DE69634122D1 - Heterocyclische amidverbindungen und deren medizinische verwendung - Google Patents
Heterocyclische amidverbindungen und deren medizinische verwendungInfo
- Publication number
- DE69634122D1 DE69634122D1 DE69634122T DE69634122T DE69634122D1 DE 69634122 D1 DE69634122 D1 DE 69634122D1 DE 69634122 T DE69634122 T DE 69634122T DE 69634122 T DE69634122 T DE 69634122T DE 69634122 D1 DE69634122 D1 DE 69634122D1
- Authority
- DE
- Germany
- Prior art keywords
- medicine
- amide compounds
- heterocyclic amide
- heterocyclic
- compounds
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/96—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/73—Unsubstituted amino or imino radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10431495 | 1995-04-27 | ||
PCT/JP1996/001171 WO1996033974A1 (fr) | 1995-04-27 | 1996-04-26 | Composes heterocycliques amides et leur utilisation medicinale |
Publications (1)
Publication Number | Publication Date |
---|---|
DE69634122D1 true DE69634122D1 (de) | 2005-02-03 |
Family
ID=14377479
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE69634122T Expired - Lifetime DE69634122D1 (de) | 1995-04-27 | 1996-04-26 | Heterocyclische amidverbindungen und deren medizinische verwendung |
Country Status (7)
Country | Link |
---|---|
US (1) | US5948785A (de) |
EP (1) | EP0826671B1 (de) |
KR (1) | KR100400639B1 (de) |
CN (2) | CN1131210C (de) |
CA (1) | CA2219364A1 (de) |
DE (1) | DE69634122D1 (de) |
WO (1) | WO1996033974A1 (de) |
Families Citing this family (77)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6271238B1 (en) | 1996-09-06 | 2001-08-07 | Nippon Kayaku Kabushiki Kaisha | Acetamide derivatives and protease inhibitors |
US6369080B2 (en) * | 1996-10-11 | 2002-04-09 | Cor Therapeutics, Inc. | Selective factor Xa inhibitors |
US6262047B1 (en) | 1996-10-11 | 2001-07-17 | Cor Therapeutics, Inc. | Selective factor Xa inhibitors |
US6194435B1 (en) | 1996-10-11 | 2001-02-27 | Cor Therapeutics, Inc. | Lactams as selective factor Xa inhibitors |
US6063794A (en) | 1996-10-11 | 2000-05-16 | Cor Therapeutics Inc. | Selective factor Xa inhibitors |
US6080738A (en) * | 1996-10-25 | 2000-06-27 | Yoshitomi Pharmaceuticals Industries, Ltd. | Heterocyclic amide compounds and medicinal uses thereof |
JP2001508796A (ja) * | 1997-01-22 | 2001-07-03 | メルク エンド カンパニー インコーポレーテッド | トロンビン阻害薬 |
NZ500352A (en) | 1997-04-14 | 2001-10-26 | Cor Therapeutics Inc | Cyclic diaza selective factor Xa inhibitors |
JP2002513412A (ja) | 1997-04-14 | 2002-05-08 | シーオーアール セラピューティクス インコーポレイテッド | 選択的Xa因子阻害剤 |
WO1998046626A1 (en) | 1997-04-14 | 1998-10-22 | Cor Therapeutics, Inc. | SELECTIVE FACTOR Xa INHIBITORS |
US6228854B1 (en) | 1997-08-11 | 2001-05-08 | Cor Therapeutics, Inc. | Selective factor Xa inhibitors |
US6333321B1 (en) | 1997-08-11 | 2001-12-25 | Cor Therapeutics, Inc. | Selective factor Xa inhibitors |
US6218382B1 (en) | 1997-08-11 | 2001-04-17 | Cor Therapeutics, Inc | Selective factor Xa inhibitors |
WO1999032459A1 (fr) * | 1997-12-22 | 1999-07-01 | Yoshitomi Pharmaceutical Industries, Ltd. | Inhibiteurs de la chymase |
AU744739B2 (en) * | 1998-02-17 | 2002-02-28 | Nippon Kayaku Kabushiki Kaisha | Novel acetamide derivative and use thereof |
US6528514B1 (en) | 1998-03-11 | 2003-03-04 | Welfide Corporation | IgE antibody production inhibitors and autoimmune diseases inhibitors |
TR200100047T2 (tr) | 1998-07-15 | 2001-10-22 | Teijin Limited | Tiyobenzimidazol türevleri |
US20050267148A1 (en) * | 1998-07-15 | 2005-12-01 | Teijin Limited | Benzimidazole derivative |
KR20010074838A (ko) * | 1998-08-20 | 2001-08-09 | 요시다 쇼지 | 안 순환 장해의 예방 또는 치료제 |
US6664255B1 (en) | 1999-05-19 | 2003-12-16 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl pyrazinones useful for selective inhibition of the coagulation cascade |
US6716838B1 (en) | 1999-05-19 | 2004-04-06 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl uracils as anticoagulative agents |
US6458952B1 (en) | 1999-05-19 | 2002-10-01 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl uracils useful for selective inhibition of the coagulation cascade |
US6750342B1 (en) | 1999-05-19 | 2004-06-15 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl pyrimidinones useful for selective inhibition of the coagulation cascade |
US7015230B1 (en) | 1999-05-19 | 2006-03-21 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl uracils useful for selective inhibition of the coagulation cascade |
US6867217B1 (en) | 1999-05-19 | 2005-03-15 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl pyridones useful for selective inhibition of the coagulation cascade |
EP1178970A1 (de) * | 1999-05-19 | 2002-02-13 | Pharmacia Corporation | Substituierte polyzyklisch aryl und heteroaryl pyrimidinonen brauchbar als gerinnungshemmende mittel |
US6653316B1 (en) | 1999-05-19 | 2003-11-25 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl pyrimidinones useful for selective inhibition of the coagulation cascade |
JP4556371B2 (ja) * | 1999-09-30 | 2010-10-06 | 三菱化学株式会社 | アシルスルホンアミド誘導体 |
AU7954900A (en) * | 1999-10-25 | 2001-05-08 | Senju Pharmaceutical Co., Ltd. | Tension-relieving agents for ciliary muscle |
CN1335778A (zh) * | 1999-11-01 | 2002-02-13 | 三得利株式会社 | 含有糜蛋白酶抑制物质的血管脂质沉积抑制剂 |
KR20010109356A (ko) | 2000-02-22 | 2001-12-08 | 도리이 신이치로 | 키마제 억제제를 유효성분으로 함유하는 피부염의 예방또는 치료제 |
CN1245978C (zh) | 2000-02-22 | 2006-03-22 | 第一阿斯比奥制药株式会社 | 含有胃促胰酶抑制剂作为活性成分的预防和治疗各种与嗜酸性粒细胞增多有关的疾病的药物 |
WO2001062292A1 (fr) | 2000-02-22 | 2001-08-30 | Suntory Limited | Medicaments preventifs ou therapeutiques pour traiter la fibrose et contenant des inhibiteurs de chymase comme ingredients actifs |
US6852761B2 (en) | 2000-03-13 | 2005-02-08 | Pharmacia Corporation | Polycyclic aryl and heteroaryl substituted benzenes useful for selective inhibition of the coagulation cascade |
US6875791B2 (en) | 2000-04-05 | 2005-04-05 | Pharmacia Corporation | Polycyclic aryl and heteroaryl substituted 4-pyrones useful for selective inhibition of the coagulation cascade |
JP2004505013A (ja) | 2000-04-05 | 2004-02-19 | ファルマシア・コーポレーション | 凝固カスケードを選択的に阻害するのに有用な多環式アリール及びヘテロアリール置換4−ピリドン類 |
WO2001079155A2 (en) | 2000-04-17 | 2001-10-25 | Pharmacia Corporation | Polycyclic aryl and heteroaryl substituted 1,4-quinones useful for selective inhibition of the coagulation cascade |
WO2001087851A1 (en) * | 2000-05-18 | 2001-11-22 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl pyrimidinones useful for selective inhibition of the coagulation cascade |
KR100850728B1 (ko) | 2000-06-12 | 2008-08-06 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 1,2-디하이드로피리딘 화합물, 그의 제조 방법 및 그의 용도 |
EP1301490A2 (de) * | 2000-07-18 | 2003-04-16 | Neurogen Corporation | 5-substituierte 2-aryl-4-pyrimidinone |
US7119094B1 (en) | 2000-11-20 | 2006-10-10 | Warner-Lambert Company | Substituted polycyclic aryl and heteroarpyl pyrazinones useful for selective inhibition of the coagulation cascade |
US7015223B1 (en) | 2000-11-20 | 2006-03-21 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl 1,2,4-triazinones useful for selective inhibition of the coagulation cascade |
EP1351686A2 (de) | 2000-11-20 | 2003-10-15 | Pharmacia Corporation | Substituierte polycyclische aryl- und heteroarylpyridine für die selektive hemmung der koagulationskaskade |
US20040063936A1 (en) * | 2000-12-26 | 2004-04-01 | Tsuneyuki Sugiura | Pyrimidine derivatives and process for preparing the same |
WO2003007964A1 (fr) * | 2001-07-18 | 2003-01-30 | Nippon Kayaku Kabushiki Kaisha | Remede ou agent preventif de cardiopathie ou d'anevrysme contenant un compose d'inhibition de la chymase |
CA2462305A1 (en) | 2001-10-03 | 2003-04-10 | Michael S. South | 6-membered heterocyclic compounds useful for selective inhibition of the coagulation cascade |
EP1432687A2 (de) | 2001-10-03 | 2004-06-30 | Pharmacia Corporation | Substitutierte fünfgliedrige polyzyclischen vebindungen für die selektive hemmung der koagulationskaskade |
GB0129260D0 (en) | 2001-12-06 | 2002-01-23 | Eisai London Res Lab Ltd | Pharmaceutical compositions and their uses |
EP1553090A4 (de) * | 2002-06-14 | 2006-07-05 | Ajinomoto Kk | Verfahren zur herstellung einer pyrimidinverbindung |
CZ20041239A3 (cs) * | 2002-07-30 | 2006-04-12 | Société de Conseil de Recherches et d´Applications Scientifique, S.A.S | Pouzití inhibitoru chymázy pro výrobu léciva pro prevenci a/nebo lécbu selhání arteriovenózního stepu |
US20050176966A1 (en) * | 2003-04-11 | 2005-08-11 | Ajinomoto Co., Inc. | Process for the preparation of pyrimidine derivative, intermediate therefor and process for the preparation thereof |
PE20050159A1 (es) * | 2003-05-27 | 2005-04-19 | Vertex Pharma | Derivados de acido 3-[2-(3-amino-2-oxo-2h-piridin-1-il)-acetilamino]-4-oxo-pentanoico como inhibidores de caspasa |
US20070032466A1 (en) * | 2003-08-22 | 2007-02-08 | Teijin Pharma Limited | Drug containing chymase inhibitor as the active ingredient |
US7358368B2 (en) | 2003-11-04 | 2008-04-15 | Ajinomoto Co., Inc. | Azlactone compound and method for preparation thereof |
EP1695967A1 (de) * | 2003-11-04 | 2006-08-30 | Ajinomoto Co., Inc. | Verfahren zur herstellung von pyrimidinderivaten und zwischenprodukten |
MY148809A (en) | 2004-07-06 | 2013-05-31 | Eisai R&D Man Co Ltd | Crystals of 1,2-dihydropyridine compound and their production process |
EP1833794B1 (de) | 2004-11-24 | 2012-02-01 | Vertex Pharmceuticals Incorporated | 3-[2-(3-azylamino-2-oxo-2h-pyridin-1-yl)acetylamino]-4-oxopentansäurederivate und deren verwendung als caspase-inhibitoren |
TWI417095B (zh) | 2006-03-15 | 2013-12-01 | Janssen Pharmaceuticals Inc | 1,4-二取代之3-氰基-吡啶酮衍生物及其作為mGluR2-受體之正向異位性調節劑之用途 |
TW200900065A (en) | 2007-03-07 | 2009-01-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-pyridinyloxy-phenyl)-pyridin-2-one derivatives |
TW200845978A (en) | 2007-03-07 | 2008-12-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-tetrahydropyran-phenyl)-pyridin-2-one derivatives |
CN103342695B (zh) | 2007-09-14 | 2015-04-22 | 杨森制药有限公司 | 1’,3’-二取代的-4-苯基-3,4,5,6-四氢-2h,1’h-[1,4’]二吡啶-2’-酮 |
MX2011002042A (es) | 2008-09-02 | 2011-06-20 | Ortho Mcneil Janssen Pharm | Derivados de 3-azabiciclo[3.1.o]hexilo como moduladores de los receptores del glutamato metabotropico. |
JP5690277B2 (ja) | 2008-11-28 | 2015-03-25 | ジャンセン ファーマシューティカルズ, インコーポレイテッド. | 代謝型グルタミン酸受容体の調節因子としてのインドールおよびベンゾオキサジン誘導体 |
WO2010088195A1 (en) | 2009-01-30 | 2010-08-05 | Boehringer Ingelheim International Gmbh | Azaquinazolinediones useful as chymase inhibitors |
MY153913A (en) | 2009-05-12 | 2015-04-15 | Janssen Pharmaceuticals Inc | 7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors |
ES2409006T3 (es) | 2009-05-12 | 2013-06-24 | Janssen Pharmaceuticals Inc. | Derivados de 1,2,4-triazolo[4,3-a]piridina y su uso como moduladores alostéricos positivos de los receptores mGluR2 |
EP2430022B1 (de) | 2009-05-12 | 2013-11-20 | Janssen Pharmaceuticals, Inc. | 1,2,4-Triazolo[4,3-a]pyridinderivate und ihre Verwendung zur Behandlung oder Vorbeugung von neurologischen oder psychiatrischen Erkrankungen |
EP2475654B1 (de) * | 2009-09-09 | 2016-12-28 | E. I. du Pont de Nemours and Company | Herbizide pyrimidonderivate |
ES2552455T3 (es) | 2010-11-08 | 2015-11-30 | Janssen Pharmaceuticals, Inc. | Derivados de 1,2,4-triazolo[4,3-a]piridina y su uso como moduladores alostéricos positivos de receptores mGluR2 |
EP2643320B1 (de) | 2010-11-08 | 2015-03-04 | Janssen Pharmaceuticals, Inc. | 1,2,4-triazolo[4,3-a]pyridinderivate und ihre verwendung als positiv allosterische modulatoren des mglur2 receptors |
CN103298809B (zh) | 2010-11-08 | 2016-08-31 | 杨森制药公司 | 1,2,4-三唑并[4,3-a]吡啶衍生物及其作为MGLUR2受体的正变构调节剂的用途 |
JO3368B1 (ar) | 2013-06-04 | 2019-03-13 | Janssen Pharmaceutica Nv | مركبات 6، 7- ثاني هيدرو بيرازولو [5،1-a] بيرازين- 4 (5 يد)- اون واستخدامها بصفة منظمات تفارغية سلبية لمستقبلات ميجلور 2 |
JO3367B1 (ar) | 2013-09-06 | 2019-03-13 | Janssen Pharmaceutica Nv | مركبات 2،1، 4- ثلاثي زولو [3،4-a] بيريدين واستخدامها بصفة منظمات تفارغية موجبة لمستقبلات ميجلور 2 |
CA2929763A1 (en) * | 2013-11-08 | 2015-05-14 | Bayer Pharma Aktiengesellschaft | Substituted uracils as chymase inhibitors |
KR20200036063A (ko) | 2014-01-21 | 2020-04-06 | 얀센 파마슈티카 엔.브이. | 대사 조절형 글루탐산 작동성 수용체 제2아형의 양성 알로스테릭 조절제 또는 오르토스테릭 작동제를 포함하는 조합 및 그 용도 |
EA202192128A1 (ru) | 2014-02-04 | 2022-02-28 | Янссен Фармацевтика Нв | Комбинации, содержащие положительные аллостерические модуляторы или ортостерические агонисты метаботропного глутаматергического рецептора 2 подтипа, и их применение |
WO2016039936A2 (en) * | 2014-09-09 | 2016-03-17 | Ptc Therapeutics, Inc. | Monocyclic substituted 2-pyridinone antibacterial compounds |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9207145D0 (en) * | 1991-04-18 | 1992-05-13 | Ici Plc | Heterocyclic amides |
GB9216272D0 (en) * | 1991-08-15 | 1992-09-09 | Ici Plc | Substituted heterocycles |
GB9307555D0 (en) * | 1992-04-16 | 1993-06-02 | Zeneca Ltd | Heterocyclic compounds |
US5486529A (en) * | 1992-04-16 | 1996-01-23 | Zeneca Limited | Certain pyridyl ketones for treating diseases involving leukocyte elastase |
US5441960A (en) * | 1992-04-16 | 1995-08-15 | Zeneca Limited | 1-pyrimidinylacetamide human leukocyte elastate inhibitors |
HU224731B1 (en) * | 1994-03-31 | 2006-01-30 | Vertex Pharma | Pyrimidinyl derivatives as interleukin inhibitors and pharmaceutical compositions containing them |
-
1996
- 1996-04-26 EP EP96912273A patent/EP0826671B1/de not_active Expired - Lifetime
- 1996-04-26 CA CA002219364A patent/CA2219364A1/en not_active Abandoned
- 1996-04-26 US US08/952,319 patent/US5948785A/en not_active Expired - Fee Related
- 1996-04-26 KR KR1019970707522A patent/KR100400639B1/ko not_active IP Right Cessation
- 1996-04-26 CN CN96194926A patent/CN1131210C/zh not_active Expired - Fee Related
- 1996-04-26 WO PCT/JP1996/001171 patent/WO1996033974A1/ja active IP Right Grant
- 1996-04-26 CN CNB001217976A patent/CN1188401C/zh not_active Expired - Fee Related
- 1996-04-26 DE DE69634122T patent/DE69634122D1/de not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
CN1188472A (zh) | 1998-07-22 |
CN1131210C (zh) | 2003-12-17 |
CN1188401C (zh) | 2005-02-09 |
WO1996033974A1 (fr) | 1996-10-31 |
EP0826671A4 (de) | 1998-09-02 |
EP0826671A1 (de) | 1998-03-04 |
US5948785A (en) | 1999-09-07 |
KR100400639B1 (ko) | 2003-12-31 |
CA2219364A1 (en) | 1996-10-31 |
KR19990007998A (ko) | 1999-01-25 |
EP0826671B1 (de) | 2004-12-29 |
CN1304931A (zh) | 2001-07-25 |
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