BRPI0418166A - compostos de bicicloeteroarilamina como ligandos de canal de ìon e usos destes - Google Patents
compostos de bicicloeteroarilamina como ligandos de canal de ìon e usos destesInfo
- Publication number
- BRPI0418166A BRPI0418166A BRPI0418166-2A BRPI0418166A BRPI0418166A BR PI0418166 A BRPI0418166 A BR PI0418166A BR PI0418166 A BRPI0418166 A BR PI0418166A BR PI0418166 A BRPI0418166 A BR PI0418166A
- Authority
- BR
- Brazil
- Prior art keywords
- compounds
- ion channel
- bicycloetheroylamine
- channel ligands
- ligands
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 3
- 102000004310 Ion Channels Human genes 0.000 title 1
- 239000003446 ligand Substances 0.000 title 1
- 206010061218 Inflammation Diseases 0.000 abstract 1
- 241000124008 Mammalia Species 0.000 abstract 1
- 208000002193 Pain Diseases 0.000 abstract 1
- -1 amine compounds Chemical class 0.000 abstract 1
- 230000004054 inflammatory process Effects 0.000 abstract 1
- 208000014674 injury Diseases 0.000 abstract 1
- 230000036407 pain Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 230000008736 traumatic injury Effects 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- 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
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Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pulmonology (AREA)
- Diabetes (AREA)
- Pain & Pain Management (AREA)
- Immunology (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Psychiatry (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Psychology (AREA)
- Otolaryngology (AREA)
- Rheumatology (AREA)
- Vascular Medicine (AREA)
- Ophthalmology & Optometry (AREA)
- Anesthesiology (AREA)
- Child & Adolescent Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Endocrinology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
Abstract
COMPOSTOS DE BICICLOETEROARILAMINA COMO LIGANDOS DE CANAL DE ìON E USOS DESTES. A presente invenção refere-se a compostos de amina que têm uma fórmula representada pela seguinte: Os compostos podem ser preparados como composições farmacêuticas e podem ser empregados para a prevenção e tratamento de uma veriedade de condições em mamíferos incluindo seres humanos, incluindo por meio de exemplos não limitantes,dor, inflamação, lesão traumática e outros.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US53237103P | 2003-12-24 | 2003-12-24 | |
| PCT/US2004/043456 WO2005066171A1 (en) | 2003-12-24 | 2004-12-23 | Bicycloheteroarylamine compounds as ion channel ligands and uses thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BRPI0418166A true BRPI0418166A (pt) | 2007-06-19 |
Family
ID=34748796
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0418166-2A BRPI0418166A (pt) | 2003-12-24 | 2004-12-23 | compostos de bicicloeteroarilamina como ligandos de canal de ìon e usos destes |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US7414131B2 (pt) |
| EP (1) | EP1697361A1 (pt) |
| JP (1) | JP2007517045A (pt) |
| AR (1) | AR051156A1 (pt) |
| BR (1) | BRPI0418166A (pt) |
| CA (1) | CA2550717A1 (pt) |
| TW (1) | TW200530235A (pt) |
| WO (1) | WO2005066171A1 (pt) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7312330B2 (en) * | 2003-12-24 | 2007-12-25 | Renovis, Inc. | Bicycloheteroarylamine compounds as ion channel ligands and uses thereof |
| US20060128710A1 (en) * | 2004-12-09 | 2006-06-15 | Chih-Hung Lee | Antagonists to the vanilloid receptor subtype 1 (VR1) and uses thereof |
| US7402596B2 (en) | 2005-03-24 | 2008-07-22 | Renovis, Inc. | Bicycloheteroaryl compounds as P2X7 modulators and uses thereof |
| CN101155787B (zh) * | 2005-04-11 | 2010-11-24 | 弗·哈夫曼-拉罗切有限公司 | (3,4-二氢-喹唑啉-2-基)-茚满-1-基-胺 |
| DE602006010540D1 (de) * | 2005-05-04 | 2009-12-31 | Hoffmann La Roche | (3,4-dihydro-chinazolin-2-yl)-(2-aryloxy-ethyl)-amine mit aktivität am 5-ht-rezeptor |
| WO2007059608A1 (en) * | 2005-11-23 | 2007-05-31 | Painceptor Pharma Corporation | Compositions and methods for modulating gated ion channels |
| US20100298285A1 (en) * | 2006-03-16 | 2010-11-25 | Kelly Michael G | Biclycloheteroaryl Compounds as P2x7 Modulators and Uses Thereof |
| TWI464148B (zh) * | 2006-03-16 | 2014-12-11 | Evotec Us Inc | 作為p2x7調節劑之雙環雜芳基化合物與其用途 |
| PE20080145A1 (es) | 2006-03-21 | 2008-02-11 | Janssen Pharmaceutica Nv | Tetrahidro-pirimidoazepinas como moduladores de trpv1 |
| CA2652307A1 (en) * | 2006-04-10 | 2007-10-18 | Painceptor Pharma Corporation | Compositions and methods for modulating gated ion channels |
| US20080095720A1 (en) * | 2006-10-18 | 2008-04-24 | Conopco, Inc., D/B/A Unilever | Skin Benefit Compositions with a Vanilloid Receptor Antagonist |
| JP2010520875A (ja) * | 2007-03-09 | 2010-06-17 | レノビス, インコーポレイテッド | P2x7調節因子としてのビシクロヘテロアリール化合物およびその使用 |
| PT2139334E (pt) * | 2007-04-17 | 2013-10-02 | Evotec Ag | Compostos heterocíclicos fusionados de 2-cianofenilo, e composições e utilizações dos mesmos |
| US8367684B2 (en) * | 2007-06-13 | 2013-02-05 | Valeant Pharmaceuticals International | Derivatives of 4-(N-azacycloalkyl) anilides as potassium channel modulators |
| JP5129812B2 (ja) * | 2007-06-15 | 2013-01-30 | Msd株式会社 | ビシクロアニリン誘導体 |
| WO2009078999A1 (en) | 2007-12-17 | 2009-06-25 | Janssen Pharmaceutica N.V. | Imidazolo-, oxazolo-, and thiazolopyrimidine modulators of trpv1 |
| US11969501B2 (en) | 2008-04-21 | 2024-04-30 | Dompé Farmaceutici S.P.A. | Auris formulations for treating otic diseases and conditions |
| EP2278999B1 (en) | 2008-04-21 | 2025-01-29 | Dompé farmaceutici S.p.A. | Auris formulations for treating otic diseases and conditions |
| EP2306975A4 (en) | 2008-07-21 | 2012-10-31 | Otonomy Inc | COMPOSITIONS WITH A TAXED RELEASE FOR MODULATING THE EARM STRUCTURE AND THE BORN IMMUNE SYSTEM, AND METHODS OF TREATING EAR OR DISEASE |
| CA2729045A1 (en) | 2008-07-31 | 2010-02-04 | Philippe Bergeron | Pyrimidine compounds, compositions and methods of use |
| JP5555236B2 (ja) | 2008-08-25 | 2014-07-23 | アイアールエム・リミテッド・ライアビリティ・カンパニー | ヘッジホッグ経路モジュレーター |
| US8759362B2 (en) * | 2008-10-24 | 2014-06-24 | Purdue Pharma L.P. | Bicycloheteroaryl compounds and their use as TRPV1 ligands |
| EP2499143B1 (en) | 2009-11-12 | 2016-03-16 | F.Hoffmann-La Roche Ag | N7-substituted purine and pyrazolopyrimidine compounds, compositions and methods of use |
| JP5579864B2 (ja) | 2009-11-12 | 2014-08-27 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | N−9−置換プリン化合物、組成物及び使用の方法 |
| WO2013134518A1 (en) * | 2012-03-09 | 2013-09-12 | Amgen Inc. | Sulfamide sodium channel inhibitors |
| CN106103434B (zh) * | 2014-05-29 | 2019-05-10 | 大鹏药品工业株式会社 | 四氢吡啶并嘧啶化合物或其盐 |
| WO2017090719A1 (ja) * | 2015-11-27 | 2017-06-01 | 大鵬薬品工業株式会社 | 縮環ピリミジン化合物又はその塩 |
| AU2017290256A1 (en) | 2016-06-29 | 2019-01-17 | Otonomy, Inc. | Triglyceride otic formulations and uses thereof |
| IL273893B2 (en) * | 2017-10-09 | 2025-11-01 | Univ Ramot | Modulators of potassium ion and trpv1 channels and uses thereof |
| AR118243A1 (es) | 2019-03-07 | 2021-09-22 | Pi Industries Ltd | Compuestos heterocíclicos fusionados y su uso como agentes de control de plagas |
| CN110256420B (zh) * | 2019-05-07 | 2020-04-28 | 江西中医药大学 | 四氢吡啶并嘧啶衍生物及其制备方法和用途 |
| AU2022361766A1 (en) * | 2021-10-08 | 2024-05-16 | Vrise Therapeutics, Inc. | Small molecules for treatement of cancer |
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| GB2338957B (en) | 1997-02-19 | 2001-08-01 | Berlex Lab | N-heterocyclic derivatives as nos inhibitors |
| SV2002000205A (es) | 1999-11-01 | 2002-06-07 | Lilly Co Eli | Compuestos farmaceuticos ref. x-01095 |
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| WO2002053558A1 (en) | 2001-01-02 | 2002-07-11 | F.Hoffman-La Roche Ag | Quinazolone derivatives as alpha 1a/b adrenergic receptor antagonists |
| WO2002088079A2 (en) | 2001-05-01 | 2002-11-07 | Bristol-Myers Squibb Company | Dual inhibitors of pde 7 and pde 4 |
| US7105667B2 (en) * | 2001-05-01 | 2006-09-12 | Bristol-Myers Squibb Co. | Fused heterocyclic compounds and use thereof |
| ATE466581T1 (de) | 2001-12-07 | 2010-05-15 | Vertex Pharma | Verbindungen auf pyrimidin-basis als gsk-3-hemmer |
| EP1470121B1 (en) | 2002-01-23 | 2012-07-11 | Bayer HealthCare LLC | Pyrimidine derivatives as rho-kinase inhibitors |
| GB0206033D0 (en) | 2002-03-14 | 2002-04-24 | Pfizer Ltd | Compounds useful in therapy |
| JPWO2003104230A1 (ja) | 2002-06-07 | 2005-10-06 | 協和醗酵工業株式会社 | 二環性ピリミジン誘導体 |
| US7208498B2 (en) | 2002-07-15 | 2007-04-24 | Merck & Co., Inc. | Piperidino pyrimidine dipeptidyl peptidase inhibitors for the treatment of diabetes |
| GB0225908D0 (en) | 2002-11-06 | 2002-12-11 | Pfizer Ltd | Treatment of female sexual dysfunction |
| US7223766B2 (en) | 2003-03-28 | 2007-05-29 | Scios, Inc. | Bi-cyclic pyrimidine inhibitors of TGFβ |
| US7419978B2 (en) | 2003-10-22 | 2008-09-02 | Bristol-Myers Squibb Company | Phenyl-aniline substituted bicyclic compounds useful as kinase inhibitors |
| MY141220A (en) | 2003-11-17 | 2010-03-31 | Astrazeneca Ab | Pyrazole derivatives as inhibitors of receptor tyrosine kinases |
| CA2553969A1 (en) | 2004-01-23 | 2005-08-04 | Amgen Inc. | Vanilloid receptor ligands and their use in treatments |
-
2004
- 2004-12-22 TW TW093139996A patent/TW200530235A/zh unknown
- 2004-12-23 JP JP2006547416A patent/JP2007517045A/ja not_active Withdrawn
- 2004-12-23 BR BRPI0418166-2A patent/BRPI0418166A/pt not_active Application Discontinuation
- 2004-12-23 US US11/022,324 patent/US7414131B2/en not_active Expired - Fee Related
- 2004-12-23 CA CA002550717A patent/CA2550717A1/en not_active Abandoned
- 2004-12-23 WO PCT/US2004/043456 patent/WO2005066171A1/en not_active Ceased
- 2004-12-23 EP EP04815521A patent/EP1697361A1/en not_active Withdrawn
- 2004-12-27 AR ARP040104919A patent/AR051156A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA2550717A1 (en) | 2005-07-21 |
| US20050215572A1 (en) | 2005-09-29 |
| JP2007517045A (ja) | 2007-06-28 |
| EP1697361A1 (en) | 2006-09-06 |
| TW200530235A (en) | 2005-09-16 |
| US7414131B2 (en) | 2008-08-19 |
| WO2005066171A1 (en) | 2005-07-21 |
| AR051156A1 (es) | 2006-12-27 |
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| B11A | Dismissal acc. art.33 of ipl - examination not requested within 36 months of filing | ||
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