TNSN08140A1 - - Google Patents
Info
- Publication number
- TNSN08140A1 TNSN08140A1 TNP2008000140A TNSN08140A TNSN08140A1 TN SN08140 A1 TNSN08140 A1 TN SN08140A1 TN P2008000140 A TNP2008000140 A TN P2008000140A TN SN08140 A TNSN08140 A TN SN08140A TN SN08140 A1 TNSN08140 A1 TN SN08140A1
- Authority
- TN
- Tunisia
- Prior art keywords
- compounds
- methods
- medicaments
- activity
- pharmaceutical compositions
- Prior art date
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
- A01N43/42—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings condensed with carbocyclic rings
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
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- C07D—HETEROCYCLIC COMPOUNDS
- 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
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 |
Publications (1)
Publication Number | Publication Date |
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TNSN08140A1 true TNSN08140A1 (fr) | 2009-07-14 |
Family
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Family Applications (1)
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TNP2008000140A TNSN08140A1 (fr) | 2005-09-27 | 2008-03-26 |
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) |
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US8193206B2 (en) | 2005-06-14 | 2012-06-05 | Taigen Biotechnology Co., Ltd. | Pyrimidine compounds |
AU2006259525B2 (en) * | 2005-06-14 | 2012-05-24 | Gpcr Therapeutics, Inc | Pyrimidine compounds |
NZ566862A (en) * | 2005-09-27 | 2010-12-24 | Irm Llc | Diarylamine-containing compounds and compositions, and their use as modulators of C-kit receptors |
EP2404905A1 (fr) * | 2006-03-31 | 2012-01-11 | Novartis AG | Nouveaux composés |
WO2008137605A1 (fr) | 2007-05-04 | 2008-11-13 | Irm Llc | Dérivés de pyrimidine et compositions utiles en tant qu'inhibiteurs des kinases c-kit et pdgfr |
JP5603770B2 (ja) | 2007-05-31 | 2014-10-08 | 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 | Ccr2受容体拮抗薬およびその使用 |
US8288540B2 (en) | 2007-08-22 | 2012-10-16 | Irm Llc | 2-heteroarylamino-pyrimidine derivatives as kinase inhibitors |
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 |
WO2009105712A1 (fr) | 2008-02-22 | 2009-08-27 | Irm Llc | Composés et compositions hétérocycliques comme inhibiteurs de c-kit et pdgfr kinase |
PT2268635E (pt) | 2008-04-21 | 2015-10-06 | Taigen Biotechnology Co Ltd | Compostos heterocíclicos |
PE20120061A1 (es) | 2008-12-19 | 2012-02-19 | Boehringer Ingelheim Int | Derivados de pirimidina como antagonistas del receptor ccr2 |
EA024397B1 (ru) | 2009-12-17 | 2016-09-30 | Сентрекшн Терапьютикс Корпорейшн | Новые антагонисты рецептора ccr2 и их применение |
JP2013526507A (ja) | 2010-05-12 | 2013-06-24 | 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受容体アンタゴニスト、その製造方法及び薬物としてのその使用 |
WO2011141477A1 (fr) | 2010-05-12 | 2011-11-17 | Boehringer Ingelheim International Gmbh | Nouveaux antagonistes du récepteur ccr2, leur procédé de production et leur utilisation en tant que médicaments |
JP5647339B2 (ja) | 2010-05-17 | 2014-12-24 | 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 | Ccr2アンタゴニスト及びこれらの使用 |
WO2011147772A1 (fr) | 2010-05-25 | 2011-12-01 | Boehringer Ingelheim International Gmbh | Antagonistes du récepteur ccr2 |
US8962656B2 (en) | 2010-06-01 | 2015-02-24 | Boehringer Ingelheim International Gmbh | CCR2 antagonists |
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 |
US8921398B2 (en) * | 2011-06-09 | 2014-12-30 | Boehringer Ingelheim International Gmbh | N-cyclopropyl-N-piperidinyl-amide derivatives, pharmaceutical compositions and uses thereof |
JP5786258B2 (ja) | 2011-07-15 | 2015-09-30 | 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 | 新規かつ選択的なccr2拮抗薬 |
RU2737434C2 (ru) | 2013-03-13 | 2020-11-30 | Форма Терапьютикс, Инк. | Новые соединения и композиции для ингибирования fasn |
JP6140373B2 (ja) | 2013-11-18 | 2017-05-31 | ノバルティス ティーアゲズントハイト アーゲー | 新規化合物 |
US10633336B2 (en) | 2014-12-19 | 2020-04-28 | The Broad Institute, Inc. | Dopamine D2 receptor ligands |
WO2016100823A1 (fr) | 2014-12-19 | 2016-06-23 | The Broad Institute, Inc. | Ligands du récepteur d2 de la dopamine |
JP6917910B2 (ja) | 2015-07-02 | 2021-08-11 | セントレクシオン セラピューティクス コーポレイション | (4−((3r,4r)−3−メトキシテトラヒドロ−ピラン−4−イルアミノ)ピペリジン−1−イル)(5−メチル−6−(((2r,6s)−6−(p−トリル)テトラヒドロ−2h−ピラン−2−イル)メチルアミノ)ピリミジン−4イル)メタノンクエン酸塩 |
US11758928B2 (en) | 2016-12-15 | 2023-09-19 | Société des Produits Nestlé S.A. | Compositions and methods that modulate phosphorus or enzymes in a companion animal |
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 |
CA3129665A1 (fr) | 2019-03-21 | 2020-09-24 | Onxeo | Molecule dbait associee a un inhibiteur de kinase pour le traitement du cancer |
EP4054579A1 (fr) | 2019-11-08 | 2022-09-14 | Institut National de la Santé et de la Recherche Médicale (INSERM) | Méthodes pour le traitement de cancers qui ont acquis une résistance aux inhibiteurs de kinase |
WO2021148581A1 (fr) | 2020-01-22 | 2021-07-29 | Onxeo | Nouvelle molécule dbait et son utilisation |
US20230080054A1 (en) * | 2021-01-22 | 2023-03-16 | Ildong Pharmaceutical Co., Ltd. | Inhibitors of anoctamin 6 protein and uses thereof |
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DE1670536B2 (de) * | 1966-11-09 | 1975-05-28 | Deutsche Gold- Und Silber-Scheideanstalt Vormals Roessler, 6000 Frankfurt | Neue 2-Anilino-5-acylamino-pyrimidlne |
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 |
ATE190608T1 (de) * | 1991-11-25 | 2000-04-15 | Pfizer | 5-(hetero- oder carbocyclylamino)-indol derivate, deren herstellung und deren verwendung als 5-ht1 agonisten |
AU5636900A (en) * | 1999-06-30 | 2001-01-31 | Merck & Co., Inc. | Src kinase inhibitor compounds |
GB0022438D0 (en) * | 2000-09-13 | 2000-11-01 | Novartis Ag | Organic Compounds |
CA2452390A1 (fr) * | 2001-06-29 | 2003-01-09 | Ab Science | Utilisation d'inhibiteurs de la tyrosine kinase dans le traitement de la perte osseuse |
WO2003011837A1 (fr) * | 2001-08-01 | 2003-02-13 | Merck & Co., Inc. | Inhibiteurs de la tyrosine kinase |
JP2005512972A (ja) * | 2001-10-12 | 2005-05-12 | アイアールエム エルエルシー | キナーゼ阻害剤足場およびそれらの調製方法 |
BRPI0510032A (pt) * | 2004-05-20 | 2007-10-02 | Sugen Inc | tiofeno heteroaril aminas |
CA2600531A1 (fr) * | 2005-03-16 | 2006-09-28 | Targegen, Inc. | Composes de pyrimidine et methodes d'utilisation |
JP2008543775A (ja) * | 2005-06-08 | 2008-12-04 | ターゲジェン インコーポレーティッド | 眼の障害を治療するための方法および組成物 |
NZ566862A (en) * | 2005-09-27 | 2010-12-24 | Irm Llc | Diarylamine-containing compounds and compositions, and their use as modulators of C-kit receptors |
-
2006
- 2006-09-26 NZ NZ566862A patent/NZ566862A/en not_active IP Right Cessation
- 2006-09-26 CA CA002622494A patent/CA2622494A1/fr not_active Abandoned
- 2006-09-26 WO PCT/US2006/037820 patent/WO2007038669A2/fr active Application Filing
- 2006-09-26 AU AU2006297089A patent/AU2006297089B2/en not_active Ceased
- 2006-09-26 ES ES06815653T patent/ES2378153T3/es active Active
- 2006-09-26 BR BRPI0616575-3A patent/BRPI0616575A2/pt not_active IP Right Cessation
- 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 US US11/535,455 patent/US7514447B2/en active Active
- 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
- 2006-09-26 EP EP06815653A patent/EP1928236B1/fr not_active Not-in-force
- 2006-09-26 CN CNA2006800355479A patent/CN101272685A/zh active Pending
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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 US11/932,986 patent/US20080139597A1/en not_active Abandoned
- 2007-10-31 US US11/933,030 patent/US7638523B2/en not_active Expired - Fee Related
-
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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