Abstract:
A high-strength cold-rolled steel sheet with dual-phase structure, recently developed by the Japanese steel producers have a low yield ratio of approximately 0.6 or lower, is free of the yield-point elongation and is of excellent press-formability. One of the production methods of this steel is a continuous annealing at a temperature range of two-phase structure of ferrite (.alpha.)+austenite (.gamma.). In order to improve the formability, the artificial-aging hardenability after forming, yield ratio and ductility over those of the known dual-phase steel, the present invention provides a method for producing a dual-phase steel, which comprise a step of cooling from the annealing temperature to a temperature not higher than 200.degree. C. at an average cooling rate (R.sub.1) in the range of 1.degree. C./second.gtoreq.R.sub.1 .ltoreq.30.degree. C./second over the primary cooling stage from the annealing temperature down to an intermediate temperature (T) in the range of 420.degree. C..ltoreq.T.ltoreq.700.degree. C., and at an average cooling rate (R.sub.2) in the range of 100.degree. C./second.ltoreq.R.sub.2 .ltoreq.300.degree. C./second over the secondary cooling stage from the intermediate temperature (T) down to the temperature not higher than 200.degree. C.
Abstract:
A method of producing a dual phase structure cold rolled steel sheet having tensile strength 35 to 50 kg/mm.sup.2, yield ratio less than 60% and high elongation which comprises hot rolling and cold rolling by conventional process a steel containing 0.01 to 0.05% C, less than 0.2% Si, 1.7 to 2.5% Mn, 0.01 to 0.10 Al with the balance being Fe and unavoidable impurities, holding the produced steel sheet for 20 seconds to 20 minutes at a temperature 720.degree. to 850.degree. C., and cooling the steel sheet at a cooling speed between 3.degree. and 50.degree. C. per second and also above a value (.degree.C. per second) shown by following formulae:12.times.[Mn(%)].sup.2 -62.times.[Mn(%)]+81.
Abstract:
A tire having excellent withstand-voltage property, wear resistance and resistance against heat build-up is disclosed. The tire has a tread, at least the contact area of the tread with road surface being made of a rubber composition containing a specifically limited softening agent and a specifically limited carbon black.
Abstract:
A broadcasting receiver suitable for receiving broadcasting signal transmitted with signal format is provided in which carrier wave is allocated in a frequency channel with certain frequency offset and signal intensity, which comprises: an information acquiring means for acquiring information related to the frequency channel in seek; and a station existence determining means for determining whether the frequency channel is station-existent or not based on information acquired by the information acquiring means; and wherein, the information acquiring means acquires information for receiving intensity of carrier wave and information for frequency offset.
Abstract:
The present invention relates to preventives or remedies for Alzheimer's disease, or to amyloid protein fibril-formation inhibitors, which include as an active ingredient a compound of general formula (I) below or a pharmacologically permitted salt thereof; and also to nitrogen-containing heteroaryl derivatives having specific substituents, or pharmacologically permitted salts thereof, which are valuable as preventives or remedies for Alzheimer's disease, or as amyloid protein fibril-formation inhibitors: (where, R1 and R2 are H or alkyl; Z1 and Z2 are H, alkyl, alkoxy, haloalkyl or halogeno; Z3 is alkoxy, SH, alkylthio, NH2, mono- or di-alkylamino, OH or halogeno; Z4 and Z5 are H or halogeno; and A is 4,6-pyrimidine-1,3-diyl, 1,3,5-triazine-2,6-diyl, etc).
Abstract translation:本发明涉及阿尔茨海默病的预防药物或补救剂,或淀粉样蛋白原纤维形成抑制剂,其包括作为活性成分的下列通式(I)的化合物或其药理学允许的盐; 以及具有特定取代基的含氮杂芳基衍生物或其药学上允许的盐,其作为阿尔茨海默氏病的预防剂或治疗剂是有价值的,或作为淀粉样蛋白原纤维形成抑制剂:(其中,R 1和R 2为H或烷基; Z 1 Z 2是H,烷基,烷氧基,卤代烷基或卤代; Z 3是烷氧基,SH,烷硫基,NH 2,一或二烷基氨基,OH或卤素; Z 4和Z 5是H或卤素; A是4,6- -1,3-二基,1,3,5-三嗪-2,6-二基等)。
Abstract:
The present invention relates to preventives or remedies for Alzheimer's disease, or to amyloid protein fibril-formation inhibitors, which include as an active ingredient a compound of general formula (I) below or a pharmacologically permitted salt thereof; and also to nitrogen-containing heteroaryl derivatives having specific substituents, or pharmacologically permitted salts thereof, which are valuable as preventives or remedies for Alzheimer's disease, or as amyloid protein fibril-formation inhibitors: (where, R1 and R2 are H or alkyl; Z1 and Z2 are H, alkyl, alkoxy, haloalkyl or halogeno; Z3 is alkoxy, SH, alkylthio, NH2, mono- or di-alkylamino, OH or halogeno; Z4 and Z5 are H or halogeno; and A is 4,6-pyrimidine-1,3-diyl, 1,3,5-triazine-2,6-diyl, etc).
Abstract translation:本发明涉及阿尔茨海默病的预防药物或补救剂,或淀粉样蛋白原纤维形成抑制剂,其包括作为活性成分的下列通式(I)的化合物或其药理学允许的盐; 以及具有特定取代基的含氮杂芳基衍生物或其药学上允许的盐,其作为阿尔茨海默氏病的预防剂或治疗剂是有价值的,或作为淀粉样蛋白原纤维形成抑制剂:(其中,R 1和R 2为H或烷基; Z 1 Z 2是H,烷基,烷氧基,卤代烷基或卤代; Z 3是烷氧基,SH,烷硫基,NH 2,一或二烷基氨基,OH或卤素; Z 4和Z 5是H或卤素; A是4,6- -1,3-二基,1,3,5-三嗪-2,6-二基等)。
Abstract:
A broadcasting receiver suitable for receiving a broadcasting signal transmitted in an IBOC signal format, comprises: a channel seek directing means for directing to start a channel seeking operation that selects selectable channel in an order of frequency; a channel seek controlling means for starting and controlling the channel seeking operation in accordance with the direction of the channel seek directing means; and a multichannel determining means for determining whether a selected frequency channel is providing multichannel digital broadcasting or not; and wherein the channel seek controlling means selects a next subchannel in an order of identification code before searching for the next frequency channel, if it is determined by the multichannel determining means that the selected frequency channel is providing the multichannel digital broadcasting.
Abstract:
A broadcasting receiver suitable for receiving broadcasting signal transmitted with signal format is provided in which carrier wave is allocated in a frequency channel with certain frequency offset and signal intensity, which comprises: an information acquiring means for acquiring information related to the frequency channel in seek; and a station existence determining means for determining whether the frequency channel is station-existent or not based on information acquired by the information acquiring means; and wherein, the information acquiring means acquires information for receiving intensity of carrier wave and information for frequency offset.
Abstract:
The present invention relates to preventives or remedies for Alzheimer's disease, or to amyloid protein fibril-formation inhibitors, which include as an active ingredient a compound of general formula (I) below or a pharmacologically permitted salt thereof; and also to nitrogen-containing heteroaryl derivatives having specific substituents, or pharmacologically permitted salts thereof, which are valuable as preventives or remedies for Alzheimer's disease, or as amyloid protein fibril-formation inhibitors: (where, R1 and R2 are H or alkyl; Z1 and Z2 are H, alkyl, alkoxy, haloalkyl or halogeno; Z3 is alkoxy, SH, alkylthio, NH2, mono- or di-alkylamino, OH or halogeno; Z4 and Z5 are H or halogeno; and A is 4,6-pyrimidine-1,3-diyl, 1,3,5-triazine-2,6-diyl, etc).
Abstract translation:本发明涉及阿尔茨海默病的预防药物或补救剂,或淀粉样蛋白原纤维形成抑制剂,其包括作为活性成分的下列通式(I)的化合物或其药理学允许的盐; 以及具有特定取代基的含氮杂芳基衍生物或其药学上允许的盐,其作为阿尔茨海默氏病的预防剂或治疗剂是有价值的,或作为淀粉样蛋白原纤维形成抑制剂:(其中,R 1和R 2为H或烷基; Z 1 Z 2是H,烷基,烷氧基,卤代烷基或卤代; Z 3是烷氧基,SH,烷硫基,NH 2,一或二烷基氨基,OH或卤素; Z 4和Z 5是H或卤素; A是4,6- -1,3-二基,1,3,5-三嗪-2,6-二基等)。
Abstract:
A compound of the formula (I): wherein R1 is a C1-C6 alkyl group, an amino group, a (C1-C6 alkyl)amino group, a di(C1-C6 alkyl)amino group or a nitrogen-containing saturated heterocyclic group; R3 is a hydrogen atom or a C1-C6 alkyl group; Arom is an unsubstituted or substituted aryl group or an unsubstituted or substituted heteroaryl group; wherein the substituted aryl group is substituted at 1 to 5 positions and the substituted heteroaryl group is substituted at 1 to 3 positions; and wherein the substituents of the aryl group and of the heteroaryl group are independently selected from the group consisting of halogen atom, C1-C6 alkyl, halogeno C1-C6 alkyl, C1-C6 alkoxy, C1-C6 alkylthio, C1-C3 alkylenedioxy, C1-C7 alkanoyl, C2-C7 alkyloxycarbonyl, amino, C1-C7 alkanoylamino, hydroxyl, mercapto, cyano, nitro and carboxyl; A is a C1-C6 alkylene group; Ra together with R2 is a C2-C3 alkylene group containing a double bond; E is a single bond, an oxygen atom, a sulfur atom or a group of the formula: —NR4—, wherein R4 is a hydrogen atom or a C1-C7 alkanoyl group; X1 and X2 are the same or different and are an oxygen atom or a sulfur atom, or a pharmacologically acceptable salt or ester thereof.