NO20081975L - Diarylamin-inneholdende forbindelser og sammensetninger, og deres anvendelse som modulatorer av C-kit-reseptorer - Google Patents
Diarylamin-inneholdende forbindelser og sammensetninger, og deres anvendelse som modulatorer av C-kit-reseptorerInfo
- Publication number
- NO20081975L NO20081975L NO20081975A NO20081975A NO20081975L NO 20081975 L NO20081975 L NO 20081975L NO 20081975 A NO20081975 A NO 20081975A NO 20081975 A NO20081975 A NO 20081975A NO 20081975 L NO20081975 L NO 20081975L
- Authority
- NO
- Norway
- Prior art keywords
- compounds
- diarylamine
- compositions
- modulators
- kit receptors
- Prior art date
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- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US72101505P | 2005-09-27 | 2005-09-27 | |
PCT/US2006/037820 WO2007038669A2 (fr) | 2005-09-27 | 2006-09-26 | Composes et compositions contenant de la diarylamine, et utilisation en tant que modulateurs de recepteurs de c-kit |
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NO20081975L true NO20081975L (no) | 2008-06-02 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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NO20081975A NO20081975L (no) | 2005-09-27 | 2008-04-24 | Diarylamin-inneholdende forbindelser og sammensetninger, og deres anvendelse som modulatorer av C-kit-reseptorer |
Country Status (19)
Country | Link |
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US (6) | US7514447B2 (fr) |
EP (1) | EP1928236B1 (fr) |
JP (1) | JP5335426B2 (fr) |
KR (1) | KR101415426B1 (fr) |
CN (1) | CN101272685A (fr) |
AT (1) | ATE534293T1 (fr) |
AU (1) | AU2006297089B2 (fr) |
BR (1) | BRPI0616575A2 (fr) |
CA (1) | CA2622494A1 (fr) |
EC (1) | ECSP088402A (fr) |
ES (1) | ES2378153T3 (fr) |
IL (1) | IL189927A0 (fr) |
MA (1) | MA29851B1 (fr) |
NO (1) | NO20081975L (fr) |
NZ (1) | NZ566862A (fr) |
RU (1) | RU2436776C2 (fr) |
TN (1) | TNSN08140A1 (fr) |
WO (1) | WO2007038669A2 (fr) |
ZA (1) | ZA200801732B (fr) |
Families Citing this family (35)
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US8193206B2 (en) | 2005-06-14 | 2012-06-05 | Taigen Biotechnology Co., Ltd. | Pyrimidine compounds |
JP5118029B2 (ja) * | 2005-06-14 | 2013-01-16 | タイゲン バイオテクノロジー カンパニー,リミテッド | ピリミジン化合物 |
CA2622494A1 (fr) * | 2005-09-27 | 2007-04-05 | Irm Llc | Composes et compositions contenant de la diarylamine, et utilisation en tant que modulateurs de recepteurs de c-kit |
PL2402319T3 (pl) | 2006-03-31 | 2018-02-28 | Novartis Ag | Inhibitory DGAT |
JP5160636B2 (ja) | 2007-05-04 | 2013-03-13 | アイアールエム・リミテッド・ライアビリティ・カンパニー | c−kitおよびPDGFRキナーゼ阻害剤としてのピリミジン誘導体および組成物 |
US8653262B2 (en) | 2007-05-31 | 2014-02-18 | Boehringer Ingelheim International Gmbh | CCR2 receptor antagonists and uses thereof |
EA017392B1 (ru) * | 2007-08-22 | 2012-12-28 | Айрм Ллк | Производные 2-гетероариламинопиримидина в качестве ингибиторов киназ |
EP2190825B1 (fr) * | 2007-08-22 | 2014-04-09 | Irm Llc | Composés et compositions de 5- (4- (haloalkoxy) phényl) pyrimidine-2-amine utilisés comme inhibiteurs de kinases |
US20090170842A1 (en) | 2007-11-14 | 2009-07-02 | University Of Kansas | Brca1-based breast or ovarian cancer prevention agents and methods of use |
BRPI0908849A2 (pt) | 2008-02-22 | 2015-08-25 | Irm Llc | Composto e composições como c-kit e inibidores de pdgfr quinase |
EP2268635B1 (fr) | 2008-04-21 | 2015-06-10 | Taigen Biotechnology Co., Ltd. | Composés hétérocycliques |
AU2009327127C1 (en) | 2008-12-19 | 2017-03-09 | Centrexion Therapeutics Corporation | Cyclic pyrimidin-4-carboxamides as CCR2 receptor antagonists for treatment of inflammation, asthma and COPD |
CN102933579B (zh) | 2009-12-17 | 2015-07-15 | 贝林格尔.英格海姆国际有限公司 | 新的ccr2受体拮抗剂及其用途 |
EP2569295B1 (fr) | 2010-05-12 | 2014-11-19 | Boehringer Ingelheim International GmbH | Nouveaux antagonistes du récepteur ccr2, son procédé de production et utilisation associée en tant que médicaments |
US8877745B2 (en) | 2010-05-12 | 2014-11-04 | Boehringer Ingelheim International Gmbh | CCR2 receptor antagonists, method for producing the same, and use thereof as medicaments |
WO2011144501A1 (fr) | 2010-05-17 | 2011-11-24 | Boehringer Ingelheim International Gmbh | Antagonistes du récepteur ccr2 et leurs utilisations |
WO2011147772A1 (fr) | 2010-05-25 | 2011-12-01 | Boehringer Ingelheim International Gmbh | Antagonistes du récepteur ccr2 |
JP5721242B2 (ja) | 2010-06-01 | 2015-05-20 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 新規ccr2アンタゴニスト |
GB201009603D0 (en) | 2010-06-08 | 2010-07-21 | Cambridge Entpr Ltd | Anti-inflammatory agent |
RU2436786C1 (ru) * | 2010-07-23 | 2011-12-20 | Александр Васильевич Иващенко | Замещенные индолы, противовирусный активный компонент, способ получения и применения |
WO2012168315A1 (fr) * | 2011-06-09 | 2012-12-13 | Boehringer Ingelheim International Gmbh | Pipéridines substituées à titre de modulateurs de gpr119 pour le traitement des troubles métaboliques |
EP2731941B1 (fr) | 2011-07-15 | 2019-05-08 | Boehringer Ingelheim International GmbH | Antagonistes ccr2, nouveaux et sélectifs |
RS59411B1 (sr) | 2013-03-13 | 2019-11-29 | Forma Therapeutics Inc | Derivati 2-hidroksi-1-{4-[(4-fenilfenil)karbonil]piperazin-1-il}etan-1-ona i srodna jedinjenja kao inhibitori sintaze masnih kiselina (fasn) za lečenje kancera |
HUE036713T2 (hu) | 2013-11-18 | 2018-07-30 | Elanco Tiergesundheit Ag | (Hetero)arilamidok endoparaziták visszaszorítására |
US10752588B2 (en) | 2014-12-19 | 2020-08-25 | The Broad Institute, Inc. | Dopamine D2 receptor ligands |
EP3233077A4 (fr) | 2014-12-19 | 2018-08-08 | The Broad Institute Inc. | Ligands des récepteurs dopaminergiques d2 |
CA2990460C (fr) | 2015-07-02 | 2023-10-17 | Centrexion Therapeutics Corporation | Citrate de (4-((3r,4r)-3-methoxytetrahydro-pyran-4-ylamino)piperidin-1-yl)(5-methyl-6-(((2r,6s)-(p-tolyl)tetrahydro-2h-pyran-2-yl)methylamino)pyrimidin-4-yl)methanone |
EP3554258B1 (fr) | 2016-12-15 | 2023-07-19 | Société des Produits Nestlé S.A. | Compositions et méthodes de modulation du phosphore ou des enzymes chez un animal de compagnie |
TWI767148B (zh) | 2018-10-10 | 2022-06-11 | 美商弗瑪治療公司 | 抑制脂肪酸合成酶(fasn) |
WO2020092395A1 (fr) | 2018-10-29 | 2020-05-07 | Forma Therapeutics, Inc. | Formes solides de (4-(2-fluoro-4-(1-méthyl-1h-benzo[d]imidazol-5-yl)benzoyl)pipérazin-1-yl)(1-hydroxycyclopropyl)méthanone |
MX2021009863A (es) | 2019-03-21 | 2021-11-12 | Onxeo | Una molecula dbait en combinacion con inhibidor de quinasa para el tratamiento del cancer. |
KR20220098759A (ko) | 2019-11-08 | 2022-07-12 | 인쎄름 (엥스띠뛰 나씨오날 드 라 쌍떼 에 드 라 흐쉐르슈 메디깔) | 키나제 억제제에 대해 내성을 획득한 암의 치료 방법 |
WO2021148581A1 (fr) | 2020-01-22 | 2021-07-29 | Onxeo | Nouvelle molécule dbait et son utilisation |
CN114763342A (zh) * | 2021-01-09 | 2022-07-19 | 江苏天士力帝益药业有限公司 | 一种高纯度4-甲基哌嗪-1-甲酸酯的合成方法 |
WO2022157686A1 (fr) * | 2021-01-22 | 2022-07-28 | Ildong Pharmaceutical Co., Ltd. | Inhibiteurs de la protéine anoctamine 6 et leurs utilisations |
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DE1670537A1 (de) * | 1966-11-09 | 1970-10-29 | Degussa | Verfahren zur Herstellung neuer substituierter Aminopyrimidine |
DE1918073A1 (de) * | 1969-04-09 | 1970-10-15 | Boehringer Sohn Ingelheim | Verfahren zur Herstellung neuer 5-Aryl-1H-1,5-benzodiazepin-2,4-dione |
GB1534593A (en) * | 1976-09-03 | 1978-12-06 | Soc D Etudes Prod Chimique | N-2,6-dichlorophenyl-2-aminopyrimidine and therapeutic compositions containing it |
EP0164204A1 (fr) | 1984-05-12 | 1985-12-11 | FISONS plc | Pyrimidines utiles dans des préparations pharmaceutiques |
ES2143992T3 (es) * | 1991-11-25 | 2000-06-01 | Pfizer | Derivados de 5-(hetero- o carbociclilamino)-indol, su preparacion y uso como 5-ht1 agonistas. |
CA2383546A1 (fr) * | 1999-06-30 | 2001-01-04 | William H. Parsons | Composes inhibiteurs de la src kinase |
GB0022438D0 (en) * | 2000-09-13 | 2000-11-01 | Novartis Ag | Organic Compounds |
US20040266771A1 (en) * | 2001-06-29 | 2004-12-30 | Alain Moussy | Use of tyrosine kinase inhibitors for treating bone loss |
US7109204B2 (en) * | 2001-08-01 | 2006-09-19 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
AU2002342051B2 (en) * | 2001-10-12 | 2009-06-11 | Irm Llc | Kinase inhibitor scaffolds and methods for their preparation |
EP1753750A1 (fr) * | 2004-05-20 | 2007-02-21 | Sugen, Inc. | Heteroarylamines de tiophene |
KR20070113288A (ko) * | 2005-03-16 | 2007-11-28 | 탈자진 인코포레이티드 | 피리미딘 화합물 및 사용 방법 |
EP1893216A4 (fr) * | 2005-06-08 | 2012-08-08 | Targegen Inc | Methodes et preparations pour le traitement de troubles oculaires |
CA2622494A1 (fr) * | 2005-09-27 | 2007-04-05 | Irm Llc | Composes et compositions contenant de la diarylamine, et utilisation en tant que modulateurs de recepteurs de c-kit |
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2006
- 2006-09-26 CA CA002622494A patent/CA2622494A1/fr not_active Abandoned
- 2006-09-26 AU AU2006297089A patent/AU2006297089B2/en not_active Ceased
- 2006-09-26 ES ES06815653T patent/ES2378153T3/es active Active
- 2006-09-26 KR KR1020087007357A patent/KR101415426B1/ko not_active IP Right Cessation
- 2006-09-26 AT AT06815653T patent/ATE534293T1/de active
- 2006-09-26 NZ NZ566862A patent/NZ566862A/en not_active IP Right Cessation
- 2006-09-26 CN CNA2006800355479A patent/CN101272685A/zh active Pending
- 2006-09-26 US US11/535,455 patent/US7514447B2/en active Active
- 2006-09-26 EP EP06815653A patent/EP1928236B1/fr not_active Not-in-force
- 2006-09-26 WO PCT/US2006/037820 patent/WO2007038669A2/fr active Application Filing
- 2006-09-26 BR BRPI0616575-3A patent/BRPI0616575A2/pt not_active IP Right Cessation
- 2006-09-26 JP JP2008533595A patent/JP5335426B2/ja not_active Expired - Fee Related
- 2006-09-26 RU RU2008116313/04A patent/RU2436776C2/ru not_active IP Right Cessation
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2007
- 2007-10-31 US US11/933,056 patent/US7592349B2/en not_active Expired - Fee Related
- 2007-10-31 US US11/932,945 patent/US7563894B2/en active Active
- 2007-10-31 US US11/933,030 patent/US7638523B2/en not_active Expired - Fee Related
- 2007-10-31 US US11/932,986 patent/US20080139597A1/en not_active Abandoned
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2008
- 2008-02-22 ZA ZA200801732A patent/ZA200801732B/xx unknown
- 2008-03-04 IL IL189927A patent/IL189927A0/en unknown
- 2008-03-26 TN TNP2008000140A patent/TNSN08140A1/fr unknown
- 2008-04-04 MA MA30814A patent/MA29851B1/fr unknown
- 2008-04-24 NO NO20081975A patent/NO20081975L/no not_active Application Discontinuation
- 2008-04-25 EC EC2008008402A patent/ECSP088402A/es unknown
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2009
- 2009-05-29 US US12/475,266 patent/US20090264649A1/en not_active Abandoned
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