JP2017502010A - 疼痛に対して多重モードの活性を有するピペリジン誘導体 - Google Patents

疼痛に対して多重モードの活性を有するピペリジン誘導体 Download PDF

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JP2017502010A
JP2017502010A JP2016539899A JP2016539899A JP2017502010A JP 2017502010 A JP2017502010 A JP 2017502010A JP 2016539899 A JP2016539899 A JP 2016539899A JP 2016539899 A JP2016539899 A JP 2016539899A JP 2017502010 A JP2017502010 A JP 2017502010A
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substituted
unsubstituted
methyl
piperidin
triazol
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JP2017502010A5 (cg-RX-API-DMAC7.html
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コルドベス，フェリックス クエバス
コルドベス，フェリックス クエバス
アルマンサ−ロサレス，カルメン
ロペス，モニカ ガルシア
ロペス，モニカ ガルシア
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ラボラトリオス・デル・デエレ・エステベ・エセ・ア
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    • 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
    • C07D401/06—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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/06—Antimigraine agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • 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
    • 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
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • 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
    • C07D417/14—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
    • 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pain & Pain Management (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
JP2016539899A 2013-12-20 2014-12-19 疼痛に対して多重モードの活性を有するピペリジン誘導体 Ceased JP2017502010A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP13384004 2013-12-20
EP13384004.1 2013-12-20
PCT/EP2014/078717 WO2015091939A1 (en) 2013-12-20 2014-12-19 Piperidine derivatives having multimodal activity against pain

Publications (2)

Publication Number Publication Date
JP2017502010A true JP2017502010A (ja) 2017-01-19
JP2017502010A5 JP2017502010A5 (cg-RX-API-DMAC7.html) 2018-02-01

Family

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JP2016539899A Ceased JP2017502010A (ja) 2013-12-20 2014-12-19 疼痛に対して多重モードの活性を有するピペリジン誘導体

Country Status (7)

Country Link
US (1) US9981942B2 (cg-RX-API-DMAC7.html)
EP (1) EP3083601B1 (cg-RX-API-DMAC7.html)
JP (1) JP2017502010A (cg-RX-API-DMAC7.html)
CN (1) CN105849096B (cg-RX-API-DMAC7.html)
CA (1) CA2931051A1 (cg-RX-API-DMAC7.html)
MX (1) MX2016006604A (cg-RX-API-DMAC7.html)
WO (1) WO2015091939A1 (cg-RX-API-DMAC7.html)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2019168164A1 (ja) * 2018-03-02 2019-09-06 国立大学法人大阪大学 タンパク質及び／又はペプチド修飾用分子

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CA2991937A1 (en) * 2015-07-29 2017-02-02 Laboratorios Del Dr. Esteve, S.A. Substituted amide derivatives having multimodal activity against pain
HK1255248A1 (zh) 2015-07-29 2019-08-09 Esteve Pharmaceuticals, S.A. 对疼痛具有多模式活性的酰胺衍生物
ES2823588T3 (es) * 2016-05-20 2021-05-07 Esteve Pharmaceuticals Sa Derivados de tetrahidropirano que tienen actividad multimodal contra el dolor
EA201990069A1 (ru) 2016-06-21 2019-06-28 ОРИОН ОФТАЛМОЛОДЖИ ЭлЭлСи Производные гетероциклического пролинамида
US10526315B2 (en) 2016-06-21 2020-01-07 Orion Ophthalmology LLC Carbocyclic prolinamide derivatives
EP3570838B1 (en) 2017-01-17 2024-06-05 Mebias Discovery, Inc. Substituted 3-dialkylaminomethyl-piperidin-4-yl-benzamides and methods of making and using same
TW202304448A (zh) * 2021-04-07 2023-02-01 西班牙商塔拉森斯調節公司 作為西格瑪配位基的新（高）哌啶基雜環
AU2023220657A1 (en) * 2022-02-16 2024-08-08 Duke Street Bio Limited Pharmaceutical compound
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 (4)

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JP2004536104A (ja) * 2001-07-05 2004-12-02 シナプティック・ファーマスーティカル・コーポレーション Ｍｃｈ選択的アンタゴニストとしての置換されたアニリン−ピペリジン誘導体
JP2009502859A (ja) * 2005-07-29 2009-01-29 エフ．ホフマン−ラ ロシュ アーゲー インドール−３−イル−カルボニル−ピペリジン及びピペラジン誘導体
JP2009542809A (ja) * 2006-07-12 2009-12-03 メルク エンド カムパニー インコーポレーテッド グレリン受容体アンタゴニストとしての置換ピラゾール
WO2011041462A2 (en) * 2009-10-01 2011-04-07 Amira Pharmaceuticals, Inc. Polycyclic compounds as lysophosphatidic acid receptor antagonists

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NL275537A (cg-RX-API-DMAC7.html) * 1961-03-06
DE2109155A1 (en) * 1971-02-26 1972-09-14 CH. Boehringer Sohn, 6507 Ingelheim 1-furylmethyl-4-phenyl-4-methoxycarbonylpiperidines - - with analgesic activity anorectic activity salt
GB9912410D0 (en) * 1999-05-28 1999-07-28 Pfizer Ltd Compounds useful in therapy
GB9912411D0 (en) * 1999-05-28 1999-07-28 Pfizer Ltd Compounds useful in therapy
US6727264B1 (en) * 2001-07-05 2004-04-27 Synaptic Pharmaceutical Corporation Substituted anilinic piperidines as MCH selective antagonists
US7381721B2 (en) 2003-03-17 2008-06-03 Adolor Corporation Substituted piperidine compounds
JPWO2005100341A1 (ja) 2004-04-15 2008-03-06 アステラス製薬株式会社 ２−アミノピリミジン誘導体
US7645755B2 (en) * 2004-10-22 2010-01-12 Janssen Pharmaceutical N.V. Inhibitors of c-fms kinase
JP5182088B2 (ja) * 2006-04-19 2013-04-10 アステラス製薬株式会社 アゾールカルボキサミド誘導体
US7842696B2 (en) 2007-06-21 2010-11-30 Forest Laboratories Holdings Limited Piperazine derivatives as inhibitors of stearoyl-CoA desaturase
EP2195313B1 (en) * 2007-08-27 2014-04-02 Theravance, Inc. Heteroarylalkyl-8-azabicyclo[3.2.1]octane compounds as mu opioid receptor antagonists
JP2011502991A (ja) * 2007-11-02 2011-01-27 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ 骨癌並びに骨癌に伴う骨喪失及び骨痛の処置又は予防のためのｃｆｍｓ阻害物質の使用
WO2010046780A2 (en) 2008-10-22 2010-04-29 Institut Pasteur Korea Anti viral compounds
JP5683489B2 (ja) 2009-01-12 2015-03-11 アレイ バイオファーマ、インコーポレイテッド ピペリジン含有化合物およびその用途
EP3263583A1 (en) 2010-02-12 2018-01-03 Pharmascience Inc. Iap bir domain binding compounds
MX2016006603A (es) 2013-12-20 2016-09-06 Esteve Labor Dr Compuestos piperidinicos con actividad multimodal contra el dolor.

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JP2004536104A (ja) * 2001-07-05 2004-12-02 シナプティック・ファーマスーティカル・コーポレーション Ｍｃｈ選択的アンタゴニストとしての置換されたアニリン−ピペリジン誘導体
JP2009502859A (ja) * 2005-07-29 2009-01-29 エフ．ホフマン−ラ ロシュ アーゲー インドール−３−イル−カルボニル−ピペリジン及びピペラジン誘導体
JP2009542809A (ja) * 2006-07-12 2009-12-03 メルク エンド カムパニー インコーポレーテッド グレリン受容体アンタゴニストとしての置換ピラゾール
WO2011041462A2 (en) * 2009-10-01 2011-04-07 Amira Pharmaceuticals, Inc. Polycyclic compounds as lysophosphatidic acid receptor antagonists

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2019168164A1 (ja) * 2018-03-02 2019-09-06 国立大学法人大阪大学 タンパク質及び／又はペプチド修飾用分子
JPWO2019168164A1 (ja) * 2018-03-02 2021-01-14 国立大学法人大阪大学 タンパク質及び／又はペプチド修飾用分子
JP7013048B2 (ja) 2018-03-02 2022-01-31 国立大学法人大阪大学 タンパク質及び／又はペプチド修飾用分子

Also Published As

Publication number Publication date
EP3083601A1 (en) 2016-10-26
EP3083601B1 (en) 2020-09-09
MX2016006604A (es) 2016-09-08
CN105849096B (zh) 2019-11-29
CN105849096A (zh) 2016-08-10
WO2015091939A1 (en) 2015-06-25
US20170001978A1 (en) 2017-01-05
CA2931051A1 (en) 2015-06-25
US9981942B2 (en) 2018-05-29

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