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Altana Pharma AG Patents
Assignee:
Altana Pharma AG
Address:
Konstanz, DE
No. of patents:
82
Patents:


1 2


Patent Number Title Of Patent Date Issued
7524973 Nitrate esters of phenylaminothiophenacetic acid derivatives April 28, 2009
The compounds of formula I ##STR00001## in which R1, R2, R3, R4 and R5 have the meanings as given in the description are novel effective antiinflammatory compounds.
7468377 Imidazopyridine-derivatives as inductible no-synthase inhibitors December 23, 2008
The compounds of Formula (I) ##STR00001## in which R1, R2, R3, R4, R5 and A have the meanings as given in the description are novel effective iNOS inhibitors.
7393860 Tetrahydropyridoethers July 1, 2008
The compound (7R,8R,9R)-2,3-Dimethyl-8-hydroxy-7-(2-methoxyethoxy)-9-phenyl-7,8,9,10-t- etrahydro-imidazo-[1,2-h] [1,7] naphthyridine inhibits the secretion of gastric acid.
7390819 Imidazo[4,5-b]quinoline-derivatives and their use as no-synthase inhibitors June 24, 2008
The compounds of formula I ##STR00001## in which R1, R2, R3 and A have the meanings as given in the description are novel effective INOS inhibitors.
7329677 Imidazo(4,5-b)pyridine-derivatives as inducible no-synthase inhibitors February 12, 2008
The compounds of formula (I) ##STR00001## in which R1, R2, R3, R4 and R11 have the meanings as given in the description are novel effective iNOS inhibitors.
7326784 Intermediates for the preparation of tricyclic dihydropyrano-imidazo-pyridines derivatives February 5, 2008
The invention relates to compounds of the formula 1, ##STR00001## in which R1, R2, R3, Arom and PG have the meanings as indicated in the description. These compounds are valuable intermediates for the preparation of pharmaceutically active compounds.
7326718 8-Substituted imidazopyridines February 5, 2008
The present invention relates to 8-substituted imidazopyridines of a certain formula (1) ##STR00001## in which the substitutents and symbols have the meanings indicated in the description. The compounds have gastric secretion inhibiting and excellent gastric and intestinal protectiv
7317021 Aminopyridine-derivatives as inductible no-synthase inhibitors January 8, 2008
The compounds of Formula (I) ##STR00001## in which R1, R2, R3 and R4 have the meanings as given in the description are novel effective iNOS inhibitors.
7314935 Tricyclic n-acyl compounds January 1, 2008
The invention relates to compounds of the formula (1) where the substituents and symbols are as defined in the description. The compounds are valuable intermediates for preparing active pharmaceutical ingredients.
7307084 Cyclic benzimidazoles December 11, 2007
The invention relates to cyclic benzimidazoles of formula 1, ##STR00001## in which the substituents and symbols have the meanings indicated in the description. The compounds have gastric secretion inhibiting and excellent gastric and intestinal protective action properties.
7256293 Imidazopyridine intermediates August 14, 2007
The invention relates to compounds of the formula 1, ##STR00001## in which the substituents and symbols have the meanings indicated in the description. The compounds are valuable intermediates for the preparation of pharmaceutical active compounds.
7247317 Compositions comprising phenylaminothiophenacetic acid derivatives for the treatment of acute or July 24, 2007
Novel compositions for the treatment of IRDS and ARDS are indicated which contain a compound of formula (I), in which R1 is hydrogen or 2-(2-hydroxyethoxy)ethyl and/or a pharmacologically tolerable salt of this compound and lung surfactant ##STR00001##
7238664 Composition comprising a pulmonary surfactant and a PDE5 inhibitor for the treatment of lung dis July 3, 2007
The invention relates to the combined administration of a pulmonary surfactant and a PDE5 inhibitor for the treatment of a disease in which pulmonary surfactant malfunction and/or phosphodiesterase 5 (PDE5) activity is detrimental.
7223771 Tricyclic imidazopyridines May 29, 2007
The invention provides compounds of the formula (I), in which the substituents and symbols are as defined in the description. The compounds inhibit the secretion of gastric acid. ##STR00001##
7220746 Pyrrolidinedione substituted piperidine-phthalazones as PDE4 inhibitors May 22, 2007
The compounds of formula I ##STR00001## in which the substituents have the meanings as indicated in the description, are novel effective PDE4 inhibitors.
7202055 Process for the production of proteins and the production of arrays of proteins April 10, 2007
Described is a novel process for the production of at least one protein of interest by secretion of the protein of interest from a pro- or eukaryotic host cell in a compartment system, which host cell is stably expressing a secretion system and capable of heterologous secretion of th
7189736 Prodrugs of imidazopyridine derivatives March 13, 2007
Compounds of formula 1, in which the substituents have the meanings mentioned in the description are suitable for the prevention and treatment of gastrointestinal diseases. ##STR00001##
7186710 Phthalazinones March 6, 2007
The compounds of formula I ##STR00001## in which R1, R2, R3, R4 and R5 have the meanings as given in the description are PDE4/7 inhibitors.
7179810 Phthalazinone-piperidino-derivatives as PDE4 inhibitors February 20, 2007
The compounds of formula I ##STR00001## in which the given substituents have the meanings as given in the description, are novel effective PDE4 inhibitors.
7175854 Pharmaceutical preparation comprising an active dispersed on a matrix February 13, 2007
The present invention relates to the field of pharmaceutical technology and describes a novel advantageous preparation for an active ingredient. The novel preparation is suitable for producing a large number of pharmaceutical dosage forms. In the new preparation an active ingredient
7173009 Surfactant protein C esters February 6, 2007
Novel surfactant protein C esters suitable for preparing pharmaceutical compositions for the treatment of infant respiratory distress syndrome and adult respiratory distress syndrome are described.
7147869 Rapidly disintegrating tablet comprising an acid-labile active ingredient December 12, 2006
A rapidly disintegrating tablet for oral administration of acid-labile active ingredients is described. The rapidly disintegrating tablet for oral administration of an acid-labile active ingredient comprises a plurality of individual active ingredient units together with pharmaceutic
7141567 Polysubstituted imidazopyridines as gastric secretion inhibitors November 28, 2006
The invention relates to imidazopyridines of a certain formula 1, in which the substituents and symbols have the meanings indicated in the description. The compounds have gastric secretion-inhibiting properties.
7138399 Alkoxypyridine-derivatives November 21, 2006
The compounds of formula I ##STR00001## in which R1 is 1 4C-alkoxy, A is 1 4C-alkylene, B represents 3H-imidazo[4,5-b]pyridin-2-yl, 3H-imidazo[4,5-b]pyridin-2-yl substituted by R2 and/or R3, 9H-purin-8-yl or 9H-purin-8-yl substituted by R4 and/or R5, are effective iNOS inhibitors.
7135452 Recombinant SP-A for the treatment or prevention of pulmonary infection and inflammation November 14, 2006
Recombinant surfactant protein A and pharmaceutical compositions based thereon are useful for the prevention or treatment of pulmonary infection and inflammation.
7105676 Tetrahydropyridoethers September 12, 2006
Compounds of formula (1) in which the substituents have the meanings mentioned in the description, are suitable for the prevention and treatment of gastrointestinal diseases.
7101911 Tryptase inhibitors September 5, 2006
Compounds of the formula I, in which M, A1, A2, K1 and K2 have the meanings given in the description are novel effective tryptase inhibitors.
7060716 Tryptase inhibitors June 13, 2006
Compounds of the formula (I), in which M is a central building block selected from the group below in which A1, A2, K1 and K2 are as defined in the description, are novel effective tryptase inhibitors.
7056936 Synergistic combination June 6, 2006
The invention relates to the combined administration of PDE inhibitors and .beta..sub.2 adrenoceptor agonists for the treatment of respiratory tract disorders.
7053176 Combination of C1-INH and lung surfactant for the treatment of respiratory disorders May 30, 2006
Pharmaceutical composition for the treatment of infant respiratory distress syndrome and acute lung injury (including adult respiratory distress syndrome) which contains C1 esterase inhibitor (C1-INH) and lung surfactant which comprises a lung surfactant protein.
7041313 Oral administration form for pyridin-2-ylmethylsulfinyl-1H-benzimidazoles May 9, 2006
The invention relates to an oral administration form for pyridin-2-ylmethylsulfinyl-1H-benzimidazoles and their salts, which comprises the active compound together with tablet disintegrants and is provided with a film coating customary per se for sustained-release compositions.
7034178 Process for the production of 3-phenylisoserine April 25, 2006
This invention is drawn to a process for the production of (R,R)-phenylisoserine or a 1 4C-alkyl ester thereof.
7022696 Piperazino-derivatives and their use as PDE4 inhibitor April 4, 2006
The compounds of formula I ##STR00001## in which R1, R2, R3, A, X, s and R9 have the meanings as given in the description are novel effective PDE4 inhibitors.
7022671 Surfactant protein C esters April 4, 2006
Novel surfactant protein C esters suitable for preparing pharmaceutical compositions for the treatment of infant respiratory distress syndrome and adult respiratory distress syndrome are described.
7015325 Tryptase inhibitors March 21, 2006
Compounds of the formula (I), in which M, A1, A2, K1 and K2 have the meanings indicated in the description are novel active tryptase inhibitors.
6998410 Compositions February 14, 2006
Novel compositions for the treatment of IRDS and ARDS are indicated which contain N-(3,5-dichloro-pyrid-4-yl)-3-cyclopropylmethoxy-4-difluoromethox- ybenzamide and/or its pharmacologically tolerable salts and lung surfactant.
6988619 Medicinal product package for eradication therapy January 24, 2006
The object of the present invention is to provide a medicinal product package which is suitable for microbe eradication therapy and with which the patient's compliance is increased and thus the result of therapy is improved.
6982075 Use of pulmonary surfactant January 3, 2006
The invention describes the novel use of pulmonary surfactant preparations in the artificial respiration of patents with toxic oxygen concentrations.
6962941 Tryptase inhibitors November 8, 2005
The compounds of formula I ##STR1##in which M, B1, B2, R1, R2, R6, R7, K1 and K2 have the meanings as indicated in the description are novel active tryptase inhibitors.
6960588 Tryptase inhibitors November 1, 2005
Compounds of formula (I) ##STR1##in which M, B1, B2, B3, B4, B5, B6, A1, A2, A3, A4, A5, A6, K1 and K2 have the meanings as indicated in the description, are novel effective tryptase inhibitors.
6953853 Phthalazinone-piperidino-derivatives as PDE4 inhibitors October 11, 2005
The compounds of a formula I, in which the given substituents have the meanings as given in the description, are novel effective PDE4 inhibitors ##STR1##
6936623 Pyrano[2,3-C]imidazo[-1,2-A]pyridine derivatives for the treatment of gastrointestinal disorders August 30, 2005
Compounds of the formula (I), in which the substituents have the meanings mentioned in the description, are suitable for the prevention and treatment of gastrointestinal diseases.
6936622 6-phenylbenzonaphthyridines August 30, 2005
Compounds of the formula (I), in which R1, R2, R3, R4 and R5 have the meanings indicated in the description, are novel effective PDE3/4 Inhibitors.
6927292 Tricyclic epoxides August 9, 2005
The invention relates to compounds of Formula (1), in which the substituents and symbols have the meanings indicated in the description. The compounds are valuable intermediates for the preparation of pharmaceutical active compounds.
6924305 Diazocine derivatives and their use as tryptase inhibitors August 2, 2005
Compounds of the formula I, in which B1, B2, R1, R2, R6, R7, K1 and K2 are as defined in the description are novel effective tryp-tase inhibitors.
6916825 Alkylated imidazopyridine derivatives July 12, 2005
Compounds of the formula 1 ##STR1##in which the substituents have the meanings mentioned in the description are suitable for the prevention and treatment of gastrointestinal diseases.
6897229 Synergistic combination comprising roflumilast and a PDE-3 inhibitor May 24, 2005
The PDE.sub.4 inhibitor N-(3,5-dichloropyrid-4-yl)-3-cyclopropylmethoxy-4-difluoromethoxy benzamide, a pharmacologically tolerable salt or N-oxide thereof, in combination with a PDE.sub.3 inhibitor is disclosed for use in inhibiting bronchospasms and treating acute obstructive bronch
6884802 6-heteroarylphenanthridines April 26, 2005
Compounds of formula 1, in which Het is an unsubstituted or R6- and/or R7-substituted pyrrolyl, furanyl, thiophenyl, pyrazolyl, imidazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, thiadiazolyl, pyrimidinyl, pyrazinyl or pyradazinyl radical, or an unsubstituted or R6- and/or R7
6869949 Polysubstituted imidazopyridines as gastric secretion inhibitors March 22, 2005
The invention relates to imidazopyridines of a certain formula 1, in which the substituents and symbols have the meanings indicated in the description. The compounds have gastric secretion-inhibiting properties.
6858223 Compositions comprising phenylaminothiophenacetic acid derivatives for the treatment of acute or February 22, 2005
A composition comprising a combination of a compound of formula I ##STR1##in which R1 is hydrogen or 2-(2-hydroxyethoxy)ethyl and/or a pharmacologically tolerable salt thereof, and lung surfactant is useful for treating patients afflicted with IRDS or ARDS.
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