AU2007243287B2 - Haloaryl substituted aminopurines, compositions thereof, and methods of treatment therewith - Google Patents
Haloaryl substituted aminopurines, compositions thereof, and methods of treatment therewith Download PDFInfo
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- AU2007243287B2 AU2007243287B2 AU2007243287A AU2007243287A AU2007243287B2 AU 2007243287 B2 AU2007243287 B2 AU 2007243287B2 AU 2007243287 A AU2007243287 A AU 2007243287A AU 2007243287 A AU2007243287 A AU 2007243287A AU 2007243287 B2 AU2007243287 B2 AU 2007243287B2
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- kinase
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- 238000011282 treatment Methods 0.000 title claims description 30
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- 150000005018 aminopurines Chemical class 0.000 title abstract description 7
- 125000003106 haloaryl group Chemical group 0.000 title 1
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 49
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 25
- 229910052736 halogen Inorganic materials 0.000 claims description 24
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- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 21
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Landscapes
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/411,413 US7521446B2 (en) | 2005-01-13 | 2006-04-26 | Haloaryl substituted aminopurines, compositions thereof, and methods of treatment therewith |
| US11/411,413 | 2006-04-26 | ||
| PCT/US2007/010258 WO2007127382A1 (en) | 2006-04-26 | 2007-04-25 | Haloaryl substituted aminopurines, compositions thereof, and methods of treatment therewith |
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| AU2007243287A1 AU2007243287A1 (en) | 2007-11-08 |
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| CA (1) | CA2684999C (OSRAM) |
| ES (1) | ES2400257T3 (OSRAM) |
| IL (1) | IL194865A (OSRAM) |
| MX (1) | MX2008013616A (OSRAM) |
| NZ (1) | NZ572467A (OSRAM) |
| WO (1) | WO2007127382A1 (OSRAM) |
| ZA (3) | ZA200809356B (OSRAM) |
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| US7256196B1 (en) * | 2003-12-09 | 2007-08-14 | The Procter & Gamble Company | Purine cytokine inhibitors |
| US7723340B2 (en) * | 2005-01-13 | 2010-05-25 | Signal Pharmaceuticals, Llc | Haloaryl substituted aminopurines, compositions thereof, and methods of treatment therewith |
| US7521446B2 (en) * | 2005-01-13 | 2009-04-21 | Signal Pharmaceuticals, Llc | Haloaryl substituted aminopurines, compositions thereof, and methods of treatment therewith |
| US7759342B2 (en) | 2005-01-13 | 2010-07-20 | Signal Pharmaceuticals, Llc | Methods of treatment and prevention using haloaryl substituted aminopurines |
| EP2017261A4 (en) * | 2006-04-28 | 2014-04-02 | Shionogi & Co | AMINE DERIVATIVE HAVING ANTAGONIST ACTIVITY OF NPY Y5 RECEPTOR |
| TWI398252B (zh) | 2006-05-26 | 2013-06-11 | Novartis Ag | 吡咯并嘧啶化合物及其用途 |
| NZ589053A (en) * | 2006-10-27 | 2012-03-30 | Signal Pharm Llc | Process of preparing 4-[9-(tetrahydro-furan-3-yl)-8-(2,4,6-trifluoro-phenylamino)-9h-purin-2-ylamino]-cyclohexan-1-ol compounds |
| EP2134738A4 (en) * | 2007-03-14 | 2010-04-21 | Univ Washington | DIAGNOSTIC PROCEDURE FOR DIABETES AND THERAPEUTICS FOR ADIPOSITAS |
| SA08290668B1 (ar) | 2007-10-25 | 2012-02-12 | شيونوجي آند كو.، ليمتد | مشتقات أمين لها نشاط مضاد لمستقبل npy y5 واستخداماتها |
| US20090156598A1 (en) * | 2007-12-17 | 2009-06-18 | Lebsack Alec D | Imidazolopyrimidine modulators of TRPV1 |
| TW200942549A (en) | 2007-12-17 | 2009-10-16 | Janssen Pharmaceutica Nv | Imidazolo-, oxazolo-, and thiazolopyrimidine modulators of TRPV1 |
| CN102186856B (zh) | 2008-08-22 | 2014-09-24 | 诺华股份有限公司 | 作为cdk抑制剂的吡咯并嘧啶化合物 |
| UY32138A (es) * | 2008-09-25 | 2010-04-30 | Boehringer Ingelheim Int | Amidas sustituidas del ácido 2-(2,6-dicloro-fenilamino)-6-fluoro-1-metil-1h-bencimidazol-5-carboxílico y sus sales farmacéuticamente aceptables |
| UY32470A (es) | 2009-03-05 | 2010-10-29 | Boehringer Ingelheim Int | Derivados de 2-{2-cloro-5-[(sustituido) metil]fenilamino} -1-metil]fenilamino}-1-metilbencimidazol-5-carboxamidas-n-(sustituidas) y sus sales fisiológicamente aceptables, composiciones conteniéndolos y aplicaciones |
| US8227618B2 (en) * | 2009-04-23 | 2012-07-24 | Shionogi & Co., Ltd. | Amine-derivatives having NPY Y5 receptor antagonistic activity and the uses thereof |
| WO2011071491A1 (en) * | 2009-12-09 | 2011-06-16 | Signal Pharmaceuticals, Llc | Isotopologues of 4-[9-(tetrahydro-furan-3-yl)-8-(2, 4, 6- trifluoro-phenylamino)-9h-purin-2-ylamino]-cyclohexan-1-ol |
| US9205577B2 (en) * | 2010-02-05 | 2015-12-08 | Allergan, Inc. | Porogen compositions, methods of making and uses |
| US9138309B2 (en) | 2010-02-05 | 2015-09-22 | Allergan, Inc. | Porous materials, methods of making and uses |
| UY33227A (es) | 2010-02-19 | 2011-09-30 | Novartis Ag | Compuestos de pirrolopirimidina como inhibidores de la cdk4/6 |
| US11202853B2 (en) * | 2010-05-11 | 2021-12-21 | Allergan, Inc. | Porogen compositions, methods of making and uses |
| US8759537B2 (en) | 2010-08-20 | 2014-06-24 | Boehringer Ingelheim International Gmbh | 3H-imidazo [4, 5-C] pyridine-6-carboxamides as anti-inflammatory agents |
| US8586604B2 (en) | 2010-08-20 | 2013-11-19 | Boehringer Ingelheim International Gmbh | Inhibitors of the microsomal prostaglandin E2 synthase-1 |
| US8680076B2 (en) | 2010-10-25 | 2014-03-25 | Signal Pharmaceuticals, Llc | Methods of treatment, improvement and prevention using haloaryl substituted aminopurines |
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| CA2684999C (en) | 2013-11-26 |
| AU2007243287A1 (en) | 2007-11-08 |
| CN103351389A (zh) | 2013-10-16 |
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