RU2005105692A - 3,4-дизамещенные циклобутен-1,2-дионы как лиганды схс-хемокинового рецептора - Google Patents
3,4-дизамещенные циклобутен-1,2-дионы как лиганды схс-хемокинового рецептора Download PDFInfo
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- RU2005105692A RU2005105692A RU2005105692/04A RU2005105692A RU2005105692A RU 2005105692 A RU2005105692 A RU 2005105692A RU 2005105692/04 A RU2005105692/04 A RU 2005105692/04A RU 2005105692 A RU2005105692 A RU 2005105692A RU 2005105692 A RU2005105692 A RU 2005105692A
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- 0 Cc1c(C)c(*)c(*)c(C)c1* Chemical compound Cc1c(C)c(*)c(*)c(C)c1* 0.000 description 6
- IXSLKMLRCXISOG-UHFFFAOYSA-N CC(C)CC(c(cccc1NC(C(C2=O)=O)=C2NC2(CC2)c2ccccc2)c1O)=O Chemical compound CC(C)CC(c(cccc1NC(C(C2=O)=O)=C2NC2(CC2)c2ccccc2)c1O)=O IXSLKMLRCXISOG-UHFFFAOYSA-N 0.000 description 1
- YEBWSRUQHMZPSX-MHPPCMCBSA-N CC([C@@H](C(N)=O)N1)[O]=C(C2=O)C1=C2Nc1cccc(C(N(C)C)=O)c1O Chemical compound CC([C@@H](C(N)=O)N1)[O]=C(C2=O)C1=C2Nc1cccc(C(N(C)C)=O)c1O YEBWSRUQHMZPSX-MHPPCMCBSA-N 0.000 description 1
- GPAIJWDRZKOGLW-UHFFFAOYSA-N CC(c1cccc(NC(C(C2=O)=O)=C2NCc2ccccc2)c1O)=O Chemical compound CC(c1cccc(NC(C(C2=O)=O)=C2NCc2ccccc2)c1O)=O GPAIJWDRZKOGLW-UHFFFAOYSA-N 0.000 description 1
- WHPJQEMKJZVBHS-UHFFFAOYSA-N CCC(CC)(C=C)NC(C(C1=O)=O)=C1Nc(cccc1C(N(C)C)=O)c1O Chemical compound CCC(CC)(C=C)NC(C(C1=O)=O)=C1Nc(cccc1C(N(C)C)=O)c1O WHPJQEMKJZVBHS-UHFFFAOYSA-N 0.000 description 1
- XOYRBACCQDGSQP-UHFFFAOYSA-N CCC(c1cccc(OC)c1)NC(C(C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O Chemical compound CCC(c1cccc(OC)c1)NC(C(C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O XOYRBACCQDGSQP-UHFFFAOYSA-N 0.000 description 1
- KXZMHPJCGOYMMR-UHFFFAOYSA-N CCC(c1cccc(OCC)c1)NC(C(C1=O)=O)=C1Nc1cccc(C(CC(C)C)=O)c1O Chemical compound CCC(c1cccc(OCC)c1)NC(C(C1=O)=O)=C1Nc1cccc(C(CC(C)C)=O)c1O KXZMHPJCGOYMMR-UHFFFAOYSA-N 0.000 description 1
- MIDBIFUTMVSOGU-UHFFFAOYSA-N CCC(c1ccccc1F)NC(C(C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O Chemical compound CCC(c1ccccc1F)NC(C(C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O MIDBIFUTMVSOGU-UHFFFAOYSA-N 0.000 description 1
- NIWIDPUKWAYMCO-UHFFFAOYSA-N CCCC(c1cc(C)c[o]1)NC(C(C1=O)=O)=C1Nc1n[s]c(S(N(C)C)(=O)=O)c1O Chemical compound CCCC(c1cc(C)c[o]1)NC(C(C1=O)=O)=C1Nc1n[s]c(S(N(C)C)(=O)=O)c1O NIWIDPUKWAYMCO-UHFFFAOYSA-N 0.000 description 1
- IAVHABRNPDEGBX-UHFFFAOYSA-N CCCC(c1ccccc1)NC(C(C1=O)=O)=C1Nc(cccc1C(N(CC2)CCN2c2ncccn2)=O)c1O Chemical compound CCCC(c1ccccc1)NC(C(C1=O)=O)=C1Nc(cccc1C(N(CC2)CCN2c2ncccn2)=O)c1O IAVHABRNPDEGBX-UHFFFAOYSA-N 0.000 description 1
- STEVBRMCBZWWSJ-UHFFFAOYSA-N CCCC(c1ccccc1)NC(C(C1=O)=O)=C1Nc1cc(C#N)cc(C(N(C)C)=O)c1O Chemical compound CCCC(c1ccccc1)NC(C(C1=O)=O)=C1Nc1cc(C#N)cc(C(N(C)C)=O)c1O STEVBRMCBZWWSJ-UHFFFAOYSA-N 0.000 description 1
- ZUHBISJJKJFVJR-NSHDSACASA-N CC[C@H](C)NC(C(C1=O)=O)=C1Nc(cc(cc1C(CC(C)C)=O)C#N)c1O Chemical compound CC[C@H](C)NC(C(C1=O)=O)=C1Nc(cc(cc1C(CC(C)C)=O)C#N)c1O ZUHBISJJKJFVJR-NSHDSACASA-N 0.000 description 1
- AMYHNXLXSQOHQV-HXUWFJFHSA-N CC[C@H](c1ccccc1)NC(C(C1=O)=O)=C1Nc(cccc1C(N(CC2)CCN2C(c2ccc[o]2)=O)=O)c1O Chemical compound CC[C@H](c1ccccc1)NC(C(C1=O)=O)=C1Nc(cccc1C(N(CC2)CCN2C(c2ccc[o]2)=O)=O)c1O AMYHNXLXSQOHQV-HXUWFJFHSA-N 0.000 description 1
- GFUQQUSTTXUMIW-UHFFFAOYSA-N CN(C)C(c(cccc1NC(C(C2=O)=O)=C2NCc2ccc[s]2)c1O)=O Chemical compound CN(C)C(c(cccc1NC(C(C2=O)=O)=C2NCc2ccc[s]2)c1O)=O GFUQQUSTTXUMIW-UHFFFAOYSA-N 0.000 description 1
- HZHOTAJKJGIIRP-UHFFFAOYSA-N OC(C1)CN1C(c(cccc1NC(C(C2=O)=O)=C2NCc2ccccc2)c1O)=O Chemical compound OC(C1)CN1C(c(cccc1NC(C(C2=O)=O)=C2NCc2ccccc2)c1O)=O HZHOTAJKJGIIRP-UHFFFAOYSA-N 0.000 description 1
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- C07C237/30—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having the nitrogen atom of the carboxamide group bound to hydrogen atoms or to acyclic carbon atoms
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| US7288563B2 (en) | 2004-02-19 | 2007-10-30 | Bristol-Myers Squibb Company | Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity |
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| US8071603B2 (en) | 2004-09-20 | 2011-12-06 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as stearoyl-CoA desaturase inhibitors |
| CN101084212A (zh) | 2004-09-20 | 2007-12-05 | 泽农医药公司 | 杂环衍生物及其作为硬脂酰CoA去饱和酶介导剂的用途 |
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| DE602006017849D1 (de) * | 2005-06-29 | 2010-12-09 | Schering Corp | 5,6-disubstituierte oxadiazolopyrazine und thiadiazolopyrazine als liganden des cxc-chemokinrezeptors |
| CN101448778A (zh) * | 2006-05-26 | 2009-06-03 | 艾博特公司 | Polo样激酶的抑制剂 |
| JP2009539990A (ja) * | 2006-06-12 | 2009-11-19 | シェーリング コーポレイション | Cxcr2またはcxcr1とcxcr2との両方のいずれかの選択的アンタゴニストの薬学的処方物および組成物ならびに炎症性障害を治療するためにそれらを使用する方法 |
| TW200813033A (en) * | 2006-07-07 | 2008-03-16 | Schering Corp | 3, 4-di-substituted cyclobutene-1, 2-diones as CXC-chemokine receptor ligands |
| BRPI0812222A2 (pt) | 2007-06-06 | 2014-12-16 | Novartis Ag | Compostos ciclobutenodiona substituídos anti-inflamatórios. |
| CA2692269A1 (en) * | 2007-07-03 | 2009-01-08 | Schering Corporation | Process and intermediates for the synthesis of 1,2-substituted 3,4-dioxo-1-cyclobutene compounds |
| 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 |
| AU2009304598B2 (en) * | 2008-10-17 | 2015-01-29 | Akaal Pharma Pty Ltd | S1P receptors modulators and their use thereof |
| CA2739901A1 (en) | 2008-10-17 | 2010-04-22 | Akaal Pharma Pty Ltd | S1p receptors modulators |
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| US20110046060A1 (en) | 2009-08-24 | 2011-02-24 | Amunix Operating, Inc., | Coagulation factor IX compositions and methods of making and using same |
| WO2010091543A1 (en) * | 2009-02-10 | 2010-08-19 | Merck Sharp & Dohme Corp. | Novel hydrazino-cyclobut-3-ene-1, 2-dione derivatives as cxcr2 antagonists |
| PT2717898T (pt) | 2011-06-10 | 2019-05-20 | Bioverativ Therapeutics Inc | Compostos pró-coagulantes e processos para a sua utilização |
| EP2760821B1 (en) | 2011-09-02 | 2017-10-11 | 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. |
| WO2013123457A1 (en) | 2012-02-15 | 2013-08-22 | Biogen Idec Ma Inc. | Recombinant factor viii proteins |
| CN119192402A (zh) | 2012-02-15 | 2024-12-27 | 比奥贝拉蒂治疗公司 | 因子viii组合物及其制备和使用方法 |
| MX2014011115A (es) | 2012-03-16 | 2015-03-13 | Axikin Pharmaceuticals Inc | Inhibidores de 3,5-diaminopirazol cinasa. |
| EP3693000B1 (en) | 2012-06-08 | 2022-03-02 | Bioverativ Therapeutics Inc. | Procoagulant compounds |
| EP2863940A4 (en) | 2012-06-08 | 2016-08-10 | Biogen Ma Inc | Chimeric clotting factors |
| CA2888806A1 (en) | 2012-10-18 | 2014-04-24 | Biogen Idec Ma Inc. | Methods of using a fixed dose of a clotting factor |
| PL2956477T5 (pl) | 2013-02-15 | 2024-05-27 | Bioverativ Therapeutics Inc. | Zoptymalizowany gen czynnika viii |
| EP4108254A1 (en) | 2013-08-14 | 2022-12-28 | Bioverativ Therapeutics Inc. | Recombinant factor viii proteins |
| WO2015023891A2 (en) | 2013-08-14 | 2015-02-19 | Biogen Idec Ma Inc. | Factor viii-xten fusions and uses thereof |
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2002
- 2002-09-11 US US10/241,326 patent/US20040106794A1/en not_active Abandoned
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2003
- 2003-07-30 CA CA2496676A patent/CA2496676C/en not_active Expired - Fee Related
- 2003-07-30 PL PL03374876A patent/PL374876A1/xx not_active Application Discontinuation
- 2003-07-30 MX MXPA05001274A patent/MXPA05001274A/es active IP Right Grant
- 2003-07-30 NZ NZ538521A patent/NZ538521A/en unknown
- 2003-07-30 EP EP03772075A patent/EP1539678B1/en not_active Expired - Lifetime
- 2003-07-30 IL IL16642703A patent/IL166427A0/xx unknown
- 2003-07-30 JP JP2004524185A patent/JP2005534684A/ja active Pending
- 2003-07-30 WO PCT/US2003/023785 patent/WO2004011418A1/en not_active Ceased
- 2003-07-30 BR BR0313109-2A patent/BR0313109A/pt not_active IP Right Cessation
- 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 RU RU2005105692/04A patent/RU2005105692A/ru not_active Application Discontinuation
- 2003-07-30 TW TW095140972A patent/TW200716520A/zh unknown
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2005
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2006
- 2006-08-08 US US11/500,739 patent/US7964646B2/en not_active Expired - Fee Related
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2009
- 2009-01-13 US US12/352,781 patent/US7947720B2/en not_active Expired - Fee Related
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2011
- 2011-05-06 US US13/102,554 patent/US20110213029A1/en not_active Abandoned
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| JP2005534684A (ja) | 2005-11-17 |
| EP1539678A1 (en) | 2005-06-15 |
| NZ538521A (en) | 2008-02-29 |
| US7947720B2 (en) | 2011-05-24 |
| BR0313109A (pt) | 2005-06-21 |
| NO20051036L (no) | 2005-04-20 |
| AU2003259302A1 (en) | 2004-02-16 |
| CA2496676A1 (en) | 2004-02-05 |
| EP1539678B1 (en) | 2012-09-05 |
| MXPA05001274A (es) | 2005-09-08 |
| CA2496676C (en) | 2011-06-14 |
| AU2003259302B2 (en) | 2008-06-26 |
| PL374876A1 (en) | 2005-11-14 |
| US7964646B2 (en) | 2011-06-21 |
| US20070021494A1 (en) | 2007-01-25 |
| IL166427A0 (en) | 2006-01-15 |
| TW200716520A (en) | 2007-05-01 |
| WO2004011418A1 (en) | 2004-02-05 |
| US20090306079A1 (en) | 2009-12-10 |
| US20040106794A1 (en) | 2004-06-03 |
| KR20050026060A (ko) | 2005-03-14 |
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| FA92 | Acknowledgement of application withdrawn (lack of supplementary materials submitted) |
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