JP2007530580A5 - - Google Patents
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- Publication number
- JP2007530580A5 JP2007530580A5 JP2007505191A JP2007505191A JP2007530580A5 JP 2007530580 A5 JP2007530580 A5 JP 2007530580A5 JP 2007505191 A JP2007505191 A JP 2007505191A JP 2007505191 A JP2007505191 A JP 2007505191A JP 2007530580 A5 JP2007530580 A5 JP 2007530580A5
- Authority
- JP
- Japan
- Prior art keywords
- compound
- pharmaceutical composition
- medicament
- inflammatory
- composition according
- 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.)
- Abandoned
Links
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US55692704P | 2004-03-26 | 2004-03-26 | |
| PCT/US2005/009899 WO2005097780A1 (en) | 2004-03-26 | 2005-03-24 | [4-(5-aminomethyl-2-fluoro-phenyl)-piperidin-1-yl]-(4-bromo-3-methyl-5-propoxy-thiophen-2-yl)-methanone hydrochloride as an inhibitor of mast cell tryptase |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007530580A JP2007530580A (ja) | 2007-11-01 |
| JP2007530580A5 true JP2007530580A5 (enExample) | 2008-05-08 |
Family
ID=34964263
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007505191A Abandoned JP2007530580A (ja) | 2004-03-26 | 2005-03-24 | 肥満細胞トリプターゼインヒビターとしての[4−(5−アミノメチル−2−フルオロ−フェニル)−ピペリジン−1−イル]−(4−ブロモ−3−メチル−5−プロポキシ−チオフェン−2−イル)−メタノンヒドロクロリド |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US20070142435A1 (enExample) |
| EP (1) | EP1737848A1 (enExample) |
| JP (1) | JP2007530580A (enExample) |
| KR (1) | KR20060130682A (enExample) |
| CN (1) | CN1956978A (enExample) |
| AR (1) | AR048336A1 (enExample) |
| AU (1) | AU2005230934A1 (enExample) |
| BR (1) | BRPI0509245A (enExample) |
| CA (1) | CA2560649A1 (enExample) |
| CR (1) | CR8603A (enExample) |
| DO (1) | DOP2005000039A (enExample) |
| EC (1) | ECSP066878A (enExample) |
| IL (1) | IL178031A0 (enExample) |
| MA (1) | MA28547B1 (enExample) |
| MX (1) | MXPA06010610A (enExample) |
| NO (1) | NO20064811L (enExample) |
| PA (1) | PA8627601A1 (enExample) |
| PE (1) | PE20060084A1 (enExample) |
| RU (1) | RU2330034C1 (enExample) |
| TN (1) | TNSN06278A1 (enExample) |
| TW (1) | TW200602035A (enExample) |
| UA (1) | UA83738C2 (enExample) |
| UY (1) | UY28821A1 (enExample) |
| WO (1) | WO2005097780A1 (enExample) |
| ZA (1) | ZA200607752B (enExample) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20071148A1 (es) * | 2006-03-29 | 2007-12-10 | Sanofi Aventis | Mejoras en la preparacion de intermedios que conducen a hidrocloruro de [4-(5-aminometil-2-fluoro-fenil)-piperidin-1-il]-(4-bromo-3-metil-5-propoxi-tiofen-2-il)-metanona |
| AR065616A1 (es) * | 2007-03-07 | 2009-06-17 | Sanofi Aventis | Sintesis regioselectiva de ullmann de acido 4- bromo-3- metil-5- propoxi- tiofeno-2- carboxilico |
| WO2008115912A1 (en) * | 2007-03-21 | 2008-09-25 | Sanofi-Aventis | Regio-specific synthesis of 4-bromo-3-methyl-5-propoxy-thiophene-2-carboxylic acid |
| AR065858A1 (es) * | 2007-03-29 | 2009-07-08 | Sanofi Aventis | Metodo para preparar el inhibidor de triptasa [ 4-(5-aminoetil-2-fluoro-fenil)-piperidin-1-il]-(4-bromo-3-metil-5-propoxi-tiofen-2-il)-metanona. |
| WO2008121669A1 (en) * | 2007-03-29 | 2008-10-09 | Sanofi-Aventis | 4-bromo-3-methyl-5-propoxythiophene-2-carboxylic acid 2,5-dioxo-pyrrolidin-1-yl ester, its regio-specific synthesis and intermediate thereto |
| ES2469824T3 (es) | 2007-11-21 | 2014-06-20 | Janssen Pharmaceutica N.V. | Espiropiperidinas para su uso como inhibidores de la triptasa |
| WO2009094641A2 (en) * | 2008-01-24 | 2009-07-30 | Dor Biopharma, Inc. | Topically active steroids for use in interstitial pulmonary fibrosis |
| WO2010022196A2 (en) * | 2008-08-22 | 2010-02-25 | Sanofi-Aventis | [4-(5-aminomethyl-2-fluoro-phenyl)-piperidin-1-yl]-[7-fluoro-1-(2-methoxy-ethyl)-4-trifluoromethoxy-1h-indol-3-yl]-methanone as an inhibitor of mast cell tryptase |
| TW201034675A (en) | 2008-12-18 | 2010-10-01 | Sanofi Aventis | Method for treating macular degeneration |
| FR2955324A1 (fr) * | 2010-01-15 | 2011-07-22 | Sanofi Aventis | [4-(5-aminomethyl-phenyl)-piperidin-1-yl]-1h-indol-3-yl]-methanones disubstituees |
| CN102574792B (zh) | 2009-09-24 | 2014-07-09 | 赛诺菲-安万特美国有限责任公司 | (4-氟-3-(哌啶-4-基)-苯甲基)-氨基甲酸叔丁酯的合成及其中间体 |
| AU2010333779A1 (en) * | 2009-12-23 | 2012-07-12 | Sanofi | Indolyl-piperidinyl benzylamines as beta-tryptase inhibitors |
| JP2013515724A (ja) * | 2009-12-23 | 2013-05-09 | サノフイ | ベータ−トリプターゼ阻害剤としてのトロピノンベンジルアミン類 |
| EP2515851A1 (en) * | 2009-12-23 | 2012-10-31 | Sanofi | Treatment for inflammatory bowel disease |
| BR112012020965A2 (pt) * | 2010-02-24 | 2016-05-03 | Sanofi Sa | tratamento de condições alérgicas dermatológicas |
| MX360706B (es) | 2011-10-07 | 2018-11-14 | Takeda Pharmaceuticals Co | Compuestos de 1-arilcarbonil-4-oxi-piperidina utiles para el tratamiento de enfermedades neurodegenerativas. |
| UA126574C2 (uk) * | 2017-02-10 | 2022-11-02 | Дженентек, Інк. | Антитіло проти триптази, його композиція та застосування |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0012362D0 (en) * | 2000-05-22 | 2000-07-12 | Aventis Pharma Ltd | Chemical compounds |
| IL152830A0 (en) * | 2000-05-22 | 2003-06-24 | Aventis Pharma Inc | Arylmethylamine derivatives for use as tryptase inhibitors |
-
2005
- 2005-03-21 DO DO2005000039A patent/DOP2005000039A/es unknown
- 2005-03-22 PE PE2005000325A patent/PE20060084A1/es not_active Application Discontinuation
- 2005-03-23 UY UY28821A patent/UY28821A1/es unknown
- 2005-03-23 AR ARP050101170A patent/AR048336A1/es not_active Application Discontinuation
- 2005-03-24 UA UAA200611261A patent/UA83738C2/ru unknown
- 2005-03-24 WO PCT/US2005/009899 patent/WO2005097780A1/en not_active Ceased
- 2005-03-24 EP EP05731154A patent/EP1737848A1/en not_active Withdrawn
- 2005-03-24 CN CNA2005800164250A patent/CN1956978A/zh active Pending
- 2005-03-24 RU RU2006137717/04A patent/RU2330034C1/ru not_active IP Right Cessation
- 2005-03-24 MX MXPA06010610A patent/MXPA06010610A/es not_active Application Discontinuation
- 2005-03-24 AU AU2005230934A patent/AU2005230934A1/en not_active Abandoned
- 2005-03-24 BR BRPI0509245-0A patent/BRPI0509245A/pt not_active IP Right Cessation
- 2005-03-24 CA CA002560649A patent/CA2560649A1/en not_active Abandoned
- 2005-03-24 JP JP2007505191A patent/JP2007530580A/ja not_active Abandoned
- 2005-03-24 KR KR1020067019886A patent/KR20060130682A/ko not_active Withdrawn
- 2005-03-25 TW TW094109209A patent/TW200602035A/zh unknown
- 2005-03-28 PA PA20058627601A patent/PA8627601A1/es unknown
-
2006
- 2006-09-07 CR CR8603A patent/CR8603A/es not_active Application Discontinuation
- 2006-09-12 IL IL178031A patent/IL178031A0/en unknown
- 2006-09-12 TN TNP2006000278A patent/TNSN06278A1/en unknown
- 2006-09-14 US US11/520,998 patent/US20070142435A1/en active Granted
- 2006-09-15 ZA ZA200607752A patent/ZA200607752B/en unknown
- 2006-09-22 EC EC2006006878A patent/ECSP066878A/es unknown
- 2006-10-20 MA MA29405A patent/MA28547B1/fr unknown
- 2006-10-23 NO NO20064811A patent/NO20064811L/no not_active Application Discontinuation
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