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 Neue Phenolderivate, diese enthaltende Arzneimittel und Verfahren zur Herstellung dieser Verbindungen und Arzneimittel EP86106126.5 1986-05-05 EP0202529B1 1989-12-13 Zimmer, Oswald, Dr.; Vollenberg, Werner, Dr.; Loschen, Gerriet, Dr.; Winter, Werner, Prof. Dr.; Kiesewetter, Erwin, Dr.; Seipp, Ulrich, Dr.
142 Salicylate assay, tracers, immunogens and antibodies EP85116063.0 1986-01-11 EP0194352A2 1986-09-17 Ungemach, Frank Schneider; Keegan, Candace Linda; Nystrom, David Donald; Stroupe, Stephen D.

The present invention is directed to a fluorescent polarization assay for salicylate, to the various components needed for preparing and carrying out such an assay, and to methods of making these components. Specifically, tracers, immunogens and antibodies are disclosed, as well as methods for making them. The tracers and the immunogens are made from substituted benzoic acid compounds. A fluorescein moiety is included in the tracer, while a poly(amino acid) forms a part of the immunogen. The antibodies are prepared in response to the immunogen. The assay is conducted by measuring the degree of polarization retention of plane polarized light that has been passed through a sample containing antiserum and tracer.

143 Dérivés de l'acide benzoique, procédé de préparation et application à titre de médicaments désinfectants ou de conservateurs EP84401675.8 1984-08-16 EP0135432A1 1985-03-27 Demarne, Henri; Filhol, Robert; Mossé, Madeleine

L'invention concerne des dérivés d'acide benzoïque de formule: dans laquelle:

  • - A représente une chaîne alkyle droite ou ramifiée comprenant de 5 à 10 atomes de carbone;
  • - X représente l'atome d'oxygène ou une liaison directe;
  • - R représente l'hydrogène ou un groupement alkyle de 2 à 6 atomes de carbone éventuellement substitué par une fonction alcool, et les sels desdits dérivés.

Ces dérivés ont une activité antimicrobienne et conviennent comme agents antiseptiques, désinfectants ou conservateurs, notamment dans les domaines de la pharmacie, la cosmétologie et l'agroalimentaire.

144 Protease inhibitors EP84105171.7 1984-05-08 EP0124905A1 1984-11-14 Müller, Richard August; Partis, Richard Allen

This invention relates to methods of preventing or reducing the degradation of elastin and other proteins and thereby preventing or retarding the disease states caused by said degradation by administering compounds of the formula: or their pharmacologically acceptable salts.

145 4-히드록시-프롤린 하부구조를 포함하는 펩티드의 합성 방법 KR1020057010600 2003-12-11 KR101018491B1 2011-03-03 비에트펠트,베른하르트; 프리코스조비흐,발터; 에르프,베른하르트; 파쉰저,베르너
본 발명은 펩티드의 제조 방법, 및 상기 방법, 예를 들면 R 12 및 R 13 이 본원에 정의된 바와 같은 화학식 VIII의 화합물의 제조 방법과 관련되는 중간체에 관한 것이다. <화학식 VIII> 4-히드록시-프롤린, 펩티드
146 2-(α-히드록시펜틸)벤조에이트, 그 제법 및 용도 KR1020047017690 2002-05-09 KR100756470B1 2007-09-07 양징후아; 왕시아올리앙; 수쯔빈; 펑잉
본 발명은 신규한 화합물 2-(α-히드록시펜틸)벤조에이트, 그 제법 및 이 화합물을 활성 성분으로 이용하는 약학 조성물에 관한 것이며; 본 발명은 또한 심장허혈, 대뇌허혈 및 심장 또는 대뇌 동맥 색전증 등의 치료 및 예방을 위한 상기 화합물의 용도에 관한 것이다.
147 2-(α-히드록시펜틸)벤조에이트, 그 제법 및 용도 KR1020047017690 2002-05-09 KR1020040106457A 2004-12-17 양징후아; 왕시아올리앙; 수쯔빈; 펑잉
본 발명은 신규한 화합물 2-(α-히드록시펜틸)벤조에이트, 그 제법 및 이 화합물을 활성 성분으로 이용하는 약학 조성물에 관한 것이며; 본 발명은 또한 심장허혈, 대뇌허혈 및 심장 또는 대뇌 동맥 색전증 등의 치료 및 예방을 위한 상기 화합물의 용도에 관한 것이다.
148 페놀 유도체의 제조방법 KR1019860004098 1986-05-24 KR1019930001324B1 1993-02-26 오스발트짐머; 베르너볼렌버그; 게리트로센; 베르너빈터; 에르빈키제베터; 율리히자이프
내용 없음.
149 항세균 활성을 갖는 벤조산 유도체의 제조방법 KR1019840004997 1984-08-18 KR1019910007365B1 1991-09-25 앙리드마른느; 로베르트삐롤; 마드랭모스
내용 없음.
150 항세균 활성을 갖는 벤조산 유도체의 제조방법 KR1019840004997 1984-08-18 KR1019850001722A 1985-04-01 앙리드마른느; 로베르트삐롤; 마드랭모스
내용없음
151 DIELS-ALDER REACTIONS CATALYZED BY LEWIS ACID CONTAINING SOLIDS: RENEWABLE PRODUCTION OF BIO-PLASTICS PCT/US2014038696 2014-05-20 WO2014197195A2 2014-12-11 DAVIS MARK E; PACHECO JOSHUA
The present disclosure is related to silica-based Lewis acid catalysts, being essentially devoid of strong Bronsted acid character, and their ability to effect the [4+2] cycloaddition and dehydrative aromatization of dienes and dienophiles containing oxygenated substituents to form substituted benzene products. In some embodiments, the processes comprise contacting biomass-derived substrates with ethylene to form terephthalic acid and its derivatives.
152 L-2-(a-HYDROXYPENTYL)BENZOATES, THE PREPARATION AND THE USE THEREOF PCT/CN2005000102 2005-01-24 WO2005123651A8 2006-04-13 LIU QUANZHI; YANG WENBIN; QIN HUA; ZHAO XINGKAI
The present invention relates to new L-2-(a-hydroxypentyl) benzoates and the preparation thereof, and to the pharmaceutical compositions in which the compounds are used as active ingredients. The invention also relates to the use of the compounds in manufacture of the medicine for preventing and treating cardioischemia, cerbroischemia, thrombotic diseases and improving the circulation in heart and brain.
153 ACID ADDITION SALT OF DONEPEZIL AND PHARMACEUTICAL COMPOSITION THEREOF PCT/IB2012001307 2012-07-03 WO2013005094A8 2014-02-20 NADKARNI SUNIL SADANAND; GUPTA ARUNKUMAR; ABRAHAM JAYA; PARIKH MANISH; SUTHAR MAHESH; MANAVADARIYA BIPIN; MISHRA VIVEK
Disclosed is an acid addition salt of donepezil, wherein acid counterion is selected from the group consisting of pamoic acid, cypionic acid, camphor sulfonic acid, enanthic acid, fusidic acid, gluceptic acid, gluconic acid, lactobionic acid, lauric acid, valeric acid, Dibenzoyl-D -Tartaric acid and terephthalic acid. Disclosed is a process for the preparation and pharmaceutical composition comprising the same. More specifically, disclosed is concerned with the pamoate acid addition salts of donepezil. Disclosed also is long acting formulation comprising the acid addition salt of donepezil and process for the preparation thereof.
154 CATALYTIC HYDROGENATION OF CARBOXYARYLALDEHYDE AND USE THEREOF FOR PURIFYING CRUDE TEREPHTHALIC ACID PCT/US2010049477 2010-09-20 WO2011041151A3 2011-05-26 NUBEL PHILIP O; BARTOS THOMAS M; TALREJA SAMEER; BRUGGE STEPHEN P
This invention provides a catalyst and the use thereof and a process for hydrogenating carboxyaryl aldehydes with selectivity to hydroxyalkylaryl monocarboxylic acids. The catalyst comprises iridium.
155 METHOD FOR PREPARING TRICYCLIC DERIVATIVES PCT/KR2010004212 2010-06-29 WO2011004980A2 2011-01-13 KIM MYUNG-HWA; YE IN-HAE; CHOI JONG-HEE
The present invention relates to a method for preparing tricyclic derivatives, and more particularly, to a method for preparing intermediates of novel tricyclic derivatives having a superior yield rate and purity, wherein the method involves esterifying 2-fluoroisophthalic acid compounds, conducting a substation reaction on the compounds to introduce a hydroxyl group, introducing a piperidyl group, conducting a reduction reaction on the compounds, introducing a hydroxyl group, and conducting a hydrolysis on the resultant compounds. The present invention also relates to a method for preparing tricyclic derivatives using the intermediates. The method of the present invention refines substances by recrystallization as opposed to conventional methods which involve refining substances by column chromatography, and thus prepares tricyclic derivatives having more excellent productivity, economical advantages, and higher purity and yield rate as compared to conventional methods, as well as to intermediates of the tricyclic derivatives. In addition, the method of the present invention uses sodium borohydride or lithium aluminum hydrate which have less risk of fire as opposed to conventional methods using lithium borohydrides which cannot be industrially used due to the high risk of fire thereof, and therefore the method of the present invention can be useful in industrial mass production.
QQ群二维码
意见反馈