KR20120081120A - 뉴로키닌 2 수용체 활성과 관련된 장애 또는 질환을 치료하기 위한 화합물 - Google Patents
뉴로키닌 2 수용체 활성과 관련된 장애 또는 질환을 치료하기 위한 화합물 Download PDFInfo
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| US5120548A (en) | 1989-11-07 | 1992-06-09 | Merck & Co., Inc. | Swelling modulated polymeric drug delivery device |
| US5733566A (en) | 1990-05-15 | 1998-03-31 | Alkermes Controlled Therapeutics Inc. Ii | Controlled release of antiparasitic agents in animals |
| US5580578A (en) | 1992-01-27 | 1996-12-03 | Euro-Celtique, S.A. | Controlled release formulations coated with aqueous dispersions of acrylic polymers |
| DE4204151A1 (de) * | 1992-02-12 | 1993-08-19 | Schneider Manfred Prof Dr | Regioisomerenreine monoglyceride sowie ein verfahren zu ihrer herstellung durch enzymatische veresterung von glycerin in organischen loesungsmitteln |
| US5591767A (en) | 1993-01-25 | 1997-01-07 | Pharmetrix Corporation | Liquid reservoir transdermal patch for the administration of ketorolac |
| IT1270594B (it) | 1994-07-07 | 1997-05-07 | Recordati Chem Pharm | Composizione farmaceutica a rilascio controllato di moguisteina in sospensione liquida |
| JPH0931020A (ja) * | 1995-07-25 | 1997-02-04 | Soda Koryo Kk | グリセロールモノ−6−ヒドロキシアルカン酸エステル、及びこれを含有する香料組成物 |
| SE9604582D0 (sv) * | 1996-12-13 | 1996-12-13 | Astra Ab | Novel compounds |
| EP1230207B1 (en) * | 1999-11-18 | 2005-06-22 | Richard L. Pederson | Metathesis syntheses of pheromones or their components |
| MY141736A (en) * | 2002-10-08 | 2010-06-15 | Elanco Animal Health Ireland | Substituted 1,4-di-piperidin-4-yi-piperazine derivatives and their use as neurokinin antagonists |
| JO2676B1 (en) * | 2004-04-06 | 2012-06-17 | جانسين فارماسوتيكا ان. في | Derivatives of second-aza-spiro- (5,4) -dikan and their use as antihistamines |
| CN1286529C (zh) * | 2004-06-11 | 2006-11-29 | 华中科技大学 | 具有皮肤靶向性的药物组合物及其制备方法和用途 |
| US7906147B2 (en) * | 2006-10-12 | 2011-03-15 | Nanoprobes, Inc. | Functional associative coatings for nanoparticles |
| BRPI0906484A2 (pt) * | 2008-01-11 | 2017-06-13 | United Paragon Ass Inc | isolado de ovo fertilizado e seus usos |
-
2010
- 2010-09-07 CA CA2773035A patent/CA2773035A1/en not_active Abandoned
- 2010-09-07 AU AU2010289276A patent/AU2010289276A1/en not_active Abandoned
- 2010-09-07 BR BR112012004988A patent/BR112012004988A2/pt not_active Application Discontinuation
- 2010-09-07 KR KR1020127008768A patent/KR20120081120A/ko not_active Withdrawn
- 2010-09-07 JP JP2012528118A patent/JP2013503908A/ja active Pending
- 2010-09-07 RU RU2012112943/04A patent/RU2012112943A/ru not_active Application Discontinuation
- 2010-09-07 SG SG2012015046A patent/SG178964A1/en unknown
- 2010-09-07 MX MX2012002551A patent/MX2012002551A/es not_active Application Discontinuation
- 2010-09-07 EP EP10814632.5A patent/EP2473038A4/en not_active Withdrawn
- 2010-09-07 US US13/394,067 patent/US20120190743A1/en not_active Abandoned
- 2010-09-07 NZ NZ599215A patent/NZ599215A/en not_active IP Right Cessation
- 2010-09-07 CN CN2010800501768A patent/CN102740693A/zh active Pending
- 2010-09-07 WO PCT/US2010/048006 patent/WO2011029099A1/en not_active Ceased
-
2012
- 2012-04-04 ZA ZA2012/02492A patent/ZA201202492B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| RU2012112943A (ru) | 2013-10-10 |
| CA2773035A1 (en) | 2011-03-10 |
| JP2013503908A (ja) | 2013-02-04 |
| NZ599215A (en) | 2014-11-28 |
| SG178964A1 (en) | 2012-04-27 |
| BR112012004988A2 (pt) | 2015-09-08 |
| EP2473038A4 (en) | 2013-10-23 |
| WO2011029099A1 (en) | 2011-03-10 |
| CN102740693A (zh) | 2012-10-17 |
| AU2010289276A1 (en) | 2012-05-03 |
| US20120190743A1 (en) | 2012-07-26 |
| ZA201202492B (en) | 2013-02-27 |
| MX2012002551A (es) | 2012-09-07 |
| EP2473038A1 (en) | 2012-07-11 |
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