摘要:
The present invention is intended to provide a method for simultaneously measuring cholesterol in low density lipoprotein and total cholesterol as test components in blood. Specifically, a method is used for simultaneously measuring cholesterol in low density lipoprotein and total cholesterol in a biological sample, whereby cholesterol in low density lipoprotein and total cholesterol in a biological sample are quantified with a single measurement.
摘要:
Disclosed is a method for quantifying cholesterol in HDL, which does not require complex fragmentation and separation operations, and by which the HDL cholesterol in test samples containing HDL and other lipoproteins such as low density lipoprotein (LDL), very low density lipoprotein (VLDL) and chylomicron (CM) may be quantified selectively, simply and accurately. The method for quantifying cholesterol in high density lipoprotein comprises a first step of erasing cholesterol in lipoproteins other than high density lipoprotein in a test sample, and a second step of adding a surfactant which specifically acts on high density lipoprotein to the product of the first step and enzymatically quantifying cholesterol in high density lipoprotein.
摘要:
Heterocyclic derivatives of the formula (I) wherein each symbol is as defined in the specification, pharmaceutically acceptable salts thereof and method of producing them. Pharmaceutical compositions containing the heterocyclic derivative or a pharmaceutically acceptable salt thereof, particularly, ACAT inhibitors and lipoperoxidation inhibitors. The heterocyclic derivatives and pharmaceutically acceptable salts thereof of the present invention show superior ACAT inhibitory activity and lipoperoxidation inhibitory activity, and are useful as ACAT inhibitors and hyperlipemia inhibitors. To be specific, they are useful for the prevention and treatment of arteriosclerotic lesions of arteriosclerosis, hyperlipemia and diabetes, as well as ischemic diseases of brain, heart and the like.
摘要:
A push and rotary operating type electronic device comprises a push switch unit 37 composed in a center of a bottom surface of a case 30, a rotary encoder unit 35 composed at a periphery of the push switch unit, a discoidal operating knob 39 mounted in a manner to be independently movable vertically, while also rotatable conjunctly with the rotary encoder unit 35, wherein the both component units 35 and 37 are operative by depression on a peripheral portion of the operating knob 39 during a rotary manipulation and a center portion of the same in a depressing manipulation. Communication terminal equipment uses this push and rotary operating type electronic device. This structure realizes a small projected area, and allows the rotary manipulation and the depressing manipulation by operating different portions of the single operating knob 39.
摘要:
A rotary-push type electronic component is provided for use in an electronic appliance such as a mobile phone. The electronic component includes a base unit, a frame mounted to the base unit, a support shaft coupling the frame to the base unit for pivotal and vertical movement of the frame relative to the base unit, a generally cylindrical operation knob rotatably mounted to the frame, a rotary operation device for emitting an electric signal upon rotation of the generally cylindrical operation knob, and a pair of self-restoring push operation parts spaced apart on the base unit below the frame so as to be operated by pivoting of the frame about the support shaft relative to the base unit. The support shaft is disposed at a rear portion of the frame, and the push operation parts are disposed beneath a front portion of the frame.
摘要:
A heterocyclic derivative of the formula (I) wherein each symbol is as defined in the specification, and pharmaceutically acceptable salts thereof. The compound (I) of the present invention and pharmaceutically acceptable salts thereof exhibit superior ACAT inhibitory activity and lipoperoxidation inhibitory activity in mammals, and are useful as ACAT inhibitors and lipoperoxidation inhibitors. Specifically, they are useful for the prophylaxis and treatment of arteriosclerosis, hyperlipemia, arteriosclerosis in diabetes, and cerebrovascular and cardiovascular ischemic diseases.
摘要:
A rotary encoder used mainly in a peripheral apparatus for computers, a portable telephone, an on-board electronic device for automobiles, and the like, in which an encoder unit and a linearly-driven type component are operable by a rotating manipulation and a tilting manipulation of an operating axle. The rotary encoder provides accuracy and is capable of producing a large number of output signals without requiring an increase in external dimensions. The rotary encoder is so constructed that flexible contacts and make resilient contact with movable contacts on a peripheral surface of a cylindrical rotor in a main unit of the encoder. The operating axle is pivotally supported by fitting it in an axle-supporting portion of the rotor in a manner that the operating axle is rotatable together with the rotor and is also tiltable. A cylindrical operating knob is attached to the operating axle that protrudes sideways from the rotor, and a push switch is disposed in a position to be in contact with a distal end of the same operating axle, and thereby making the main unit of the encoder operable by rotating manipulation and the push switch by tilting manipulation of the operating axle.
摘要:
A heterocyclic derivative of the formula (I) ##STR1## wherein each symbol is as defined in the specification, and pharmaceutically acceptable salts thereof. The compound (I) of the present invention and pharmaceutically acceptable salts thereof exhibit superior ACAT inhibitory activity and lipoperoxidation inhibitory activity in mammals, and are useful as ACAT inhibitors and lipoperoxidation inhibitors. Specifically, they are useful for the prophylaxis and treatment of arteriosclerosis, hyperlipemia, arteriosclerosis in diabetes, and cerebrovascular and cardiovascular ischemic diseases.
摘要:
Heterocyclic derivatives of the formula (I) ##STR1## wherein each symbol is as defined in the specification, pharmaceutically acceptable salts thereof and method of producing them. Pharmaceutical compositions containing the heterocyclic derivative or a pharmaceutically acceptable salt thereof, particularly, ACAT inhibitors and lipoperoxidation inhibitors. The heterocyclic derivatives and pharmaceutically acceptable salts thereof of the present invention show superior ACAT inhibitory activity and lipoperoxidation inhibitory activity, and are useful as ACAT inhibitors and hyperlipemia inhibitors. To be specific, they are useful for the prevention and treatment of arteriosclerotic lesions of arteriosclerosis, hyperlipemia and diabetes, as well as ischemic diseases of brain, heart and the like.