JP6872550B2 - 架橋されたピペリジン誘導体 - Google Patents
架橋されたピペリジン誘導体 Download PDFInfo
- Publication number
- JP6872550B2 JP6872550B2 JP2018529006A JP2018529006A JP6872550B2 JP 6872550 B2 JP6872550 B2 JP 6872550B2 JP 2018529006 A JP2018529006 A JP 2018529006A JP 2018529006 A JP2018529006 A JP 2018529006A JP 6872550 B2 JP6872550 B2 JP 6872550B2
- Authority
- JP
- Japan
- Prior art keywords
- azabicyclo
- octane
- triazolo
- amine
- pyridin
- 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.)
- Active
Links
- 0 CC=CN1N=C(NC(C(CC2)C3)C2CN3c2nnc(C)[o]2)N[C@]1C(O*)=*C=C* Chemical compound CC=CN1N=C(NC(C(CC2)C3)C2CN3c2nnc(C)[o]2)N[C@]1C(O*)=*C=C* 0.000 description 7
- MMERROPKZFZEAL-UHFFFAOYSA-N CC(C(F)(F)F)Oc1ccc(C(F)(F)F)[n]2nc(N)nc12 Chemical compound CC(C(F)(F)F)Oc1ccc(C(F)(F)F)[n]2nc(N)nc12 MMERROPKZFZEAL-UHFFFAOYSA-N 0.000 description 1
- CQKFAVNVIQGNST-VSUJBEPISA-N CC(C(F)(F)F)Oc1ccc[n]2nc(N[C@@H]([C@@H](CC3)C4)C3CN4c3cc(C)n[s]3)nc12 Chemical compound CC(C(F)(F)F)Oc1ccc[n]2nc(N[C@@H]([C@@H](CC3)C4)C3CN4c3cc(C)n[s]3)nc12 CQKFAVNVIQGNST-VSUJBEPISA-N 0.000 description 1
- ROPTZEWCEBXLSL-NJQDXXEXSA-N CC(C(F)(F)F)Oc1ccc[n]2nc(N[C@H]([C@H](CC3)C4)[C@@H]3CN4c3cnc(C)[s]3)nc12 Chemical compound CC(C(F)(F)F)Oc1ccc[n]2nc(N[C@H]([C@H](CC3)C4)[C@@H]3CN4c3cnc(C)[s]3)nc12 ROPTZEWCEBXLSL-NJQDXXEXSA-N 0.000 description 1
- UQZWFZCEABXERF-UHFFFAOYSA-N CC(Nc(nc(C)cc1)c1OCC(F)(F)F)=O Chemical compound CC(Nc(nc(C)cc1)c1OCC(F)(F)F)=O UQZWFZCEABXERF-UHFFFAOYSA-N 0.000 description 1
- RATLSCMFCROEPA-ZXWBDNALSA-N CC[C@H](C(C1)[C@H]2CN1C(OC(C)(C)C)=O)[C@H]2Nc1n[n](cccc2OCC3(CC3)C(F)(F)F)c2n1 Chemical compound CC[C@H](C(C1)[C@H]2CN1C(OC(C)(C)C)=O)[C@H]2Nc1n[n](cccc2OCC3(CC3)C(F)(F)F)c2n1 RATLSCMFCROEPA-ZXWBDNALSA-N 0.000 description 1
- PXQPZJQQRXHZHQ-QFGYEDSMSA-N CC[C@H](C(C1)[C@H]2CN1c1cc(C)n[o]1)[C@H]2Nc(nc12)n[n]1c(C(F)(F)F)ccc2OCC(F)(F)F Chemical compound CC[C@H](C(C1)[C@H]2CN1c1cc(C)n[o]1)[C@H]2Nc(nc12)n[n]1c(C(F)(F)F)ccc2OCC(F)(F)F PXQPZJQQRXHZHQ-QFGYEDSMSA-N 0.000 description 1
- SZQBAIOCMHKWEP-FVNJLXPISA-N CC[C@H](C(C1)[C@H]2CN1c1ccncc1F)[C@H]2Nc(nc12)n[n]1c(C(C)(C)O)ccc2OCC(F)(F)F Chemical compound CC[C@H](C(C1)[C@H]2CN1c1ccncc1F)[C@H]2Nc(nc12)n[n]1c(C(C)(C)O)ccc2OCC(F)(F)F SZQBAIOCMHKWEP-FVNJLXPISA-N 0.000 description 1
- MHSPLKBWKCJRFJ-UHFFFAOYSA-N COC(c([n]1nc(N)nc11)ccc1OCC(F)(F)F)=O Chemical compound COC(c([n]1nc(N)nc11)ccc1OCC(F)(F)F)=O MHSPLKBWKCJRFJ-UHFFFAOYSA-N 0.000 description 1
- ANAWZIZMEJPUNV-UHFFFAOYSA-N COC(c(nc1N)ccc1OCC(F)(F)F)=O Chemical compound COC(c(nc1N)ccc1OCC(F)(F)F)=O ANAWZIZMEJPUNV-UHFFFAOYSA-N 0.000 description 1
- QOIXGDNEWDXUMJ-UHFFFAOYSA-N COc1cc(F)c[n]2nc(N)nc12 Chemical compound COc1cc(F)c[n]2nc(N)nc12 QOIXGDNEWDXUMJ-UHFFFAOYSA-N 0.000 description 1
- NIALRUWNTFTGFQ-AKABHXMESA-N COc1ncnc(N(C2)CC3([C@H]4CC3)[C@H]2CCC4=N)c1 Chemical compound COc1ncnc(N(C2)CC3([C@H]4CC3)[C@H]2CCC4=N)c1 NIALRUWNTFTGFQ-AKABHXMESA-N 0.000 description 1
- LWPNPNYFFHHQME-BZBKMWRSSA-N COc1ncnc(N(C[C@H]2CC3)C[C@H]3[C@@H]2N)c1 Chemical compound COc1ncnc(N(C[C@H]2CC3)C[C@H]3[C@@H]2N)c1 LWPNPNYFFHHQME-BZBKMWRSSA-N 0.000 description 1
- IRXLGVTVIKWXJB-UZSMEQOGSA-N C[C@@H](C(F)(F)F)Oc1ccc[n]2nc(N[C@H]([C@H](CC3)CN(C4)C5=NC(C)NS5)[C@@]34N)nc12 Chemical compound C[C@@H](C(F)(F)F)Oc1ccc[n]2nc(N[C@H]([C@H](CC3)CN(C4)C5=NC(C)NS5)[C@@]34N)nc12 IRXLGVTVIKWXJB-UZSMEQOGSA-N 0.000 description 1
- ZCSQTGRKLUUFKT-DRXBFXEBSA-N C[n]1ncc(N(C[C@H]2CC3)C[C@H]3[C@@H]2Nc(nc23)n[n]2c(C(F)(F)F)ccc3OCC(F)(F)F)c1 Chemical compound C[n]1ncc(N(C[C@H]2CC3)C[C@H]3[C@@H]2Nc(nc23)n[n]2c(C(F)(F)F)ccc3OCC(F)(F)F)c1 ZCSQTGRKLUUFKT-DRXBFXEBSA-N 0.000 description 1
- WTIBMXCTMHKOHG-UHFFFAOYSA-N Cc([n]1nc(N)nc11)ccc1OCC(F)(F)F Chemical compound Cc([n]1nc(N)nc11)ccc1OCC(F)(F)F WTIBMXCTMHKOHG-UHFFFAOYSA-N 0.000 description 1
- PDCCSFXLWXUKNV-DDFAGTSDSA-N Cc(cc1N(C[C@H]2CC3)C[C@H]3[C@@H]2N)ncc1F Chemical compound Cc(cc1N(C[C@H]2CC3)C[C@H]3[C@@H]2N)ncc1F PDCCSFXLWXUKNV-DDFAGTSDSA-N 0.000 description 1
- AENHEFDZKPSDCK-UHFFFAOYSA-N Cc(nc1[N+]([O-])=O)ccc1OCC(F)(F)F Chemical compound Cc(nc1[N+]([O-])=O)ccc1OCC(F)(F)F AENHEFDZKPSDCK-UHFFFAOYSA-N 0.000 description 1
- OOYSIUPAGYSLKF-WUEBVRTOSA-N Cc1n[s]c(N(C2)CC3(C4CC3)[C@@H]2[C@@H]4Nc2n[n](cccc3OCCCC(F)(F)F)c3n2)n1 Chemical compound Cc1n[s]c(N(C2)CC3(C4CC3)[C@@H]2[C@@H]4Nc2n[n](cccc3OCCCC(F)(F)F)c3n2)n1 OOYSIUPAGYSLKF-WUEBVRTOSA-N 0.000 description 1
- ONBGPUYSPIJKCI-SFIRGFGWSA-N Cc1n[s]c(N(C[C@@H]2CC3)CC3[C@H]2Nc2n[n](cccc3OCCCC(F)(F)F)c3n2)n1 Chemical compound Cc1n[s]c(N(C[C@@H]2CC3)CC3[C@H]2Nc2n[n](cccc3OCCCC(F)(F)F)c3n2)n1 ONBGPUYSPIJKCI-SFIRGFGWSA-N 0.000 description 1
- XRTKBFJTGVQLFD-HPNRGHHYSA-N Cc1n[s]c(N2CC(CC3)[C@@H](CNc4n[n](ccnc5OCC(F)F)c5n4)[C@@H]3C2)c1 Chemical compound Cc1n[s]c(N2CC(CC3)[C@@H](CNc4n[n](ccnc5OCC(F)F)c5n4)[C@@H]3C2)c1 XRTKBFJTGVQLFD-HPNRGHHYSA-N 0.000 description 1
- OVLXIJQZTDOQOD-LVURXURCSA-N Cc1ncnc(N(C2)CC3(C4C3)[C@@H]2[C@@H]4Nc2n[n](cccc3OCCCC(F)(F)F)c3n2)c1 Chemical compound Cc1ncnc(N(C2)CC3(C4C3)[C@@H]2[C@@H]4Nc2n[n](cccc3OCCCC(F)(F)F)c3n2)c1 OVLXIJQZTDOQOD-LVURXURCSA-N 0.000 description 1
- SBIKCUDPZRLNAC-IVWMJMPLSA-N Cc1ncnc(N(C[C@H]2CC3)C[C@H]3[C@@H]2Nc(nc23)n[n]2c(C(F)(F)F)ccc3OCC(F)F)c1 Chemical compound Cc1ncnc(N(C[C@H]2CC3)C[C@H]3[C@@H]2Nc(nc23)n[n]2c(C(F)(F)F)ccc3OCC(F)F)c1 SBIKCUDPZRLNAC-IVWMJMPLSA-N 0.000 description 1
- SVYZUHSGVZDUDT-UHFFFAOYSA-N FC(COc(c1n2)ccc[n]1nc2Br)(F)F Chemical compound FC(COc(c1n2)ccc[n]1nc2Br)(F)F SVYZUHSGVZDUDT-UHFFFAOYSA-N 0.000 description 1
- OSGWEELMNPDYHT-IVWMJMPLSA-N FCCOc1ccc(C(F)(F)F)[n]2nc(N[C@H]([C@H](CC3)C4)[C@@H]3CN4c3cc(Cl)ncc3)nc12 Chemical compound FCCOc1ccc(C(F)(F)F)[n]2nc(N[C@H]([C@H](CC3)C4)[C@@H]3CN4c3cc(Cl)ncc3)nc12 OSGWEELMNPDYHT-IVWMJMPLSA-N 0.000 description 1
- HRCKNYWKHBWFJH-UHFFFAOYSA-N Nc(nc12)n[n]1c(C(F)(F)F)ccc2Br Chemical compound Nc(nc12)n[n]1c(C(F)(F)F)ccc2Br HRCKNYWKHBWFJH-UHFFFAOYSA-N 0.000 description 1
- UIWJIQYXUKFLSE-UHFFFAOYSA-N Nc(nc12)n[n]1c(C(F)(F)F)ccc2OCC(F)(F)F Chemical compound Nc(nc12)n[n]1c(C(F)(F)F)ccc2OCC(F)(F)F UIWJIQYXUKFLSE-UHFFFAOYSA-N 0.000 description 1
- YGKKBLOKOLYQQT-UHFFFAOYSA-N Oc(c1n2)cc(F)c[n]1nc2Br Chemical compound Oc(c1n2)cc(F)c[n]1nc2Br YGKKBLOKOLYQQT-UHFFFAOYSA-N 0.000 description 1
- AJSRUPTXYSCBFT-UHFFFAOYSA-N [O-][N+](c(nc(cc1)Br)c1OCC(F)(F)F)=O Chemical compound [O-][N+](c(nc(cc1)Br)c1OCC(F)(F)F)=O AJSRUPTXYSCBFT-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—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
- 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
- C07D471/04—Ortho-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Neurosurgery (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hospice & Palliative Care (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Psychiatry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP15199260 | 2015-12-10 | ||
| EP15199260.9 | 2015-12-10 | ||
| PCT/EP2016/079816 WO2017097728A1 (en) | 2015-12-10 | 2016-12-06 | Bridged piperidine derivatives |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018536671A JP2018536671A (ja) | 2018-12-13 |
| JP2018536671A5 JP2018536671A5 (https=) | 2019-12-12 |
| JP6872550B2 true JP6872550B2 (ja) | 2021-05-19 |
Family
ID=54848457
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018529006A Active JP6872550B2 (ja) | 2015-12-10 | 2016-12-06 | 架橋されたピペリジン誘導体 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US10562903B2 (https=) |
| EP (1) | EP3386978B1 (https=) |
| JP (1) | JP6872550B2 (https=) |
| CN (1) | CN108137579B (https=) |
| AR (1) | AR107010A1 (https=) |
| TW (1) | TWI629278B (https=) |
| WO (1) | WO2017097728A1 (https=) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ739090A (en) | 2015-10-02 | 2025-06-27 | Hoffmann La Roche | Bispecific antibodies specific for pd1 and tim3 |
| EA201800367A1 (ru) | 2015-12-10 | 2019-02-28 | ПиТиСи ТЕРАПЬЮТИКС, ИНК. | Способы лечения болезни хантингтона |
| JP7012715B2 (ja) * | 2016-06-27 | 2022-01-28 | エフ.ホフマン-ラ ロシュ アーゲー | γ-セクレターゼモジュレーターとしてのトリアゾロピリジン |
| AR109829A1 (es) * | 2016-09-29 | 2019-01-30 | Hoffmann La Roche | Derivados de piperidina puenteados |
| WO2018083050A1 (en) * | 2016-11-01 | 2018-05-11 | F. Hoffmann-La Roche Ag | Bicyclic heteroaryl derivatives |
| RU2761377C2 (ru) | 2017-04-03 | 2021-12-07 | Ф. Хоффманн-Ля Рош Аг | Иммуноконъюгаты антитела к pd-1 с мутантом il-2 или с il-15 |
| TWI690538B (zh) | 2017-04-05 | 2020-04-11 | 瑞士商赫孚孟拉羅股份公司 | 特異性結合至pd1至lag3的雙特異性抗體 |
| EP3634953B1 (en) | 2017-06-05 | 2024-01-03 | PTC Therapeutics, Inc. | Compounds for treating huntington's disease |
| MX2019015580A (es) | 2017-06-28 | 2020-07-28 | Ptc Therapeutics Inc | Metodos para tratar la enfermedad de huntington. |
| CN111182898B (zh) | 2017-06-28 | 2024-04-16 | Ptc医疗公司 | 用于治疗亨廷顿氏病的方法 |
| EA202092001A1 (ru) | 2018-03-27 | 2021-01-29 | ПиТиСи ТЕРАПЬЮТИКС, ИНК. | Соединения для лечения болезни гентингтона |
| WO2020005877A1 (en) | 2018-06-27 | 2020-01-02 | Ptc Therapeutics, Inc. | Heteroaryl compounds for treating huntington's disease |
| HRP20240935T1 (hr) | 2018-06-27 | 2024-11-22 | Ptc Therapeutics, Inc. | Heterociklični i heteroaril spojevi za liječenje huntingtonove bolesti |
| DK3846903T3 (da) | 2018-09-03 | 2024-01-02 | Hoffmann La Roche | Bicykliske heteroarylderivater |
| CN117946116A (zh) | 2018-12-13 | 2024-04-30 | 豪夫迈·罗氏有限公司 | 6,7-二氢-5h-吡咯并[1,2-b][1,2,4]三唑-2-胺衍生物 |
| ES2940185T3 (es) | 2018-12-27 | 2023-05-04 | Hoffmann La Roche | Procedimiento para la preparación de exo-N-(3-azabiciclo[3.2.1]octan-8-il)carbamato de terc-butilo |
| JP7649257B2 (ja) | 2019-05-13 | 2025-03-19 | ピーティーシー セラピューティクス, インコーポレイテッド | ハンチントン病を処置するための化合物 |
| CN117396490A (zh) * | 2021-05-14 | 2024-01-12 | Bm医药咨询有限公司 | 用于预防和治疗病毒感染的双环杂环化合物 |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1383409A (en) | 1972-09-09 | 1974-02-12 | Pfizer Ltd | Derivatives of 2-amino- and 4-amino-quinazoline and pharmaceutical compositions containing them |
| US6774134B2 (en) | 2000-12-20 | 2004-08-10 | Bristol-Myers Squibb Company | Heterocyclic substituted 2-methyl-benzimidazole antiviral agents |
| BRPI0418127A (pt) | 2003-12-24 | 2007-04-27 | Biota Scient Management | uso de um composto, seus sais, e derivados farmaceuticamente aceitáveis dos mesmos, método para o tratamento de infecções envolvendo vìrus da sub-famìlia pneumovirinae, formulação farmacêutica, métodos para tratar mamìferos infectados e para prevenir a infecção de mamìferos com vìrus da sub-famìlia pneumovirinae, composto, seus sais, e derivados farmaceuticamente aceitáveis dos mesmos, composto e a forma n-óxido e sal piridìnio do mesmo, e, método de separação de enantiÈmeros de um composto |
| US8338607B2 (en) * | 2005-10-06 | 2012-12-25 | Nippon Soda Co., Ltd. | Cyclic amine compounds and agents for pest control |
| FR2914188B1 (fr) | 2007-03-28 | 2012-06-22 | Trophos | Nouvelle composition a base d'oxime de cholest-4-en-3-one |
| WO2009151546A2 (en) | 2008-05-27 | 2009-12-17 | Ptc Therapeutics, Inc. | Methods for treating spinal muscular atrophy |
| EP2337609B1 (en) | 2008-08-14 | 2016-08-17 | Cardiac Pacemakers, Inc. | Performance assessment and adaptation of an acoustic communication link |
| US8486967B2 (en) * | 2010-02-17 | 2013-07-16 | Hoffmann-La Roche Inc. | Heteroaryl substituted piperidines |
| US8703763B2 (en) * | 2011-03-02 | 2014-04-22 | Hoffmann-La Roche Inc. | Bridged piperidine derivatives |
| US8871756B2 (en) | 2011-08-11 | 2014-10-28 | Hoffmann-La Roche Inc. | Compounds for the treatment and prophylaxis of Respiratory Syncytial Virus disease |
| GB201119538D0 (en) | 2011-11-10 | 2011-12-21 | Viral Ltd | Pharmaceutical compounds |
| MX352861B (es) | 2011-12-30 | 2017-12-13 | Ptc Therapeutics Inc | Compuestos para tratar la atrofia muscular espinal. |
| MX357834B (es) | 2012-01-26 | 2018-07-26 | Ptc Therapeutics Inc | Compuestos de tipo isocumarina sustituidos para tratar la atrofia muscular espinal. |
| EP2812004B1 (en) | 2012-02-10 | 2018-06-27 | PTC Therapeutics, Inc. | Compounds for treating spinal muscular atrophy |
| US9212209B2 (en) | 2012-07-13 | 2015-12-15 | Indiana University Research And Technology Corporation | Screening methods for spinal muscular atrophy |
| EP2997028A1 (en) | 2013-05-14 | 2016-03-23 | F.Hoffmann-La Roche Ag | Aza-oxo-indoles for the treatment and prophylaxis of respiratory syncytial virus infection |
| CA2913785C (en) | 2013-06-25 | 2021-08-31 | F. Hoffmann-La Roche Ag | Compounds for treating spinal muscular atrophy |
| AR099134A1 (es) | 2014-01-24 | 2016-06-29 | Hoffmann La Roche | Procedimiento para la preparación de n-[(3-aminooxetán-3-il)metil]-2-(1,1-dioxo-3,5-dihidro-1,4-benzotiazepín-4-il)-6-metil-quinazolín-4-amina |
| ES2761423T3 (es) | 2014-05-15 | 2020-05-19 | Hoffmann La Roche | Compuestos para tratar la atrofia muscular espinal |
| EA036399B1 (ru) | 2015-11-12 | 2020-11-06 | Ф. Хоффманн-Ля Рош Аг | Композиции для лечения спинальной мышечной атрофии |
-
2016
- 2016-12-06 WO PCT/EP2016/079816 patent/WO2017097728A1/en not_active Ceased
- 2016-12-06 CN CN201680057010.6A patent/CN108137579B/zh active Active
- 2016-12-06 JP JP2018529006A patent/JP6872550B2/ja active Active
- 2016-12-06 EP EP16805853.5A patent/EP3386978B1/en active Active
- 2016-12-07 AR ARP160103753A patent/AR107010A1/es unknown
- 2016-12-09 TW TW105140951A patent/TWI629278B/zh not_active IP Right Cessation
-
2018
- 2018-06-08 US US16/004,145 patent/US10562903B2/en active Active
-
2020
- 2020-02-13 US US16/790,629 patent/US20200291034A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| EP3386978B1 (en) | 2021-01-27 |
| US10562903B2 (en) | 2020-02-18 |
| CN108137579A (zh) | 2018-06-08 |
| US20200291034A1 (en) | 2020-09-17 |
| TW201725209A (zh) | 2017-07-16 |
| AR107010A1 (es) | 2018-03-14 |
| WO2017097728A1 (en) | 2017-06-15 |
| EP3386978A1 (en) | 2018-10-17 |
| CN108137579B (zh) | 2022-01-07 |
| US20190010156A1 (en) | 2019-01-10 |
| TWI629278B (zh) | 2018-07-11 |
| JP2018536671A (ja) | 2018-12-13 |
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