WO2009108551A3 - Heteroaryl amide analogues - Google Patents
Heteroaryl amide analogues Download PDFInfo
- Publication number
- WO2009108551A3 WO2009108551A3 PCT/US2009/034379 US2009034379W WO2009108551A3 WO 2009108551 A3 WO2009108551 A3 WO 2009108551A3 US 2009034379 W US2009034379 W US 2009034379W WO 2009108551 A3 WO2009108551 A3 WO 2009108551A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- heteroaryl amide
- disorder
- amide analogues
- analogues
- heteroaryl
- Prior art date
Links
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/42—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
- 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
- C07D401/12—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 chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
- C07D401/14—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 three or more hetero rings
-
- 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
- C07D403/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/08—Bridged systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Compounds, pharmaceutical compositions, and methods of use are disclosed for heteroaryl amide analogues of formula Ia and/or Ib. In certain embodiments, the heteroaryl amide analogues are agonists and/or ligands of dopamine receptors and may be useful, inter alia, for the treatment of a condition responsive to P2X7 receptor modulation, for example, pain, inflammation, a neurological or neurodegenerative disorder, a cardiovascular disorder, an ocular disorder or an immune system disorder.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US3108208P | 2008-02-25 | 2008-02-25 | |
US61/031,082 | 2008-02-25 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2009108551A2 WO2009108551A2 (en) | 2009-09-03 |
WO2009108551A3 true WO2009108551A3 (en) | 2009-11-26 |
Family
ID=41016676
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2009/034379 WO2009108551A2 (en) | 2008-02-25 | 2009-02-18 | Heteroaryl amide analogues |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2009108551A2 (en) |
Families Citing this family (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MX336731B (en) | 2010-01-28 | 2016-01-28 | Harvard College | Compositions and methods for enhancing proteasome activity. |
GB201004311D0 (en) * | 2010-03-15 | 2010-04-28 | Proximagen Ltd | New enzyme inhibitor compounds |
PL2707101T3 (en) | 2011-05-12 | 2019-10-31 | Proteostasis Therapeutics Inc | Proteostasis regulators |
CN103687860B (en) | 2011-07-22 | 2016-06-08 | 埃科特莱茵药品有限公司 | As P2X7The heterocyclic amide derivative of receptor antagonist |
GB201115853D0 (en) * | 2011-09-14 | 2011-10-26 | Proximagen Ltd | New enzyme inhibitor compounds |
IN2014DN01883A (en) | 2011-09-14 | 2015-05-15 | Proximagen Ltd | |
WO2013108227A1 (en) | 2012-01-20 | 2013-07-25 | Actelion Pharmaceuticals Ltd | Heterocyclic amide derivatives as p2x7 receptor antagonists |
JOP20130213B1 (en) | 2012-07-17 | 2021-08-17 | Takeda Pharmaceuticals Co | 5-ht3 receptor antagonists |
SG11201504369SA (en) | 2012-12-12 | 2015-07-30 | Actelion Pharmaceuticals Ltd | Indole carboxamide derivatives as p2x7 receptor antagonists |
JP6295270B2 (en) * | 2012-12-18 | 2018-03-14 | イドーシア ファーマシューティカルズ リミテッドIdorsia Pharmaceuticals Ltd | Indole carboxamide derivatives as P2X7 receptor antagonists |
ES2616883T3 (en) | 2013-01-22 | 2017-06-14 | Actelion Pharmaceuticals Ltd. | Heterocyclic amide derivatives as P2X7 receptor antagonists |
EP2956135B1 (en) | 2013-01-22 | 2016-11-16 | Actelion Pharmaceuticals Ltd. | Heterocyclic amide derivatives as p2x7 receptor antagonists |
US9849135B2 (en) | 2013-01-25 | 2017-12-26 | President And Fellows Of Harvard College | USP14 inhibitors for treating or preventing viral infections |
MD20150071A2 (en) | 2013-02-19 | 2016-02-29 | Pfizer Inc. | Azabenzimidazole compounds as inhibitors of PDE4 isozymes for the treatment of CNS and other disorders |
WO2015073528A1 (en) | 2013-11-12 | 2015-05-21 | Proteostasis Therapeutics, Inc. | Proteasome activity enhancing compounds |
EP2905282A1 (en) | 2014-02-05 | 2015-08-12 | AXXAM S.p.A. | Substituted thiazole or oxazole as P2X7 receptor antagonists |
US10131669B2 (en) | 2014-07-24 | 2018-11-20 | Pfizer Inc. | Pyrazolopyrimidine compounds |
CR20170035A (en) | 2014-08-06 | 2017-04-28 | Pfizer | IMIDAZOPIRIDAZINE COMPOUNDS |
PL3201203T3 (en) | 2014-09-29 | 2021-11-22 | Takeda Pharmaceutical Company Limited | Crystalline form of 1-(1-methyl-1h-pyrazol-4-yl)-n-((1r,5s,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1h-indole-3-carboxamide |
JP6673932B2 (en) * | 2014-12-15 | 2020-03-25 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | Indole and azaindole derivatives and their use in neurodegenerative diseases |
EP3954685A1 (en) | 2014-12-29 | 2022-02-16 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Small molecule inhibitors of lactate dehydrogenase and methods of use thereof |
KR102630013B1 (en) | 2015-08-06 | 2024-01-25 | 키메릭스 인크. | Pyrrolopyrimidine nucleosides and analogues thereof useful as antiviral agents |
EP3402780A1 (en) | 2016-01-14 | 2018-11-21 | Beth Israel Deaconess Medical Center, Inc. | Mast-cell modulators and uses thereof |
EP3290416A1 (en) | 2016-08-31 | 2018-03-07 | AXXAM S.p.A. | Substituted n-[2-(4-phenoxypiperidin-1-yl)-2-(1,3-thiazol-5-yl)ethyl]benzamide and n-[2-(4-benzyloxypiperidin-1-yl)-2-(1,3-thiazol-5-yl)ethyl]benzamide derivatives and their use as p2x7 receptor antagonist |
EP3290417A1 (en) | 2016-08-31 | 2018-03-07 | AXXAM S.p.A. | 2-chloro-n-[2-(1,3-thiazol-5-yl)ethyl]-5-(5-fluoropyrimidin-2-yl)-benzamides and their use as p2x7 receptor antagonists |
TW201819361A (en) | 2016-09-03 | 2018-06-01 | 印度商托仁特生技有限公司 | Novel indazole compounds |
EP3398941A1 (en) | 2017-05-03 | 2018-11-07 | AXXAM S.p.A. | Heterocyclic p2x7 antagonists |
EP3684771A1 (en) | 2017-09-21 | 2020-07-29 | Chimerix, Inc. | MORPHIC FORMS OF 4-AMINO-7-(3,4-DIHYDROXY-5-(HYDROXYMETHYL)TETRAHYDROFURAN-2-YL)-2-METHYL-7H-PYRROLO[2,3-d]PYRIMIDINE-5-CARBOXAMIDE AND USES THEREOF |
EP4015039A1 (en) | 2020-12-18 | 2022-06-22 | AXXAM S.p.A. | Heterocyclic derivatives as p2x7 receptor antagonists |
US20240174606A1 (en) * | 2021-09-03 | 2024-05-30 | Shenzhen 01 Life Science And Technology Co., Ltd. | Indole compounds, and preparation methods, and uses thereof |
EP4396181A1 (en) | 2021-09-03 | 2024-07-10 | Breye Therapeutics ApS | 2,4-dihydro-3h-1,2,4-triazol-3-one p2x7 antagonists |
WO2023198199A1 (en) * | 2022-04-15 | 2023-10-19 | 先声再明医药有限公司 | Myt1 kinase inhibitor |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004018461A2 (en) * | 2002-08-23 | 2004-03-04 | Pharmacia & Upjohn Company Llc | Antibacterial benzoic acid derivatives |
US6812226B2 (en) * | 1999-12-17 | 2004-11-02 | Astrazeneca Ab | P2X7 receptor antagonists for use in the treatment of inflammatory, immune or cardiovascular disease |
US6927219B2 (en) * | 2001-11-12 | 2005-08-09 | Pfizer Inc. | N-alkyl-adamantyl triazinyl benzamide derivatives |
US20060293337A1 (en) * | 2003-06-02 | 2006-12-28 | Richard Evans | P2x7 receptor antagonists and their use |
WO2007088277A1 (en) * | 2006-02-03 | 2007-08-09 | Sanofi-Aventis | Tricyclic ν-heteroaryl-carboxamide derivatives containing a benzimidazole unit, method for preparing same and their therapeutic use |
US20070203209A1 (en) * | 2005-08-18 | 2007-08-30 | Wilmin Bartolini | Useful indole compounds |
US20080027092A1 (en) * | 2003-11-26 | 2008-01-31 | Roger Victor Bonnert | 1-Acetic Acid-Indole, -Indazole and -Benzimidazole Derivatives Useful for the Treatment of Respiratory Disorders |
-
2009
- 2009-02-18 WO PCT/US2009/034379 patent/WO2009108551A2/en active Application Filing
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6812226B2 (en) * | 1999-12-17 | 2004-11-02 | Astrazeneca Ab | P2X7 receptor antagonists for use in the treatment of inflammatory, immune or cardiovascular disease |
US6927219B2 (en) * | 2001-11-12 | 2005-08-09 | Pfizer Inc. | N-alkyl-adamantyl triazinyl benzamide derivatives |
WO2004018461A2 (en) * | 2002-08-23 | 2004-03-04 | Pharmacia & Upjohn Company Llc | Antibacterial benzoic acid derivatives |
US20060293337A1 (en) * | 2003-06-02 | 2006-12-28 | Richard Evans | P2x7 receptor antagonists and their use |
US20080027092A1 (en) * | 2003-11-26 | 2008-01-31 | Roger Victor Bonnert | 1-Acetic Acid-Indole, -Indazole and -Benzimidazole Derivatives Useful for the Treatment of Respiratory Disorders |
US20070203209A1 (en) * | 2005-08-18 | 2007-08-30 | Wilmin Bartolini | Useful indole compounds |
WO2007088277A1 (en) * | 2006-02-03 | 2007-08-09 | Sanofi-Aventis | Tricyclic ν-heteroaryl-carboxamide derivatives containing a benzimidazole unit, method for preparing same and their therapeutic use |
Also Published As
Publication number | Publication date |
---|---|
WO2009108551A2 (en) | 2009-09-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2009108551A3 (en) | Heteroaryl amide analogues | |
UA99729C2 (en) | Heteroaryl amide analogues | |
WO2012021629A3 (en) | Novel d3 dopamine receptor agonists to treat dyskinesia in parkinson's disease | |
WO2010037059A3 (en) | Heteroaryl antagonists of prostaglandin d2 receptors | |
WO2010057118A3 (en) | Heterocyclic antagonists of prostaglandin d2 receptors | |
UA104869C2 (en) | Normal;heading 1;heading 2;heading 3;PHARMACEUTICAL FORMULATIONS CONTAINING DOPAMINE RECEPTOR LIGANDS | |
EP4268814A3 (en) | Pharmaceutical composition for the treatment of dry eye | |
WO2008064353A3 (en) | 7,8-saturated-4,5-epoxy-morphinanium analogs | |
WO2010039977A3 (en) | Heteroaryl antagonists of prostaglandin d2 receptors | |
WO2007067616A3 (en) | Uses of myostatin antagonists | |
WO2008152099A3 (en) | Aryl/hetarylamides as modulators of the ep2 receptor | |
WO2010148007A3 (en) | Nanoparticle and polymer formulations for thyroid hormone, analogs, antagonists, and formulations and uses thereof | |
WO2009100294A3 (en) | Amide derivatives as positive allosteric modulators and methods of use thereof | |
WO2010077883A3 (en) | Antagonists of lysophosphatidic acid receptors | |
WO2008140507A3 (en) | Nanoparticle and polymer formulations for thyroid hormone analogs, antagonists, and formulations and uses thereof | |
IL225198A (en) | Aminotetrahydropyran compounds, pharmaceutical compositions comprising the same and the use thereof for the treatment of diabetes | |
WO2009145996A3 (en) | Amide derivatives as positive allosteric modulators and methods of use thereof | |
WO2008121348A8 (en) | Peripheral opioid receptor antagonists and uses thereof | |
WO2010141761A3 (en) | Polycyclic antagonists of lysophosphatidic acid receptors | |
WO2008021851A3 (en) | Novel compounds as antagonists or inverse agonists for opioid receptors | |
WO2010008831A3 (en) | Compounds and methods for modulating g protein-coupled receptors | |
IL207001A0 (en) | Parenteral formulations for the administration of dopamine agonists | |
WO2010068775A3 (en) | Alkyne antagonists of lysophosphatidic acid receptors | |
WO2007087518A3 (en) | 2-substituted benzimidazoles as selective androgen receptor modulators (sarms) | |
WO2009145989A3 (en) | Aminoalkylphenyl antagonists of prostaglandin d2 receptors |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 09715672 Country of ref document: EP Kind code of ref document: A2 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 09715672 Country of ref document: EP Kind code of ref document: A2 |