JP2019510006A5 - - Google Patents

Download PDF

Info

Publication number
JP2019510006A5
JP2019510006A5 JP2018544466A JP2018544466A JP2019510006A5 JP 2019510006 A5 JP2019510006 A5 JP 2019510006A5 JP 2018544466 A JP2018544466 A JP 2018544466A JP 2018544466 A JP2018544466 A JP 2018544466A JP 2019510006 A5 JP2019510006 A5 JP 2019510006A5
Authority
JP
Japan
Prior art keywords
hal
disease
replaced
compound
carbon atoms
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Withdrawn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
JP2018544466A
Other languages
English (en)
Japanese (ja)
Other versions
JP2019510006A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2017/054268 external-priority patent/WO2017144633A1/en
Publication of JP2019510006A publication Critical patent/JP2019510006A/ja
Publication of JP2019510006A5 publication Critical patent/JP2019510006A5/ja
Withdrawn legal-status Critical Current

Links

JP2018544466A 2016-02-25 2017-02-24 グリコシダーゼ阻害剤 Withdrawn JP2019510006A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
IN201621006636 2016-02-25
IN201621006636 2016-02-25
PCT/EP2017/054268 WO2017144633A1 (en) 2016-02-25 2017-02-24 Glycosidase inhibitors

Publications (2)

Publication Number Publication Date
JP2019510006A JP2019510006A (ja) 2019-04-11
JP2019510006A5 true JP2019510006A5 (enExample) 2020-03-26

Family

ID=58159073

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2018544466A Withdrawn JP2019510006A (ja) 2016-02-25 2017-02-24 グリコシダーゼ阻害剤
JP2019545961A Active JP7082446B2 (ja) 2016-02-25 2017-08-24 スルホキシイミングリコシダーゼ阻害剤

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2019545961A Active JP7082446B2 (ja) 2016-02-25 2017-08-24 スルホキシイミングリコシダーゼ阻害剤

Country Status (12)

Country Link
US (1) US11612599B2 (enExample)
EP (1) EP3419971B1 (enExample)
JP (2) JP2019510006A (enExample)
KR (1) KR20180132629A (enExample)
CN (2) CN108884077A (enExample)
AU (1) AU2017222958B2 (enExample)
CA (1) CA3012560A1 (enExample)
EA (1) EA201991697A1 (enExample)
MA (1) MA43677A (enExample)
MX (1) MX2018010192A (enExample)
WO (1) WO2017144633A1 (enExample)
ZA (1) ZA201905405B (enExample)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102043337B1 (ko) 2014-08-28 2019-11-11 아셰뉴론 에스아 글리코시다제 저해제
KR102800480B1 (ko) 2016-02-25 2025-04-25 아셰뉴론 에스아 피페라진 유도체의 산 부가 염
US11261183B2 (en) 2016-02-25 2022-03-01 Asceneuron Sa Sulfoximine glycosidase inhibitors
MA43680A (fr) * 2016-02-25 2018-11-28 Asceneuron Sa Inhibiteurs de glycosidases
JP2020503298A (ja) 2016-12-16 2020-01-30 ヤンセン ファーマシューティカ エヌ.ベー. 単環式oga阻害剤化合物
EP3585779A1 (en) * 2017-02-24 2020-01-01 Asceneuron S.A. Substituted dihydrobenzofuran glycosidase inhibitors
EP3672959A1 (en) 2017-08-24 2020-07-01 Asceneuron SA Linear glycosidase inhibitors
JP2021514010A (ja) * 2018-02-20 2021-06-03 エッジワイズ セラピューティクス, インコーポレイテッド 運動障害を処置するための方法および組成物
EP3810612A1 (en) * 2018-06-20 2021-04-28 Janssen Pharmaceutica NV Oga inhibitor compounds
CA3102903A1 (en) * 2018-06-20 2019-12-26 Janssen Pharmaceutica Nv Oga inhibitor compounds
US20210277003A1 (en) * 2018-06-21 2021-09-09 Janssen Pharmaceutica Nv Oga inhibitor compounds
EP3810608B1 (en) * 2018-06-21 2022-08-10 Janssen Pharmaceutica NV Oga inhibitor compounds
TWI726329B (zh) 2018-06-22 2021-05-01 美商美國禮來大藥廠 2,3-二氫呋喃并[2,3-b]吡啶化合物
WO2020039029A1 (en) 2018-08-22 2020-02-27 Asceneuron S. A. Spiro compounds as glycosidase inhibitors
US11795165B2 (en) 2018-08-22 2023-10-24 Asceneuron Sa Tetrahydro-benzoazepine glycosidase inhibitors
SG11202101651RA (en) * 2018-08-22 2021-03-30 Asceneuron S A Succinate and fumarate acid addition salts of piperazine derivatives useful as glycosidase inhibitors
US12016852B2 (en) 2018-08-22 2024-06-25 Asceneuron Sa Pyrrolidine glycosidase inhibitors
TWI716107B (zh) * 2018-09-26 2021-01-11 美商美國禮來大藥廠 6-氟-2-甲基苯并[d]噻唑-5-基化合物
CN111039946A (zh) * 2018-10-15 2020-04-21 上海轶诺药业有限公司 一类咪唑并芳环类化合物的制备和应用
WO2020163689A1 (en) * 2019-02-08 2020-08-13 University Of Pittsburgh - Of The Commonwealth System Of Higher Education 20-hete formation inhibitors
WO2021094312A1 (en) 2019-11-11 2021-05-20 Janssen Pharmaceutica Nv Pyrrolidine and bicycloheteroaryl containing oga inhibitor compounds
WO2021110656A1 (en) 2019-12-02 2021-06-10 Janssen Pharmaceutica Nv Oga inhibitor compounds
CN114867725A (zh) 2019-12-18 2022-08-05 詹森药业有限公司 Oga抑制剂化合物
IL293929A (en) * 2019-12-18 2022-08-01 Janssen Pharmaceutica Nv Oga inhibitor compounds
WO2021123291A1 (en) 2019-12-18 2021-06-24 Janssen Pharmaceutica Nv Oga inhibitor compounds
WO2021247862A1 (en) * 2020-06-03 2021-12-09 Yumanity Therapeutics, Inc. Bicyclic heteroarenes and methods of their use
CN112028839B (zh) * 2020-09-30 2022-04-12 中国海洋大学 一种医药中间体环烷烃并嘧啶二酮化合物的合成方法
JP2024518530A (ja) * 2021-05-14 2024-05-01 ビーエム ファーマ コンサルティング ピーティーワイ リミテッド ウイルス感染の予防及び治療のための二環式複素環化合物

Family Cites Families (102)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1311316A (fr) 1961-04-12 1962-12-07 Science Union Et Compagnie Soc Nouveaux dérivés de la pipérazine et leurs préparations
NL127996C (enExample) 1963-11-19
US3485757A (en) 1964-11-23 1969-12-23 Atomic Energy Commission Thermoelectric composition comprising doped bismuth telluride,silicon and boron
DE1595923A1 (de) * 1965-02-20 1969-11-27 Merck Ag E 1-Aralkyl-4-(thiazolyl-2)-piperazine und Verfahren zu ihrer Herstellung
GB1165283A (en) 1967-01-17 1969-09-24 Science Union & Cie New Purine Derivatives and processes for prepararing them
US4600025A (en) 1982-11-18 1986-07-15 Grigg Ronald E Smoking products comprising nicotine substitutes
WO1993021181A1 (en) 1992-04-15 1993-10-28 Merck Sharp & Dohme Limited Azacyclic compounds
IL118768A (en) 1995-07-12 2000-10-31 Akzo Nobel Nv Diphenylmethane piperidine derivatives pharmaceutical compositions containing them and a method for their preparation
TW504510B (en) 1996-05-10 2002-10-01 Janssen Pharmaceutica Nv 2,4-diaminopyrimidine derivatives
US6534496B1 (en) 1997-04-17 2003-03-18 Takeda Chemical Industries, Inc. Thermogenic composition and benzazepine thermogenics
WO1999021850A1 (en) 1997-10-24 1999-05-06 Neurogen Corporation 1-(2-naphthyl) and 1-(2-azanaphthyl)-4-(1-phenylmethyl)piperazines being dopamine d4 receptor subtype ligands
EP1389189A2 (en) * 2001-05-22 2004-02-18 Neurogen Corporation Melanin concentrating hormone receptor ligands: substituted 1-benzyl-4-aryl piperazine analogues
US6982259B2 (en) 2002-04-30 2006-01-03 Schering Aktiengesellschaft N-heterocyclic derivatives as NOS inhibitors
JP2005532368A (ja) 2002-06-12 2005-10-27 アボット・ラボラトリーズ メラニン濃縮ホルモン受容体の拮抗薬
EP1531815B1 (en) 2002-06-27 2014-09-24 Novo Nordisk A/S Glucokinase activators
EA009789B1 (ru) 2002-07-05 2008-04-28 Таргасепт, Инк. N-арилдиазаспирациклические соединения и способы их получения и применения
KR20050043935A (ko) 2002-09-09 2005-05-11 얀센 파마슈티카 엔.브이. Orl-1 수용체 매개 장애의 치료에 유용한 하이드록시 알킬 치환된 1,3,8-트리아자스피로[4.5]데칸-4-온 유도체
WO2004094380A1 (en) 2003-04-18 2004-11-04 Eli Lilly And Company (piperidinyloxy)phenyl, (piperidinyloxy)pyridinyl, (piperidinylsulfanyl)phenyl and (piperidinylsulfanyl)pyridinyl compounds as 5-ht1f agonists
JP4552854B2 (ja) 2003-05-21 2010-09-29 萬有製薬株式会社 2−アミノキノリン誘導体
WO2005066145A1 (en) 2004-01-06 2005-07-21 Novo Nordisk A/S Heteroaryl-ureas and their use as glucokinase activators
US7253168B2 (en) 2004-04-07 2007-08-07 Neurogen Corporation Substituted 1-benzyl-4-substituted piperazine analogues
HU227119B1 (en) 2004-07-29 2010-07-28 Richter Gedeon Nyrt Indole and benzimidazole carboxylic acid amide derivatives and pharmaceutical compositions containing them
HUP0401522A2 (en) 2004-07-29 2006-04-28 Richter Gedeon Vegyeszet New 4-benzylidene-piperidine derivatives, pharmaceutical compositions containing the same and process for their preparation
EP1869060B1 (en) 2005-03-01 2012-08-15 Simon Fraser University Selective glycosidase inhibitors, methods of making inhibitors, and uses thereof
EP1705177A1 (en) * 2005-03-23 2006-09-27 Schering Aktiengesellschaft N-aryl-sulfoximine-substituted pyrimidines as CDK- and/or VEGF inhibitors, their production and use as pharmaceutical agents
TW200724140A (en) 2005-05-27 2007-07-01 Eisai Co Ltd Hydantoin compounds
BRPI0613591A2 (pt) 2005-07-08 2011-01-18 Novo Nordisk As ativadores de dicicloalquil uréia glicocinase
WO2007008541A2 (en) 2005-07-08 2007-01-18 Kalypsys, Inc. Cellular cholesterol absorption modifiers
CA2646755A1 (en) 2006-03-31 2007-10-11 Astrazeneca Ab Bicyclic benzimidazole compounds and their use as metabotropic glutamate receptor potentiators
EP2029593A1 (en) 2006-05-22 2009-03-04 AstraZeneca AB Indole derivatives
US20080051387A1 (en) 2006-06-09 2008-02-28 Yuelian Xu Tetrahydropyrido[3,4-d]pyrimidines and related analogues
WO2008012623A1 (en) 2006-07-25 2008-01-31 Pfizer Products Inc. Benzimidazolyl compounds as potentiators of mglur2 subtype of glutamate receptor
CA2661582C (en) 2006-08-31 2015-09-29 Simon Fraser University Selective glycosidase inhibitors and uses thereof
US20100022517A1 (en) 2006-12-18 2010-01-28 Richards Lori A Ophthalmic formulation of rho kinase inhibitor compound
US8148369B2 (en) 2007-05-10 2012-04-03 Janssen Pharmaceutica Nv Fused pyrazine compounds useful for the treatment of degenerative and inflammatory diseases
WO2009011904A1 (en) 2007-07-19 2009-01-22 Renovis, Inc. Compounds useful as faah modulators and uses thereof
EP2215075B1 (en) 2007-10-26 2013-12-11 Janssen Pharmaceutica, N.V. Quinolinone derivatives as parp inhibitors
US8642660B2 (en) 2007-12-21 2014-02-04 The University Of Rochester Method for altering the lifespan of eukaryotic organisms
JP2011518142A (ja) 2008-04-17 2011-06-23 ファイザー・インク Faah阻害剤として有用なエーテルベンジリデンピペリジン5員アリールカルボキサミド化合物
US20110060012A1 (en) 2008-04-17 2011-03-10 Pfizer Inc. 4-[3-(aryloxy)benzylidene]-3-methyl piperidine 5-membered aryl carboxamide compounds useful as faah inhibitors
US7863291B2 (en) 2008-04-23 2011-01-04 Bristol-Myers Squibb Company Quinuclidine compounds as alpha-7 nicotinic acetylcholine receptor ligands
AU2009261248A1 (en) 2008-06-19 2009-12-23 Banyu Pharmaceutical Co., Ltd. Spirodiamine-diarylketoxime derivative
JP2010065024A (ja) 2008-08-14 2010-03-25 Ishihara Sangyo Kaisha Ltd トリアゾロピリミジン誘導体又はその塩を含有する有害生物防除剤
WO2010021381A1 (ja) 2008-08-22 2010-02-25 武田薬品工業株式会社 縮合複素環誘導体およびその用途
WO2010022517A1 (en) 2008-08-29 2010-03-04 Saint Mary's University Use of gluconacetobacter with reduced use of nitrogen fertilizer to improve beet crop production
EP2336104A4 (en) 2008-09-02 2012-01-25 Nissan Chemical Ind Ltd ORTHOSUBSTITUTED HALOALKYL SULFONANILIDE DERIVATIVE AND HERBICIDE
TW201030007A (en) 2009-02-06 2010-08-16 Gruenenthal Gmbh Substituted spiro-amides as b1r modulators
WO2010101949A1 (en) 2009-03-02 2010-09-10 Sirtris Pharmaceuticals, Inc. 8-substituted quinolines and related analogs as sirtuin modulators
US20100240720A1 (en) 2009-03-20 2010-09-23 Burnham Institute For Medical Research Allosteric jnk inhibitors
WO2010108268A1 (en) 2009-03-23 2010-09-30 Merck Frosst Canada Ltd. Heterocyclic compounds as inhibitors of stearoyl-coenzyme a delta-9 desaturase
JP2010270034A (ja) 2009-05-20 2010-12-02 Sumitomo Chemical Co Ltd アミド化合物並びにその植物病害防除用途
US9096518B2 (en) 2009-06-22 2015-08-04 Millennium Pharmaceuticals, Inc. Substituted hydroxamic acids and uses thereof
DE102009049679A1 (de) 2009-10-19 2011-04-21 Merck Patent Gmbh Pyrazolopyrimidinderivate
WO2011140640A1 (en) 2010-05-11 2011-11-17 Simon Fraser University Selective glycosidase inhibitors and uses thereof
EP2615918A4 (en) 2010-09-17 2014-01-29 Glaxosmithkline Ip Dev Ltd INHIBITORS OF ACID GRAS SYNTHASE
WO2012061972A1 (en) 2010-11-08 2012-05-18 Alectos Therapeutics Inc. Selective glycosidase inhibitors and uses thereof
CA2815002C (en) 2010-11-08 2019-10-22 Janssen Pharmaceuticals, Inc. 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors
US8933040B2 (en) 2010-11-08 2015-01-13 Craig A. Coburn Selective glycosidase inhibitors and uses thereof
LT2655388T (lt) 2010-12-23 2016-11-10 Alectos Therapeutics Inc. Selektyvieji glikozidazės inhibitoriai ir jų panaudojimas
GB201103526D0 (en) 2011-03-02 2011-04-13 Summit Corp Plc Selective glycosidase inhibitors and uses thereof
WO2012124744A1 (ja) 2011-03-14 2012-09-20 大正製薬株式会社 含窒素縮合複素環化合物
HUE029390T2 (en) 2011-08-25 2017-02-28 Merck Patent Gmbh Pirano [3,2-d] [1,3] thiazole derivatives as glucosidase inhibitors
US9221809B2 (en) 2011-10-31 2015-12-29 Merck Sharp & Dohme Corp. Aminopyrimidinones as interleukin receptor-associated kinase inhibitors
AR092031A1 (es) 2012-07-26 2015-03-18 Merck Sharp & Dohme Inhibidores del canal de potasio medular externo renal
PT2882733T (pt) 2012-08-08 2017-07-13 Novartis Tiergesundheit Ag Azinas substituídas como pesticidas
WO2014032187A1 (en) 2012-08-31 2014-03-06 Alectos Therapeutics Inc. Glycosidase inhibitors and uses thereof
HUE043398T2 (hu) 2013-03-14 2019-08-28 Merck Patent Gmbh Glikozidáz inhibítorok
CN103435606A (zh) 2013-08-22 2013-12-11 中国药科大学 CDK2与GSK3β双重抑制剂及用途
NZ720092A (en) 2013-12-05 2019-05-31 Pfizer Pyrrolo[2,3-d]pyrimidinyl, pyrrolo[2,3-b]pyrazinyl and pyrrolo[2,3-d]pyridinyl acrylamides
EP2913330A1 (en) 2014-02-27 2015-09-02 Laboratoire Biodim Condensed derivatives of imidazole useful as pharmaceuticals
HRP20212035T1 (hr) 2014-04-23 2022-04-01 Dart Neuroscience Llc Pripravci koji sadrže supstituirane [1,2,4]triazolo[1,5-a]pirimidin-7-il spojeve kao inhibitore pde2
AR101197A1 (es) * 2014-07-16 2016-11-30 Gruenenthal Gmbh Pirimidinas 2,5-sustituidas
KR102043337B1 (ko) * 2014-08-28 2019-11-11 아셰뉴론 에스아 글리코시다제 저해제
RS60933B1 (sr) * 2014-10-08 2020-11-30 UCB Biopharma SRL Derivati tetrahidroizohinolina
ES2729490T3 (es) * 2014-10-08 2019-11-04 Ucb Biopharma Sprl Derivados de isoindolina
SG11201702741SA (en) * 2014-11-20 2017-04-27 Merck Patent Gmbh Heteroaryl compounds as irak inhibitors and uses thereof
TWI770525B (zh) * 2014-12-30 2022-07-11 美商瓦洛健康公司 作為泛素特異性蛋白酶7抑制劑之吡咯并及吡唑并嘧啶
MA42293A (fr) 2015-07-02 2018-05-09 Janssen Sciences Ireland Uc Composés antibactériens
MX2018005342A (es) 2015-11-02 2018-08-15 Janseen Pharmaceutica Nv Compuesto de [1,2,4]triazolo[1,5-a]pirimidin-7-ilo.
AR106595A1 (es) * 2015-11-06 2018-01-31 Incyte Corp COMPUESTOS HETEROCÍCLICOS COMO INHIBIDORES DE PI3K-g
WO2017087858A1 (en) 2015-11-20 2017-05-26 Abide Therapeutics, Inc. Pyrazole compounds and methods of making and using same
US10323038B2 (en) 2015-11-20 2019-06-18 Abide Therapeutics, Inc. Pyrazole compounds and methods of making and using same
ES2893613T3 (es) 2015-11-25 2022-02-09 Lieber Inst Inc Dba Lieber Inst For Brain Development Tetrahidro-8H-pirido[1,2-a]pirazin-8-onas como inhibidores de COMT para el tratamiento de trastornos neurodegenerativos
WO2017106254A1 (en) 2015-12-18 2017-06-22 Merck Sharp & Dohme Corp. Glycosidase inhibitors and uses thereof
MA43680A (fr) * 2016-02-25 2018-11-28 Asceneuron Sa Inhibiteurs de glycosidases
US11261183B2 (en) 2016-02-25 2022-03-01 Asceneuron Sa Sulfoximine glycosidase inhibitors
KR102800480B1 (ko) 2016-02-25 2025-04-25 아셰뉴론 에스아 피페라진 유도체의 산 부가 염
JP2019510007A (ja) 2016-02-25 2019-04-11 エースニューロン・ソシエテ・アノニム ピペラジン誘導体のエナンチオマーの分離方法
WO2017223243A1 (en) 2016-06-21 2017-12-28 X4 Pharmaceuticals, Inc. Cxcr4 inhibitors and uses thereof
US11186564B2 (en) 2016-08-04 2021-11-30 Sunovion Pharmaceuticals Inc. Dual NAV1.2/5HT2a inhibitors for treating CNS disorders
JP2020503298A (ja) 2016-12-16 2020-01-30 ヤンセン ファーマシューティカ エヌ.ベー. 単環式oga阻害剤化合物
CA3044762A1 (en) 2016-12-16 2018-06-21 Janssen Pharmaceutica Nv Bicyclic oga inhibitor compounds
AR110747A1 (es) 2017-01-27 2019-05-02 Lilly Co Eli Compuestos de 5-metil-1,2,4-oxadiazol-3-ilo
MA47420A (fr) 2017-02-06 2019-12-11 Janssen Pharmaceutica Nv Composés inhibiteurs d'oga
EP3585779A1 (en) 2017-02-24 2020-01-01 Asceneuron S.A. Substituted dihydrobenzofuran glycosidase inhibitors
WO2018154133A1 (en) 2017-02-27 2018-08-30 Janssen Pharmaceutica Nv [1,2,4]-triazolo [1,5-a]-pyrimidinyl derivatives substituted with piperidine, morpholine or piperazine as oga inhibitors
TWI669302B (zh) 2017-05-25 2019-08-21 美商美國禮來大藥廠 5-甲基-1,3,4-<img align="absmiddle" height="18px" width="27px" file="d10999.TIF" alt="其他非圖式 ed10999.png" img-content="tif" orientation="portrait" inline="yes" giffile="ed10999.png"></img>二唑-2-基化合物
EP3672959A1 (en) 2017-08-24 2020-07-01 Asceneuron SA Linear glycosidase inhibitors
SG11202101651RA (en) 2018-08-22 2021-03-30 Asceneuron S A Succinate and fumarate acid addition salts of piperazine derivatives useful as glycosidase inhibitors
US12016852B2 (en) 2018-08-22 2024-06-25 Asceneuron Sa Pyrrolidine glycosidase inhibitors
WO2020039029A1 (en) 2018-08-22 2020-02-27 Asceneuron S. A. Spiro compounds as glycosidase inhibitors
WO2020169804A1 (en) 2019-02-22 2020-08-27 Asceneuron Sa Fused glycosidase inhibitors

Similar Documents

Publication Publication Date Title
JP2019510006A5 (enExample)
JP2019506430A5 (enExample)
JP2014527060A5 (enExample)
JP2014503527A5 (enExample)
NZ788543A (en) Dimethyltryptamine derivatives and their use in psychedelic-assisted psychotherapy
CN115768750B (zh) Gcn2调节剂化合物
AU2016373533B2 (en) Novel compounds
JP7341034B2 (ja) プロテオパチーの処置のためのベンジリデングアニジン誘導体の新規な治療的使用
JP2018536641A5 (enExample)
JP2013010793A5 (enExample)
CA2800405C (en) Antidepressant, neuroprotectant, amyloid .beta. deposition inhibitor or age retardant containing heterocyclic compound having specific structure
HRP20160334T1 (hr) Pirano [3, 2 - d][1, 3]tiazol kao inhibitori glikozidaze
GB2571950A8 (en) New polymorph and new path to synthesize tafamidis
JP2010531345A5 (enExample)
RU2014141579A (ru) Гетероциклические соединения в качестве ингибиторов бета-лактамаз
JP2019503362A5 (enExample)
JP2016172757A (ja) カゼインキナーゼ1デルタ(ck1デルタ)阻害剤
JP2016509047A5 (enExample)
HRP20230628T1 (hr) Primjena i doziranje diaminofenotiazina
JP2013500314A5 (enExample)
JP2012532125A5 (enExample)
US8815914B2 (en) Positive allosteric modulators of nicotinic acetylcholine receptor
RU2011152516A (ru) Производные 2-карбоксамид-7-пиперазинил-бензофурана 774
CA3182424A1 (en) Hydroxynorketamine analogues, compositions comprising same and methods of use thereof
JP2017522370A (ja) O−アルキル−ベンジリデングアニジン誘導体、及びミスフォールドタンパク質の蓄積と関連する障害の処置のための治療的使用