JP2008534672A5 - - Google Patents

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Publication number
JP2008534672A5
JP2008534672A5 JP2008504870A JP2008504870A JP2008534672A5 JP 2008534672 A5 JP2008534672 A5 JP 2008534672A5 JP 2008504870 A JP2008504870 A JP 2008504870A JP 2008504870 A JP2008504870 A JP 2008504870A JP 2008534672 A5 JP2008534672 A5 JP 2008534672A5
Authority
JP
Japan
Prior art keywords
pharmaceutically acceptable
pharmaceutical composition
compound
acceptable salt
composition according
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.)
Withdrawn
Application number
JP2008504870A
Other languages
English (en)
Japanese (ja)
Other versions
JP2008534672A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/IB2006/000954 external-priority patent/WO2006106427A1/en
Publication of JP2008534672A publication Critical patent/JP2008534672A/ja
Publication of JP2008534672A5 publication Critical patent/JP2008534672A5/ja
Withdrawn legal-status Critical Current

Links

JP2008504870A 2005-04-06 2006-03-27 抗菌剤としての7−フルオロ−1,3−ジヒドロ−インドール−2−オンオキサゾリジノン Withdrawn JP2008534672A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US66871505P 2005-04-06 2005-04-06
US68403305P 2005-05-24 2005-05-24
PCT/IB2006/000954 WO2006106427A1 (en) 2005-04-06 2006-03-27 7-fluoro-1,3-dihydro-indol-2-one oxazolidinones as antibacterial agents

Publications (2)

Publication Number Publication Date
JP2008534672A JP2008534672A (ja) 2008-08-28
JP2008534672A5 true JP2008534672A5 (enExample) 2009-05-14

Family

ID=36636389

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008504870A Withdrawn JP2008534672A (ja) 2005-04-06 2006-03-27 抗菌剤としての7−フルオロ−1,3−ジヒドロ−インドール−2−オンオキサゾリジノン

Country Status (21)

Country Link
US (1) US7435751B2 (enExample)
EP (1) EP1869030A1 (enExample)
JP (1) JP2008534672A (enExample)
KR (1) KR20070108938A (enExample)
AP (1) AP2007004172A0 (enExample)
AR (1) AR053839A1 (enExample)
AU (1) AU2006231919A1 (enExample)
BR (1) BRPI0610533A2 (enExample)
CA (1) CA2603899A1 (enExample)
CR (1) CR9417A (enExample)
DO (1) DOP2006000080A (enExample)
GT (1) GT200600133A (enExample)
IL (1) IL186119A0 (enExample)
MX (1) MX2007012386A (enExample)
NL (1) NL1031525C2 (enExample)
NO (1) NO20075505L (enExample)
PE (1) PE20061301A1 (enExample)
TN (1) TNSN07373A1 (enExample)
TW (1) TW200716101A (enExample)
UY (1) UY29452A1 (enExample)
WO (1) WO2006106427A1 (enExample)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1781643A1 (en) * 2004-08-06 2007-05-09 Pharmacia & Upjohn Company LLC Oxindole oxazolidinones as antibacterial agents
KR100891485B1 (ko) 2007-10-29 2009-04-02 주식회사 만도 디스크 브레이크의 주차브레이크 장치
US20090124737A1 (en) * 2007-11-12 2009-05-14 Eastman Chemical Company Acrylic plastisol viscosity reducers

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5164510A (en) 1988-09-15 1992-11-17 The Upjohn Company 5'Indolinyl-5β-amidomethyloxazolidin-2-ones
ATE112773T1 (de) 1988-09-15 1994-10-15 Upjohn Co 5-indolinyl-5-beta-amidomethyloxazolidin-2-one, 3-(substituierte kondensierte)phenyl-5-beta amidomethyloxazolidin-2-one und 3-(nitrogen- substituierte)phenyl-5-beta-amidomethyloxazolid n-2-one.
DE4425613A1 (de) 1994-07-20 1996-01-25 Bayer Ag 5-gliedrige Heteroaryl-oxazolidinone
DE4425612A1 (de) 1994-07-20 1996-04-04 Bayer Ag 6-gliedrige stickstoffhaltige Heteroaryl-oxazolidinone
US6015429A (en) * 1994-09-08 2000-01-18 Gore Enterprise Holdings, Inc. Procedures for introducing stents and stent-grafts
DE19604223A1 (de) 1996-02-06 1997-08-07 Bayer Ag Neue substituierte Oxazolidinone
DE19649095A1 (de) 1996-02-06 1997-08-07 Bayer Ag Neue Heteroaryl-Oxazolidinone
CN1288462A (zh) 1998-01-23 2001-03-21 法玛西雅厄普约翰美国公司 噁唑烷酮组合库、组合物和制备方法
CN1301248A (zh) 1998-04-14 2001-06-27 三星精密化学株式会社 手性(s)-2,3-二取代-1-丙胺衍生物的制备方法
AU1379900A (en) 1998-11-17 2000-06-05 Bayer Aktiengesellschaft Novel substituted phenyloxazolidone derivatives
AU764980B2 (en) 1998-11-27 2003-09-04 Pharmacia & Upjohn Company Oxazolidinone antibacterial agents having a thiocarbonyl functionality
JP2003501351A (ja) 1999-05-27 2003-01-14 ファルマシア・アンド・アップジョン・カンパニー 抗菌剤としての二環系オキサゾリジノン
ATE321024T1 (de) 2000-10-17 2006-04-15 Pharmacia & Upjohn Co Llc Verfahren zur herstellung von oxazolidinonverbindungen
ES2268011T3 (es) 2001-04-07 2007-03-16 Astrazeneca Ab Oxazolidinonas que contienen un grupo sulfonimida como antibioticos.
EP1380121B1 (en) 2001-04-20 2007-09-26 Pharmacia & Upjohn Company LLC Process to prepare oxazolidinones
AR038536A1 (es) 2002-02-25 2005-01-19 Upjohn Co N-aril-2-oxazolidinona-5- carboxamidas y sus derivados
US7012088B2 (en) * 2003-02-24 2006-03-14 Pharmacia & Upjohn Company Indolone oxazolidinones and derivatives thereof
EP1781643A1 (en) * 2004-08-06 2007-05-09 Pharmacia & Upjohn Company LLC Oxindole oxazolidinones as antibacterial agents

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