NO923695L - Leukotrien-biosyntese-inhibitorer - Google Patents
Leukotrien-biosyntese-inhibitorerInfo
- Publication number
- NO923695L NO923695L NO92923695A NO923695A NO923695L NO 923695 L NO923695 L NO 923695L NO 92923695 A NO92923695 A NO 92923695A NO 923695 A NO923695 A NO 923695A NO 923695 L NO923695 L NO 923695L
- Authority
- NO
- Norway
- Prior art keywords
- biosynthesis inhibitors
- leukotriene biosynthesis
- leukotriene
- oxazolopyridines
- thiazolopyridines
- Prior art date
Links
- 230000015572 biosynthetic process Effects 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 150000002617 leukotrienes Chemical class 0.000 title abstract 2
- 150000000183 1,3-benzoxazoles Chemical class 0.000 abstract 1
- 241001465754 Metazoa Species 0.000 abstract 1
- BFPLMTPHDFFMTG-UHFFFAOYSA-N [1,3]oxazolo[5,4-b]pyridine Chemical class C1=CN=C2OC=NC2=C1 BFPLMTPHDFFMTG-UHFFFAOYSA-N 0.000 abstract 1
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 230000003389 potentiating effect Effects 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/28—Radicals substituted by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
- C07D263/58—Benzoxazoles; Hydrogenated benzoxazoles 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 in position 2
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/16—Otologicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles 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 in position 2
- C07D277/82—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US76459191A | 1991-09-24 | 1991-09-24 | |
| US07/937,315 US5296486A (en) | 1991-09-24 | 1992-09-04 | Leukotriene biosynthesis inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO923695D0 NO923695D0 (no) | 1992-09-23 |
| NO923695L true NO923695L (no) | 1993-03-25 |
Family
ID=27117489
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO92923695A NO923695L (no) | 1991-09-24 | 1992-09-23 | Leukotrien-biosyntese-inhibitorer |
Country Status (19)
| Country | Link |
|---|---|
| US (2) | US5296486A (cs) |
| EP (1) | EP0535521A3 (cs) |
| JP (1) | JPH05213911A (cs) |
| KR (1) | KR930005992A (cs) |
| AU (1) | AU661034B2 (cs) |
| CA (1) | CA2078810A1 (cs) |
| CZ (1) | CZ293392A3 (cs) |
| FI (1) | FI924277A7 (cs) |
| HU (2) | HU213113B (cs) |
| IL (1) | IL103251A (cs) |
| LV (1) | LV11181B (cs) |
| MX (1) | MX9205432A (cs) |
| NO (1) | NO923695L (cs) |
| NZ (1) | NZ244429A (cs) |
| PL (1) | PL296038A1 (cs) |
| RU (1) | RU2080321C1 (cs) |
| SG (1) | SG46381A1 (cs) |
| SK (1) | SK293392A3 (cs) |
| TW (1) | TW218877B (cs) |
Families Citing this family (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5698550A (en) * | 1993-06-14 | 1997-12-16 | Pfizer Inc. | Tetralin and chroman derivatives useful in the treatment of asthma, arthritis and related diseases |
| CO4520280A1 (es) * | 1993-10-26 | 1997-10-15 | Boehringer Ingelheim Pharma | Derivados de pirrolidina, inhibidores de la bioscientesis de leucotrienos |
| DE4428531A1 (de) | 1994-08-12 | 1996-02-15 | Boehringer Ingelheim Kg | Neue enantiomerenreine Pyridylcycloalkylethylamine und deren Salze sowie Verfahren zu ihrer Herstellung |
| US5616717A (en) * | 1995-04-20 | 1997-04-01 | Boehringer Ingelheim Pharmaceuticals, Inc. | Process for the preparation of pure enantiomers of 1-(2-pyridyl)-2-cyclohexylethylamine |
| US5856497A (en) * | 1995-12-11 | 1999-01-05 | Boehringer Ingelheim Pharmaceuticals, Inc. | Asymmetric synthesis of α-cycloalkylalkyl substituted methanamines |
| CN1290165A (zh) | 1997-11-10 | 2001-04-04 | 布里斯托尔-迈尔斯斯奎布公司 | 苯并噻唑蛋白酪氨酸激酶抑制剂 |
| US5952326A (en) * | 1997-12-10 | 1999-09-14 | Pfizer Inc. | Tetralin and chroman derivatives useful in the treatment of asthma, arthritis and related diseases |
| US6329372B1 (en) | 1998-01-27 | 2001-12-11 | Celltech Therapeutics Limited | Phenylalanine derivatives |
| JP2002504534A (ja) | 1998-02-26 | 2002-02-12 | セルテック・セラピューティクス・リミテッド | α４インテグリンの阻害剤としてのフェニルアラニン誘導体 |
| GB9805655D0 (en) | 1998-03-16 | 1998-05-13 | Celltech Therapeutics Ltd | Chemical compounds |
| US6521626B1 (en) | 1998-03-24 | 2003-02-18 | Celltech R&D Limited | Thiocarboxamide derivatives |
| GB9811159D0 (en) | 1998-05-22 | 1998-07-22 | Celltech Therapeutics Ltd | Chemical compounds |
| GB9811969D0 (en) | 1998-06-03 | 1998-07-29 | Celltech Therapeutics Ltd | Chemical compounds |
| GB9812088D0 (en) | 1998-06-05 | 1998-08-05 | Celltech Therapeutics Ltd | Chemical compounds |
| GB9814414D0 (en) | 1998-07-03 | 1998-09-02 | Celltech Therapeutics Ltd | Chemical compounds |
| GB9821061D0 (en) | 1998-09-28 | 1998-11-18 | Celltech Therapeutics Ltd | Chemical compounds |
| GB9821222D0 (en) | 1998-09-30 | 1998-11-25 | Celltech Therapeutics Ltd | Chemical compounds |
| GB9825652D0 (en) | 1998-11-23 | 1999-01-13 | Celltech Therapeutics Ltd | Chemical compounds |
| GB9826174D0 (en) | 1998-11-30 | 1999-01-20 | Celltech Therapeutics Ltd | Chemical compounds |
| US6800486B1 (en) | 1998-12-07 | 2004-10-05 | Smithkline Beecham Corporation | Method for quantitative determination of amino acids |
| WO2000034251A1 (en) * | 1998-12-07 | 2000-06-15 | Smithkline Beecham Corporation | A method for quantitative determination of amino acids |
| JP4754693B2 (ja) | 1999-01-22 | 2011-08-24 | エラン ファーマシューティカルズ，インコーポレイテッド | Ｖｌａ−４関連障害を処置するアシル誘導体 |
| US6545003B1 (en) * | 1999-01-22 | 2003-04-08 | Elan Pharmaceuticals, Inc. | Fused ring heteroaryl and heterocyclic compounds which inhibit leukocyte adhesion mediated by VLA-4 |
| US6436904B1 (en) | 1999-01-25 | 2002-08-20 | Elan Pharmaceuticals, Inc. | Compounds which inhibit leukocyte adhesion mediated by VLA-4 |
| AU3487500A (en) * | 1999-02-08 | 2000-08-25 | Lion Bioscience Ag | Thiazole derivatives and combinatorial libraries thereof |
| US6518283B1 (en) | 1999-05-28 | 2003-02-11 | Celltech R&D Limited | Squaric acid derivatives |
| US6534513B1 (en) | 1999-09-29 | 2003-03-18 | Celltech R&D Limited | Phenylalkanoic acid derivatives |
| US6436977B1 (en) | 1999-09-29 | 2002-08-20 | Pfizer Inc. | Dosing regimens for lasofoxifene |
| US6455539B2 (en) | 1999-12-23 | 2002-09-24 | Celltech R&D Limited | Squaric acid derivates |
| ES2295150T3 (es) | 2000-04-17 | 2008-04-16 | Ucb Pharma, S.A. | Derivados de enamina como moleculas de adhesion celular. |
| FR2808798A1 (fr) * | 2000-05-09 | 2001-11-16 | Hoechst Marion Roussel Inc | Nouveaux derives antagonistes du recepteur de la vitronectine |
| US6545013B2 (en) | 2000-05-30 | 2003-04-08 | Celltech R&D Limited | 2,7-naphthyridine derivatives |
| US6403608B1 (en) | 2000-05-30 | 2002-06-11 | Celltech R&D, Ltd. | 3-Substituted isoquinolin-1-yl derivatives |
| AU2001267753A1 (en) | 2000-07-07 | 2002-01-21 | Celltech R And D Limited | Squaric acid derivatives containing a bicyclic heteroaromatic ring as integrin antagonists |
| CA2417059A1 (en) | 2000-08-02 | 2002-02-07 | Celltech R&D Limited | 3-substituted isoquinolin-1-yl derivatives |
| EP1341769B1 (en) | 2000-12-15 | 2007-10-17 | Vertex Pharmaceuticals Incorporated | Bacterial gyrase inhibitors and uses thereof |
| TWI281470B (en) | 2002-05-24 | 2007-05-21 | Elan Pharm Inc | Heterocyclic compounds which inhibit leukocyte adhesion mediated by alpha4 integrins |
| TW200307671A (en) | 2002-05-24 | 2003-12-16 | Elan Pharm Inc | Heteroaryl compounds which inhibit leukocyte adhesion mediated by α 4 integrins |
| SE0202429D0 (sv) * | 2002-08-14 | 2002-08-14 | Astrazeneca Ab | Novel Compounds |
| CN100406446C (zh) * | 2003-01-13 | 2008-07-30 | 弗·哈夫曼-拉罗切有限公司 | 苯并唑衍生物及其作为腺苷受体配体的用途 |
| PL371841A1 (pl) * | 2004-12-20 | 2006-06-26 | ADAMED Sp.z o.o. | Nowe związki pochodne kwasu 3-fenylopropionowego |
| PL372332A1 (pl) * | 2005-01-19 | 2006-07-24 | ADAMED Sp.z o.o. | Nowe związki, pochodne kwasu 3-fenylopropionowego |
| PL372356A1 (pl) * | 2005-01-20 | 2006-07-24 | ADAMED Sp.z o.o. | Nowe związki, pochodne kwasu 3-fenylopropionowego |
| CA2624450C (en) | 2005-09-29 | 2014-02-04 | Elan Pharmaceuticals, Inc. | Pyrimidinyl amide compounds which inhibit leukocyte adhesion mediated by vla-4 |
| EP1940827B1 (en) | 2005-09-29 | 2011-03-16 | Elan Pharmaceuticals Inc. | Carbamate compounds which inhibit leukocyte adhesion mediated by vla-4 |
| WO2007101165A1 (en) | 2006-02-27 | 2007-09-07 | Elan Pharmaceuticals, Inc. | Pyrimidinyl sulfonamide compounds which inhibit leukocyte adhesion mediated by vla-4 |
| DE102006021878A1 (de) * | 2006-05-11 | 2007-11-15 | Sanofi-Aventis | Phenylamino-benzoxazol substituierte Carbonsäuren, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| TW200811166A (en) * | 2006-06-30 | 2008-03-01 | Basf Ag | Substituted 1-(azolin-2-yl)-amino-2-aryl-1-hetaryl-ethane compounds |
| US20090258907A1 (en) * | 2008-04-09 | 2009-10-15 | Abbott Laboratories | Compounds useful as inhibitors of rock kinases |
| RS53081B (sr) * | 2008-04-11 | 2014-06-30 | Janssen Pharmaceutica N.V. | Thiazolopiridin-2-iloksi-fenil i amini thiazolopiridin-2-iloksi fenila kao modulatori leukotrien a4 hidrolaze |
| US8969577B2 (en) | 2008-11-24 | 2015-03-03 | Basf Se | Curable composition comprising a thermolatent base |
| CN102459179A (zh) | 2009-04-27 | 2012-05-16 | 艾伦药物公司 | α-4整联蛋白的吡啶酮拮抗剂 |
| UY35592A (es) * | 2013-06-03 | 2014-12-31 | Bayer Pharma AG | Benzoxazoles sustituidos |
| CA2913958A1 (en) | 2013-06-03 | 2014-12-11 | Bayer Pharma Aktiengesellschaft | Substituted benzoxazoles |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3419994A1 (de) * | 1984-05-29 | 1985-12-05 | Hoechst Ag, 6230 Frankfurt | Benzoxazolyl- und benzthiazolyl-aminosaeuren, ihre herstellung und verwendung im pflanzenschutz |
| DE3533331A1 (de) * | 1985-09-18 | 1987-03-26 | Heumann Ludwig & Co Gmbh | Pyridothiazolderivate, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel |
| US4873346A (en) * | 1985-09-20 | 1989-10-10 | The Upjohn Company | Substituted benzothiazoles, benzimidazoles, and benzoxazoles |
| FI91859C (fi) * | 1987-06-17 | 1994-08-25 | Eisai Co Ltd | Analogiamenetelmä antiallergisena aineena aktiivisen bentsotiatsolijohdannaisen valmistamiseksi |
| AU653349B2 (en) * | 1990-07-24 | 1994-09-29 | Agilent Technologies Australia (M) Pty Ltd | Inductively coupled plasma spectroscopy |
| IE920921A1 (en) * | 1991-04-04 | 1992-10-07 | Eisai Co Ltd | Benzothiazole derivative |
-
1992
- 1992-09-04 US US07/937,315 patent/US5296486A/en not_active Expired - Lifetime
- 1992-09-22 CA CA002078810A patent/CA2078810A1/en not_active Abandoned
- 1992-09-23 EP EP19920116249 patent/EP0535521A3/en not_active Withdrawn
- 1992-09-23 NO NO92923695A patent/NO923695L/no unknown
- 1992-09-23 RU SU925052823A patent/RU2080321C1/ru active
- 1992-09-23 AU AU25274/92A patent/AU661034B2/en not_active Ceased
- 1992-09-23 IL IL10325192A patent/IL103251A/en not_active IP Right Cessation
- 1992-09-23 SG SG1996003973A patent/SG46381A1/en unknown
- 1992-09-23 HU HU9203033A patent/HU213113B/hu not_active IP Right Cessation
- 1992-09-23 NZ NZ244429A patent/NZ244429A/en unknown
- 1992-09-24 PL PL29603892A patent/PL296038A1/xx unknown
- 1992-09-24 FI FI924277A patent/FI924277A7/fi not_active Application Discontinuation
- 1992-09-24 JP JP4255123A patent/JPH05213911A/ja active Pending
- 1992-09-24 KR KR1019920017495A patent/KR930005992A/ko not_active Ceased
- 1992-09-24 TW TW081107568A patent/TW218877B/zh active
- 1992-09-24 SK SK2933-92A patent/SK293392A3/sk unknown
- 1992-09-24 LV LVP-92-133A patent/LV11181B/en unknown
- 1992-09-24 MX MX9205432A patent/MX9205432A/es unknown
- 1992-09-24 CZ CS922933A patent/CZ293392A3/cs unknown
-
1995
- 1995-04-06 US US08/417,547 patent/US5552421A/en not_active Expired - Fee Related
- 1995-04-12 HU HU95P/P00102P patent/HU210881A9/hu unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US5296486A (en) | 1994-03-22 |
| LV11181A (lv) | 1996-04-20 |
| EP0535521A2 (en) | 1993-04-07 |
| SG46381A1 (en) | 1998-02-20 |
| EP0535521A3 (en) | 1993-06-16 |
| AU2527492A (en) | 1993-03-25 |
| CA2078810A1 (en) | 1993-03-25 |
| HUT64951A (en) | 1994-03-28 |
| US5552421A (en) | 1996-09-03 |
| IL103251A (en) | 1996-09-12 |
| NZ244429A (en) | 1995-07-26 |
| CZ293392A3 (en) | 1993-12-15 |
| PL296038A1 (en) | 1993-10-18 |
| HU213113B (en) | 1997-02-28 |
| FI924277L (fi) | 1993-03-25 |
| LV11181B (en) | 1996-08-20 |
| FI924277A0 (fi) | 1992-09-24 |
| AU661034B2 (en) | 1995-07-13 |
| KR930005992A (ko) | 1993-04-20 |
| NO923695D0 (no) | 1992-09-23 |
| MX9205432A (es) | 1993-03-31 |
| FI924277A7 (fi) | 1993-03-25 |
| HU9203033D0 (en) | 1992-12-28 |
| SK293392A3 (en) | 1995-09-13 |
| HU210881A9 (en) | 1995-09-28 |
| RU2080321C1 (ru) | 1997-05-27 |
| TW218877B (cs) | 1994-01-11 |
| JPH05213911A (ja) | 1993-08-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO923695L (no) | Leukotrien-biosyntese-inhibitorer | |
| NO20010628L (no) | Substituerte oksazol- og thiazolderivater som hPPAR <gamma> og hPPAR <alfa> aktivatorer | |
| TR199700844T1 (xx) | Pirazolil-Benzoil T�revleri. | |
| NZ233735A (en) | Heterocyclic substituted aminophenol derivatives | |
| DE69325454D1 (de) | Taxol-derivate | |
| ATE216360T1 (de) | Sulfinsäurederivate und deren herstellung und verwendung | |
| TW325458B (en) | Stilbene derivatives and pharmaceutical compositions comprising the same for anti-cancer | |
| YU49312B (sh) | Kristalni hidratni derivati 3,4,4-trisupstituisanih - peperidinil-n-alkilkarboksilata, njihovi intermedijari i postupak za dobijanje | |
| ATE269290T1 (de) | Benzoylderivate | |
| ATE47845T1 (de) | Guanidin-derivate. | |
| DK0977741T3 (da) | Substituerede phenylderivater, deres fremstilling og anvendelse | |
| YU68792A (sh) | Postupak za dobivanje derivata bakatina iii i 10-dezacetil-bakatina iii | |
| MX9301783A (es) | Derivados de 1-[2-arilsulfonilamino)-etil-1-oxo]-piperidina, su preparacion y su aplicacion en terapeutica. | |
| DK537389D0 (da) | Glycosidase-inhibitoren salbostatin, dens fremstilling og anvendelse | |
| DE69314942D1 (de) | N-acylglutamin-derivate | |
| TR199700206A2 (xx) | Floralkil- ve floralkoksi ikame edilmi� heterosiklik bradikinin-antagonistleri, bunlar�n imal edilmesine mahsus usul ve bunlar�n kullan�lmalar�. | |
| YU78092A (sh) | Postupak za dobijanje derivata beta-fenilizoserina i njihova primena | |
| NO971142L (no) | Bis-(2-halogenetyl)aminofenylsubstituerte distamycinderivater som antitumor- og antivirale midler | |
| RU95106653A (ru) | Производные 2-имидазолин-5-онов и 2-имидазолин-5-тионов и фунгицидные композиции на их основе | |
| DK0490816T3 (da) | Fluorforbindelser som aromatase-inhibitorer. | |
| FI923679A0 (fi) | Ny b-fenylisoserinderivat, dess framstaellning och anvaendning. | |
| TR200100133T2 (tr) | FKBP İnhibitörleri | |
| TR199701298T1 (xx) | Tetralinler. | |
| NO942668L (no) | Alkylderivater av trazodon med CNS-aktivitet | |
| NO179755C (no) | Fremgangsmåte for fremstilling av deoksymulundocandin |