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1. 发明申请

WO9904822A3 NEW SALTS WITH BENEFICIAL ORGANOLEPTIC PROPERTIES 审中-公开
标题翻译：新的盐与有益的有机物质性能
公开(公告)号：WO9904822A3
公开(公告)日：1999-08-12
申请号：PCT/HU9800066
申请日：1998-07-22
申请人： CHINOIN GYOGYSZER ES VEGYESZET , LEDNICZKY LASZLO , SERES ISTVAN
发明人： LEDNICZKY LASZLO , SERES ISTVAN
IPC分类号： A61K31/33 , A61K47/20 , A61K47/22 , A61K47/48 , A61P13/06
CPC分类号： A61K47/541
摘要： The invention relates to new salts of known drugs which have pleasant taste.
摘要翻译：本发明涉及具有令人愉快的味道的已知药物的新盐。

2. 发明申请

WO03011849A8 PROCESS FOR THE PRODUCTION OF BERAPROST AND ITS SALTS 审中-公开
标题翻译：生产BERAPROST及其销售的方法
公开(公告)号：WO03011849A8
公开(公告)日：2004-03-11
申请号：PCT/HU0200074
申请日：2002-07-25
申请人： CHINOIN GYOGYSZER ES VEGYESZET , SZABO TIBOR , BODI JOZSEF , DALMADI GYULA , BALOGHNE KARDOS ZSUZSANNA , SZEVERENYI ZOLTAN
发明人： SZABO TIBOR , BODI JOZSEF , DALMADI GYULA , BALOGHNE KARDOS ZSUZSANNA , SZEVERENYI ZOLTAN
IPC分类号： C07D307/93 , C07F7/08 , C07F7/18
CPC分类号： C07D307/93 , C07F7/1856 , Y02P20/55
摘要： The present invention relates to a new process for the preparation of beraprost of formula (I) using new intermediates.
摘要翻译：本发明涉及使用新的中间体制备式（I）的贝前列素的新方法。

3. 发明申请

WO9719040A2 PESTICIDE COMPOUNDS, COMPOSITIONS AND PROCESS FOR THE PREPARATION THEREOF 审中-公开
标题翻译：杀虫剂化合物，其制备方法及其制备方法
公开(公告)号：WO9719040A2
公开(公告)日：1997-05-29
申请号：PCT/HU9600069
申请日：1996-11-19
申请人： CHINOIN GYOGYSZER ES VEGYESZET , ARVAI GEZA , BAKONYVARI ILDIKO , BERTOK BELA , CSIZ LASZLO , CZUDOR IREN , KURUCZNE R ZSUZSA , PAP LASZLO , SZEKELY ISTVAN
发明人： ARVAI GEZA , BAKONYVARI ILDIKO , BERTOK BELA , CSIZ LASZLO , CZUDOR IREN , KURUCZNE R ZSUZSA , PAP LASZLO , SZEKELY ISTVAN
IPC分类号： C07D317/54 , A01N31/04 , A01N31/06 , A01N31/14 , A01N31/16 , A01N33/04 , A01N33/22 , A01N35/10 , A01N37/18 , A01N37/32 , A01N43/12 , A01N43/16 , A01N43/30 , A01N43/32 , C07C41/16 , C07C43/166 , C07C43/176 , C07C43/178 , C07C43/188 , C07C43/196 , C07C43/215 , C07C205/37 , C07C211/30 , C07C231/02 , C07C233/65 , C07C249/12 , C07C251/40 , C07C251/48 , C07D231/12 , C07D307/79 , C07D307/80 , C07D319/18 , C07C
CPC分类号： C07C43/215 , A01N31/04 , A01N31/06 , A01N31/14 , A01N31/16 , A01N33/04 , A01N33/22 , A01N35/10 , A01N37/18 , A01N37/32 , A01N43/12 , A01N43/30 , A01N43/32 , C07C43/166 , C07C43/176 , C07C43/188 , C07C205/37 , C07C211/30 , C07C233/65 , C07C251/48 , C07C2602/08 , C07C2602/10
摘要： The invention relates to compounds of general formula (I), their optically active isomers and salts wherein Ar = alycyclic, aromatic or one or more heteroatom containing heterocyclic moiety, optionally substituted by one or more alkoxy-, methylenedioxy-, alkyl-, halogen-, haloalkyl-, or nitro-group and/or condensed with a benzene ring; R , R = independently H, alkyl, alkenyl, haloalkyl, phenyl, substituted phenyl, cycloalkyl, R , R = independently H, alkyl, alkenyl, haloalkyl, phenyl, substituted phenyl, cycloalkyl, or R , R are together =O, Y = C; PO, or YR R together (a) group; X = -O-; -NR -, R = H, alkyl, phenyl, substituded phenyl; R = H, alkyl; R5, R6, R7, R8 are independently H, alkyl, alkenyl, haloalkyl, or Ar-(CR R )m-(YR R )n-X- form together a carboximide group; E = H, halogen, methyl; m = 0, 1, 2; n = 0, 1; o = 0, 1, 2; p = 0, 1, 2, with the proviso, that the sum of the atoms or groups of the -(CR R )m-(CR R )n-X-(CR R )o-(CR R )p bridge skeleton is 3 and the -CC-E skeleton forms with the atoms of the bridge a linear chain, consisting of 6 atoms ending preferably in a methyl group, furthermore with the proviso, that if Ar stands for a naphthyl group, Y means C-atom, X means O-atom, R and R together cannot mean =O. The compounds of general formula (I) according to the invention can be applied as active ingredients of pesticide, preferably arthropodicide compositions, and as synergists of other arthropodicide active ingredients.
摘要翻译：本发明涉及通式（I）的化合物，它们的旋光异构体和盐，其中Ar =亚环，芳族或一个或多个含杂原子的杂环部分，任选被一个或多个烷氧基，亚甲二氧基，烷基 - ，卤代烷基 - 或硝基和/或与苯环缩合; R 1，R 2独立地为H，烷基，烯基，卤代烷基，苯基，取代的苯基，环烷基，R 3，R 4独立地为H，烷基，烯基，卤代烷基，苯基，取代的苯基，环烷基或R 3，R 4一起= O，Y = C; PO或YR 3 R 4一起（a）基团; X = -O-; -NR 10 - ，R 9 = H，烷基，苯基，取代苯基; R 10 = H，烷基; R 5，R 6，R 7，R 8独立地是H，烷基，链烯基，卤代烷基或Ar-（CR 1 R 2）m - （YR 3 R 4） E = H，卤素，甲基; m = 0,1,2; n = 0,1; o = 0,1,2; p = 0,1,2，条件是 - （CR 1 R 2）m - （CR 3 R 4）n X-（CR 3）的原子或基团的和，（CR 7 R 8）p桥骨架是3，并且-CC-E骨架与桥的原子形成直链，由6个原子组成，优选在甲基，此外条件是，如果Ar表示萘基，则Y表示C原子，X表示O原子，R 3和R 4一起不能表示= O。根据本发明的通式（I）的化合物可以作为农药的活性成分，优选节肢杀鼠剂组合物，以及作为其他节肢动物杀真菌剂活性成分的增效剂。

4. 发明申请

WO0107024A3 PARACETAMOL AND DROTAVERINE CONTAINING COMPOSITION 审中-公开
标题翻译：帕拉米托和含有组合物的DROTAVERINE
公开(公告)号：WO0107024A3
公开(公告)日：2001-03-29
申请号：PCT/HU0000086
申请日：2000-07-28
申请人： CHINOIN GYOGYSZER ES VEGYESZET , VITANYINE MORVAI MAGDOLNA , KOVACS PETERNE , KALMANNE MATHE IRMA , JAKAB BOGLARKA , VEGELI ERZSEBET
发明人： VITANYINE MORVAI MAGDOLNA , KOVACS PETERNE , KALMANNE MATHE IRMA , JAKAB BOGLARKA , VEGELI ERZSEBET
IPC分类号： A61K31/47 , A61K31/00 , A61K31/165 , A61K31/167 , A61K31/485 , A61P29/00
CPC分类号： A61K31/47 , A61K31/167 , A61K31/485 , A61K2300/00
摘要： The invention relates to a stable, solid pharmaceutical composition comprising as active ingredients paracetamol and drotaverine hydrochloride in a mixture with one or more organic acid or potassium sorbate as stabilizers, one or more usually used pharmaceutical auxiliary materials and optionally additional active ingredient. As additional active ingredient codein phosphate may be used.
摘要翻译：本发明涉及一种稳定的固体药物组合物，其包含与一种或多种有机酸或山梨酸钾作为稳定剂，一种或多种通常使用的药物辅助材料和任选的其它活性成分的混合物中的扑热息痛和盐酸屈麦丹的活性成分。作为另外的活性成分可以使用磷酸可待因。

5. 发明申请

WO1982001821A1 ANTIMYCOTIC SYNERGISTIC PHARMACEUTICAL COMPOSITIONS AND PROCESS FOR THE PREPARATION THEREOF 审中-公开
标题翻译：抗菌协同药物组合物及其制备方法
公开(公告)号：WO1982001821A1
公开(公告)日：1982-06-10
申请号：PCT/HU1980000005
申请日：1980-11-27
申请人： CHINOIN GYOGYSZER ES VEGYESZET , KOVACS ANDRAS , SZEBENI RUDOLF , NEMES JOZSEF , NGYKALDI ATTILA
发明人： CHINOIN GYOGYSZER ES VEGYESZET
IPC分类号： A61K31/71
CPC分类号： A61K31/70 , A61K31/12 , A61K2300/00
摘要： Antimycotic synergistic pharmaceutical compositions comprising nystatine and a 2-lower alkyl-l, 4-naphthoquinone or an addition product thereof in admixture with suitable inert pharmaceutical carriers. The invention also relates to a process for the above compositions by admixing the active ingredients with suitable inert carriers. It is preferred to use 2-methyl-1, -naphthoquinone or the sodium bisulfite adduct thereof. The ratio of the active ingredients is preferably 20.000 to 100.000 IU of nystatine for 1 mg of 2-methyl-1,4-naphthoquinone-sodium bisulfite adduct. The compositions show strong synergism in the treatment of infections caused by Candida albicans and Trichomonas vaginalis and are active against resistant strains too. The compositions may be finished in forms suitable for topical use, such as suppository, aerosol, jelly or vaginal tablets.
摘要翻译：抗微生物协同药物组合物，其包含与合适的惰性药物载体混合的营养素和2-低级烷基-1,4-萘醌或其加成产物。本发明还涉及通过将活性成分与合适的惰性载体混合而获得的上述组合物的方法。优选使用2-甲基-1'-萘醌或其亚硫酸氢钠加成物。对于1mg 2-甲基-1,4-萘醌 - 亚硫酸氢钠加合物，活性成分的比例优选为20.000〜100.000IU的营养元素。该组合物在治疗由白色念珠菌和阴道毛滴虫引起的感染中表现出强烈的协同作用，并且对抗性菌株也具有活性。组合物可以以适于局部使用的形式，例如栓剂，气雾剂，果冻或阴道片剂来完成。

6. 发明授权

KR870001002B1 선택적으로 생리활성인 7-옥소-프로스타사이클린 유도체의 제조방법 失效
公开(公告)号：KR870001002B1
公开(公告)日：1987-05-18
申请号：KR870002970
申请日：1987-03-30
申请人： CHINOIN GYOGYSZER ES VEGYESZET
发明人： GYORY PETER , GELANBOS GEZA , KANAI KAROLY , IVANICHS JOSEPH , DORMAN GYORGY , KAVACHS GABOR
IPC分类号： C07D307/00 , C07D307/935

7. 发明申请

WO2012093271A8 A NEW PALLADIUM CATALYST, METHOD FOR ITS PREPARATION AND ITS USE 审中-公开
标题翻译：一种新的钯催化剂，其制备方法及其用途
公开(公告)号：WO2012093271A8
公开(公告)日：2013-09-12
申请号：PCT/HU2011000122
申请日：2011-12-13
申请人： H4SEP KFT , CHINOIN GYOGYSZER ES VEGYESZET , DALICSEK ZOLTAN , SOOS TIBOR , FINTA ZOLTAN , TIMARI GEZA , VLAD GABOR
发明人： DALICSEK ZOLTAN , SOOS TIBOR , FINTA ZOLTAN , TIMARI GEZA , VLAD GABOR
IPC分类号： C07B35/02 , B01J31/24 , C07B37/04 , C07C15/52 , C07C15/54 , C07C41/30 , C07C43/205 , C07C43/215 , C07C201/12 , C07C205/06 , C07D213/30 , C07D217/02 , C07D217/16
CPC分类号： B01J31/2404 , B01J31/2409 , B01J31/2447 , C07B35/02 , C07B37/04 , C07C2/66 , C07C2/88 , C07C15/52 , C07C15/54 , C07C17/26 , C07C41/30 , C07C201/12 , C07C205/06 , C07D209/08 , C07D213/127 , C07D213/14 , C07D213/26 , C07D213/30 , C07D215/06 , C07D215/12 , C07D215/14 , C07D217/02 , C07D217/16 , C07D217/18 , C07D217/20 , C07D295/023
摘要： The invention relates to palladium(0)-tetrakis{tri-[3,5-bis(trifluoromethyl)- phenylj-phosphine} complex of formula (I), as well as to its preparation and use. This compound is outstandingly stable, and can be used as catalyst with excellent results.
摘要翻译：本发明涉及式（I）的钯（0） - 四（三 - [3,5-双（三氟甲基）苯基]膦基）络合物，以及其制备和用途。该化合物稳定，可用作催化剂，效果优异。

8. 发明申请

WO0107033A3 NEUROPROTECTIVE PHARMACEUTICAL REPARATIONS COMPRISING P-FLUOROSELEGILINE 审中-公开
标题翻译：包含对氟菊酯的神经保护性药物报道
公开(公告)号：WO0107033A3
公开(公告)日：2001-08-16
申请号：PCT/HU0000084
申请日：2000-07-21
申请人： CHINOIN GYOGYSZER ES VEGYESZET , BARANYI ATTILANE HF , BARANYI KRISZTINA HF , ARANYI PETER , ERDOE FRANCISKA , SCHRAMMELNE MIHALKA CSILLA , VENEKEINE LOSONCZI OLGA
发明人： BARANYI ATTILA DI , ARANYI PETER , ERDOE FRANCISKA , SCHRAMMELNE MIHALKA CSILLA , VENEKEINE LOSONCZI OLGA
IPC分类号： A61K9/28 , A61K9/70 , A61K31/137 , C07K5/078 , A61K31/135 , A61P25/28
CPC分类号： C07K5/06139 , A61K9/2826 , A61K9/7023 , A61K31/137
摘要： The invention relates to the use of racemic or optically active p-fluoro-selegiline and/or its salts of formula (I) for the protection of neurons and/or for the promotion of the regeneration of damaged neurons.
摘要翻译：本发明涉及外消旋或光学活性的对 - 氟 - 司来吉兰和/或其式（I）的盐用于保护神经元和/或促进受损神经元的再生。

9. 发明申请

WO9633615A3 PESTICIDE FORMULATIONS AND PROCESS FOR THE MANUFACPESTICIDE FORMULATIONS AND PROCESS FOR THE MANUFACTURE THEREOF TURE THEREOF 审中-公开
标题翻译：杀虫剂制剂及其制备方法及其制备方法
公开(公告)号：WO9633615A3
公开(公告)日：1997-01-09
申请号：PCT/HU9600020
申请日：1996-04-19
申请人： CHINOIN GYOGYSZER ES VEGYESZET , SZEKELY ISTVAN , BOTAR SANDOR , BERTOK BELA , HAJIMICHAEL JANIS , KIRALY JENO , HADOBAS JANOSME , PAP LASZLO , MENESINE B ILDIKO
发明人： SZEKELY ISTVAN , BOTAR SANDOR , BERTOK BELA , HAJIMICHAEL JANIS , KIRALY JENO , HADOBAS JANOSME , PAP LASZLO , MENESINE B ILDIKO
IPC分类号： A01N25/04 , A01N25/08 , A01N25/22 , A01N25/30 , A01N53/00 , A01N53/02 , A01N53/08
CPC分类号： A01N53/00 , Y10S514/937 , Y10S514/941 , Y10S514/949 , Y10S514/97 , A01N25/04 , A01N2300/00
摘要： PCT No. PCT/HU96/00020 Sec. 371 Date Dec. 23, 1997 Sec. 102(e) Date Dec. 23, 1997 PCT Filed Apr. 19, 1996 PCT Pub. No. WO96/33615 PCT Pub. Date Oct. 31, 1996The subject of the invention is an aqueous suspension containing: 0.1-20% by mass beta-cypermethrin, 0-40% by mass other pesticide substance, 1-10% by mass surface active substances in total and within this, 1-5% by mass ethoxylated polyaryl-phenol-phosphate or sulfate, 0.1-25% by mass mineral and/or synthetic silicates, 0.1-1% by mass synthetic silicic acid and up to 100% by mass other auxiliary materials and water as dispersant.

10. 发明授权

KR880000002B1 살균 조성물 失效
公开(公告)号：KR880000002B1
公开(公告)日：1988-02-15
申请号：KR850004748
申请日：1985-07-02
申请人： CHINOIN GYOGYSZER ES VEGYESZET
发明人： SANDOS ANGIAN , ESTBAN RAKZ , ANDRAS SZEGO , GYULA SZUK , TAMAS SZUTK , OYS SEF , KATARIN MARMAROSI
IPC分类号： A01N33/08 , A01N43/50 , A01N43/82

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