序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
141 CYCLOHEXANDIONECARBOXYLIC ACID DERIVATIVES HAVING A HERBICIDAL AND PLANT GROWTH-REGULATING ACTION. MYPI19872263 1987-09-29 MY102084A 1992-03-31 HANS-GEORG BRUNNER
NEW CYCLOHEXANEDIONECARBOXYLIC ACID DERIVATIVES EXHIBIT A HERBICIDAL AND PLANT GROWTH-REGULATING ACTION. THE CYCLOHEXANEDIONECARBOXYLIC ACID DERIVATIVES CORRESPONDING (SIC) TO THE FORMULA 1 WHEREIN A DENOTES A RADICAL -OR2 OR -NR3R4,B DENOTES HYDROXYL, A RADICAL -NHOR1 OR A METAL OR AMMONIUM SALT THEREOF R DENOTES C1-C6-ALKYL, C1-C6-CYCLOALKYL WHICH IS UNSUBSTITUTED OR SUBSTITUTED BY HALOGEN, C1-C4-ALKOXYL OR C1-C4 ALKYLTHIO,R1 DENOTES C1-C6-ALKYL, C1-C6-HALOGENOALKYL, C3-C6-ALKENYL, C3-C6-HALOGENOALKENYL OR C3-C6-ALKYNYL,R2 R3 AND R4 INDEPENDENTLY OF ONE ANOTHER EACH DENOTEHYDROGEN; CI-C6 ALKYL, C1-C6-HALOGENOALKYL, C2-C10-ALKOXYALKYL OR C2-C10-ALKYLTHIOALKYL; C3-C6-ALKENYL WHICH IS UNSUBSTITUTED OR SUBSTITUTED BY HALOGEN, C1-C4-ALKOXY OR C1-C4-ALKYLTHIO; C3-C6-ALKYNYL; OR PHENYL OR C1-C6 ARALKYL WHEREIN THE PHENYL NUCLEUS IS UNSUBSTITUTED OR SUBSTITUTED BY HYDROGEN, C1-C4-ALKYL, C1-C4-ALKOXY, C1-C4-HALOGENOALKYL, NITRO OR CYANO, AND R3 ANDR4, TOGETHER WITH THE NITROGEN ATOM TO WHICH THEY ARE ATTACHED, ALSO FORM A 5-MEMBERED TO 6-MEMBERED HETEROCYCLIC STRUCTURE WHICH CAN BE ALSO CONTAIN AN OXYGEN OR SULFUR ATOM IN THE RING.
142 Inhibitors of slow reacting substance anaphylactic. DE3585377 1985-07-11 DE3585377D1 1992-03-26 SAKSENA ANIL KUMAR; WONG JESSE KWOK-KEUNG; MANGIARACINA PIETRO
143 RETINOIDS,THEIR MANUFACTURE AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM IL8404187 1987-09-30 IL84041A 1992-02-16
144 NO841687 1984-04-27 NO168526B 1991-11-25 CRAWLEY GRAHAM CHARLES; EDWARDS PHILIP NEIL; HILL GEORGE BERESFORD; TAIT BRIAN STEELE; YOUNG DEREK WILLIAM; PILGRIM WILLIAM ROBERT
145 ORGANIC SULFIDE ANTIOXIDANTS CA2027829 1990-10-17 CA2027829A1 1991-05-01 BOHEN JOSEPH M; REILLY JAMES L
ORGANIC SULFIDE ANTIOXIDANTS Organic sulfide antioxidants useful for stabilizing polyolefins against oxidative and thermal degradation during processing and use represented by Formula I: (I) wherein n is an integer of 2 to 15; R is an integer group of 2 to 30 carbons, or a cycloalkyl group of 5 to 20 carbons, R is a substituted or unsubstituted alkyl group of 2 to 30 carbons, a substituted or unsubstituted cycloalkyl group of 5 to 20 carbons, a substituted or unsubstituted alkyl group of 2 to 30 carbons where any of up to 6 carbon atoms are replaced with an O or S heteroatom, a substituted or unsubstituted cycloalkyl group of 5 to 20 carbons where any of up to 6 carbon atoms are replaced with an O or S heteroatom, with the proviso that the heteroatoms must be separated from each other and from the portion of the compound to which the R group is bonded by at least one carbon atom, the substituents for R being -OH, -SR4 or -OR4, wherein R4 is an alkyl group of 1 to 3 0 carbons or a cycloalkyl group of 5 to 20 carbons; R1 and R2 are independently H or an alkyl group of 1 to 4 carbons; and R3 is an alkyl group of 1 to 24 carbons or a cycloalkyl group of 5 to 20 carbons.
146 RETROVIRAL PROTEASE INHIBITING COMPOUNDS AU5571190 1990-05-18 AU5571190A 1990-11-29 NAME NOT GIVEN
147 AT86303299 1986-04-30 ATE56951T1 1990-10-15 KOJIMA KOICHI; AMEMIYA SHIGEO; KOYAMA KAZUO; IWATA NOBUYOSHI; OSHIMA TAKESHI
148 PROSTAGLANDIN DERIVATIVES, THEIR PREPARATION AND USE CA508019 1986-04-30 CA1273919A 1990-09-11 KOJIMA KOICHI; AMEMIYA SHIGEO; KOYAMA KAZUO; IWATA NOBUYOSHI; OSHIMA TAKASHI
Prostaglandin derivatives, and specifically derivatives of isocarbacyclin, have an optionally substituted methylene group as a substituent on the .alpha.-carbon atom of the .alpha.-side chain. They have a variety of physiological effects, notably a strong ability to inhibit blood platelet aggregation and a strong anti-ulcer activity. They may be prepared from a carbacyclin derivative.
149 HERBICIDES AND REGULATING THE GROWTH OF PLANTS COMPOSITIONS CONTAINING AS ACTIVE SUBSTANCE DERIVATIVES OF CYCLOHEXAN-DION-CARBONIC ACID AND PROCESS FOR PRODUCTION OF THE ACTIVE SUBSTANCES HU190384 1984-05-17 HU199770B 1990-03-28 BRUNNER HANS-GEORG
150 PROCESS FOR PRODUCING FLUOROALLYLAMINE MONOAMINEOXIDASE INHIBITORS HU502586 1986-12-04 HU199394B 1990-02-28 BEY PHILIPPE; MCDONALD IAN A; PALFREYMAN MICHAEL G
151 NO844570 1984-11-15 NO160361C 1989-04-12 BRUNNER HANS-GEORG
152 ES557713 1987-09-01 ES557713A0 1989-03-16
153 CYCLOHEXANEDIONE-CARBOXYLIC-ACID DERIVATIVES HAVING A HERBICIDAL AND PLANT GROWTH REGULATING ACTIVITY DE3476195 1984-05-14 DE3476195D1 1989-02-23 BRUNNER HANS-GEORG
154 PT8386486 1986-12-03 PT83864B 1989-01-17 BEY PHILIPPE; PALFREYMAN MICHAEL G; MCDONALD IAN A
155 DERIVATIVES OF 4-ACYL-3,5-DIOXOCYCLO HEXANECARBOXYLIC ACID,THEIR PREPARATION AND THEIR USE AS HERBICIDES AND PLANT GROWTH REGULATORS IL7184984 1984-05-16 IL71849A 1988-06-30
156 UN PROCEDIMIENTO PARA LA PREPARACION DE NUEVOS DERIVADOS DE PROSTAGLANDINA ES557711 1987-09-01 ES8802418A1 1988-06-01
LOS DERIVADOS DE PROSTAGLANDINA (I), DONDE NO EXCLUSIVAMENTE R ELEVADO A 1 ES CARBOXI O TETRAZOLILO, R ELEVADO A 2, R ELEVADO A 3 Y R ELEVADO A 6 ALQUILO C1-4, R ELEVADO A 4 Y R ELEVADO A 5 ACILO ALIFATICO C2-5, O ACILO AROMATICO, R ELEVADO A 7 ALQUILO C1-12, B ES -CH2-CH2 O -CH=CH-, E OXIGENO O AZUFRE, P VA DE 0 A 3 Y Q DE 1 A 3, Y LA LINEA DISCONTINUA REPRESENTA UN DOBLE ENLACE EN 2 O 3; SE OBTIENE HACIENDO REACCIONAR UN COMPUESTO (II) CON HALOGENURO (III) O AGENTE SULFONILANTE (IV) CUANDO E ES AZUFRE Y OPCIONALMENTE TRANSFORMAR LOS GRUPOS R ELEVADO A 15-, -OR ELEVADO A 11 Y OTROS EN R ELEVADO A 1, -OR ELEVADO A 4 Y OTROS. ESTOS DERIVADOS, ESPECIFICAMENTE LOS DE ISOCARBACICLINA, INHIBEN FUERTEMENTE LA AGRUPACION DE PLAQUETAS EN SANGRE Y PRESENTAN FUERTE ACTIVIDAD ANTIULCERA. *FORMULA*
157 ES557712 1987-09-01 ES557712A0 1988-06-01
158 HERBICIDE AND GROWTH-CONTROLLING COMPOSITIONS CONTAINING ACYL-CYCLOHEXANE-DIONS AND OKSIMETHERS THEREOF AS ACTIVE COMPONENTS AND PROCESS FOR PRODUCING THE ACTIVE COMPONENTS HU175887 1987-04-23 HUT44121A 1988-02-29 TOBLER HANS
159 PHENOL DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS NZ20797584 1984-04-27 NZ207975A 1987-11-27 CRAWLEY G C; EDWARDS P N; HILL G B; PILGRIM W R; TAIT B S; YOUNG D W
160 UN PROCEDIMIENTO PARA LA PREPARACION DE NUEVOS DERIVADOS DE PROSTAGLANDINA. ES554621 1986-04-30 ES8800665A1 1987-11-16
PROCEDIMIENTO PARA PREPARAR NUEVOS DERIVADOS DE PROSTAGLANDINA. COMPRENDE: A) HACER REACCIONAR A (III) CON CLORURO DE BENCENO, EN PRESENCIA DE TRIETILAMINA EN HEXANO Y ENTRE C30J Y B50JC; B) TRATAR AL COMPUESTO DE A) CON TRIETILAMINA, EN HEXANO Y ENTRE 0J Y 80JC, PARA DAR A (III) Y C) REDUCIR A (III) CON SULFURO SODICO, EN ALCOHOL Y ENTRE 0J Y 100JC, PARA OBTENER A (I) Y SUS SALES Y ESTERES FARMACEUTICAMENTE ACEPTABLES. SIENDO: AK, ALQUILENO DE CADENA LINEAL Y DE C 1 A 4; B, -CH2-CH2O -CHFCN-; R1, CARBOXI, TETRAZOLILO Y OTROS; R2, R3 Y R6, H O ALQUILO DE C 1 A 4; R4 Y R5, -R10; R7 Y R7A, ALQUILO DE C 1 A 12; R11 Y R12 GRUPO PROTECTOR DE HIDROXI Y R14, TETRAZOLILO. SE UTILIZAN COMO ANTIULCEROSOS.
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