OBJECT IMAGE DISPLAY APPARATUS, OBJECT IMAGE DISPLAY METHOD AND OBJECT IMAGE DISPLAY PROGRAM

The total number of object images is “N”. Object images whose the number is less than “N” are displayed on a display among the N-object images according to a previously defined display rule. When a selected object image is shifted by n-object images, a position obtained by shifting by a distance becomes a new position of the selected object image, wherein the distance is obtained by multiplying by “n” a value obtained by dividing the distance between a display position of an object image and a display position of the selected object image by a value obtained by subtracting “1” from “N”. 19-. (canceled)10. An object image display apparatus comprising:an object image generator that generates object images corresponding to N-objects to be used to select any object from among the N-objects, wherein the number “N” is a natural number more than “1”; anda controller that controls to display on a display object images whose the number is less than “N” among the N-object images according to a previously defined display rule,wherein as the display rule, the controllerdisplays as a selected object image, at the time of selecting a first object image corresponding to a first object having the highest rank in an arrangement sequence in which the N-objects are arranged according to a certain order, the first object image on a first position in the display, and arranges and displays as non-selected object images, object images corresponding to objects having ranks below the first object by a certain number,displays as a selected object image, at the time of selecting a second object image corresponding to a second object having the lowest rank in the arrangement sequence in which the N-objects are arranged according to a certain order, the second object image on a second position in the display, and arranges and displays as non-selected object images, object images corresponding objects having ranks above the second object by a certain number,arranges and displays as non-selected ...

Vertical magnetic head

(57)【要約】本公報は電子出願前の出願データであるた め要約のデータは記録されません。

Patent JPS6152815B2

Novel amino acid derivatives having n,n-dialkylaminophenyl group

The present invention relates to novel amino acid derivatives having an N, N-dialkylaminophenyl group represented by the general formula [I]. wherein R 1 represents a hydrogen atom, a lower alkyl group, a phenyl-lower alkyl group, a lower alkanoyl group or a benzoyl group, and each phenyl ring in the phenyl-lower alkyl group and the benzoyl group can be substituted by a halogen atom, a lower alkyl group or a lower alkoxy group; R 2 represents a carboxyl group which can be converted into an ester, an amide or a hydroxamic acid; R 3 represents a lower alkyl group; R 4 represents a lower alkyl group; A 1 represents a lower alkylene group which can be substituted by a phenyl group, and the phenyl group can be substituted by a halogen atom, a lower alkyl group or a lower alkoxy group; A 2 represents a lower alkylene group; A 3 represents a lower alkylene group; and "Z" represents a sulfur atom or an oxygen atom. The compounds have inhibitory effects on LTA 4 hydrolase and are useful as medicines, in particular, therapeutic agents for inflammatory diseases such as rheumatic diseases, psoriasis, inflammatory intestinal diseases, gout and cystic fibrosis, in which LTB 4 is concerned.

Tnf-alpha production inhibitors

New polyimide copolymer and molded article of polyimide obtained by molding the same

【課題】 高透明性、高靭性及び高耐熱性を有する新規なポリイミド樹脂の提供、及び各種電子デバイスの電気絶縁膜やガラス基板代替用として有用なプラスチック基板を提供する。 【解決手段】 ピロメリット酸二無水物及び９，９−ビス(４’−ヒドロキシフェニル)フルオレン−ビス（トリメリテート アンハイドライド）からなる群より選ばれる少なくとも一種と、４，４’−メチレンビス(シクロヘキシルアミン)及びイソホロンジアミンを、４，４’−メチレンビス(シクロヘキシルアミン)とイソホロンジアミンとのモル比が５：９５〜９５：５の範囲でイミド化反応する。得られたポリイミド樹脂は、透明性、靭性及び耐熱性を有しているので、ガラス基板代替用プラスチック基板、電子デバイスの電気絶縁膜、光学材料、太陽電池パネル等の保護フィルム、光導波路など種々の用途に使用可能である。

Novel amino acid derivatives having n,n-dialkylaminophenyl group

Novel amino acid derivatives having an N,N-dialkylaminophenyl group represented by general formula (I), wherein R1 represents hydrogen, lower alkyl, phenyl lower alkyl, lower alkanoyl or benzoyl, provided that the phenyl ring in the phenyl lower alkyl or benzoyl may be substituted by halogeno, lower alkyl or lower alkoxy; R2 represents carboxyl optionally converted into ester, amide or hydroxamic acid; R3 represents lower alkyl; R4 represents lower alkyl; A1 represents lower alkylene optionally substituted by phenyl, provided that the phenyl group may be substituted by halogeno, lower alkyl or lower alkoxy; A2 represents lower alkylene; A3 represents lower alkylene; and Z represents S or O. The compounds have inhibitory effects on LTA and hydrolase and are useful as a drug, in particular, a remedy for diseases in which LTB¿4? participates such as rheumatism, psoriasis, inflammatory intestinal diseases, gout, cystic fibrosis, etc.

(pyridin-4-yl)alkyl-amides as TNF-alpha production inhibitors

A purpose of the present invention is to provide TNF-α production inhibitors being useful as therapeutic agents for autoimmune diseases such as rheumatoid arthritis. Novel compounds having the structure represented by the general formula [1] or salts thereof according to the present invention have excellent TNF-α production inhibitory activities,    wherein "A" is ―(NR 4 )―, ―(CR 5 R 6 )― or ―O―, "B" is alkylene or alkenylene, R 1 , R 2 , R 4 , R 5 and R 6 are hydrogen, alkyl, alkenyl or the like, R 3 is aryl or unsaturated heterocycle, R 7 is hydrogen or alkyl, "X" is O or S, and "n" is an integer of 1 to 5.

Purification of methacrylamide

N-substituted-n'-substituted urea derivatives and the use thereof as tnf-.alpha production inhibitory agents

The N-substituted-N'-substituted urea derivative of formula (1), analogues o f the same, or medicinally acceptable salts of both, having a TNF-.alpha. production inhibiting effect.

Tnf-.alpha. production inhibitors

A purpose of the present invention is to provide TNF-.alpha. production inhibitors being useful as therapeutic agents for autoimmune diseases such as rheumatoid arthritis. Novel compounds having the structure represented by the general formula [1] or salts thereof according to the present invention have excellent TNF-.alpha. production inhibitory activities, (see formula 1) wherein "A" is -(NR4)- , -(CR5R6)- or -O-, "B" is alkylene or alkenylene, R1, R2, R4, R5 and R6 are hydrogen, alkyl, alkenyl, adamantyl or the like, R3 is aryl or an unsaturated heterocycle, and "X" is oxygen or sulfer respectively.

TNF-alpha production inhibitors

N-substituted-N′-substituted urea derivatives and pharmaceutical compositions containing the derivatives

N-Substituted-N'-substituted urea derivatives represented by the following formula, analogs thereof or pharmaceutically acceptable salts thereof are herein provided. These compounds show a TNF-alpha production inhibitory activity.

Production of butyl methacrylate

Preparation of tertiary-butylaminoethyl methacrylate

Preparation of acrylic alkali salt dispersion

Recording and reproducing tester

(57)【要約】本公報は電子出願前の出願データであるた め要約のデータは記録されません。

Thin film magnetic head

Conveyor equipment

(57)【要約】本公報は電子出願前の出願データであるた め要約のデータは記録されません。

Urea derivatives having tnf- .alpha. production inhibitory effects

Objects of the present invention are to create compounds having urea structure as basic structure and having a sulfur atom and an amide bond in side chains and to find pharmacological effects thereof, particularly TNF-.alpha. production inhibitory effects. The present invention provides compounds represented by the following formula [I] wherein R' is H, alkyl, aromatic, R A-CO-, R C-S- or the formula [II]; R2, R3 and R4 are H, alkyl, alkenyl, cycloalkyl, cycloalkenyl or aromatic; R5 and R5 are H, alkyl, alkenyl, cycloalkyl, cycloalkenyl or aromatic; R5 and R6 can together form a nonaromatic heterocyclic ring; R7 is H, alkyl, cycloalkyl, hydroxy, mercapto, phenyl, R B-O-, R C-S-, R D-COS-, R E-OCO-, R F-N(R G)- or -CONHOH; and A1 and A2 are alkylene.

Inhibitoren der tnf-alpha bildung zur behandlung von autoimmunerkrankungen

1-ä(adamantyl)alkylü-3- ä(pyridinyl)alkylüharnstoff-verbindungen als tnf- .alpha hemmer zur behandlung von autoimmunerkrankungen

(pyridinyl)alkyl-amide oder -harnstoffe als tnf- alpha bildung inhibitoren

Preparation of methacrylamide

[UNK]

[UNK]

カラオケシステム

【課題】 伝送時の時間遅れを解消して相互に相手の歌声を聴きながら同期歌唱することができるカラオケシステムを提供する。 【解決手段】 カラオケ装置は、カラオケコンテンツを復号する復号手段と、カラオケ音声データを音声出力させる音声出力手段と、音声出力されたカラオケ音声データを第１のカラオケ音声データに符号化する符号化手段と、第１のカラオケ音声データを他のカラオケ装置に送信する音声送信手段と、他のカラオケ装置から供給された第２のカラオケ音声データと第１のカラオケ音声データとに基づき、カラオケコンテンツの相対的な伝送遅延量を測定する遅延量測定手段と、配信サーバに対して、伝送遅延量に基づいたカラオケコンテンツの配信タイミング調整要求信号を出力する制御手段とを備え、配信サーバは配信タイミング調整要求信号に基づき、複数の配信先カラオケ装置ごとにカラオケコンテンツの配信タイミングを調整する。 【選択図】 図１

Ａｖ装置の制御システム及び制御方法

【課題】所望の放送局や番組を覚えることが容易に、しかも短時間で選択操作を行い得るＡＶ装置の制御システム及び制御方法を提供する。 【解決手段】表示画面に表示された見出し語情報の中から所望の見出し語情報を指定し、指定された見出し語情報に対応する全チャネルを検出し、検出された全チャネルを表示画面にザッピングにより表示してザッピングによる表示画面から任意のチャネルを選択する。または、ザッピング選択モードを指定し、ザッピングモードに従って表示画面に全チャネルをザッピングにより表示させてザッピングによる表示画面から任意のチャネルを選択する。さらに、操作部として、キー入力、音声認識、身振り手振りの検出、表情の検出のうちの少なくとも一つを含み、リモートコントロール装置で構成する。 【選択図】図２

Nuevos derivados de aminoacidos que contienen azufre.

LA INVENCION SE REFIERE A NUEVOS DERIVADOS DE AMINOACIDOS QUE CONTIENEN AZUFRE, LOS CUALES PRESENTAN ACTIVIDADES INHIBITORIAS DE HIDROLASA LTA 4 . DICHOS DERIVADOS ESTAN REPRESEN TADOS POR LA FORMULA SIGUIENTE [I]: DONDE R 1 REPRESENTA H, ALQUILO, FENILALQUILO (SUSTITUIDO), ALCANOILO O BENZOILO (SUSTITUIDO), R 2 REPRESENTA ESTER, AMIDA O CARBOXILO, R SU P,3 REPRESENTA HIDROXILO, ALQUILO, HALOGENOALQUILO, ALCOXI, HALOGENOALCOXI, ALQUILTIO, FENILO (SUSTITUIDO), FENOXI (SUSTITUIDO), FENILTIO (SUSTITUIDO), ATOMO DE HALOGENO, ALQUILSULFONILO, HALOGENOALQUILSULFONILO, NITRO O CIANO, R 4 REPRESENTA ALQUILO, A 1 REPRESENTA ALQUILENO Y A 2 REPRESENTA ALQUILENO.

Faerbende zusammensetzung zur bestimmung von cystin

Werkwijze voor het bereiden van een kleurvormend reagens en werkwijze voor het aantonen van cystine of cysteine.

Werkwijze voor het bereiden van een kleurvormend reagens en werkwijze voor het aantonen van cystine of cysteine.

Schwefel enthaltende aminosäurederivate

Ｎ−置換−ｎ’−置換−ウレア誘導体及び該誘導体を含有する医薬組成物

(57)【要約】 【課題】 ＴＮＦ−α産生阻害活性を有する新規化合物 を提供すること。 【解決手段】 下記式で表されるＮ−置換−Ｎ’−置換 −ウレア誘導体、その類縁体又はこれらの医薬上許容さ れる塩。 【化１９】

Schwefel enthaltende aminosäurederivate

Inhibitoren der leukotrien a4 hydrolase

Inhibidores de la leucotrieno a4 hidrolasa.

La presente invención se refiere a inhibidores de leucotrieno A{sub, 4} hidrolasa que contienen compuestos representados por la fórmula [I] o sales de los mismos como ingredientes activos, (fórmula) en la que R{sup, 1}{sub, a} representa hidrógeno, alquilo, fenilalquilo, alcanoílo o benzoílo; cada uno de R{sup, 2}{sub, a} y R{sup, 3}{sub, a} representa hidrógeno o alquilo; R{sup,1}{sub,a} representa hidroxilo, alcoxi, fenilalcoxi, amino, alquilamino o fenilalquilamino;R{sup, 5}{sub, a} representa fenilalquilo o naftilalquilo; "Z" representa azufre u oxígeno; "A" representa alquileno; y "n" representa 0, 1 ó 2; con la condición de que el anillo fenilo en R{sup, 1}{sub, a} pueda sustituirse con alquilo, alcoxi o halógeno, y de que el anillo de fenilo o el anillo de naftilo en R{sup, 5}{sub, a} pueda sustituirse con alquilo, cicloalquilo, alcoxi, alquiltio o halógeno.

Inhibiteurs de leucotriene a4 hydrolase

重量物のスライド装置およびそれに用いるｗｃチップの施工方法

【課題】重量物を移動させる移動体と、該移動体を案内するガイドレールと摺動面の磨耗を低減させて長寿命化することができる重量物のスライド装置およびそれに用いるWCチップの施工方法を提供する。 【解決手段】シフトシリンダを用いて重量物をスライドさせる装置であって、前記重量物を移動させる移動体と、該移動体を案内するガイドレールとを有し、該移動体とガイドレールとの摺動面にWCチップを配置することを特徴とする重量物のスライド装置。 【選択図】 図３

Inhibitoren der leukotrien a4 hydrolase