摘要:
The present invention relates to the identification, functionality and use of domains from the N terminus of the receptor for Advanced Glycation End Products (AGER). These domains, called receptor multimerization epitope (RME), are highly conserved in all AGER protein sequences. They represent the mediators for AGER self-association and heteromerization with other proteins. The invention likewise relates to the identification, functionality and use of peptides derived from the C domain of AGER (AGER-CDP). The AGER RMEs and AGER-CDPs of the invention are suitable as target for identifying AGER ligands which modulate the natural ligand interaction; as immunogen for active or passive immunization of individuals, as diagnostic means for identifying immunogenic reactions, and as peptide ligands for modulating protein-protein interactions involving AGER.
摘要:
The present invention relates to the identification, functionality and use of domains from the N terminus of the receptor for Advanced Glycation End Products (AGER). These domains, called receptor mulitimerization epitope (RME), are highly conserved in all AGER protein sequences. They represent the mediators for AGER self-association and heteromerization with other proteins. The invention likewise relates to the identification, functionality and use of peptides derived from the C domain of AGER (AGER-CDP). The AGER RMEs and AGER-CDPs of the invention are suitable as target for identifying AGER ligands which modulate the natural ligand interaction; as immunogen for active or passive immunization of individuals, as diagnostic means for identifying immunogenic reactions, and as peptide ligands for modulating protein-protein interactions involving AGER.
摘要:
The invention relates to the hetaryl-substituted guanidine compounds of general formula (I), enantiomeres, diastereomeres and/or tautomeres thereof, in addition to the pharmaceutically acceptable salts thereof and the prodrugs of the known compounds. The invention also relates to the use of said hetaryl-substituted guanidine compounds as binding partners for 5-HT5-receptors for treating and/or for the prophylaxis of illnesses which are modulated by a 5-HT5-receptor activity, in particular, for treating and/or for the prophylaxis of neurodegenerative and neuropsychiatric disorders, and signs, symptoms and dysfunctions associated with said disorders.
摘要:
The present invention relates to novel quinoline compounds. The compounds possess valuable therapeutic properties and are particularly suitable, for treating diseases that respond to modulation of the serotonin 5-HT6 receptor. wherein R is a moiety of the formula wherein A, R1 to R4 are as defined in the claims and the specification, n is 0, 1 or 2; m is 0, 1, 2 or 3; Ra, Rb are independently selected from the group consisting of halogen, CN, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy, C(O)Raa, C(O)NRccRbb and NRccRbb; X is CH2, C(O), S, S(O) or S(O)2; which is located in the 3- or 4-position of the quinoline ring; Ar is a radical Ar1, Ar2—Ar3 or Ar2—O—Ar3, wherein Ar1, Ar2 and Ar3 are each independently selected from the group consisting of aryl or hetaryl wherein aryl or hetaryl moieties may be unsubstituted or may carry 1, 2, 3 substituents Rx, wherein and physiologically tolerated acid addition salts and the N-oxides thereof.
摘要翻译:本发明涉及新颖的喹啉化合物。 该化合物具有有价值的治疗特性,特别适用于治疗对血清素5-HT 6受体调节作出反应的疾病。 其中R是下式的部分,其中A,R 1至R 4如权利要求和说明书中所定义,n为0,1或2; m为0,1,2或3; R a,R b独立地选自卤素,CN,C 1 -C 4 - 烷基,C 1 -C 4卤代烷基,C 1 -C 4 - 烷氧基,C 1 -C 4卤代烷氧基,C(O)R aa,C(O)NR c R b b 和NRccRbb; X是CH 2,C(O),S,S(O)或S(O)2; 其位于喹啉环的3-或4-位; Ar是Ar1,Ar2-Ar3或Ar2-O-Ar3基团,其中Ar1,Ar2和Ar3各自独立地选自芳基或杂芳基,其中芳基或杂芳基部分可以是未取代的或可以携带1,2,3 取代基Rx,其中和生理上耐受的酸加成盐及其N-氧化物。
摘要:
The invention relates to 5-ring heteroaromatic compounds of general formula (I), their use for the treatment and/or prevention of diseases, and medicaments containing same.
摘要:
A support apparatus for supporting and positioning a patient during a medical examination includes a patient support plate and a combination of elements for lifting and pivoting the support plate which operate to pivot the support plate around a stationary, virtual (i.e., non-load bearing) axis disposed at an end region of the support plate.
摘要:
The invention relates to an apparatus for the contactless fragmentation of a concrement present in the body of a living being. A shock wave generator is aimed at a target region in the body and includes a coil having the form of a spherical segment. In front of the coil is arranged a mating radiator element, which closes off a liquid filled space and generates therein a shock wave focused on the centers of curvature of the coil and element upon brief connection of the coil to a high voltage. The concrement to be fragmented is positioned to lie at these centers of curvature.
摘要:
A primary-beam collimator for a stereo radiographic x-ray diagnostic installation has an x-ray tube with dual focal points (F1, F2) arranged at a distance from each other. Shutter leaves (1a, 1b, 2a, 2b, 3a, 3b, 4a, 4b) are provided, and adjustable so that two beam pyramids (I from focal point F1, and II from focal point F2) can be individually controlled. Two internal shutter leaves (4a, 4b) are provided for restricting the beam in planes perpendicular to the stereo base F1-F2. These are adjustable between two external shutter leaves--each in the direction of its corresponding external shutter leaf. The internal shutter leaves (4a, 4b) are constructed so that, when adjusted to their external positions, they permit the emission of a central beam-pyramid from a central focal point (FN) and, together with the external shutter leaves (2a, 2b), they close the external shutter openings.
摘要:
An x-ray examination table having a trestle on which a patient support platform is height-adjustably mounted, characterized by the trestle having a liftable member on which the table is mounted being connected to a base by a double-jointed support arrangement and being movable to the base by a lifting arrangement. The double-jointed support arrangement includes a pair of brackets pivotally connected together and having one of the pair being pivotally connected to the liftable member and the other being pivotally connected to the base. The pivotal connections are shafts which extend parallel to each other for each linkage arrangement and perpendicular to the shafts of the adjacent linkage arrangement so that the double-jointed supports guide the liftable member as it is moved between the upper and lowermost positions.
摘要:
The present invention relates to engineered multivalent and multispecific binding proteins, methods of making, and specifically to their uses in the prevention, diagnosis, and/or treatment of disease.