JP2008502689A - 抗菌剤 - Google Patents
抗菌剤 Download PDFInfo
- Publication number
- JP2008502689A JP2008502689A JP2007516640A JP2007516640A JP2008502689A JP 2008502689 A JP2008502689 A JP 2008502689A JP 2007516640 A JP2007516640 A JP 2007516640A JP 2007516640 A JP2007516640 A JP 2007516640A JP 2008502689 A JP2008502689 A JP 2008502689A
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- methyloxy
- ethyl
- pyrrolidinyl
- fluoro
- 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.)
- Pending
Links
- 0 COc1ccc2ncc(F)c(CCN3C[C@](CN*)C(*)C3)c2n1 Chemical compound COc1ccc2ncc(F)c(CCN3C[C@](CN*)C(*)C3)c2n1 0.000 description 5
- VBFYXYSBQYVMQX-UQPPLGOBSA-N CC(C)(C)OC(N(C[C@@H]1CNC(OCc2ccccc2)=O)CC1O)O Chemical compound CC(C)(C)OC(N(C[C@@H]1CNC(OCc2ccccc2)=O)CC1O)O VBFYXYSBQYVMQX-UQPPLGOBSA-N 0.000 description 1
- AXCFIJFQUMHJRG-UHFFFAOYSA-N CC(C)(C)OC(NCC1(C)CNCC1)=O Chemical compound CC(C)(C)OC(NCC1(C)CNCC1)=O AXCFIJFQUMHJRG-UHFFFAOYSA-N 0.000 description 1
- OTAKZEXNJOXEJV-UHFFFAOYSA-N CC(CNCc(nc1N2)ccc1SCC2=O)(CN(CCc(c1nc(OC)ccc1nc1)c1F)C1)C1O Chemical compound CC(CNCc(nc1N2)ccc1SCC2=O)(CN(CCc(c1nc(OC)ccc1nc1)c1F)C1)C1O OTAKZEXNJOXEJV-UHFFFAOYSA-N 0.000 description 1
- LMHNNPSLUPAFFW-UHFFFAOYSA-N CC1(CNCc(nc2)cc3c2OCS3)CN(CCc(c(F)cnc2cc3)c2nc3OC)CC1 Chemical compound CC1(CNCc(nc2)cc3c2OCS3)CN(CCc(c(F)cnc2cc3)c2nc3OC)CC1 LMHNNPSLUPAFFW-UHFFFAOYSA-N 0.000 description 1
- RTNRCBBYEVAJQR-UHFFFAOYSA-N CC1(CNCc(nc2N3)ccc2OCC3=O)CN(CCc(c(F)cnc2cc3)c2nc3OC)CC1 Chemical compound CC1(CNCc(nc2N3)ccc2OCC3=O)CN(CCc(c(F)cnc2cc3)c2nc3OC)CC1 RTNRCBBYEVAJQR-UHFFFAOYSA-N 0.000 description 1
- ZHPLQENDVLYPCY-UJONTBEJSA-N CN(C1[C@H](CNCc(nc2)cc3c2OCCO3)CN(CCc(c2nc(OC)ccc2nc2)c2F)C1)O Chemical compound CN(C1[C@H](CNCc(nc2)cc3c2OCCO3)CN(CCc(c2nc(OC)ccc2nc2)c2F)C1)O ZHPLQENDVLYPCY-UJONTBEJSA-N 0.000 description 1
- VPMXUOVMCBAXEQ-CAWMZFRYSA-N COc(cc1F)cc2c1nccc2CCN(CC1CNCc(nc2N3)ccc2SCC3=O)C[C@H]1O Chemical compound COc(cc1F)cc2c1nccc2CCN(CC1CNCc(nc2N3)ccc2SCC3=O)C[C@H]1O VPMXUOVMCBAXEQ-CAWMZFRYSA-N 0.000 description 1
- WDUIWEXAJFYVRE-HRAATJIYSA-N COc(cc1F)cc2c1nccc2CCN(C[C@@H]1CNCc(nc2N3)ccc2OCC3=O)C[C@H]1O Chemical compound COc(cc1F)cc2c1nccc2CCN(C[C@@H]1CNCc(nc2N3)ccc2OCC3=O)C[C@H]1O WDUIWEXAJFYVRE-HRAATJIYSA-N 0.000 description 1
- VWPZCEWHEMYMEQ-UHFFFAOYSA-N COc1c(c(C=C)ccn2)c2ccc1F Chemical compound COc1c(c(C=C)ccn2)c2ccc1F VWPZCEWHEMYMEQ-UHFFFAOYSA-N 0.000 description 1
- HZOMNKYBWZXILX-IINYFYTJSA-N COc1ccc2ncc(F)c(CCN(C[C@@H]3CN)C[C@H]3O)c2n1 Chemical compound COc1ccc2ncc(F)c(CCN(C[C@@H]3CN)C[C@H]3O)c2n1 HZOMNKYBWZXILX-IINYFYTJSA-N 0.000 description 1
- PHBJPXOVFMFBMC-SCLBCKFNSA-N COc1ccc2ncc(F)c(CCN(C[C@@H]3CNC(c(cc4)nc(N5)c4OCC5=O)=O)C[C@H]3O)c2n1 Chemical compound COc1ccc2ncc(F)c(CCN(C[C@@H]3CNC(c(cc4)nc(N5)c4OCC5=O)=O)C[C@H]3O)c2n1 PHBJPXOVFMFBMC-SCLBCKFNSA-N 0.000 description 1
- NJRYQMQXELIPEV-HRAATJIYSA-N COc1ccc2ncc(F)c(CCN(C[C@@H]3CNCc(cc4OCCOc4c4)c4F)C[C@H]3O)c2n1 Chemical compound COc1ccc2ncc(F)c(CCN(C[C@@H]3CNCc(cc4OCCOc4c4)c4F)C[C@H]3O)c2n1 NJRYQMQXELIPEV-HRAATJIYSA-N 0.000 description 1
- DJWPRIZZEJMOIW-OEMAIJDKSA-N COc1ccc2ncc(F)c(CCN3C[C@H](CO)C(CNCc(nc4N5)ccc4OCC5=O)C3)c2n1 Chemical compound COc1ccc2ncc(F)c(CCN3C[C@H](CO)C(CNCc(nc4N5)ccc4OCC5=O)C3)c2n1 DJWPRIZZEJMOIW-OEMAIJDKSA-N 0.000 description 1
- QMJFZPVEZZYXHU-MRVPVSSYSA-N COc1ccc2ncc(F)c([C@@H]3OC3)c2n1 Chemical compound COc1ccc2ncc(F)c([C@@H]3OC3)c2n1 QMJFZPVEZZYXHU-MRVPVSSYSA-N 0.000 description 1
- MYXOEAOZEKNPRT-GHTZIAJQSA-N COc1ccc2nccc(CCN(C[C@@H]3CNCc(cc4OCCOc4c4)c4F)C[C@H]3O)c2n1 Chemical compound COc1ccc2nccc(CCN(C[C@@H]3CNCc(cc4OCCOc4c4)c4F)C[C@H]3O)c2n1 MYXOEAOZEKNPRT-GHTZIAJQSA-N 0.000 description 1
- KKFHYWHZDXEZBV-FSWLIYMRSA-N COc1nc2c(CCN(C[C@@H]3CNC(O)OCc4ccccc4)C[C@H]3O)c(F)cnc2cc1 Chemical compound COc1nc2c(CCN(C[C@@H]3CNC(O)OCc4ccccc4)C[C@H]3O)c(F)cnc2cc1 KKFHYWHZDXEZBV-FSWLIYMRSA-N 0.000 description 1
- HTKGTXYWJIZZLQ-OAHLLOKOSA-N COc1nc2c(CCN3C[C@@H](CNS(c(cc4N5)ccc4SCC5=O)(=O)=O)CC3)c(F)cnc2cc1 Chemical compound COc1nc2c(CCN3C[C@@H](CNS(c(cc4N5)ccc4SCC5=O)(=O)=O)CC3)c(F)cnc2cc1 HTKGTXYWJIZZLQ-OAHLLOKOSA-N 0.000 description 1
- NVEIHQIBSICSFB-INIZCTEOSA-N COc1nc2c(CCN3C[C@H](CNCc(cc4OCCOc4c4)c4F)CC3)c(F)cnc2cc1 Chemical compound COc1nc2c(CCN3C[C@H](CNCc(cc4OCCOc4c4)c4F)CC3)c(F)cnc2cc1 NVEIHQIBSICSFB-INIZCTEOSA-N 0.000 description 1
- KPYAYPOLIYEFMN-HNNXBMFYSA-N COc1nc2c(CCN3C[C@H](CNCc(nc4)cc5c4OCS5)CC3)c(F)cnc2cc1 Chemical compound COc1nc2c(CCN3C[C@H](CNCc(nc4)cc5c4OCS5)CC3)c(F)cnc2cc1 KPYAYPOLIYEFMN-HNNXBMFYSA-N 0.000 description 1
- HEXIHVLAGMRYGG-XCWJXAQQSA-N COc1nc2c([C@@H](CN3CC(CNCc(nc4N5)ccc4SCC5=O)CC3)O)ccnc2cc1 Chemical compound COc1nc2c([C@@H](CN3CC(CNCc(nc4N5)ccc4SCC5=O)CC3)O)ccnc2cc1 HEXIHVLAGMRYGG-XCWJXAQQSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
-
- 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
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D497/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms
- C07D497/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D497/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US57987304P | 2004-06-15 | 2004-06-15 | |
| PCT/US2005/020950 WO2006002047A2 (en) | 2004-06-15 | 2005-06-15 | Antibacterial agents |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008502689A true JP2008502689A (ja) | 2008-01-31 |
| JP2008502689A5 JP2008502689A5 (enExample) | 2008-08-14 |
Family
ID=35782248
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007516640A Pending JP2008502689A (ja) | 2004-06-15 | 2005-06-15 | 抗菌剤 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US7691850B2 (enExample) |
| EP (1) | EP1796466A4 (enExample) |
| JP (1) | JP2008502689A (enExample) |
| WO (1) | WO2006002047A2 (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011083858A1 (ja) * | 2010-01-08 | 2011-07-14 | 杏林製薬株式会社 | 3,4-ジ置換ピロリジン誘導体の製造方法及び製造中間体 |
| JP2015512426A (ja) * | 2012-04-04 | 2015-04-27 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | Metap−2インヒビターとしての環状アミド |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE602005024151D1 (de) | 2004-08-02 | 2010-11-25 | Glaxo Group Ltd | Antibakterielle mittel |
| WO2006081179A1 (en) | 2005-01-25 | 2006-08-03 | Glaxo Group Limited | Antibacterial agents |
| MY150958A (en) | 2005-06-16 | 2014-03-31 | Astrazeneca Ab | Compounds for the treatment of multi-drug resistant bacterial infections |
| EP1954697B1 (en) * | 2005-10-21 | 2010-02-24 | Glaxo Group Limited | Peri condensed tricyclic compounds useful as antibacterial agents |
| EP1790342A1 (de) | 2005-11-11 | 2007-05-30 | Zentaris GmbH | Pyridopyrazin-Derivate und deren Verwendung als Modulatoren der Signaltransduktionswege |
| US8217042B2 (en) | 2005-11-11 | 2012-07-10 | Zentaris Gmbh | Pyridopyrazines and their use as modulators of kinases |
| EP2001887B1 (en) | 2006-04-06 | 2010-09-15 | Glaxo Group Limited | Pyrrolo-quinoxalinone derivatives as antibacterials |
| EP2007377A4 (en) | 2006-04-06 | 2011-08-17 | Glaxo Group Ltd | ANTIBACTERIAL ACTIVE SUBSTANCES |
| EP1992628A1 (en) | 2007-05-18 | 2008-11-19 | Glaxo Group Limited | Derivatives and analogs of N-ethylquinolones and N-ethylazaquinolones |
| CL2008001003A1 (es) | 2007-04-11 | 2008-10-17 | Actelion Pharmaceuticals Ltd | Compuestos derivados de oxazolidinona; composicion farmaceutica que comprende a dichos compuestos; y su uso para preparar un medicamento para tratar una infeccion bacteriana. |
| CA2684659C (en) | 2007-04-20 | 2015-11-24 | Glaxo Group Limited | Tricyclic nitrogen containing compounds as antibacterial agents |
| EP2080761A1 (en) | 2008-01-18 | 2009-07-22 | Glaxo Group Limited | Compounds |
| WO2009128019A1 (en) | 2008-04-15 | 2009-10-22 | Actelion Pharmaceuticals Ltd | Tricyclic antibiotics |
| WO2010043714A1 (en) | 2008-10-17 | 2010-04-22 | Glaxo Group Limited | Tricyclic nitrogen compounds used as antibacterials |
| JP5653935B2 (ja) | 2009-01-15 | 2015-01-14 | グラクソ グループ リミテッドGlaxo Group Limited | 抗菌薬として有用なナフチリジン―2(1h)−オン化合物 |
| CN102361863B (zh) | 2009-01-21 | 2014-12-03 | 巴斯利尔药物股份公司 | 新的二环抗生素 |
| AR076222A1 (es) | 2009-04-09 | 2011-05-26 | Actelion Pharmaceuticals Ltd | Derivados 2-hidroxietil-1h-quinolin-ona y sus analogos azaisotericos con actividad antibacteriana y composiciones farmaceuticas que los contienen |
| MX2012007935A (es) | 2010-01-07 | 2012-08-15 | Du Pont | Compuestos heterociclicos fungicidas. |
| EP2640366A2 (en) | 2010-11-15 | 2013-09-25 | Exelixis, Inc. | Benzoxazepines as inhibitors of pi3k/mtor and methods of their use and manufacture |
| CN103958525A (zh) | 2011-11-30 | 2014-07-30 | 埃科特莱茵药品有限公司 | 3,7-二取代八氢-2H-吡啶并[4,3-e][1,3]噁嗪-2-酮抗生素 |
| CN102702098A (zh) * | 2012-05-24 | 2012-10-03 | 盛世泰科生物医药技术(苏州)有限公司 | 6-甲氧基-1,2,3,4四氢喹啉-5羧酸甲酯的合成 |
| WO2014057415A2 (en) * | 2012-10-10 | 2014-04-17 | Vitas Pharma Research Pvt Ltd | Inhibitors of dna gyrase for the treatment of bacterial infections |
| WO2016027249A1 (en) | 2014-08-22 | 2016-02-25 | Glaxosmithkline Intellectual Property Development Limited | Tricyclic nitrogen containing compounds for treating neisseria gonorrhoea infection |
| GB201509006D0 (en) | 2015-05-26 | 2015-07-08 | Redx Pharma Plc | Antibacterial compounds |
| TW201722965A (zh) | 2015-08-16 | 2017-07-01 | 葛蘭素史密斯克藍智慧財產發展有限公司 | 用於抗菌應用之化合物 |
| US9957233B1 (en) | 2016-08-05 | 2018-05-01 | Calitor Sciences, Llc | Process for preparing substituted quinolin-4-ol compounds |
| CA3093189A1 (en) | 2018-03-07 | 2019-09-12 | Bayer Aktiengesellschaft | Identification and use of erk5 inhibitors |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002008224A1 (en) * | 2000-07-26 | 2002-01-31 | Smithkline Beecham P.L.C. | Aminopiperidine quinolines and their azaisosteric analogues with antibacterial activity |
| WO2002056882A1 (en) * | 2001-01-22 | 2002-07-25 | Smithkline Beecham P.L.C. | Quinolines and nitrogenated derivaive thereof substituted in 4-position by a piperidine-containing moiety and their use as antibacterial agents |
| WO2003064421A1 (en) * | 2002-01-29 | 2003-08-07 | Glaxo Group Limited | Aminopiperidine derivatives |
| WO2004002490A2 (en) * | 2002-06-26 | 2004-01-08 | Glaxo Group Limited | Piperidine compounds as antibacterials |
| WO2004035569A2 (de) * | 2002-10-10 | 2004-04-29 | Morphochem Aktiengesellschaft für kombinatorische Chemie | Neue verbindungen mit antibakterieller aktivität |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2679906B1 (fr) | 1991-07-31 | 1995-01-20 | Adir | Nouvelles (isoquinolein-5 yl) sulfonamides, leur procede de preparation et les compositions pharmaceutiques qui les contiennent. |
| JP2000500467A (ja) | 1995-11-13 | 2000-01-18 | スミスクライン・ビーチャム・コーポレイション | 血液調節化合物 |
| US6489354B1 (en) | 1999-03-02 | 2002-12-03 | Merck & Co., Inc. | 3-alkyl substituted pyrrolidine modulators of chemokine receptor activity |
| GB9917408D0 (en) | 1999-07-23 | 1999-09-22 | Smithkline Beecham Plc | Compounds |
| US6362177B1 (en) * | 2000-05-16 | 2002-03-26 | Teijin Limited | Cyclic amine derivatives and their use as drugs |
| JP2002047272A (ja) | 2000-07-26 | 2002-02-12 | Dai Ichi Seiyaku Co Ltd | ポリアミンアミド誘導体 |
| WO2003064431A2 (en) | 2002-01-29 | 2003-08-07 | Glaxo Group Limited | Aminopiperidine compounds, process for their preparation, and pharmaceutical compositions containing them |
| AR040335A1 (es) * | 2002-06-26 | 2005-03-30 | Glaxo Group Ltd | Compuesto de ciclohexano o ciclohexeno, uso del mismo para preparar un medicamento, composicion farmaceutica que lo comprende, procedimiento y compuestos intermediarios de utilidad para preparar dicho compuesto |
| GB0217294D0 (en) | 2002-07-25 | 2002-09-04 | Glaxo Group Ltd | Medicaments |
| DE60331849D1 (de) | 2002-11-05 | 2010-05-06 | Glaxosmithkline Llc | Antibakterielle wirkstoffe |
| AU2003291227A1 (en) | 2002-11-05 | 2004-06-07 | Smithkline Beecham Corporation | Antibacterial agents |
| WO2004050036A2 (en) | 2002-12-04 | 2004-06-17 | Glaxo Group Limited | Quinolines and nitrogenated derivatives thereof and their use as antibacterial agents |
| TW200427688A (en) | 2002-12-18 | 2004-12-16 | Glaxo Group Ltd | Antibacterial agents |
| TW200507841A (en) | 2003-03-27 | 2005-03-01 | Glaxo Group Ltd | Antibacterial agents |
| US7232833B2 (en) * | 2003-03-28 | 2007-06-19 | Novexel | 4-substituted quinoline derivatives, method and intermediates for their preparation and pharmaceutical compositions containing them |
| FR2852954B1 (fr) | 2003-03-28 | 2006-07-14 | Aventis Pharma Sa | Derives de quinoleines-4-substituees, leurs procede et intermediaires de preparation et les compositions pharmaceutiques qui les contiennent |
| DE10316081A1 (de) * | 2003-04-08 | 2004-10-21 | Morphochem AG Aktiengesellschaft für kombinatorische Chemie | Neue Verbindungen mit antibakterieller Aktivität |
| FR2858619B1 (fr) | 2003-08-08 | 2006-12-22 | Aventis Pharma Sa | Derives de quinoleines-4-substituees, leurs procede et intermediaires de preparation et les compositions pharmaceutiques qui les contiennent |
| US7348434B2 (en) * | 2003-08-08 | 2008-03-25 | Antony Bigot | 4-substituted quinoline derivatives, method and intermediates for their preparation and pharmaceutical compositions containing them |
| FR2872164B1 (fr) | 2004-06-29 | 2006-11-17 | Aventis Pharma Sa | Derives de quinoleines-4-substituees, leur procede et intermediaires de preparation et les compositions pharmaceutiques qui les contiennent |
| EP1773831A1 (en) * | 2004-07-08 | 2007-04-18 | Glaxo Group Limited | Antibacterial agents |
| DE102004041163A1 (de) | 2004-08-25 | 2006-03-02 | Morphochem Aktiengesellschaft für kombinatorische Chemie | Neue Verbindungen mit antibakterieller Aktivität |
| WO2006046552A1 (ja) | 2004-10-27 | 2006-05-04 | Toyama Chemical Co., Ltd. | 新規な含窒素複素環化合物およびその塩 |
| EP1863483A4 (en) | 2005-03-31 | 2010-03-31 | Janssen Pharmaceutica Nv | Bicyclic pyrazole compounds as anti-bacteriostatic agents |
-
2005
- 2005-06-15 US US11/628,705 patent/US7691850B2/en not_active Expired - Fee Related
- 2005-06-15 WO PCT/US2005/020950 patent/WO2006002047A2/en not_active Ceased
- 2005-06-15 JP JP2007516640A patent/JP2008502689A/ja active Pending
- 2005-06-15 EP EP05785327A patent/EP1796466A4/en not_active Withdrawn
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002008224A1 (en) * | 2000-07-26 | 2002-01-31 | Smithkline Beecham P.L.C. | Aminopiperidine quinolines and their azaisosteric analogues with antibacterial activity |
| WO2002056882A1 (en) * | 2001-01-22 | 2002-07-25 | Smithkline Beecham P.L.C. | Quinolines and nitrogenated derivaive thereof substituted in 4-position by a piperidine-containing moiety and their use as antibacterial agents |
| WO2003064421A1 (en) * | 2002-01-29 | 2003-08-07 | Glaxo Group Limited | Aminopiperidine derivatives |
| WO2004002490A2 (en) * | 2002-06-26 | 2004-01-08 | Glaxo Group Limited | Piperidine compounds as antibacterials |
| WO2004035569A2 (de) * | 2002-10-10 | 2004-04-29 | Morphochem Aktiengesellschaft für kombinatorische Chemie | Neue verbindungen mit antibakterieller aktivität |
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| WO2011083858A1 (ja) * | 2010-01-08 | 2011-07-14 | 杏林製薬株式会社 | 3,4-ジ置換ピロリジン誘導体の製造方法及び製造中間体 |
| AU2011204131B2 (en) * | 2010-01-08 | 2014-05-08 | Kyorin Pharmaceutical Co., Ltd. | Method for producing 3,4-disubstituted pyrrolidine derivative and production intermediate thereof |
| JP2015512426A (ja) * | 2012-04-04 | 2015-04-27 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | Metap−2インヒビターとしての環状アミド |
| JP2017149724A (ja) * | 2012-04-04 | 2017-08-31 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | Metap−2インヒビターとしての環状アミド |
| US10093623B2 (en) | 2012-04-04 | 2018-10-09 | Merck Patent Gmbh | Cyclic amides as MetAP-2 inhibitors |
Also Published As
| Publication number | Publication date |
|---|---|
| US7691850B2 (en) | 2010-04-06 |
| WO2006002047A3 (en) | 2006-03-23 |
| WO2006002047A2 (en) | 2006-01-05 |
| US20070287701A1 (en) | 2007-12-13 |
| EP1796466A2 (en) | 2007-06-20 |
| EP1796466A4 (en) | 2009-09-02 |
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