|
GB581334A
(en)
|
1943-09-29 |
1946-10-09 |
Francis Henry Swinden Curd |
New pyrimidine compounds
|
|
JPS4921148B1
(enExample)
|
1970-12-28 |
1974-05-30 |
|
|
|
JPS4921149B1
(enExample)
|
1970-12-28 |
1974-05-30 |
|
|
|
DE2341925A1
(de)
|
1973-08-20 |
1975-03-06 |
Thomae Gmbh Dr K |
Neue pyrimidinderivate und verfahren zu ihrer herstellung
|
|
AT340933B
(de)
|
1973-08-20 |
1978-01-10 |
Thomae Gmbh Dr K |
Verfahren zur herstellung neuer pyrimidinderivate und ihrer saureadditionssalze
|
|
US4994386A
(en)
|
1987-07-13 |
1991-02-19 |
Pharmacia Diagnostics, Inc. |
Production of HBLV virus in the HSB-2 cell line
|
|
US4929726A
(en)
|
1988-02-09 |
1990-05-29 |
Georgia State University Foundation, Inc. |
Novel diazines and their method of preparation
|
|
EP0330263A1
(en)
|
1988-02-25 |
1989-08-30 |
Merck & Co. Inc. |
Piperazinylalkylpyrimidines as hypoglycemic agents
|
|
GB9012311D0
(en)
|
1990-06-01 |
1990-07-18 |
Wellcome Found |
Pharmacologically active cns compounds
|
|
DE69120221T2
(de)
|
1990-07-03 |
1996-11-21 |
Mitsui Petrochemical Ind |
Pyrimidin-verbindung und ihr pharmazeutisch annehmbares salz
|
|
AU692090B2
(en)
|
1995-04-13 |
1998-05-28 |
Taiho Pharmaceutical Co., Ltd. |
Novel 4,6-diarylpyrimidine derivatives and salts thereof
|
|
JP3734907B2
(ja)
|
1996-12-19 |
2006-01-11 |
富士写真フイルム株式会社 |
現像処理方法
|
|
DK1020462T3
(da)
|
1997-07-24 |
2004-04-26 |
Zenyaku Kogyo Kk |
Heterocykliske forbindelser og antitumormiddel indeholdende disse som aktiv ingrediens
|
|
JPH11158073A
(ja)
|
1997-09-26 |
1999-06-15 |
Takeda Chem Ind Ltd |
アデノシンa3拮抗剤
|
|
US6440965B1
(en)
|
1997-10-15 |
2002-08-27 |
Krenitsky Pharmaceuticals, Inc. |
Substituted pyrimidine derivatives, their preparation and their use in the treatment of neurodegenerative or neurological disorders of the central nervous system
|
|
US6150362A
(en)
|
1997-12-12 |
2000-11-21 |
Henkin; Jack |
Triazine angiogenesis inhibitors
|
|
ES2193607T3
(es)
|
1998-01-16 |
2003-11-01 |
Hoffmann La Roche |
Derivados de benzosulfona .
|
|
WO1999065897A1
(en)
|
1998-06-19 |
1999-12-23 |
Chiron Corporation |
Inhibitors of glycogen synthase kinase 3
|
|
US7045519B2
(en)
|
1998-06-19 |
2006-05-16 |
Chiron Corporation |
Inhibitors of glycogen synthase kinase 3
|
|
JP2002535318A
(ja)
|
1999-01-22 |
2002-10-22 |
アムジエン・インコーポレーテツド |
キナーゼ阻害薬
|
|
US6495558B1
(en)
|
1999-01-22 |
2002-12-17 |
Amgen Inc. |
Kinase inhibitors
|
|
EP1206265B1
(en)
|
1999-06-30 |
2003-11-12 |
Merck & Co., Inc. |
Src kinase inhibitor compounds
|
|
JP2003503354A
(ja)
|
1999-06-30 |
2003-01-28 |
メルク エンド カムパニー インコーポレーテッド |
Srcキナーゼ阻害剤化合物
|
|
US6329380B1
(en)
|
1999-06-30 |
2001-12-11 |
Merck & Co., Inc. |
SRC kinase inhibitor compounds
|
|
ATE250053T1
(de)
|
1999-07-15 |
2003-10-15 |
Pharmacopeia Inc |
Bradikinin b1 rezeptor antagonisten
|
|
JP2001089452A
(ja)
|
1999-09-22 |
2001-04-03 |
Sankyo Co Ltd |
ピリミジン誘導体
|
|
AU2001237041B9
(en)
|
2000-02-17 |
2005-07-28 |
Amgen Inc. |
Kinase inhibitors
|
|
WO2001072745A1
(en)
|
2000-03-29 |
2001-10-04 |
Cyclacel Limited |
2-substituted 4-heteroaryl-pyrimidines and their use in the treatmetn of proliferative disorders
|
|
ES2360933T3
(es)
|
2000-04-27 |
2011-06-10 |
Astellas Pharma Inc. |
Derivados de heteroarilo condensados.
|
|
KR100711042B1
(ko)
|
2000-04-28 |
2007-04-24 |
다나베 세이야꾸 가부시키가이샤 |
환상 화합물
|
|
WO2002000647A1
(en)
|
2000-06-23 |
2002-01-03 |
Bristol-Myers Squibb Pharma Company |
Heteroaryl-phenyl substituted factor xa inhibitors
|
|
EP1317433A2
(en)
|
2000-09-06 |
2003-06-11 |
Chiron Corporation |
Inhibitors of glycogen synthase kinase 3
|
|
EP1318814B1
(en)
|
2000-09-15 |
2007-05-30 |
Vertex Pharmaceuticals Incorporated |
Triazole compounds useful as protein kinase inhibitors
|
|
SE0004053D0
(sv)
|
2000-11-06 |
2000-11-06 |
Astrazeneca Ab |
N-type calcium channel antagonists for the treatment of pain
|
|
US7625913B2
(en)
|
2000-12-21 |
2009-12-01 |
Vertex Pharmaceuticals Incorporated |
Pyrazole compounds useful as protein kinase inhibitors
|
|
WO2002062766A2
(en)
|
2001-02-07 |
2002-08-15 |
Millennium Pharmaceuticals, Inc. |
Melanocortin-4 receptor binding compounds and methods of use thereof
|
|
US20030130264A1
(en)
|
2001-02-16 |
2003-07-10 |
Tularik Inc. |
Methods of using pyrimidine-based antiviral agents
|
|
MXPA03010724A
(es)
|
2001-05-25 |
2004-03-02 |
Boehringer Ingelheim Pharma |
Compuestos de carbamato y oxamida como inhibidores de la produccion de citocina.
|
|
JP2005500294A
(ja)
|
2001-06-19 |
2005-01-06 |
ブリストル−マイヤーズ スクイブ カンパニー |
ホスホジエステラーゼ7に対するピリミジン阻害剤
|
|
US6603000B2
(en)
|
2001-07-11 |
2003-08-05 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Synthesis for heteroarylamine compounds
|
|
WO2003030909A1
(en)
|
2001-09-25 |
2003-04-17 |
Bayer Pharmaceuticals Corporation |
2- and 4-aminopyrimidines n-substtituded by a bicyclic ring for use as kinase inhibitors in the treatment of cancer
|
|
DE60314603T2
(de)
|
2002-03-15 |
2008-02-28 |
Vertex Pharmaceuticals Inc., Cambridge |
Zusammensetzungen brauchbar als protein-kinase-inhibitoren
|
|
ATE466580T1
(de)
|
2002-03-15 |
2010-05-15 |
Vertex Pharma |
Azolylaminoazine als proteinkinasehemmer
|
|
AU2003225800A1
(en)
|
2002-03-15 |
2003-09-29 |
Hayley Binch |
Azolylaminoazine as inhibitors of protein kinases
|
|
DE60332604D1
(de)
|
2002-03-15 |
2010-07-01 |
Vertex Pharma |
Azolylaminoazine als proteinkinasehemmer
|
|
AU2003245669A1
(en)
|
2002-06-21 |
2004-01-06 |
Cellular Genomics, Inc. |
Certain aromatic monocycles as kinase modulators
|
|
US7405221B2
(en)
|
2002-09-27 |
2008-07-29 |
Merck & Co., Inc. |
Substituted pyrimidines
|
|
AU2003288925A1
(en)
|
2002-10-08 |
2004-05-04 |
Massachusetts Institute Of Technology |
Compounds for modulation of cholesterol transport
|
|
US7223870B2
(en)
|
2002-11-01 |
2007-05-29 |
Pfizer Inc. |
Methods for preparing N-arylated oxazolidinones via a copper catalyzed cross coupling reaction
|
|
ES2412273T3
(es)
|
2002-11-21 |
2013-07-10 |
Novartis Ag |
Inhibidores de 2-morfolín-4-pirimidinas como inhibidores de fosfotidilinositol (PI) 3-quinasa y su uso en el tratamiento del cáncer.
|
|
EP1631260A2
(en)
|
2003-02-28 |
2006-03-08 |
Transform Pharmaceuticals, Inc. |
Pharmaceutical co-crystal compositions of drugs such as carbamazepine, celecoxib, olanzapine, itraconazole, topiramate, modafinil, 5-fluorouracil, hydrochlorothazide, acetaminophen, aspirin, flurbiprofen, phenytoin and ibuprofen
|
|
AU2004224392A1
(en)
|
2003-03-24 |
2004-10-07 |
Merck & Co., Inc. |
Biaryl substituted 6-membered heterocyles as sodium channel blockers
|
|
US20050014753A1
(en)
|
2003-04-04 |
2005-01-20 |
Irm Llc |
Novel compounds and compositions as protein kinase inhibitors
|
|
US7763627B2
(en)
|
2003-04-09 |
2010-07-27 |
Exelixis, Inc. |
Tie-2 modulators and methods of use
|
|
WO2005009977A1
(en)
|
2003-07-15 |
2005-02-03 |
Neurogen Corporation |
Substituted pyrimidin-4-ylamina analogues as vanilloid receptor ligands
|
|
EP1644358A2
(en)
|
2003-07-16 |
2006-04-12 |
Neurogen Corporation |
Biaryl piperazinyl-pyridine analogues
|
|
PE20050952A1
(es)
*
|
2003-09-24 |
2005-12-19 |
Novartis Ag |
Derivados de isoquinolina como inhibidores de b-raf
|
|
ATE485824T1
(de)
|
2004-04-13 |
2010-11-15 |
Icagen Inc |
Polycyclische pyrimidine als kaliumionenkanal- modulatoren
|
|
GB0415364D0
(en)
|
2004-07-09 |
2004-08-11 |
Astrazeneca Ab |
Pyrimidine derivatives
|
|
GB0415365D0
(en)
|
2004-07-09 |
2004-08-11 |
Astrazeneca Ab |
Pyrimidine derivatives
|
|
MY145822A
(en)
|
2004-08-13 |
2012-04-30 |
Neurogen Corp |
Substituted biaryl piperazinyl-pyridine analogues
|
|
US7652009B2
(en)
*
|
2004-11-30 |
2010-01-26 |
Amgem Inc. |
Substituted heterocycles and methods of use
|
|
CA2590299A1
(en)
|
2004-12-13 |
2006-06-22 |
Neurogen Corporation |
Piperazinyl-pyridine analogues
|
|
AU2005322328A1
(en)
|
2004-12-13 |
2006-07-06 |
Neurogen Corporation |
Substituted biaryl analogues
|
|
EP1836169B9
(en)
|
2004-12-28 |
2012-07-04 |
Kinex Pharmaceuticals, LLC |
Compositions and methods of treating cell proliferation disorders
|
|
US20080124384A1
(en)
|
2005-01-19 |
2008-05-29 |
Blum Charles A |
Heteroaryl Substituted Piperazinyl-Pyridine Analogues
|
|
EP1877388A2
(en)
|
2005-02-25 |
2008-01-16 |
Kudos Pharmaceuticals Ltd |
Hydrazinomethyl, hydrazonomethyl and 5-membered heterocylic compounds which act as mtor inhibitors and their use as anti cancer agents
|
|
JP2008536950A
(ja)
|
2005-04-18 |
2008-09-11 |
ニューロジェン・コーポレーション |
置換ヘテロアリールのcb1拮抗薬
|
|
GB2431156A
(en)
|
2005-10-11 |
2007-04-18 |
Piramed Ltd |
1-cyclyl-3-substituted- -benzenes and -azines as inhibitors of phosphatidylinositol 3-kinase
|
|
CA2635997A1
(en)
|
2006-01-11 |
2007-07-19 |
Astrazeneca Ab |
Morpholino pyrimidine derivatives and their use in therapy
|
|
JO2660B1
(en)
|
2006-01-20 |
2012-06-17 |
نوفارتيس ايه جي |
Pi-3 inhibitors and methods of use
|
|
EP2012794B1
(en)
*
|
2006-04-13 |
2014-09-17 |
The Trustees of Columbia University in the City of New York |
Compositions and intraluminal devices for inhibiting vascular stenosis
|
|
WO2008080937A1
(en)
|
2006-12-28 |
2008-07-10 |
Basf Se |
2-substituted pyrimidines i in therapy
|
|
JP2010518107A
(ja)
|
2007-02-06 |
2010-05-27 |
ノバルティス アーゲー |
Pi3−キナーゼ阻害剤およびその使用方法
|
|
US7957951B2
(en)
|
2007-03-16 |
2011-06-07 |
Robert Bosch Gmbh |
Address translation system for use in a simulation environment
|
|
BRPI0814818A2
(pt)
|
2007-07-09 |
2019-09-10 |
Astrazeneca Ab |
composto, uso de um composto, métodos para produzir um efeito anti-proliferativo e um efeito inibitório de mtor quinase em uma animal de sangue quente, método para tratar doenças, e, composição farmacêutica
|
|
WO2009066084A1
(en)
|
2007-11-21 |
2009-05-28 |
F. Hoffmann-La Roche Ag |
2 -morpholinopyrimidines and their use as pi3 kinase inhibitors
|
|
RU2496500C2
(ru)
|
2008-03-05 |
2013-10-27 |
Новартис Аг |
Применение производных пиримидина для лечения egfr-зависимых заболеваний или заболеваний с приобретенной резистентностью к агентам, направленным против членов семейства egfr
|
|
AU2009228797B2
(en)
|
2008-03-26 |
2012-07-19 |
Novartis Ag |
5imidazoquinolines and pyrimidine derivatives as potent modulators of VEGF-driven angiogenic processes
|
|
US20110053907A1
(en)
|
2008-03-27 |
2011-03-03 |
Auckland Uniservices Limited |
Substituted pyrimidines and triazines and their use in cancer therapy
|
|
WO2009125870A1
(en)
|
2008-04-09 |
2009-10-15 |
Mitsubishi Tanabe Pharma Corporation |
Pyrimidine, pyridine and triazine derivatives as maxi-k channel openers.
|
|
GB0815369D0
(en)
|
2008-08-22 |
2008-10-01 |
Summit Corp Plc |
Compounds for treatment of duchenne muscular dystrophy
|
|
EP2349275B1
(en)
|
2008-10-31 |
2017-03-08 |
Novartis AG |
Combination of a phosphatidylinositol-3-kinase (pi3k) inhibitor and a mtor inhibitor.
|
|
GB2465405A
(en)
|
2008-11-10 |
2010-05-19 |
Univ Basel |
Triazine, pyrimidine and pyridine analogues and their use in therapy
|
|
WO2010068863A2
(en)
|
2008-12-12 |
2010-06-17 |
Cystic Fibrosis Foundation Therapeutics, Inc. |
Pyrimidine compounds and methods of making and using same
|
|
JP5263304B2
(ja)
|
2009-02-06 |
2013-08-14 |
日本新薬株式会社 |
アミノピラジン誘導体及び医薬
|
|
JP5747440B2
(ja)
|
2009-02-06 |
2015-07-15 |
住友化学株式会社 |
ヒドラジド化合物及びその有害生物防除用途
|
|
AU2010223919B2
(en)
|
2009-03-13 |
2016-03-31 |
Les Laboratoires Servier |
Methods and compositions for cell-proliferation-related disorders
|
|
WO2010120994A2
(en)
|
2009-04-17 |
2010-10-21 |
Wyeth Llc |
Ureidoaryl-and carbamoylaryl-morpholino- pyrimidine compounds, their use as mtor kinase and pi3 kinase inhibitors, and their synthesis
|
|
JP2012527461A
(ja)
|
2009-05-19 |
2012-11-08 |
ダウ アグロサイエンシィズ エルエルシー |
真菌を防除するための化合物および方法
|
|
TW201105662A
(en)
|
2009-07-07 |
2011-02-16 |
Pathway Therapeutics Ltd |
Pyrimidinyl and 1,3,5-triazinyl benzimidazoles and their use in cancer therapy
|
|
TWI393716B
(zh)
|
2009-08-04 |
2013-04-21 |
Merck Sharp & Dohme |
作為ixa因子抑制劑之雜環化合物
|
|
AR077999A1
(es)
|
2009-09-02 |
2011-10-05 |
Vifor Int Ag |
Antagonistas de pirimidin y triazin-hepcidina
|
|
AU2010292198A1
(en)
|
2009-09-09 |
2012-04-05 |
Celgene Avilomics Research, Inc. |
PI3 kinase inhibitors and uses thereof
|
|
ES2642109T3
(es)
|
2009-12-09 |
2017-11-15 |
Agios Pharmaceuticals, Inc. |
Compuestos terapéuticamente activos para su uso en el tratamiento de cáncer caracterizados por tener una mutación de IDH
|
|
GB201004200D0
(en)
|
2010-03-15 |
2010-04-28 |
Univ Basel |
Spirocyclic compounds and their use as therapeutic agents and diagnostic probes
|
|
AR081626A1
(es)
|
2010-04-23 |
2012-10-10 |
Cytokinetics Inc |
Compuestos amino-piridazinicos, composiciones farmaceuticas que los contienen y uso de los mismos para tratar trastornos musculares cardiacos y esqueleticos
|
|
AR081331A1
(es)
|
2010-04-23 |
2012-08-08 |
Cytokinetics Inc |
Amino- pirimidinas composiciones de las mismas y metodos para el uso de los mismos
|
|
EP2560488B1
(en)
|
2010-04-23 |
2015-10-28 |
Cytokinetics, Inc. |
Certain amino-pyridines and amino-triazines, compositions thereof, and methods for their use
|
|
US20130109643A1
(en)
|
2010-05-10 |
2013-05-02 |
The Johns Hopkins University |
Metabolic inhibitor against tumors having an idh mutation
|
|
CN103097340B
(zh)
|
2010-07-16 |
2018-03-16 |
安吉奥斯医药品有限公司 |
治疗活性组合物及其使用方法
|
|
AR083213A1
(es)
|
2010-10-01 |
2013-02-06 |
Novartis Ag |
Proceso de preparacion de derivados pirimidinicos, compuestos intermediarios y proceso para prepararlos
|
|
WO2012054535A2
(en)
|
2010-10-18 |
2012-04-26 |
Cerenis Therapeutics Sa |
Compounds, compositions and methods useful for cholesterol mobilisation
|
|
GB201106829D0
(en)
|
2011-04-21 |
2011-06-01 |
Proximagen Ltd |
Heterocyclic compounds
|
|
WO2012109423A1
(en)
|
2011-02-11 |
2012-08-16 |
Dana-Farber Cancer Institute, Inc. |
Method of inhibiting hamartoma tumor cells
|
|
CN102827073A
(zh)
|
2011-06-17 |
2012-12-19 |
安吉奥斯医药品有限公司 |
治疗活性组合物和它们的使用方法
|
|
AU2012300835A1
(en)
|
2011-09-01 |
2014-03-13 |
Novartis Ag |
PI3K inhibitor for use in the treatment of bone cancer or for preventing metastatic dissemination primary cancer cells into the bone
|
|
CU24269B1
(es)
|
2011-09-27 |
2017-08-08 |
Novartis Ag |
3- pirimidin- 4-il- oxazolidin- 2- onas inhibidores de la idh mutante
|
|
JP2014528446A
(ja)
|
2011-10-06 |
2014-10-27 |
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. |
1,3−置換アゼチジンpde10阻害剤
|
|
UY34632A
(es)
|
2012-02-24 |
2013-05-31 |
Novartis Ag |
Compuestos de oxazolidin- 2- ona y usos de los mismos
|
|
SG11201406550QA
(en)
*
|
2012-05-16 |
2014-11-27 |
Novartis Ag |
Dosage regimen for a pi-3 kinase inhibitor
|
|
WO2013184621A1
(en)
|
2012-06-06 |
2013-12-12 |
Novartis Ag |
Combination of a 17 -alpha -hydroxylase (c17, 20 - lyase) inhibitor and a specific pi-3k inhibitor for treating a tumor disease
|
|
JP2015529194A
(ja)
|
2012-08-16 |
2015-10-05 |
ノバルティス アーゲー |
PI3Kインヒビターとc−Metインヒビターの組み合わせ
|
|
MX360703B
(es)
|
2012-10-23 |
2018-11-14 |
Novartis Ag |
Proceso mejorado para la elaboración de 5-(2, 6-di-4-morfolinil-4-pirimidinil)-4-trifluoro-metil-piridin-2-amin a.
|
|
US9296733B2
(en)
|
2012-11-12 |
2016-03-29 |
Novartis Ag |
Oxazolidin-2-one-pyrimidine derivative and use thereof for the treatment of conditions, diseases and disorders dependent upon PI3 kinases
|
|
KR20150127197A
(ko)
|
2013-03-14 |
2015-11-16 |
노파르티스 아게 |
돌연변이 idh의 억제제로서의 3-피리미딘-4-일-옥사졸리딘-2-온
|
|
CA2903979A1
(en)
|
2013-03-14 |
2014-09-18 |
Novartis Ag |
3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh
|
|
CN103483345B
(zh)
|
2013-09-25 |
2016-07-06 |
中山大学 |
Pi3k激酶抑制剂、包含其的药物组合物及其应用
|
|
CN103694218B
(zh)
|
2013-12-05 |
2016-04-27 |
中山大学 |
嘧啶化合物、pi3k抑制剂、包含pi3k抑制剂的药物组合物及应用
|