Abstract:
Compounds represented by the general formula (1) or salts thereof or solvates of both; PAR-2 antagonists containing the compounds; and preventive or therapeutic agents for PAR-2 related diseases containing the antagonists as the active ingredient: (1) wherein R1 is hydrogen, halogeno, or a group represented by the general formula (2): (wherein R11 is straight-chain or branched C1-6 alkylene or the like; and R12 and R13 together with the nitrogen atom adjacent to them form a 5- to 7-membered ring); R2 is straight-chain or branched C1-6 alkyl or the like; R3 and R4 are each independently hydrogen, one to three halogen atoms, or the like; and A1-A2-A3 is a tripeptide residue composed of α-amino acids each independently selected from the group consisting of glycine, alanine, cyclohexylalanine, and so on.
Abstract translation:由通式(1)表示的化合物或其盐或两者的溶剂合物; 含有这些化合物的PAR-2拮抗剂; 以及含有拮抗剂作为活性成分的PAR-2相关疾病的预防或治疗剂:(1)其中R1是氢,卤素或由通式(2)表示的基团:(其中R11是直链或支链的 C 1-6亚烷基等; R 12和R 13与它们相邻的氮原子一起形成5-至7-元环); R2是直链或支链C 1-6烷基等; R3和R4各自独立地为氢,一至三个卤素原子等; 并且A1-A2-A3是由各自独立地选自甘氨酸,丙氨酸,环己基丙氨酸等的α-氨基酸组成的三肽残基。
Abstract:
It is intended to provide a novel pharmaceutical effect of HMG-COA reductase inhibitors, in particular, (+)-(3R, 5S, 6E)-7-[2-cyclopropyl-4-(4-fluorophenyl)-3-quinolyl]-3,5-di hydroxy-6-heptenoic acid or its salt. Namely, TM expression promoters, more specifically speaking, antithrombotic drugs, preventive/remedies for sepsis, antiplatelet drugs and anticoagulants comprising as the active ingredient an HMG-COA reductase inhibitor, in particular, (+)-(3R, 5S, 6E)-7-[2-cyclopropyl-4-(4-fluorophenyl)-3-quinolyl]-3,5-dihydroxy-6-heptenoic acid or its salt.
Abstract:
Attenuation compensation volume computing means (60, 61, 62, 63, 67, 68, 69, 70) of a signal receiver computes attenuation compensation volume of a video signal (GL, GH) on the basis of attenuation of pulses which are arranged in a digital sound signal LRD from the signal transmitter, and video signal attenuation compensation means (60, 61) of the signal receiver compensates the attenuation of the video signal (RAT, GAT, BAT) on the basis of the computed attenuation compensation volume (GL, GH), thereby stably compensating the attenuation of the video signal irrespective of kinds of displays or resolution of an image, and outputting good sounds to a video output machine as well as good videos.
Abstract:
An intraocular tension measuring method comprising vibrating an eyeball to be examined by a sound wave, measuring vibration of the eyeball to be examined by a noninvasive means to determine a Q value of resonance of the eyeball to be examined, and calculating intraocular tension from the Q value, and an intraocular tension measuring device comprising a vibrating means for vibrating an eyeball to be examined by a sound wave, a measuring means for noninvasively measuring vibration of the eyeball to be examined, a Q value calculating means for calculating a Q value of resonance of the eyeball to be examined from the vibration measured by the measuring means, and an intraocular tension calculating means for calculating intraocular tension from the Q value.
Abstract:
A model eye that models the optical characteristics of a human eye and is endowed with a grayscale pattern on the ocular fundus model surface is stereographically photographed with a parallax via a stereo photographic optical system. Photographed images are processed to provide calibration data for correcting the shape distortions of the stereo photographic optical system. The calibration data is used to correct a distortion-affected shape data and parallax images obtained in stereographic photography of the actual ocular fundus of a subject's eye. The shape distortion-corrected parallax image is used for a three-dimensional measurement process and 3D display on a stereo monitor. This allows an accurate three-dimensional measurement to be carried out and an accurate fundus image to be produced. The examiner can accurately evaluate the stereo shape of the ocular fundus of the subject's eye.
Abstract:
The present invention provides to a novel compound having an ACAT inhibiting activity.The present invention relates to compounds represented by formula (I) wherein represents an optionally substituted divalent residue such as benzene, pyridine, cyclohexane or naphthalene, or a group, Het represents a 5- to 8-membered, substituted or unsubstituted heterocyclic group containing at least one heteroatom selected from the group consisting of a nitrogen atom, an oxygen atom and a sulfur atom, such as a monocyclic group, a polycyclic group or a group of a fused ring, X represents —NH—, an oxygen atom or a sulfur atom, Y represents —NR4—, an oxygen atom, a sulfur atom, a sulfoxide or a sulfone, Z represents a single bond or —NR5—, R4 represents a hydrogen atom, a lower alkyl group, an aryl group or an optionally substituted silyl lower alkyl group, R5 represents a hydrogen atom, a lower alkyl group, an aryl group or an optionally substituted silyl lower alkyl group, and n is an integer of from 1 to 15, or salts or solvates thereof, and a pharmaceutical composition containing at least one of these compounds.
Abstract:
An antibody against a peptide having an amino acid sequence AVQGPEETVT QDC (expressed in single letter amino acid code) corresponding to the 134- to 146-positions in human BAFF (B cell activating factor belonging to the TNF family) protein which is preferably a monoclonal antibody; a method of producing the above antibody; a medicinal composition containing the antibody; utilization of the antibody; and a method of screening an inhibitory effect or an activating effect on BAFF with the use of the antibody.
Abstract:
There is provided a perimeter that allows a reliability evaluation to be performed in a kinetic visual field examination. A stimulus for examination is displayed onto an inner surface of a visual field dome and moved at a constant speed on a meridian toward the center of the dome. A subject responds to the stimulus for examination when he visually recognized the moving stimulus. There is displayed a false-negative stimulus, which is more visible than the stimulus for examination, or a false-positive stimulus, which corresponds to the operating sound of the perimeter without any stimulus display. The visual field examination results are evaluated on the basis of a response made by the subject to the false-negative and the false-positive stimuli.This arrangement allows the reliability of the examination results in a kinetic visual field examination to be satisfactorily evaluated.
Abstract:
A perimeter is comprised of means for setting a second visual field coordinate system on a fundus image displayed on a monitor wherein an origin is a macula lutea, means for provisionally determining a blind spot position on the second visual field coordinate system, means for searching a coordinate position of a blind spot on the first visual field coordinate system by presenting a stimulus on the visual field dome, means for changing a scale of the second visual field coordinate system so as to correspond the coordinate value of the blind spot on the first visual field coordinate system and the coordinate position of the blind spot on the second visual field coordinate system with each other, and means for conducting a perimetry by presenting the stimulus at a position on the first visual field coordinate system having the same coordinate value as one on the second coordinate system of a predetermined test point.
Abstract:
A nuclear transfer promoter for Cdc42 protein comprising an isoprenoid synthesis inhibitor and/or a geranylgeranyl transferase inhibitor such as an HMG-CoA synthase inhibitor, an HMG-CoA reductase inhibitor, an AMPK activator or a farnesyl pyrophosphoric acid synthase preparation; utilization thereof; a method therefor; a blood vessel remedy comprising the nuclear transfer promoter for Cdc42 protein as the active ingredient; and a method of screening a blood vessel remedy which comprises assaying the ability of Cdc42 protein to transfer into nucleus.