JP2005534684A5 - - Google Patents
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- JP2005534684A5 JP2005534684A5 JP2004524185A JP2004524185A JP2005534684A5 JP 2005534684 A5 JP2005534684 A5 JP 2005534684A5 JP 2004524185 A JP2004524185 A JP 2004524185A JP 2004524185 A JP2004524185 A JP 2004524185A JP 2005534684 A5 JP2005534684 A5 JP 2005534684A5
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- JP
- Japan
- Prior art keywords
- group
- substituted
- unsubstituted
- alkyl
- independently selected
- 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.)
- Pending
Links
- 0 CC(*)(*)Cc1c(cccn2)c2ccc1 Chemical compound CC(*)(*)Cc1c(cccn2)c2ccc1 0.000 description 27
- AUQGAQQMGDCJRI-UHFFFAOYSA-O CC(C)C(C([NH2+]C(C)c1ccccc1)=O)NC(C(C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O Chemical compound CC(C)C(C([NH2+]C(C)c1ccccc1)=O)NC(C(C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O AUQGAQQMGDCJRI-UHFFFAOYSA-O 0.000 description 1
- AUQGAQQMGDCJRI-DNVCBOLYSA-N CC(C)[C@H](C(N[C@H](C)c1ccccc1)=O)NC(C(C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O Chemical compound CC(C)[C@H](C(N[C@H](C)c1ccccc1)=O)NC(C(C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O AUQGAQQMGDCJRI-DNVCBOLYSA-N 0.000 description 1
- LTNCYCKOTJDBMA-UHFFFAOYSA-N CC(c1ccc[o]1)NC(C(C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O Chemical compound CC(c1ccc[o]1)NC(C(C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O LTNCYCKOTJDBMA-UHFFFAOYSA-N 0.000 description 1
- JZUARMCNZIOGMA-UHFFFAOYSA-N CN(C)C(c(cccc1NC(C(C2=O)O)=C2NC2(CC2)c2ccccc2)c1O)=O Chemical compound CN(C)C(c(cccc1NC(C(C2=O)O)=C2NC2(CC2)c2ccccc2)c1O)=O JZUARMCNZIOGMA-UHFFFAOYSA-N 0.000 description 1
- IIFTXCCQGXWRHG-UHFFFAOYSA-N CN(C)C(c1cccc(NC(C(C2=O)=O)=C2NC2CCCCCC2)c1O)=O Chemical compound CN(C)C(c1cccc(NC(C(C2=O)=O)=C2NC2CCCCCC2)c1O)=O IIFTXCCQGXWRHG-UHFFFAOYSA-N 0.000 description 1
- PWBSHAALNNETET-OCCSQVGLSA-N CN(C)C(c1cccc(NC(C(C2=O)=O)=C2N[C@@H]2[C@@H](COC)CCCC2)c1O)=O Chemical compound CN(C)C(c1cccc(NC(C(C2=O)=O)=C2N[C@@H]2[C@@H](COC)CCCC2)c1O)=O PWBSHAALNNETET-OCCSQVGLSA-N 0.000 description 1
- SMWDFEZZVXVKRB-UHFFFAOYSA-N c1ccc2ncccc2c1 Chemical compound c1ccc2ncccc2c1 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/208,412 US20040097547A1 (en) | 2001-04-16 | 2002-07-30 | 3,4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor ligands |
| US10/241,326 US20040106794A1 (en) | 2001-04-16 | 2002-09-11 | 3,4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor ligands |
| PCT/US2003/023785 WO2004011418A1 (en) | 2002-07-30 | 2003-07-30 | 3,4-di-substituted cyclobutene-1, 2-diones as cxc-chemokine receptor ligands |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010217953A Division JP2011063591A (ja) | 2002-07-30 | 2010-09-28 | Cxcケモカインレセプタ配位子としての3,4−二置換シクロブテン−1,2−ジオン |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005534684A JP2005534684A (ja) | 2005-11-17 |
| JP2005534684A5 true JP2005534684A5 (enExample) | 2006-09-14 |
Family
ID=31190690
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004524185A Pending JP2005534684A (ja) | 2002-07-30 | 2003-07-30 | Cxcケモカインレセプタ配位子としての3,4−二置換シクロブテン−1,2−ジオン |
Country Status (15)
| Country | Link |
|---|---|
| US (4) | US20040106794A1 (enExample) |
| EP (1) | EP1539678B1 (enExample) |
| JP (1) | JP2005534684A (enExample) |
| KR (1) | KR20050026060A (enExample) |
| AU (1) | AU2003259302B2 (enExample) |
| BR (1) | BR0313109A (enExample) |
| CA (1) | CA2496676C (enExample) |
| IL (1) | IL166427A0 (enExample) |
| MX (1) | MXPA05001274A (enExample) |
| NO (1) | NO20051036L (enExample) |
| NZ (1) | NZ538521A (enExample) |
| PL (1) | PL374876A1 (enExample) |
| RU (1) | RU2005105692A (enExample) |
| TW (1) | TW200716520A (enExample) |
| WO (1) | WO2004011418A1 (enExample) |
Families Citing this family (63)
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| US20040106794A1 (en) * | 2001-04-16 | 2004-06-03 | Schering Corporation | 3,4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor ligands |
| GB0302094D0 (en) | 2003-01-29 | 2003-02-26 | Pharmagene Lab Ltd | EP4 receptor antagonists |
| MXPA05011183A (es) | 2003-04-18 | 2005-12-14 | Schering Corp | Sintesis de 2-hidroxi-n, n-dimetil- 3-[[2-[1(r) -(5-metil -2-furanil) propil]amino]-3, 4-dioxo-1 -ciclobuten-1 -il]amino] benzamida. |
| GB0324269D0 (en) | 2003-10-16 | 2003-11-19 | Pharmagene Lab Ltd | EP4 receptor antagonists |
| US7230022B2 (en) | 2004-02-19 | 2007-06-12 | Bristol-Myers Squibb Company | Substituted fused bicyclic amines as modulators of chemokine receptor activity |
| US7288563B2 (en) | 2004-02-19 | 2007-10-30 | Bristol-Myers Squibb Company | Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity |
| US7479496B2 (en) | 2004-02-19 | 2009-01-20 | Bristol-Myers Squibb Company | Substituted spiro azabicyclics as modulators of chemokine receptor activity |
| US7381738B2 (en) | 2004-02-19 | 2008-06-03 | Bristol-Myers Squibb Company | Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity |
| CN1946690A (zh) * | 2004-02-27 | 2007-04-11 | 先灵公司 | 用作丙型肝炎病毒ns3丝氨酸蛋白酶抑制剂的含环丁烯二酮基团化合物 |
| CA2565519A1 (en) * | 2004-05-12 | 2005-12-01 | Schering Corporation | Cxcr1 and cxcr2 chemokine antagonists |
| TW200626155A (en) | 2004-09-20 | 2006-08-01 | Xenon Pharmaceuticals Inc | Heterocyclic derivatives and their use as therapeutic agents |
| CN101084211A (zh) | 2004-09-20 | 2007-12-05 | 泽农医药公司 | 杂环衍生物及其作为治疗剂的用途 |
| AU2005286728A1 (en) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as mediators of stearoyl-CoA desaturase |
| JP4958785B2 (ja) | 2004-09-20 | 2012-06-20 | ゼノン・ファーマシューティカルズ・インコーポレイテッド | 複素環誘導体およびステアロイル−CoAデサチュラーゼインヒビターとしてのそれらの使用 |
| BRPI0515483A (pt) | 2004-09-20 | 2008-07-22 | Xenon Pharmaceuticals Inc | derivados heterocìclicos para o tratamento de doenças mediadas por enzimas estearoil-coa desaturase |
| WO2006034441A1 (en) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors |
| WO2007130075A1 (en) | 2005-06-03 | 2007-11-15 | Xenon Pharmaceuticals Inc. | Aminothiazole derivatives as human stearoyl-coa desaturase inhibitors |
| CN101253180B (zh) | 2005-06-29 | 2011-08-03 | 先灵公司 | 作为cxc-化学活素受体配体的5,6-二取代的*二唑吡嗪和噻二唑吡嗪 |
| MX2008015004A (es) * | 2006-05-26 | 2008-12-05 | Abbott Lab | Inhibidores de cinasas de tipo polo. |
| CN101500544B (zh) * | 2006-06-12 | 2012-08-08 | 先灵公司 | Cxcr2或cxcr1与cxcr2两者的选择性拮抗剂的药物制剂和组合物及其用于治疗炎性疾病的使用方法 |
| KR20090028811A (ko) * | 2006-07-07 | 2009-03-19 | 쉐링 코포레이션 | Cxc-케모카인 수용체 리간드로서의 3,4-이치환된 사이클로부텐-1,2-디온 |
| KR20100031718A (ko) | 2007-06-06 | 2010-03-24 | 노파르티스 아게 | 항-염증성 치환된 시클로부텐디온 화합물 |
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| WO2009012375A2 (en) * | 2007-07-19 | 2009-01-22 | Wyeth | Squarate kinase inhibitors |
| UA103198C2 (en) | 2008-08-04 | 2013-09-25 | Новартис Аг | Squaramide derivatives as cxcr2 antagonists |
| EP2344446A4 (en) | 2008-10-17 | 2012-04-04 | Akaal Pharma Pty Ltd | S1P RECEPTOR MODULATORS |
| CN102186845B (zh) * | 2008-10-17 | 2016-09-07 | 阿卡制药有限公司 | S1p受体调节剂以及它们的用途 |
| WO2010063802A1 (en) * | 2008-12-05 | 2010-06-10 | Novartis Ag | 3, 4-di-substituted cyclobutene- 1, 2 -diones as cxcr2 receptor antagonists |
| WO2010091543A1 (en) * | 2009-02-10 | 2010-08-19 | Merck Sharp & Dohme Corp. | Novel hydrazino-cyclobut-3-ene-1, 2-dione derivatives as cxcr2 antagonists |
| US20120263701A1 (en) | 2009-08-24 | 2012-10-18 | Volker Schellenberger | Coagulation factor vii compositions and methods of making and using same |
| HUE043894T2 (hu) | 2011-06-10 | 2019-09-30 | Bioverativ Therapeutics Inc | Koagulációt elõsegítõ vegyületek és alkalmazásuk módszerei |
| PT2760821T (pt) | 2011-09-02 | 2018-01-11 | Novartis Ag | Sal de colina de um composto anti-inflamatório de ciclobutenodiona substituída |
| FR2981936B1 (fr) | 2011-10-28 | 2013-12-20 | Galderma Res & Dev | Nouveaux composes di-substitues de la diamino-3,4-cyclobutene-3-dione-1,2 utiles dans le traitement de pathologies mediees par des chimiokines. |
| MX369862B (es) | 2012-02-15 | 2019-11-25 | Bioverativ Therapeutics Inc | Composiciones del factor viii y metodos para hacerlas y usarlas. |
| NZ628014A (en) | 2012-02-15 | 2016-09-30 | Biogen Ma Inc | Recombinant factor viii proteins |
| JP6120941B2 (ja) | 2012-03-16 | 2017-04-26 | アクシキン ファーマシューティカルズ インコーポレーテッド | 3,5−ジアミノピラゾールキナーゼ阻害剤 |
| AU2013270682A1 (en) | 2012-06-08 | 2014-12-11 | Biogen Ma Inc. | Procoagulant compounds |
| CA2875247A1 (en) | 2012-06-08 | 2013-12-12 | Biogen Idec Ma Inc. | Chimeric clotting factors |
| EP2908847B1 (en) | 2012-10-18 | 2022-03-30 | Bioverativ Therapeutics Inc. | Methods of using a fixed dose of a clotting factor |
| ES2959747T3 (es) | 2013-02-15 | 2024-02-28 | Bioverativ Therapeutics Inc | Gen del factor VIII optimizado |
| WO2015023894A1 (en) | 2013-08-14 | 2015-02-19 | Biogen Idec Ma Inc. | Recombinant factor viii proteins |
| EP3033097B1 (en) | 2013-08-14 | 2021-03-10 | Bioverativ Therapeutics Inc. | Factor viii-xten fusions and uses thereof |
| NZ631142A (en) | 2013-09-18 | 2016-03-31 | Axikin Pharmaceuticals Inc | Pharmaceutically acceptable salts of 3,5-diaminopyrazole kinase inhibitors |
| EP3048899B1 (en) | 2013-09-25 | 2021-09-08 | Bioverativ Therapeutics Inc. | On-column viral inactivation methods |
| EP3197481A1 (en) | 2014-09-26 | 2017-08-02 | Bayer Pharma Aktiengesellschaft | Stabilized adrenomedullin derivatives and use thereof |
| EA201700181A1 (ru) | 2014-10-14 | 2017-09-29 | Галозим, Инк. | Композиции аденозиндеаминазы-2 (ада-2), их варианты и способы использования |
| KR102034202B1 (ko) | 2014-12-23 | 2019-10-18 | 에스엠에이 세라퓨틱스 아이엔씨. | 3,5-디아미노피라졸 키나제 억제제 |
| EP3309146A4 (en) | 2015-06-12 | 2019-02-27 | University of Tsukuba | SULPHONAMID DERIVATIVE AND PHARMACEUTICALLY ACCEPTABLE ACID ADDITIVE SALT THEREOF |
| CA2994547A1 (en) | 2015-08-03 | 2017-02-09 | Bioverativ Therapeutics Inc. | Factor ix fusion proteins and methods of making and using same |
| TWI724056B (zh) * | 2015-11-19 | 2021-04-11 | 美商卡默森屈有限公司 | Cxcr2抑制劑 |
| TWI734715B (zh) | 2015-11-19 | 2021-08-01 | 美商卡默森屈有限公司 | 趨化因子受體調節劑 |
| EP3411478B1 (en) | 2016-02-01 | 2022-06-08 | Bioverativ Therapeutics Inc. | Optimized factor viii genes |
| WO2018102743A1 (en) | 2016-12-02 | 2018-06-07 | Bioverativ Therapeutics Inc. | Methods of treating hemophilic arthropathy using chimeric clotting factors |
| GB201708856D0 (en) * | 2017-06-02 | 2017-07-19 | Ucb Biopharma Sprl | Seletalisib crystalline forms |
| EP3668832A1 (en) | 2017-08-14 | 2020-06-24 | Allergan, Inc. | 3,4-disubstituted 3-cyclobutene-1,2-diones and use thereof |
| JP7322036B2 (ja) | 2018-01-08 | 2023-08-07 | ケモセントリックス,インコーポレイティド | Ccr6またはcxcr2のアンタゴニストを用いて汎発性膿疱性乾癬を治療する方法 |
| SG11202010767SA (en) | 2018-05-18 | 2020-11-27 | Bioverativ Therapeutics Inc | Methods of treating hemophilia a |
| CN110577472B (zh) * | 2018-06-11 | 2023-06-02 | 重庆博腾制药科技股份有限公司 | 一种(1r,3s)-3-氨基-1-环戊醇盐酸盐的制备方法 |
| US12226451B2 (en) | 2018-07-03 | 2025-02-18 | Bristol-Myers Squibb Company | FGF-21 formulations |
| EP3852879A1 (en) | 2018-09-21 | 2021-07-28 | Pfizer Inc. | N-substituted-dioxocyclobutenylamino-3-hydroxy-picolinamides useful as ccr6 inhibitors |
| EP4015501A1 (en) * | 2020-12-16 | 2022-06-22 | Consejo Superior de Investigaciones Científicas (CSIC) | N-benzyl-alpha-aminoamides as anaphase-promoting complex/cyclosome (apc/c) inhibitors |
| WO2024222865A1 (zh) * | 2023-04-28 | 2024-10-31 | 武汉朗来科技发展有限公司 | 作为ccr6拮抗剂的化合物、其药物组合物和用途 |
| WO2025092968A1 (zh) * | 2023-11-03 | 2025-05-08 | 武汉朗来科技发展有限公司 | 作为ccr6拮抗剂的化合物、其药物组合物和用途 |
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| US20040132694A1 (en) | 2001-01-16 | 2004-07-08 | Palovich Michael R. | Il-8 receptor antagonists |
| RU2003126913A (ru) | 2001-02-02 | 2005-03-10 | Шеринг Корпорейшн (US) | 3,4-дизамещенные циклобутен-1,2-дионы, как антагонисты хемокинового рецептора схс |
| US20030204085A1 (en) | 2001-02-02 | 2003-10-30 | Taveras Arthur G. | 3, 4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor antagonists |
| US20040097547A1 (en) * | 2001-04-16 | 2004-05-20 | Taveras Arthur G. | 3,4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor ligands |
| PT1818325E (pt) * | 2001-04-16 | 2010-05-12 | Schering Corp | Ciclobuteno-1,2-dionas 3,4-di-substituídas como ligandos de receptor de quimoquina cxc |
| US7132445B2 (en) * | 2001-04-16 | 2006-11-07 | Schering Corporation | 3,4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor ligands |
| US20040106794A1 (en) * | 2001-04-16 | 2004-06-03 | Schering Corporation | 3,4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor ligands |
| EP1434775A1 (en) | 2001-10-12 | 2004-07-07 | Schering Corporation | 3,4-di-substituted maleimide compounds as cxc-chemokine receptor antagonists |
| US6878709B2 (en) | 2002-01-04 | 2005-04-12 | Schering Corporation | 3,4-di-substituted pyridazinediones as CXC chemokine receptor antagonists |
| BR0308739A (pt) * | 2002-03-18 | 2005-01-11 | Schering Corp | Tratamentos em combinação para doenças mediadas por quimiocina |
| US20040186142A1 (en) | 2002-10-09 | 2004-09-23 | Schering Corporation Pharmacopeia, Inc. | Thiadiazoledioxides and thiadiazoleoxides as CXC- and CC- chemokine receptor ligands |
| MXPA05011183A (es) * | 2003-04-18 | 2005-12-14 | Schering Corp | Sintesis de 2-hidroxi-n, n-dimetil- 3-[[2-[1(r) -(5-metil -2-furanil) propil]amino]-3, 4-dioxo-1 -ciclobuten-1 -il]amino] benzamida. |
| DE602005022986D1 (de) | 2004-01-30 | 2010-09-30 | Schering Corp | Kristalline polymorphe eines cxc-chemokinrezeptorliganden |
| US20080190441A1 (en) * | 2007-02-13 | 2008-08-14 | Michael Victor Vecchiola | Ergonomic hair brush |
-
2002
- 2002-09-11 US US10/241,326 patent/US20040106794A1/en not_active Abandoned
-
2003
- 2003-07-30 MX MXPA05001274A patent/MXPA05001274A/es active IP Right Grant
- 2003-07-30 JP JP2004524185A patent/JP2005534684A/ja active Pending
- 2003-07-30 EP EP03772075A patent/EP1539678B1/en not_active Expired - Lifetime
- 2003-07-30 PL PL03374876A patent/PL374876A1/xx not_active Application Discontinuation
- 2003-07-30 KR KR1020057001672A patent/KR20050026060A/ko not_active Ceased
- 2003-07-30 RU RU2005105692/04A patent/RU2005105692A/ru not_active Application Discontinuation
- 2003-07-30 IL IL16642703A patent/IL166427A0/xx unknown
- 2003-07-30 WO PCT/US2003/023785 patent/WO2004011418A1/en not_active Ceased
- 2003-07-30 CA CA2496676A patent/CA2496676C/en not_active Expired - Fee Related
- 2003-07-30 AU AU2003259302A patent/AU2003259302B2/en not_active Ceased
- 2003-07-30 NZ NZ538521A patent/NZ538521A/en unknown
- 2003-07-30 TW TW095140972A patent/TW200716520A/zh unknown
- 2003-07-30 BR BR0313109-2A patent/BR0313109A/pt not_active IP Right Cessation
-
2005
- 2005-02-25 NO NO20051036A patent/NO20051036L/no not_active Application Discontinuation
-
2006
- 2006-08-08 US US11/500,739 patent/US7964646B2/en not_active Expired - Fee Related
-
2009
- 2009-01-13 US US12/352,781 patent/US7947720B2/en not_active Expired - Fee Related
-
2011
- 2011-05-06 US US13/102,554 patent/US20110213029A1/en not_active Abandoned
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