KR20110027817A - Mglur 조절제를 포함하는 파킨슨병 치료용 조합물 - Google Patents
Mglur 조절제를 포함하는 파킨슨병 치료용 조합물 Download PDFInfo
- Publication number
- KR20110027817A KR20110027817A KR1020117002251A KR20117002251A KR20110027817A KR 20110027817 A KR20110027817 A KR 20110027817A KR 1020117002251 A KR1020117002251 A KR 1020117002251A KR 20117002251 A KR20117002251 A KR 20117002251A KR 20110027817 A KR20110027817 A KR 20110027817A
- Authority
- KR
- South Korea
- Prior art keywords
- phenylethynyl
- chloro
- hydroxy
- parkinson
- cyclohexyl
- 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
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- 101000963131 Homo sapiens Membralin Proteins 0.000 title 1
- 102100039605 Membralin Human genes 0.000 title 1
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- WTDRDQBEARUVNC-UHFFFAOYSA-N L-Dopa Natural products OC(=O)C(N)CC1=CC=C(O)C(O)=C1 WTDRDQBEARUVNC-UHFFFAOYSA-N 0.000 claims abstract description 74
- 102000016193 Metabotropic glutamate receptors Human genes 0.000 claims abstract description 62
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- 238000011282 treatment Methods 0.000 claims abstract description 40
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 39
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- 239000000534 dopa decarboxylase inhibitor Substances 0.000 claims abstract description 19
- 239000003136 dopamine receptor stimulating agent Substances 0.000 claims abstract description 15
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- 150000001875 compounds Chemical class 0.000 claims description 66
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- TZFNLOMSOLWIDK-JTQLQIEISA-N carbidopa (anhydrous) Chemical group NN[C@@](C(O)=O)(C)CC1=CC=C(O)C(O)=C1 TZFNLOMSOLWIDK-JTQLQIEISA-N 0.000 claims description 9
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- OZVBMTJYIDMWIL-AYFBDAFISA-N bromocriptine Chemical group C1=CC(C=2[C@H](N(C)C[C@@H](C=2)C(=O)N[C@]2(C(=O)N3[C@H](C(N4CCC[C@H]4[C@]3(O)O2)=O)CC(C)C)C(C)C)C2)=C3C2=C(Br)NC3=C1 OZVBMTJYIDMWIL-AYFBDAFISA-N 0.000 claims description 5
- 229960002802 bromocriptine Drugs 0.000 claims description 5
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 5
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- 125000003107 substituted aryl group Chemical group 0.000 claims description 5
- 229940099362 Catechol O methyltransferase inhibitor Drugs 0.000 claims description 4
- BNQDCRGUHNALGH-UHFFFAOYSA-N benserazide Chemical compound OCC(N)C(=O)NNCC1=CC=C(O)C(O)=C1O BNQDCRGUHNALGH-UHFFFAOYSA-N 0.000 claims description 4
- 229960000911 benserazide Drugs 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 229940124807 mGLUR antagonist Drugs 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 4
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical group 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 description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 claims description 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 2
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims description 2
- BKRGVLQUQGGVSM-KBXCAEBGSA-N Revanil Chemical compound C1=CC(C=2[C@H](N(C)C[C@H](C=2)NC(=O)N(CC)CC)C2)=C3C2=CNC3=C1 BKRGVLQUQGGVSM-KBXCAEBGSA-N 0.000 claims description 2
- 125000003282 alkyl amino group Chemical group 0.000 claims description 2
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 2
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 2
- 229960003587 lisuride Drugs 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- YEHCICAEULNIGD-MZMPZRCHSA-N pergolide Chemical compound C1=CC([C@H]2C[C@@H](CSC)CN([C@@H]2C2)CCC)=C3C2=CNC3=C1 YEHCICAEULNIGD-MZMPZRCHSA-N 0.000 claims 1
- VYFYYTLLBUKUHU-UHFFFAOYSA-N dopamine Chemical compound NCCC1=CC=C(O)C(O)=C1 VYFYYTLLBUKUHU-UHFFFAOYSA-N 0.000 abstract description 10
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- 125000003118 aryl group Chemical group 0.000 description 12
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Applications Claiming Priority (2)
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| US7677208P | 2008-06-30 | 2008-06-30 | |
| US61/076,772 | 2008-06-30 |
Publications (1)
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| KR20110027817A true KR20110027817A (ko) | 2011-03-16 |
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Family Applications (1)
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| KR1020117002251A Ceased KR20110027817A (ko) | 2008-06-30 | 2009-06-30 | Mglur 조절제를 포함하는 파킨슨병 치료용 조합물 |
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|---|---|
| US (2) | US8703809B2 (enExample) |
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| JP (1) | JP2011526596A (enExample) |
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Families Citing this family (11)
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| BRPI0818560A2 (pt) * | 2007-10-12 | 2019-09-24 | Novartis Ag | compostos orgânicos |
| NZ590753A (en) * | 2008-08-12 | 2012-06-29 | Novartis Ag | Processes for the preparation of 4-oxo-octahydro-indole-1-carbocylic acid methyl ester and derivatives thereof |
| US20130274294A1 (en) * | 2010-12-20 | 2013-10-17 | David Carcache | 4-(Hetero)Aryl-Ethynyl-Octahydro-Indole-1-Esters |
| GB201204962D0 (en) | 2012-03-21 | 2012-05-02 | Addex Pharmaceuticals Sa | Pharmaceutical combination products for parkinsons disease |
| MX390106B (es) | 2012-10-22 | 2025-03-20 | Merz Pharmaceuticals Llc | Formulaciones de levodopa para el alivio rapido de la enfermedad de parkinson |
| JP5744112B2 (ja) * | 2013-06-11 | 2015-07-01 | デクセリアルズ株式会社 | パターン形成体の製造方法 |
| GB201312800D0 (en) | 2013-07-17 | 2013-08-28 | Heptares Therapeutics Ltd | mGlu5 modulators |
| SG11201608608PA (en) * | 2014-04-21 | 2016-11-29 | Civitas Therapeutics Inc | Rapid relief of motor fluctuations in parkinson's disease |
| CA3066711A1 (en) * | 2017-07-31 | 2019-02-07 | Novartis Ag | Use of mavoglurant in the reduction of cocaine use or in preventing relapse into cocaine use |
| US12201612B2 (en) | 2017-07-31 | 2025-01-21 | Novartis Ag | Use of mavoglurant in the reduction of alcohol use or in preventing relapse into alcohol use |
| EP3870292A4 (en) | 2018-10-26 | 2022-11-09 | The Research Foundation for The State University of New York | COMBINATION OF SEROTONIN-SPECIFIC RESUPPUT INHIBITOR AND SEROTONIN 1A RECEPTOR PARTIAL AGONIST TO REDUCE L-DOPA-INDUCED DYSKINESIA |
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| US3769424A (en) * | 1970-10-01 | 1973-10-30 | Merck & Co Inc | Composition and method of treating dopamine deficiency in brain tissue |
| US5521297A (en) | 1993-06-04 | 1996-05-28 | Salk Institute Biotechnology/Industrial Associates | Nucleic acids encoding human metabotropic glutamate receptors |
| FR2777781B1 (fr) * | 1998-04-24 | 2004-04-09 | Rhone Poulenc Rorer Sa | Associations riluzole et l-dopa pour le traitement de la maladie de parkinson |
| GB0007193D0 (en) * | 2000-03-25 | 2000-05-17 | Univ Manchester | Treatment of movrmrnt disorders |
| GB0128996D0 (en) * | 2001-12-04 | 2002-01-23 | Novartis Ag | Organic compounds |
| SE0201943D0 (sv) | 2002-06-20 | 2002-06-20 | Astrazeneca Ab | New use |
| IL166510A0 (en) | 2002-08-09 | 2006-01-15 | Nps Pharma Inc | 1,2,4"oxadiazole as modulators of metabotropic glutamate receptor-5 |
| US7105533B2 (en) * | 2002-09-13 | 2006-09-12 | Merck & Co., Inc. | Fused heterobicyclo substituted phenyl metabotropic glutamate-5 modulators |
| US7393959B2 (en) * | 2003-04-04 | 2008-07-01 | Merck & Co. Inc. | Di-aryl substituted pyrrole modulators of metabotropic glutamate receptor-5 |
| MY142655A (en) | 2003-06-12 | 2010-12-15 | Euro Celtique Sa | Therapeutic agents useful for treating pain |
| EP1667983A4 (en) * | 2003-09-23 | 2010-07-21 | Merck Sharp & Dohme | PYRAZOL MODULATORS OF METABOTROPIC GLUTAMATE RECEPTORS |
| CA2549965A1 (en) | 2003-10-31 | 2005-05-19 | Astrazeneca Ab | Alkynes iii |
| CA2549967A1 (en) | 2003-10-31 | 2005-05-19 | Astrazeneca Ab | Alkynes i |
| WO2005044267A1 (en) | 2003-10-31 | 2005-05-19 | Astrazeneca Ab | Alkynes ii |
| CN1933838A (zh) | 2004-02-12 | 2007-03-21 | 默克公司 | 作为代谢型谷氨酸受体-5调节剂的联吡啶酰胺 |
| JP2007533037A (ja) | 2004-04-14 | 2007-11-15 | デジタル リバー、インコーポレイテッド | 地理的位置に基づくライセンスシステム |
| GB0508319D0 (en) * | 2005-04-25 | 2005-06-01 | Novartis Ag | Organic compounds |
| TW200801005A (en) | 2005-08-15 | 2008-01-01 | Astrazeneca Ab | Acetylenic piperazines as metabotropic glutamate receptor antagonists |
| AU2006329007A1 (en) * | 2005-12-20 | 2007-06-28 | Novartis Ag | Nicotinic acid derivatives as modulators of metabotropic glutamate receptors |
| WO2007143422A2 (en) * | 2006-05-30 | 2007-12-13 | Janssen Pharmaceutica N.V. | Substituted pyridyl amide compounds as modulators of the histamine h3 receptor |
| KR20090033871A (ko) * | 2006-06-16 | 2009-04-06 | 솔베이 파마슈티칼스 비. 브이 | 비페프루녹스 및 l-dopa를 포함하는 병용 제제 |
| ATE494289T1 (de) * | 2006-08-04 | 2011-01-15 | Merz Pharma Gmbh & Co Kgaa | Substituierte pyrazolopyrimidine, ein verfahren zu ihrer herstellung und ihre verwendung als medizin |
| KR20090061041A (ko) * | 2006-09-11 | 2009-06-15 | 노파르티스 아게 | 대사성 글루타메이트 수용체의 조절제로서의 니코틴산 유도체 |
| BRPI0818560A2 (pt) * | 2007-10-12 | 2019-09-24 | Novartis Ag | compostos orgânicos |
-
2009
- 2009-06-30 EP EP14167553.8A patent/EP2826478A1/en not_active Withdrawn
- 2009-06-30 AU AU2009265760A patent/AU2009265760B2/en not_active Ceased
- 2009-06-30 KR KR1020117002251A patent/KR20110027817A/ko not_active Ceased
- 2009-06-30 RU RU2011103083/15A patent/RU2496494C2/ru not_active IP Right Cessation
- 2009-06-30 MX MX2010014222A patent/MX2010014222A/es not_active Application Discontinuation
- 2009-06-30 WO PCT/EP2009/058230 patent/WO2010000763A2/en not_active Ceased
- 2009-06-30 US US12/999,634 patent/US8703809B2/en not_active Expired - Fee Related
- 2009-06-30 JP JP2011515445A patent/JP2011526596A/ja active Pending
- 2009-06-30 CN CN2013101485895A patent/CN103212078A/zh active Pending
- 2009-06-30 CA CA2729595A patent/CA2729595C/en not_active Expired - Fee Related
- 2009-06-30 EP EP09772463A patent/EP2320892A2/en not_active Withdrawn
- 2009-06-30 BR BRPI0913642A patent/BRPI0913642A2/pt not_active IP Right Cessation
- 2009-06-30 CN CN2009801331117A patent/CN102131503A/zh active Pending
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2014
- 2014-03-04 US US14/195,947 patent/US20140194423A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0913642A2 (pt) | 2015-11-24 |
| US20140194423A1 (en) | 2014-07-10 |
| CA2729595A1 (en) | 2010-01-07 |
| CN103212078A (zh) | 2013-07-24 |
| AU2009265760B2 (en) | 2013-07-18 |
| MX2010014222A (es) | 2011-03-29 |
| CN102131503A (zh) | 2011-07-20 |
| WO2010000763A3 (en) | 2010-02-25 |
| US20120122878A1 (en) | 2012-05-17 |
| CA2729595C (en) | 2017-01-03 |
| AU2009265760A1 (en) | 2010-01-07 |
| EP2826478A1 (en) | 2015-01-21 |
| WO2010000763A2 (en) | 2010-01-07 |
| RU2011103083A (ru) | 2012-08-10 |
| US8703809B2 (en) | 2014-04-22 |
| EP2320892A2 (en) | 2011-05-18 |
| RU2496494C2 (ru) | 2013-10-27 |
| JP2011526596A (ja) | 2011-10-13 |
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