|
TW200300350A
(en)
*
|
2001-11-14 |
2003-06-01 |
Bristol Myers Squibb Co |
C-5 modified indazolylpyrrolotriazines
|
|
TW200306841A
(en)
|
2002-04-23 |
2003-12-01 |
Bristol Myers Squibb Co |
Aryl ketone pyrrolo-triazine compounds useful as kinase inhibitors
|
|
PT1497019E
(pt)
|
2002-04-23 |
2015-09-10 |
Bristol Myers Squibb Co |
Compostos de pirrolotriazina anilina úteis como inibidores de quinase
|
|
TW200401638A
(en)
*
|
2002-06-20 |
2004-02-01 |
Bristol Myers Squibb Co |
Heterocyclic inhibitors of kinases
|
|
TWI329112B
(en)
*
|
2002-07-19 |
2010-08-21 |
Bristol Myers Squibb Co |
Novel inhibitors of kinases
|
|
AU2003265349A1
(en)
*
|
2002-08-02 |
2004-02-23 |
Bristol-Myers Squibb Company |
Pyrrolotriazine kinase inhibitors
|
|
TW200420565A
(en)
*
|
2002-12-13 |
2004-10-16 |
Bristol Myers Squibb Co |
C-6 modified indazolylpyrrolotriazines
|
|
JP2006516653A
(ja)
|
2003-02-05 |
2006-07-06 |
ブリストル−マイヤーズ スクイブ カンパニー |
キナーゼ阻害剤ピロロトリアジンの製造方法
|
|
US7419978B2
(en)
*
|
2003-10-22 |
2008-09-02 |
Bristol-Myers Squibb Company |
Phenyl-aniline substituted bicyclic compounds useful as kinase inhibitors
|
|
AU2004309420B2
(en)
*
|
2003-12-23 |
2008-10-30 |
Novartis Ag |
Bicyclic heterocyclic p-38 kinase inhibitors
|
|
RU2006134022A
(ru)
|
2004-02-27 |
2008-04-10 |
Ф.Хоффманн-Ля Рош Аг (Ch) |
Производные индазола и содержащие их фармацевтические композиции
|
|
WO2005085249A1
(en)
|
2004-02-27 |
2005-09-15 |
F. Hoffmann-La Roche Ag |
Fused derivatives of pyrazole
|
|
CN1934111A
(zh)
|
2004-02-27 |
2007-03-21 |
霍夫曼-拉罗奇有限公司 |
杂芳基稠合的吡唑并衍生物
|
|
US7067659B2
(en)
*
|
2004-04-23 |
2006-06-27 |
Duke University |
Reactive oxygen generating enzyme inhibitor with nitric oxide bioactivity and uses thereof
|
|
US7439246B2
(en)
*
|
2004-06-28 |
2008-10-21 |
Bristol-Myers Squibb Company |
Fused heterocyclic kinase inhibitors
|
|
TW200600513A
(en)
*
|
2004-06-30 |
2006-01-01 |
Bristol Myers Squibb Co |
A method for preparing pyrrolotriazine compounds
|
|
US7253167B2
(en)
*
|
2004-06-30 |
2007-08-07 |
Bristol-Myers Squibb Company |
Tricyclic-heteroaryl compounds useful as kinase inhibitors
|
|
US7504521B2
(en)
*
|
2004-08-05 |
2009-03-17 |
Bristol-Myers Squibb Co. |
Methods for the preparation of pyrrolotriazine compounds
|
|
TW200618803A
(en)
|
2004-08-12 |
2006-06-16 |
Bristol Myers Squibb Co |
Process for preparing pyrrolotriazine aniline compounds useful as kinase inhibitors
|
|
ES2368930T3
(es)
|
2004-09-06 |
2011-11-23 |
Bayer Pharma Aktiengesellschaft |
Pirazolopirimidinas como inhibidores de proteína cinasa b (akt).
|
|
GB0425035D0
(en)
*
|
2004-11-12 |
2004-12-15 |
Novartis Ag |
Organic compounds
|
|
GB0427604D0
(en)
*
|
2004-12-16 |
2005-01-19 |
Novartis Ag |
Organic compounds
|
|
EP1846408B1
(en)
|
2005-01-14 |
2013-03-20 |
Janssen Pharmaceutica NV |
5-membered annelated heterocyclic pyrimidines as kinase inhibitors
|
|
WO2006074984A1
(en)
*
|
2005-01-14 |
2006-07-20 |
Janssen Pharmaceutica N.V. |
Pyrazolopyrimidines as cell cycle kinase inhibitors
|
|
US20060178388A1
(en)
|
2005-02-04 |
2006-08-10 |
Wrobleski Stephen T |
Phenyl-substituted pyrimidine compounds useful as kinase inhibitors
|
|
GB0507575D0
(en)
|
2005-04-14 |
2005-05-18 |
Novartis Ag |
Organic compounds
|
|
WO2006122230A1
(en)
*
|
2005-05-11 |
2006-11-16 |
Array Biopharma Inc. |
P38 inhibitors and methods of use thereof
|
|
KR101011958B1
(ko)
|
2005-08-25 |
2011-01-31 |
에프. 호프만-라 로슈 아게 |
p38 MAP 키나아제 저해제로서의 융합형 피라졸
|
|
BRPI0614884A2
(pt)
|
2005-08-25 |
2011-04-19 |
Hoffmann La Roche |
inibidores de p38 map cinase e métodos para uso dos mesmos
|
|
KR101011956B1
(ko)
*
|
2005-08-25 |
2011-01-31 |
에프. 호프만-라 로슈 아게 |
P38 mαp 키나아제 저해제 및 이의 사용 방법
|
|
GB0522880D0
(en)
*
|
2005-11-09 |
2005-12-21 |
Glaxo Group Ltd |
Novel compounds
|
|
GB0524436D0
(en)
*
|
2005-11-30 |
2006-01-11 |
Novartis Ag |
Organic compounds
|
|
WO2007095161A2
(en)
*
|
2006-02-14 |
2007-08-23 |
New York University |
Methods and compositions for treating disorders associated with increased bone turnover and osteopenia
|
|
WO2007103308A2
(en)
*
|
2006-03-07 |
2007-09-13 |
Array Biopharma Inc. |
Heterobicyclic pyrazole compounds and methods of use
|
|
CN101405283B
(zh)
|
2006-03-30 |
2014-06-18 |
泰博特克药品有限公司 |
Hiv抑制性5-酰氨基取代的嘧啶类化合物
|
|
WO2007139778A2
(en)
*
|
2006-05-22 |
2007-12-06 |
University Of Virginia Patent Foundation |
Rhamnose substituents of sl0101 and therapeutic uses thereof
|
|
KR20090064602A
(ko)
*
|
2006-10-16 |
2009-06-19 |
노파르티스 아게 |
단백질 키나제 억제제로서 유용한 페닐아세트아미드
|
|
US8148361B2
(en)
|
2006-11-10 |
2012-04-03 |
Bristol-Myers Squibb Company |
Kinase inhibitors
|
|
EP2091952A1
(en)
*
|
2006-12-19 |
2009-08-26 |
F. Hoffmann-Roche AG |
Pyrazolo ý3, 4 -d¨pyrimidine p38 map kinase inhibitors
|
|
WO2009023053A2
(en)
*
|
2007-05-18 |
2009-02-19 |
University Of Virginia Patent Foundation |
Use of rsk inhibitors to impede intracellular pathogen infections
|
|
EA019869B1
(ru)
*
|
2007-11-28 |
2014-06-30 |
Дана Фарбер Кансер Инститьют, Инк. |
Низкомолекулярные миристатные ингибиторы тирозинкиназы bcr-abl и способы их применения
|
|
US8987280B2
(en)
*
|
2008-01-30 |
2015-03-24 |
Genentech, Inc. |
Pyrazolopyrimidine PI3K inhibitor compounds and methods of use
|
|
US8188098B2
(en)
|
2008-05-19 |
2012-05-29 |
Hoffmann-La Roche Inc. |
GPR119 receptor agonists
|
|
CN104592231A
(zh)
*
|
2008-06-10 |
2015-05-06 |
Abbvie公司 |
新的三环化合物
|
|
WO2010011620A1
(en)
*
|
2008-07-21 |
2010-01-28 |
Wyeth |
4-phenoxy-6-aryl-1h-pyrazolo[3,4-d]pyrimidine and n-aryl-6-aryl-1h-pyrazolo[3,4-d]pyrimidin-4-amine compounds, their use as mtor kinase and pi3 kinase inhibitors, and their syntheses
|
|
WO2010059788A1
(en)
|
2008-11-20 |
2010-05-27 |
Genentech, Inc. |
Pyrazolopyridine pi3k inhibitor compounds and methods of use
|
|
US8343961B2
(en)
|
2009-03-31 |
2013-01-01 |
Arqule, Inc. |
Substituted heterocyclic compounds
|
|
PH12012501000A1
(en)
*
|
2009-12-01 |
2013-02-11 |
Abbvie Inc |
Novel tricyclic compounds
|
|
RU2711869C3
(ru)
|
2009-12-01 |
2022-02-02 |
Эббви Инк. |
Имидазопирролопиразиновые производные, полезные для лечения заболеваний, вызванных аномальной активностью протеинкиназ Jak1, Jak3 или Syk
|
|
WO2011156698A2
(en)
*
|
2010-06-11 |
2011-12-15 |
Abbott Laboratories |
NOVEL PYRAZOLO[3,4-d]PYRIMIDINE COMPOUNDS
|
|
BR112013011520A2
(pt)
*
|
2010-11-19 |
2019-09-24 |
Hoffmann La Roche |
pirazolo piridinas e pirazolo piridinas e seu uso como inibidores de tyk2
|
|
TWI399205B
(zh)
*
|
2011-01-14 |
2013-06-21 |
Univ Kaohsiung Medical |
茶鹼化合物之抑制骨質疏鬆症活性
|
|
EP2548878A1
(en)
*
|
2011-07-21 |
2013-01-23 |
Laboratorios Del. Dr. Esteve, S.A. |
Pyrazolo[3,4-d]pyrimidine compounds, their preparation and use as sigma ligands
|
|
CN102746306B
(zh)
*
|
2012-07-09 |
2014-11-19 |
四川国康药业有限公司 |
别嘌醇类衍生物及其制备方法和用途
|
|
CN103570723B
(zh)
*
|
2012-07-27 |
2016-07-13 |
广西梧州制药(集团)股份有限公司 |
吡唑并嘧啶衍生物及其制备方法和在药物制备中的用途
|
|
AU2013343105B2
(en)
|
2012-11-08 |
2016-04-14 |
Pfizer Inc. |
Heteroaromatic compounds as dopamine D1 ligands
|
|
CN103601722B
(zh)
*
|
2013-09-13 |
2016-03-02 |
南京华威医药科技开发有限公司 |
新型抗肿瘤化合物
|
|
SG11201607586UA
(en)
|
2014-03-13 |
2016-10-28 |
Agency Science Tech & Res |
Fused pyrimidine-based hydroxamate derivatives
|
|
US11773106B2
(en)
|
2015-10-16 |
2023-10-03 |
Abbvie Inc. |
Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
|
|
US10550126B2
(en)
|
2015-10-16 |
2020-02-04 |
Abbvie Inc. |
Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-A]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
|
|
US11524964B2
(en)
|
2015-10-16 |
2022-12-13 |
Abbvie Inc. |
Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
|
|
SG10201913990RA
(en)
|
2015-10-16 |
2020-03-30 |
Abbvie Inc |
PROCESSES FOR THE PREPARATION OF (3S,4R)-3-ETHYL-4-(3H-IMIDAZO[1,2-a]PYRROLO[2,3-e]-PYRAZIN-8-YL)-N-(2,2,2-TRIFLUOROETHYL)PYRROLIDINE-1-CARBOXAMIDE AND SOLID STATE FORMS THEREOF
|
|
US12365689B2
(en)
|
2015-10-16 |
2025-07-22 |
Abbvie Inc. |
Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
|
|
US11512092B2
(en)
|
2015-10-16 |
2022-11-29 |
Abbvie Inc. |
Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
|
|
US11365198B2
(en)
|
2015-10-16 |
2022-06-21 |
Abbvie Inc. |
Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
|
|
WO2018081451A1
(en)
|
2016-10-26 |
2018-05-03 |
Indiana University Research And Technology Corporation |
Small molecule protein arginine methyltransferase 5 (prmt5) inhibitors and methods of treatment
|
|
BR112020006677A2
(pt)
|
2017-10-05 |
2020-10-06 |
Fulcrum Therapeutics, Inc. |
uso de inibidores p38 para reduzir a expressão de dux4
|
|
US10342786B2
(en)
|
2017-10-05 |
2019-07-09 |
Fulcrum Therapeutics, Inc. |
P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD
|
|
MX2024007009A
(es)
*
|
2021-12-08 |
2024-08-22 |
Kineta Inc |
Heteroarenos bicíclicos y métodos para su uso.
|
|
CN117865965B
(zh)
*
|
2024-01-08 |
2024-06-28 |
贵州省天然产物研究中心 |
吡咯并嘧啶-4-胺和吡唑并嘧啶-4-胺衍生物及制备方法和应用
|