AU2015306643B2 - Soluble epoxide hydrolase inhibitors and uses thereof - Google Patents

Soluble epoxide hydrolase inhibitors and uses thereof Download PDF

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Publication number
AU2015306643B2
AU2015306643B2 AU2015306643A AU2015306643A AU2015306643B2 AU 2015306643 B2 AU2015306643 B2 AU 2015306643B2 AU 2015306643 A AU2015306643 A AU 2015306643A AU 2015306643 A AU2015306643 A AU 2015306643A AU 2015306643 B2 AU2015306643 B2 AU 2015306643B2
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AU
Australia
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compound
alkyl
compounds
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groups
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AU2015306643A
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English (en)
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AU2015306643A1 (en
Inventor
Christoph Dumelin
Anthony D. Keefe
Ying Zhang
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X Chem Inc
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X Chem Inc
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Publication of AU2015306643A1 publication Critical patent/AU2015306643A1/en
Application granted granted Critical
Publication of AU2015306643B2 publication Critical patent/AU2015306643B2/en
Priority to AU2020207828A priority Critical patent/AU2020207828A1/en
Ceased legal-status Critical Current
Anticipated expiration legal-status Critical

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4412Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81Amides; Imides

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
AU2015306643A 2014-08-28 2015-08-26 Soluble epoxide hydrolase inhibitors and uses thereof Ceased AU2015306643B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU2020207828A AU2020207828A1 (en) 2014-08-28 2020-07-22 Soluble epoxide hydrolase inhibitors and uses thereof

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201462043275P 2014-08-28 2014-08-28
US62/043,275 2014-08-28
PCT/US2015/046878 WO2016033150A1 (en) 2014-08-28 2015-08-26 Soluble epoxide hydrolase inhibitors and uses thereof

Related Child Applications (1)

Application Number Title Priority Date Filing Date
AU2020207828A Division AU2020207828A1 (en) 2014-08-28 2020-07-22 Soluble epoxide hydrolase inhibitors and uses thereof

Publications (2)

Publication Number Publication Date
AU2015306643A1 AU2015306643A1 (en) 2017-03-16
AU2015306643B2 true AU2015306643B2 (en) 2020-05-07

Family

ID=55400481

Family Applications (2)

Application Number Title Priority Date Filing Date
AU2015306643A Ceased AU2015306643B2 (en) 2014-08-28 2015-08-26 Soluble epoxide hydrolase inhibitors and uses thereof
AU2020207828A Abandoned AU2020207828A1 (en) 2014-08-28 2020-07-22 Soluble epoxide hydrolase inhibitors and uses thereof

Family Applications After (1)

Application Number Title Priority Date Filing Date
AU2020207828A Abandoned AU2020207828A1 (en) 2014-08-28 2020-07-22 Soluble epoxide hydrolase inhibitors and uses thereof

Country Status (8)

Country Link
US (2) US10081616B2 (enExample)
EP (1) EP3186228A4 (enExample)
JP (1) JP2017525777A (enExample)
CN (2) CN107074771B (enExample)
AU (2) AU2015306643B2 (enExample)
CA (1) CA2958881A1 (enExample)
MA (1) MA40538A (enExample)
WO (1) WO2016033150A1 (enExample)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2017525777A (ja) * 2014-08-28 2017-09-07 エックス−ケム,インコーポレーテッド 可溶性エポキシドヒドロラーゼ阻害剤及びこれらの使用
EP3600266B1 (en) * 2017-03-30 2022-07-27 INSERM (Institut National de la Santé et de la Recherche Médicale) Pharmaceutical compositions for use in the treatment of cardiovascular calcification
US20230071934A1 (en) * 2019-12-18 2023-03-09 Intra-Cellular Therapies, Inc. Novel uses
WO2024105225A1 (en) 2022-11-18 2024-05-23 Universitat De Barcelona Synergistic combinations of a sigma receptor 1 (s1r) antagonist and a soluble epoxide hydrolase inhibitor (sehi) and their use in the treatment of pain

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3245950A1 (de) * 1981-12-24 1983-07-07 Byk Gulden Lomberg Chemische Fabrik Gmbh, 7750 Konstanz Verfahren zur herstellung substituierter pyridine
US20030055088A1 (en) * 2001-09-07 2003-03-20 Euro-Celtique S.A. Aryl substituted pyridines and the use thereof
WO2007098352A2 (en) * 2006-02-16 2007-08-30 Boehringer Ingelheim International Gmbh Substituted pyridineamide compounds useful as soluble epoxide hydrolase inhibitors
WO2008152099A2 (en) * 2007-06-13 2008-12-18 Bayer Schering Pharma Aktiengesellschaft Aryl/hetarylamides as modulators of the ep2 receptor
US20100113512A1 (en) * 2008-10-30 2010-05-06 Diane Michele Ignar Method of treatment using novel antagonists or inverse agonists at opioid receptors
WO2011091410A1 (en) * 2010-01-25 2011-07-28 Glaxos Smithkline Llc Trpv4 antagonists
WO2013057251A2 (en) * 2011-10-21 2013-04-25 F. Hoffmann-La Roche Ag Heteroaryl hydroxamic acid derivatives and their use in the treatment, amelioration or prevention of a viral disease
WO2014075754A1 (en) * 2012-11-16 2014-05-22 Merck Patent Gmbh 3-aminocyclopentane carboxamide derivatives

Family Cites Families (15)

* Cited by examiner, † Cited by third party
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US20040067985A1 (en) * 2002-10-04 2004-04-08 Fortuna Haviv Method of inhibiting angiogenesis
CA2643859A1 (en) 2006-03-10 2007-09-20 Boehringer Ingelheim International Gmbh Soluble epoxide hydrolase inhibitors and methods of using same
CN102516115B (zh) * 2006-08-09 2016-05-11 史密丝克莱恩比彻姆公司 作为阿片样物质受体的拮抗剂或反向激动剂的新型化合物
CA2672373C (en) * 2006-12-19 2011-08-30 Pfizer Products Inc. Nicotinamide derivatives as inhibitors of h-pgds and their use for treating prostaglandin d2 mediated diseases
WO2009151800A1 (en) * 2008-05-07 2009-12-17 Merck & Co., Inc. Soluble epoxide hydrolase inhibitors, compositions containing such compounds and methods of treatment
US20110306597A1 (en) * 2008-06-18 2011-12-15 James Michael Crawforth Nicotinamide Derivatives
TW201010997A (en) * 2008-06-18 2010-03-16 Pfizer Ltd Nicotinamide derivatives
EP2149552A1 (de) * 2008-07-30 2010-02-03 Bayer Schering Pharma AG 5,6 substituierte Benzamid-Derivate als Modulatoren des EP2-Rezeptors
EP2149551A1 (de) * 2008-07-30 2010-02-03 Bayer Schering Pharma AG N-(Indol-3-ylalkyl)-(hetero)arylamidderivate als Modulatoren des EP2-Rezeptors
WO2010080183A1 (en) 2009-01-08 2010-07-15 The Trustees Of Columbia University In The City Of New York Potent non-urea inhibitors of soluble epoxide hydrolase
US20130102601A1 (en) * 2011-10-21 2013-04-25 F. Hoffmann-La Roche Ltd Pyrimidin-4-one derivatives and their use in the treatment, amelioration or prevention of a viral disease
US8809552B2 (en) * 2011-11-01 2014-08-19 Hoffmann-La Roche Inc. Azetidine compounds, compositions and methods of use
WO2013112751A1 (en) * 2012-01-25 2013-08-01 The Trustees Of Columbia University In The City Of New York Potent non-urea inhibitors of soluble epoxide hydrolase
CN104016914B (zh) * 2014-05-27 2016-03-30 苏州科技学院 一种酰胺化合物的制备方法
JP2017525777A (ja) * 2014-08-28 2017-09-07 エックス−ケム,インコーポレーテッド 可溶性エポキシドヒドロラーゼ阻害剤及びこれらの使用

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3245950A1 (de) * 1981-12-24 1983-07-07 Byk Gulden Lomberg Chemische Fabrik Gmbh, 7750 Konstanz Verfahren zur herstellung substituierter pyridine
US20030055088A1 (en) * 2001-09-07 2003-03-20 Euro-Celtique S.A. Aryl substituted pyridines and the use thereof
WO2007098352A2 (en) * 2006-02-16 2007-08-30 Boehringer Ingelheim International Gmbh Substituted pyridineamide compounds useful as soluble epoxide hydrolase inhibitors
WO2008152099A2 (en) * 2007-06-13 2008-12-18 Bayer Schering Pharma Aktiengesellschaft Aryl/hetarylamides as modulators of the ep2 receptor
US20100113512A1 (en) * 2008-10-30 2010-05-06 Diane Michele Ignar Method of treatment using novel antagonists or inverse agonists at opioid receptors
WO2011091410A1 (en) * 2010-01-25 2011-07-28 Glaxos Smithkline Llc Trpv4 antagonists
WO2013057251A2 (en) * 2011-10-21 2013-04-25 F. Hoffmann-La Roche Ag Heteroaryl hydroxamic acid derivatives and their use in the treatment, amelioration or prevention of a viral disease
WO2014075754A1 (en) * 2012-11-16 2014-05-22 Merck Patent Gmbh 3-aminocyclopentane carboxamide derivatives

Also Published As

Publication number Publication date
AU2015306643A1 (en) 2017-03-16
CN111454246A (zh) 2020-07-28
JP2017525777A (ja) 2017-09-07
EP3186228A1 (en) 2017-07-05
AU2020207828A1 (en) 2020-08-13
CN107074771A (zh) 2017-08-18
US20180362499A1 (en) 2018-12-20
US10081616B2 (en) 2018-09-25
EP3186228A4 (en) 2018-04-18
WO2016033150A1 (en) 2016-03-03
CN107074771B (zh) 2020-03-20
US20170240526A1 (en) 2017-08-24
MA40538A (fr) 2021-04-07
CA2958881A1 (en) 2016-03-03

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