JP2020506899A5 - - Google Patents

Download PDF

Info

Publication number
JP2020506899A5
JP2020506899A5 JP2019538407A JP2019538407A JP2020506899A5 JP 2020506899 A5 JP2020506899 A5 JP 2020506899A5 JP 2019538407 A JP2019538407 A JP 2019538407A JP 2019538407 A JP2019538407 A JP 2019538407A JP 2020506899 A5 JP2020506899 A5 JP 2020506899A5
Authority
JP
Japan
Prior art keywords
alkyl
pharmaceutically acceptable
disease
acceptable salt
pain
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
JP2019538407A
Other languages
English (en)
Japanese (ja)
Other versions
JP2020506899A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/IB2018/050103 external-priority patent/WO2018134695A1/en
Publication of JP2020506899A publication Critical patent/JP2020506899A/ja
Publication of JP2020506899A5 publication Critical patent/JP2020506899A5/ja
Withdrawn legal-status Critical Current

Links

JP2019538407A 2017-01-20 2018-01-08 Magl阻害薬としての1,1,1−トリフルオロ−3−ヒドロキシプロパン−2−イルカルバマート誘導体 Withdrawn JP2020506899A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201762448498P 2017-01-20 2017-01-20
US62/448,498 2017-01-20
PCT/IB2018/050103 WO2018134695A1 (en) 2017-01-20 2018-01-08 1,1,1-trifluoro-3-hydroxypropan-2-yl carbamate derivatives as magl inhibitors

Publications (2)

Publication Number Publication Date
JP2020506899A JP2020506899A (ja) 2020-03-05
JP2020506899A5 true JP2020506899A5 (cg-RX-API-DMAC7.html) 2021-02-04

Family

ID=61168134

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2019538407A Withdrawn JP2020506899A (ja) 2017-01-20 2018-01-08 Magl阻害薬としての1,1,1−トリフルオロ−3−ヒドロキシプロパン−2−イルカルバマート誘導体

Country Status (14)

Country Link
US (2) US10329308B2 (cg-RX-API-DMAC7.html)
EP (1) EP3571191A1 (cg-RX-API-DMAC7.html)
JP (1) JP2020506899A (cg-RX-API-DMAC7.html)
KR (1) KR20190104405A (cg-RX-API-DMAC7.html)
CN (1) CN110382479A (cg-RX-API-DMAC7.html)
AU (1) AU2018208846A1 (cg-RX-API-DMAC7.html)
BR (1) BR112019014688A2 (cg-RX-API-DMAC7.html)
CA (1) CA3050625C (cg-RX-API-DMAC7.html)
IL (1) IL267899A (cg-RX-API-DMAC7.html)
MX (1) MX2019008626A (cg-RX-API-DMAC7.html)
RU (1) RU2720203C1 (cg-RX-API-DMAC7.html)
SG (1) SG11201906417RA (cg-RX-API-DMAC7.html)
TW (1) TWI660946B (cg-RX-API-DMAC7.html)
WO (1) WO2018134695A1 (cg-RX-API-DMAC7.html)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX375424B (es) * 2015-07-31 2025-03-06 Pfizer Derivados de 1,1,1-trifluoro-3-hidroxipropan-2-il carbamato y derivados de 1,1,1-trifluoro-4- hidroxibutan-2-il carbamato como inhibidores de magl
MX2019008626A (es) 2017-01-20 2019-09-19 Pfizer Derivados de 1,1,1-trifluoro-3-hidroxipropan-2-ilcarbamato como inhibidores de monoacilglicerol lipasa (magl).
US10662159B2 (en) * 2017-11-22 2020-05-26 Makscientific, Llc ABHD6 and dual ABHD6/MGL inhibitors and their uses
US20220098159A1 (en) * 2019-01-25 2022-03-31 NodThera Limited Carbamate derivatives and uses thereof
WO2021191390A1 (en) * 2020-03-26 2021-09-30 Janssen Pharmaceutica Nv Azaspirocycles as monoacylglycerol lipase modulators
HRP20241177T1 (hr) * 2020-06-09 2024-11-22 Pfizer Inc. Spiro-spojevi kao antagonisti melanokortinskog receptora 4 i njihova upotreba
CA3192236A1 (en) 2020-09-10 2022-03-17 Tony Lahoutte Antibody fragment against fap
WO2022063784A1 (en) * 2020-09-22 2022-03-31 Janssen Pharmaceutica Nv Cyclobutyl amide monoacylglycerol lipase modulators
WO2022135462A1 (zh) * 2020-12-22 2022-06-30 鲁南制药集团股份有限公司 Magl抑制剂的医药用途
KR20240128870A (ko) 2021-12-29 2024-08-27 싸이 테라퓨틱스, 인크. 모노아실글리세롤 리파아제(magl) 억제
WO2023203135A1 (en) 2022-04-22 2023-10-26 Precirix N.V. Improved radiolabelled antibody
JP2025517625A (ja) 2022-05-02 2025-06-10 プレシリックス・ナームローゼ・ベンノートシヤープ プレターゲティング
WO2024168426A1 (en) 2023-02-13 2024-08-22 Apogee Pharmaceuticals, Inc. Small molecules as monoacylglycerol lipase (magl) inhibitors, compositions and use thereof
CN116621792B (zh) * 2023-05-16 2025-02-25 常州大学 一种制备n-正丁基-1,2-苯并异噻唑啉-3-酮-1-氧化物的方法
CN118191332B (zh) * 2024-03-19 2024-10-29 暨南大学 一种用于诊断术后认知功能障碍的血浆生物标志物及其应用

Family Cites Families (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0273659A1 (en) 1986-12-27 1988-07-06 Takeda Chemical Industries, Ltd. Azaspiro compounds, their production and use
US5376645A (en) 1990-01-23 1994-12-27 University Of Kansas Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof
KR0166088B1 (ko) 1990-01-23 1999-01-15 . 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도
CA2195107A1 (en) 1994-08-02 1996-02-15 Richard Alexander Jelley Azetidine, pyrrolidine and piperidine derivatives
GB9518953D0 (en) 1995-09-15 1995-11-15 Pfizer Ltd Pharmaceutical formulations
WO2000035298A1 (en) 1996-11-27 2000-06-22 Wm. Wrigley Jr. Company Chewing gum containing medicament active agents
GB9711643D0 (en) 1997-06-05 1997-07-30 Janssen Pharmaceutica Nv Glass thermoplastic systems
CA2369695A1 (en) 1999-04-09 2000-10-19 Manabu Itoh Agent for treating neuropathic pain
JP2003506468A (ja) 1999-08-13 2003-02-18 アベンティス・クロップサイエンス・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング 農薬としての複素環式スピロ化合物
US20020151712A1 (en) 1999-09-14 2002-10-17 Nan-Horng Lin 3-pyrrolidinyloxy-3'-pyridyl ether compounds useful for controlling chemical synaptic transmission
ES2279837T3 (es) 2000-11-20 2007-09-01 Scios Inc. Inhibidores de tipo piperidina/piperazina de la quinasa p38.
CA2447329C (en) 2001-05-14 2009-07-28 F.Hoffmann-La Roche Ag 1-oxa-3,9-diaza-spiro[5,5]undecan-2-ones derivatives and its use as antagonist of the neurikinin receptor
NZ545748A (en) 2003-08-29 2010-03-26 Ranbaxy Lab Ltd Isoxazoline derivatives as inhibitors of phosphodiesterase type-IV
SE0302811D0 (sv) 2003-10-23 2003-10-23 Astrazeneca Ab Novel compounds
AR046756A1 (es) 2003-12-12 2005-12-21 Solvay Pharm Gmbh Derivados de hidronopol como agonistas de receptores orl-1 humanos.
JP3912400B2 (ja) 2004-03-30 2007-05-09 株式会社デンソー 圧力センサ
ES2370788T3 (es) 2005-02-07 2011-12-22 Aerocrine Ab Controlar flujo de aliento exhalado durante análisis.
BRPI0611498B1 (pt) 2005-05-25 2015-10-13 Basf Ag composto, processos para a preparação de compostos e de agentes, e para combater vegetação indesejada, agente, e, uso de compostos
BRPI0611497A2 (pt) 2005-05-25 2011-02-22 Basf Ag composto, processos para a preparação de compostos, e de agentes, e para combater vegetação indesejada, agente, e, uso do composto
JP2008545009A (ja) 2005-06-30 2008-12-11 プロシディオン・リミテッド Gpcrアゴニスト
AR055395A1 (es) 2005-08-26 2007-08-22 Vertex Pharma Compuestos inhibidores de la actividad de la serina proteasa ns3-ns4a del virus de la hepatitis c
WO2008068265A1 (en) 2006-12-05 2008-06-12 Janssen Pharmaceutica N.V. Novel substituted diaza spiro pyridinone derivatives for use in mch-1 mediated diseases
FR2915198B1 (fr) 2007-04-18 2009-12-18 Sanofi Aventis Derives de triazolopyridine-carboxamides et triazolopyridine -carboxamides, leur preparation et leur application en therapeutique.
MX2009011358A (es) 2007-04-20 2009-11-05 Schering Corp Derivados de pirimidinona y metodos para su uso.
EP2058306A1 (en) 2007-11-08 2009-05-13 Schwarz Pharma Ag Heteroaryl-substituted 2-pyridinyl-methylamine derivatives
MX2011000664A (es) 2008-07-16 2011-02-24 Schering Corp Derivados biciclicos heterociclicos y uso de los mismos como moduladores de gpr119.
WO2010049146A1 (en) 2008-10-29 2010-05-06 Grünenthal GmbH Substituted spiroamines
EP2373315A4 (en) 2008-11-14 2012-06-27 Scripps Research Inst METHOD AND COMPOSITIONS RELATED TO TARGETING OF MONOACYLGLYCEROLLIPASE
BR122013027950A2 (pt) * 2008-12-24 2019-12-10 BIAL PORTELA & Cª S A compostos farmacêuticos
KR20120035146A (ko) 2009-04-22 2012-04-13 얀센 파마슈티카 엔.브이. 모노아실글리세롤 리파아제 억제제로서의 아제티디닐 다이아미드
US8435977B2 (en) 2009-04-22 2013-05-07 Janssen Pharmaceutica, Nv Heteroaromatic and aromatic piperazinyl azetidinyl amides as monoacylglycerol lipase inhibitors
FR2945531A1 (fr) * 2009-05-12 2010-11-19 Sanofi Aventis Derives de 7-aza-spiro°3,5!nonane-7-carboxylates, leur preparation et leur application en therapeutique
WO2011142359A1 (ja) 2010-05-10 2011-11-17 日産化学工業株式会社 スピロ化合物及びアディポネクチン受容体活性化薬
FR2960875B1 (fr) 2010-06-04 2012-12-28 Sanofi Aventis Derives de carbamates d'hexafluoroisopropyle, leur preparation et leur application en therapeutique
EP2621918A1 (en) 2010-09-27 2013-08-07 Janssen Pharmaceutica, N.V. Oxopiperazine-azetidine amides and oxodiazepine-azetidine amides as monoacylglycerol lipase inhibitors
US8513423B2 (en) 2010-10-22 2013-08-20 Janssen Pharmaceutica, Nv Piperidin-4-yl-azetidine diamides as monoacylglycerol lipase inhibitors
JP2013540160A (ja) 2010-10-22 2013-10-31 ヤンセン ファーマシューティカ エヌ.ベー. モノアシルグリセロールリパーゼ阻害剤としてのアミノ−ピロリジン−アゼチジンジアミド
MX347982B (es) 2011-03-14 2017-05-22 Vertex Pharma Morfolina-piperidina espirociclica-amidas como moduladores de canales ionicos.
JP2014159376A (ja) 2011-06-17 2014-09-04 Taisho Pharmaceutical Co Ltd アザスピロアルカン化合物
EA028085B1 (ru) 2012-01-06 2017-10-31 Эбайд Терапьютикс, Инк. Карбаматные соединения и их применение
WO2013131010A2 (en) 2012-03-02 2013-09-06 Icahn School Of Medicine At Mount Sinai Function of chemokine receptor ccr8 in melanoma metastasis
EP2872899B1 (en) 2012-07-13 2018-07-11 Pain Therapeutics, Inc. Alzheimer's disease assay in a living patient
WO2014074715A1 (en) * 2012-11-07 2014-05-15 Genentech, Inc. Cyclopropyl amide derivatives
JP6647592B2 (ja) * 2013-07-03 2020-02-14 ルンドベック ラ ホーヤ リサーチ センター,インク. ピロロピロールカルバメート、および関連する有機化合物、医薬組成物、ならびにその医学的使用
CN107660199B (zh) * 2015-03-18 2021-11-23 H.隆德贝克有限公司 哌嗪氨基甲酸酯及其制备和使用方法
MX375424B (es) 2015-07-31 2025-03-06 Pfizer Derivados de 1,1,1-trifluoro-3-hidroxipropan-2-il carbamato y derivados de 1,1,1-trifluoro-4- hidroxibutan-2-il carbamato como inhibidores de magl
MX2019008626A (es) 2017-01-20 2019-09-19 Pfizer Derivados de 1,1,1-trifluoro-3-hidroxipropan-2-ilcarbamato como inhibidores de monoacilglicerol lipasa (magl).
SG11201906427QA (en) * 2017-01-23 2019-08-27 Pfizer Heterocyclic spiro compounds as magl inhibitors

Similar Documents

Publication Publication Date Title
JP2020506899A5 (cg-RX-API-DMAC7.html)
JP2020506903A5 (cg-RX-API-DMAC7.html)
JP6982376B2 (ja) Rorガンマ調節物質としての置換型テトラヒドロキノリン化合物
JP2019526582A5 (cg-RX-API-DMAC7.html)
TWI583681B (zh) 胺基嘧啶基化合物
US11584732B2 (en) Methods of treatment using 4-(3-cyanophenyl)-6-pyridinylpyrimidine mGlu5 modulators
CN110573501A (zh) Rho相关蛋白激酶抑制剂、包含其的药物组合物及其制备方法和用途
JP2018534326A5 (cg-RX-API-DMAC7.html)
JP2006514006A (ja) Jakインヒビターとしてのヘテロアリール−ピリミジン誘導体
IL235051A (en) A heterocyclic compound containing nitrogen or its salt
MD3419978T2 (ro) Derivaţi de pirazolo[1,5-a]pirazin-4-il
JP2008503492A (ja) Rho−キナーゼの新規阻害剤
US9238644B2 (en) VEGFR3 inhibitors
JP2009518444A (ja) ケモカイン受容体のピリジニルスルホンアミドモジュレーター
JP2007507540A (ja) タンパク質キナーゼ阻害剤としての化合物および組成物
KR20070085609A (ko) 혈관 내피 성장 인자 (vegf) 수용체 키나제 억제제로서니코틴아미드 피리딘우레아
CN119039379B (zh) 一种蛋白降解靶向嵌合体分子及其应用
HK1241857B (zh) 作为jak抑制剂的氨基嘧啶基化合物
OA18225A (en) Aminopyrimidinyl compounds as Jak inhibitors.
HK1224662B (en) 4-(3-cyanophenyl)-6-pyridinylpyrimidine mglu5 modulators
HK1224662A1 (en) 4-(3-cyanophenyl)-6-pyridinylpyrimidine mglu5 modulators