JP2017527559A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2017527559A5 JP2017527559A5 JP2017511927A JP2017511927A JP2017527559A5 JP 2017527559 A5 JP2017527559 A5 JP 2017527559A5 JP 2017511927 A JP2017511927 A JP 2017511927A JP 2017511927 A JP2017511927 A JP 2017511927A JP 2017527559 A5 JP2017527559 A5 JP 2017527559A5
- Authority
- JP
- Japan
- Prior art keywords
- dihydro
- isoindol
- pyridin
- imaging agent
- methoxy
- 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.)
- Ceased
Links
- 239000012216 imaging agent Substances 0.000 claims description 56
- -1 cyano, methyl Chemical group 0.000 claims description 42
- 125000000217 alkyl group Chemical group 0.000 claims description 30
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 20
- 125000001072 heteroaryl group Chemical group 0.000 claims description 14
- 125000003545 alkoxy group Chemical group 0.000 claims description 12
- 125000001475 halogen functional group Chemical group 0.000 claims description 12
- 125000003118 aryl group Chemical group 0.000 claims description 10
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
- 238000012636 positron electron tomography Methods 0.000 claims description 10
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 8
- 125000000304 alkynyl group Chemical group 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 8
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 6
- 208000023105 Huntington disease Diseases 0.000 claims description 6
- 150000002431 hydrogen Chemical group 0.000 claims description 6
- 230000004770 neurodegeneration Effects 0.000 claims description 6
- 208000015122 neurodegenerative disease Diseases 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 102000004169 proteins and genes Human genes 0.000 claims description 6
- 108090000623 proteins and genes Proteins 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 5
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 208000037273 Pathologic Processes Diseases 0.000 claims description 4
- 210000004556 brain Anatomy 0.000 claims description 4
- 125000004366 heterocycloalkenyl group Chemical group 0.000 claims description 4
- 238000002595 magnetic resonance imaging Methods 0.000 claims description 4
- 239000000178 monomer Substances 0.000 claims description 4
- 230000009054 pathological process Effects 0.000 claims description 4
- 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 claims description 4
- 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 claims description 4
- RWEYYSNPCVRJSQ-UHFFFAOYSA-N C(C1=CC=CC=C1)OC=1C=C2CN(CC2=CC=1)C1=NC=NC=C1C#N Chemical compound C(C1=CC=CC=C1)OC=1C=C2CN(CC2=CC=1)C1=NC=NC=C1C#N RWEYYSNPCVRJSQ-UHFFFAOYSA-N 0.000 claims description 3
- AEFGEBPXNMNFPY-UHFFFAOYSA-N COC=1C=C2CN(CC2=CC=1)C1=C(C=NC=C1)C#N Chemical compound COC=1C=C2CN(CC2=CC=1)C1=C(C=NC=C1)C#N AEFGEBPXNMNFPY-UHFFFAOYSA-N 0.000 claims description 3
- JQYYMDQPSVKGEV-UHFFFAOYSA-N COC=1C=C2CN(CC2=CC=1)C1=NC=CC=C1C#N Chemical compound COC=1C=C2CN(CC2=CC=1)C1=NC=CC=C1C#N JQYYMDQPSVKGEV-UHFFFAOYSA-N 0.000 claims description 3
- PETGGGCVQOSNIP-UHFFFAOYSA-N COC=1C=C2CN(CC2=CC=1)C1=NC=NC=C1C#N Chemical compound COC=1C=C2CN(CC2=CC=1)C1=NC=NC=C1C#N PETGGGCVQOSNIP-UHFFFAOYSA-N 0.000 claims description 3
- HUGKALXNRWBIQE-UHFFFAOYSA-N COC=1C=CC(=NC=1)COC=1C=C2CN(C(C2=CC=1)=O)C1=CC=NC=C1 Chemical compound COC=1C=CC(=NC=1)COC=1C=C2CN(C(C2=CC=1)=O)C1=CC=NC=C1 HUGKALXNRWBIQE-UHFFFAOYSA-N 0.000 claims description 3
- REHYONXLVUWYNH-UHFFFAOYSA-N COC=1C=CC(=NC=1)COC=1C=C2CN(CC2=CC=1)C1=C(C=NC=C1)C#N Chemical compound COC=1C=CC(=NC=1)COC=1C=C2CN(CC2=CC=1)C1=C(C=NC=C1)C#N REHYONXLVUWYNH-UHFFFAOYSA-N 0.000 claims description 3
- BEDGSVZKCWBILF-UHFFFAOYSA-N COC=1C=CC(=NC=1)COC=1C=C2CN(CC2=CC=1)C1=NC=CC=C1C#N Chemical compound COC=1C=CC(=NC=1)COC=1C=C2CN(CC2=CC=1)C1=NC=CC=C1C#N BEDGSVZKCWBILF-UHFFFAOYSA-N 0.000 claims description 3
- KQORCPPKKYMCPM-UHFFFAOYSA-N COC=1C=CC(=NC=1)COC=1C=C2CN(CC2=CC=1)C1=NC=NC=C1C#N Chemical compound COC=1C=CC(=NC=1)COC=1C=C2CN(CC2=CC=1)C1=NC=NC=C1C#N KQORCPPKKYMCPM-UHFFFAOYSA-N 0.000 claims description 3
- AMAXXQKKZCHDNG-UHFFFAOYSA-N COC=1C=CC(=NC=1)COC=1C=C2CN(CC2=CC=1)C=1C=CC(N(N=1)C)=O Chemical compound COC=1C=CC(=NC=1)COC=1C=C2CN(CC2=CC=1)C=1C=CC(N(N=1)C)=O AMAXXQKKZCHDNG-UHFFFAOYSA-N 0.000 claims description 3
- QRTPOXXFPDZCES-UHFFFAOYSA-N COC=1N=CC(=NC=1)COC=1C=C2CN(CC2=CC=1)C1=CC=NC=C1 Chemical compound COC=1N=CC(=NC=1)COC=1C=C2CN(CC2=CC=1)C1=CC=NC=C1 QRTPOXXFPDZCES-UHFFFAOYSA-N 0.000 claims description 3
- VNSRTBKAWDJHOP-UHFFFAOYSA-N N1=CN=CC(=C1)COC=1C=C2CN(CC2=CC=1)C1=C(C=NC=C1)C#N Chemical compound N1=CN=CC(=C1)COC=1C=C2CN(CC2=CC=1)C1=C(C=NC=C1)C#N VNSRTBKAWDJHOP-UHFFFAOYSA-N 0.000 claims description 3
- NVXYCFAAMKMACA-UHFFFAOYSA-N N1=CN=CC(=C1)COC=1C=C2CN(CC2=CC=1)C1=NC=CC=C1C#N Chemical compound N1=CN=CC(=C1)COC=1C=C2CN(CC2=CC=1)C1=NC=CC=C1C#N NVXYCFAAMKMACA-UHFFFAOYSA-N 0.000 claims description 3
- DCRUQOOGKROGBZ-UHFFFAOYSA-N OC=1C=CC(=NC=1)COC=1C=C2CN(CC2=CC=1)C1=C(C=NC=C1)C#N Chemical compound OC=1C=CC(=NC=1)COC=1C=C2CN(CC2=CC=1)C1=C(C=NC=C1)C#N DCRUQOOGKROGBZ-UHFFFAOYSA-N 0.000 claims description 3
- JWFNVWRPBFZRLQ-UHFFFAOYSA-N OC=1C=CC(=NC=1)COC=1C=C2CN(CC2=CC=1)C1=NC=NC=C1C#N Chemical compound OC=1C=CC(=NC=1)COC=1C=C2CN(CC2=CC=1)C1=NC=NC=C1C#N JWFNVWRPBFZRLQ-UHFFFAOYSA-N 0.000 claims description 3
- 208000024827 Alzheimer disease Diseases 0.000 claims description 2
- 102000014461 Ataxins Human genes 0.000 claims description 2
- 108010078286 Ataxins Proteins 0.000 claims description 2
- 206010008025 Cerebellar ataxia Diseases 0.000 claims description 2
- 238000012879 PET imaging Methods 0.000 claims description 2
- 208000018737 Parkinson disease Diseases 0.000 claims description 2
- 208000024777 Prion disease Diseases 0.000 claims description 2
- 208000009415 Spinocerebellar Ataxias Diseases 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 claims description 2
- 201000004562 autosomal dominant cerebellar ataxia Diseases 0.000 claims description 2
- 210000004227 basal ganglia Anatomy 0.000 claims description 2
- 238000013170 computed tomography imaging Methods 0.000 claims description 2
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 2
- 238000003384 imaging method Methods 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000004043 oxo group Chemical group O=* 0.000 claims description 2
- 238000012831 peritoneal equilibrium test Methods 0.000 claims description 2
- 238000012877 positron emission topography Methods 0.000 claims description 2
- 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 238000003325 tomography Methods 0.000 claims description 2
- FHMPYHRBAHQOCN-UHFFFAOYSA-N COC=1C=C2CN(C(C2=CC=1)=O)C1=CC=NC=C1 Chemical compound COC=1C=C2CN(C(C2=CC=1)=O)C1=CC=NC=C1 FHMPYHRBAHQOCN-UHFFFAOYSA-N 0.000 claims 2
- HPKKNWCMDLWNOE-UHFFFAOYSA-N COC=1C=C2CN(CC2=CC=1)C=1C=CC(N(N=1)C)=O Chemical compound COC=1C=C2CN(CC2=CC=1)C=1C=CC(N(N=1)C)=O HPKKNWCMDLWNOE-UHFFFAOYSA-N 0.000 claims 2
- VHYBOSRPUOCKTJ-UHFFFAOYSA-N OC=1C=C2CN(CC2=CC=1)C1=C(C=NC=C1)C#N Chemical group OC=1C=C2CN(CC2=CC=1)C1=C(C=NC=C1)C#N VHYBOSRPUOCKTJ-UHFFFAOYSA-N 0.000 claims 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000007792 addition Methods 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462043644P | 2014-08-29 | 2014-08-29 | |
| US62/043,644 | 2014-08-29 | ||
| PCT/US2015/047396 WO2016033436A1 (en) | 2014-08-29 | 2015-08-28 | Probes for imaging huntingtin protein |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020016705A Division JP6843282B2 (ja) | 2014-08-29 | 2020-02-04 | ハンチントンタンパク質のイメージング用プローブ |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2017527559A JP2017527559A (ja) | 2017-09-21 |
| JP2017527559A5 true JP2017527559A5 (enExample) | 2018-10-04 |
Family
ID=55400644
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017511927A Ceased JP2017527559A (ja) | 2014-08-29 | 2015-08-28 | ハンチントンタンパク質のイメージング用プローブ |
| JP2020016705A Active JP6843282B2 (ja) | 2014-08-29 | 2020-02-04 | ハンチントンタンパク質のイメージング用プローブ |
| JP2021026146A Active JP7042940B2 (ja) | 2014-08-29 | 2021-02-22 | ハンチントンタンパク質のイメージング用プローブ |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020016705A Active JP6843282B2 (ja) | 2014-08-29 | 2020-02-04 | ハンチントンタンパク質のイメージング用プローブ |
| JP2021026146A Active JP7042940B2 (ja) | 2014-08-29 | 2021-02-22 | ハンチントンタンパク質のイメージング用プローブ |
Country Status (20)
| Country | Link |
|---|---|
| US (2) | US11071793B2 (enExample) |
| EP (1) | EP3186241B1 (enExample) |
| JP (3) | JP2017527559A (enExample) |
| KR (1) | KR102410760B1 (enExample) |
| CN (2) | CN107074817B (enExample) |
| AU (1) | AU2015308765B2 (enExample) |
| BR (1) | BR112017004136B1 (enExample) |
| CA (1) | CA2959531C (enExample) |
| DK (1) | DK3186241T3 (enExample) |
| EA (1) | EA037275B1 (enExample) |
| ES (1) | ES2841746T3 (enExample) |
| HR (1) | HRP20202032T1 (enExample) |
| HU (1) | HUE052892T2 (enExample) |
| IL (1) | IL250805B (enExample) |
| MX (2) | MX383202B (enExample) |
| PL (1) | PL3186241T3 (enExample) |
| PT (1) | PT3186241T (enExample) |
| SG (1) | SG11201701578YA (enExample) |
| SI (1) | SI3186241T1 (enExample) |
| WO (1) | WO2016033436A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11104691B2 (en) | 2014-08-29 | 2021-08-31 | Chdi Foundation, Inc. | Probes for imaging huntingtin protein |
| EP3186233B8 (en) | 2014-08-29 | 2021-09-29 | CHDI Foundation, Inc. | Probes for imaging huntingtin protein |
| EA037275B1 (ru) | 2014-08-29 | 2021-03-03 | Сиэйчдиай Фаундэйшн, Инк. | Зонды для визуализации белка хантингтина |
| SG11201701580XA (en) | 2014-08-29 | 2017-03-30 | Chdi Foundation Inc | Probes for imaging huntingtin protein |
| DK3340796T3 (da) | 2015-08-28 | 2021-07-26 | Chdi Foundation Inc | Sonder til afbildning af huntingtin-protein |
| US10865201B2 (en) | 2016-09-12 | 2020-12-15 | Valo Health, Inc. | Bicyclic compounds useful as GPR120 modulators |
| EP3509587B1 (en) | 2016-09-12 | 2023-12-06 | Valo Health, Inc. | Monocyclic compounds useful as gpr120 modulators |
| WO2020176424A1 (en) | 2019-02-25 | 2020-09-03 | Chdi Foundation, Inc. | Compounds for targeting mutant huntingtin protein and uses thereof |
| US11992535B2 (en) | 2019-12-18 | 2024-05-28 | Chdi Foundation, Inc. | Compounds and probes for imaging huntingtin protein |
| BR112022025238A2 (pt) * | 2020-06-11 | 2023-02-14 | Chdi Foundation Inc | Compostos heterocíclicos e agentes de imageamento para formar imagem da proteína huntingtina |
| WO2022216947A1 (en) * | 2021-04-08 | 2022-10-13 | Chdi Foundation, Inc. | Isoindolinone compounds and imaging agents for imaging huntingtin protein |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5726197A (en) * | 1992-11-02 | 1998-03-10 | Syntex (U.S.A.) Inc. | Isoindolinyl derivatives |
| IL146455A0 (en) | 1999-06-10 | 2002-07-25 | Warner Lambert Co | Method of inhibiting amyloid protein aggregation and imaging amyloid deposits using isoindoline derivatives |
| KR101011657B1 (ko) * | 2002-03-01 | 2011-01-28 | 다케다 야쿠힌 고교 가부시키가이샤 | 항우울제 |
| US7968569B2 (en) | 2002-05-17 | 2011-06-28 | Celgene Corporation | Methods for treatment of multiple myeloma using 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione |
| US7320992B2 (en) * | 2003-08-25 | 2008-01-22 | Amgen Inc. | Substituted 2,3-dihydro-1h-isoindol-1-one derivatives and methods of use |
| US8110681B2 (en) * | 2006-03-17 | 2012-02-07 | The United States Of America As Represented By The Secretary, Department Of Health And Human Services | Compounds for the treatment of spinal muscular atrophy and other uses |
| EP2215074B1 (en) * | 2007-09-27 | 2014-02-19 | The United States of America, as Represented by the Secretary, Department of Health and Human Services | Isoindoline compounds for the treatment of spinal muscular atrophy and other uses |
| WO2009072581A1 (ja) * | 2007-12-05 | 2009-06-11 | Aska Pharmaceutical Co., Ltd. | ラクタム化合物又はその塩及びｐｐａｒ活性化剤 |
| WO2010104324A2 (ko) * | 2009-03-10 | 2010-09-16 | 한국과학기술연구원 | 베타-아밀로이드 집적체 및 피브릴에 우수한 결합 친화도를 가지는 할로겐화 이소인돌론 화합물, 및 이의 제조 방법 및 용도 |
| BR112014026283B1 (pt) * | 2012-04-25 | 2022-08-02 | Raqualia Pharma Inc | Compostos da fórmula (i), (ii), (iii), uso dos mesmos, composição farmacêutica, e processo para a preparação de uma composição farmacêutica |
| WO2015054317A1 (en) * | 2013-10-07 | 2015-04-16 | Kadmon Corporation, Llc | Rho kinase inhibitors |
| EP3186233B8 (en) | 2014-08-29 | 2021-09-29 | CHDI Foundation, Inc. | Probes for imaging huntingtin protein |
| EA037275B1 (ru) | 2014-08-29 | 2021-03-03 | Сиэйчдиай Фаундэйшн, Инк. | Зонды для визуализации белка хантингтина |
| US11104691B2 (en) | 2014-08-29 | 2021-08-31 | Chdi Foundation, Inc. | Probes for imaging huntingtin protein |
| SG11201701580XA (en) | 2014-08-29 | 2017-03-30 | Chdi Foundation Inc | Probes for imaging huntingtin protein |
| DK3340796T3 (da) | 2015-08-28 | 2021-07-26 | Chdi Foundation Inc | Sonder til afbildning af huntingtin-protein |
-
2015
- 2015-08-28 EA EA201790432A patent/EA037275B1/ru unknown
- 2015-08-28 HR HRP20202032TT patent/HRP20202032T1/hr unknown
- 2015-08-28 JP JP2017511927A patent/JP2017527559A/ja not_active Ceased
- 2015-08-28 MX MX2017002704A patent/MX383202B/es unknown
- 2015-08-28 HU HUE15836970A patent/HUE052892T2/hu unknown
- 2015-08-28 SG SG11201701578YA patent/SG11201701578YA/en unknown
- 2015-08-28 CN CN201580058254.1A patent/CN107074817B/zh active Active
- 2015-08-28 DK DK15836970.2T patent/DK3186241T3/da active
- 2015-08-28 AU AU2015308765A patent/AU2015308765B2/en active Active
- 2015-08-28 CA CA2959531A patent/CA2959531C/en active Active
- 2015-08-28 ES ES15836970T patent/ES2841746T3/es active Active
- 2015-08-28 WO PCT/US2015/047396 patent/WO2016033436A1/en not_active Ceased
- 2015-08-28 BR BR112017004136-7A patent/BR112017004136B1/pt active IP Right Grant
- 2015-08-28 PL PL15836970T patent/PL3186241T3/pl unknown
- 2015-08-28 CN CN202311625463.2A patent/CN118005611A/zh active Pending
- 2015-08-28 EP EP15836970.2A patent/EP3186241B1/en active Active
- 2015-08-28 US US15/507,214 patent/US11071793B2/en active Active
- 2015-08-28 KR KR1020177008418A patent/KR102410760B1/ko active Active
- 2015-08-28 PT PT158369702T patent/PT3186241T/pt unknown
- 2015-08-28 SI SI201531461T patent/SI3186241T1/sl unknown
-
2017
- 2017-02-27 IL IL250805A patent/IL250805B/en active IP Right Grant
- 2017-02-28 MX MX2021005891A patent/MX2021005891A/es unknown
-
2020
- 2020-02-04 JP JP2020016705A patent/JP6843282B2/ja active Active
-
2021
- 2021-02-22 JP JP2021026146A patent/JP7042940B2/ja active Active
- 2021-06-21 US US17/353,611 patent/US12036291B2/en active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2017527559A5 (enExample) | ||
| HRP20202032T1 (hr) | Probe za snimanje huntingtonovog proteina | |
| JP2017529340A5 (enExample) | ||
| JP4751957B2 (ja) | アミロイドの凝集及び／又は沈着に起因する疾患の診断薬及び治療薬 | |
| JP2017528519A5 (enExample) | ||
| JP2017528520A5 (enExample) | ||
| RU2007124935A (ru) | АМИНОПИРИДИНЫ В КАЧЕСТВЕ ИНГИБИТОРОВ β-СЕКТРЕТАЗЫ | |
| JP2016539180A5 (enExample) | ||
| US7670591B2 (en) | Heteroaryl substituted benzoxazoles | |
| RU2019121871A (ru) | Новые производные фенилпропионовой кислоты и их применение | |
| US20140363830A1 (en) | Compounds that modulate hsp90 activity and methods for identifying same | |
| RU2015138964A (ru) | Полициклические модуляторы рецептора эстрогена и их применения | |
| JP2009541311A5 (enExample) | ||
| JP2014503528A5 (enExample) | ||
| JP2008503591A5 (enExample) | ||
| JP2016518328A5 (enExample) | ||
| JP2017513894A5 (enExample) | ||
| JP2012514007A5 (enExample) | ||
| NZ601794A (en) | Di - substituted pyridine derivatives as anticancers | |
| US20140094436A1 (en) | Imidazole compounds that modulate hsp90 activity | |
| US20220056052A1 (en) | Quinazoline derivatives as ectonucleotide pyrophosphatase phosphodiesterase 1 inhibitors | |
| NZ593848A (en) | Synthesis of 18f-radiolabeled styrylpyridines from tosylate precursors and stable pharmaceutical compositions thereof | |
| US20150126499A1 (en) | Triazole Compounds that Modulate HSP90 Activity | |
| JP2010526800A5 (enExample) | ||
| PE20170664A1 (es) | Agonistas del receptor de apelina(apj) y usos de los mismos |