JP2017502069A5 - - Google Patents
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- JP2017502069A5 JP2017502069A5 JP2016545898A JP2016545898A JP2017502069A5 JP 2017502069 A5 JP2017502069 A5 JP 2017502069A5 JP 2016545898 A JP2016545898 A JP 2016545898A JP 2016545898 A JP2016545898 A JP 2016545898A JP 2017502069 A5 JP2017502069 A5 JP 2017502069A5
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- Prior art keywords
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- 150000001875 compounds Chemical class 0.000 claims 37
- 150000003839 salts Chemical group 0.000 claims 19
- 206010012289 Dementia Diseases 0.000 claims 17
- 208000010877 cognitive disease Diseases 0.000 claims 15
- 208000028698 Cognitive impairment Diseases 0.000 claims 13
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 13
- 208000035475 disorder Diseases 0.000 claims 13
- 208000020925 Bipolar disease Diseases 0.000 claims 9
- 201000011240 Frontotemporal dementia Diseases 0.000 claims 9
- 208000002193 Pain Diseases 0.000 claims 8
- 125000000217 alkyl group Chemical group 0.000 claims 8
- 208000019888 Circadian rhythm sleep disease Diseases 0.000 claims 7
- 239000003814 drug Substances 0.000 claims 7
- 208000024827 Alzheimer disease Diseases 0.000 claims 6
- 208000036864 Attention deficit/hyperactivity disease Diseases 0.000 claims 6
- 208000019695 Migraine disease Diseases 0.000 claims 6
- 208000019022 Mood disease Diseases 0.000 claims 6
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- 208000015802 attention deficit-hyperactivity disease Diseases 0.000 claims 6
- 230000027288 circadian rhythm Effects 0.000 claims 6
- ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 claims 6
- 206010027599 migraine Diseases 0.000 claims 6
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- 208000011580 syndromic disease Diseases 0.000 claims 5
- 239000008194 pharmaceutical composition Substances 0.000 claims 4
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 claims 3
- SVUOLADPCWQTTE-UHFFFAOYSA-N 1h-1,2-benzodiazepine Chemical compound N1N=CC=CC2=CC=CC=C12 SVUOLADPCWQTTE-UHFFFAOYSA-N 0.000 claims 3
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- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 3
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- 229960002715 nicotine Drugs 0.000 claims 3
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 claims 3
- 235000020824 obesity Nutrition 0.000 claims 3
- 208000019906 panic disease Diseases 0.000 claims 3
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- 101150047910 CSNK1D gene Proteins 0.000 claims 2
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- 206010044688 Trisomy 21 Diseases 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
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- 229940035676 analgesics Drugs 0.000 claims 2
- 239000000730 antalgic agent Substances 0.000 claims 2
- 239000008280 blood Substances 0.000 claims 2
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 230000010370 hearing loss Effects 0.000 claims 2
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- 125000001072 heteroaryl group Chemical group 0.000 claims 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 2
- 208000027061 mild cognitive impairment Diseases 0.000 claims 2
- 239000006187 pill Substances 0.000 claims 2
- 125000004193 piperazinyl group Chemical group 0.000 claims 2
- 238000011321 prophylaxis Methods 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- 230000036280 sedation Effects 0.000 claims 2
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 2
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 1
- 125000004195 4-methylpiperazin-1-yl group Chemical group [H]C([H])([H])N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 208000000094 Chronic Pain Diseases 0.000 claims 1
- 208000012661 Dyskinesia Diseases 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- ZCYVEMRRCGMTRW-AHCXROLUSA-N Iodine-123 Chemical compound [123I] ZCYVEMRRCGMTRW-AHCXROLUSA-N 0.000 claims 1
- 241000124008 Mammalia Species 0.000 claims 1
- 208000018737 Parkinson disease Diseases 0.000 claims 1
- 208000027089 Parkinsonian disease Diseases 0.000 claims 1
- 206010034010 Parkinsonism Diseases 0.000 claims 1
- GKLVYJBZJHMRIY-OUBTZVSYSA-N Technetium-99 Chemical compound [99Tc] GKLVYJBZJHMRIY-OUBTZVSYSA-N 0.000 claims 1
- 201000004810 Vascular dementia Diseases 0.000 claims 1
- KRHYYFGTRYWZRS-BJUDXGSMSA-N ac1l2y5h Chemical compound [18FH] KRHYYFGTRYWZRS-BJUDXGSMSA-N 0.000 claims 1
- 208000005298 acute pain Diseases 0.000 claims 1
- 201000007034 advanced sleep phase syndrome Diseases 0.000 claims 1
- 230000032683 aging Effects 0.000 claims 1
- 230000000202 analgesic effect Effects 0.000 claims 1
- 230000003542 behavioural effect Effects 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- OKTJSMMVPCPJKN-BJUDXGSMSA-N carbon-11 Chemical group [11C] OKTJSMMVPCPJKN-BJUDXGSMSA-N 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 231100000895 deafness Toxicity 0.000 claims 1
- 230000003111 delayed effect Effects 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- APFVFJFRJDLVQX-AHCXROLUSA-N indium-111 Chemical compound [111In] APFVFJFRJDLVQX-AHCXROLUSA-N 0.000 claims 1
- 229940055742 indium-111 Drugs 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
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- 239000000203 mixture Substances 0.000 claims 1
- 125000002950 monocyclic group Chemical group 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- 239000000932 sedative agent Substances 0.000 claims 1
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- 208000024891 symptom Diseases 0.000 claims 1
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 0 *c(cc1)ccc1-c1n[n](ccc(N(*)*)n2)c2c1-c1ccncc1 Chemical compound *c(cc1)ccc1-c1n[n](ccc(N(*)*)n2)c2c1-c1ccncc1 0.000 description 9
- NDYIDNFYFMCFSD-UHFFFAOYSA-N CN(CC1)CCN1c(cc[n]1nc2-c(cc3)ccc3F)nc1c2-c1ccncc1 Chemical compound CN(CC1)CCN1c(cc[n]1nc2-c(cc3)ccc3F)nc1c2-c1ccncc1 NDYIDNFYFMCFSD-UHFFFAOYSA-N 0.000 description 2
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- NCGPQHYINHQFQO-UHFFFAOYSA-N CC(C)(C)c1ccc2nc(NC(Cc(cc3)ccc3NC(C)=O)=O)[s]c2c1 Chemical compound CC(C)(C)c1ccc2nc(NC(Cc(cc3)ccc3NC(C)=O)=O)[s]c2c1 NCGPQHYINHQFQO-UHFFFAOYSA-N 0.000 description 1
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- VNFGFTRQFPELFE-UHFFFAOYSA-N N/C(/Nc1nc2ccccc2[nH]1)=N\C(Cc1ccncc1)=O Chemical compound N/C(/Nc1nc2ccccc2[nH]1)=N\C(Cc1ccncc1)=O VNFGFTRQFPELFE-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201461925608P | 2014-01-09 | 2014-01-09 | |
| US61/925,608 | 2014-01-09 | ||
| PCT/US2015/010901 WO2015106158A1 (en) | 2014-01-09 | 2015-01-09 | Organic compounds |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017502069A JP2017502069A (ja) | 2017-01-19 |
| JP2017502069A5 true JP2017502069A5 (enExample) | 2018-02-15 |
| JP6542236B2 JP6542236B2 (ja) | 2019-07-10 |
Family
ID=53524387
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016545898A Active JP6542236B2 (ja) | 2014-01-09 | 2015-01-09 | 有機化合物 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US9944648B2 (enExample) |
| EP (1) | EP3091982B1 (enExample) |
| JP (1) | JP6542236B2 (enExample) |
| KR (1) | KR20160101197A (enExample) |
| CN (1) | CN106029075A (enExample) |
| AU (1) | AU2015204566A1 (enExample) |
| BR (1) | BR112016016098A2 (enExample) |
| CA (1) | CA2935985A1 (enExample) |
| ES (1) | ES2728932T3 (enExample) |
| MX (1) | MX2016008968A (enExample) |
| RU (1) | RU2016132574A (enExample) |
| WO (1) | WO2015106158A1 (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR112016016098A2 (pt) | 2014-01-09 | 2017-08-08 | Intracellular Therapies Inc | Compostos orgânicos |
| US10647689B2 (en) * | 2015-04-28 | 2020-05-12 | Sanford Burnham Prebys Medical Discovery Institute | Apelin receptor agonists and methods of use thereof |
| CN115335057A (zh) * | 2020-03-27 | 2022-11-11 | 北京原基华毅生物科技有限公司 | 抑制酪蛋白激酶的方法 |
| CN115298183A (zh) * | 2020-03-27 | 2022-11-04 | 北京原基华毅生物科技有限公司 | 作为酪蛋白激酶抑制剂的化合物 |
| BR112022022437A2 (pt) * | 2020-05-07 | 2023-01-03 | Adorx Therapeutics Ltd | Antagonistas do receptor a2a de adenosina |
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| US4376110A (en) | 1980-08-04 | 1983-03-08 | Hybritech, Incorporated | Immunometric assays using monoclonal antibodies |
| US4946778A (en) | 1987-09-21 | 1990-08-07 | Genex Corporation | Single polypeptide chain binding molecules |
| EP0413751A4 (en) * | 1988-05-02 | 1992-07-22 | N. Eric Naftchi | Neurologically active compounds |
| US5530101A (en) | 1988-12-28 | 1996-06-25 | Protein Design Labs, Inc. | Humanized immunoglobulins |
| US5661016A (en) | 1990-08-29 | 1997-08-26 | Genpharm International Inc. | Transgenic non-human animals capable of producing heterologous antibodies of various isotypes |
| US5789650A (en) | 1990-08-29 | 1998-08-04 | Genpharm International, Inc. | Transgenic non-human animals for producing heterologous antibodies |
| US5625126A (en) | 1990-08-29 | 1997-04-29 | Genpharm International, Inc. | Transgenic non-human animals for producing heterologous antibodies |
| US5633425A (en) | 1990-08-29 | 1997-05-27 | Genpharm International, Inc. | Transgenic non-human animals capable of producing heterologous antibodies |
| US5770429A (en) | 1990-08-29 | 1998-06-23 | Genpharm International, Inc. | Transgenic non-human animals capable of producing heterologous antibodies |
| AU8507191A (en) | 1990-08-29 | 1992-03-30 | Genpharm International, Inc. | Transgenic non-human animals capable of producing heterologous antibodies |
| US6060296A (en) | 1991-07-03 | 2000-05-09 | The Salk Institute For Biological Studies | Protein kinases |
| US5157378A (en) | 1991-08-06 | 1992-10-20 | North-South Corporation | Integrated firefighter safety monitoring and alarm system |
| US5932448A (en) | 1991-11-29 | 1999-08-03 | Protein Design Labs., Inc. | Bispecific antibody heterodimers |
| US5880141A (en) | 1995-06-07 | 1999-03-09 | Sugen, Inc. | Benzylidene-Z-indoline compounds for the treatment of disease |
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| US6506559B1 (en) | 1997-12-23 | 2003-01-14 | Carnegie Institute Of Washington | Genetic inhibition by double-stranded RNA |
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| JP2002541253A (ja) | 1999-04-09 | 2002-12-03 | スミスクライン・ビーチャム・コーポレイション | トリアリールイミダゾール |
| KR100722176B1 (ko) | 1999-06-08 | 2007-05-29 | 아벤티스 파마슈티칼스 인크. | 일주기 리듬 단백질을 변화시키기 위한 스크리닝 방법 |
| ES2213996T3 (es) | 1999-12-08 | 2004-09-01 | Centre National De La Recherche Scientifique (Cnrs) | Uso de himenialdisina o sus derivados en la fabricacion de medicamentos. |
| US6448057B1 (en) | 2001-03-22 | 2002-09-10 | Applera Corporation | Isolated human casein kinase proteins, nucleic acid molecules encoding human casein kinase proteins, and uses thereof |
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| US7320785B2 (en) | 2001-08-10 | 2008-01-22 | The Rockefeller University | Compositions and methods for modulation of DARPP-32 phosphorylation |
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| FR2918061B1 (fr) * | 2007-06-28 | 2010-10-22 | Sanofi Aventis | Derives de 6-cycloamino-3-(pyridin-4-yl)imidazo°1,2-b!- pyridazine,leur preparation et leur application en therapeutique. |
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| US8591943B2 (en) * | 2009-04-09 | 2013-11-26 | Merck Sharp & Dohme Corp. | Pyrazolo[1,5-a]pyrimidine derivatives as mTOR inhibitors |
| US8633200B2 (en) * | 2010-09-08 | 2014-01-21 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
| JP5997763B2 (ja) * | 2011-05-19 | 2016-09-28 | フンダシオン セントロ ナシオナル デ インベスティガシオネス オンコロヒカス カルロス ザ サードＦｕｎｄａｃｉｏｎ Ｃｅｎｔｒｏ Ｎａｃｉｏｎａｌ ｄｅ Ｉｎｖｅｓｔｉｇａｃｉｏｎｅｓ Ｏｎｃｏｌｏｇｉｃａｓ Ｃａｒｌｏｓ ＩＩＩ | タンパク質キナーゼ阻害剤としての大環状化合物 |
| CN104159904B (zh) * | 2012-01-10 | 2016-12-14 | 霍夫曼-拉罗奇有限公司 | 噻吩并嘧啶化合物 |
| GB201205669D0 (en) * | 2012-03-30 | 2012-05-16 | Agency Science Tech & Res | Bicyclic heterocyclic derivatives as mnk2 and mnk2 modulators and uses thereof |
| BR112016016098A2 (pt) | 2014-01-09 | 2017-08-08 | Intracellular Therapies Inc | Compostos orgânicos |
-
2015
- 2015-01-09 BR BR112016016098A patent/BR112016016098A2/pt not_active IP Right Cessation
- 2015-01-09 WO PCT/US2015/010901 patent/WO2015106158A1/en not_active Ceased
- 2015-01-09 MX MX2016008968A patent/MX2016008968A/es unknown
- 2015-01-09 AU AU2015204566A patent/AU2015204566A1/en not_active Abandoned
- 2015-01-09 JP JP2016545898A patent/JP6542236B2/ja active Active
- 2015-01-09 KR KR1020167021570A patent/KR20160101197A/ko not_active Withdrawn
- 2015-01-09 ES ES15735265T patent/ES2728932T3/es active Active
- 2015-01-09 CA CA2935985A patent/CA2935985A1/en not_active Abandoned
- 2015-01-09 US US15/110,613 patent/US9944648B2/en active Active
- 2015-01-09 EP EP15735265.9A patent/EP3091982B1/en active Active
- 2015-01-09 RU RU2016132574A patent/RU2016132574A/ru unknown
- 2015-01-09 CN CN201580009759.9A patent/CN106029075A/zh active Pending
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