Patents by Inventor Ulrich Demuth

Ulrich Demuth has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Patent number: 7053055
    Abstract: Novel compounds of unstable inhibitors of the serine peptidase dipeptidyl peptidase IV, are used in the treatment of various disorders, especially of metabolic disorders. The compounds can be used in the treatment of impaired glucose tolerance, glucosuria, hyperlipidaemia, metabolic acidoses, diabetes mellitus, diabetic neuropathy and nephropathy.
    Type: Grant
    Filed: December 21, 2000
    Date of Patent: May 30, 2006
    Assignee: Prosidion Ltd.
    Inventors: Hans-Ulrich Demuth, Jorn Schmidt, Torsten Hoffmann, Konrad Glund
  • Publication number: 20060100253
    Abstract: The present invention relates to novel inhibitors of prolyl endopeptidase of formula 1 W—KCONH—X—CON—Y—CO—Z ??(1) wherein K, W, X, Y and Z are specified in the description. The compounds are useful for the treatment of diseases such as mild cognitive impairment (MCI), Alzheimer's disease, Down Syndrome, Parkinson disease and Chorea Huntington.
    Type: Application
    Filed: November 30, 2005
    Publication date: May 11, 2006
    Inventors: Andre Niestroj, Ulrich Heiser, Ingo Schulz, Jens-Ulrich Rahfeld, Joachim Baer, Hans-Ulrich Demuth
  • Patent number: 7025610
    Abstract: An electrical connector arrangement having a first connector which is arranged in a housing and may be brought into an electrical connection with a mating connector by the actuation of an actuation lever arranged movably on the first connector. The actuation lever being movable between a free position in which the two connectors are not fully mated and a coupled position in which the two connectors are fully mated. A portion of the actuation lever is disposed between the first connector and the housing with a clamping projection on the lever that is in engagement with a mating clamping projection on the housing when the actuation lever is in the coupled position.
    Type: Grant
    Filed: April 13, 2004
    Date of Patent: April 11, 2006
    Assignee: Tyco Electronics AMP GmbH
    Inventor: Ulrich Demuth
  • Publication number: 20050233978
    Abstract: The present invention relates to new compounds that act as specific inhibitors of the cysteine protease dipeptidyl peptidase I (DP I). Those compounds are represented by the general formula and the pharmaceutical salts thereof, in which R is an acyl-residue including urethane and peptide, or a branched or unbranched C1-C9 alkyl chain, a branched or unbranched C2-C9 alkenyl chain, a branched or unbranched C2-C9 alkynyl chain, a C3-C9 cycloalkyl, C4-C9 carbocyclic, C5-C14 aryl, C3-C9 heteroaryl, C3-C9 heterocyclic, all of the above residues may be optionally substituted, or is H, AS is an amino acid or a peptide mimetic thereof. The amino acid is peptide bound with R and R? is a branched or unbranched C1-C9 alkyl chain, a branched or unbranched C2-C9 alkenyl chain, a branched or unbranched.
    Type: Application
    Filed: November 24, 2004
    Publication date: October 20, 2005
    Inventors: Andre Niestroj, Ulrich Heiser, Hans-Ulrich Demuth
  • Publication number: 20050222221
    Abstract: The present invention discloses a method for therapeutically treating mammals, including but not limited to humans, to increase the relative insulin producing performance of endogenous pancreatic ?-cells and to cause differentiation of pancreatic epithelial cells into insulin producing ?-cells. Oral administration a DP IV inhibitor causes the active form of GLP-1 to be preserved longer under physiological conditions. The extended presence of GLP-1, in particular in the pancreatic tissue facilitates differentiation and regeneration of the ?-cells already present that are in need of repair. These repaired insulin producing cells can contribute to the correction and maintenance of normal physiological glycemic levels.
    Type: Application
    Filed: October 1, 2003
    Publication date: October 6, 2005
    Inventors: Hans-Ulrich Demuth, Konrad Glund
  • Publication number: 20050215573
    Abstract: The present invention relates to novel inhibitors of glutaminyl cyclase and combinations thereof for the treatment of neuronal disorders, especially Alzheimer's disease, Down Syndrome, Parkinson disease, Chorea Huntington, pathogenic psychotic conditions, schizophrenia, impaired food intake, sleep-wakefulness, impaired homeostatic regulation of energy metabolism, impaired autonomic function, impaired hormonal balance, impaired regulation, body fluids, hypertension, fever, sleep dysregulation, anorexia, anxiety related disorders including depression, seizures including epilepsy, drug withdrawal and alcoholism, neurodegenerative disorders including cognitive dysfunction and dementia.
    Type: Application
    Filed: February 4, 2005
    Publication date: September 29, 2005
    Inventors: Stephan Schilling, Mirko Buchholz, Andre Niestroj, Ulrich Heiser, Hans-Ulrich Demuth
  • Patent number: 6949515
    Abstract: The invention relates to compounds for topically influencing the activity of dipeptidyl peptidase of the general formula wherein A is an amino acid having at least one functional group in the side chain; B is a chemical compound covalently bound to a functional group of the side chain of A, chosen from the group consisting of (a) oligopeptides having a chain length of up to 20 amino acids, (b) homopolymers of glycine consisting of up to 6 glycine monomers, and (c) polyethylene glycols having molar masses of up to 20 000 g/mol; and C is a group amide-bonded to A chosen from the group consisting of thiazolidine, pyrrolidine, cyanopyrrolidine, hydroxyproline, dehydroproline or piperidine.
    Type: Grant
    Filed: February 22, 2002
    Date of Patent: September 27, 2005
    Assignee: Probiodrug AG
    Inventors: Hans-Ulrich Demuth, Torsten Hoffmann, Dagmar Schlenzig, Ulrich Heiser
  • Publication number: 20050209159
    Abstract: The invention relates to compounds for topically influencing the activity of dipeptidyl peptidase of the general formula wherein A is an amino acid having at least one functional group in the side chain; B is a chemical compound covalently bound to a functional group of the side chain of A, chosen from the group consisting of (a) oligopeptides having a chain length of up to 20 amino acids, (b) homopolymers of glycine consisting of up to 6 glycine monomers, and (c) polyethylene glycols having molar masses of up to 20 000 g/mol; and C is a group amide-bonded to A chosen from the group consisting of thiazolidine, pyrrolidine, cyanopyrrolidine, hydroxyproline, dehydroproline or piperidine.
    Type: Application
    Filed: March 1, 2005
    Publication date: September 22, 2005
    Inventors: Hans-Ulrich Demuth, Torsten Hoffmann, Dagmar Schlenzig, Ulrich Heiser
  • Patent number: 6946480
    Abstract: The present invention provides compounds of the formula: wherein X?CH2 or S or pharmaceutical acceptable salts thereof useful for treating conditions mediated by DPIV or DPIV-like enzymes, such as arthritis, obesity, immune and autoimmune disorders, allograft transplantation, cancer, neuronal disorders and dermal diseases.
    Type: Grant
    Filed: September 16, 2002
    Date of Patent: September 20, 2005
    Inventors: Hans-Ulrich Demuth, Torsten Hoffmann, Ulrich Heiser
  • Publication number: 20050203030
    Abstract: Dipeptide compounds and compounds analogous to dipeptide compounds that are formed from an amino acid and a thiazolidine or pyrrolidine group, and salts thereof used in the treatment of impaired glucose tolerance, glycosuria, hyperlipidaemia, metabolic acidoses, diabetes mellitus, diabetic neuropathy and nephropathy and also of sequelae of diabetes mellitus in mammals.
    Type: Application
    Filed: December 2, 2003
    Publication date: September 15, 2005
    Inventors: Hans-Ulrich Demuth, Konrad Glund, Dagmar Schlenzig, Susanne Kruber
  • Publication number: 20050176622
    Abstract: The present application relates to the secondary binding site of dipeptidyl peptidase IV, its relationship amongst substrates and to the modulation of substrate specificity of dipeptidyl peptidase IV (DP IV, synonym: DPP IV, CD26, EC 3.4.14.5). The application relates further to compounds that bind to the secondary binding site of DP IV and their use to modulate the substrate specificity of DP IV; methods of treatment of various DP IV mediated disorders; and screening methods for the identification of secondary binding sites on DP IV and DP IV-like enzymes.
    Type: Application
    Filed: September 18, 2003
    Publication date: August 11, 2005
    Inventors: Kerstin Kuhn-Wache, Joachim Bar, Hans-Ulrich Demuth, Torsten Hoffmann, Ulrich Heiser, Wolfgang Brandt
  • Publication number: 20050171025
    Abstract: The present invention provides new uses of DPIV-inhibitors of the present invention, and their corresponding pharmaceutically acceptable acid addition salt forms, for treating conditions mediated by DPIV or DPIV-like enzymes, such as cancer and tumors. In a more preferred embodiment, the compounds of the present invention are useful for the treatment of metastasis and tumor colonization.
    Type: Application
    Filed: March 30, 2005
    Publication date: August 4, 2005
    Inventors: Stephan von Hoersten, Hans-Ulrich Demuth, Torsten Hoffmann
  • Publication number: 20050171112
    Abstract: The present invention provides a method for the treatment of neuronal disorders, in a mammal such as a human, which method comprises administering an effective, non-toxic and pharmaceutically acceptable amount of at least one QC-inhibitor, optionally in combination with at least one agent, selected from the group consisting of PEP-inhibitors, LiCl, inhibitors of DP IV/DP IV-like enzymes, NPY-receptor ligands, NPY agonists, NPY antagonists, ACE-inhibitors, PIMT enhancers, inhibitors of beta secretases, inhibitors of gamma secretases and inhibitors of neutral endopeptidase, to a mammal in need thereof.
    Type: Application
    Filed: December 2, 2004
    Publication date: August 4, 2005
    Inventors: Ingo Schulz, Stephan Schilling, Andre Niestroj, Ulrich Heiser, Hans-Ulrich Demuth, Steffen Rossner
  • Publication number: 20050137142
    Abstract: The present invention provides a method for the treatment of neuronal disorders, in a mammal such as a human, which method comprises administering an effective, non-toxic and pharmaceutically acceptable amount of at least one QC-inhibitor, optionally in combination with at least one agent, selected from the group consisting of PEP-inhibitors, inhibitors of DP IV/DP IV-like enzymes, NPY-receptor ligands, NPY agonists, NPY antagonists, ACE-inhibitors, PIMT enhancers, inhibitors of beta secretases, inhibitors of gamma secretases and inhibitors of neutral endopeptidase, to a mammal in need thereof.
    Type: Application
    Filed: October 29, 2004
    Publication date: June 23, 2005
    Inventors: Ingo Schulz, Stephan Schilling, Andre Niestroj, Hans-Ulrich Demuth, Steffen Rossner
  • Publication number: 20050137135
    Abstract: The present invention relates to novel C-terminal truncated fragments and novel N-terminal modified analogues of gastric inhibitory polypeptide as well as various GIP analogues with a reduced peptide bond or alterations of the amino acids close to the dipeptidyl peptidase IV (DPIV)-specific cleavage site providing improved DPIV-resistance and prolonged half-life. Further the invention relates to novel analogs with different linkers between potential receptor binding sites of GIP. The compounds of the present invention and their pharmaceutically acceptable salts are useful in treating GIP-receptor mediated conditions, such as non-insulin dependent diabetes mellitus and obesity.
    Type: Application
    Filed: January 25, 2005
    Publication date: June 23, 2005
    Inventors: Simon Hinke, Susanne Manhart, Jan Ehses, Christopher McIntosh, Hans-Ulrich Demuth, Raymond Pederson
  • Publication number: 20050107309
    Abstract: The present invention comprises the use of activity-reducing effectors of dipeptidyl peptidase (DP IV) and DP IV-analogous enzyme activity in the blood of a mammal to lower elevated post-prandial and basal blood glucose levels in mammalian organisms. The invention further comprises the use of activity-reducing effectors of dipeptidyl peptidase (DP IV) and DP IV-analogous enzyme activity in the blood of a mammal to increase the half-life of incretins in vivo.
    Type: Application
    Filed: December 22, 2004
    Publication date: May 19, 2005
    Inventors: Hans-Ulrich Demuth, Fred Rosche, Joem Schmidt, Robert Pauly, Christopher McIntosh, Ray Pederson
  • Publication number: 20050107308
    Abstract: The present invention provides new uses of DPIV-inhibitors of the present invention, and their corresponding pharmaceutically acceptable acid addition salt forms, for lowering blood pressure levels.
    Type: Application
    Filed: October 21, 2004
    Publication date: May 19, 2005
    Inventors: Andrew Pospisilik, Hans-Ulrich Demuth, Kourad Glund, Matthias Hoffmann, Christopher McIntosh, Ray Pederson
  • Patent number: 6890905
    Abstract: The present invention discloses methods for therapeutically treating mammals, including but not limited to humans, to increase the relative insulin producing performance of endogenous pancreatic ?-cells, to cause differentiation of pancreatic epithelial cells into insulin producing ?-cells, to improve muscle sensitivity to insulin and other weight control efforts by the chronic oral administration of a DP IV-inhibitor. The administration causes the active form of GLP-1 and other non-nutrient stimulated growth hormones to remain biologically active longer under physiological conditions. The extended presence of such hormones, in particular in the pancreatic tissue can also facilitate differentiation and regeneration of the ?-cells already present that are in need of repair.
    Type: Grant
    Filed: August 9, 2002
    Date of Patent: May 10, 2005
    Assignee: Prosidion Limited
    Inventors: Hans-Ulrich Demuth, Konrad Glund, Andrew J. Pospisilik, Kerstin Kuehn-Wache
  • Publication number: 20050058635
    Abstract: The present invention provides novel physiological substrates of mammalian glutaminyl cyclase (QC, EC 2.3.2.5), new effectors of QC, methods for screeing for such effectors, and the use of such effectors and pharmaceutical compositions comprising such effectors for the treatment of conditions that can be treated by modulation of QC-activity. Preferred compositions additionally comprise inhibitors of DP IV or DP IV-like enzymes for the treatment or alleviation of conditions that can be treated by modulation of QC- and DP IV-activity.
    Type: Application
    Filed: May 5, 2004
    Publication date: March 17, 2005
    Inventors: Hans-Ulrich Demuth, Torsten Hoffmann, Andre Niestroj, Stephan Schilling, Ulrich Heiser
  • Publication number: 20050026484
    Abstract: An electrical connector arrangement having a first connector which is arranged in a housing and may be brought into an electrical connection with a mating connector by the actuation of an actuation lever arranged movably on the first connector. The actuation lever being movable between a free position in which the two connectors are not fully mated and a coupled position in which the two connectors are fully mated. A portion of the actuation lever is disposed between the first connector and the housing with a clamping projection on the lever that is in engagement with a mating clamping projection on the housing when the actuation lever is in the coupled position.
    Type: Application
    Filed: April 13, 2004
    Publication date: February 3, 2005
    Inventor: Ulrich Demuth