.3, R.sup.6, R.sup.7, R.sup.8, R.sup.9, X, Y, Z, t and u have the meanings described in the specification, as well as the preparation and use thereof. The novel compounds are valuable neurokinin (tachykinin) antagonists.
Type:
Grant
Filed:
July 8, 1998
Date of Patent:
November 14, 2000
Assignee:
Boehringer Ingelheim KG
Inventors:
Franz Esser, Gerd Schnorrenberg, Horst Dollinger, Birgit Jung, Erich Burger
Abstract: A process for the re-racemisation of a (-)-2-phenylmethyl-3,3-dimethyl-piperidin-4-on derivative wherein a (-)-2-phenylmethyl-3,3-dimethyl-piperidin-4-on derivative of the formula 8.sub.BwhereinR.sub.2 denotes hydrogen C.sub.1 -C.sub.6 -alkyl, halogen, C.sub.1 -C.sub.8 -alkoxy, a benzoyl group bound via an oxygen or an alkylcarboxyl group having a straight chained or branched C.sub.1 -C.sub.6 -lower alkyl group--wherein the alkyl group may optionally be substituted by one or more halogen atoms which may be identical or different;is heated to yield a racemic mixture of compounds of the formulae 8.sub.A and 8.sub.
Type:
Grant
Filed:
November 18, 1999
Date of Patent:
October 31, 2000
Assignee:
Boehringer Ingelheim KG
Inventors:
Matthias Grauert, Herbert Merz, Hanfried Baltes
Abstract: The present invention relates to new processes for preparing norbenzomorphan, the central intermediate step in the preparation of pharmaceutically useful benzomorphan derivatives of general formula 1 ##STR1## especially (-)-(1R,5S,2"R)-3'-hydroxy-2-(2-methoxypropyl)-5,9,9-trimethyl-6,7-benzomo rphan or [(-)-(2R, 6S,2'R)-3-(2-methoxypropyl)-6,11,11-trimethyl-1,2,3,4,5,6-hexahydro-2,6-me thano-benzo[.alpha.]oxacin-9-ol] (BIII 277).
Type:
Grant
Filed:
November 18, 1999
Date of Patent:
October 24, 2000
Assignee:
Boehringer Ingelheim KG
Inventors:
Matthias Grauert, Herbert Merz, Hanfried Baltes
Abstract: The invention refers to a transcorneal system for the actively controlled transcorneal delivery of a medicament into a subject comprising an active substance reservoir and a device provided with a plurality of micro-pins or micro-blades adapted in use to penetrate the stratum corneum of the subject and connected with reservoir via a liquid conveying connection and thereby allow active substance to pass from the reservoir through capillary openings of the micro-pins or along the micro-blades into the subject.
Abstract: The invention relates to new arylglycinamide derivatives of general formula I ##STR1## and the pharmaceutically acceptable salts thereof, wherein R.sup.1 and R.sup.2 together with the N to which they are bound form a ring of the formula ##STR2## wherein p is 2 or 3 andX denotes oxygen, N(CH.sub.2).sub.n R.sup.6 or CR.sup.7 R.sup.8,and R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7, R.sup.8, Ar and n have the meanings given in the specification, and the preparation and use thereof. The new compounds are valuable neurokinin (tachykinin)-antagonists.
Type:
Grant
Filed:
October 29, 1997
Date of Patent:
September 26, 2000
Assignee:
Boehringer Ingelheim KG
Inventors:
Gerd Schnorrenberg, Horst Dollinger, Franz Esser, Hans Briem, Birgit Jung, Georg Speck
Abstract: Phenylacetic acid benzylamides having the following general structure
wherein the substituents are defined herein, are disclosed, which compounds are hypoglcemic agents.
Type:
Grant
Filed:
October 7, 1997
Date of Patent:
January 30, 2001
Assignee:
Boehringer Ingelheim KG
Inventors:
Wolfgang Grell, Rudolf Hurnaus, Gerhart Griss, Robert Sauter, Manfred Reiffen, Eckhard Rupprecht