EA201270666A1 - Соединения и фармацевтические композиции для снижения уровня мочевой кислоты - Google Patents
Соединения и фармацевтические композиции для снижения уровня мочевой кислотыInfo
- Publication number
- EA201270666A1 EA201270666A1 EA201270666A EA201270666A EA201270666A1 EA 201270666 A1 EA201270666 A1 EA 201270666A1 EA 201270666 A EA201270666 A EA 201270666A EA 201270666 A EA201270666 A EA 201270666A EA 201270666 A1 EA201270666 A1 EA 201270666A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- compounds
- uric acid
- pharmaceutical compositions
- acid level
- reducing uric
- Prior art date
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- 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
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- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7068—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
- A61K31/7072—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid having two oxo groups directly attached to the pyrimidine ring, e.g. uridine, uridylic acid, thymidine, zidovudine
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- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7076—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid
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Abstract
Изобретение относится к соединениям общей формулы (I), которые пригодны для модулирования уровня мочевой кислоты в крови, лекарственным составам, содержащим эти соединения, и их применению. В некоторых вариантах осуществления настоящего изобретения соединения, описанные в настоящем документе, применяются для лечения или предупреждения заболеваний, связанных с аномальным уровнем мочевой кислоты.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US99057407P | 2007-11-27 | 2007-11-27 | |
US9438808P | 2008-09-04 | 2008-09-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
EA201270666A1 true EA201270666A1 (ru) | 2012-12-28 |
Family
ID=40679222
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA201000897A EA018193B3 (ru) | 2007-11-27 | 2008-11-26 | Соединения и фармацевтические композиции для снижения уровня мочевой кислоты |
EA201270666A EA201270666A1 (ru) | 2007-11-27 | 2008-11-26 | Соединения и фармацевтические композиции для снижения уровня мочевой кислоты |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA201000897A EA018193B3 (ru) | 2007-11-27 | 2008-11-26 | Соединения и фармацевтические композиции для снижения уровня мочевой кислоты |
Country Status (36)
Country | Link |
---|---|
US (8) | US8084483B2 (ru) |
EP (2) | EP2217577B1 (ru) |
JP (3) | JP5099794B2 (ru) |
KR (2) | KR101291643B1 (ru) |
CN (3) | CN101918377A (ru) |
AR (1) | AR069753A1 (ru) |
AU (2) | AU2008329673C1 (ru) |
BR (1) | BRPI0819847B1 (ru) |
CA (1) | CA2706858C (ru) |
CL (1) | CL2008003529A1 (ru) |
CY (1) | CY2019010I1 (ru) |
DK (1) | DK2217577T3 (ru) |
EA (2) | EA018193B3 (ru) |
EC (1) | ECSP10010310A (ru) |
ES (1) | ES2513390T3 (ru) |
HK (2) | HK1180337A1 (ru) |
HR (1) | HRP20140950T1 (ru) |
HU (1) | HUS1900009I1 (ru) |
IL (1) | IL205974A (ru) |
LT (1) | LTPA2019003I1 (ru) |
LU (1) | LUC00103I2 (ru) |
MA (1) | MA31936B1 (ru) |
ME (2) | ME01294B (ru) |
MX (1) | MX2010005776A (ru) |
MY (1) | MY147370A (ru) |
NO (1) | NO2016016I2 (ru) |
NZ (4) | NZ601786A (ru) |
PL (1) | PL2217577T3 (ru) |
PT (1) | PT2217577E (ru) |
RS (1) | RS53569B1 (ru) |
SG (1) | SG183721A1 (ru) |
SI (1) | SI2217577T1 (ru) |
TN (1) | TN2010000237A1 (ru) |
TW (1) | TWI415840B (ru) |
WO (1) | WO2009070740A2 (ru) |
ZA (1) | ZA201003769B (ru) |
Families Citing this family (97)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SG185992A1 (en) | 2004-08-25 | 2012-12-28 | Ardea Biosciences Inc | S-TRIAZOLYL α-MERCAPTOACETANILIDES AS INHIBITORS OF HIV REVERSE TRANSCRIPTASE |
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 |
AR069753A1 (es) | 2007-11-27 | 2010-02-17 | Ardea Biosciences Inc | Compuestos de 1,2,4-triazol y composiciones, utiles en la modulacion de los niveles de acido urico sanguineo |
US8173690B2 (en) * | 2008-09-04 | 2012-05-08 | Ardea Biosciences, Inc. | Compounds, compositions and methods of using same for modulating uric acid levels |
US8242154B2 (en) | 2008-09-04 | 2012-08-14 | Ardea Biosciences, Inc. | Compounds, compositions and methods of using same for modulating uric acid levels |
CA2736117C (en) * | 2008-09-04 | 2013-11-19 | Ardea Biosciences, Inc. | Compounds, compositions and methods of using same for modulating uric acid levels |
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 |
WO2010048593A1 (en) * | 2008-10-24 | 2010-04-29 | 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 |
WO2010071865A1 (en) | 2008-12-19 | 2010-06-24 | Nuon Therapeutics, Inc. | Pharmaceutical compositions and methods for treating hyperuricemia and related disorders |
US20100160351A1 (en) * | 2008-12-19 | 2010-06-24 | Nuon Therapeutics, Inc. | Pharmaceutical compositions and methods for treating hyperuricemia and related disorders |
EP2432774A4 (en) * | 2009-05-20 | 2013-01-02 | Ardea Biosciences Inc | COMPOUNDS, COMPOSITIONS AND METHODS FOR MODULATING URIC ACID RATES |
EP2432468A2 (en) | 2009-05-20 | 2012-03-28 | Ardea Biosciences, Inc. | Methods of modulating uric acid levels |
CN102741234B (zh) * | 2010-01-08 | 2015-11-25 | 亚德生化公司 | 2-(5-溴-4-(4-环丙基萘-1-基)-4h-1,2,4-***-3-基硫基)乙酸钠的多晶型、结晶型及中间相型与其用途 |
EP2560642A4 (en) * | 2010-03-30 | 2013-12-18 | Ardea Biosciences Inc | TREATMENT OF GICHT |
ES2670700T3 (es) * | 2010-06-15 | 2018-05-31 | Ardea Biosciences, Inc. | Tratamiento de gota e hiperuricemia |
JP5709146B2 (ja) * | 2010-06-16 | 2015-04-30 | アルデア バイオサイエンシーズ インク. | フェニルチオ酢酸化合物、組成物、および、その使用方法 |
AR081930A1 (es) | 2010-06-16 | 2012-10-31 | Ardea Biosciences Inc | Compuestos de tioacetato |
CA2813555C (en) * | 2010-10-15 | 2014-11-25 | Ardea Biosciences, Inc. | Methods for treating hyperuricemia and related diseases |
WO2012056442A1 (en) * | 2010-10-28 | 2012-05-03 | Mapi Pharma Holdings (Cyprus) Limited | Polymorphs of febuxostat |
EP2658846B1 (en) | 2010-12-30 | 2016-12-14 | Ardea Biosciences, Inc. | Polymorphic forms of 2-(5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-4h-1,2,4-triazol-3-ylthio) acetic acid and uses thereof |
WO2012122532A2 (en) * | 2011-03-09 | 2012-09-13 | Biocryst Pharmaceuticals, Inc. | Compositions and methods for treatment of hyperuricemia |
EP2714669B1 (en) * | 2011-05-24 | 2017-04-26 | Ardea Biosciences, Inc. | Hypertension and hyperuricemia |
EP2567959B1 (en) | 2011-09-12 | 2014-04-16 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
EA026101B1 (ru) | 2011-11-03 | 2017-03-31 | Ардеа Биосайнсиз, Инк. | Применение 3,4-дизамещенного пиридинового соединения для снижения уровня мочевой кислоты в сыворотке крови |
US9060987B2 (en) | 2011-11-04 | 2015-06-23 | Cymabay Therapeutics, Inc. | Methods for treating gout flares |
US9023856B2 (en) | 2011-11-04 | 2015-05-05 | Cymabay Therapeutics, Inc. | Methods for treating hyperuricemia in patients with gout using halofenate or halogenic acid and a second urate-lowering agent |
BR112014010729A2 (pt) * | 2011-11-04 | 2018-03-20 | Cymabay Therapeutics Inc | métodos para tratamento de ataques de gota |
CN104066323A (zh) * | 2011-11-04 | 2014-09-24 | 西玛贝医药公司 | 用于治疗患者亚群中痛风的方法 |
MX2014008484A (es) * | 2012-01-27 | 2014-10-14 | Teijin Pharma Ltd | Agente terapeutico para la diabetes mellitus. |
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 |
HUE037736T2 (hu) * | 2012-11-14 | 2018-09-28 | Teijin Pharma Ltd | Piridin származékok |
CN102973530B (zh) * | 2012-12-14 | 2016-08-03 | 贵州信邦制药股份有限公司 | 一种非布索坦双层肠溶片剂及其制备方法 |
TR201807104T4 (tr) | 2013-05-13 | 2018-06-21 | Jiangsu Hengrui Medicine Co | Sikloalkil asit türevi, bunun hazırlanış yöntemi ve farmasötik uygulaması. |
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 |
CN104447589B (zh) * | 2013-11-20 | 2017-01-11 | 广东东阳光药业有限公司 | 一种尿酸调节剂的制备方法及其中间体 |
CN103588716A (zh) * | 2013-11-22 | 2014-02-19 | 苏州晶云药物科技有限公司 | 2-(5-溴-4-(4-环丙基萘-1-基)-4h-1,2,4-***-3-基硫基)乙酸的新晶型及其制备方法 |
ES2704198T3 (es) * | 2013-11-22 | 2019-03-14 | Crystal Pharmatech Co Ltd | Formas cristalinas de lesinurad |
CN103613552A (zh) * | 2013-12-02 | 2014-03-05 | 苏州晶云药物科技有限公司 | 2-(5-溴-4-(4-环丙基萘-1-基)-4h-1,2,4-***-3-基硫基)乙酸钠的新晶型及其制备方法 |
CN103626710A (zh) * | 2013-12-20 | 2014-03-12 | 苏州晶云药物科技有限公司 | 2-(5-溴-4-(4-环丙基萘-1-基)-4h-1,2,4-***-3-基硫基)乙酸的共晶及其制备方法 |
US9969701B2 (en) * | 2013-12-20 | 2018-05-15 | Crystal Pharmatech Co., Ltd. | Salts and co-crystals of lesinurad |
CN103755651A (zh) * | 2013-12-23 | 2014-04-30 | 苏州晶云药物科技有限公司 | 2-(5-溴-4-(4-环丙基萘-1-基)-4h-1,2,4-***-3-基硫基)乙酸的盐的新晶型及其制备方法 |
CN105294585B (zh) * | 2014-07-02 | 2019-02-12 | 成都海创药业有限公司 | 一种治疗痛风的化合物 |
CN104068288B (zh) * | 2014-07-25 | 2016-08-24 | 许伟琦 | 一种防***的饲料添加剂 |
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 |
CN104326994A (zh) * | 2014-10-27 | 2015-02-04 | 张远强 | 一种腈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 |
CN104341365A (zh) * | 2014-10-27 | 2015-02-11 | 张远强 | 卤代三氮唑丙二酸类化合物、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 |
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 |
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 |
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 |
CN104326996A (zh) * | 2014-10-27 | 2015-02-04 | 张远强 | 一种硝基取代三氮唑丙二酸类化合物、其制备方法及用途 |
CN104326995A (zh) * | 2014-10-27 | 2015-02-04 | 张远强 | 一种腈基取代的三氮唑丙二酸类化合物、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 |
CN104341364A (zh) * | 2014-10-27 | 2015-02-11 | 张远强 | 三氮唑丙二酸类化合物、其制备方法及用途 |
CN104529848A (zh) * | 2014-11-10 | 2015-04-22 | 安徽万邦医药科技有限公司 | 一种1-环丙基-4-异硫氰酰基萘的合成方法 |
EP3915542B1 (en) | 2014-12-23 | 2023-11-22 | Dyve Biosciences, Inc. | Formulations for transdermal administration |
WO2016108282A1 (ja) * | 2014-12-29 | 2016-07-07 | 日本ケミファ株式会社 | Urat1阻害剤 |
CN105985295B (zh) * | 2015-02-17 | 2018-11-20 | 华润赛科药业有限责任公司 | 一种旋光纯的硫代乙酸类化合物 |
CN105622531A (zh) | 2015-04-03 | 2016-06-01 | 南京明德新药研发股份有限公司 | 轴手性异构体及其制备方法和制药用途 |
CN104710374A (zh) * | 2015-04-14 | 2015-06-17 | 安徽省逸欣铭医药科技有限公司 | 一种痛风新化合物及制备方法、用途及其药物制剂 |
CN106187926B (zh) * | 2015-04-30 | 2018-11-27 | 天津药物研究院有限公司 | 含二芳基甲烷结构的羧酸类urat1抑制剂、制备方法及其在高尿酸血症和痛风治疗上的用途 |
WO2016203436A1 (en) * | 2015-06-19 | 2016-12-22 | Dr. Reddy's Laboratories Limited | Amorphous and amorphous solid dispersion of lesinurad and their preparation |
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]***-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]***-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]***-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]***-3-基硫烷基]-乙酸甲酯的新制备方法 |
RU2728722C2 (ru) * | 2015-08-26 | 2020-07-30 | Стаджен Ко., Лтд. | Усилитель внутриклеточного атф |
WO2017036884A1 (en) | 2015-08-28 | 2017-03-09 | Sandoz Ag | A lesinurad, free form / lesinurad ethyl ester co-crystal |
CN105301126B (zh) * | 2015-10-10 | 2021-02-12 | 大道隆达(北京)医药科技发展有限公司 | 一种托匹司他有关物质的分析方法 |
EP3380970B1 (en) | 2015-11-24 | 2023-01-04 | Sanford Burnham Prebys Medical Discovery Institute | Novel azole derivatives as apelin receptor agonist |
JP6898330B2 (ja) | 2015-12-28 | 2021-07-07 | シャンハイ フォチョン ファーマシューティカル カンパニー リミテッド | インドリジン誘導体、組成物、及び使用方法 |
US20170319552A1 (en) * | 2016-02-24 | 2017-11-09 | Ardea Biosciences, Inc. | Atropisomers of triazole derivative |
CN107176930B (zh) * | 2016-03-11 | 2020-12-01 | 广东赛烽医药科技有限公司 | 2-[5-溴-4-(4-氟代环丙基萘-1-基)-4h-1,2,4-***-3-基硫基]乙酸化合物及其应用 |
CN107337649B (zh) * | 2016-04-29 | 2020-10-16 | 四川科伦药物研究院有限公司 | 一种乙酸钠水合物无定型及其制备方法和用途 |
CN109790155B (zh) * | 2016-05-23 | 2022-02-18 | 东宝紫星(杭州)生物医药有限公司 | 噻吩化合物及其合成方法和其在医药上的应用 |
CN106074540B (zh) * | 2016-06-10 | 2018-10-16 | 江西博屾医疗器械有限公司 | 一种用于高尿酸血症治疗的药物组合物及其应用 |
JP7050009B2 (ja) * | 2016-06-17 | 2022-04-07 | メッドシャイン ディスカバリー インコーポレイテッド | ハロゲン化合物およびその軸性キラリティ異性体 |
CN105943552A (zh) * | 2016-06-17 | 2016-09-21 | 王枝宝 | 一种氢氧化钾的医药用途 |
CN106083847B (zh) * | 2016-08-03 | 2018-10-30 | 山东大学 | 一种咪唑并吡啶巯乙酸类衍生物及其制备方法与应用 |
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 |
CZ307277B6 (cs) * | 2016-09-30 | 2018-05-09 | Zentiva, K.S. | Způsob výroby 2-(5-brom-4-(1-cyklopropylnaftalen-4-yl)-4H-1,2,4-triazol-3-ylthio)octové kyseliny - lesinuradu |
CN108014108A (zh) * | 2016-11-03 | 2018-05-11 | 江苏万邦生化医药股份有限公司 | lesinurad或其医药上可接受的盐在制备治疗或预防库欣综合征的药物中的应用 |
CA3042738A1 (en) | 2016-11-10 | 2018-05-17 | Apotex Inc. | Novel crystalline forms of lesinurad |
CN110121359A (zh) | 2016-11-11 | 2019-08-13 | 怀特黑德生物制剂研究所 | 人血浆培养基 |
CN108164471B (zh) * | 2016-12-07 | 2019-09-13 | 浙江京新药业股份有限公司 | Lesinurad衍生物及其制备方法和用途 |
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 |
US10538808B2 (en) | 2017-05-26 | 2020-01-21 | Vibrant Holdings, Llc | Photoactive compounds and methods for biomolecule detection and sequencing |
JP2020534285A (ja) | 2017-09-15 | 2020-11-26 | アンパサンド バイオファーマシューティカルズ インコーポレイテッドAmpersand Biopharmaceuticals Inc. | 投与および処置の方法 |
NZ765226A (en) | 2017-11-23 | 2022-11-25 | Medshine Discovery Inc | Crystal form of urat1 inhibitor, and preparation method therefor |
EP3498697A1 (en) | 2017-12-12 | 2019-06-19 | Química Sintética, S.A. | Novel salts and polymorphs of lesinurad |
KR102660247B1 (ko) * | 2017-12-15 | 2024-04-25 | 지앙수 카니온 파마수티컬 씨오., 엘티디. | 4-(나프탈렌-1-일)-4h-1, 2, 4-트리아졸계 화합물의 결정 형태, 염 형태 및 이의 제조방법 |
CN109369783B (zh) * | 2018-11-30 | 2021-09-10 | 昆明医科大学 | 一种多肽rdp1及其提纯方法与应用 |
CN111320588B (zh) * | 2018-12-14 | 2024-02-09 | 上海奥博生物医药股份有限公司 | 一种纯化Lesinurad的方法 |
Family Cites Families (50)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2006101A (en) | 1932-07-05 | 1935-06-25 | Meaf Mach En Apparaten Fab Nv | Reversing mechanism for dry gas meters |
NL7112373A (ru) * | 1970-09-25 | 1972-03-28 | ||
US4198513A (en) | 1970-09-25 | 1980-04-15 | Merck & Co., Inc. | 1,2,4-Triazoles |
JPS5641637B2 (ru) | 1973-11-26 | 1981-09-29 | ||
US4889868A (en) | 1984-12-20 | 1989-12-26 | Rorer Pharmaceutical Corporation | Bis-imidazolinoamino derivatives as antiallergy compounds |
US5260322A (en) * | 1990-10-08 | 1993-11-09 | Merck & Co., Inc. | Angiotension II antagonists in the treatment of hyperuricemia |
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 |
WO1995029897A1 (en) | 1994-04-29 | 1995-11-09 | G.D. Searle & Co. | METHOD OF USING (H+/K+) ATPase INHIBITORS AS ANTIVIRAL AGENTS |
JP3964478B2 (ja) | 1995-06-30 | 2007-08-22 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | ヘテロ環含有カルボン酸誘導体及びそれを含有する医薬 |
US6017925A (en) | 1997-01-17 | 2000-01-25 | Merck & Co., Inc. | Integrin antagonists |
US6245817B1 (en) | 1997-02-14 | 2001-06-12 | Bayer Corporation | NPY5 receptor antagonists and methods for using same |
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 |
BRPI9909191B8 (pt) | 1998-03-27 | 2021-07-06 | Janssen Pharmaceutica Nv | derivados de pirimidina inibidores do hiv, seu uso e composição farmacêutica que os compreende |
WO2000027850A2 (en) | 1998-11-12 | 2000-05-18 | Neurocrine Biosciences, Inc. | Crf receptor antagonists and methods relating thereto |
WO2000037471A1 (en) | 1998-12-23 | 2000-06-29 | Neurogen Corporation | 2-amino-9-alkylpurines: gaba brain receptor ligands |
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 |
US6624194B1 (en) * | 1999-06-04 | 2003-09-23 | Metabolex, Inc. | Use of (−) (3-trihalomethylphenoxy) (4-halophenyl) acetic acid derivatives for treatment of insulin resistance, type 2 diabetes, hyperlipidemia and hyperuricemia |
NZ527864A (en) | 2001-03-02 | 2004-05-28 | Smithkline Beecham Corp | Benzophenones as inhibitors of reverse transcriptase |
JO3429B1 (ar) | 2001-08-13 | 2019-10-20 | Janssen Pharmaceutica Nv | مشتقات برميدينات مثبطة فيروس الايدز |
US7074816B2 (en) * | 2002-01-28 | 2006-07-11 | Fuji Yakuhin Co., Ltd. | 1 2 4-triazole compound |
CA2484233A1 (en) | 2002-05-13 | 2003-11-27 | Eli Lilly And Company | Multicyclic compounds for use as melanin concentrating hormone antagonists in the treatment of obesity and diabetes |
JP4413781B2 (ja) | 2002-08-23 | 2010-02-10 | アーディア・バイオサイエンシーズ・インコーポレイテッド | 非ヌクレオシド逆転写酵素インヒビター |
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 |
EP1668011B1 (en) | 2003-09-25 | 2011-03-02 | Janssen Pharmaceutica NV | Hiv replication inhibiting purine derivatives |
US20080031901A1 (en) * | 2004-09-24 | 2008-02-07 | Abbott Laboratories | Sustained release monoeximic formulations of opioid and nonopioid analgesics |
EP1698348A4 (en) | 2003-11-14 | 2008-02-27 | Human Cell Systems Inc | CURATIVE OR PREVENTIVE REMEDY FOR VASCULAR DISORDERS AND HYPERTENSION AND SCREENING METHOD THEREOF |
US20050250794A1 (en) | 2003-12-19 | 2005-11-10 | Andrew Napper | Methods of treating a disorder |
CN1934095A (zh) * | 2004-03-08 | 2007-03-21 | 惠氏公司 | 离子通道调节剂 |
BRPI0508537A (pt) * | 2004-03-08 | 2007-08-14 | Wyeth Corp | moduladores do canal de ìon |
JP2008500357A (ja) | 2004-05-25 | 2008-01-10 | メタボレックス インコーポレーティッド | Pparのモジュレーターとしての置換されたトリアゾールおよびこれらの調製方法 |
US20060013556A1 (en) | 2004-07-01 | 2006-01-19 | Thomas Poslinski | Commercial information and guide |
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 |
SG185992A1 (en) | 2004-08-25 | 2012-12-28 | Ardea Biosciences Inc | S-TRIAZOLYL α-MERCAPTOACETANILIDES AS INHIBITORS OF HIV REVERSE TRANSCRIPTASE |
GB0422057D0 (en) | 2004-10-05 | 2004-11-03 | Astrazeneca Ab | Novel compounds |
US7947707B2 (en) * | 2005-10-07 | 2011-05-24 | Kissei Pharmaceutical Co., Ltd. | Nitrogenated heterocyclic compound and pharmaceutical composition comprising the same |
WO2007077042A1 (en) | 2006-01-06 | 2007-07-12 | Topotarget Switzerland Sa | New method for the treatment of gout or pseudogout |
JP2009530399A (ja) | 2006-03-22 | 2009-08-27 | シンデクサ ファーマシューティカルズ コーポレーション | Erストレスに関連する疾病の治療のための化合物及び方法 |
AU2007267843B2 (en) | 2006-05-25 | 2011-10-13 | Synta Pharmaceuticals Corp. | Method for treating proliferative disorders associated with protooncogene products |
EP2026797A2 (en) | 2006-05-25 | 2009-02-25 | Synta Pharmaceuticals Corporation | Method for treating non-hodgkin's lymphoma |
AU2007292816B2 (en) | 2006-09-07 | 2011-11-17 | Amgen Inc. | Benzo-fused compounds for use in treating metabolic disorders |
EP1939181A1 (en) | 2006-12-27 | 2008-07-02 | sanofi-aventis | Heteroaryl-substituted carboxamides and use thereof for the stimulation of the expression of NO synthase |
EP2120956A4 (en) | 2007-01-19 | 2010-01-20 | Takeda Pharmaceuticals North A | METHODS FOR PREVENTING OR REDUCING THE NUMBER OF DROUGHT ERYTHEMES USING XANTHINE OXYDOREDUCTASE INHIBITORS AND INFLAMMATORY AGENTS |
AR069753A1 (es) | 2007-11-27 | 2010-02-17 | Ardea Biosciences Inc | Compuestos de 1,2,4-triazol y composiciones, utiles en la modulacion de los niveles de acido urico sanguineo |
US8173690B2 (en) * | 2008-09-04 | 2012-05-08 | Ardea Biosciences, Inc. | Compounds, compositions and methods of using same for modulating uric acid levels |
US8242154B2 (en) * | 2008-09-04 | 2012-08-14 | Ardea Biosciences, Inc. | Compounds, compositions and methods of using same for modulating uric acid levels |
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 |
WO2010071865A1 (en) | 2008-12-19 | 2010-06-24 | Nuon Therapeutics, Inc. | Pharmaceutical compositions and methods for treating hyperuricemia and related disorders |
EP2714669B1 (en) | 2011-05-24 | 2017-04-26 | Ardea Biosciences, Inc. | Hypertension and hyperuricemia |
-
2008
- 2008-11-26 AR ARP080105142A patent/AR069753A1/es unknown
- 2008-11-26 EP EP08853900.2A patent/EP2217577B1/en active Active
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