JP4574112B2 - アデノシンa2aレセプターアンタゴニスト - Google Patents
アデノシンa2aレセプターアンタゴニスト Download PDFInfo
- Publication number
- JP4574112B2 JP4574112B2 JP2002500877A JP2002500877A JP4574112B2 JP 4574112 B2 JP4574112 B2 JP 4574112B2 JP 2002500877 A JP2002500877 A JP 2002500877A JP 2002500877 A JP2002500877 A JP 2002500877A JP 4574112 B2 JP4574112 B2 JP 4574112B2
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- alkoxy
- compound
- mmol
- phenyl
- 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.)
- Expired - Lifetime
Links
- 0 CCC(C)CCC(C)C(C)CC(C1CC1)*1C[C@@](**CC2=C(**CC3C(C(C4)C4=C(C4CC4)*4*=*(*)*C44)=C4C=*3)CC3C2C3)CC1 Chemical compound CCC(C)CCC(C)C(C)CC(C1CC1)*1C[C@@](**CC2=C(**CC3C(C(C4)C4=C(C4CC4)*4*=*(*)*C44)=C4C=*3)CC3C2C3)CC1 0.000 description 5
- LHVYTKQPBYJZOB-UHFFFAOYSA-O CC(C)c(cc1)cc(F)c1N1CCN(CCNc2nc(N)nc(Cl)c2C=[NH2+])CC1 Chemical compound CC(C)c(cc1)cc(F)c1N1CCN(CCNc2nc(N)nc(Cl)c2C=[NH2+])CC1 LHVYTKQPBYJZOB-UHFFFAOYSA-O 0.000 description 1
- WEESZZFDAJMZSG-UHFFFAOYSA-N CC(C1)C=CC=C1N1CCN(CCC[n]2ncc3c2nc(N)[n]2nc(-c4ccc[o]4)nc32)CC1 Chemical compound CC(C1)C=CC=C1N1CCN(CCC[n]2ncc3c2nc(N)[n]2nc(-c4ccc[o]4)nc32)CC1 WEESZZFDAJMZSG-UHFFFAOYSA-N 0.000 description 1
- GGSJHKVRBJLCQD-LIFCSCCISA-N CC/C(/C(/C=C\C)=C/C)=C\NC Chemical compound CC/C(/C(/C=C\C)=C/C)=C\NC GGSJHKVRBJLCQD-LIFCSCCISA-N 0.000 description 1
- KCVVRRWNOVMZBA-UHFFFAOYSA-N CC=C1CN(C)C1 Chemical compound CC=C1CN(C)C1 KCVVRRWNOVMZBA-UHFFFAOYSA-N 0.000 description 1
- YSBGEFRYHMIQFE-UHFFFAOYSA-N CCC(CN(C)C)=[NH+][O-] Chemical compound CCC(CN(C)C)=[NH+][O-] YSBGEFRYHMIQFE-UHFFFAOYSA-N 0.000 description 1
- ZEDNMYPSRVIRSG-UHFFFAOYSA-N CCC(CNC)(C(NC1)=O)N1c1ccccc1 Chemical compound CCC(CNC)(C(NC1)=O)N1c1ccccc1 ZEDNMYPSRVIRSG-UHFFFAOYSA-N 0.000 description 1
- LTHAIAJHDPJXLG-UHFFFAOYSA-N CCCC(C)c1ccccc1 Chemical compound CCCC(C)c1ccccc1 LTHAIAJHDPJXLG-UHFFFAOYSA-N 0.000 description 1
- SRCLUWIRIAYUQH-UHFFFAOYSA-N CN(C1)C2=C1c1ccccc1N2 Chemical compound CN(C1)C2=C1c1ccccc1N2 SRCLUWIRIAYUQH-UHFFFAOYSA-N 0.000 description 1
- ISJUKQAQAXXZNJ-UHFFFAOYSA-N CN(C1)CC11OC(C=C=C2)=C2O1 Chemical compound CN(C1)CC11OC(C=C=C2)=C2O1 ISJUKQAQAXXZNJ-UHFFFAOYSA-N 0.000 description 1
- HGSXZTCIYCAXSQ-UHFFFAOYSA-N Cc(cc1)ccc1C1=NCCCC=C1 Chemical compound Cc(cc1)ccc1C1=NCCCC=C1 HGSXZTCIYCAXSQ-UHFFFAOYSA-N 0.000 description 1
- URLKBWYHVLBVBO-UHFFFAOYSA-N Cc1ccc(C)cc1 Chemical compound Cc1ccc(C)cc1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 1
- WHYSXRRCJYAVIL-UHFFFAOYSA-N Fc(cc1F)ccc1N1CCN(CCCl)CC1 Chemical compound Fc(cc1F)ccc1N1CCN(CCCl)CC1 WHYSXRRCJYAVIL-UHFFFAOYSA-N 0.000 description 1
- KVONYNAPEKNVBP-UHFFFAOYSA-N Nc1c(C=N)c(Cl)nc(N)n1 Chemical compound Nc1c(C=N)c(Cl)nc(N)n1 KVONYNAPEKNVBP-UHFFFAOYSA-N 0.000 description 1
- WVJCIGSGLCAJKA-UHFFFAOYSA-N Nc1nc(NN)c(C=N)c(NCCN(CC2)CCN2c(ccc(F)c2)c2F)n1 Chemical compound Nc1nc(NN)c(C=N)c(NCCN(CC2)CCN2c(ccc(F)c2)c2F)n1 WVJCIGSGLCAJKA-UHFFFAOYSA-N 0.000 description 1
- QIQITDHWZYEEPA-UHFFFAOYSA-N O=C(c1ccc[s]1)Cl Chemical compound O=C(c1ccc[s]1)Cl QIQITDHWZYEEPA-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
- C07D487/12—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 three hetero rings
- C07D487/14—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
-
- 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
- A61P25/08—Antiepileptics; Anticonvulsants
-
- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P25/24—Antidepressants
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Hospice & Palliative Care (AREA)
- Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US20714300P | 2000-05-26 | 2000-05-26 | |
| US60/207,143 | 2000-05-26 | ||
| PCT/US2001/016954 WO2001092264A1 (en) | 2000-05-26 | 2001-05-24 | Adenosine a2a receptor antagonists |
Related Child Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006128415A Division JP4938348B2 (ja) | 2000-05-26 | 2006-05-02 | アデノシンa2aレセプターアンタゴニスト |
| JP2007069618A Division JP2007145875A (ja) | 2000-05-26 | 2007-03-16 | アデノシンa2aレセプターアンタゴニスト |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2003535094A JP2003535094A (ja) | 2003-11-25 |
| JP2003535094A5 JP2003535094A5 (enExample) | 2006-06-22 |
| JP4574112B2 true JP4574112B2 (ja) | 2010-11-04 |
Family
ID=22769372
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002500877A Expired - Lifetime JP4574112B2 (ja) | 2000-05-26 | 2001-05-24 | アデノシンa2aレセプターアンタゴニスト |
| JP2006128415A Expired - Lifetime JP4938348B2 (ja) | 2000-05-26 | 2006-05-02 | アデノシンa2aレセプターアンタゴニスト |
| JP2007069618A Withdrawn JP2007145875A (ja) | 2000-05-26 | 2007-03-16 | アデノシンa2aレセプターアンタゴニスト |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006128415A Expired - Lifetime JP4938348B2 (ja) | 2000-05-26 | 2006-05-02 | アデノシンa2aレセプターアンタゴニスト |
| JP2007069618A Withdrawn JP2007145875A (ja) | 2000-05-26 | 2007-03-16 | アデノシンa2aレセプターアンタゴニスト |
Country Status (31)
| Country | Link |
|---|---|
| US (4) | US6630475B2 (enExample) |
| EP (1) | EP1283839B1 (enExample) |
| JP (3) | JP4574112B2 (enExample) |
| KR (1) | KR100520907B1 (enExample) |
| CN (2) | CN100384847C (enExample) |
| AR (1) | AR028621A1 (enExample) |
| AT (1) | ATE293627T1 (enExample) |
| AU (2) | AU2001268089C1 (enExample) |
| BR (1) | BRPI0111015B8 (enExample) |
| CA (1) | CA2410237C (enExample) |
| CZ (1) | CZ303790B6 (enExample) |
| DE (1) | DE60110219T2 (enExample) |
| DK (1) | DK1283839T3 (enExample) |
| EC (1) | ECSP024364A (enExample) |
| ES (1) | ES2237576T3 (enExample) |
| HK (1) | HK1049007B (enExample) |
| HU (1) | HU230420B1 (enExample) |
| IL (3) | IL152726A0 (enExample) |
| MX (1) | MXPA02011625A (enExample) |
| MY (1) | MY132006A (enExample) |
| NO (1) | NO325008B1 (enExample) |
| NZ (1) | NZ522326A (enExample) |
| PE (1) | PE20020062A1 (enExample) |
| PL (1) | PL218764B1 (enExample) |
| PT (1) | PT1283839E (enExample) |
| RU (1) | RU2315053C2 (enExample) |
| SI (1) | SI1283839T1 (enExample) |
| SK (1) | SK287748B6 (enExample) |
| TW (1) | TWI288137B (enExample) |
| WO (1) | WO2001092264A1 (enExample) |
| ZA (1) | ZA200208898B (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007145875A (ja) * | 2000-05-26 | 2007-06-14 | Schering Plough Corp | アデノシンa2aレセプターアンタゴニスト |
Families Citing this family (88)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1425017A1 (en) * | 2001-09-13 | 2004-06-09 | Schering Corporation | Combination of an adenosine a2a receptor antagonist and an antidepressant or anxiolytic |
| JP4545437B2 (ja) | 2001-10-15 | 2010-09-15 | シェーリング コーポレイション | アデノシンa2a受容体アンタゴニストとしてのイミダゾ(4,3−e)−1,2,4−トリアゾロ(1,5−c)ピリミジン |
| FR2832405B1 (fr) * | 2001-11-19 | 2004-12-10 | Sanofi Synthelabo | Tetrahydropyridyl-alkyl-heterocycles azotes, procede pour leur preparation et compositions pharmaceutiques les contenant |
| AU2002346503A1 (en) * | 2001-11-30 | 2003-06-17 | Schering Corporation | Adenosine A2a receptor antagonists |
| CA2468658C (en) | 2001-11-30 | 2009-04-14 | Schering Corporation | [1,2,4]-triazole bicyclic adenosine a2a receptor antagonists |
| TW200300686A (en) | 2001-11-30 | 2003-06-16 | Schering Corp | Adenosine A2a receptor antagonists |
| ES2716404T3 (es) | 2002-01-28 | 2019-06-12 | Kyowa Hakko Kogyo Kk | Antagonistas de receptores A2A para su uso en el tratamiento de trastornos del movimiento |
| MXPA04000908A (es) * | 2002-05-30 | 2004-03-26 | King Pharmaceuticals Res & Dev | Compuestos farmaceuticamente activos que tienen estructura de anillo de pirazolotriazolopirimidina triciclica y metodos de uso. |
| MXPA05006790A (es) * | 2002-12-19 | 2005-09-08 | Schering Corp | Usos de antagonistas del receptor adenosina a2a. |
| US20060106040A1 (en) * | 2002-12-19 | 2006-05-18 | Michael Grzelak | Adenosine A2a receptor antagonists for the treatment of extra-pyramidal syndrome and other movement disorders |
| EP1618109A2 (en) | 2003-04-09 | 2006-01-25 | Biogen Idec MA Inc. | Triazolo[1,5-c]pyrimidines and pyrazolo[1,5-c]pyrimidines useful as a2a adenosine receptor antagonists |
| EP1622912B1 (en) * | 2003-04-23 | 2009-05-27 | Schering Corporation | 2-alkynyl-and 2-alkenyl-pyrazolo- [4,3-e ] -1,2,4-triazolo- [1,5-c] -pyrimidine adenosine a2a receptor antagonists |
| EA200501924A1 (ru) * | 2003-06-10 | 2006-06-30 | Киова Хакко Когио Ко., Лтд. | Способ лечения тревожного расстройства |
| JP2006527212A (ja) * | 2003-06-12 | 2006-11-30 | ノボ ノルディスク アクティーゼルスカブ | ホルモン感受性リパーゼの阻害剤として使用するための、置換ピペラジンカルバメート |
| US7816353B2 (en) * | 2003-10-24 | 2010-10-19 | Exelixis, Inc. | P70S6 kinase modulators and method of use |
| DK1678182T3 (da) | 2003-10-28 | 2007-06-04 | Schering Corp | Fremgangsmåde til fremstilling af substituerede 5-amino-pyrazolo[4,3-E]-1,2,4-triazolo-[1,5-C]pyrimidiner |
| ATE377599T1 (de) * | 2003-12-01 | 2007-11-15 | Schering Corp | Verfahren zur herstellung von substituierten 5- aminopyrazolo(4,3-e)-1,2,4-triazolo(1,5- c)pyrimidinen |
| CA2550071A1 (en) * | 2003-12-19 | 2005-07-07 | Schering Corporation | Pharmaceutical compositions |
| ATE461932T1 (de) * | 2004-04-21 | 2010-04-15 | Schering Corp | Pyrazoloä4,3-eü-1,2,4-triazoloä1,5-cüpyrimidine als antagonisten des adenosin-a2a-rezeptors |
| JPWO2006132275A1 (ja) * | 2005-06-07 | 2009-01-08 | 協和醗酵工業株式会社 | 運動障害の予防および/または治療剤 |
| AR057817A1 (es) * | 2005-09-19 | 2007-12-19 | Schering Corp | Antagonistas del receptor a2a de 2-heteroaril-pirazolo-[4,3-e]-1,2,4-triazolo-[1,5-c]-pirimidin adenosina. composiciones farmaceuticas |
| AR056080A1 (es) * | 2005-09-23 | 2007-09-19 | Schering Corp | 7-[2-[4-(6-fluoro-3-metil-1,2-benciosoxazol-5-il)-1-piperazinil]etil]-2-(1-propinil)-7h-pirazol-[4,3-e]-[1,2,4]-triazol-[1,5-c] -pirimidin-5-amine |
| ES2273599B1 (es) | 2005-10-14 | 2008-06-01 | Universidad De Barcelona | Compuestos para el tratamiento de la fibrilacion auricular. |
| EP2040698A4 (en) * | 2006-07-14 | 2011-08-10 | Shionogi & Co | OXIM CONNECTIONS AND ITS USE |
| TW200840566A (en) * | 2006-12-22 | 2008-10-16 | Esteve Labor Dr | Heterocyclyl-substituted-ethylamino-phenyl derivatives, their preparation and use as medicaments |
| US7691869B2 (en) | 2007-03-30 | 2010-04-06 | King Pharmaceuticals Research And Development, Inc. | Pyrrolotriazolopyrimidine derivatives, pharmaceutical compositions containing them and methods of treating conditions and diseases mediated by the adenosine A2A receptor activity |
| WO2009110955A2 (en) * | 2008-02-29 | 2009-09-11 | Albert Einstein College Of Medicine Of Yeshiva University | Ketoconazole-derivative antagonists of human pregnane x receptor and uses thereof |
| JP2011513417A (ja) | 2008-03-04 | 2011-04-28 | シェーリング コーポレイション | アデノシンA2a受容体アンタゴニストとして使用するための1,2,4−トリアゾロ[4,3−c]ピリミジン−3−オンおよびピラゾロ[4,3−e]−1,2,4−トリアゾロ[4,3−c]ピリミジン−3−オン化合物 |
| US20110064671A1 (en) | 2008-03-10 | 2011-03-17 | Cornell University | Modulation of blood brain barrier permeability |
| TWI473614B (zh) * | 2008-05-29 | 2015-02-21 | Kyowa Hakko Kirin Co Ltd | Anti-analgesic inhibitors |
| NZ590793A (en) * | 2008-07-23 | 2012-07-27 | Kyowa Hakko Kirin Co Ltd | Therapeutic agent for migraine |
| US20100093702A1 (en) * | 2008-10-13 | 2010-04-15 | Barbay J Kent | METHYLENE AMINES OF THIENO[2,3-d]PYRIMIDINE AND THEIR USE AS ADENOSINE A2a RECEPTOR ANTAGONISTS |
| TW201036614A (en) | 2008-12-30 | 2010-10-16 | Arqule Inc | Substituted 1H-pyrazolo[3,4-d]pyrimidine-6-amine compounds |
| AU2010207004A1 (en) | 2009-01-20 | 2011-07-28 | Merck Sharp & Dohme Corp. | Methods of alleviating or treating signs and/or symptoms associated with moderate to severe Parkinson's disease |
| US8993808B2 (en) | 2009-01-21 | 2015-03-31 | Oryzon Genomics, S.A. | Phenylcyclopropylamine derivatives and their medical use |
| BRPI1009398A2 (pt) | 2009-03-13 | 2016-03-08 | Advinus Therapeutics Private Ltd | compostos de pirimidina fundida substituída |
| EP2414361A1 (en) | 2009-03-31 | 2012-02-08 | ArQule, Inc. | Substituted heterocyclic compounds |
| WO2010147941A1 (en) | 2009-06-15 | 2010-12-23 | Marvell World Trade Ltd. | System and methods for gamut bounded saturation adaptive color enhancement |
| EP2462144B1 (en) | 2009-08-07 | 2017-09-20 | Merck Sharp & Dohme Corp. | PROCESS FOR PREPARING A 2-ALKYNYL SUBSTITUTED 5-AMINO-PYRAZOLO-[4,3-e]-1,2,4-TRIAZOLO[1,5-c]PYRIMIDINE |
| WO2011035941A1 (en) | 2009-09-25 | 2011-03-31 | Oryzon Genomics S.A. | Lysine specific demethylase-1 inhibitors and their use |
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| WO2011101861A1 (en) | 2010-01-29 | 2011-08-25 | Msn Laboratories Limited | Process for preparation of dpp-iv inhibitors |
| WO2011106106A2 (en) | 2010-02-24 | 2011-09-01 | Oryzon Genomics, S.A. | Lysine demethylase inhibitors for diseases and disorders associated with hepadnaviridae |
| WO2011106574A2 (en) | 2010-02-24 | 2011-09-01 | Oryzon Genomics, S.A. | Inhibitors for antiviral use |
| RS55348B1 (sr) | 2010-04-19 | 2017-03-31 | Oryzon Gnomics S A | Inhibitori lizin specifične demetilaze-1 i njihova upotreba |
| DK2598482T3 (en) | 2010-07-29 | 2018-06-14 | Oryzon Genomics Sa | ARYLCYCLOPROPYLAMINE-BASED DEMETHYLASE INHIBITORS OF LSD1 AND THEIR MEDICAL USE |
| EP2598480B1 (en) | 2010-07-29 | 2019-04-24 | Oryzon Genomics, S.A. | Cyclopropylamine derivatives useful as lsd1 inhibitors |
| CN103261202B (zh) * | 2010-09-24 | 2016-01-20 | 阿迪维纳斯疗法有限公司 | 作为腺苷受体拮抗剂的稠合三环化合物 |
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| WO2012129381A1 (en) * | 2011-03-22 | 2012-09-27 | Concert Pharmaceuticals Inc. | Deuterated preladenant |
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| AU2012324803B9 (en) | 2011-10-20 | 2017-08-24 | Oryzon Genomics, S.A. | (hetero)aryl cyclopropylamine compounds as LSD1 inhibitors |
| WO2014071512A1 (en) * | 2012-11-06 | 2014-05-15 | Universite Laval | Combination therapy and methods for the treatment of respiratory diseases |
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| AU2015350315B2 (en) | 2014-11-18 | 2020-06-25 | Merck Sharp & Dohme Corp. | Aminopyrazine compounds with A2A antagonist properties |
| WO2016126570A1 (en) | 2015-02-06 | 2016-08-11 | Merck Sharp & Dohme Corp. | Aminoquinazoline compounds as a2a antagonist |
| EP3307067B1 (en) | 2015-06-11 | 2022-11-02 | Merck Sharp & Dohme LLC | Aminopyrazine compounds with a2a antagonist properties |
| WO2017008205A1 (en) | 2015-07-10 | 2017-01-19 | Merck Sharp & Dohme Corp. | Substituted aminoquinazoline compounds as a2a antagonist |
| US9687475B1 (en) | 2016-03-24 | 2017-06-27 | Ezra Pharma Llc | Extended release pharmaceutical formulations with controlled impurity levels |
| US9675585B1 (en) | 2016-03-24 | 2017-06-13 | Ezra Pharma | Extended release pharmaceutical formulations |
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| AR057817A1 (es) * | 2005-09-19 | 2007-12-19 | Schering Corp | Antagonistas del receptor a2a de 2-heteroaril-pirazolo-[4,3-e]-1,2,4-triazolo-[1,5-c]-pirimidin adenosina. composiciones farmaceuticas |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007145875A (ja) * | 2000-05-26 | 2007-06-14 | Schering Plough Corp | アデノシンa2aレセプターアンタゴニスト |
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