|
GB9601666D0
(en)
*
|
1996-01-27 |
1996-03-27 |
Zeneca Ltd |
Chemical compounds
|
|
GB9702213D0
(en)
|
1996-02-24 |
1997-03-26 |
Zeneca Ltd |
Chemical compounds
|
|
GB9609919D0
(en)
|
1996-05-11 |
1996-07-17 |
Zeneca Ltd |
Chemical compounds
|
|
WO1999002525A1
(en)
*
|
1997-07-11 |
1999-01-21 |
Pharmacia & Upjohn Company |
Thiadiazolyl and oxadiazolyl phenyl oxazolidinone antibacterial agents
|
|
GB9717804D0
(en)
|
1997-08-22 |
1997-10-29 |
Zeneca Ltd |
Chemical compounds
|
|
GB9717807D0
(en)
|
1997-08-22 |
1997-10-29 |
Zeneca Ltd |
Chemical compounds
|
|
GB9725244D0
(en)
|
1997-11-29 |
1998-01-28 |
Zeneca Ltd |
Chemical compounds
|
|
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
|
|
US7002020B1
(en)
|
1998-01-23 |
2006-02-21 |
Pharmacia & Upjohn Company |
Oxazolidinone combinatorial libraries, compositions and methods of preparation
|
|
US6562844B2
(en)
|
1998-01-23 |
2003-05-13 |
Pharmacia & Upjohn Company |
Oxazolidinone combinatorial libraries, compositions and methods of preparation
|
|
WO1999064417A2
(en)
|
1998-06-05 |
1999-12-16 |
Astrazeneca Ab |
Oxazolidinone derivatives, process for their preparation and pharmaceutical compositions containing them
|
|
EP1102536B1
(de)
*
|
1998-08-04 |
2003-05-02 |
Ciba SC Holding AG |
Verwendung von Oxathiazolonen als Mikrobizide
|
|
JP2002535680A
(ja)
|
1999-01-27 |
2002-10-22 |
ファルマシア・アンド・アップジョン・カンパニー |
延長因子ｐ活性モジュレーターのアッセイ方法
|
|
GB9928568D0
(en)
|
1999-12-03 |
2000-02-02 |
Zeneca Ltd |
Chemical compounds
|
|
PE20010851A1
(es)
*
|
1999-12-14 |
2001-08-17 |
Upjohn Co |
Esteres del acido benzoico de oxazolidinonas que tienen un substituyente hidroxiacetilpiperazina
|
|
GB0009803D0
(en)
*
|
2000-04-25 |
2000-06-07 |
Astrazeneca Ab |
Chemical compounds
|
|
WO2003008389A1
(en)
*
|
2001-07-16 |
2003-01-30 |
Ranbaxy Laboratories Limited |
Oxazolidinone derivatives as potential antimicrobials
|
|
PL363960A1
(en)
*
|
2000-07-17 |
2004-11-29 |
Ranbaxy Laboratories Limited |
Oxazolidinone derivatives as antimicrobials
|
|
JP2005503435A
(ja)
*
|
2001-04-17 |
2005-02-03 |
メルク アンド カンパニー インコーポレーテッド |
ビシクロ［３．１．０］ヘキサン含有オキサゾリジノン抗生物質及びその誘導体
|
|
JP2005529924A
(ja)
*
|
2002-05-15 |
2005-10-06 |
ランバクシー ラボラトリーズ リミテッド |
フェニルオキサゾリジノン誘導体
|
|
CN1668308A
(zh)
*
|
2002-07-29 |
2005-09-14 |
兰贝克赛实验室有限公司 |
作为抗菌剂的噁唑烷酮衍生物
|
|
CA2491287A1
(en)
|
2002-08-12 |
2004-02-19 |
Pharmacia & Upjohn Company |
N-aryl-2-oxazolidinones and their derivatives
|
|
AU2002339721A1
(en)
*
|
2002-09-20 |
2004-04-08 |
Lupin Limited |
Oxazolidinone derivatives, process for their preperation and their use as antimycobacterial agents
|
|
CA2502017A1
(en)
|
2002-11-21 |
2004-06-03 |
Pharmacia & Upjohn Company Llc |
N-(4-(piperazin-1-yl)-phenyl-2-oxazolidinone-5-carboxamide derivates and related compounds as antibacterial agents
|
|
RU2348628C2
(ru)
*
|
2003-07-02 |
2009-03-10 |
Мерк Энд Ко., Инк. |
Замещенные циклопропильной группой оксазолидиноновые антибиотики и их производные
|
|
WO2005005422A1
(en)
*
|
2003-07-02 |
2005-01-20 |
Merck & Co., Inc. |
Oxazolidinone antibiotics and derivatives thereof
|
|
EP1654259A1
(en)
*
|
2003-07-02 |
2006-05-10 |
Merck & Co., Inc. |
Cyclopropyl group substituted oxazolidinone antibiotics and derivatives thereof
|
|
WO2005005399A1
(en)
*
|
2003-07-02 |
2005-01-20 |
Merck & Co., Inc. |
Oxazolidinone antibiotics and derivatives thereof
|
|
WO2005051933A1
(en)
*
|
2003-11-28 |
2005-06-09 |
Ranbaxy Laboratories Limited |
An improved process for the synthesis of 4-(4-benzyloxy-carbonylamino-2-fluorophenyl)-piperazine-1-carboxylic acid tert-butyl ester, a key intermediate for oxazolidinone antimicrobials and compounds prepared thereby
|
|
WO2005082899A1
(en)
*
|
2004-01-28 |
2005-09-09 |
Ranbaxy Laboratories Limited |
Oxazolidinone derivatives as antimicrobials
|
|
US8686011B2
(en)
|
2004-05-24 |
2014-04-01 |
Amgen Inc. |
Inhibitors of 11-β-hydroxy steroid dehydrogenase type 1
|
|
WO2005116002A2
(en)
*
|
2004-05-24 |
2005-12-08 |
Amgen Inc. |
Inhibitors of 11-beta-hydroxy steroid dehydrogenase type 1
|
|
WO2006035283A1
(en)
*
|
2004-09-27 |
2006-04-06 |
Ranbaxy Laboratories Limited |
Oxazolidinone derivatives as antimicrobials
|
|
WO2006043121A1
(en)
*
|
2004-10-20 |
2006-04-27 |
Ranbaxy Laboratories Limited |
Oxazolidinone derivatives as antimicrobials
|
|
WO2006051408A1
(en)
*
|
2004-11-11 |
2006-05-18 |
Ranbaxy Laboratories Limited |
Oxazolidinone derivatives as antimicrobials
|
|
WO2007023507A2
(en)
*
|
2005-06-20 |
2007-03-01 |
Wockhardt Limited |
Oxazolidinones bearing antimicrobial activity composition and methods of preparation
|
|
JO2769B1
(en)
|
2005-10-26 |
2014-03-15 |
جانسين فارماسوتيكا ان. في |
Rapid decomposition of physiologically antagonistic agents of the 2-dopamine receptor
|
|
CN100406455C
(zh)
*
|
2006-02-20 |
2008-07-30 |
中国科学院上海药物研究所 |
含三氮唑基的噁唑烷酮类化合物及其制备方法和用途
|
|
JO2642B1
(en)
*
|
2006-12-08 |
2012-06-17 |
جانسين فارماسوتيكا ان. في |
Dopamine 2 receptor antagonists are rapidly hydrolyzed
|
|
JO2849B1
(en)
|
2007-02-13 |
2015-03-15 |
جانسين فارماسوتيكا ان. في |
Dopamine 2 receptor antagonists are rapidly hydrolyzed
|
|
PL2148873T3
(pl)
*
|
2007-04-23 |
2013-01-31 |
Janssen Pharmaceutica Nv |
Pochodne 4-alkoksypirydazynowe jako szybko dysocjujący antagoniści receptora dopaminowego 2
|
|
CN101663299A
(zh)
*
|
2007-04-23 |
2010-03-03 |
詹森药业有限公司 |
作为快速解离性多巴胺2受体拮抗剂的噻(二)唑类化合物
|
|
KR20100016498A
(ko)
*
|
2007-04-23 |
2010-02-12 |
얀센 파마슈티카 엔.브이. |
속해리성 도파민 2 수용체 길항제로서의 피리딘 유도체
|
|
WO2009120789A1
(en)
*
|
2008-03-26 |
2009-10-01 |
Global Alliance For Tb Drug Development |
Bicyclic nitroimidazoles covalently linked to substituted phenyl oxazolidinones
|
|
EP2310374B1
(en)
*
|
2008-07-03 |
2012-10-31 |
Janssen Pharmaceutica N.V. |
Substituted 6- (1-piperazinyl) -pyridazines as 5-ht6 receptor antagonists
|
|
KR101609218B1
(ko)
*
|
2008-07-31 |
2016-04-05 |
얀센 파마슈티카 엔.브이. |
속해리성 도파민 2 수용체 길항제로서의 피페라진-1-일-트리플루오로메틸-치환된-피리딘
|
|
WO2011152442A1
(ja)
*
|
2010-06-03 |
2011-12-08 |
塩野義製薬株式会社 |
2－クロロ－6－フルオロベンゾオキサゾールの製造方法
|
|
CN102079730B
(zh)
*
|
2010-09-06 |
2013-10-16 |
贵州大学 |
一类含2,5-取代杂环基砜类衍生物及其合成方法和应用
|
|
CN103450173B
(zh)
*
|
2013-09-07 |
2015-06-03 |
吉首大学 |
吡咯酮-苯基-噁唑烷酮型化合物及其制法和用途
|
|
CN103709119B
(zh)
*
|
2013-12-04 |
2015-05-20 |
上海应用技术学院 |
一种制备5-氨基噻唑-4-甲酰胺的方法
|
|
CN104202835A
(zh)
*
|
2014-09-03 |
2014-12-10 |
苏州微站通信科技有限公司 |
Ue进入静默期时让基站及时释放时频资源的方法
|
|
JP7175481B2
(ja)
*
|
2018-04-27 |
2022-11-21 |
国立大学法人大阪大学 |
ベンゾイソオキサゾール化合物
|
|
US12479816B2
(en)
|
2019-02-08 |
2025-11-25 |
University of Pittsburgh—of the Commonwealth System of Higher Education |
20-HETE formation inhibitors
|