子分类：
| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 421 | Drugs to improved synaptic transmission | AU3407695 | 1995-08-16 | AU3407695A | 1996-04-09 | SUMIKAWA KATUMI; ITO KENICHI; MCGAUGH JAMES L |
| 422 | CYCLOPENTANE DERIVATIVES, PROCESS FOR PRODUCING THEM AND THEIR PHARMACEUTICAL USE. | GR950403488 | 1995-12-12 | GR3018360T3 | 1996-03-31 | KLAR ULRICH; REHWINKEL HARTMUT; VORBRUEGGEN HELMUT; THIERAUCH KARL-HEINZ; VERHALLEN PETER |
| 423 | DRUGS TO IMPROVE SYNAPTIC TRANSMISSION | CA2197673 | 1995-08-16 | CA2197673A1 | 1996-03-28 | SUMIKAWA KATUMI; ITO KEN-ICHI; MCGAUGH JAMES L |
| Brefeldine A et ses analogues et dérivés, administrés de manière périphérique pour stimuler le potentiel d'apprentissage et stopper les troubles de la mémoire grâce à une potentialisation induite à long terme dans les tissus hippocampiques. | ||||||
| 424 | Carbamoyl carboxylic acid amides | AU3470995 | 1995-08-19 | AU3470995A | 1996-03-27 | WETTERICH FRANK; WAGNER OLIVER; EICKEN KARL; AMMERMANN EBERHARD; LORENZ GISELA |
| 425 | CARBAMOYLCARBOXAMIDES | CA2198638 | 1995-08-19 | CA2198638A1 | 1996-03-14 | WETTERICH FRANK; WAGNER OLIVER; EICKEN KARL; AMMERMANN EBERHARD; LORENZ GISELA |
| Carbamoyl carboxylic acid amides of general formula (I) and salts thereof are disclosed. In said formula (I), R1 represents optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl or an optionally substituted nonaromatic carbo- or heterocycle; R2 represents H or optionally substituted alkyl or cycloalkyl; R3 represents optionally halogenated alkyl, cycloalkyl or phenylalkyl; R4 represents H or one of the groups R3; or R3 and R4, together with the C atom to which they are attached, represent an optionally substituted carbo- or heterocycle; R5 independently of the latter represents one of the groups R2; X represents independently of one another hydrogen or optionally substituted alkyl and/or alkenyl; Y represents independently of each other and of the latter one of the groups X; p and q independently of one another are 0, 1 or 2; R6 represents halogen, cyano, nitro, or optionally substituted alkyl, alkoxy, alkylthio, or an optionally substituted phenyl group bound by oxygen or sulphur; r is 0, 1, 2 or 3. Also disclosed are agents containing these compounds, processes for producing them and the use of formula (I) compounds and of said agents. | ||||||
| 426 | Caramoylcarbonsäureamide | DE4431467 | 1994-09-03 | DE4431467A1 | 1996-03-07 | |
| Carbamoyl carboxylic acid amides of general formula (I) and salts thereof are disclosed. In said formula (I), R<1> represents optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl or an optionally substituted non-aromatic carbo- or heterocycle; R<2> represents H or optionally substituted alkyl or cycloalkyl; R<3> represents optionally halogenated alkyl, cycloalkyl or phenylalkyl; R<4> represents H or one of the groups R<3>; or R<3> and R<4>, together with the C atom to which they are attached, represent an optionally substituted carbo- or heterocycle; R<5> independently of the latter represents one of the groups R<2>; X represents independently of one another hydrogen or optionally substituted alkyl and/or alkenyl; Y represents independently of each other and of the latter one of the groups X; p and q independently of one another are 0, 1 or 2; R<6> represents halogen, cyano, nitro, or optionally substituted alkyl, alkoxy, alkylthio, or an optionally substituted phenyl group bound by oxygen or sulphur; r is 0, 1, 2 or 3. Also disclosed are agents containing these compounds, processes for producing them and the use of formula (I) compounds and of said agents. | ||||||
| 427 | Process for the preparation of 3-(methylthio)propanal | AU3093995 | 1995-07-06 | AU3093995A | 1996-02-09 | HSU YUNG C; RUEST DENNIS A |
| 428 | BR9406478 | 1994-04-13 | BR9406478A | 1996-01-02 | BAUMANN ERNST; RHEINHEIMER JOACHIM; VOLGELBACHER UWE JOSEF; BRATZ MATTHIAS; THEOBALD HANS; GERBER MATTHIAS; WESTPHALEN KARL-OTTO; WALTER HELMUT; RADEMACHER WILHELM | |
| 429 | 3-(HETERO)ARYL CARBOXYLIC ACID DERIVATIVES, METHODS OF PREPARING THEM AND INTERMEDIATES USED IN THEIR PREPARATION | HU9503040 | 1994-04-13 | HU9503040D0 | 1995-12-28 | RADEMACHER WILHELM; WALTER HELMUT; BRATZ MATTHIAS; GERBER MATTHIAS; WESTPHALEN KARL-OTTO; BAUMANN ERNST; THEOBALD HANS; RHEINHEIMER JOACHIM; VOGELBACHER UWE JOSEF |
| 430 | DERIVATIVE OF GLUTAMIC ACID, PROCESS OF ITS PREPARATION AND PHARMACEUTICAL COMPOSITION CONTAINING THEREOF | CZ294794 | 1994-11-29 | CZ294794A3 | 1995-12-13 | HEINZ LAWRENCE JOSEPH; LUNN WILLIAM HENRY WALKER; SCHOEPP DARRYLE DARWIN |
| 431 | ANTAGONISTA DE AMINOACIDOS EXCITATORIOS A NIVEL DE SU RECEPTOR | PE25583694 | 1994-11-28 | PE42595A1 | 1995-12-12 | HEINZ LAWRENCE JOSEPH; WALKER LUNN WILLIAM HENRY; SCHOEPP DARRYLE DARWIN |
| SE REFIERE A UN COMPUESTO DE FORMULA I DONDE: 1) Z ES NR5, O, S; 2) W ES CH(3-p), -(CH2)q-, -(CH2)q-CH(3-p), -(CH2)q-CO-, -(CH2)qO-, -(CH2)q-CH=CH(CH2)q-, -(CH2)q-CH=CH-, -CH=CH-CO-, -CH=CH-COR6, -(CH2)q-CHOH-R6, -(CH2)q-CHOH-, -(CH2)q-COR6, -O(CH2)q-, NR5, O, S, SO u SO2; 3) n, m Y s, VARIAN DE 0 A 1; 4) p VARIA DE 0 A 3; 5) q VARIA DE 0 A 6; 6) R1 Y R2 SON INDEPENDIENTEMENTE ARILO Y/O HETEROCICLO OPCIONALMENTE SUSTITUDOS. TALES COMO TETRAZOLILO, TRIAZOLILO, PIRIDILO, FENILO, NAFTILO Y OTROS; 7) R3 Y R4 SON HIDROGENOS Y/O GRUPOS PROTECTORES DEL CARBOXILO; 8) R5 ES HIDROGENO, ALQUILO C1-C10, ACILO, SO2-(ALQUILO C1-C4); 9) R6 ES ALQUILO C1-C10; EL CUAL ACTUA SOBRE RECEPTORES DE AMINOACIDOS EXCITATORIOS A NIVEL DE NEURONAS; TAL COMO EL RECEPTOR PARA EL GLUTAMATO; Y PUEDE SER UTIL EN EL TRATAMIENTO DE DESORDENES NEUROLOGICOS | ||||||
| 432 | Carbamoylcarboxamides their preparation and use | IL11508495 | 1995-08-28 | IL115084A0 | 1995-12-08 | |
| 433 | ACETIC ACID DERIVATIVES | HU9403441 | 1994-11-30 | HUT71332A | 1995-11-28 | MUELLER MARCEL; HUERZELER MUELLER MARIANNE; STEINER BEAT; HADVARY PAUL; ALIG LEO; WELLER THOMAS |
| 434 | Process for the preparation of novel organic nitrates, | FI894350 | 1989-09-14 | FI95569B | 1995-11-15 | HUETTER JOACHIM; NOACK EIKE; SANDROCK KLAUS |
| 435 | Fungicides Acylamidobenamide. | DE69110365 | 1991-07-16 | DE69110365T2 | 1995-11-09 | GLEN ALASDAIR THOMAS; SPENCE ROSAMUND ALISON; LAWSON KEVIN ROBERT; CROWLEY PATRICK JELF |
| 436 | AT91912996 | 1991-07-22 | ATE127788T1 | 1995-09-15 | KLAR ULRICH; REHWINKEL HARTMUT; VORBRUEGGEN HELMUT; THIERAUCH KARL-HEINZ; VERHALLEN PETER | |
| 437 | Aromatic esters of phenylenedialkanoates as inhibitors of human neutrophil elastase | AU3151093 | 1992-12-01 | AU662379B2 | 1995-08-31 | OLEKSYSZYN JOZEF; KIRSCHENHEUTER GARY P |
| 438 | Fungicides. | ES91306446 | 1991-07-16 | ES2073123T3 | 1995-08-01 | GLEN ALASDAIR THOMAS; SPENCE ROSAMUND ALISON; LAWSON KEVIN ROBERT; CROWLEY PATRICK JELF |
| COMPUESTOS FUNGICIDICOS QUE TIENEN LA FORMULA (I): EN QUE DYE SON INDEPENDIENTEMENTE HOF; XEY SON OOS; R ELEVADO 1 AR ELEVADO 4 TIENEN VARIOS VALORES ESPECIFICOS; AYB SON INDEPENDIENTEMENTE H, IODO, NITRO, CIANO, ALCOXICARBONILO C SUB 1-4, ALCOXI (C SUB 1-4) ALQUILO C SUB 1-4, ALQUILTIO (C SUB 1-4)-ALQUILO C SUB 1-4, FORMILO, ALQUILTIO C SUB 1-4, HALO (C SUB 1-4) ALQUILITIO, HALO (C SUB 1-4) ALCOXI, ALQUILCARBONILO C SUB 1-4, -CR ELEVADO 5=NOR ELEVADO 6 (DONDE R ELEVADO 5 YR ELEVADO 6 SON INDEPENDIENTEMENTE HO ALQUILO C SUB 1-4), ALQUENILO C SUB 2-4 O ALQUINILO C SUB 2-4, SIEMPRE Y CUANDO AYB NO SON LOS DOS H. | ||||||
| 439 | Acyloxymethyl phenylglyoxylic acid oxime derivatives and fungicidal compositions containing them | IL9103589 | 1989-07-19 | IL91035A | 1995-07-31 | |
| 440 | PREPARATION OF A ZINC MERCAPTOESTER BY HEATING A MERCAPTOESTER WITH ZINC OXIDE IN THE PRESENCE OF PARAFFIN WAX; HEAT STABILISER COMPRISING THE ABOVE REACTION PRODUCT AND CALCIUM STEARATE; POLYMER COMPOSITIONS | NZ25069894 | 1994-01-18 | NZ250698A | 1995-07-26 | BEEKMAN GEORGE F; PRICE LIONEL R; MESCH KEITH A |
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