JP2019506430A - グリコシダーゼ阻害剤 - Google Patents
グリコシダーゼ阻害剤 Download PDFInfo
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- JP2019506430A JP2019506430A JP2018544555A JP2018544555A JP2019506430A JP 2019506430 A JP2019506430 A JP 2019506430A JP 2018544555 A JP2018544555 A JP 2018544555A JP 2018544555 A JP2018544555 A JP 2018544555A JP 2019506430 A JP2019506430 A JP 2019506430A
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- 0 Cc1c(C=*)nccc1 Chemical compound Cc1c(C=*)nccc1 0.000 description 3
- XAKLVBKPMJRVAX-UHFFFAOYSA-N C1C(C=C[I]=N2)=C2OC1 Chemical compound C1C(C=C[I]=N2)=C2OC1 XAKLVBKPMJRVAX-UHFFFAOYSA-N 0.000 description 1
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- WIEMWLGSWIIWEG-LBPRGKRZSA-N C[C@@H](c1cc(OCC2)c2cc1)N(CC1)CCN1c1nnc(NC(C)=O)[s]1 Chemical compound C[C@@H](c1cc(OCC2)c2cc1)N(CC1)CCN1c1nnc(NC(C)=O)[s]1 WIEMWLGSWIIWEG-LBPRGKRZSA-N 0.000 description 1
- CCYHSWGUDVNJBB-CQSZACIVSA-N C[C@H](c1cc(OCC2)c2cc1)N(CC1)CCN1c1nc(CCNC2)c2[s]1 Chemical compound C[C@H](c1cc(OCC2)c2cc1)N(CC1)CCN1c1nc(CCNC2)c2[s]1 CCYHSWGUDVNJBB-CQSZACIVSA-N 0.000 description 1
- WIEMWLGSWIIWEG-GFCCVEGCSA-N C[C@H](c1cc(OCC2)c2cc1)N(CC1)CCN1c1nnc(NC(C)=O)[s]1 Chemical compound C[C@H](c1cc(OCC2)c2cc1)N(CC1)CCN1c1nnc(NC(C)=O)[s]1 WIEMWLGSWIIWEG-GFCCVEGCSA-N 0.000 description 1
- IQRWUQVVQPBSQZ-UHFFFAOYSA-N Cc(cc1)nc2c1[s]cn2 Chemical compound Cc(cc1)nc2c1[s]cn2 IQRWUQVVQPBSQZ-UHFFFAOYSA-N 0.000 description 1
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- CKTRBJQDVBLQPF-UHFFFAOYSA-N Cc1nc(cc(C)cn2)c2[s]1 Chemical compound Cc1nc(cc(C)cn2)c2[s]1 CKTRBJQDVBLQPF-UHFFFAOYSA-N 0.000 description 1
- QHFLHFHJVNMPBL-UHFFFAOYSA-N Cc1nc(nc(C)cc2)c2[s]1 Chemical compound Cc1nc(nc(C)cc2)c2[s]1 QHFLHFHJVNMPBL-UHFFFAOYSA-N 0.000 description 1
- UPCQCZXLRXNCMP-UHFFFAOYSA-N FC1=C[I]=Nc2ncccc12 Chemical compound FC1=C[I]=Nc2ncccc12 UPCQCZXLRXNCMP-UHFFFAOYSA-N 0.000 description 1
- DSCYVCLBSVVQDH-UHFFFAOYSA-N Fc1c2nccnc2ccc1 Chemical compound Fc1c2nccnc2ccc1 DSCYVCLBSVVQDH-UHFFFAOYSA-N 0.000 description 1
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- NYBJDWOMBJJWSN-UHFFFAOYSA-N OC1(CCOCC1)c(cn1)cnc1Cl Chemical compound OC1(CCOCC1)c(cn1)cnc1Cl NYBJDWOMBJJWSN-UHFFFAOYSA-N 0.000 description 1
- MHZLMQFZGQYNJK-UHFFFAOYSA-N [IH]=Nc1c(N=[IH])nccc1 Chemical compound [IH]=Nc1c(N=[IH])nccc1 MHZLMQFZGQYNJK-UHFFFAOYSA-N 0.000 description 1
- XVAOXPHOWWIJMU-UHFFFAOYSA-N c1cnc(C=C[I]=N2)c2c1 Chemical compound c1cnc(C=C[I]=N2)c2c1 XVAOXPHOWWIJMU-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
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- 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
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- 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
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| JP2019510006A (ja) * | 2016-02-25 | 2019-04-11 | エースニューロン・ソシエテ・アノニム | グリコシダーゼ阻害剤 |
| JP2023538434A (ja) * | 2020-08-19 | 2023-09-07 | ユニヴァーシティ・オブ・オックスフォード | Lmo2タンパク質阻害剤 |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6563017B2 (ja) | 2014-08-28 | 2019-08-21 | エースニューロン・ソシエテ・アノニム | グリコシダーゼ阻害剤 |
| EP3419976B1 (en) | 2016-02-25 | 2021-04-07 | Asceneuron SA | Acid addition salts of piperazine derivatives |
| CA3012624A1 (en) | 2016-02-25 | 2017-08-31 | Asceneuron S.A. | Glycosidase inhibitors |
| US11261183B2 (en) | 2016-02-25 | 2022-03-01 | Asceneuron Sa | Sulfoximine glycosidase inhibitors |
| US20200079766A1 (en) | 2016-12-16 | 2020-03-12 | Janssen Pharmaceutica Nv | Monocyclic oga inhibitor compounds |
| MX2019010085A (es) * | 2017-02-24 | 2019-11-21 | Asceneuron S A | Inhibidores de la glicosidasa de sulfoximina. |
| JP2020509004A (ja) * | 2017-02-27 | 2020-03-26 | ヤンセン ファーマシューティカ エヌ.ベー. | Oga阻害剤としての、ピペリジン、モルホリンまたはピペラジンで置換されている[1,2,4]−トリアゾロ[1,5−a]−ピリミジニル誘導体 |
| WO2019037860A1 (en) | 2017-08-24 | 2019-02-28 | Asceneuron S.A. | LINEAR INHIBITORS OF GLYCOSIDASE |
| 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 |
| CN112469476B (zh) | 2018-07-31 | 2024-07-16 | 伊莱利利公司 | 5-甲基-4-氟-噻唑-2-基化合物 |
| US12016852B2 (en) | 2018-08-22 | 2024-06-25 | Asceneuron Sa | Pyrrolidine glycosidase inhibitors |
| WO2020039028A1 (en) * | 2018-08-22 | 2020-02-27 | Asceneuron S. A. | Tetrahydro-benzoazepine glycosidase inhibitors |
| US11731972B2 (en) | 2018-08-22 | 2023-08-22 | Asceneuron Sa | Spiro compounds as glycosidase inhibitors |
| KR102839500B1 (ko) * | 2018-08-22 | 2025-07-28 | 아셰뉴론 에스아 | 글리코시다제 억제제로서 유용한 피페라진 유도체의 숙시네이트 및 푸마레이트 산 부가염 |
| 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 |
| WO2021123291A1 (en) * | 2019-12-18 | 2021-06-24 | Janssen Pharmaceutica Nv | Oga inhibitor compounds |
| WO2024083820A1 (en) | 2022-10-18 | 2024-04-25 | Institut National de la Santé et de la Recherche Médicale | Method and composition for determining the level of o-glcnacylation in horses |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014159234A1 (en) * | 2013-03-14 | 2014-10-02 | Merck Patent Gmbh | Glycosidase inhibitors |
| JP2019510006A (ja) * | 2016-02-25 | 2019-04-11 | エースニューロン・ソシエテ・アノニム | グリコシダーゼ阻害剤 |
Family Cites Families (84)
| 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 |
| EP0636130A1 (en) | 1992-04-15 | 1995-02-01 | Merck Sharp & Dohme Ltd. | 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 |
| CA2282390A1 (en) | 1997-04-17 | 1998-10-22 | Yukio Fujisawa | Thermogenic composition and benzazepine thermogenics |
| EP1025097B1 (en) | 1997-10-24 | 2005-04-27 | Neurogen Corporation | 1-(2-naphthyl) and 1-(2-azanaphthyl)-4-(1-phenylmethyl)piperazines being dopamine d 4? receptor subtype ligands |
| US6953801B2 (en) * | 2001-05-22 | 2005-10-11 | 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 |
| WO2003106452A2 (en) | 2002-06-12 | 2003-12-24 | Millennium Pharmaceuticals, Inc. | Antagonists of melanin concentrating hormone receptor |
| KR101116627B1 (ko) | 2002-06-27 | 2012-10-09 | 노보 노르디스크 에이/에스 | 치료제로서 아릴 카르보닐 유도체 |
| IL165829A0 (en) | 2002-07-05 | 2006-01-15 | Targacept Inc | N-aryl diazaspiracyclic compounds and methods of preparation and use thereof |
| JP4712384B2 (ja) | 2002-09-09 | 2011-06-29 | 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 | Orl−1受容体介在障害の治療に有用なヒドロキシアルキル置換1,3,8−トリアザスピロ[4.5]デカン−4−オン誘導体 |
| AU2004232799A1 (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 |
| CN100448870C (zh) | 2003-05-21 | 2009-01-07 | 万有制药株式会社 | 2-氨基喹啉衍生物 |
| MXPA06007667A (es) | 2004-01-06 | 2006-09-01 | Novo Nordisk As | Heteroaril-ureas y su uso como activadores de glucocinasa. |
| 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 |
| AU2006220187B2 (en) | 2005-03-01 | 2012-11-08 | Simon Fraser University | Selective glycosidase inhibitors, methods of making inhibitors, and uses thereof |
| MX2008000294A (es) | 2005-07-08 | 2008-04-04 | Novo Nordisk As | Activadores de dicicloalquil urea glucocinasa. |
| MX2008011968A (es) | 2006-03-31 | 2008-10-01 | Astrazeneca Ab | Compuestos biciclicos de bencimidazol y su uso como potenciadores del receptor metabotropico de glutamato. |
| US20090306126A1 (en) | 2006-05-22 | 2009-12-10 | 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 |
| EP2057171A4 (en) | 2006-08-31 | 2010-04-21 | Univ Fraser Simon | SELECTIVE GLYCOSIDASE INHIBITORS AND APPLICATIONS THEREOF |
| US20100022517A1 (en) | 2006-12-18 | 2010-01-28 | Richards Lori A | Ophthalmic formulation of rho kinase inhibitor compound |
| WO2008138842A1 (en) | 2007-05-10 | 2008-11-20 | Galapagos N.V. | Imidazopyrazines and triazolopyrazine for the treatment of joint 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 |
| AU2008345225A1 (en) | 2007-12-21 | 2009-07-09 | University Of Rochester | Method for altering the lifespan of eukaryotic organisms |
| WO2009127943A1 (en) | 2008-04-17 | 2009-10-22 | Pfizer Inc. | Ether benzylidene piperidine 5-membered aryl carboxamide compounds useful as faah inhibitors |
| WO2009127948A1 (en) | 2008-04-17 | 2009-10-22 | 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 |
| WO2009154132A1 (ja) | 2008-06-19 | 2009-12-23 | 萬有製薬株式会社 | スピロジアミン-ジアリールケトオキシム誘導体 |
| 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 |
| CN102137841B (zh) | 2008-09-02 | 2014-05-14 | 日产化学工业株式会社 | 邻位取代卤代烷基磺酰苯胺衍生物及除草剂 |
| TW201030007A (en) | 2009-02-06 | 2010-08-16 | Gruenenthal Gmbh | Substituted spiro-amides as b1r modulators |
| MX2011009213A (es) | 2009-03-02 | 2011-12-14 | Sirtris Pharmaceuticals Inc | Quinolinas 8-sustituidas y analogos relacionados como moduladores de sirtuina. |
| WO2010108115A1 (en) | 2009-03-20 | 2010-09-23 | Sanford-Burnham Medical Research Institute | Allosteric jnk inhibitors |
| US20120010186A1 (en) | 2009-03-23 | 2012-01-12 | 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 |
| WO2010151318A1 (en) | 2009-06-22 | 2010-12-29 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
| DE102009049679A1 (de) | 2009-10-19 | 2011-04-21 | Merck Patent Gmbh | Pyrazolopyrimidinderivate |
| US9120781B2 (en) | 2010-05-11 | 2015-09-01 | Simon Fraser University | Selective glycosidase inhibitors and uses thereof |
| JP2013537233A (ja) | 2010-09-17 | 2013-09-30 | グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッド | 脂肪酸合成酵素阻害剤 |
| EP2638052B1 (en) | 2010-11-08 | 2017-03-22 | Alectos Therapeutics, Inc. | Selective glycosidase inhibitors and uses thereof |
| WO2012062759A1 (en) | 2010-11-08 | 2012-05-18 | Janssen Pharmaceuticals, Inc. | 1,2,4-TRIAZOLO[4,3-a]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS |
| WO2012061972A1 (en) | 2010-11-08 | 2012-05-18 | Alectos Therapeutics Inc. | Selective glycosidase inhibitors and uses thereof |
| PL2655388T3 (pl) | 2010-12-23 | 2016-12-30 | Selektywne inhibitory glikozydazy i ich zastosowania | |
| GB201103526D0 (en) | 2011-03-02 | 2011-04-13 | Summit Corp Plc | Selective glycosidase inhibitors and uses thereof |
| TW201300358A (zh) | 2011-03-14 | 2013-01-01 | 大正製藥股份有限公司 | 含氮縮合雜環化合物 |
| EA022562B1 (ru) | 2011-08-25 | 2016-01-29 | Мерк Патент Гмбх | ПИРАНО[3,2-d][1,3]ТИАЗОЛ В КАЧЕСТВЕ ИНГИБИТОРОВ ГЛИКОЗИДАЗЫ |
| US9221809B2 (en) | 2011-10-31 | 2015-12-29 | Merck Sharp & Dohme Corp. | Aminopyrimidinones as interleukin receptor-associated kinase inhibitors |
| JP6233855B2 (ja) | 2012-08-08 | 2017-11-22 | ノバルティス・ティーアゲズントハイト・アクチェンゲゼルシャフトNovartis Tiergesundheit Ag | 殺虫剤としての置換されたアジン類 |
| WO2014032187A1 (en) | 2012-08-31 | 2014-03-06 | Alectos Therapeutics Inc. | Glycosidase inhibitors and uses thereof |
| 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 |
| MA39092B1 (fr) | 2013-12-05 | 2018-09-28 | Pfizer | Pyrrolo[2,3-d]pyrimidinyle, pyrrolo[2,3-b]pyrazinyle et pyrollo[2,3-d]pyridinyle acrylamides |
| EP2913330A1 (en) | 2014-02-27 | 2015-09-02 | Laboratoire Biodim | Condensed derivatives of imidazole useful as pharmaceuticals |
| MA50375A (fr) | 2014-04-23 | 2021-05-26 | Dart Neuroscience Cayman Ltd | Compositions contenant des composés substitués de [1,2,4]triazolo[1,5-a]pyrimidine-7-yl utilisés en tant qu'inhibiteurs pde2 |
| JP6563017B2 (ja) | 2014-08-28 | 2019-08-21 | エースニューロン・ソシエテ・アノニム | グリコシダーゼ阻害剤 |
| PL3316969T3 (pl) | 2015-07-02 | 2022-06-20 | Janssen Sciences Ireland Unlimited Company | Związki przeciwbakteryjne |
| SG11201803605YA (en) | 2015-11-02 | 2018-05-30 | Janssen Pharmaceutica Nv | [1,2,4]TRIAZOLO[1,5-a]PYRIMIDIN-7-YL COMPOUND |
| US10385057B2 (en) | 2015-11-20 | 2019-08-20 | Lundbeck La Jolla Research Center, Inc. | Pyrazole compounds and methods of making and using same |
| WO2017087863A1 (en) | 2015-11-20 | 2017-05-26 | Abide Therapeutics, Inc. | Pyrazole compounds and methods of making and using same |
| HUE056356T2 (hu) | 2015-11-25 | 2022-02-28 | Lieber Inst Inc | Tetrahidro-8H-pirido[1,2-a]pirazin-8-on vegyületek, mint COMT inhibitorok neurodegeneratív rendellenességek kezelésére |
| US10913733B2 (en) | 2015-12-18 | 2021-02-09 | Alectos Therapeutics Inc. | Substituted piperidines thiazolyl acetamides as glycosidase inhibitors and uses thereof |
| EP3419976B1 (en) | 2016-02-25 | 2021-04-07 | Asceneuron SA | Acid addition salts of piperazine derivatives |
| CA3012624A1 (en) | 2016-02-25 | 2017-08-31 | Asceneuron S.A. | Glycosidase inhibitors |
| EP3419974B1 (en) | 2016-02-25 | 2021-05-05 | Asceneuron SA | Process for the separation of enantiomers of piperazine derivatives |
| US11186564B2 (en) | 2016-08-04 | 2021-11-30 | Sunovion Pharmaceuticals Inc. | Dual NAV1.2/5HT2a inhibitors for treating CNS disorders |
| US20190359609A1 (en) | 2016-12-16 | 2019-11-28 | Janssen Pharmaceutica Nv | Bicyclic oga inhibitor compounds |
| US20200079766A1 (en) | 2016-12-16 | 2020-03-12 | Janssen Pharmaceutica Nv | Monocyclic 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 |
| MX2019010085A (es) | 2017-02-24 | 2019-11-21 | Asceneuron S A | Inhibidores de la glicosidasa de sulfoximina. |
| JP2020509004A (ja) | 2017-02-27 | 2020-03-26 | ヤンセン ファーマシューティカ エヌ.ベー. | Oga阻害剤としての、ピペリジン、モルホリンまたはピペラジンで置換されている[1,2,4]−トリアゾロ[1,5−a]−ピリミジニル誘導体 |
| 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 |
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- 2017-02-24 MA MA043680A patent/MA43680A/fr unknown
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- 2017-02-24 KR KR1020187025755A patent/KR20180132626A/ko not_active Withdrawn
- 2017-02-24 WO PCT/EP2017/054280 patent/WO2017144639A1/en not_active Ceased
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- 2017-08-24 MA MA047574A patent/MA47574A/fr unknown
- 2017-08-24 MA MA047573A patent/MA47573A/fr unknown
- 2017-08-24 KR KR1020197027278A patent/KR20190118184A/ko not_active Abandoned
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- 2017-08-24 US US16/488,163 patent/US10995090B2/en active Active
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Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014159234A1 (en) * | 2013-03-14 | 2014-10-02 | Merck Patent Gmbh | Glycosidase inhibitors |
| JP2019510006A (ja) * | 2016-02-25 | 2019-04-11 | エースニューロン・ソシエテ・アノニム | グリコシダーゼ阻害剤 |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2019510006A (ja) * | 2016-02-25 | 2019-04-11 | エースニューロン・ソシエテ・アノニム | グリコシダーゼ阻害剤 |
| JP2023538434A (ja) * | 2020-08-19 | 2023-09-07 | ユニヴァーシティ・オブ・オックスフォード | Lmo2タンパク質阻害剤 |
Also Published As
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| MA43680A (fr) | 2018-11-28 |
| CA3053200A1 (en) | 2018-08-30 |
| CA3012624A1 (en) | 2017-08-31 |
| US10556902B2 (en) | 2020-02-11 |
| MA47573A (fr) | 2021-04-28 |
| US10995090B2 (en) | 2021-05-04 |
| MX2018010191A (es) | 2019-05-20 |
| AU2017222964B2 (en) | 2020-01-02 |
| CA3053200C (en) | 2023-03-14 |
| IL268501A (en) | 2019-09-26 |
| EP3419972A1 (en) | 2019-01-02 |
| WO2017144639A1 (en) | 2017-08-31 |
| US20190388415A1 (en) | 2019-12-26 |
| AU2017222964A1 (en) | 2018-08-02 |
| KR20230026541A (ko) | 2023-02-24 |
| KR20190118184A (ko) | 2019-10-17 |
| MA47574A (fr) | 2020-01-01 |
| US20190055239A1 (en) | 2019-02-21 |
| KR20180132626A (ko) | 2018-12-12 |
| KR102620279B1 (ko) | 2024-01-03 |
| CN108884078A (zh) | 2018-11-23 |
| EP3419972B1 (en) | 2023-07-26 |
| BR112019017514A2 (pt) | 2020-03-31 |
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