MA25809A1 - Derives d'arylmethylamine pour usage comme inhibiteurs de tryptase - Google Patents
Derives d'arylmethylamine pour usage comme inhibiteurs de tryptaseInfo
- Publication number
- MA25809A1 MA25809A1 MA26919A MA26919A MA25809A1 MA 25809 A1 MA25809 A1 MA 25809A1 MA 26919 A MA26919 A MA 26919A MA 26919 A MA26919 A MA 26919A MA 25809 A1 MA25809 A1 MA 25809A1
- Authority
- MA
- Morocco
- Prior art keywords
- tryptase
- tryptase inhibitors
- arylmethylamine
- derivatives
- arylmethylamine derivatives
- Prior art date
Links
- 239000002750 tryptase inhibitor Substances 0.000 title 1
- 102000001400 Tryptase Human genes 0.000 abstract 2
- 108060005989 Tryptase Proteins 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 230000001668 ameliorated effect Effects 0.000 abstract 1
- 208000006673 asthma Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
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- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physical Education & Sports Medicine (AREA)
- Pulmonology (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Heart & Thoracic Surgery (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Hematology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Virology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Ophthalmology & Optometry (AREA)
- Urology & Nephrology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Gastroenterology & Hepatology (AREA)
- Obesity (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0012362.0A GB0012362D0 (en) | 2000-05-22 | 2000-05-22 | Chemical compounds |
| US09/843,126 US6977263B2 (en) | 2000-05-22 | 2001-04-26 | Chemical compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA25809A1 true MA25809A1 (fr) | 2003-07-01 |
Family
ID=26244322
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA26919A MA25809A1 (fr) | 2000-05-22 | 2002-11-21 | Derives d'arylmethylamine pour usage comme inhibiteurs de tryptase |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US20050228018A1 (fr) |
| EP (1) | EP1296972B1 (fr) |
| KR (1) | KR100858642B1 (fr) |
| CN (1) | CN1230431C (fr) |
| AR (1) | AR033525A1 (fr) |
| AU (2) | AU2001257413B2 (fr) |
| BR (1) | BR0111206A (fr) |
| CA (1) | CA2409827C (fr) |
| DZ (1) | DZ3347A1 (fr) |
| HR (1) | HRP20020926B1 (fr) |
| HU (1) | HU227630B1 (fr) |
| IL (1) | IL152830A0 (fr) |
| MA (1) | MA25809A1 (fr) |
| MX (1) | MXPA02011400A (fr) |
| NO (1) | NO327378B1 (fr) |
| OA (1) | OA12274A (fr) |
| PL (1) | PL360495A1 (fr) |
| WO (1) | WO2001090101A1 (fr) |
Families Citing this family (57)
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| KR20040097375A (ko) * | 2002-04-23 | 2004-11-17 | 시오노기 앤드 컴파니, 리미티드 | 피라졸로[1, 5-에이]피리미딘 유도체 및 이를 함유한엔에이디(피)에이취 산화효소 저해제 |
| PL378268A1 (pl) | 2002-11-26 | 2006-03-20 | Pfizer Products Inc. | Aktywatory PPAR |
| GB0308613D0 (en) * | 2002-12-26 | 2003-05-21 | Aventis Pharma Inc | 4-(3-Aminomethylphenyl) piperidin-1-yl- 5-(2-fluorophenylethynyl) furan-2-yl- methanone as an inhibitor of mast cell tryptase |
| ES2770035T3 (es) | 2003-04-11 | 2020-06-30 | Ptc Therapeutics Inc | Compuesto de ácido 1,2,4-oxadiazol benzoico y su uso para la supresión sin sentido y el tratamiento de enfermedades |
| CA2525325A1 (fr) * | 2003-05-01 | 2004-11-18 | Abbott Laboratories | Pyrazole-amides et sulfonamides modulateurs des canaux sodiques |
| EP1648879B1 (fr) | 2003-07-24 | 2008-10-22 | Euro-Celtique S.A. | Composes de 4-heteroaryle-tetrahydropyridyle utiles pour le traitement ou la prevention de la douleur |
| KR101182690B1 (ko) * | 2004-03-02 | 2012-09-14 | 아벤티스 파마슈티칼스 인크. | 트립타제 억제제의 제조방법 |
| EP1571150A1 (fr) * | 2004-03-02 | 2005-09-07 | Aventis Pharma Deutschland GmbH | Procédé pour la prparation des inhibiteurs de tryptase |
| DE602005017129D1 (de) * | 2004-03-22 | 2009-11-26 | Lilly Co Eli | Pyridyl-derivate und ihre verwendung als mglu5-rezeptorantagonisten |
| DOP2005000039A (es) * | 2004-03-26 | 2005-10-31 | Aventis Pharma Inc | Hidrocloruro de [4-(5-aminometil-2-fluoro-fenil)- piperidin-1-il]-(4-bomo-3-metil-5-propoxi-tiofen-2-il)-metanona como un inhibidor de la triptasa de mastocitos |
| CA2569530C (fr) | 2004-07-01 | 2013-07-30 | Daiichi Asubio Pharma Co.,Ltd. | Derive de thienopyrazole ayant une activite d'inhibition de la pde 7 |
| US8188277B2 (en) | 2004-08-06 | 2012-05-29 | Otsuka Pharmaceutical Co., Ltd. | Aromatic compounds for suppressing the generation of collagen |
| JP2008515992A (ja) * | 2004-10-13 | 2008-05-15 | ピーティーシー セラピューティクス,インコーポレーテッド | 体細胞変異に起因する疾患の阻止/治療用医薬を製造するための規定化合物の使用 |
| WO2006058294A2 (fr) | 2004-11-29 | 2006-06-01 | Vertex Pharmaceuticals Incorporated | Modulateurs des recepteurs muscariniques |
| AU2005318465A1 (en) * | 2004-12-21 | 2006-06-29 | Devgen N.V. | Compounds with Kv4 ion channel activity |
| US7576218B2 (en) * | 2005-10-11 | 2009-08-18 | Chemocentryx, Inc. | 4-phenylpiperdine-pyrazole CCR1 antagonists |
| MY146514A (en) | 2005-12-05 | 2012-08-15 | Otsuka Pharma Co Ltd | Diarylether derivatives as antitumor agents |
| WO2007117438A2 (fr) | 2006-03-30 | 2007-10-18 | Ptc Therapeutics, Inc. | Méthodes de production d'une protéine fonctionnelle à partir d'un adn présentant une mutation non-sens et traitement des troubles associés |
| WO2008019302A1 (fr) * | 2006-08-04 | 2008-02-14 | Decode Genetics Ehf | Inhibiteurs pyrazolylphényliques et pyrrolylphényliques de la lta4h pour le traitement de l'inflammation |
| UA95978C2 (ru) | 2006-10-02 | 2011-09-26 | Оцука Фармас'Ютікел Ко., Лтд. | Ингибитор активации stat3/5 |
| TW200833663A (en) * | 2006-12-21 | 2008-08-16 | Astrazeneca Ab | Therapeutic agents |
| WO2008075077A1 (fr) * | 2006-12-21 | 2008-06-26 | Astrazeneca Ab | Dérivés de pipéridine destinés au traitement de l'obésité |
| 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 |
| WO2009044403A2 (fr) * | 2007-10-05 | 2009-04-09 | Juvenis Ltd. | Compositions polymères biodégradables injectables pour la réparation et l'augmentation des tissus mous |
| US8158792B2 (en) | 2007-11-21 | 2012-04-17 | Janssen Pharmaceutica N.V. | Spiropiperidines for use as tryptase inhibitors |
| EP2234485B1 (fr) * | 2007-12-20 | 2013-11-13 | Teva Pharmaceutical Industries, Ltd. | Préparations de laquinimod stables |
| HRP20151338T1 (hr) * | 2008-08-22 | 2016-01-15 | Sanofi | [4-(5-aminometil-2-fluoro-fenil)-piperidin-1-il]-[7-fluoro-1-(2-metoksi-etil)-4trifluorometoksi-1h-indol-3-il]metanon kao inhibitor triptaze mastocita |
| US20120053164A1 (en) | 2008-12-19 | 2012-03-01 | Boehringer Ingelheim International Gmbh | Cyclic pyrimidin-4-carboxamides as ccr2 receptor antagonists for treatment of inflammation, asthma and copd |
| FR2955324A1 (fr) * | 2010-01-15 | 2011-07-22 | Sanofi Aventis | [4-(5-aminomethyl-phenyl)-piperidin-1-yl]-1h-indol-3-yl]-methanones disubstituees |
| EP2513093B1 (fr) | 2009-12-17 | 2014-08-27 | Boehringer Ingelheim International GmbH | Nouveaux antagonistes du récepteur CCR2 et leurs utilisations |
| MX2012006805A (es) * | 2009-12-23 | 2012-07-10 | Sanofi Sa | Indolil-piperidinil bencilaminas como inhibidores de beta-triptasa. |
| WO2011078983A1 (fr) * | 2009-12-23 | 2011-06-30 | Sanofi | Traitement des maladies inflammatoires intestinales |
| EP2516418B1 (fr) * | 2009-12-23 | 2014-05-14 | Sanofi | Promédicaments de [4[4-(5-aminométhyl-2-fluoro-phényl)-pipéridin-1-yl]-(1h-pyrrolo-pyridin-yl)-méthanones et leur synthèse |
| WO2011079103A1 (fr) * | 2009-12-23 | 2011-06-30 | Sanofi | Spiropipéridine benzylaminesutiles comme inhibitrices de la bêta-tryptase |
| RU2012131280A (ru) * | 2009-12-23 | 2014-02-10 | Санофи | [4-(5-аминометил-2-фторфенил)пиперидин-1-ил]-(1н-пирролопиридинил)метаноны и их синтез |
| US9492439B2 (en) * | 2010-03-11 | 2016-11-15 | New York University | Amido compounds as RORγt modulators and uses thereof |
| US8946218B2 (en) | 2010-05-12 | 2015-02-03 | Boehringer Ingelheim International Gmbh | CCR2 receptor antagonists, method for producing the same, and use thereof as medicaments |
| WO2011141474A1 (fr) | 2010-05-12 | 2011-11-17 | Boehringer Ingelheim International Gmbh | Nouveaux antagonistes des récepteurs ccr2, procédé de production associé et application comme médicaments |
| EP2571870B1 (fr) | 2010-05-17 | 2015-01-21 | Boehringer Ingelheim International GmbH | Antagonistes de ccr2 et leurs utilisations |
| US9018212B2 (en) | 2010-05-25 | 2015-04-28 | Boehringer Ingelheim International Gmbh | Pyridazine carboxamides as CCR2 receptor antagonists |
| EP2576538B1 (fr) | 2010-06-01 | 2015-10-28 | Boehringer Ingelheim International GmbH | Nouveaux antagonistes de CCR2 |
| US20140194383A1 (en) | 2011-04-07 | 2014-07-10 | Cornell University | Monomers capable of dimerizing in an aqueous solution, and methods of using same |
| EP2731941B1 (fr) | 2011-07-15 | 2019-05-08 | Boehringer Ingelheim International GmbH | Antagonistes ccr2, nouveaux et sélectifs |
| US10092574B2 (en) | 2012-09-26 | 2018-10-09 | Valorisation-Recherche, Limited Partnership | Inhibitors of polynucleotide repeat-associated RNA foci and uses thereof |
| TW201439066A (zh) | 2012-11-30 | 2014-10-16 | Kyowa Hakko Kirin Co Ltd | 含氮雜環化合物 |
| TW201441193A (zh) * | 2012-12-06 | 2014-11-01 | Kyowa Hakko Kirin Co Ltd | 吡啶酮化合物 |
| BR112016011079A2 (pt) | 2013-11-15 | 2017-12-05 | Wistar Inst | ?inibidores de ebna1 e seu método de uso? |
| CA2942147C (fr) | 2014-03-06 | 2022-12-13 | Ptc Therapeutics, Inc. | Compositions pharmaceutiques et sels d'un acide benzoique 1,2,4-oxadiazole |
| KR102616818B1 (ko) | 2015-05-14 | 2023-12-22 | 더 위스타 인스티튜트 오브 아나토미 앤드 바이올로지 | Ebna1 억제제 및 그의 사용 방법 |
| WO2017004537A1 (fr) | 2015-07-02 | 2017-01-05 | Centrexion Therapeutics Corporation | Citrate de (4-((3r,4r)-3-méthoxytétrahydro-pyran-4-ylamino)pipéridin-1-yl)(5-méthyl-6-(((2r,6s)-(p-tolyl)tétrahydro-2h-pyran-2-yl)méthylamino)pyrimidin-4-yl)méthanone |
| CN108348527A (zh) | 2015-10-30 | 2018-07-31 | Ptc医疗公司 | 用于治疗癫痫的方法 |
| CN112543634A (zh) | 2018-05-17 | 2021-03-23 | 威斯达研究所 | Ebna1抑制剂晶体形式及其制备和使用方法 |
| WO2020163689A1 (fr) | 2019-02-08 | 2020-08-13 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | Inhibiteurs de formation de 20-hete |
| CN110357833B (zh) * | 2019-06-03 | 2022-05-24 | 杭州维坦医药科技有限公司 | 芳杂乙酰胺类衍生物及其制备和应用 |
| TW202115086A (zh) * | 2019-06-28 | 2021-04-16 | 美商輝瑞大藥廠 | Bckdk抑制劑 |
| BR112022024300A2 (pt) * | 2020-06-04 | 2023-01-24 | Pillai Universal Llc | Moléculas pequenas para degradação direcionada de kras não direcionado na terapia de câncer |
| WO2025195508A1 (fr) * | 2024-03-22 | 2025-09-25 | 润尔眼科药物(广州)有限公司 | Composé de phényle hétérocyclique et son utilisation |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4407139A1 (de) * | 1994-03-04 | 1995-09-07 | Thomae Gmbh Dr K | Aryl-1-azacycloalkane und deren Salze, diese Verbindungen enthaltende Arzneimittel und deren Verwendung sowie Verfahren zu ihrer Herstellung |
| US6673908B1 (en) * | 1999-02-22 | 2004-01-06 | Nuvelo, Inc. | Tumor necrosis factor receptor 2 |
-
2001
- 2001-04-27 AU AU2001257413A patent/AU2001257413B2/en not_active Ceased
- 2001-04-27 CA CA2409827A patent/CA2409827C/fr not_active Expired - Lifetime
- 2001-04-27 KR KR1020027015683A patent/KR100858642B1/ko not_active Expired - Fee Related
- 2001-04-27 WO PCT/US2001/013811 patent/WO2001090101A1/fr not_active Ceased
- 2001-04-27 EP EP01930925A patent/EP1296972B1/fr not_active Expired - Lifetime
- 2001-04-27 IL IL15283001A patent/IL152830A0/xx unknown
- 2001-04-27 OA OA1200200357A patent/OA12274A/en unknown
- 2001-04-27 HR HR20020926A patent/HRP20020926B1/xx not_active IP Right Cessation
- 2001-04-27 PL PL36049501A patent/PL360495A1/xx not_active Application Discontinuation
- 2001-04-27 CN CNB018119522A patent/CN1230431C/zh not_active Expired - Lifetime
- 2001-04-27 MX MXPA02011400A patent/MXPA02011400A/es active IP Right Grant
- 2001-04-27 DZ DZ013347A patent/DZ3347A1/fr active
- 2001-04-27 HU HU0302485A patent/HU227630B1/hu not_active IP Right Cessation
- 2001-04-27 BR BR0111206-6A patent/BR0111206A/pt not_active IP Right Cessation
- 2001-04-27 AR ARP010102009A patent/AR033525A1/es active IP Right Grant
- 2001-04-27 AU AU5741301A patent/AU5741301A/xx active Pending
-
2002
- 2002-11-21 MA MA26919A patent/MA25809A1/fr unknown
- 2002-11-21 NO NO20025601A patent/NO327378B1/no not_active IP Right Cessation
-
2005
- 2005-02-14 US US11/057,809 patent/US20050228018A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| WO2001090101A1 (fr) | 2001-11-29 |
| KR20030003294A (ko) | 2003-01-09 |
| EP1296972B1 (fr) | 2009-12-23 |
| NO20025601D0 (no) | 2002-11-21 |
| HUP0302485A2 (hu) | 2003-12-29 |
| AU5741301A (en) | 2001-12-03 |
| US20050228018A1 (en) | 2005-10-13 |
| BR0111206A (pt) | 2003-04-15 |
| MXPA02011400A (es) | 2003-05-23 |
| IL152830A0 (en) | 2003-06-24 |
| NO20025601L (no) | 2003-01-06 |
| EP1296972A1 (fr) | 2003-04-02 |
| CA2409827A1 (fr) | 2001-11-29 |
| HRP20020926A2 (en) | 2005-02-28 |
| KR100858642B1 (ko) | 2008-09-17 |
| HUP0302485A3 (en) | 2007-09-28 |
| CA2409827C (fr) | 2010-06-01 |
| PL360495A1 (en) | 2004-09-06 |
| DZ3347A1 (fr) | 2001-11-29 |
| HU227630B1 (hu) | 2011-10-28 |
| OA12274A (en) | 2006-05-09 |
| CN1230431C (zh) | 2005-12-07 |
| HRP20020926B1 (en) | 2011-01-31 |
| NO327378B1 (no) | 2009-06-22 |
| HK1057899A1 (en) | 2004-04-23 |
| AR033525A1 (es) | 2003-12-26 |
| CN1439003A (zh) | 2003-08-27 |
| AU2001257413B2 (en) | 2007-01-18 |
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