FR16C0031I1 - - Google Patents
Info
- Publication number
- FR16C0031I1 FR16C0031I1 FR16C0031C FR16C0031I1 FR 16C0031 I1 FR16C0031 I1 FR 16C0031I1 FR 16C0031 C FR16C0031 C FR 16C0031C FR 16C0031 I1 FR16C0031 I1 FR 16C0031I1
- Authority
- FR
- France
- Prior art keywords
- hiv
- mercaptoacetanilides
- conr
- triazolyl
- useful
- 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.)
- Active
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles 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 to ring carbon atoms
- C07D249/12—Oxygen or sulfur atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4196—1,2,4-Triazoles
-
- 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
-
- 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
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles 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 to ring carbon atoms
- C07D249/14—Nitrogen atoms
-
- 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
-
- 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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US60421904P | 2004-08-25 | 2004-08-25 | |
US60422004P | 2004-08-25 | 2004-08-25 | |
US68635105P | 2005-05-31 | 2005-05-31 | |
EP05790722A EP1789039B1 (en) | 2004-08-25 | 2005-08-25 | S-triazolyl alpha -mercaptoacetanildes as inhibitors of hiv reverse transcriptase |
Publications (2)
Publication Number | Publication Date |
---|---|
FR16C0031I1 true FR16C0031I1 (zh) | 2016-09-23 |
FR16C0031I2 FR16C0031I2 (fr) | 2017-03-31 |
Family
ID=36000576
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR16C0031C Active FR16C0031I2 (fr) | 2004-08-25 | 2016-07-29 | S-triazolyl alpha -mercaptoacetanilides en tant qu'inhibiteurs de la transcriptase inverse du vih |
Country Status (32)
Country | Link |
---|---|
US (8) | US7947721B2 (zh) |
EP (5) | EP2135608B8 (zh) |
JP (2) | JP4952943B2 (zh) |
KR (1) | KR101241716B1 (zh) |
CN (2) | CN101083987B (zh) |
AT (2) | ATE528001T1 (zh) |
AU (2) | AU2005280130C9 (zh) |
BR (2) | BRPI0520870B8 (zh) |
CA (1) | CA2578068C (zh) |
CY (2) | CY1112221T1 (zh) |
DK (1) | DK2135608T3 (zh) |
EA (2) | EA014737B1 (zh) |
EC (1) | ECSP077322A (zh) |
ES (2) | ES2374773T3 (zh) |
FR (1) | FR16C0031I2 (zh) |
HK (1) | HK1133582A1 (zh) |
HR (1) | HRP20130075T1 (zh) |
HU (1) | HUS1600034I1 (zh) |
IL (3) | IL181523A (zh) |
IN (1) | IN2014CN03762A (zh) |
LT (1) | LTC2135608I2 (zh) |
LU (1) | LU93169I2 (zh) |
ME (1) | ME01512B (zh) |
MX (1) | MX2007002236A (zh) |
NL (1) | NL300825I2 (zh) |
NZ (2) | NZ581376A (zh) |
PL (1) | PL2135608T3 (zh) |
PT (1) | PT2135608E (zh) |
RS (1) | RS52632B (zh) |
SG (2) | SG185992A1 (zh) |
SI (1) | SI2135608T1 (zh) |
WO (1) | WO2006026356A2 (zh) |
Families Citing this family (51)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007050087A1 (en) * | 2004-08-25 | 2007-05-03 | Ardea Biosciences, Inc. | N[S(4-aryl-triazol-3-yl)α -mercaptoacetyl]-p-amino benozoic acids AS HIV REVERSE TRANSCRIPTASE INHIBITORS |
EP2135608B8 (en) | 2004-08-25 | 2012-03-21 | Ardea Biosciences, Inc. | S-triazolyl alpha -mercaptoacetanilides as inhibitors of HIV reverse transcriptase |
KR101542629B1 (ko) | 2007-05-30 | 2015-08-06 | 에프. 호프만-라 로슈 아게 | 비-뉴클레오사이드 역전사효소 억제제 |
WO2009030996A1 (en) * | 2007-09-05 | 2009-03-12 | Coley Pharmaceutical Group, Inc. | Triazole compounds as toll-like receptor (tlr) agonists |
SI2217577T1 (sl) | 2007-11-27 | 2014-11-28 | Ardea Biosciences, Inc. | Nove spojine in sestavki ter metode uporabe |
US8242154B2 (en) | 2008-09-04 | 2012-08-14 | Ardea Biosciences, Inc. | Compounds, compositions and methods of using same for modulating uric acid levels |
AU2009289647C1 (en) | 2008-09-04 | 2013-03-21 | Ardea Biosciences, Inc. | Compounds, compositions and methods of using same for modulating uric acid levels |
US8173690B2 (en) * | 2008-09-04 | 2012-05-08 | Ardea Biosciences, Inc. | Compounds, compositions and methods of using same for modulating uric acid levels |
EP2349258A1 (en) * | 2008-10-24 | 2011-08-03 | Ardea Biosciences, Inc. | Compositions comprising 4- (2- ( 5-br0m0-4- ( l-cyclopropylnaphthalen-4-yl) -4h-1, 2, 4-triazol-3-ylthio) acetamido -3-chlorobenzoic acid and pharmaceutically acceptable salts thereof |
WO2010048592A1 (en) * | 2008-10-24 | 2010-04-29 | Ardea Biosciences, Inc. | Compositions comprising 4- (2- ( 5-br0m0-4- ( 1-cyclopropylnaphthalen-4-yl) -4h-1, 2, 4-triaz0l-3-ylthi0) acetamido -3-chlorobenzoic acid and pharmaceutically acceptable salts thereof |
CA2760940A1 (en) | 2009-05-20 | 2010-11-25 | Ardea Biosciences, Inc. | Methods of modulating uric acid levels |
CN102040546B (zh) * | 2009-10-10 | 2014-10-15 | 台州市华南医化有限公司 | 一种4-环丙基-1-异硫氰基萘的制备方法及中间体4-环丙基-1-萘甲醛肟/卤化物 |
SG182404A1 (en) * | 2010-01-08 | 2012-08-30 | Ardea Biosciences Inc | Polymorphic, crystalline and mesophase forms of sodium 2-(5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-4h-1,2,4-triazol-3-ylthio)acetate, and uses thereof |
CA2794798C (en) | 2010-03-30 | 2017-05-30 | Ardea Biosciences, Inc. | Treatment of gout |
LT2582683T (lt) | 2010-06-15 | 2018-06-11 | Ardea Biosciences, Inc. | Podagros ir hiperuricemijos gydymas |
CA2802692C (en) | 2010-06-16 | 2016-01-05 | Ardea Biosciences, Inc. | Phenylthioacetate compounds useful as uricosuric agents |
AR081930A1 (es) | 2010-06-16 | 2012-10-31 | Ardea Biosciences Inc | Compuestos de tioacetato |
CN101899013B (zh) * | 2010-07-12 | 2012-07-25 | 山东大学 | 2-(2-取代芳基-2h-1,2,4-三唑-3-巯基)乙酰胺衍生物及其制备方法与应用 |
EP2627331A4 (en) * | 2010-10-15 | 2014-03-12 | Ardea Biosciences Inc | METHODS OF TREATING HYPERURICEMIA AND RELATED DISEASES |
MX2013007505A (es) | 2010-12-30 | 2013-08-01 | Ardea Biosciences Inc | Formas polimorficas de acido 2-(5-bromo-4-(4-ciclopropilnaftalen-1 -il)-4h-1,2,4-triazol-3-iltio)acetico y usos de los mismos. |
WO2013067425A1 (en) | 2011-11-03 | 2013-05-10 | Ardea Biosciences Inc. | 3,4-di-substituted pyridine compound, methods of using and compositions comprising the same |
AR091651A1 (es) * | 2012-07-03 | 2015-02-18 | Ardea Biosciences Inc | Elaboracion de acido 2-(5-bromo-4-(4-ciclopropilnaftalen-1-il)-4h-1,2,4-triazol-3-iltio)acetico |
WO2014198241A1 (en) * | 2013-06-14 | 2014-12-18 | Sunshine Lake Pharma Co., Ltd. | Thio-1,2,4-triazole derivatives and method for preparing the same |
CN103524440B (zh) * | 2013-10-15 | 2015-09-09 | 苏州鹏旭医药科技有限公司 | 痛风治疗药Lesinurad的制备方法及Lesinurad中间体 |
JP6470761B2 (ja) * | 2013-11-22 | 2019-02-13 | クリスタル ファーマテック カンパニー、リミテッドCrystal Pharmatech Co., Ltd. | レシヌラドおよびそのナトリウム塩の結晶形態 |
CN104557748A (zh) * | 2014-01-25 | 2015-04-29 | 广东东阳光药业有限公司 | 硫代-1,2,4-三唑衍生物的新的固体形态 |
CN105315218A (zh) * | 2014-07-17 | 2016-02-10 | 天津药物研究院 | 一种制备lesinurad中间体1-萘基三唑硫酮的方法 |
CN104341362B (zh) * | 2014-10-27 | 2016-07-13 | 张远强 | 三氮唑磺酰丙二酸类化合物、其制备方法及用途 |
CN104326998B (zh) * | 2014-10-27 | 2016-08-17 | 张远强 | 苯基取代的三氮唑丙二酸类化合物、其制备方法及用途 |
CN104326993B (zh) * | 2014-10-27 | 2016-08-17 | 张远强 | 一种硝基取代三氮唑亚磺酰丙二酸类化合物、其制备方法及用途 |
CN104341363B (zh) * | 2014-10-27 | 2016-08-17 | 张远强 | 一种硝基取代的三氮唑磺酰丙二酸类化合物、其制备方法及用途 |
CN104370842B (zh) * | 2014-10-27 | 2016-07-13 | 张远强 | 苯基取代的三氮唑磺酰丙二酸类化合物、其制备方法及用途 |
CN104341361B (zh) * | 2014-10-27 | 2017-01-11 | 张远强 | 一种腈基取代三氮唑亚磺酰丙二酸类化合物、其制备方法及用途 |
CN104370841B (zh) * | 2014-10-27 | 2016-07-13 | 张远强 | 三氮唑亚磺酰丙二酸类化合物、其制备方法及用途 |
CN104311498B (zh) * | 2014-10-27 | 2016-04-06 | 张远强 | 烷氧基取代的三氮唑磺酰丙二酸类化合物、其制备方法及用途 |
CN104327000B (zh) * | 2014-10-27 | 2016-08-17 | 张远强 | 苯基取代的三氮唑亚磺酰丙二酸类化合物、其制备方法及用途 |
EP3112334A1 (en) | 2015-06-29 | 2017-01-04 | DPx Fine Chemicals Austria GmbH & CoKG | Process for manufacturing 1-cyclopropyl-naphthalenes |
CN104987311A (zh) * | 2015-06-30 | 2015-10-21 | 安徽万邦医药科技有限公司 | 一种[4-(4-环丙基萘-1-基)-5-硝基- 4h-[1,2,4]三唑-3-基硫烷基]-乙酸乙酯的制备方法及其中间体(5-硝基-4h-[1,2,4]三唑-3-基硫基)-乙酸乙酯 |
CN105017168A (zh) * | 2015-07-01 | 2015-11-04 | 安徽万邦医药科技有限公司 | 一种[5-溴-4-(4-环丙基萘-1-基)-4h-[1,2,4]三唑-3-基硫烷基]-乙酸甲酯的新制备方法 |
CN105153056A (zh) * | 2015-07-01 | 2015-12-16 | 安徽万邦医药科技有限公司 | 一种[5-溴-4-(4-环丙基萘-1-基)-4h-[1,2,4]三唑-3-基硫烷基]-乙酸甲酯的新制备方法 |
WO2017036884A1 (en) | 2015-08-28 | 2017-03-09 | Sandoz Ag | A lesinurad, free form / lesinurad ethyl ester co-crystal |
CN105566237B (zh) * | 2016-03-01 | 2018-05-18 | 山东大学 | 一种治疗痛风的三唑巯乙酸类化合物的制备方法 |
EP3473617B1 (en) * | 2016-06-17 | 2022-09-07 | Medshine Discovery Inc. | Halogenated compound and axially chiral isomers thereof |
EP3281941B1 (en) | 2016-08-11 | 2019-07-24 | Zentiva K.S. | Process for preparing 2-(5-bromo-4-(1-cyclopropylnaphthalen-4-yl)-4h-1,2,4-triazol-3-ylthio)acetic acid |
EP3372592A1 (en) | 2017-03-07 | 2018-09-12 | Zentiva, k.s. | Solid forms of lesinurad amine salts |
US10351537B2 (en) * | 2017-03-10 | 2019-07-16 | Apotex Inc. | Processes for the preparation of lesinurad and intermediates thereof |
EP3315494A1 (en) | 2017-04-19 | 2018-05-02 | Química Sintética, S.A. | Amorphous form of lesinurad and processes for its preparation |
CN108947919B (zh) | 2017-05-17 | 2023-05-02 | 上海奥博生物医药股份有限公司 | 一种抗痛风药Lesinurad的新型制备方法及其关键中间体 |
WO2019001325A1 (zh) * | 2017-06-28 | 2019-01-03 | 苏州科睿思制药有限公司 | 雷西纳得的晶型xv及其制备方法 |
EP3498697A1 (en) | 2017-12-12 | 2019-06-19 | Química Sintética, S.A. | Novel salts and polymorphs of lesinurad |
DE112022002825T5 (de) | 2021-05-28 | 2024-03-14 | Sumitomo Chemical Company, Limited | Verfahren zur Herstellung von Cycloalkylbromid |
Family Cites Families (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US226186A (en) | 1880-04-06 | Car-coupling | ||
US2006A (en) * | 1841-03-16 | Clamp for crimping leather | ||
US2009A (en) * | 1841-03-18 | Improvement in machines for boring war-rockets | ||
US2008A (en) * | 1841-03-18 | Gas-lamp eok conducting gas pkom ah elevated buhner to one below it | ||
JPS5641637B2 (zh) | 1973-11-26 | 1981-09-29 | ||
US6832996B2 (en) * | 1995-06-07 | 2004-12-21 | Arthrocare Corporation | Electrosurgical systems and methods for treating tissue |
JPH07215940A (ja) | 1994-01-27 | 1995-08-15 | Torii Yakuhin Kk | 抗ウイルス活性を有する化合物 |
JP2000510164A (ja) | 1997-02-14 | 2000-08-08 | バイエル・コーポレーシヨン | 選択的神経ペプチドy受容体アンタゴニストとしてのアミド誘導体 |
US6245817B1 (en) * | 1997-02-14 | 2001-06-12 | Bayer Corporation | NPY5 receptor antagonists and methods for using same |
JPH10243033A (ja) * | 1997-02-28 | 1998-09-11 | Oki Electric Ind Co Ltd | 復調装置 |
ES2361146T3 (es) * | 1998-03-27 | 2011-06-14 | Janssen Pharmaceutica Nv | Derivados de la piramidina inhibitatoria de vih. |
PT1129096E (pt) | 1998-11-12 | 2003-09-30 | Neurocrine Biosciences Inc | Antagonistas de receptor de crf e metodos de tratamento relacionados com os mesmos |
WO2000037471A1 (en) * | 1998-12-23 | 2000-06-29 | Neurogen Corporation | 2-amino-9-alkylpurines: gaba brain receptor ligands |
CN1178913C (zh) * | 1998-12-25 | 2004-12-08 | 盐野义制药株式会社 | 具有hiv整合酶抑制活性的芳族杂环化合物 |
US6593077B2 (en) * | 1999-03-22 | 2003-07-15 | Special Materials Research And Technology, Inc. | Method of making thin films dielectrics using a process for room temperature wet chemical growth of SiO based oxides on a substrate |
PL364658A1 (en) | 2001-03-02 | 2004-12-13 | Smithkline Beecham Corporation | Benzophenones as inhibitors of reverse transcriptase |
JO3429B1 (ar) | 2001-08-13 | 2019-10-20 | Janssen Pharmaceutica Nv | مشتقات برميدينات مثبطة فيروس الايدز |
JP2005529923A (ja) | 2002-05-13 | 2005-10-06 | イーライ・リリー・アンド・カンパニー | 肥満および糖尿病の治療におけるメラニン凝集ホルモンアンタゴニストとして使用するための多環式化合物 |
EA009478B1 (ru) * | 2002-08-23 | 2008-02-28 | Ардеа Байосайенсиз, Инк. | Ненуклеозидные ингибиторы обратной транскриптазы |
US7642277B2 (en) | 2002-12-04 | 2010-01-05 | Boehringer Ingelheim International Gmbh | Non-nucleoside reverse transcriptase inhibitors |
PL227577B1 (pl) | 2003-02-07 | 2017-12-29 | Janssen Pharmaceutica Nv | Zastosowanie pochodnych pirymidyny do wytwarzania leku do zapobiegania zakażeniu wirusem HIV oraz kompozycja farmaceutyczna |
DE602004031641D1 (de) | 2003-09-25 | 2011-04-14 | Janssen Pharmaceutica Nv | Die replikation von hiv hemmende purinderivate |
US20080031901A1 (en) * | 2004-09-24 | 2008-02-07 | Abbott Laboratories | Sustained release monoeximic formulations of opioid and nonopioid analgesics |
US7517998B2 (en) | 2004-06-01 | 2009-04-14 | Boehringer Ingelheim International Gmbh | Non nucleoside reverse transcriptase inhibitors |
WO2007050087A1 (en) * | 2004-08-25 | 2007-05-03 | Ardea Biosciences, Inc. | N[S(4-aryl-triazol-3-yl)α -mercaptoacetyl]-p-amino benozoic acids AS HIV REVERSE TRANSCRIPTASE INHIBITORS |
EP2135608B8 (en) * | 2004-08-25 | 2012-03-21 | Ardea Biosciences, Inc. | S-triazolyl alpha -mercaptoacetanilides as inhibitors of HIV reverse transcriptase |
SI2217577T1 (sl) * | 2007-11-27 | 2014-11-28 | Ardea Biosciences, Inc. | Nove spojine in sestavki ter metode uporabe |
EP2349258A1 (en) | 2008-10-24 | 2011-08-03 | Ardea Biosciences, Inc. | Compositions comprising 4- (2- ( 5-br0m0-4- ( l-cyclopropylnaphthalen-4-yl) -4h-1, 2, 4-triazol-3-ylthio) acetamido -3-chlorobenzoic acid and pharmaceutically acceptable salts thereof |
WO2010048592A1 (en) | 2008-10-24 | 2010-04-29 | Ardea Biosciences, Inc. | Compositions comprising 4- (2- ( 5-br0m0-4- ( 1-cyclopropylnaphthalen-4-yl) -4h-1, 2, 4-triaz0l-3-ylthi0) acetamido -3-chlorobenzoic acid and pharmaceutically acceptable salts thereof |
TWM377707U (en) * | 2009-09-16 | 2010-04-01 | Nat Energy Technology Co Ltd | Assembly of power supply |
-
2005
- 2005-08-25 EP EP09170772A patent/EP2135608B8/en active Active
- 2005-08-25 KR KR1020077006746A patent/KR101241716B1/ko active IP Right Grant
- 2005-08-25 EA EA200700488A patent/EA014737B1/ru not_active IP Right Cessation
- 2005-08-25 SG SG2012083366A patent/SG185992A1/en unknown
- 2005-08-25 CN CN2005800363729A patent/CN101083987B/zh active Active
- 2005-08-25 ES ES09170772T patent/ES2374773T3/es active Active
- 2005-08-25 CA CA2578068A patent/CA2578068C/en active Active
- 2005-08-25 ES ES05790722T patent/ES2380604T3/es active Active
- 2005-08-25 BR BRPI0520870A patent/BRPI0520870B8/pt active IP Right Grant
- 2005-08-25 IN IN3762CHN2014 patent/IN2014CN03762A/en unknown
- 2005-08-25 EP EP11177941A patent/EP2402011B1/en active Active
- 2005-08-25 SI SI200531426T patent/SI2135608T1/sl unknown
- 2005-08-25 SG SG200905668-0A patent/SG155246A1/en unknown
- 2005-08-25 MX MX2007002236A patent/MX2007002236A/es active IP Right Grant
- 2005-08-25 EP EP11184025A patent/EP2433633A1/en not_active Withdrawn
- 2005-08-25 EA EA200901186A patent/EA015846B1/ru not_active IP Right Cessation
- 2005-08-25 CN CN200910205213.7A patent/CN101817793B/zh active Active
- 2005-08-25 EP EP12187096.8A patent/EP2609917A1/en not_active Withdrawn
- 2005-08-25 NZ NZ581376A patent/NZ581376A/en not_active IP Right Cessation
- 2005-08-25 BR BRPI0514630A patent/BRPI0514630B8/pt active IP Right Grant
- 2005-08-25 EP EP05790722A patent/EP1789039B1/en active Active
- 2005-08-25 PL PL09170772T patent/PL2135608T3/pl unknown
- 2005-08-25 WO PCT/US2005/030259 patent/WO2006026356A2/en active Application Filing
- 2005-08-25 US US11/661,079 patent/US7947721B2/en active Active
- 2005-08-25 DK DK09170772.9T patent/DK2135608T3/da active
- 2005-08-25 PT PT09170772T patent/PT2135608E/pt unknown
- 2005-08-25 NZ NZ553534A patent/NZ553534A/en not_active IP Right Cessation
- 2005-08-25 AT AT09170772T patent/ATE528001T1/de active
- 2005-08-25 RS RS20130029A patent/RS52632B/en unknown
- 2005-08-25 JP JP2007530127A patent/JP4952943B2/ja active Active
- 2005-08-25 ME MEP-2013-18A patent/ME01512B/me unknown
- 2005-08-25 AT AT05790722T patent/ATE540677T1/de active
- 2005-08-25 AU AU2005280130A patent/AU2005280130C9/en active Active
-
2007
- 2007-02-22 IL IL181523A patent/IL181523A/en active IP Right Grant
- 2007-03-15 EC EC2007007322A patent/ECSP077322A/es unknown
-
2009
- 2009-09-23 AU AU2009217458A patent/AU2009217458B2/en active Active
- 2009-10-15 IL IL201546A patent/IL201546A/en not_active IP Right Cessation
- 2009-11-13 US US12/618,604 patent/US20100069645A1/en not_active Abandoned
- 2009-12-08 US US12/633,638 patent/US8003681B2/en active Active
-
2010
- 2010-01-22 HK HK10100716.1A patent/HK1133582A1/xx unknown
-
2011
- 2011-04-06 US US13/081,398 patent/US8946273B2/en active Active
- 2011-06-30 US US13/174,538 patent/US8252828B2/en active Active
-
2012
- 2012-01-05 JP JP2012000790A patent/JP5457472B2/ja active Active
- 2012-01-11 CY CY20121100023T patent/CY1112221T1/el unknown
- 2012-04-15 IL IL219131A patent/IL219131A0/en unknown
- 2012-07-18 US US13/552,443 patent/US8481581B2/en active Active
-
2013
- 2013-01-29 HR HRP20130075TT patent/HRP20130075T1/hr unknown
-
2014
- 2014-12-03 US US14/559,803 patent/US20150094284A1/en not_active Abandoned
-
2016
- 2016-07-26 LT LTPA2016024C patent/LTC2135608I2/lt unknown
- 2016-07-28 NL NL300825C patent/NL300825I2/nl unknown
- 2016-07-29 FR FR16C0031C patent/FR16C0031I2/fr active Active
- 2016-08-10 CY CY2016028C patent/CY2016028I2/el unknown
- 2016-08-10 LU LU93169C patent/LU93169I2/fr unknown
- 2016-08-17 HU HUS1600034C patent/HUS1600034I1/hu unknown
-
2017
- 2017-02-16 US US15/435,119 patent/US20180002296A1/en not_active Abandoned
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
FR16C0031I1 (zh) | ||
GB2371066B8 (en) | Tubulars with expandable cells and locking mechanisms | |
WO2005032488A3 (en) | 2,4-dioxo-3-quinazolinylaryl sulfonylureas | |
WO2003037864A1 (fr) | Compose indolique, et utilisation a des fins therapeutiques | |
DE602005011031D1 (en) | Phosphoindole als hiv-inhibitoren | |
AU2003243765A8 (en) | 2,4-disubstituted-pyridine n-oxides useful as hiv reverse transcriptase inhibitors | |
USD522907S1 (en) | Gemstone (I) | |
USD483954S1 (en) | Fabric | |
UA89200C2 (ru) | S-ТРИАЗОЛИЛ-б-МЕРКАПТОАЦЕТАНИЛИДЫ КАК ИНГИБИТОРЫ ОБРАТНОЙ ТРАНСКРИПТАЗЫ ВИЧ | |
DK1399142T3 (da) | Anvendelse af acetyl-L-carnitin i kombination med biotin til behandlingen af patienter med type-2 insulinresistent diabetes mellitus | |
USD521586S1 (en) | Billiard table | |
USD475098S1 (en) | Craft kit construction component—leg form | |
WO2004096147A3 (en) | Oxo-pyrimidine compounds | |
USD472406S1 (en) | Table | |
AR028458A1 (es) | Un estuche de combinacion usado en el tratamiento del paludismo | |
RU2006146820A (ru) | Средство связи | |
TH54449EX (th) | อุปกรณ์ควบคุมไร้สาย | |
JP2003334596A5 (zh) | ||
AP2005003429A0 (en) | 5,7-Diaminopyrazolo Ä4,3-DÜ pyrimidines useful in the treatment of hypertension. |