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序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
161 新穎化合物、潛在性添加劑及含該添加劑之組合物 TW105128858 2016-09-07 TW201713670A 2017-04-16 松井依純; MATSUI, IZUMI; 鈴木智美; SUZUKI, TOMOMI; 岡田光裕; OKADA, MITSUHIRO
本發明係一種下述通式(1)所表示之化合物。下述通式(1)中,R1 、R2 、R3 及R4 較佳為-CO-O-R11 ,尤佳為R11 係第三丁基之-CO-O-R11 。下述通式(1)中,R1 、R2 、R3 及R4 較佳為以-CO-O-R11 所表示之基。下述通式(1)所表示之化合物可適宜地用作潛在性添加劑。上述潛在性添加劑適宜用於感光性組合物。
162 MATERIALS FOR ORGANIC ELECTROLUMINESCENT DEVICES EP20800954.8 2020-11-10 EP4058462A1 2022-09-21 STENGEL, Ilona; LACKNER, Aaron; RODRIGUEZ, Lara-Isabel; WALTER, Charlotte; MEKIC, Amel
The present invention relates to compounds of the formula (1) which are suitable for use in electronic devices, in particular organic electroluminescent devices, and to electronic devices which comprise these compounds.
163 NOVEL BENZIMIDAMIDES COMPOUNDS COMPRISING AN OXABORININ RING EP19729249.3 2019-06-05 EP3802550A1 2021-04-14 LIDDLE, John; WALKER, Ann Louise; WHITE, Gemma Victoria
164 NITROGEN-CONTAINING MACROCYCLIC CONJUGATES AS RADIOPHARMACEUTICALS EP09829884.7 2009-12-02 EP2370447B1 2016-07-27 DONNELLY, Paul, Stephen; MA, Michelle, Therese; SCANLON, Denis, Bernard
The present invention relates to compounds that are useful as metal ligands and which either contain a molecular recognition moiety or can be bound to a molecular recognition moiety and methods of making these compounds. Once the compounds that contain a molecular recognition moiety are coordinated with a suitable metallic radionuclide, the coordinated compounds are useful as radiopharmaceuticals in the areas of radiotherapy and diagnostic imaging. The invention therefore also relates to methods of diagnosis and therapy utilising the radiolabelled compounds of the invention.
165 PLATELET ADP RECEPTOR INHIBITORS EP10183633.6 2002-07-25 EP2314593B1 2016-05-04 Scarborough, Robert; Jantzen, Hans-Michael; Huang, Wolin; Sedlock, David; Marlowe, Charles; Kane-Maguire, Kim
166 NITROGEN-CONTAINING MACROCYCLIC CONJUGATES AS RADIOPHARMACEUTICALS EP09829884 2009-12-02 EP2370447A4 2013-08-14 DONNELLY PAUL STEPHEN; MA MICHELLE THERESE; SCANLON DENIS BERNARD
The present invention relates to compounds that are useful as metal ligands and which either contain a molecular recognition moiety or can be bound to a molecular recognition moiety and methods of making these compounds. Once the compounds that contain a molecular recognition moiety are coordinated with a suitable metallic radionuclide, the coordinated compounds are useful as radiopharmaceuticals in the areas of radiotherapy and diagnostic imaging. The invention therefore also relates to methods of diagnosis and therapy utilising the radiolabelled compounds of the invention.
167 Structural variants of mycolactones for use in modulating inflammation, immunity and pain EP11306521.3 2011-11-18 EP2594561A1 2013-05-22 Demangel, Caroline; Blanchard, Nicolas; Bismuth, Georges; Eustache, Jacques; Casarotto, Virginie; Chany, Anne-Caroline

The present invention is related to variants of mycolactones of formula (I), processes for the preparation thereof, pharmaceutical compositions thereof and their use in modulating inflammation, immunity and pain.



         Y-O-W     (I)



wherein Y and W are as defined in claim 1.

168 NEW ORGANIC COMPOUND AND ORGANIC LIGHT EMITTING DEVICE USING THE SAME EP04774798.5 2004-10-18 EP1680479B1 2012-11-28 KIM, Kong-Kyeom; LEE, Min-Jeong; KIM, Yeon-Hwan, 1612-801, Munchonmaul 16 Danji Apt; JANG, Jun-Gi, 7-401 LG Chemical Apartment
169 Dérivés de paraphénylènediamine à groupement pyrrolidinyle substitués par un radical cationique et utilisation de ces dérivés pour la coloration de fibres kératiniques EP03290597.8 2003-03-11 EP1348695B1 2012-04-25 Sabelle, Stéphane; Ramos, Laure; Leduc, Madeleine, Rés. Les Chèvrefeuilles; Philippe, Michel
170 INHIBITORS OF HISTONE DEACETYLASE EP08748100 2008-04-09 EP2139850A4 2011-07-20 TESSIER PIERRE; LEIT SILVANA; SMIL DAVID; DEZIEL ROBERT; AJAMIAN ALAIN; CHANTIGNY YVES ANDRE; DOMINGUEZ CELIA
This invention relates to compounds for the inhibition of histone deacetylase. More particularly, the invention provides for compounds of the Formula (I) and N-oxides, hydrates, solvates, pharmaceutically acceptable salts, prodrugs and complexes thereof, and racemic and scalemic mixtures, diastereomers and enantiomers thereof, wherein groups L, M, X and Y are as defined herein.
171 DERIVES D'UREE CYCLIQUE, LEUR PREPARATION ET LEUR UTILISATION PHARMACEUTIQUE COMME INHIBITEURS DE KINASES EP04705838.3 2004-01-28 EP1599464B1 2010-09-22 PATEK, Marcel; NAIR, Anil; HITTINGER, Augustin; NEMECEK, Conception; BOND, Daniel; HARLOW, Greg; BOUCHARD, Hervé; MAUGER, Jacques; MALLERON, Jean-Luc; PALERMO, Mark; AL-OBEIDI, Fahad; FAITG, Thomas; STROBEL, Hartmut; RUF, Sven; RITTER, Kurt; EL-AHMAD, Youssef; LESUISSE, Dominique; BENARD, Didier
The invention relates to novel products having formula (I), wherein: p denotes 0 to 2; R and R1 denote O or NH; R2 and R3 denote hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, aryl and heteroaryl, or R2 and R3, together with the carbon atom to which they are bound, form a carbocyclic or heterocyclic radical, all of said radicals being optionally substituted; A1 denotes a single bond, alkyl, allyl and propynyl; Y and Y1 denote H, OCF3, S(O)nCF3, S(O)nAlk, SO2CHF2, SO2CF2CF3, -O-CF2-CHF2, -O-CHF2, -O-CH2-CF3, SF5 and SO2NR5R6, whereby R5 and R6 are selected from among hydrogen, alkyl, alkenyl, cycloalkyl, cycloalkenyl, heterocycloalkyl, aryl and heteroaryl, which are optionally substituted, or R5 and R6, together with N to which they are bound, form a heterocyclic radical; A2 denotes Al, CO and SO2; B2 denotes a heterocyclic radical which is optionally substituted with one or more substituents which are selected from the values of Y2; Y2 denotes hydrogen, halogen, hydroxyl, cyano, alkyl, alkoxy, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, -O-alkenyl, -O-alkynyl, O-cycloalkyl, S(O)n-alkyl, -S(O)n-alkenyl, -S(O)n-alkynyl, S(O)n-cycloalkyl, -COOR13,-OCOR13, NR5R6, CONR5R6, S(O)n-NR5R6,-NR10-CO-R13, -NR10-SO2-R13, -NH-SO2-NR5R6, -NR10-CO-NR5R6, -NR10-CS-NR5R6, -NR10-COOR13, all of said radicals being optionally substituted; and n denotes an integer of between 0 and 2. The aforementioned products are in all the isomeric forms and the salts thereof for use as medicaments.
172 THIAZOLO-PYRAMIDINE / PYRIDINE UREA DERIVATIVES AS ADENOSINE A2B RECEPTOR ANTAGONISTS EP07728869.4 2007-05-08 EP2027132B1 2010-09-15 BRINKMAN, John A.; CHEUNG, Adrian Wai-Hing; FIROOZNIA, Fariborz; GUERTIN, Kevin Richard; MARCOPULOS, Nicholas; QI, Lida; RACHA, Jagdish Kumar; SARABU, Ramakanth; TAN, Jenny; TILLEY, Jefferson Wright
There are presented compounds of the formula (I) wherein R1, R2, R3 and R4 are as defined in the description and claims, or a pharmaceutically acceptable salt thereof, which are active adenosine A2B receptor antagonists and useful in the treatment of diabetes, diabetic retinopathy, asthma and diarrhea.
173 NOVEL TYROSINE KINASES INHIBITORS EP03774510 2003-10-01 EP1545543A4 2010-03-10 WITTMAN MARK D; BALASUBRAMANIAN NEELAKANTAN; VELAPARTHI UPENDER; ZIMMERMANN KURT; SAULNIER MARK G; LIU PEIYING; SANG XIAOPENG; FRENNESSON DAVID B; STOFFAN KAREN M; TARRANT JAMES G; MARINIER ANNE; ROY STEPHAN
174 INHIBITORS OF HISTONE DEACETYLASE EP08748100.8 2008-04-09 EP2139850A1 2010-01-06 TESSIER, Pierre; LEIT, Silvana; SMIL, David; DÉZIEL, Robert; AJAMIAN, Alain; CHANTIGNY, Yves, Andre; DOMINGUEZ, Celia
This invention relates to compounds for the inhibition of histone deacetylase. More particularly, the invention provides for compounds of formula compounds of the Formula (I) and N-oxides, hydrates, solvates, pharmaceutically acceptable salts, prodrugs and complexes thereof, and racemic and scalemic mixtures, diastereomers and enantiomers thereof, wherein groups L, M, X and Y are as defined herein.
175 METHOD FOR DETECTING PATHOGENIC MICROORGANISMS AND ANTIMICROBIAL AGENTS, METHOD FOR EVALUATING THE DRUG EFFECT OF ANTIMICROBIAL AGENTS, AND ANTIMICROBIAL AGENTS EP00944390.4 2000-07-11 EP1205559B1 2009-06-24 TATSUMI, Yoshiyuki; YOKOO, Mamoru; NAKAMURA, Kosho; ARIKA, Tadashi
A novel method for evaluating the drug effect of an antimicrobial agent which comprises eliminating the antimicrobial agent remaining in a biological sample, etc. to thereby accurately evaluate the drug effect of the antimicrobial agent without being affected by the remaining antimicrobial agent. Remedies for nail mycosis which can be obtained by the drug effect evaluation method as described above.
176 Dihydrothienopyrimidine zur Behandlung von entzündlichen Erkrankungen EP09152706.9 2006-04-19 EP2060575A1 2009-05-20 Pouzet, Pascale; Hoenke, Christoph; Martyres, Domnic; Nickolaus, Peter; Jung, Birgit

Die Erfindung betrifft neue Dihydrothienopyrimidine der Formel 1, sowie pharmakologisch verträgliche Salze, Diastereomere, Enantiomere, Racemate, Hydrate oder Solvate davon, die geeignet sind zur Behandlung von Atemwegs- oder gastrointestinalen Beschwerden oder Erkrankungen, entzündlichen Erkrankungen der Gelenke, der Haut oder der Augen, Erkrankungen des periphären oder zentralen Nervensystems oder Krebserkrankungen, sowie pharmazeutische Zusammensetzungen die diese Verbindungen beinhalten.

177 BETA-SECRETASE INHIBITORS AND METHODS OF USE EP02793826 2002-10-23 EP1448218A4 2009-01-14 GHOSH ARUN K; TANG JORDAN; BILCER GEOFFREY; CHANG WANPIN; HONG LIN; KOELSCH GERALD; LOY JEFF; TURNER ROBERT T III
178 SUBSTITUTED BENZOFURANS, BENZOTHIOPHENES, BENZOSELENOPHENES AND INDOLES AND THEIR USE AS TUBULIN POLYMERISATION INHIBITORS EP07701434.8 2007-02-02 EP1984333A1 2008-10-29 CHAPLIN, Jason, Hugh; GILL, Gurmit, Singh; GROBELNY, Damian, Wojciech; FLYNN, Bernard, Luke; KREMMIDIOTIS, Gabriel
The present invention relates generally to substituted benzofurans, benzothiophenes, and indoles and their use as tubulin polymerisation inhibitors.
179 USE OF COMPOUNDS HAVING AN AMINE NUCLEUS IN MANUFACTURE OF A MEDICAMENT USEFUL FOR TREATING FACTOR VIIA-ASSOCIATED CONDITIONS EP03742043 2003-06-17 EP1532103A4 2008-03-05 HERPIN TIMOTHY; BISACCHI GREGORY S; PI ZULAN; PRIESTLEY E SCOTT; DHAR T G MURALI
180 N-THIO-NICOTINAMID DERIVATE UND VERWANDTE VERBINDUNGEN ZUR VERWENDUNG ALS SCHÄDLINGSBEKÄMPFUNGSMITTEL EP02762475.8 2002-09-13 EP1432313B1 2008-01-23 BECKMANN, Marion; ORT, Oswald; DÖLLER, Uwe; KRAUTSTRUNK, Gerhard; SCHAPER, Wolfgang; LÜMMEN, Peter; JANS, Daniela; HEMPEL, Waltraud; WAIBEL, Jutta, Maria; KÜHN, Barbara
The invention relates to compounds of formulas (I) and (II), wherein the symbols and indices have the meaning cited in the description. Said compounds are suitable for the control of animal pests.
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