|
JP4642766B2
(ja)
*
|
2003-05-28 |
2011-03-02 |
ユニバーシタ・デグリ・スタディ・ディ・シエナ |
ピラゾロ[3,4−d]ピリミジン及びピロロ[2,3−d]ピリミジンの4−置換誘導体並びにそれらの使用
|
|
WO2005060970A1
(en)
*
|
2003-12-24 |
2005-07-07 |
Astrazeneca Ab |
Pyrimidines with tie2 (tek) activity
|
|
TW200530236A
(en)
*
|
2004-02-23 |
2005-09-16 |
Chugai Pharmaceutical Co Ltd |
Heteroaryl phenylurea
|
|
JP2007523938A
(ja)
|
2004-02-27 |
2007-08-23 |
エフ.ホフマン−ラ ロシュ アーゲー |
ピラゾールの縮合誘導体
|
|
CN1922150A
(zh)
|
2004-02-27 |
2007-02-28 |
霍夫曼-拉罗奇有限公司 |
吲唑衍生物以及含有它们的药物组合物
|
|
MXPA06009462A
(es)
*
|
2004-02-27 |
2007-03-15 |
Hoffmann La Roche |
Derivados pirazolo heteroaril fusionados.
|
|
US7405220B2
(en)
*
|
2004-06-09 |
2008-07-29 |
Hoffmann-La Roche Inc. |
Pyrazolopyrimidines
|
|
ES2368930T3
(es)
|
2004-09-06 |
2011-11-23 |
Bayer Pharma Aktiengesellschaft |
Pirazolopirimidinas como inhibidores de proteína cinasa b (akt).
|
|
GB0420722D0
(en)
|
2004-09-17 |
2004-10-20 |
Addex Pharmaceuticals Sa |
Novel allosteric modulators
|
|
GB0427604D0
(en)
*
|
2004-12-16 |
2005-01-19 |
Novartis Ag |
Organic compounds
|
|
EP1863805A1
(de)
*
|
2005-02-01 |
2007-12-12 |
AstraZeneca AB |
Pyrimidinverbindungen mit tie2- (tek-) hemmender wirkung
|
|
WO2006082371A1
(en)
*
|
2005-02-01 |
2006-08-10 |
Astrazeneca Ab |
Pyrimidine compounds having tie2 (tek) inhibitory activity
|
|
GB0502418D0
(en)
*
|
2005-02-05 |
2005-03-16 |
Astrazeneca Ab |
Compounds
|
|
DE102005037499A1
(de)
*
|
2005-08-09 |
2007-02-15 |
Merck Patent Gmbh |
Pyrazolderivate
|
|
MX2008002588A
(es)
*
|
2005-08-25 |
2008-03-18 |
Hoffmann La Roche |
Inhibidores de p38-map-cinasa y los metodos para utilizarlos.
|
|
GB0524436D0
(en)
*
|
2005-11-30 |
2006-01-11 |
Novartis Ag |
Organic compounds
|
|
TWI417095B
(zh)
|
2006-03-15 |
2013-12-01 |
Janssen Pharmaceuticals Inc |
1,4-二取代之3-氰基-吡啶酮衍生物及其作為mGluR2-受體之正向異位性調節劑之用途
|
|
GB0610242D0
(en)
|
2006-05-23 |
2006-07-05 |
Novartis Ag |
Organic compounds
|
|
EP1949894B1
(de)
*
|
2007-01-25 |
2016-06-29 |
Roche Diagnostics GmbH |
Verstärkung von vanadiumhaltigen Phosphatasehemmern mit Polyole
|
|
US8008035B2
(en)
|
2007-01-25 |
2011-08-30 |
Roche Diagnostics Operations, Inc. |
Enhancement of vanadium-containing phosphatase inhibitors
|
|
TW200900065A
(en)
|
2007-03-07 |
2009-01-01 |
Janssen Pharmaceutica Nv |
3-cyano-4-(4-pyridinyloxy-phenyl)-pyridin-2-one derivatives
|
|
TW200845978A
(en)
|
2007-03-07 |
2008-12-01 |
Janssen Pharmaceutica Nv |
3-cyano-4-(4-tetrahydropyran-phenyl)-pyridin-2-one derivatives
|
|
WO2009033702A1
(en)
|
2007-09-14 |
2009-03-19 |
Ortho-Mcneil-Janssen Pharmaceuticals, Inc. |
1,3-disubstituted 4-(aryl-x-phenyl)-1h-pyridin-2-ones
|
|
PL2203439T3
(pl)
|
2007-09-14 |
2011-06-30 |
Addex Pharmaceuticals Sa |
1',3'-dipodstawione-4-fenylo-3,4,5,6-tetrahydro-2H, 1'H-[1, 4']bipirydynylo-2'-ketony
|
|
CA2711759A1
(en)
*
|
2008-01-30 |
2009-08-06 |
Genentech, Inc. |
Pyrazolopyrimidine pi3k inhibitor compounds and methods of use
|
|
WO2009114870A2
(en)
*
|
2008-03-14 |
2009-09-17 |
Intellikine, Inc. |
Kinase inhibitors and methods of use
|
|
WO2010006072A2
(en)
|
2008-07-08 |
2010-01-14 |
The Regents Of The University Of California |
Mtor modulators and uses thereof
|
|
ES2439291T3
(es)
|
2008-09-02 |
2014-01-22 |
Janssen Pharmaceuticals, Inc. |
Derivados de 3-azabiciclo[3.1.0]hexilo como moduladores de receptores de glutamato metabotrópicos
|
|
US8220787B2
(en)
*
|
2008-09-19 |
2012-07-17 |
Panasonic Corporation |
Part mounting device
|
|
ES2392488T3
(es)
|
2008-11-20 |
2012-12-11 |
Genentech, Inc. |
Compuestos inhibidores de PI3K de tipo pirazolopiridina y sus procedimientos de uso
|
|
ES2401691T3
(es)
|
2008-11-28 |
2013-04-23 |
Ortho-Mcneil-Janssen Pharmaceuticals, Inc. |
Derivados de indol y de benzoxacina como moduladores de los receptores metabotrópicos de glutamato
|
|
JP5634506B2
(ja)
|
2009-05-12 |
2014-12-03 |
ジャンセン ファーマシューティカルズ, インコーポレイテッド |
1,2,3−トリアゾロ[4,3−a]ピリジン誘導体ならびに神経障害および精神障害の治療または予防のためのその使用
|
|
MY153913A
(en)
|
2009-05-12 |
2015-04-15 |
Janssen Pharmaceuticals Inc |
7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors
|
|
AU2010246607B2
(en)
|
2009-05-12 |
2012-09-27 |
Addex Pharma S.A. |
1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mGluR2 receptors
|
|
EA021595B1
(ru)
|
2009-06-29 |
2015-07-30 |
Инсайт Корпорейшн |
Пиримидиноны в качестве ингибиторов pi3k
|
|
WO2011075643A1
(en)
|
2009-12-18 |
2011-06-23 |
Incyte Corporation |
Substituted heteroaryl fused derivatives as pi3k inhibitors
|
|
GB201004311D0
(en)
|
2010-03-15 |
2010-04-28 |
Proximagen Ltd |
New enzyme inhibitor compounds
|
|
AR081823A1
(es)
|
2010-04-14 |
2012-10-24 |
Incyte Corp |
DERIVADOS FUSIONADOS COMO INHIBIDORES DE PI3Kd
|
|
US9290499B2
(en)
|
2010-05-19 |
2016-03-22 |
The University Of North Carolina At Chapel Hill |
Pyrazolopyrimidine compounds for the treatment of cancer
|
|
WO2011163195A1
(en)
|
2010-06-21 |
2011-12-29 |
Incyte Corporation |
Fused pyrrole derivatives as pi3k inhibitors
|
|
JP5852666B2
(ja)
|
2010-11-08 |
2016-02-03 |
ジヤンセン・フアーマシユーチカルズ・インコーポレーテツド |
1,2,4−トリアゾロ[4,3−a]ピリジン誘導体およびmGluR2受容体のポジティブアロステリックモジュレーターとしてのそれらの使用
|
|
ES2552455T3
(es)
|
2010-11-08 |
2015-11-30 |
Janssen Pharmaceuticals, Inc. |
Derivados de 1,2,4-triazolo[4,3-a]piridina y su uso como moduladores alostéricos positivos de receptores mGluR2
|
|
JP5852665B2
(ja)
|
2010-11-08 |
2016-02-03 |
ジヤンセン・フアーマシユーチカルズ・インコーポレーテツド |
1,2,4−トリアゾロ[4,3−a]ピリジン誘導体およびmGluR2受容体のポジティブアロステリックモジュレーターとしてのそれらの使用
|
|
TW201249844A
(en)
|
2010-12-20 |
2012-12-16 |
Incyte Corp |
N-(1-(substituted-phenyl)ethyl)-9H-purin-6-amines as PI3K inhibitors
|
|
US8362023B2
(en)
|
2011-01-19 |
2013-01-29 |
Hoffmann-La Roche Inc. |
Pyrazolo pyrimidines
|
|
WO2012125629A1
(en)
|
2011-03-14 |
2012-09-20 |
Incyte Corporation |
Substituted diamino-pyrimidine and diamino-pyridine derivatives as pi3k inhibitors
|
|
US9126948B2
(en)
|
2011-03-25 |
2015-09-08 |
Incyte Holdings Corporation |
Pyrimidine-4,6-diamine derivatives as PI3K inhibitors
|
|
TWI543980B
(zh)
|
2011-09-02 |
2016-08-01 |
英塞特控股公司 |
作為pi3k抑制劑之雜環基胺
|
|
AU2011376717A1
(en)
|
2011-09-14 |
2014-03-20 |
Proximagen Limited |
New enzyme inhibitor compounds
|
|
GB201115853D0
(en)
*
|
2011-09-14 |
2011-10-26 |
Proximagen Ltd |
New enzyme inhibitor compounds
|
|
ES2650630T3
(es)
|
2011-10-03 |
2018-01-19 |
The University Of North Carolina At Chapel Hill |
Compuestos de pirrolopirimidina para el tratamiento del cáncer
|
|
AR090548A1
(es)
|
2012-04-02 |
2014-11-19 |
Incyte Corp |
Azaheterociclobencilaminas biciclicas como inhibidores de pi3k
|
|
KR20150018789A
(ko)
|
2012-05-22 |
2015-02-24 |
더 유니버시티 오브 노쓰 캐롤라이나 엣 채플 힐 |
암의 치료를 위한 피리미딘 화합물
|
|
US9562047B2
(en)
|
2012-10-17 |
2017-02-07 |
The University Of North Carolina At Chapel Hill |
Pyrazolopyrimidine compounds for the treatment of cancer
|
|
WO2014085225A1
(en)
|
2012-11-27 |
2014-06-05 |
The University Of North Carolina At Chapel Hill |
Pyrimidine compounds for the treatment of cancer
|
|
TWI629275B
(zh)
*
|
2013-03-13 |
2018-07-11 |
賽諾菲公司 |
N-(4-(氮雜吲唑-6-基)-苯基)-磺醯胺及其作為醫藥之用途
|
|
JO3368B1
(ar)
|
2013-06-04 |
2019-03-13 |
Janssen Pharmaceutica Nv |
مركبات 6، 7- ثاني هيدرو بيرازولو [5،1-a] بيرازين- 4 (5 يد)- اون واستخدامها بصفة منظمات تفارغية سلبية لمستقبلات ميجلور 2
|
|
JO3367B1
(ar)
|
2013-09-06 |
2019-03-13 |
Janssen Pharmaceutica Nv |
مركبات 2،1، 4- ثلاثي زولو [3،4-a] بيريدين واستخدامها بصفة منظمات تفارغية موجبة لمستقبلات ميجلور 2
|
|
KR20220038826A
(ko)
|
2014-01-21 |
2022-03-29 |
얀센 파마슈티카 엔.브이. |
대사 조절형 글루탐산 작동성 수용체 제2아형의 양성 알로스테릭 조절제 또는 오르토스테릭 작동제를 포함하는 조합 및 그 용도
|
|
KR20200036063A
(ko)
|
2014-01-21 |
2020-04-06 |
얀센 파마슈티카 엔.브이. |
대사 조절형 글루탐산 작동성 수용체 제2아형의 양성 알로스테릭 조절제 또는 오르토스테릭 작동제를 포함하는 조합 및 그 용도
|
|
US20150291609A1
(en)
|
2014-04-11 |
2015-10-15 |
The University Of North Carolina At Chapel Hill |
Mertk-specific pyrimidine compounds
|
|
WO2015191677A1
(en)
|
2014-06-11 |
2015-12-17 |
Incyte Corporation |
Bicyclic heteroarylaminoalkyl phenyl derivatives as pi3k inhibitors
|
|
ES2747249T3
(es)
|
2014-07-17 |
2020-03-10 |
Sunshine Lake Pharma Co Ltd |
Derivados de 1-(5-(terc-butil)isoxazol-3-il)-3-(4-((fenil)etinil)fenil)urea y compuestos relacionados como inhibidores de FLT3 para el tratamiento de cáncer
|
|
MA55193B1
(fr)
|
2015-02-27 |
2022-10-31 |
Incyte Holdings Corp |
Procédés de préparation d'un inhibiteur de pi3k
|
|
US9732097B2
(en)
|
2015-05-11 |
2017-08-15 |
Incyte Corporation |
Process for the synthesis of a phosphoinositide 3-kinase inhibitor
|
|
US9988401B2
(en)
|
2015-05-11 |
2018-06-05 |
Incyte Corporation |
Crystalline forms of a PI3K inhibitor
|
|
US10709708B2
(en)
|
2016-03-17 |
2020-07-14 |
The University Of North Carolina At Chapel Hill |
Method of treating cancer with a combination of MER tyrosine kinase inhibitor and an epidermal growth factor receptor (EGFR) inhibitor
|
|
GB201801562D0
(en)
|
2018-01-31 |
2018-03-14 |
Almac Diagnostics Ltd |
Pharmaceutical compounds
|
|
EP3801533B1
(de)
|
2018-06-01 |
2026-03-04 |
Incyte Corporation |
Dosierungsschema zur behandlung von störungen im zusammenhang mit pi3k
|
|
JP2021527051A
(ja)
*
|
2018-06-05 |
2021-10-11 |
ラプト・セラピューティクス・インコーポレイテッド |
ピラゾロ−ピリミジン−アミノ−シクロアルキル化合物及びその治療的使用
|
|
JP2022512128A
(ja)
|
2018-12-06 |
2022-02-02 |
アルマック・ディスカバリー・リミテッド |
医薬化合物およびユビキチン特異的プロテアーゼ19(usp19)阻害剤としてのその使用
|