JP2011519865A5 - - Google Patents

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Publication number
JP2011519865A5
JP2011519865A5 JP2011507641A JP2011507641A JP2011519865A5 JP 2011519865 A5 JP2011519865 A5 JP 2011519865A5 JP 2011507641 A JP2011507641 A JP 2011507641A JP 2011507641 A JP2011507641 A JP 2011507641A JP 2011519865 A5 JP2011519865 A5 JP 2011519865A5
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JP
Japan
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carbon atoms
group
compound
ring
pharmaceutical composition
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JP2011507641A
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English (en)
Japanese (ja)
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JP2011519865A (ja
JP5431457B2 (ja
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Priority claimed from PCT/US2009/042298 external-priority patent/WO2009134995A2/en
Publication of JP2011519865A publication Critical patent/JP2011519865A/ja
Publication of JP2011519865A5 publication Critical patent/JP2011519865A5/ja
Application granted granted Critical
Publication of JP5431457B2 publication Critical patent/JP5431457B2/ja
Expired - Fee Related legal-status Critical Current
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JP2011507641A 2008-04-30 2009-04-30 尿酸を減少させるテトラゾール化合物 Expired - Fee Related JP5431457B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US4916708P 2008-04-30 2008-04-30
US61/049,167 2008-04-30
US9374308P 2008-09-03 2008-09-03
US61/093,743 2008-09-03
PCT/US2009/042298 WO2009134995A2 (en) 2008-04-30 2009-04-30 Tetrazole compounds for reducing uric acid

Publications (3)

Publication Number Publication Date
JP2011519865A JP2011519865A (ja) 2011-07-14
JP2011519865A5 true JP2011519865A5 (cg-RX-API-DMAC7.html) 2013-04-11
JP5431457B2 JP5431457B2 (ja) 2014-03-05

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ID=41255799

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2011507641A Expired - Fee Related JP5431457B2 (ja) 2008-04-30 2009-04-30 尿酸を減少させるテトラゾール化合物

Country Status (15)

Country Link
US (2) US8410154B2 (cg-RX-API-DMAC7.html)
EP (1) EP2282736B1 (cg-RX-API-DMAC7.html)
JP (1) JP5431457B2 (cg-RX-API-DMAC7.html)
KR (1) KR101613611B1 (cg-RX-API-DMAC7.html)
CN (1) CN102014898B (cg-RX-API-DMAC7.html)
AU (1) AU2009243028B2 (cg-RX-API-DMAC7.html)
BR (1) BRPI0910541B8 (cg-RX-API-DMAC7.html)
CA (1) CA2722624C (cg-RX-API-DMAC7.html)
ES (1) ES2561039T3 (cg-RX-API-DMAC7.html)
IL (1) IL209004A (cg-RX-API-DMAC7.html)
MX (1) MX2010011603A (cg-RX-API-DMAC7.html)
NZ (1) NZ588374A (cg-RX-API-DMAC7.html)
RU (1) RU2522458C2 (cg-RX-API-DMAC7.html)
WO (1) WO2009134995A2 (cg-RX-API-DMAC7.html)
ZA (1) ZA201006929B (cg-RX-API-DMAC7.html)

Families Citing this family (15)

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BRPI0924547B1 (pt) 2008-03-13 2021-08-17 Wellstat Therapeutics Corporation Composto ácido 2-(3-(2,6-dimetilbenzilóxi)-4-metilfenil)acético, sua composição, bem como seu uso
AU2009243028B2 (en) 2008-04-30 2015-01-29 Wellstat Therapeutics Corporation Tetrazole compounds for reducing uric acid
CN102573462B (zh) * 2009-10-13 2014-04-16 维尔斯达医疗公司 用于降低尿酸的3位取代的化合物
US20130331452A1 (en) * 2010-09-08 2013-12-12 Wellstat Therapeutics Corporation Benzoic acid compounds for reducing uric acid
EP3501520A1 (en) * 2011-11-03 2019-06-26 Ardea Biosciences, Inc. 3,4-di-substituted pyridine compound, methods of using and compositions comprising the same
CA2859693C (en) * 2011-11-04 2018-05-22 Cymabay Therapeutics, Inc. Methods for treating gout flares
MX2014008484A (es) * 2012-01-27 2014-10-14 Teijin Pharma Ltd Agente terapeutico para la diabetes mellitus.
TW201443025A (zh) * 2013-04-19 2014-11-16 Pfizer Ltd 化學化合物
CN104292176B (zh) * 2014-10-07 2016-06-29 张远强 一种含卤代苯的四氮唑乙酸类化合物、其制备方法和用途
CN104292177B (zh) * 2014-10-07 2016-08-17 张远强 含腈基和卤苯取代的四氮唑乙酸类化合物、其制备方法及用途
CN104262277B (zh) * 2014-10-07 2016-06-22 张远强 含硝基和卤苯取代的四氮唑乙酸类化合物、其制备方法及用途
JP6192142B2 (ja) * 2016-09-13 2017-09-06 サイマベイ・セラピューティクス・インコーポレイテッドCymaBay Therapeutics,Inc. 痛風発赤の治療方法
RU2683570C1 (ru) * 2018-05-23 2019-03-29 Евгений Иванович Верещагин Композиция из растительных компонентов, обладающая способностью снижать уровень мочевой кислоты сыворотки крови
CN111943957B (zh) * 2019-05-17 2023-01-06 中国医学科学院药物研究所 喹啉甲酰胺类化合物及其制备方法和用途
CN114805233A (zh) * 2022-03-30 2022-07-29 华南理工大学 苯基四氮唑类xor抑制剂及其制备方法与应用

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US4024253A (en) 1973-04-20 1977-05-17 Zaidan Hojin Biseibutsu Kagaku Kenkyu Kai Treatment of elevated histamine and uric acid levels
US4182764A (en) * 1973-10-11 1980-01-08 Merck & Co., Inc. Tetrazole derivatives of [1-oxo-2-aryl or thienyl-2-substituted-5-indanyloxy(or thio)]alkanoic acids
US4874777A (en) 1987-04-10 1989-10-17 Eli Lilly And Company Leukotriene antagonists
US4845231A (en) 1988-02-12 1989-07-04 American Home Products Corporation Tetrazoles and their use as hypoglycemic agents
FR2631827B1 (fr) 1988-05-27 1992-03-27 Delalande Sa Nouveaux derives d'(hetero)aryl-5 tetrazole, leur procede de preparation et leur application en therapeutique
US5260322A (en) 1990-10-08 1993-11-09 Merck & Co., Inc. Angiotension II antagonists in the treatment of hyperuricemia
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JP2002503202A (ja) 1996-02-02 2002-01-29 メルク エンド カンパニー インコーポレーテッド 抗糖尿病薬
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BRPI0924547B1 (pt) 2008-03-13 2021-08-17 Wellstat Therapeutics Corporation Composto ácido 2-(3-(2,6-dimetilbenzilóxi)-4-metilfenil)acético, sua composição, bem como seu uso
AU2009243028B2 (en) 2008-04-30 2015-01-29 Wellstat Therapeutics Corporation Tetrazole compounds for reducing uric acid

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