|
SI1283839T1
(enExample)
*
|
2000-05-26 |
2005-08-31 |
Schering Corp |
|
|
WO2003022283A1
(en)
*
|
2001-09-13 |
2003-03-20 |
Schering Corporation |
Combination of an adenosine a2a receptor antagonist and an antidepressant or anxiolytic
|
|
AR037243A1
(es)
|
2001-10-15 |
2004-11-03 |
Schering Corp |
Antagonistas del receptor de adenosina a2a,a5-amino-imidazolo-[4,3-e]-1,2,4-triazolo-[1,5-c]pirimidina, composiciones farmaceuticas y el uso de dichos compuestos para la preparacion de un medicamento
|
|
FR2832405B1
(fr)
*
|
2001-11-19 |
2004-12-10 |
Sanofi Synthelabo |
Tetrahydropyridyl-alkyl-heterocycles azotes, procede pour leur preparation et compositions pharmaceutiques les contenant
|
|
ES2283625T3
(es)
|
2001-11-30 |
2007-11-01 |
Schering Corporation |
Antagonistas del receptopr a2a de adenosina de (1,2,4)-triazol biciclicos.
|
|
US6916811B2
(en)
*
|
2001-11-30 |
2005-07-12 |
Schering Corporation |
Adenosine A2a receptor antagonists
|
|
TW200300686A
(en)
|
2001-11-30 |
2003-06-16 |
Schering Corp |
Adenosine A2a receptor antagonists
|
|
ES2686123T3
(es)
|
2002-01-28 |
2018-10-16 |
Kyowa Hakko Kogyo Co., Ltd |
Antagonistas del receptor A2A para su uso en el tratamiento de trastornos del movimiento
|
|
IL160133A0
(en)
*
|
2002-05-30 |
2004-06-20 |
King Pharmaceuticals Res & Dev |
Pharmaceutically active compounds having a tricyclic pyrazolotriazolopyrimidine ring structure and methods of use
|
|
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
|
|
AU2003304527B2
(en)
*
|
2002-12-19 |
2010-09-09 |
Merck Sharp & Dohme Corp. |
Uses of adenosine A2a receptor antagonists
|
|
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
|
|
CN1787821A
(zh)
*
|
2003-06-10 |
2006-06-14 |
协和发酵工业株式会社 |
一种治疗焦虑症的方法
|
|
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
|
|
JP4800216B2
(ja)
*
|
2003-10-24 |
2011-10-26 |
エグゼリクシス, インコーポレイテッド |
p70S6キナーゼモジュレーターおよび使用方法
|
|
PT1678182E
(pt)
|
2003-10-28 |
2007-04-30 |
Schering Corp |
Processo para preparar 5-amino-pirazolo-[4,3-e]-1,2,4-triazolo[1,5-c]pirimidinas
|
|
JP2007513091A
(ja)
*
|
2003-12-01 |
2007-05-24 |
シェーリング コーポレイション |
置換された5−アミノ−ピラゾロ−[4,3−e]−1,2,4−トリアゾロ[1,5−c]ピリミジンを調製するための方法
|
|
EP1701699B1
(en)
*
|
2003-12-19 |
2011-07-13 |
Schering Corporation |
Pharmaceutical compositions of an A2a receptor antagonist
|
|
KR20060135901A
(ko)
|
2004-04-21 |
2006-12-29 |
쉐링 코포레이션 |
피라졸로-[4,3-e]-1,2,4-트리아졸로-[1,5-c]피리미딘아데노신 A2a 수용체 길항제
|
|
EP1902716A4
(en)
*
|
2005-06-07 |
2009-05-13 |
Kyowa Hakko Kirin Co Ltd |
PROPHYLACTIC AND / OR THERAPEUTIC AGENT FOR MOTOR TROUBLESHOOTING
|
|
CA2622741A1
(en)
|
2005-09-19 |
2007-03-29 |
Schering Corporation |
2-heteroaryl-pyrazolo-[4, 3-e]-1, 2, 4-triazolo-[1,5-c]-pyrimidine as adenosine a2a receptor antagonists
|
|
PE20070521A1
(es)
*
|
2005-09-23 |
2007-07-13 |
Schering Corp |
7-[2-[4-(6-FLUORO-3-METIL-1,2-BENCISOXAZOL-5-IL)-1-PIPERAZINIL]ETIL]-2-(1-PROPINIL)-7H-PIRAZOL-[4,3-E]-[1,2,4]-TRIAZOL-[1,5-C]-PIRIMIDIN-5-AMINA COMO ANTAGONISTA DEL RECEPTOR DE ADENOSINA A2a
|
|
ES2273599B1
(es)
|
2005-10-14 |
2008-06-01 |
Universidad De Barcelona |
Compuestos para el tratamiento de la fibrilacion auricular.
|
|
WO2008008398A2
(en)
*
|
2006-07-14 |
2008-01-17 |
Shionogi & Co., Ltd. |
Oxime compounds and the use thereof
|
|
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
|
|
AU2009222047A1
(en)
|
2008-03-04 |
2009-09-11 |
Schering Corporation |
1,2,4-triazolo[4,3-c]pyrimidin-3-one and pyrazolo [4,3-e] -1,2,4-triazolo [4,3-c] pyrimidin-3-one compounds for use as adenosine A2a receptor antagonists
|
|
CN102014959B
(zh)
|
2008-03-10 |
2016-01-20 |
康奈尔大学 |
血脑屏障通透性的调节
|
|
TWI473614B
(zh)
*
|
2008-05-29 |
2015-02-21 |
Kyowa Hakko Kirin Co Ltd |
Anti-analgesic inhibitors
|
|
JP5599311B2
(ja)
|
2008-07-23 |
2014-10-01 |
協和発酵キリン株式会社 |
片頭痛治療剤
|
|
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
|
|
EP2379556A1
(en)
|
2008-12-30 |
2011-10-26 |
ArQule, Inc. |
Substituted 1h-pyrazolo[3,4-d]pyrimidine-6-amine compounds
|
|
CA2750265A1
(en)
|
2009-01-20 |
2010-07-29 |
Marc Cantillon |
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
|
|
JP5765239B2
(ja)
|
2009-03-13 |
2015-08-19 |
アドヴィナス・セラピューティックス・リミテッド |
置換縮合ピリミジン化合物
|
|
WO2010114894A1
(en)
|
2009-03-31 |
2010-10-07 |
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
|
|
US8859555B2
(en)
|
2009-09-25 |
2014-10-14 |
Oryzon Genomics S.A. |
Lysine Specific Demethylase-1 inhibitors and their use
|
|
EP2486002B1
(en)
|
2009-10-09 |
2019-03-27 |
Oryzon Genomics, S.A. |
Substituted heteroaryl- and aryl- cyclopropylamine acetamides and their use
|
|
WO2011101861A1
(en)
|
2010-01-29 |
2011-08-25 |
Msn Laboratories Limited |
Process for preparation of dpp-iv inhibitors
|
|
US9616058B2
(en)
|
2010-02-24 |
2017-04-11 |
Oryzon Genomics, S.A. |
Potent selective LSD1 inhibitors and dual LSD1/MAO-B inhibitors for antiviral use
|
|
WO2011106573A2
(en)
|
2010-02-24 |
2011-09-01 |
Oryzon Genomics, S.A. |
Lysine demethylase inhibitors for diseases and disorders associated with hepadnaviridae
|
|
MX2012012111A
(es)
|
2010-04-19 |
2013-05-30 |
Oryzon Genomics Sa |
Inhibidores de demetilasa-1 especifica de lisina y su uso.
|
|
WO2012013727A1
(en)
|
2010-07-29 |
2012-02-02 |
Oryzon Genomics S.A. |
Cyclopropylamine derivatives useful as lsd1 inhibitors
|
|
SI2598482T1
(sl)
|
2010-07-29 |
2018-09-28 |
Oryzon Genomics, S.A. |
Inhibitorji demetilaze lsd1 na osnovi arilciklopropilamina in njihova medicinska uporaba
|
|
JP5843869B2
(ja)
*
|
2010-09-24 |
2016-01-13 |
アドヴィナス・セラピューティックス・リミテッド |
アデノシン受容体拮抗薬としての縮合三環化合物
|
|
WO2012045883A1
(en)
|
2010-10-08 |
2012-04-12 |
Oryzon Genomics S.A. |
Cyclopropylamine inhibitors of oxidases
|
|
WO2012072713A2
(en)
|
2010-11-30 |
2012-06-07 |
Oryzon Genomics, S.A. |
Lysine demethylase inhibitors for diseases and disorders associated with flaviviridae
|
|
WO2012107498A1
(en)
|
2011-02-08 |
2012-08-16 |
Oryzon Genomics S.A. |
Lysine demethylase inhibitors for myeloproliferative disorders
|
|
WO2012127472A1
(en)
*
|
2011-03-22 |
2012-09-27 |
Mapi Pharma Ltd. |
Process and intermediates for the preparation of preladenant and related compounds
|
|
WO2012129381A1
(en)
*
|
2011-03-22 |
2012-09-27 |
Concert Pharmaceuticals Inc. |
Deuterated preladenant
|
|
WO2013024474A1
(en)
*
|
2011-08-18 |
2013-02-21 |
Mapi Phrarma Ltd. |
Polymorphs of preladenant
|
|
CN107266345B
(zh)
|
2011-10-20 |
2021-08-17 |
奥瑞泽恩基因组学股份有限公司 |
作为lsd1抑制剂的(杂)芳基环丙胺化合物
|
|
RS58475B1
(sr)
|
2011-10-20 |
2019-04-30 |
Oryzon Genomics Sa |
Jedinjenja (hetero)aril ciklopropilamina kao lsd1 inhibitori
|
|
WO2014071512A1
(en)
*
|
2012-11-06 |
2014-05-15 |
Universite Laval |
Combination therapy and methods for the treatment of respiratory diseases
|
|
WO2014101120A1
(en)
|
2012-12-28 |
2014-07-03 |
Merck Sharp & Dohme Corp. |
Heterobicyclo-substituted-7-methoxy-[1,2,4]triazolo[1,5-c]quinazolin-5-amine compounds with a2a antagonist properties
|
|
JP6779204B2
(ja)
|
2014-11-18 |
2020-11-04 |
メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. |
A2a拮抗薬特性を有するアミノピラジン化合物
|
|
US10138212B2
(en)
|
2015-02-06 |
2018-11-27 |
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
|
|
CN115873022A
(zh)
*
|
2017-03-30 |
2023-03-31 |
伊忒欧斯比利时股份公司 |
作为a2a抑制剂的2-氧代噻唑衍生物和用于治疗癌症的化合物
|
|
WO2018178338A1
(en)
*
|
2017-03-30 |
2018-10-04 |
Iteos Therapeutics |
2-oxo-thiazole derivatives as a2a inhibitors and compounds for use in the treatment of cancers
|
|
US11498923B2
(en)
|
2017-12-13 |
2022-11-15 |
Merck Sharp & Dohme Llc |
Substituted imidazo[1,2-c]quinazolines as A2A antagonists
|
|
IL275817B2
(en)
*
|
2018-01-04 |
2024-04-01 |
Impetis Biosciences Ltd |
Tricyclic compounds, compositions and medicinal applications thereof
|
|
BR122023024273A2
(pt)
|
2018-02-27 |
2024-02-20 |
Incyte Corporation |
Compostos imidazopirimidinas e triazolopirimidinas, seus usos, método para inibir uma atividade de um receptor de adenosina e composição farmacêutica dos mesmos
|
|
CN108276345A
(zh)
*
|
2018-03-22 |
2018-07-13 |
重庆奥舍生物化工有限公司 |
一种药物中间体嘧啶-5-甲醛的制备方法
|
|
JP2021520392A
(ja)
*
|
2018-04-08 |
2021-08-19 |
ベイジーン リミテッド |
A2a受容体アンタゴニストとしてのピラゾロトリアゾロピリミジン誘導体
|
|
EP3810610A1
(en)
|
2018-05-18 |
2021-04-28 |
Incyte Corporation |
Fused pyrimidine derivatives as a2a / a2b inhibitors
|
|
CN108864114B
(zh)
|
2018-06-04 |
2020-11-06 |
应世生物科技(南京)有限公司 |
选择性a2a受体拮抗剂
|
|
AU2019297361B2
(en)
|
2018-07-05 |
2024-06-27 |
Incyte Corporation |
Fused pyrazine derivatives as A2A / A2B inhibitors
|
|
CN110742893B
(zh)
*
|
2018-07-23 |
2024-04-05 |
百济神州(北京)生物科技有限公司 |
A2a受体拮抗剂治疗癌症的方法
|
|
CR20210271A
(es)
|
2018-11-30 |
2021-07-14 |
Merck Sharp & Dohme |
Derivados de amino triazolo quinazolina 9-sustituidos como antagonistas del receptor de adenosina, composiciones farmacéuticas y su uso
|
|
AU2019401649B2
(en)
|
2018-12-20 |
2025-08-28 |
Incyte Corporation |
Imidazopyridazine and imidazopyridine compounds as inhibitors of activin receptor-like kinase-2
|
|
TWI829857B
(zh)
|
2019-01-29 |
2024-01-21 |
美商英塞特公司 |
作為a2a / a2b抑制劑之吡唑并吡啶及三唑并吡啶
|
|
WO2020227156A1
(en)
*
|
2019-05-03 |
2020-11-12 |
Nektar Therapeutics |
Adenosine 2 receptor antagonists
|
|
DE102019116986A1
(de)
|
2019-06-24 |
2020-12-24 |
Helmholtz-Zentrum Dresden-Rossendorf E. V. |
Deuterierte 7-(3-(4-(2-([18F]Fluor)ethoxy)phenyl)propyl)-2-(furan-2-yl)-7H-pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidin-5-amin-Derivate
|
|
CN114667287A
(zh)
*
|
2019-07-17 |
2022-06-24 |
泰昂治疗公司 |
腺苷a2a受体拮抗剂及其用途
|
|
CN112479956A
(zh)
|
2019-07-30 |
2021-03-12 |
杭州阿诺生物医药科技有限公司 |
一种用于制备腺苷受体抑制剂中间体的方法
|
|
CN112608330B
(zh)
|
2019-07-30 |
2021-09-28 |
杭州阿诺生物医药科技有限公司 |
A2a和/或a2b受体抑制剂
|
|
CN111072675A
(zh)
*
|
2019-12-12 |
2020-04-28 |
广东东阳光药业有限公司 |
含氮稠合三环衍生物及其用途
|
|
CN113773327B
(zh)
*
|
2021-09-13 |
2022-07-15 |
八叶草健康产业研究院(厦门)有限公司 |
一种吡唑并嘧啶并三唑环类化合物的制备方法
|
|
CN117946123A
(zh)
*
|
2024-01-26 |
2024-04-30 |
北京脑重大疾病研究院 |
放射性三氮唑并嘧啶基衍生物及其制备方法和应用
|
|
CN118812539B
(zh)
*
|
2024-06-19 |
2025-11-28 |
苏州大学 |
一种5-氨基三唑并嘧啶衍生物及其制备方法
|
|
CN118812544A
(zh)
*
|
2024-06-19 |
2024-10-22 |
厦门大学 |
一种腺苷a2ar靶向小分子化合物、核素标记探针及其制备方法、应用和药物组合物
|