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
- Authority
- 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 (65)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| DE602004025458D1 (de) | 2003-04-18 | 2010-03-25 | Schering Corp | SYNTHESE VON 2-HYDROXY-N,N-DIMETHYL-3-ii2-i1(R)-(5-METHYL-2-FURANYL)PROPYL AMINO -3,4-DIOXO-1-CYCLOBUTEN-1-YL AMINO BENZAMID |
| 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 |
| US7381738B2 (en) | 2004-02-19 | 2008-06-03 | 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 |
| US7288563B2 (en) | 2004-02-19 | 2007-10-30 | Bristol-Myers Squibb Company | Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity |
| EP1742914A1 (en) * | 2004-02-27 | 2007-01-17 | Schering Corporation | Cyclobutenedione groups-containing compounds as inhibitors of hepatitis c virus ns3 serine protease |
| CN1984899B (zh) * | 2004-05-12 | 2011-07-27 | 先灵公司 | Cxcr1和cxcr2趋化因子拮抗剂 |
| EP1804799B1 (en) | 2004-09-20 | 2013-08-21 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors |
| EP1799667B1 (en) | 2004-09-20 | 2013-03-20 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as therapeutic agents |
| EP2289510A1 (en) | 2004-09-20 | 2011-03-02 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives for the treatment of diseases mediated by stearoyl-coa desaturase enzymes |
| EP2316458A1 (en) | 2004-09-20 | 2011-05-04 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives for inhibiting human stearoyl-coa-desaturase |
| US7951805B2 (en) | 2004-09-20 | 2011-05-31 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as mediators of stearoyl-CoA desaturase |
| CA2580856A1 (en) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors |
| EP2029138A1 (en) | 2005-06-03 | 2009-03-04 | Xenon Pharmaceuticals Inc. | Aminothiazole derivatives as human stearoyl-coa desaturase inhibitors |
| ATE486078T1 (de) | 2005-06-29 | 2010-11-15 | Schering Corp | 5,6-disubstituierte oxadiazolopyrazine und thiadiazolopyrazine als liganden des cxc- chemokinrezeptors |
| JP5437061B2 (ja) * | 2006-05-26 | 2014-03-12 | アッヴィ・インコーポレイテッド | ポロ様キナーゼの阻害薬 |
| WO2007146296A1 (en) * | 2006-06-12 | 2007-12-21 | Schering Corporation | Pharmaceutical formulations and compositions of a selective antagonist of either cxcr2 or both cxcr1 and cxcr2 and methods of using the same for treating inflammatory disorders |
| JP2009542700A (ja) * | 2006-07-07 | 2009-12-03 | シェーリング コーポレイション | Cxcケモカイン受容体リガンドとしての3,4−ジ置換シクロブテン−1,2−ジオン |
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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 |
| 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 |
| CA2739901A1 (en) | 2008-10-17 | 2010-04-22 | Akaal Pharma Pty Ltd | S1p receptors modulators |
| 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 |
| CA2771999A1 (en) | 2009-08-24 | 2011-03-10 | Amunix Operating Inc. | Coagulation factor vii compositions and methods of making and using same |
| CA2838833A1 (en) | 2011-06-10 | 2012-12-13 | Biogen Idec Ma Inc. | Pro-coagulant compounds and methods of use thereof |
| WO2013030803A1 (en) | 2011-09-02 | 2013-03-07 | Novartis Ag | Choline salt of an anti - inflammatory substituted cyclobutenedione compound |
| 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. |
| HRP20191920T1 (hr) | 2012-01-12 | 2020-01-10 | Bioverativ Therapeutics Inc. | Kimerni polipeptidi faktora viii i njihova uporaba |
| WO2013123457A1 (en) | 2012-02-15 | 2013-08-22 | Biogen Idec Ma Inc. | Recombinant factor viii proteins |
| CN111548418A (zh) | 2012-02-15 | 2020-08-18 | 比奥贝拉蒂治疗公司 | 因子viii组合物及其制备和使用方法 |
| CN104302640A (zh) | 2012-03-16 | 2015-01-21 | 埃克希金医药品有限公司 | 3,5-二氨基吡唑激酶抑制剂 |
| AU2013270683A1 (en) | 2012-06-08 | 2014-12-11 | Biogen Ma Inc. | Chimeric clotting factors |
| AU2013270682A1 (en) | 2012-06-08 | 2014-12-11 | Biogen Ma Inc. | Procoagulant compounds |
| AU2013331000B2 (en) | 2012-10-18 | 2018-04-19 | Bioverativ Therapeutics Inc. | Methods of using a fixed dose of a clotting factor |
| RS61387B2 (sr) | 2013-02-15 | 2024-06-28 | Bioverativ Therapeutics Inc | Gen optimizovanog faktora viii |
| US10548953B2 (en) | 2013-08-14 | 2020-02-04 | Bioverativ Therapeutics Inc. | Factor VIII-XTEN fusions and uses thereof |
| US20160311885A1 (en) | 2013-08-14 | 2016-10-27 | Biogen Ma Inc. | Recombinant factor viii proteins |
| NZ631142A (en) | 2013-09-18 | 2016-03-31 | Axikin Pharmaceuticals Inc | Pharmaceutically acceptable salts of 3,5-diaminopyrazole kinase inhibitors |
| US10611794B2 (en) | 2013-09-25 | 2020-04-07 | Bioverativ Therapeutics Inc. | On-column viral inactivation methods |
| EA201691111A1 (ru) | 2014-01-10 | 2017-01-30 | Байоджен Ма Инк. | Химерные белки фактора viii и их применение |
| CN107001440A (zh) | 2014-09-26 | 2017-08-01 | 拜耳制药股份公司 | 稳定化的肾上腺髓质素衍生物及其用途 |
| AU2015332533B2 (en) | 2014-10-14 | 2018-08-30 | Halozyme, Inc. | Compositions of adenosine deaminase-2 (ADA2), variants thereof and methods of using same |
| MY191736A (en) | 2014-12-23 | 2022-07-13 | Axikin Pharmaceuticals Inc | 3,5-diaminopyrazole kinase inhibitors |
| CA2989146A1 (en) | 2015-06-12 | 2016-12-15 | Board Of Regents, The University Of Texas System | Sulfonamide derivative and pharmaceutically acceptable acid addition salt thereof |
| UA126016C2 (uk) | 2015-08-03 | 2022-08-03 | Біовератів Терапеутікс Інк. | Злитий білок фактора іх |
| 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 |
| TWI724056B (zh) * | 2015-11-19 | 2021-04-11 | 美商卡默森屈有限公司 | Cxcr2抑制劑 |
| KR20180118659A (ko) | 2016-02-01 | 2018-10-31 | 바이오버라티브 테라퓨틱스 인크. | 최적화된 viii 인자 유전자 |
| KR20190090827A (ko) | 2016-12-02 | 2019-08-02 | 바이오버라티브 테라퓨틱스 인크. | 키메라 응고 인자를 사용해 혈우병성 관절증을 치료하는 방법 |
| GB201708856D0 (en) * | 2017-06-02 | 2017-07-19 | Ucb Biopharma Sprl | Seletalisib crystalline forms |
| KR20200037857A (ko) | 2017-08-14 | 2020-04-09 | 알러간, 인코포레이티드 | 3,4-이치환된 3-시클로부텐-1,2-디온 및 그의 용도 |
| ES3067325T3 (en) | 2018-01-08 | 2026-05-21 | Chemocentryx Inc | Methods of treating generalized pustular psoriasis with an antagonist of ccr6 or cxcr2 |
| KR102914074B1 (ko) | 2018-05-18 | 2026-01-16 | 바이오버라티브 테라퓨틱스 인크. | A형 혈우병의 치료 방법 |
| 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 |
| KR20210027426A (ko) | 2018-07-03 | 2021-03-10 | 브리스톨-마이어스 스큅 컴퍼니 | Fgf21 제제 |
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| 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 |
| KR20260005351A (ko) * | 2023-04-28 | 2026-01-09 | 우한 크리에이터나 사이언스 앤드 테크놀로지 컴퍼니, 리미티드 | Ccr6 길항제로서의 화합물, 이의 약학 조성물 및 용도 |
| CN121693497A (zh) * | 2023-11-03 | 2026-03-17 | 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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| GB0006050D0 (en) | 2000-03-14 | 2000-05-03 | Johnson Matthey Plc | Liquid gold compositions |
| WO2001092202A1 (en) | 2000-05-30 | 2001-12-06 | Smithkline Beecham Corporation | Il-8 receptor antagonists |
| CA2417059A1 (en) * | 2000-08-02 | 2002-02-07 | Celltech R&D Limited | 3-substituted isoquinolin-1-yl derivatives |
| AU2002223492A1 (en) * | 2000-11-14 | 2002-05-27 | Neurosearch A/S | Use of malaria parasite anion channel blockers for treating malaria |
| US20040048897A1 (en) | 2001-01-16 | 2004-03-11 | Mccleland Brent | Il-8 receptor antagonists |
| DE60230722D1 (de) | 2001-01-16 | 2009-02-26 | Smithkline Beecham Corp | Il-8-rezeptor-antagonisten |
| EP1355875A1 (en) | 2001-02-02 | 2003-10-29 | Schering Corporation | 3,4-di-substituted cyclobutene-1, 2-diones as cxc chemokine receptor antagonists |
| 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 |
| KR20100008794A (ko) | 2001-04-16 | 2010-01-26 | 쉐링 코포레이션 | Cxc-케모카인 수용체 리간드로서의 3,4-이치환된 사이클로부텐-1,2-디온 |
| 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 |
| JP2005505595A (ja) | 2001-10-12 | 2005-02-24 | シェーリング コーポレイション | Cxc−ケモカインレセプターアンタゴニストとしての3,4−二置換マレイミド化合物 |
| US6878709B2 (en) * | 2002-01-04 | 2005-04-12 | Schering Corporation | 3,4-di-substituted pyridazinediones as CXC chemokine receptor antagonists |
| NZ535314A (en) * | 2002-03-18 | 2007-08-31 | Schering Corp | Combination treatments for chemokine-mediated diseases |
| EP1551818B1 (en) * | 2002-10-09 | 2009-02-04 | Schering Corporation | Thiadiazoledioxides and thiadiazoleoxides as cxc- and cc-chemokine receptor ligands |
| DE602004025458D1 (de) * | 2003-04-18 | 2010-03-25 | Schering Corp | SYNTHESE VON 2-HYDROXY-N,N-DIMETHYL-3-ii2-i1(R)-(5-METHYL-2-FURANYL)PROPYL AMINO -3,4-DIOXO-1-CYCLOBUTEN-1-YL AMINO BENZAMID |
| CN1914187B (zh) | 2004-01-30 | 2012-01-25 | 先灵公司 | Cxc趋化因子受体配位体的结晶多晶型物 |
| 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 TW TW095140972A patent/TW200716520A/zh unknown
- 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 IL IL16642703A patent/IL166427A0/xx unknown
- 2003-07-30 RU RU2005105692/04A patent/RU2005105692A/ru not_active Application Discontinuation
- 2003-07-30 NZ NZ538521A patent/NZ538521A/en unknown
- 2003-07-30 MX MXPA05001274A patent/MXPA05001274A/es active IP Right Grant
- 2003-07-30 BR BR0313109-2A patent/BR0313109A/pt not_active IP Right Cessation
- 2003-07-30 JP JP2004524185A patent/JP2005534684A/ja active Pending
- 2003-07-30 AU AU2003259302A patent/AU2003259302B2/en not_active Ceased
- 2003-07-30 KR KR1020057001672A patent/KR20050026060A/ko not_active Ceased
- 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
-
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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