AR031809A1 - Quinolonas antimicrobianas, sus composiciones y usos - Google Patents
Quinolonas antimicrobianas, sus composiciones y usosInfo
- Publication number
- AR031809A1 AR031809A1 ARP010105794A ARP010105794A AR031809A1 AR 031809 A1 AR031809 A1 AR 031809A1 AR P010105794 A ARP010105794 A AR P010105794A AR P010105794 A ARP010105794 A AR P010105794A AR 031809 A1 AR031809 A1 AR 031809A1
- Authority
- AR
- Argentina
- Prior art keywords
- hydrogen
- compound
- joined
- fluoro
- hydroxy
- Prior art date
Links
- 230000000845 anti-microbial effect Effects 0.000 title 1
- 239000000203 mixture Substances 0.000 title 1
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 5
- 125000001153 fluoro group Chemical group F* 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- -1 quinolone compound Chemical class 0.000 abstract 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 abstract 1
- 241000124008 Mammalia Species 0.000 abstract 1
- 150000001336 alkenes Chemical class 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 125000002618 bicyclic heterocycle group Chemical group 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 1
- 150000003949 imides Chemical class 0.000 abstract 1
- 208000015181 infectious disease Diseases 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 230000000813 microbial effect Effects 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 230000003287 optical effect Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000000546 pharmaceutical excipient Substances 0.000 abstract 1
- 125000003386 piperidinyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
- A01N43/42—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings condensed with carbocyclic rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D455/00—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine
- C07D455/02—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing not further condensed quinolizine ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Environmental Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Un compuesto quinolona que tiene una estructura segun la formula (1) en donde: (A) A1 se selecciona de -N- y -C(R8)- donde R8 es como se define en la memoria; X se selecciona de -C- y -N-, donde (i) si X es -C-, a es un enlace doble y b un enlace individual, y (ii) si X es -N-, a es un enlace individual y b un enlace doble; e Y se selecciona de -N(R1)- y -C(R1)-; siempre Y es -N(R1)- solamente si X es -C- e Y es -C(R1)- solamente si X es -N-; R1 es como se define en la memoria; R2 es hidrogeno; R3 se selecciona de hidrogeno e hidroxi; R5 se selecciona de hidrogeno, hidroxi, amino, halo, alquilo C1-6, alqueno C1-6 y alcoxi C1-6; R6 se selecciona de fluoro y cloro; R7 es -Q-C(R11)(R11')(R11''), donde Q, R11, R11' y R11'', y R12 y R12' son como se definen en la memoria; R9 y R9' cada uno independientemente se selecciona de hidrogeno y alquilo C1-15, o R9 y R9' se unen para formar un anillo heterocíclico que contienen el átomo de nitrogeno al que están unidos; y R10 representa las mitades en el anillo de piperidina diferentes a R7 y -NR9R9', donde cada R10 independientemente se selecciona de hidrogeno, alquilo C1-6 y fluoro; (B) si A1 es -(R8)-, X es -C- e Y es -N(R1)-, entonces R8 y R1 se pueden unir para formar un anillo heterocíclico de 6 miembros, donde R2, R3, R5, R6, R7, R8, R9, R9' y R10 son como se describen en (A); o (C) si A1es -C(R8)-, X es -C- e Y es -N(R1)-, entonces R1 y R2 se pueden unir para formar un anillo heterocíclico monocíclico o bicíclico, donde R3, R5, R6, R7, R8, R9, R9' y R10 son como se describen en (A); o (D) si A1 es -C(R8)-, X es -C- e Y es -N(R1)-, entonces R3 y R2 se pueden unir para formar un heterocicloalquilo de 5 miembros que es sustituido con una mitad carbonilo, donde R1, R5, R6, R7, R8, R9, R9' y R10 son como de describen en (A); o un isomero optico, diasteromero o enantiomero de éstos; una sal farmacéuticamente aceptable, hidrato, o éster biohidrolizable, amida o imida de éstos. Compuestos segun las formulas (2) y (3). Un método de utilizar un compuesto que tiene una estructura segun la formula (4) en donde R13 se selecciona de metilo, fluoro e hidroxi; en un proceso de elaborar un compuesto que tiene una estructura segun la formula (1). Una composicion farmacéutica que comprende: (a) una cantidad segura y eficaz de dicho compuesto; y (b) un excipiente farmacéuticamente aceptable. El uso de dicho compuesto en la fabricacion de un medicamento para tratar una infeccion microbiana en un humano u otro mamífero.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25563400P | 2000-12-14 | 2000-12-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR031809A1 true AR031809A1 (es) | 2003-10-01 |
Family
ID=22969211
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP010105794A AR031809A1 (es) | 2000-12-14 | 2001-12-14 | Quinolonas antimicrobianas, sus composiciones y usos |
Country Status (18)
| Country | Link |
|---|---|
| US (2) | US6645981B2 (es) |
| EP (1) | EP1341781B1 (es) |
| JP (1) | JP2004515548A (es) |
| AR (1) | AR031809A1 (es) |
| AT (1) | ATE304539T1 (es) |
| AU (2) | AU2002230891B2 (es) |
| BR (1) | BR0116217A (es) |
| CA (1) | CA2429951A1 (es) |
| DE (1) | DE60113450T2 (es) |
| DK (1) | DK1341781T3 (es) |
| ES (1) | ES2249489T3 (es) |
| HU (1) | HUP0303410A3 (es) |
| IL (1) | IL155679A0 (es) |
| NO (1) | NO20032665L (es) |
| NZ (1) | NZ525571A (es) |
| PE (1) | PE20020592A1 (es) |
| PL (1) | PL363323A1 (es) |
| WO (1) | WO2002048138A1 (es) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4669607B2 (ja) | 1997-09-15 | 2011-04-13 | ザ プロクター アンド ギャンブル カンパニー | 抗微生物キノロン類、その組成物およびその使用 |
| US6900224B2 (en) | 2002-07-31 | 2005-05-31 | The Procter & Gamble Company | Antimicrobial quinolones, their compositions and uses |
| EP1610759A4 (en) * | 2003-04-07 | 2007-04-25 | Cylene Pharmaceuticals Inc | SUBSTITUTED QUINOBENZOXAZINE ANALOGUES |
| US7354916B2 (en) * | 2003-04-07 | 2008-04-08 | Cylene Pharmaceuticals | Substituted quinobenzoxazine analogs |
| US7507727B2 (en) * | 2003-04-07 | 2009-03-24 | Cylene Pharmaceuticals, Inc. | Substituted quinobenzoxazine analogs and methods of using thereof |
| US7163948B2 (en) * | 2003-04-07 | 2007-01-16 | Cylene Pharmaceuticals, Inc. | Heterocyclic substituted 1,4-dihydri-4ox9-1,8-naphthyridine analogs |
| US7652134B2 (en) * | 2004-09-17 | 2010-01-26 | Cylene Pharmaceuticals, Inc. | Methods for converting quinolone esters into quinolone amides |
| KR100989029B1 (ko) * | 2004-09-17 | 2010-10-25 | 사일린 파마슈티칼스, 인크 | 세포 증식 억제제로서의 퀴놀론 동족체 |
| US20060100215A1 (en) * | 2004-11-11 | 2006-05-11 | Bradbury Barton J | 8A,9-dihydro-4aH-isothiazolo[5,4-b]quinoline-3,4-diones and related compounds as anti-infective agents |
| WO2006113509A2 (en) * | 2005-04-15 | 2006-10-26 | Cylene Pharmaceuticals, Inc. | Quinobenzoxazine analogs and methods of using thereof |
| NZ566209A (en) | 2005-07-27 | 2011-03-31 | Achillion Pharmaceuticals Inc | 8-methoxy-9H-isothiazolo[5,4-b]quinoline-3,4-diones and related compounds as anti-infective agents |
| US7456279B2 (en) | 2006-03-28 | 2008-11-25 | The Procter & Gamble Company | Coupling process for preparing quinolone intermediates |
| HRP20110558T1 (hr) | 2006-03-28 | 2011-09-30 | Warner Chilcott Company | Malatne soli i polimorfi od (3s, 5s)-7-[3-amino-5-metil-piperidinil]-1-ciklopropil-1, 4-dihidro-8-metoksi-4-okso-3-kinolinkarboksilne kiseline |
| WO2008071405A1 (en) | 2006-12-14 | 2008-06-19 | Syngenta Participations Ag | 4-phenyl-pyrane-3,5-diones, 4-phenyl-thiopyrane-3,5-diones and cyclohexanetriones as novel herbicides |
| US7902227B2 (en) | 2007-07-27 | 2011-03-08 | Janssen Pharmaceutica Nv. | C-7 isoxazolinyl quinolone / naphthyridine derivatives useful as antibacterial agents |
| FR2928150A1 (fr) * | 2008-02-29 | 2009-09-04 | Vetoquinol Sa Sa | Nouveaux derives 7-substitues de 3-carboxy-oxadiazino-quinolones, leur preparation et leur application comme anti-bacteriens |
| FR2936798B1 (fr) * | 2008-10-03 | 2012-09-28 | Novexel | Nouveaux composes heterocycliques azotes, leur preparation et leur utilisation comme medicaments antibacteriens. |
| FR2937034B1 (fr) * | 2008-10-10 | 2012-11-23 | Novexel | Nouveaux composes heterocycliques azotes, leur preparation et leur utilisation comme medicaments antibacteriens |
| FR2936951B1 (fr) * | 2008-10-10 | 2010-12-03 | Novexel | Nouvelles combinaisons de composes heterocycliques azotes antibacteriens avec d'autres composes antibacteriens et leur utilisation comme medicaments |
| MX2011010434A (es) | 2009-04-03 | 2012-01-20 | Achillion Pharmaceuticals Inc | Hidroxitienoquinolonas y compuestos relacionados como agentes antiinfecciosos. |
| WO2011031745A1 (en) | 2009-09-09 | 2011-03-17 | Achaogen, Inc. | Antibacterial fluoroquinolone analogs |
| CA2777739A1 (en) | 2009-10-16 | 2011-04-21 | Rib-X Pharmaceuticals, Inc. | Antimicrobial compounds and methods of making and using the same |
| CN102725274A (zh) | 2009-10-16 | 2012-10-10 | Rib-X制药公司 | 抗微生物化合物和其制备和使用方法 |
| TW201125566A (en) * | 2009-10-16 | 2011-08-01 | Rib X Pharmaceuticals Inc | Antimicrobial compounds and methods of making and using the same |
| CN102617568B (zh) * | 2012-03-06 | 2014-06-25 | 天津市汉康医药生物技术有限公司 | 一种稳定的盐酸莫西沙星化合物、其制备方法 |
| CN103360409B (zh) * | 2012-04-06 | 2016-02-10 | 天方药业有限公司 | 氧氟羧酸制备方法 |
| EP3038623A4 (en) | 2013-09-09 | 2017-04-19 | Melinta Therapeutics, Inc. | Antimicrobial compounds and methods of making and using the same |
| CA2923214A1 (en) | 2013-09-09 | 2015-03-12 | Melinta Therapeutics, Inc. | Antimicrobial compounds and methods of making and using the same |
| CN105732660B (zh) * | 2014-12-10 | 2017-11-21 | 浙江京新药业股份有限公司 | 左氧氟沙星中间体的制备方法 |
| JP2018507881A (ja) | 2015-03-11 | 2018-03-22 | メリンタ セラピューティクス,インコーポレイテッド | 抗微生物化合物ならびにこれらを作製および使用する方法 |
| EP3452479A1 (en) | 2016-05-06 | 2019-03-13 | Melinta Therapeutics, Inc. | Antimicrobials and methods of making and using same |
| CN108440562A (zh) * | 2018-05-08 | 2018-08-24 | 邳州易萨新型材料有限公司 | 一种左氟沙星药物中间体的合成方法 |
| CN111253241B (zh) * | 2018-11-30 | 2022-11-04 | 浙江新和成股份有限公司 | 一种2,4,5-三氟-3-甲氧基苯甲酰氯及其中间体的制备方法 |
| CN110878047A (zh) * | 2019-12-09 | 2020-03-13 | 怀化学院 | 加替沙星羧酸及其合成方法 |
| CN119569650A (zh) * | 2024-12-05 | 2025-03-07 | 凯美克(上海)医药科技有限公司 | 一种7-溴-2-氯喹啉-4-醇的合成方法 |
Family Cites Families (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0717608B2 (ja) | 1986-04-25 | 1995-03-01 | 杏林製薬株式会社 | 6−アルコキシキノロンカルボン酸誘導体 |
| DE3704907A1 (de) | 1987-02-17 | 1988-08-25 | Bayer Ag | Topisch anwendbare zubereitungen von gyrase-inhibitoren in kombination mit kortikosteroiden |
| US4921857A (en) | 1987-09-18 | 1990-05-01 | Merck & Co., Inc. | 4-Oxo-4h-quinolizine-3-carboxylic acids and derivatives thereof |
| US5328908A (en) | 1988-10-24 | 1994-07-12 | Procter & Gamble Pharmaceuticals, Inc. | Antimicrobial quinolone thioureas |
| HU219403B (hu) | 1989-08-16 | 2001-04-28 | Pfizer Inc. | Azabiciklo-csoporttal helyettesített kinolon- és naftiridon-karbonsavak és eljárás ezek előállítására |
| US5164402A (en) | 1989-08-16 | 1992-11-17 | Pfizer Inc | Azabicyclo quinolone and naphthyridinone carboxylic acids |
| JPH03115277A (ja) | 1989-09-28 | 1991-05-16 | Banyu Pharmaceut Co Ltd | ピリドンカルボン酸誘導体 |
| US5580872A (en) | 1990-05-02 | 1996-12-03 | Abbott Laboratories | Quinolizinone type compounds |
| EP0527889B1 (en) | 1990-05-02 | 2000-08-02 | Abbott Laboratories | Quinolizinone type compounds |
| US5726182A (en) | 1990-05-02 | 1998-03-10 | Abbott Laboratories | Quinolizinone type compounds |
| US5072001A (en) | 1990-11-30 | 1991-12-10 | Warner-Lambert Company | Certain optically active substituted 3-pyrraidine acetic acid derivatives useful as intermediates |
| US5412098A (en) | 1991-12-27 | 1995-05-02 | Wakunaga Seiyaku Kabushiki Kaisha | Quinolone derivative or salt thereof and antibacterial containing the same |
| JPH05112554A (ja) * | 1992-02-19 | 1993-05-07 | Chugai Pharmaceut Co Ltd | 新規なキノロンカルボン酸誘導体 |
| NO304832B1 (no) | 1992-05-27 | 1999-02-22 | Ube Industries | Aminokinolonderivater samt middel mot HIV |
| DE4230804A1 (de) | 1992-09-15 | 1994-03-17 | Bayer Ag | 7-Isoindolinyl-chinolon- und -naphthyridon-Derivate |
| DE4301246A1 (de) | 1993-01-19 | 1994-07-21 | Bayer Ag | Chinolon- und Naphthyridoncarbonsäurederivate |
| ATE217309T1 (de) | 1993-10-14 | 2002-05-15 | Abbott Lab | Verbindungen des chinolizinon-typs |
| AU692583B2 (en) | 1994-08-12 | 1998-06-11 | Toyama Chemical Co. Ltd. | Novel quinolone- or naphthyridonecarboxylic acid derivative or salt thereof |
| JPH092953A (ja) * | 1995-06-16 | 1997-01-07 | Chugai Pharmaceut Co Ltd | バルフロキサシン製剤 |
| JP3833738B2 (ja) | 1995-11-15 | 2006-10-18 | 第一製薬株式会社 | 置換アミノメチルピロリジン誘導体 |
| US6384050B1 (en) | 1996-10-25 | 2002-05-07 | Daiichi Pharmaceutical Co., Ltd. | Tricyclic amine derivatives |
| JPH10287669A (ja) | 1997-04-10 | 1998-10-27 | Dai Ichi Seiyaku Co Ltd | 置換アミノメチルピロリジン誘導体 |
| DE69829682T2 (de) | 1997-05-21 | 2006-03-09 | Daiichi Pharmaceutical Co., Ltd. | Cis-disubstituierte aminocycloalkyl-pyrrolidin-derivate |
| ZA984527B (en) | 1997-05-30 | 1998-12-03 | Daiichi Seiyaku Co | Substituted cyclobutylamine derivative |
| KR100241673B1 (ko) | 1997-08-09 | 2000-03-02 | 김충섭 | 퀴놀리진 카르복실산 유도체 |
| JP4669607B2 (ja) * | 1997-09-15 | 2011-04-13 | ザ プロクター アンド ギャンブル カンパニー | 抗微生物キノロン類、その組成物およびその使用 |
-
2001
- 2001-12-07 AU AU2002230891A patent/AU2002230891B2/en not_active Ceased
- 2001-12-07 CA CA002429951A patent/CA2429951A1/en not_active Abandoned
- 2001-12-07 EP EP01991148A patent/EP1341781B1/en not_active Expired - Lifetime
- 2001-12-07 IL IL15567901A patent/IL155679A0/xx unknown
- 2001-12-07 BR BR0116217-9A patent/BR0116217A/pt not_active IP Right Cessation
- 2001-12-07 DE DE60113450T patent/DE60113450T2/de not_active Expired - Fee Related
- 2001-12-07 JP JP2002549669A patent/JP2004515548A/ja not_active Withdrawn
- 2001-12-07 NZ NZ525571A patent/NZ525571A/en unknown
- 2001-12-07 AT AT01991148T patent/ATE304539T1/de not_active IP Right Cessation
- 2001-12-07 HU HU0303410A patent/HUP0303410A3/hu unknown
- 2001-12-07 PL PL01363323A patent/PL363323A1/xx not_active Application Discontinuation
- 2001-12-07 WO PCT/US2001/048532 patent/WO2002048138A1/en not_active Ceased
- 2001-12-07 ES ES01991148T patent/ES2249489T3/es not_active Expired - Lifetime
- 2001-12-07 AU AU3089102A patent/AU3089102A/xx active Pending
- 2001-12-07 DK DK01991148T patent/DK1341781T3/da active
- 2001-12-13 PE PE2001001250A patent/PE20020592A1/es not_active Application Discontinuation
- 2001-12-14 AR ARP010105794A patent/AR031809A1/es unknown
- 2001-12-14 US US10/017,969 patent/US6645981B2/en not_active Expired - Fee Related
-
2003
- 2003-06-12 NO NO20032665A patent/NO20032665L/no not_active Application Discontinuation
- 2003-07-30 US US10/630,998 patent/US20040029882A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| EP1341781A1 (en) | 2003-09-10 |
| HUP0303410A2 (hu) | 2004-01-28 |
| ES2249489T3 (es) | 2006-04-01 |
| CA2429951A1 (en) | 2002-06-20 |
| HUP0303410A3 (en) | 2005-12-28 |
| NO20032665L (no) | 2003-08-07 |
| US20030008894A1 (en) | 2003-01-09 |
| NZ525571A (en) | 2004-09-24 |
| US20040029882A1 (en) | 2004-02-12 |
| WO2002048138A1 (en) | 2002-06-20 |
| IL155679A0 (en) | 2003-11-23 |
| AU3089102A (en) | 2002-06-24 |
| EP1341781B1 (en) | 2005-09-14 |
| BR0116217A (pt) | 2003-12-30 |
| ATE304539T1 (de) | 2005-09-15 |
| PL363323A1 (en) | 2004-11-15 |
| DK1341781T3 (da) | 2005-12-05 |
| PE20020592A1 (es) | 2002-08-14 |
| JP2004515548A (ja) | 2004-05-27 |
| AU2002230891B2 (en) | 2005-04-07 |
| US6645981B2 (en) | 2003-11-11 |
| NO20032665D0 (no) | 2003-06-12 |
| DE60113450D1 (de) | 2005-10-20 |
| DE60113450T2 (de) | 2006-07-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR031809A1 (es) | Quinolonas antimicrobianas, sus composiciones y usos | |
| PE20220931A1 (es) | Inhibidores de shp2 fosfatasa de tipo pirazolo[3,4-b]pirazina | |
| PE20250021A1 (es) | Cicloalquil 3-oxopiperazin carboxamidas y cicloheteroalquil 3-oxopiperazin carboxamidas como inhibidores de nav1.8 | |
| AR102722A2 (es) | Un derivado de pirazolo-quinazolina, su uso, un procedimiento para prepararlos, composiciones farmacéuticas que los comprenden, compuestos utilizables en su preparación, una biblioteca de dos o más compuestos, y un producto o kit | |
| NO962811D0 (no) | Nye heterosykliske forbindelser | |
| AR030186A1 (es) | Compuesto antibacteriano 3-aminoquinazolina-2,4-diona, composicion farmaceutica que lo comprende y su uso para fabricarla | |
| AR028619A1 (es) | Un compuesto inhibidor de caspasas | |
| AR041303A1 (es) | Compuestos de piperidinil-imidazopiridina n-sustituidos como moduladores del receptor 5-ht4" | |
| AR061838A1 (es) | Moduladores de propiedades farmacocineticas de terapeuticos | |
| PE20090276A1 (es) | Compuestos derivados de imidazoquinolina como moduladores de tlr7 | |
| PE20030062A1 (es) | Derivados aralquilsulfonil-3-(pirrol-2-ilmetiliden)-2-indolinona como inhibidores de quinasas | |
| CY1112603T1 (el) | Μυκητοκτονος συνθεση η οποια περιεχει ενα παραγωγο οξινου αμιδιου | |
| AR046711A1 (es) | 5-7-diaminopirazolo[4,3d]pirimidinas como inhibidores de la pde-5,composiciones farmaceuticas que las contienen y usos en el tratamiento de hipertensiones | |
| AR016429A1 (es) | Compuesto derivado de acido hidroxamico como inhibidores de metaloproteasa de matriz (mmp), composiciones farmaceuticas y formulaciones veterinarias, usopara la preparacion de composiciones y formulaciones, compuesto intermediario, procedimiento de preparacion del compuesto. | |
| KR960014121A (ko) | 아로일-피페리딘 유도체 | |
| AR033306A1 (es) | Compuestos | |
| HUP0202787A2 (hu) | 5-HT1B antagonista piperazinszármazékok, eljárás az előállításukra és ezeket tartalmazó gyógyszerkészítmények | |
| AR066103A1 (es) | Derivados de triazolopiridin - carboxamidas, su preparacion y su aplicacion en terapeutica | |
| AR055303A1 (es) | Derivados de triazol sustituidos como antagonistas de oxitocina, composicion farmaceutica y uso del compuesto para preparar un medicamento | |
| PA8495101A1 (es) | Derivados de 13-metileritromicina | |
| SE9703377D0 (sv) | New compounds | |
| PE20220704A1 (es) | Derivados de 3,6-diamino-piridazin-3-ilo, composiciones farmaceuticas que los contienen y sus usos como agentes proapoptoticos | |
| AR029742A1 (es) | Derivados de eter propargilico, proceso para su preparacion, composicion para controlar y proteger contra microorganismos fitopatogenos, uso de dichos derivados para la proteccion de plantas contra la infestacion por microorganismos fitopatogenos, y metodo para controlar y prevenir una infestacion d | |
| BG94282A (bg) | 2,9-дизаместени-4н-пиридо/1,2,-а/пиримидин-4-они | |
| NO20091486L (no) | Nye imidazolonderivater, deres fremstilling som medikamenter, farmasoytiske preparater og anvendelse derav som proteinkinaseinhibitorer, saerlig CDC7 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |