US4522811A
(en)
|
1982-07-08 |
1985-06-11 |
Syntex (U.S.A.) Inc. |
Serial injection of muramyldipeptides and liposomes enhances the anti-infective activity of muramyldipeptides
|
US5593992A
(en)
|
1993-07-16 |
1997-01-14 |
Smithkline Beecham Corporation |
Compounds
|
US5670527A
(en)
|
1993-07-16 |
1997-09-23 |
Smithkline Beecham Corporation |
Pyridyl imidazole compounds and compositions
|
US5658903A
(en)
|
1995-06-07 |
1997-08-19 |
Smithkline Beecham Corporation |
Imidazole compounds, compositions and use
|
US6369068B1
(en)
|
1995-06-07 |
2002-04-09 |
Smithkline Beecham Corporation |
Amino substituted pyrimidine containing compounds
|
EP0883402A4
(en)
|
1996-01-11 |
1999-08-11 |
Smithkline Beecham Corp |
NEW CYCLOALKYL-SUBSTITUTED IMIDAZOLES
|
AP9700912A0
(en)
|
1996-01-11 |
1997-01-31 |
Smithkline Beecham Corp |
Novel cycloalkyl substituted imidazoles
|
ZA97175B
(en)
|
1996-01-11 |
1997-11-04 |
Smithkline Beecham Corp |
Novel substituted imidazole compounds.
|
JP2000507224A
(ja)
|
1996-03-08 |
2000-06-13 |
スミスクライン・ビーチャム・コーポレイション |
Csaid化合物の血管形成の抑制物質としての使用
|
JP2000510327A
(ja)
|
1996-03-12 |
2000-08-15 |
スミスクライン・ビーチャム・コーポレイション |
医薬的に活性な化合物の同定方法
|
US6096748A
(en)
|
1996-03-13 |
2000-08-01 |
Smithkline Beecham Corporation |
Pyrimidine compounds useful in treating cytokine mediated diseases
|
JP2000507545A
(ja)
|
1996-03-25 |
2000-06-20 |
スミスクライン・ビーチャム・コーポレイション |
Cns損傷についての新規な治療
|
US6096739A
(en)
|
1996-03-25 |
2000-08-01 |
Smithkline Beecham Corporation |
Treatment for CNS injuries
|
WO1998007425A1
(en)
|
1996-08-21 |
1998-02-26 |
Smithkline Beecham Corporation |
Imidazole compounds, compositions and use
|
US6096753A
(en)
|
1996-12-05 |
2000-08-01 |
Amgen Inc. |
Substituted pyrimidinone and pyridone compounds and methods of use
|
US6147080A
(en)
|
1996-12-18 |
2000-11-14 |
Vertex Pharmaceuticals Incorporated |
Inhibitors of p38
|
WO1998028292A1
(en)
|
1996-12-23 |
1998-07-02 |
Smithkline Beecham Corporation |
Novel piperidine containing compounds
|
NZ500447A
(en)
|
1997-04-24 |
2001-09-28 |
Ortho Mcneil Pharm Inc |
Substituted imidazoles that inhibit cytokine production and are useful in the treatment of inflammatory disease
|
US6514977B1
(en)
|
1997-05-22 |
2003-02-04 |
G.D. Searle & Company |
Substituted pyrazoles as p38 kinase inhibitors
|
JP2002504909A
(ja)
|
1997-06-13 |
2002-02-12 |
スミスクライン・ビーチャム・コーポレイション |
新規な置換ピラゾールおよびピラゾリン化合物
|
CA2294137A1
(en)
|
1997-06-19 |
1998-12-23 |
Smithkline Beecham Corporation |
Novel aryloxy substituted pyrimidine imidazole compounds
|
US6093742A
(en)
|
1997-06-27 |
2000-07-25 |
Vertex Pharmaceuticals, Inc. |
Inhibitors of p38
|
TW517055B
(en)
|
1997-07-02 |
2003-01-11 |
Smithkline Beecham Corp |
Novel substituted imidazole compounds
|
AR016294A1
(es)
|
1997-07-02 |
2001-07-04 |
Smithkline Beecham Corp |
Compuesto de imidazol sustituido, composicion farmaceutica que la contiene, su uso en la fabricacion de un medicamento y procedimiento para supreparacion
|
GB9721437D0
(en)
|
1997-10-10 |
1997-12-10 |
Glaxo Group Ltd |
Heteroaromatic compounds and their use in medicine
|
EP1025102B1
(en)
|
1997-10-20 |
2004-05-19 |
F. Hoffmann-La Roche Ag |
Bicyclic kinase inhibitors
|
US6162613A
(en)
|
1998-02-18 |
2000-12-19 |
Vertex Pharmaceuticals, Inc. |
Methods for designing inhibitors of serine/threonine-kinases and tyrosine kinases
|
PL344004A1
(en)
|
1998-05-05 |
2001-09-10 |
Hoffmann La Roche |
Pyrazole derivatives as p-38 map kinase inhibitors
|
US6316466B1
(en)
|
1998-05-05 |
2001-11-13 |
Syntex (U.S.A.) Llc |
Pyrazole derivatives P-38 MAP kinase inhibitors
|
MY132496A
(en)
|
1998-05-11 |
2007-10-31 |
Vertex Pharma |
Inhibitors of p38
|
US6340685B1
(en)
|
1998-05-22 |
2002-01-22 |
Scios, Inc. |
Compounds and methods to treat cardiac failure and other disorders
|
PL344330A1
(en)
|
1998-05-22 |
2001-10-22 |
Smithkline Beecham Corp |
Novel 2-alkyl substituted imidazole compounds
|
US6589954B1
(en)
|
1998-05-22 |
2003-07-08 |
Scios, Inc. |
Compounds and methods to treat cardiac failure and other disorders
|
US6448257B1
(en)
|
1998-05-22 |
2002-09-10 |
Scios, Inc. |
Compounds and methods to treat cardiac failure and other disorders
|
CN1229351C
(zh)
|
1998-05-22 |
2005-11-30 |
西奥斯股份有限公司 |
杂环化合物和治疗心力衰竭及其它疾病的方法
|
US6867209B1
(en)
|
1998-05-22 |
2005-03-15 |
Scios, Inc. |
Indole-type derivatives as inhibitors of p38 kinase
|
WO1999064400A1
(en)
|
1998-06-12 |
1999-12-16 |
Vertex Pharmaceuticals Incorporated |
INHIBITORS OF p38
|
EP1112070B1
(en)
|
1998-08-20 |
2004-05-12 |
Smithkline Beecham Corporation |
Novel substituted triazole compounds
|
US6184226B1
(en)
|
1998-08-28 |
2001-02-06 |
Scios Inc. |
Quinazoline derivatives as inhibitors of P-38 α
|
EP1114039A1
(en)
|
1998-09-18 |
2001-07-11 |
Vertex Pharmaceuticals Incorporated |
INHIBITORS OF p38
|
WO2000019824A1
(en)
|
1998-10-07 |
2000-04-13 |
Smithkline Beecham Corporation |
Novel treatment for stroke management
|
JP2002528506A
(ja)
|
1998-11-04 |
2002-09-03 |
スミスクライン・ビーチャム・コーポレイション |
ピリジン−4−イルまたはピリミジン−4−イル置換ピラジン
|
UA73492C2
(en)
|
1999-01-19 |
2005-08-15 |
|
Aromatic heterocyclic compounds as antiinflammatory agents
|
PL351148A1
(en)
|
1999-04-23 |
2003-03-24 |
Takeda Chemical Industries Ltd |
5-pyridyl-1,3-azole compounds, process for producing the same and use thereof
|
AU772295B2
(en)
|
1999-05-21 |
2004-04-22 |
Scios Inc. |
Indole-type derivatives as inhibitors of p38 kinase
|
JP4162406B2
(ja)
|
1999-07-09 |
2008-10-08 |
ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド |
ヘテロアリール置換ウレア化合物の新規合成方法
|
US6541477B2
(en)
|
1999-08-27 |
2003-04-01 |
Scios, Inc. |
Inhibitors of p38-a kinase
|
BR0014041A
(pt)
|
1999-09-17 |
2003-07-15 |
Smithkline Beecham Corp |
Utilização de csaids em infecção por rinovìrus
|
BR0014973A
(pt)
|
1999-10-21 |
2002-07-16 |
Hoffmann La Roche Ag G |
Heterociclos de nitrogênio bicìclico de alquilamino substituìdo como inibidores de proteìna quinase p38
|
HUP0203564A3
(en)
|
1999-10-21 |
2004-07-28 |
Hoffmann La Roche |
Heteroalkylamino-substituted bicyclic nitrogen heterocycles as inhibitors of p38 protein kinease, process for their preparation and pharmaceutical compositions containing them
|
JP2003514900A
(ja)
|
1999-11-23 |
2003-04-22 |
スミスクライン・ビーチャム・コーポレイション |
CSBP/p38キナーゼ阻害剤としての3,4−ジヒドロ−(1H)−キナゾリン−2−オン化合物
|
AU1782301A
(en)
|
1999-11-23 |
2001-06-04 |
Smithkline Beecham Corporation |
3,4-dihydro-(1h)quinazolin-2-one compounds as csbp/p39 kinase inhibitors
|
DE60015599T2
(de)
|
1999-11-23 |
2005-11-03 |
Smithkline Beecham Corp. |
3,4-DIHYDRO-(1H)CHINAZOLIN-2-ON-VERBINDUNGEN ALS CSBP/p38-KINASE-INHIBITOREN
|
WO2001037837A1
(en)
|
1999-11-23 |
2001-05-31 |
Smithkline Beecham Corporation |
3,4-DIHYDRO-(1H)-QUINAZOLIN-2-ONES AND THEIR USE AS CSBP/p38 KINASE INHIBITORS
|
US6906067B2
(en)
|
1999-12-28 |
2005-06-14 |
Bristol-Myers Squibb Company |
N-heterocyclic inhibitors of TNF-α expression
|
DE60043397D1
(de)
|
1999-12-28 |
2010-01-07 |
Pharmacopeia Inc |
Cytokine, insbesondere tnf-alpha, hemmer
|
WO2001064676A2
(en)
|
2000-02-28 |
2001-09-07 |
Scios, Inc. |
INHIBITORS OF p38-α KINASE
|
AR030053A1
(es)
|
2000-03-02 |
2003-08-13 |
Smithkline Beecham Corp |
1h-pirimido [4,5-d] pirimidin-2-onas y sales, composiciones farmaceuticas, uso para la fabricacion de un medicamento y procedimiento para producirlas
|
MXPA02012909A
(es)
|
2000-07-24 |
2004-05-05 |
Boehringer Ingelheim Pharma |
Formulaciones mejoradas de dosis oral de 1-(5-ter-butil -2-p-tiolil2h -pirazol-3 -il)-3-(4-2 (2-morfolin-4-il -etoxi) -naftalen -1-il) -urea.
|
PE20020506A1
(es)
|
2000-08-22 |
2002-07-09 |
Glaxo Group Ltd |
Derivados de pirazol fusionados como inhibidores de la proteina cinasa
|
BR0113628A
(pt)
|
2000-08-31 |
2003-07-01 |
Hoffmann La Roche |
7-oxo-piridopirimidinas como inibidores de uma proliferação celular
|
CN1303072C
(zh)
|
2000-08-31 |
2007-03-07 |
霍夫曼-拉罗奇有限公司 |
7-氧代吡啶并嘧啶
|
AU2002231283A1
(en)
|
2000-10-19 |
2002-04-29 |
Smith Kline Beecham Corporation |
Use of p38 inhibitors for the treatment of smoke inhalation
|
JP2004530648A
(ja)
|
2000-10-19 |
2004-10-07 |
スミスクライン・ビーチャム・コーポレイション |
炎症により促進される咳の治療のためのp38阻害剤の使用
|
EP1333833B1
(en)
|
2000-10-23 |
2011-08-24 |
GlaxoSmithKline LLC |
Novel trisubstituted-8H-pyrido[2,3-d]pyrimidin-7-one compound for the treatment of CSBP/p38 kinase mediated diseases
|
PL366376A1
(pl)
|
2000-11-17 |
2005-01-24 |
Bristol-Myers Squibb Company |
Sposoby leczenia stanów związanych z kinazą p38 izwiązki pirolotriazynowe użyteczne jako inhibitory kinazy
|
WO2002044168A2
(en)
|
2000-11-20 |
2002-06-06 |
Scios Inc. |
Indole-type inhibitors of p38 kinase
|
CA2429605A1
(en)
|
2000-11-20 |
2002-05-30 |
Scios Inc. |
Indol derivative and their use as inhibitors of p38 kinase
|
WO2002046158A2
(en)
|
2000-11-20 |
2002-06-13 |
Scios Inc. |
Piperidine/piperazine-type inhibitors of p38 kinase
|
US20020165286A1
(en)
|
2000-12-08 |
2002-11-07 |
Hanne Hedeman |
Dermal anti-inflammatory composition
|
EP1345603A4
(en)
|
2000-12-20 |
2004-09-08 |
Merck & Co Inc |
P38 KINASE INHIBITORS (HALO-BENZO CARBONYL) HETEROCYCLO- FUSIONNES PHENYL
|
ATE305303T1
(de)
|
2001-02-12 |
2005-10-15 |
Hoffmann La Roche |
6-substituierte pyridopyrimidine
|
ATE406881T1
(de)
|
2001-02-28 |
2008-09-15 |
Univ Temple |
Verwendung von alpha, beta ungesättigten arylsulfonen zum schutz von zellen und geweben vor toxizität ionischer strahlung
|
DE60210755T2
(de)
|
2001-03-09 |
2006-11-16 |
Pfizer Products Inc., Groton |
Triazolopyridine als entzündungshemmende mittel
|
WO2002072576A1
(en)
|
2001-03-09 |
2002-09-19 |
Pfizer Products Inc. |
Benzimidazole anti-inflammatory compounds
|
WO2002076984A1
(en)
|
2001-03-23 |
2002-10-03 |
Smithkline Beecham Corporation |
Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases
|
WO2002076985A1
(en)
|
2001-03-23 |
2002-10-03 |
Smithkline Beecham Corporation |
Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases
|
AU2002303145A1
(en)
|
2001-03-23 |
2002-10-08 |
Smithkline Beecham Corporation |
Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases
|
WO2002076463A1
(en)
|
2001-03-23 |
2002-10-03 |
Smithkline Beecham Corporation |
Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases
|
WO2002076954A1
(en)
|
2001-03-23 |
2002-10-03 |
Smithkline Beecham Corporation |
Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases
|
ES2247271T3
(es)
|
2001-04-04 |
2006-03-01 |
Pfizer Products Inc. |
Nuevos benzotriazoles como compuestos antiinflamatorios.
|
ES2366775T3
(es)
|
2001-04-24 |
2011-10-25 |
Merck Patent Gmbh |
POLITERAPIA UTILIZANDO AGENTES ANTIANGIOGÉNICOS Y TNF(alfa).
|
WO2002090360A1
(en)
|
2001-05-10 |
2002-11-14 |
Smithkline Beecham Corporation |
Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases
|
MXPA03010269A
(es)
|
2001-05-11 |
2004-05-05 |
Vertex Pharma |
Derivados de 2,5-disubstituida piridina, pirimidina, piridazina y 1,2,4-triazina para usarse como inhibidores de p38.
|
ES2289116T3
(es)
|
2001-05-24 |
2008-02-01 |
Eli Lilly And Company |
Nuevos derivados de pirrol como agentes farmaceuticos.
|
EP1414455B1
(en)
|
2001-06-11 |
2008-11-26 |
Vertex Pharmaceuticals Incorporated |
Isoquinoline inhibitors of p38
|
US7196095B2
(en)
|
2001-06-25 |
2007-03-27 |
Merck & Co., Inc. |
(Pyrimidinyl) (phenyl) substituted fused heteroaryl p38 inhibiting and PKG kinase inhibiting compounds
|
US20030139435A1
(en)
|
2001-06-26 |
2003-07-24 |
Gulzar Ahmed |
N-heterocyclic inhibitors of TNF-alpha expression
|
ATE360417T1
(de)
|
2001-07-11 |
2007-05-15 |
Boehringer Ingelheim Pharma |
Methode zur behandlung von zytokinvermittelten erkrankungen
|
CA2454913A1
(en)
|
2001-08-20 |
2003-02-27 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Parenteral formulations of 1-(5-tert-butyl-2-p-tolyl-2h-pryrazol-3-yl)-3-¬4-(2-morpholin-4-yl-ethoxy)-naphthalen-1-yl|-urea and a cyclodextrin
|
RU2315045C2
(ru)
|
2001-08-30 |
2008-01-20 |
Ф.Хоффманн-Ля Рош Аг |
Производные аминопиррола, способ их получения, их применение и фармацевтическая композиция, обладающая противовоспалительной активностью
|
AU2002330031B2
(en)
|
2001-09-21 |
2007-07-05 |
Merck & Co., Inc. |
Androstanes as androgen receptor modulators
|
US7205275B2
(en)
|
2001-10-11 |
2007-04-17 |
Amgen Inc. |
Methods of treatment using specific binding agents of human angiopoietin-2
|
WO2003032894A2
(en)
|
2001-10-12 |
2003-04-24 |
Pfizer Products Inc. |
Method of monitoring neuroprotective treatment
|
GB0124933D0
(en)
|
2001-10-17 |
2001-12-05 |
Glaxo Group Ltd |
Chemical compounds
|
GB0124931D0
(en)
|
2001-10-17 |
2001-12-05 |
Glaxo Group Ltd |
Chemical compounds
|
GB0124928D0
(en)
|
2001-10-17 |
2001-12-05 |
Glaxo Group Ltd |
Chemical compounds
|
GB0124939D0
(en)
|
2001-10-17 |
2001-12-05 |
Glaxo Group Ltd |
Chemical compounds
|
GB0124936D0
(en)
|
2001-10-17 |
2001-12-05 |
Glaxo Group Ltd |
Chemical compounds
|
GB0124938D0
(en)
|
2001-10-17 |
2001-12-05 |
Glaxo Group Ltd |
Chemical compounds
|
GB0124932D0
(en)
|
2001-10-17 |
2001-12-05 |
Glaxo Group Ltd |
Chemical compounds
|
GB0124941D0
(en)
|
2001-10-17 |
2001-12-05 |
Glaxo Group Ltd |
Chemical compounds
|
US20040235728A1
(en)
|
2001-11-08 |
2004-11-25 |
Stoch Selwyn Aubrey |
Compositions and methods for treating osteoporosis
|
PL369019A1
(pl)
|
2001-11-09 |
2005-04-18 |
Scios Inc. |
Sposób leczenia zwłóknienia torbielowatego
|
US20050261836A1
(en)
|
2001-12-05 |
2005-11-24 |
Wuyi Meng |
Crystal structure of mitogen-activated protein kinase-activated protein kinase 2 and binding pockets thereof
|
EP1455791A1
(en)
|
2001-12-11 |
2004-09-15 |
Boehringer Ingelheim Pharmaceuticals Inc. |
Method for administering birb 796 bs
|
MXPA04006545A
(es)
|
2002-01-03 |
2004-10-04 |
Smithkline Beecham Corp |
Nuevas formas de dosificacion farmaceutica y metodo para producir las mismas.
|
AU2003219656B2
(en)
|
2002-01-15 |
2007-05-17 |
Merck Sharp & Dohme Corp. |
17-hydroxy-4-aza-androstan-3-ones as androgen receptor modulators
|
DE10203749A1
(de)
|
2002-01-31 |
2003-08-14 |
Boehringer Ingelheim Pharma |
Neue Anticholinergika, Verfahren zu deren Herstellung sowie deren Verwendung als Arzneimittel
|
DE10203753A1
(de)
|
2002-01-31 |
2003-08-14 |
Boehringer Ingelheim Pharma |
Neue Xanthencarbonsäureester, Verfahren zu deren Herstellung sowie deren Verwendung als Arzneimittel
|
DE10203741A1
(de)
|
2002-01-31 |
2003-08-14 |
Boehringer Ingelheim Pharma |
Neue Fluorencarbonsäureester, Verfahren zu deren Herstellung sowie deren Verwendung als Arzneimittel
|
US20040023961A1
(en)
|
2002-02-11 |
2004-02-05 |
Bayer Corporation |
Aryl ureas with raf kinase and angiogenisis inhibiting activity
|
EP1864975B1
(en)
|
2002-02-12 |
2010-10-20 |
GlaxoSmithKline LLC |
Nicotinamide derivates useful as P38 inhibitors
|
EP1485390B1
(en)
|
2002-03-07 |
2008-10-08 |
F. Hoffman-la Roche AG |
Bicyclic pyridine and pyrimidine p38 kinase inhibitors
|
PL372920A1
(pl)
|
2002-03-13 |
2005-08-08 |
Merck & Co,Inc. |
Fluorowane pochodne 4-azasteroidowe jako modulatory receptora androgenowego
|
WO2003079986A2
(en)
|
2002-03-18 |
2003-10-02 |
Bristol-Myers Squibb Company |
Uracil derivatives as inhibitors of tnf-alpha converting enzyme (tace) and matrix metalloproteinases
|
US20040122008A1
(en)
|
2002-09-05 |
2004-06-24 |
Protter Andrew A. |
Treatment of pain by inhibition of p38 MAP kinase
|
US6900208B2
(en)
|
2002-03-28 |
2005-05-31 |
Bristol Myers Squibb Company |
Pyrrolopyridazine compounds and methods of use thereof for the treatment of proliferative disorders
|
PL374544A1
(pl)
|
2002-04-03 |
2005-10-31 |
F.Hoffmann-La Roche Ag |
Związki imidazo-skondensowane
|
WO2003084503A2
(en)
|
2002-04-05 |
2003-10-16 |
Boehringer Ingelheim Pharma Gmbh & Co. Kg |
P38 kinase inhibitors for treating mucus hypersecretion_
|
US20030225089A1
(en)
|
2002-04-10 |
2003-12-04 |
Boehringer Ingelheim Pharma Gmbh & Co. Kg |
Pharmaceutical compositions based on anticholinergics and p38 kinase inhibitors
|
DE10216339A1
(de)
|
2002-04-13 |
2003-10-23 |
Boehringer Ingelheim Pharma |
Neue Ester hydroxy-substituierter Stickstoffheterocyclen, Verfahren zu deren Herstellung sowie deren Verwendung als Arzneimittel
|
WO2003087394A1
(en)
|
2002-04-15 |
2003-10-23 |
Glaxo Group Limited |
A method of identifying a modudator for a serine/theronine kinase
|
ES2291630T3
(es)
|
2002-04-19 |
2008-03-01 |
Smithkline Beecham Corporation |
Nuevos compuestos.
|
PL373371A1
(pl)
|
2002-04-23 |
2005-08-22 |
Bristol-Myers Squibb Company |
Związki aryloketonopirolotriazyny użyteczne jako inhibitory kinazy
|
US7388009B2
(en)
|
2002-04-23 |
2008-06-17 |
Bristol-Myers Squibb Company |
Heteroaryl-substituted pyrrolo-triazine compounds useful as kinase inhibitors
|
SI1497019T1
(sl)
|
2002-04-23 |
2015-08-31 |
Bristol-Myers Squibb Company |
Pirolo-triazin anilin spojine uporabne kot inhibitorji kinaze
|
US20050131005A1
(en)
|
2002-04-30 |
2005-06-16 |
Jiabing Wang |
4-azasteroid derivatives as androgen receptor modulators
|
GB0209891D0
(en)
|
2002-04-30 |
2002-06-05 |
Glaxo Group Ltd |
Novel compounds
|
WO2003097615A1
(en)
|
2002-05-17 |
2003-11-27 |
Scios, Inc. |
TREATMENT OF FIBROPROLIFERATIVE DISORDERS USING TGF-β INHIBITORS
|
TW200400034A
(en)
|
2002-05-20 |
2004-01-01 |
Bristol Myers Squibb Co |
Pyrazolo-pyrimidine aniline compounds useful as kinase inhibitors
|
US7008958B2
(en)
|
2002-05-21 |
2006-03-07 |
Bristol-Myers Squibb Company |
2-substituted 5-oxazolyl indole compounds useful as IMPDH inhibitors and pharmaceutical compositions comprising same
|
JP4245561B2
(ja)
|
2002-06-11 |
2009-03-25 |
メルク エンド カムパニー インコーポレーテッド |
(ハロ−ベンゾカルボニル)複素2環p38キナーゼ阻害剤
|
EP1534282B1
(en)
|
2002-07-09 |
2006-12-27 |
Boehringer Ingelheim Pharma GmbH & Co.KG |
Pharmaceutical compositions of anticholinergics and p38 kinase inhibitors in the treatment of respiratory diseases
|
WO2004010929A2
(en)
|
2002-07-25 |
2004-02-05 |
Scios, Inc. |
METHODS FOR IMPROVEMENT OF LUNG FUNCTION USING TGF-β INHIBITORS
|
GB0217757D0
(en)
|
2002-07-31 |
2002-09-11 |
Glaxo Group Ltd |
Novel compounds
|
RU2324695C2
(ru)
|
2002-08-06 |
2008-05-20 |
Ф.Хоффманн-Ля Рош Аг |
6-АЛКОКСИПИРИДОПИРИМИДИНЫ И ФАРМАЦЕВТИЧЕСКАЯ КОМПОЗИЦИЯ, ОБЛАДАЮЩАЯ АКТИВНОСТЬЮ ИНГИБИТОРОВ КИНАЗЫ МАР р38
|
US6872726B2
(en)
|
2002-08-08 |
2005-03-29 |
Boehringer Ingelheim Pharmaceuticals Inc. |
Fluorinated di-aryl urea compounds
|
US7320995B2
(en)
|
2002-08-09 |
2008-01-22 |
Eli Lilly And Company |
Benzimidazoles and benzothiazoles as inhibitors of map kinase
|
US20040110755A1
(en)
|
2002-08-13 |
2004-06-10 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Combination therapy with p38 MAP kinase inhibitors and their pharmaceutical compositions
|
US20040033222A1
(en)
|
2002-08-14 |
2004-02-19 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Anticoagulant and fibrinolytic therapy uning p38 MAP kinase inhibitors
|
AU2003262911A1
(en)
|
2002-08-29 |
2004-03-19 |
Scios Inc. |
Methods of promoting osteogenesis
|
US7005523B2
(en)
|
2002-08-30 |
2006-02-28 |
Pfizer Inc. |
Cycloalkyl-[4-(trifluorophenyl)-oxazol-5yl]-triazolo-pyridines
|
US7037923B2
(en)
|
2002-08-30 |
2006-05-02 |
Pfizer, Inc. |
Alkyl-[4-(trifluorophenyl)-oxazol-5-yl]-triazolo-pyridines
|
WO2004020438A2
(en)
|
2002-08-30 |
2004-03-11 |
Pfizer Products Inc. |
Novel processes and intermediates for preparing triazolo-pyridines
|
US7012143B2
(en)
|
2002-08-30 |
2006-03-14 |
Dombroski Mark A |
Cycloalkyl-[4-(difluorophenyl)-oxazol-5-yl]-triazolo-pyridines
|
US20040092547A1
(en)
|
2002-08-30 |
2004-05-13 |
Pfizer Inc |
Alkyl-[4-(difluorophenyl)-oxazol-5-yl]-triazolo-pyridines
|
PA8579601A1
(es)
|
2002-08-30 |
2004-05-07 |
Pfizer Prod Inc |
Compuestos antiinflamatorios de di y trifloruro-triazolo-piridinas
|
JP2006506346A
(ja)
|
2002-09-03 |
2006-02-23 |
サイオス インク. |
p38キナーゼ阻害剤としてのインドール系誘導体
|
US20050288503A1
(en)
|
2002-09-06 |
2005-12-29 |
Adams Jerry L |
Novel compounds
|
US7115644B2
(en)
|
2002-09-13 |
2006-10-03 |
Boehringer Ingelheim Pharmaceuticals Inc. |
Heterocyclic compounds
|
WO2004026871A1
(en)
|
2002-09-17 |
2004-04-01 |
Eli Lilly And Company |
Novel pyrazolopyridine derivatves as pharmaceutical agents
|
CN1701069A
(zh)
|
2002-09-27 |
2005-11-23 |
詹森药业有限公司 |
3,4-二取代吡咯及其在治疗炎性疾病中的应用
|
US7041693B2
(en)
|
2002-10-04 |
2006-05-09 |
Bristol-Myers Squibb Company |
Hydantoin derivatives as inhibitors of matrix metalloproteinases and/or TNF-α converting enzyme (TACE)
|
CN1713910A
(zh)
|
2002-10-09 |
2005-12-28 |
西奥斯股份有限公司 |
作为p38激酶抑制剂的氮杂吲哚衍生物
|
US20050288299A1
(en)
|
2002-10-09 |
2005-12-29 |
Mavunkel Babu J |
Azaindole derivatives as inhibitors of p38 kinase
|
US7622592B2
(en)
|
2002-11-01 |
2009-11-24 |
Merck & Co., Inc. |
Carbonylamino-benzimidazole derivatives as androgen receptor modulators
|
DE60327097D1
(de)
|
2002-11-18 |
2009-05-20 |
Hoffmann La Roche |
Diazinopyrimidine und ihre verwendung als proteinkinaseinhibitoren
|
DE10255040A1
(de)
|
2002-11-26 |
2004-06-03 |
Boehringer Ingelheim Pharma Gmbh & Co. Kg |
Neue Carbaminsäureester mit anticholinerger Wirksamkeit
|
WO2004053107A2
(en)
|
2002-12-06 |
2004-06-24 |
Scios Inc. |
Methods for treating diabetes
|
US7105537B2
(en)
|
2003-01-28 |
2006-09-12 |
Bristol-Myers Squibb Company |
2-substituted cyclic amines as calcium sensing receptor modulators
|
CA2515218A1
(en)
|
2003-02-05 |
2004-08-26 |
Bristol-Myers Squibb Company |
Process for preparing pyrrolotriazine kinase inhibitors
|
MXPA05008450A
(es)
|
2003-02-10 |
2005-10-18 |
Vertex Pharma |
Procesos para la preparacion de n-heteroaril-n-aril-aminas mediante reaccion de un ester de acido n-aril-carbamico con un halo-heteroarilo y procesos analogos.
|
US7205322B2
(en)
|
2003-02-12 |
2007-04-17 |
Bristol-Myers Squibb Company |
Thiazolidine compounds as calcium sensing receptor modulators
|
MXPA05008568A
(es)
|
2003-02-14 |
2005-11-04 |
Pfizer Prod Inc |
Nuevos compuestos anti-inflamatorios triazolo-piridinas.
|
US7550480B2
(en)
|
2003-02-14 |
2009-06-23 |
Smithkline Beecham Corporation |
Compounds
|
AR043416A1
(es)
|
2003-02-27 |
2005-07-27 |
Uriach Y Compania S A J |
Un compuesto que comprende derivados de pirazolopiridina, procedimiento para preparar dicho compuesto y sus usos en la manufactura de medicamentos y composiciones farmaceuticas
|
US7135575B2
(en)
|
2003-03-03 |
2006-11-14 |
Array Biopharma, Inc. |
P38 inhibitors and methods of use thereof
|
AU2004218463B2
(en)
|
2003-03-03 |
2009-07-16 |
Array Biopharma, Inc. |
p38 inhibitors and methods of use thereof
|
US7030112B2
(en)
|
2003-03-25 |
2006-04-18 |
Bristol-Myers Squibb Company |
Pyrrolopyridazine compounds and methods of use thereof for the treatment of proliferative disorders
|
GB0308201D0
(en)
|
2003-04-09 |
2003-05-14 |
Smithkline Beecham Corp |
Novel compounds
|
GB0308185D0
(en)
|
2003-04-09 |
2003-05-14 |
Smithkline Beecham Corp |
Novel compounds
|
GB0308186D0
(en)
|
2003-04-09 |
2003-05-14 |
Smithkline Beecham Corp |
Novel compounds
|
AU2004229163A1
(en)
|
2003-04-16 |
2004-10-28 |
F. Hoffmann-La Roche Ag |
(6-(phenoxy)-pyrido`3,4-d! PYRIMIDIN-2-YL)-AMINE DERIVATIVES AS P38 KINASE INHIBITORS FOR THE TREATMENT OF INFLAMMATORYY CONDITIONS SUCH AS RHEUMATOIS ARTRITIS
|
MXPA05011103A
(es)
|
2003-04-16 |
2005-12-12 |
Hoffmann La Roche |
Compuestos de quinazolina.
|
WO2004098518A2
(en)
|
2003-05-01 |
2004-11-18 |
Bristol-Myers Squibb Company |
Pyrazole-amide compounds useful as kinase inhibitors
|
GB0320244D0
(en)
|
2003-05-06 |
2003-10-01 |
Aventis Pharma Inc |
Pyrazoles as inhibitors of tumour necrosis factor
|
US7351698B2
(en)
|
2003-05-07 |
2008-04-01 |
Merck & Co., Inc. |
Androgen receptor modulators and methods of use thereof
|
EP1633714B1
(en)
|
2003-06-04 |
2008-01-23 |
Pfizer Limited |
2-amino-pyridine derivatives as beta-2 adrenoreceptor agonists
|
PL1641764T3
(pl)
|
2003-06-26 |
2011-12-30 |
Novartis Ag |
Inhibitory kinazy P38 na bazie 5-członowych heterocykli
|
US7482357B2
(en)
|
2003-06-30 |
2009-01-27 |
Merck & Co., Inc. |
17-acetamido-4-azasteroid derivatives as androgen receptor modulators
|
CN1816370A
(zh)
|
2003-06-30 |
2006-08-09 |
麦克公司 |
用作雄激素受体调节剂的17-乙酰氨基-4-氮杂甾族化合物衍生物
|
WO2005009367A2
(en)
|
2003-07-17 |
2005-02-03 |
Ambit Biosciences Corporation |
Treatment of diseases with kinase inhibitors
|
US7153870B2
(en)
|
2003-07-25 |
2006-12-26 |
Pfizer Inc. |
Nicotinamide derivatives useful as PDE4 inhibitors
|
GB0317516D0
(en)
|
2003-07-25 |
2003-08-27 |
Pfizer Ltd |
Nicotinamide derivatives useful as PDE4 inhibitors
|
GB0317484D0
(en)
|
2003-07-25 |
2003-08-27 |
Pfizer Ltd |
Nicotinamide derivatives useful as pde4 inhibitors
|
US20050020587A1
(en)
|
2003-07-25 |
2005-01-27 |
Pfizer Inc |
Nicotinamide derivatives useful as PDE4 inhibitors
|
GB0317482D0
(en)
|
2003-07-25 |
2003-08-27 |
Pfizer Ltd |
Nicotinamide derivatives useful as pde4 inhibitors
|
US20070105114A1
(en)
|
2003-07-29 |
2007-05-10 |
Martha Li |
Biomarkers of cyclin-dependent kinase modulation
|
GB0318814D0
(en)
|
2003-08-11 |
2003-09-10 |
Smithkline Beecham Corp |
Novel compounds
|
CL2004002050A1
(es)
|
2003-08-13 |
2005-06-03 |
Pharmacia Corp Sa Organizada B |
Compuestos derivados de piridinonas sustituidas; su uso en el tratamiento de afecciones causadas o exacerbadas por actividad p38 map kinasa y/o tnf no regulada, tales como inflamaciones, tumores, sida y otros.
|
AU2004266719A1
(en)
|
2003-08-22 |
2005-03-03 |
Boehringer Ingelheim France S.A.S. |
Methods of treating COPD and pulmonary hypertension
|
US20050053600A1
(en)
|
2003-09-09 |
2005-03-10 |
Lane Thomas E. |
Methods for treating rheumatoid arthritis
|
US7446110B2
(en)
|
2003-09-10 |
2008-11-04 |
Merck & Co., Inc. |
17-Heterocyclic-4-azasteroid derivatives as androgen receptor modulators
|
BRPI0414313A
(pt)
|
2003-09-11 |
2006-11-07 |
Kemia Inc |
inibidores de citocinas
|
WO2005032481A2
(en)
|
2003-09-30 |
2005-04-14 |
Scios Inc. |
Quinazoline derivatives as medicaments
|
US20060019971A1
(en)
|
2003-09-30 |
2006-01-26 |
Higgins Linda S |
Treatment of cardiovascular disease with inhibitors of p38 kinase
|
JP2007507529A
(ja)
|
2003-09-30 |
2007-03-29 |
サイオス・インコーポレーテツド |
複素環式アミドおよびスルホンアミド
|
US7419978B2
(en)
|
2003-10-22 |
2008-09-02 |
Bristol-Myers Squibb Company |
Phenyl-aniline substituted bicyclic compounds useful as kinase inhibitors
|
ATE356124T1
(de)
|
2003-11-13 |
2007-03-15 |
Hoffmann La Roche |
Hydroxyalkylsubstituierte pyrido-7-pyrimidin-7- one
|
EP1538201A1
(en)
|
2003-12-02 |
2005-06-08 |
F.Hoffmann-La Roche Ag |
Method for the recombinant production and purification of protein kinases
|
CN1893950A
(zh)
|
2003-12-18 |
2007-01-10 |
辉瑞产品公司 |
用p38 MAP激酶抑制剂治疗动物急性炎症的方法
|
JP2007514791A
(ja)
|
2003-12-18 |
2007-06-07 |
ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド |
P38mapキナーゼインヒビターであるbirb796の多形
|
GB0329275D0
(en)
|
2003-12-18 |
2004-01-21 |
Merck Sharp & Dohme |
Therapeutic treatment
|
US20060079461A1
(en)
|
2003-12-24 |
2006-04-13 |
Scios, Inc. |
Treatment of multiple myeloma by inhibition of p38 MAP kinase
|
US20060052390A1
(en)
|
2003-12-24 |
2006-03-09 |
Scios, Inc. |
Treatment of multiple myeloma by p38 MAP kinase and proteasome inhibition
|
US20060058296A1
(en)
|
2003-12-24 |
2006-03-16 |
Scios, Inc. |
Treatment of osteolytic lesions associated with multiple myeloma by inhibition of p38 map kinase
|
WO2005065691A1
(en)
|
2003-12-24 |
2005-07-21 |
Scios, Inc. |
Treatment of malignant gliomas with tgf-beta inhibitors
|
TWI332003B
(en)
|
2004-01-30 |
2010-10-21 |
Lilly Co Eli |
Kinase inhibitors
|
GB0402140D0
(en)
|
2004-01-30 |
2004-03-03 |
Smithkline Beecham Corp |
Novel compounds
|
US20070161677A1
(en)
|
2004-01-30 |
2007-07-12 |
Merck Patent Gmbh |
Bisarylurea derivatives
|
GB0402138D0
(en)
|
2004-01-30 |
2004-03-03 |
Smithkline Beecham Corp |
Novel compounds
|
GB0402137D0
(en)
|
2004-01-30 |
2004-03-03 |
Smithkline Beecham Corp |
Novel compounds
|
GB0402143D0
(en)
|
2004-01-30 |
2004-03-03 |
Smithkline Beecham Corp |
Novel compounds
|
EP1720862A1
(en)
|
2004-02-03 |
2006-11-15 |
Eli Lilly And Company |
Kinase inhibitors
|
TWI338004B
(en)
|
2004-02-06 |
2011-03-01 |
Bristol Myers Squibb Co |
Process for preparing 2-aminothiazole-5-aromatic carboxamides as kinase inhibitors
|
US7652146B2
(en)
|
2004-02-06 |
2010-01-26 |
Bristol-Myers Squibb Company |
Process for preparing 2-aminothiazole-5-carboxamides useful as kinase inhibitors
|
US20070191444A1
(en)
|
2004-02-26 |
2007-08-16 |
Hans-Peter Buchstaller |
Benzimidazolyl derivatives
|
RU2006134022A
(ru)
|
2004-02-27 |
2008-04-10 |
Ф.Хоффманн-Ля Рош Аг (Ch) |
Производные индазола и содержащие их фармацевтические композиции
|
WO2005085248A1
(en)
|
2004-02-27 |
2005-09-15 |
F.Hoffmann-La Roche Ag |
Heteroaryl-fused pyrazolo derivatives
|
EP1574501A1
(en)
|
2004-03-11 |
2005-09-14 |
Pfizer Limited |
Quinolinone derivatives, pharmaceutical compositions containing them and their use
|
WO2005091891A2
(en)
|
2004-03-11 |
2005-10-06 |
Kythera Biopharmaceuticals, Inc. |
Compositions and methods for preventing and treating skin and hair conditions
|
EP1577292A1
(en)
|
2004-03-17 |
2005-09-21 |
Pfizer Limited |
Phenylaminoethanol derivatives as beta2 receptor agonists
|
EP1577291A1
(en)
|
2004-03-17 |
2005-09-21 |
Pfizer Limited |
Phenylethanolamine derivatives as beta-2 agonists
|
US7410977B2
(en)
|
2004-04-28 |
2008-08-12 |
Merck & Co., Inc. |
Fluorinated 4-azasteroids as androgen receptor modulators
|
CA2566677A1
(en)
|
2004-05-13 |
2005-11-24 |
Intermune, Inc. |
Combination therapy for treating hepatitis virus infection
|
UA87854C2
(en)
|
2004-06-07 |
2009-08-25 |
Мерк Энд Ко., Инк. |
N-(2-benzyl)-2-phenylbutanamides as androgen receptor modulators
|
ES2308523T3
(es)
|
2004-06-23 |
2008-12-01 |
Eli Lilly And Company |
Inhibidores de quinasa.
|
EP1609789A1
(en)
|
2004-06-23 |
2005-12-28 |
Eli Lilly And Company |
Ureido-pyrazole derivatives and their use as kinase inhibitors
|
US7253167B2
(en)
|
2004-06-30 |
2007-08-07 |
Bristol-Myers Squibb Company |
Tricyclic-heteroaryl compounds useful as kinase inhibitors
|
US20060035893A1
(en)
|
2004-08-07 |
2006-02-16 |
Boehringer Ingelheim International Gmbh |
Pharmaceutical compositions for treatment of respiratory and gastrointestinal disorders
|
US7148348B2
(en)
|
2004-08-12 |
2006-12-12 |
Bristol-Myers Squibb Company |
Process for preparing pyrrolotriazine aniline compounds useful as kinase inhibitors
|
JP4084836B2
(ja)
|
2004-08-12 |
2008-04-30 |
ファイザー・インク |
p38MAPキナーゼインヒビターとしてのトリアゾロピリジニルスルファニル誘導体
|
AU2005280334A1
(en)
|
2004-08-25 |
2006-03-09 |
Merck Sharp & Dohme Corp. |
Androgen receptor modulators
|
US20070054916A1
(en)
|
2004-10-01 |
2007-03-08 |
Amgen Inc. |
Aryl nitrogen-containing bicyclic compounds and methods of use
|
AR055271A1
(es)
|
2004-10-05 |
2007-08-15 |
Smithkline Beecham Corp |
Compuesto del acido bifenil carboxilico, composicion farmaceutica que lo comprende, su uso para preparar esta ultima y proceso para prepararlo
|
KR20070062998A
(ko)
|
2004-10-13 |
2007-06-18 |
메르크 파텐트 게엠베하 |
키나제 억제제로서의 복소환 치환된 비스아릴우레아 유도체
|
KR20070073791A
(ko)
|
2004-10-18 |
2007-07-10 |
암젠 인코포레이티드 |
티아디아졸 화합물 및 이의 사용방법
|
AU2005310238A1
(en)
|
2004-10-29 |
2006-06-08 |
Merck Sharp & Dohme Corp. |
N-(pyridin-3-yl)-2-phenylbutanamides as androgen receptor modulators
|
US20060258582A1
(en)
|
2004-11-04 |
2006-11-16 |
Scios, Inc. |
Method of treating myelodysplastic syndromes
|
WO2006048266A2
(en)
|
2004-11-04 |
2006-05-11 |
Roche Diagnostics Gmbh |
Gene expression profiling of leukemias with mll gene rearrangements
|
WO2006051373A1
(en)
|
2004-11-12 |
2006-05-18 |
Pfizer Limited |
Compounds for the treatment of diseases
|
GB0425057D0
(en)
|
2004-11-12 |
2004-12-15 |
Pfizer Ltd |
L-tartrate salt of N-1-adamantyl-2-{3-[(2R)-2-hydroxy-2-[4-hydroxy-3-(hydroxymethyl)phenyl]eth yl}amino)propyl]phenyl}acetamide
|
AU2005306741A1
(en)
|
2004-11-16 |
2006-05-26 |
Merck & Co., Inc. |
Prodrugs of (2R)-2-propyloctanoic acid for treatment of stroke
|
WO2006058023A2
(en)
|
2004-11-23 |
2006-06-01 |
Merck & Co., Inc. |
Treatment of stroke with histamine h3 inverse agonists or histamine h3 antagonists
|
US20060111416A1
(en)
|
2004-11-24 |
2006-05-25 |
Lane Charlotte A L |
Octahydropyrrolo[3,4-C]pyrrole derivatives
|
US20070224662A1
(en)
|
2004-12-17 |
2007-09-27 |
Jun Luo |
Post-translational modification of proteins in cell-free expression systems
|
US20060154939A1
(en)
|
2004-12-24 |
2006-07-13 |
Boehringer Ingelheim International Gmbh |
Medicaments for the Treatment or Prevention of Fibrotic Diseases
|
PE20060777A1
(es)
|
2004-12-24 |
2006-10-06 |
Boehringer Ingelheim Int |
Derivados de indolinona para el tratamiento o la prevencion de enfermedades fibroticas
|
PE20061155A1
(es)
|
2004-12-24 |
2006-12-16 |
Boehringer Ingelheim Int |
Derivados de indolinona como agentes para el tratamiento o la prevencion de enfermedades fibroticas
|
WO2006070927A1
(ja)
|
2004-12-28 |
2006-07-06 |
Aska Pharmaceutical Co., Ltd. |
ピリミジニルイソオキサゾール誘導体
|
US20060178388A1
(en)
|
2005-02-04 |
2006-08-10 |
Wrobleski Stephen T |
Phenyl-substituted pyrimidine compounds useful as kinase inhibitors
|
EP1853581B1
(en)
|
2005-02-28 |
2010-06-02 |
Merckle Gmbh |
2-sulfinyl- and 2-sulfonyl-substituted imidazole derivatives and their use as cytokine inhibitors
|
US7759337B2
(en)
|
2005-03-03 |
2010-07-20 |
Amgen Inc. |
Phthalazine compounds and methods of use
|
MY145281A
(en)
|
2005-03-25 |
2012-01-13 |
Glaxo Group Ltd |
Novel compounds
|
PE20061193A1
(es)
|
2005-03-25 |
2006-12-02 |
Glaxo Group Ltd |
DERIVADOS DE 3,4-DIHIDROPIRIMIDO[4,5-d]PIRIMIDIN-2-[1H]-0NA COMO INHIBIDORES DE QUINASA p38
|
EP1868612A4
(en)
|
2005-03-25 |
2010-03-24 |
Glaxo Group Ltd |
NOVEL CONNECTIONS
|
US20060235020A1
(en)
|
2005-04-18 |
2006-10-19 |
Soojin Kim |
Process for preparing salts of 4-[[5-[(cyclopropylamino)carbonyl]-2-methylphenyl]amino]-5-methyl-N-propylpyrrolo[2,1-f][1,2,4]triazine-6-carboxamide and novel stable forms produced therein
|
WO2006122230A1
(en)
|
2005-05-11 |
2006-11-16 |
Array Biopharma Inc. |
P38 inhibitors and methods of use thereof
|
WO2006127678A2
(en)
|
2005-05-23 |
2006-11-30 |
Smithkline Beecham Corporation |
Inhibition of p38 mark for treatment of obesity
|
GB0512429D0
(en)
|
2005-06-17 |
2005-07-27 |
Smithkline Beecham Corp |
Novel compound
|
US20070032506A1
(en)
|
2005-07-02 |
2007-02-08 |
Peter Giannousis |
Crystalline forms of (2r-trans)-6-chloro-5[[4-[(4-fluorophenyl)methyl]-2,5-dimethyl-1-piperazinyl]carbonyl]-n,n, 1-trimethyl-alpha-oxo-1h-indole-3-acetamide monohydrochloride
|
US7473784B2
(en)
|
2005-08-01 |
2009-01-06 |
Bristol-Myers Squibb Company |
Benzothiazole and azabenzothiazole compounds useful as kinase inhibitors
|
WO2007016358A1
(en)
|
2005-08-02 |
2007-02-08 |
Merck & Co., Inc. |
N-(pyridin-4-yl)-2-phenylbutanamides as androgen receptor modulators
|
US7879875B2
(en)
|
2005-08-12 |
2011-02-01 |
Merk Sharp & Dohme Corp. |
P38 kinase inhibiting agents
|
EP1928843A1
(en)
|
2005-08-22 |
2008-06-11 |
Amgen, Inc |
Bis-aryl urea compounds for the treatment of protein kinase-mediated diseaes
|
WO2007023114A1
(en)
|
2005-08-25 |
2007-03-01 |
F. Hoffmann-La Roche Ag |
P38 map kinase inhibitors and methods for using the same
|
AU2006283945A1
(en)
|
2005-08-25 |
2007-03-01 |
F. Hoffmann-La Roche Ag |
P38 MAP kinase inhibitors and methods for using the same
|
AU2006283940A1
(en)
|
2005-08-25 |
2007-03-01 |
F. Hoffmann-La Roche Ag |
P38 MAP kinase inhibitors and methods for using the same
|
MX2008002588A
(es)
|
2005-08-25 |
2008-03-18 |
Hoffmann La Roche |
Inhibidores de p38-map-cinasa y los metodos para utilizarlos.
|
CN101242832B
(zh)
|
2005-08-25 |
2011-08-10 |
霍夫曼-拉罗奇有限公司 |
用作p38 MAP激酶抑制剂的稠合吡唑
|
AU2006285599A1
(en)
|
2005-09-01 |
2007-03-08 |
Astellas Pharma Inc. |
Pyridazinone derivatives used for the treatment of pain
|
CN101268046B
(zh)
|
2005-09-21 |
2012-07-25 |
辉瑞有限公司 |
作为毒蕈碱性受体拮抗剂的碳酰胺衍生物
|
JP2009509969A
(ja)
|
2005-09-26 |
2009-03-12 |
メルク エンド カムパニー インコーポレーテッド |
アンドロゲン受容体モジュレーターとしてのn−(4−オキソ−3,4−ジヒドロキナゾリン−2−イル)ブタンアミド
|
WO2007045989A1
(en)
|
2005-10-20 |
2007-04-26 |
Pfizer Limited |
Pyridyl derivatives useful as h3 ligands
|
DOP2006000233A
(es)
|
2005-10-28 |
2007-06-15 |
Lilly Co Eli |
Inhibidores de cinasa
|
AR056582A1
(es)
|
2005-10-28 |
2007-10-10 |
Lilly Co Eli |
COMPUESTOS DE PIRAZOLIL UREA CON ACTIVIDAD INHIBITORIA DE CINASA P38 Y FORMULACIoN FARMACÉUTICA QUE LO COMPRENDE
|
WO2007056016A2
(en)
|
2005-11-02 |
2007-05-18 |
Kemia, Inc. |
Bisamide cytokine inhibitors
|
JP2009514846A
(ja)
|
2005-11-04 |
2009-04-09 |
ファイザー・リミテッド |
テトラヒドロナフチリジン誘導体
|
EP1948599A1
(en)
|
2005-11-08 |
2008-07-30 |
Ranbaxy Laboratories Limited |
Process for (3r, 5r)-7-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4- [(4-hydroxy methyl phenyl amino) carbonyl]-pyrrol-1-yl]-3, 5-dihydroxy-heptanoic acid hemi calcium salt
|
PE20100742A1
(es)
|
2005-11-15 |
2010-11-25 |
Glaxo Group Ltd |
Nuevos procedimientos y formulaciones
|
NL2000323C2
(nl)
|
2005-12-20 |
2007-11-20 |
Pfizer Ltd |
Pyrimidine-derivaten.
|
WO2007075896A2
(en)
|
2005-12-22 |
2007-07-05 |
Kemia, Inc. |
Heterocyclic cytokine inhibitors
|
EA200801716A1
(ru)
|
2006-01-18 |
2009-04-28 |
Амген Инк. |
Тиазольные соединения и их применение
|
SG175599A1
(en)
|
2006-01-31 |
2011-11-28 |
Array Biopharma Inc |
Kinase inhibitors and methods of use thereof
|
EP1984363A1
(en)
|
2006-02-09 |
2008-10-29 |
Pfizer Limited |
Triazolopyridine compounds
|
US20090270350A1
(en)
|
2006-02-10 |
2009-10-29 |
Pfizer Inc. |
Pyridinone Pyrazole Urea and Pyrimidinone Pyrazole Urea Derivatives
|
GB0603684D0
(en)
|
2006-02-23 |
2006-04-05 |
Novartis Ag |
Organic compounds
|
TW200808313A
(en)
|
2006-03-07 |
2008-02-16 |
Vertex Pharma |
Compositions and methods for treating rheumatoid arthritis
|
BRPI0708644A2
(pt)
|
2006-03-07 |
2011-06-07 |
Bristol-Myers Squibb Company |
compostos de pró-fármaco de anilina de pirrolotriazina úteis como inibidores de cinase
|
NZ570693A
(en)
|
2006-03-20 |
2011-02-25 |
Pfizer Ltd |
Amine derivatives
|
CN101454313A
(zh)
|
2006-03-29 |
2009-06-10 |
阿雷生物药品公司 |
P38抑制剂及其使用方法
|
JP2009533362A
(ja)
|
2006-04-12 |
2009-09-17 |
メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング |
キナーゼ媒介性疾患を治療するための複素環式置換ビスアリール尿素のn−オキシド
|
EP2038289A2
(en)
|
2006-04-21 |
2009-03-25 |
Amgen Inc. |
Thieno-[2,3-d]pyrimidine and thieno-pyridazine compounds and methods of use
|
CA2691214A1
(en)
|
2006-06-09 |
2007-12-21 |
Kemia, Inc. |
Therapy using cytokine inhibitors
|
US20100069409A1
(en)
|
2006-06-16 |
2010-03-18 |
Glaxo Group Limited |
"novel compounds"
|
WO2007147109A2
(en)
|
2006-06-16 |
2007-12-21 |
Glaxo Group Limited |
Novel compounds
|
JP2009542816A
(ja)
|
2006-06-16 |
2009-12-03 |
グラクソ グループ リミテッド |
新規化合物
|
GB0612026D0
(en)
|
2006-06-16 |
2006-07-26 |
Smithkline Beecham Corp |
New use
|
WO2008001930A1
(fr)
|
2006-06-28 |
2008-01-03 |
Aska Pharmaceutical Co., Ltd. |
Dérivé de pyridylisoxazole
|
CN101478989A
(zh)
|
2006-06-28 |
2009-07-08 |
Aska制药株式会社 |
炎性肠病的处置剂
|
CA2656507C
(en)
|
2006-07-17 |
2012-03-20 |
Amgen Inc. |
Quinazoline and pyridopyrimidine derivatives as p38 kinase inhibitors
|
WO2008013823A2
(en)
|
2006-07-26 |
2008-01-31 |
Scios Inc. |
Co-crystals of (2r-trans)-6-chloro-5-[[4-[(4-fluorophenyl)methyl]-2,5-dimethyl-1-piperazinyl]carbonyl]-n,n,1-trimethyl-alpha-oxo-1h-indole-3-acetamide
|
EP2046343B1
(en)
|
2006-07-28 |
2014-05-14 |
Onconova Therapeutics, Inc. |
Formulations of radioprotective alpha, beta unsaturated aryl sulfones
|
PE20080906A1
(es)
|
2006-08-17 |
2008-07-05 |
Kemia Inc |
Derivados heteroarilo como inhibidores de citocina
|
WO2008024391A1
(en)
|
2006-08-22 |
2008-02-28 |
Scios Inc. |
Pharmaceutical formulations of an indole-type derivative and related methods of use
|
AU2007303909A1
(en)
|
2006-10-04 |
2008-04-10 |
Pfizer Limited |
Sulfonamide derivatives as adrenergic agonists and muscarinic antagonists
|
CA2665195C
(en)
|
2006-10-11 |
2011-08-09 |
Amgen Inc. |
Imidazo- and triazolo-pyridine compounds and methods of use thereof
|
US20090275515A1
(en)
|
2006-10-18 |
2009-11-05 |
Yuntae Kim |
2-hydroxy-2-phenylthiophenylpropionamides as androgen receptor modulators
|
WO2008049842A2
(en)
|
2006-10-26 |
2008-05-02 |
Boehringer Ingelheim International Gmbh |
Egfr kinase inhibitor combinations for the treatment of respiratory and gastrointestinal disorders
|
US7943617B2
(en)
|
2006-11-27 |
2011-05-17 |
Bristol-Myers Squibb Company |
Heterobicyclic compounds useful as kinase inhibitors
|
WO2008071665A1
(en)
|
2006-12-12 |
2008-06-19 |
Smithkline Beecham Corporation |
A nicotinamide derivative useful as p38 kinase inhibitor
|
WO2008071664A1
(en)
|
2006-12-12 |
2008-06-19 |
Smithkline Beecham Corporation |
Nicotinamide derivative used as a p38 kinase inhibitor
|
ATE556055T1
(de)
|
2006-12-13 |
2012-05-15 |
Pfizer Prod Inc |
Verfahren zur herstellung von 3-(4-(2,4- difluorbenzyloxy)-3-brom-6-methyl- 2-oxopyridin- 1(2h)-yl)-n,4-dimethylbenzamid
|
CN101657460A
(zh)
|
2006-12-13 |
2010-02-24 |
基利得科学公司 |
用于治疗肺炎症和支气管收缩的作为抗炎性信号转导调节剂(AISTM’S)和β-激动剂的相互前药的单磷酸酯
|
CA2672719A1
(en)
|
2006-12-19 |
2008-06-26 |
F. Hoffmann-La Roche Ag |
Pyrazolo [3, 4 -d] pyrimidine p38 map kinase inhibitors
|
EP2099779A1
(en)
|
2006-12-20 |
2009-09-16 |
Brystol-Myers Squibb Company |
Crystalline forms of aryl-substituted pyrazole-amide compounds
|
WO2008089034A2
(en)
|
2007-01-11 |
2008-07-24 |
Kemia, Inc. |
Cytokine inhibitors
|
WO2008098096A1
(en)
|
2007-02-08 |
2008-08-14 |
Boehringer Ingelheim International Gmbh |
Anti-cytokine heterocyclic compounds
|
WO2008099615A1
(ja)
|
2007-02-16 |
2008-08-21 |
Aska Pharmaceutical Co., Ltd. |
微粒子油性懸濁液を含む医薬組成物
|
JP2010519203A
(ja)
|
2007-02-16 |
2010-06-03 |
メルク・シャープ・エンド・ドーム・コーポレイション |
生物活性分子の活性を強化するための組成物及び方法
|
WO2008104473A2
(en)
|
2007-02-28 |
2008-09-04 |
F. Hoffmann-La Roche Ag |
Pyrazolopyriidine derivatives and their use as kinase inhibitors
|
SI2125714T1
(sl)
|
2007-03-16 |
2011-10-28 |
Pfizer Ltd |
Hidrokloridna sol 5-(3-(3-hidroksifenoksi)azetidin-1-il)-5-metil-2,2-difenilheksanamida
|
AU2008248073B2
(en)
|
2007-05-07 |
2011-03-24 |
Amgen Inc. |
Pyrazolo-pyridinone compounds, process for their preparation, and their pharmaceutical use
|
AU2008248296B2
(en)
|
2007-05-07 |
2011-12-01 |
Amgen Inc. |
Pyrazolo-pyridinone and pyrazolo-pyrazinone compounds as P38 modulators, process for their preparation, and their pharmaceutical use
|
AU2008276512A1
(en)
|
2007-07-17 |
2009-01-22 |
Amgen Inc. |
Thiadiazole modulators of PKB
|
AU2008276521B2
(en)
|
2007-07-17 |
2011-11-03 |
Amgen Inc. |
Heterocyclic modulators of PKB
|
US7943658B2
(en)
|
2007-07-23 |
2011-05-17 |
Bristol-Myers Squibb Company |
Indole indane amide compounds useful as CB2 agonists and method
|
US8202899B2
(en)
|
2007-07-25 |
2012-06-19 |
Array Biopharma Inc. |
Pyrazole urea derivatives used as kinase inhibitors
|
WO2009034432A2
(en)
|
2007-09-14 |
2009-03-19 |
Pfizer Limited |
Novel compounds active as muscarinic receptor antagonists
|
WO2009038784A1
(en)
|
2007-09-21 |
2009-03-26 |
Amgen Inc. |
Triazole fused heteroaryl compounds as p38 kinase inhibitors
|
ES2399945T3
(es)
|
2007-11-30 |
2013-04-04 |
Pfizer Limited |
Agonistas novedosos de los receptores de glucocorticoides
|
GB0724258D0
(en)
|
2007-12-12 |
2008-01-30 |
Glaxo Group Ltd |
Novel combinations
|
WO2009074518A1
(en)
|
2007-12-12 |
2009-06-18 |
Glaxo Group Limited |
Combinations of prolinamide p2x7 modulators with further therapeutic agents
|
WO2009078992A1
(en)
|
2007-12-17 |
2009-06-25 |
Amgen Inc. |
Linear tricyclic compounds as p38 kinase inhibitors
|
WO2009094556A2
(en)
|
2008-01-25 |
2009-07-30 |
Bristol-Myers Squibb Pharma Company |
Identification of predictive markers of response to dasatinib in human colon cancer
|
EP2254630A1
(de)
|
2008-02-20 |
2010-12-01 |
Boehringer Ingelheim International GmbH |
Pulverinhalatoren
|
US8367671B2
(en)
|
2008-03-21 |
2013-02-05 |
Amgen Inc. |
Pyrazolo[3.4-B]pyrazine compounds as p38 modulators and methods of use as anti-inflamatory agents
|
JP2009263234A
(ja)
|
2008-04-21 |
2009-11-12 |
Ranbaxy Lab Ltd |
ホスホジエステラーゼタイプiv阻害剤の組成物
|
AR072008A1
(es)
|
2008-06-13 |
2010-07-28 |
Merck & Co Inc |
Compuestos heterobiciclicos como agentes de inhibicion de quinasa p38
|
CN102131806A
(zh)
|
2008-06-20 |
2011-07-20 |
百时美施贵宝公司 |
用作激酶抑制剂的三唑并吡啶化合物
|
EP2300466B1
(en)
|
2008-06-20 |
2014-08-06 |
Bristol-Myers Squibb Company |
Imidazopyridine and imidazopyrazine compounds useful as kinase inhibitors
|
WO2009158450A1
(en)
|
2008-06-25 |
2009-12-30 |
Bristol-Myers Squibb Company |
Crystalline forms of ((((4-((5-(cyclopropylcarbamoyl)-2-methylphenyl)amino)-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yl)carbonyl)(propyl)carbamoyl)oxy)methyl (4-(phosphonooxy)phenyl)acetate, preparation and use thereof
|
WO2009158446A2
(en)
|
2008-06-25 |
2009-12-30 |
Bristol-Myers Squibb Company |
Crystalline forms of ((((4-((5-(cyclopropylcarbamoyl)-2-methylphenyl)amino)-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yl)carbonyl)(propyl)carbamoyl)oxy)methyl (4-(phosphonooxy)phenyl)acetate, method of preparation and use thereof
|
US8263623B2
(en)
|
2008-07-11 |
2012-09-11 |
Pfizer Inc. |
Triazol derivatives useful for the treatment of diseases
|
WO2010007561A1
(en)
|
2008-07-15 |
2010-01-21 |
Pfizer Limited |
Novel compounds active as muscarinic receptor antagonists
|
PE20110312A1
(es)
|
2008-07-15 |
2011-06-25 |
Pfizer Ltd |
Compuestos piperidinicos de esteres del acido bifenil-2-ilcarbamico como antagonistas del receptor muscarinico m3
|
WO2010025202A1
(en)
|
2008-08-29 |
2010-03-04 |
Amgen Inc. |
PYRIDO[3,2-d]PYRIDAZINE-2(1H)-ONE COMPOUNDS AS P38 MODULATORS AND METHODS OF USE THEREOF
|
US8455495B2
(en)
|
2008-08-29 |
2013-06-04 |
Amgen Inc. |
Pyridazino-pyridinone compounds and methods of use
|
WO2010038428A1
(ja)
|
2008-09-30 |
2010-04-08 |
武田薬品工業株式会社 |
タキサン系抗がん剤の置き換え薬
|
EP2206534A1
(de)
|
2008-10-09 |
2010-07-14 |
c-a-i-r biosciences GmbH |
Dibenzocycloheptanonderivate und pharmazeutische Mittel, welche diese Verbindungen enthalten
|
WO2010042646A1
(en)
|
2008-10-10 |
2010-04-15 |
Amgen Inc. |
Aza- and diaza-phthalazine compounds as p38 map kinase modulators and methods of use thereof
|
US8497269B2
(en)
|
2008-10-10 |
2013-07-30 |
Amgen Inc. |
Phthalazine compounds as p38 map kinase modulators and methods of use thereof
|
US20110263647A1
(en)
|
2009-01-15 |
2011-10-27 |
Amgen Inc. |
Fluoroisoquinoline substituted thiazole compounds and methods of use
|
EP2393492A1
(en)
|
2009-02-09 |
2011-12-14 |
Boehringer Ingelheim International GmbH |
New pharmaceutical compositions for treatment of respiratory and gastrointestinal disorders
|
EP2396303A2
(en)
|
2009-02-13 |
2011-12-21 |
Vertex Pharmaceuticals Incorporated |
Solid forms of 2-(2, 4-difluorophenyl)-6-(1-(2,6-difluorophenyl)ureido)nicotinamide
|
EP2396302A2
(en)
|
2009-02-13 |
2011-12-21 |
Vertex Pharmceuticals Incorporated |
Processes for producing phenyl-6-(1-(phenyl)ureido)nicotinamides)
|
GB0902648D0
(en)
|
2009-02-17 |
2009-04-01 |
Argenta Discovery Ltd |
Pharmaceutical compounds and compositions
|
US8557797B2
(en)
|
2009-02-17 |
2013-10-15 |
Chiesi Farmaceutici S.P.A. |
Triazolopyridine derivatives and their therapeutic use
|
WO2010120963A1
(en)
|
2009-04-16 |
2010-10-21 |
Bristol-Myers Squibb Company |
Tablet formulation for p38 inhibitor and method
|
AU2010245072B2
(en)
|
2009-05-05 |
2013-11-28 |
Merck Sharp & Dohme Corp. |
p38 kinase inhibiting agents
|
US20120157500A1
(en)
|
2009-08-24 |
2012-06-21 |
Weikang Tao |
Jak inhibition blocks rna interference associated toxicities
|
KR20120102642A
(ko)
|
2009-10-22 |
2012-09-18 |
제넨테크, 인크. |
축삭 변성의 조절
|
WO2011063076A1
(en)
|
2009-11-19 |
2011-05-26 |
Itherx Pharmaceuticals, Inc. |
Methods of treating hepatitis c virus with oxoacetamide compounds
|
WO2011083387A1
(en)
|
2010-01-07 |
2011-07-14 |
Pfizer Limited |
Hydrochloride salt of biphenyl-2-yl-carbamic acid 1-{9-[(3-fluoro-4-hydroxy-benzoyl)-methyl-amino]-nonyl}-piperidin-4-yl ester
|
EA022360B1
(ru)
|
2010-03-24 |
2015-12-30 |
Онконова Терапьютикс, Инк. |
Композиции и способы для профилактики и лечения ран
|
SI2552199T1
(sl)
|
2010-03-26 |
2015-10-30 |
Onconova Therapeutics, Inc. |
Izboljšana stabilna vodna formulacija (e)-4-karboksistiril-4-klorobenzil sulfona
|
GB201009731D0
(en)
|
2010-06-10 |
2010-07-21 |
Pulmagen Therapeutics Inflamma |
Kinase inhibitors
|
SG186855A1
(en)
|
2010-06-28 |
2013-02-28 |
Merck Patent Gmbh |
2,4- diaryl - substituted [1,8] naphthyridines as kinase inhibitors for use against cancer
|
CN102971293A
(zh)
|
2010-07-05 |
2013-03-13 |
默克专利有限公司 |
用于治疗激酶诱导的疾病的联吡啶衍生物
|
WO2012031057A1
(en)
|
2010-09-01 |
2012-03-08 |
Bristol-Myers Squibb Company |
Bms- 582949 for the treatment of resistant rheumatic disease
|
BR112013012943A2
(pt)
|
2010-11-29 |
2020-08-11 |
Genentech, Inc |
método de diagnóstico de uma disfunção neurodegenerativa em um sujeito, método de monitoramento de doença, método de avaliação de predisposição e kit
|
TWI410425B
(zh)
|
2010-12-03 |
2013-10-01 |
Lilly Co Eli |
唑并[5,4-b]吡啶-5-基化合物
|
MX2013010163A
(es)
|
2011-03-09 |
2013-10-30 |
Merck Patent Gmbh |
Derivados de pirido[2,3-b] pirazina y sus usos terapeuticos.
|
EP2707369B1
(en)
|
2011-05-09 |
2016-07-27 |
Eip Pharma, LLC |
Compositions and methods for treating alzheimer's disease
|
PT2718280E
(pt)
|
2011-06-10 |
2015-11-25 |
Chiesi Farma Spa |
Compostos possuindo uma atividade antagonista de um recetor muscarínico e agonista de um recetor beta2 adrenérgico
|
ES2627120T3
(es)
|
2011-07-08 |
2017-07-26 |
Helmholtz-Zentrum für Infektionsforschung GmbH |
Medicamento para el tratamiento del cáncer de hígado
|
JP6055481B2
(ja)
|
2011-11-11 |
2016-12-27 |
イーライ リリー アンド カンパニー |
卵巣癌のための併用療法
|
WO2013086002A1
(en)
|
2011-12-05 |
2013-06-13 |
Cellworks Research India Private Limited |
Compositions, process of preparation of said compositions and method of treating cancer
|
CA2858447C
(en)
|
2011-12-09 |
2020-10-27 |
Monique Bodil Van Niel |
Tryazolopyridine derivatives as kinase inhibitors
|
EP2788345B1
(en)
|
2011-12-09 |
2020-06-10 |
Chiesi Farmaceutici S.p.A. |
Derivatives of 4-hydroxy-1,2,3,4-tetrahydronaphtalen-1-yl urea and their use in the treatment of, inter alia, diseases of the respiratory tract
|
CN103974953B
(zh)
|
2011-12-09 |
2016-06-29 |
奇斯药制品公司 |
激酶抑制剂
|
RU2666530C2
(ru)
|
2012-01-12 |
2018-09-11 |
Йейл Юниверсити |
Соединения и способы усиления деградации белков-мишеней и других полипептидов с помощью е3 убиквитин лигазы
|
SG11201405357SA
(en)
|
2012-03-01 |
2014-10-30 |
Array Biopharma Inc |
Crystalline forms of 1- (3 -tert-butyl- 1 - p-tolyl- 1h- pyrazol- 5 -yl) -3- (5-fluoro-2- (1- ( 2 - hydroxyethyl) - indazol- 5 -yloxy) benzyl) urea hydrochloride
|
WO2013139809A1
(en)
|
2012-03-20 |
2013-09-26 |
Novartis Ag |
Use of a pyrazole derivative in the treatment of acute exacerbations of chronic obstructive pulmonary disease
|
EP2852584B1
(en)
|
2012-05-22 |
2018-02-28 |
F. Hoffmann-La Roche AG |
Substituted dipyridylamines and uses thereof
|
JP2015522612A
(ja)
|
2012-07-17 |
2015-08-06 |
グラクソスミスクライン・リミテッド・ライアビリティ・カンパニーGlaxoSmithKline LLC |
急性冠症候群の治療におけるニコチンアミド誘導体
|
GB201214750D0
(en)
|
2012-08-17 |
2012-10-03 |
Respivert Ltd |
Compounds
|
GB201215357D0
(en)
|
2012-08-29 |
2012-10-10 |
Respivert Ltd |
Compounds
|
EP2890695A2
(en)
|
2012-08-29 |
2015-07-08 |
Respivert Limited |
Kinase inhibitors
|
WO2014033449A1
(en)
|
2012-08-29 |
2014-03-06 |
Respivert Limited |
Kinase inhibitors
|
WO2014033446A1
(en)
|
2012-08-29 |
2014-03-06 |
Respivert Limited |
Kinase inhibitors
|
US9155747B2
(en)
|
2012-09-13 |
2015-10-13 |
Chiesi Farmaceutici S.P.A. |
Isoxazolidine derivatives
|
EP2925742B1
(en)
|
2012-11-16 |
2016-10-26 |
Respivert Limited |
Kinase inhibitors
|
EP2925323B1
(en)
|
2012-11-30 |
2017-05-17 |
F. Hoffmann-La Roche AG |
An inhibitor of bruton's tyrosine kinase
|
US9370527B2
(en)
|
2012-12-28 |
2016-06-21 |
The Regents Of The University Of Michigan |
Amelioration of intestinal fibrosis and treatment of Crohn's disease
|
JP6433922B2
(ja)
|
2013-02-27 |
2018-12-05 |
アレイ バイオファーマ、インコーポレイテッド |
インダゾール誘導体の調製に使用するための中間体およびその調製方法
|
US20160016934A1
(en)
|
2013-03-14 |
2016-01-21 |
Respivert Limited |
Kinase inhibitors
|
GB201305714D0
(en)
|
2013-03-28 |
2013-05-15 |
Ucl Business Plc |
Method
|
BR112015024671A2
(pt)
|
2013-04-02 |
2017-07-18 |
Respivert Ltd |
derivados de ureia úteis como inibidores de quinase
|
WO2014181213A1
(en)
|
2013-05-10 |
2014-11-13 |
Pfizer Inc. |
Crystalline form of (sa)-(-)-3-(3-bromo-4-((2,4-difluorobenzyl)oxy)-6-methyl-2-oxopyridin-1 (2h)-yl)-n,4-dimethylbenzamide
|
WO2014195402A1
(en)
|
2013-06-06 |
2014-12-11 |
Chiesi Farmaceutici S.P.A. |
Kinase inhibitors
|
RU2637944C2
(ru)
|
2013-06-06 |
2017-12-08 |
КЬЕЗИ ФАРМАЧЕУТИЧИ С.п.А. |
Ингибиторы киназы
|
WO2014195400A1
(en)
|
2013-06-06 |
2014-12-11 |
Chiesi Farmaceutici S.P.A. |
Kinase inhibitors
|
US9707219B2
(en)
|
2013-07-10 |
2017-07-18 |
Glaxosmithkline Intellectual Property (No.2) Limited |
Losmapimod for use in treating glomerular disease
|
WO2015006753A2
(en)
|
2013-07-12 |
2015-01-15 |
The Regents Of The University Of California |
Therapies for diseases caused by arthropod-borne parasites
|
US9814728B2
(en)
*
|
2013-09-20 |
2017-11-14 |
Saint Louis University |
Inhibition of DUX4 expression using bromodomain and extra-terminal domain protein inhibitors (BETi)
|
CA2928626C
(en)
*
|
2013-11-14 |
2023-03-14 |
The Doshisha |
Drug for treating corneal endothelium by promoting cell proliferation or inhibiting cell damage
|
EP3083604A1
(en)
|
2013-12-20 |
2016-10-26 |
Respivert Limited |
Urea derivatives useful as kinase inhibitors
|
MX2016008110A
(es)
|
2013-12-20 |
2016-08-19 |
Hoffmann La Roche |
Derivados de pirazol como inhibidores de la cinasa de cremallera de leucina dual (dlk) y usos de los mismos.
|
CN110522731B
(zh)
|
2014-02-14 |
2022-08-02 |
瑞斯比维特有限公司 |
作为抗炎化合物的芳族杂环化合物
|
TW201609700A
(zh)
|
2014-02-19 |
2016-03-16 |
H 朗德貝克公司 |
2-胺基-3,5,5-三氟-3,4,5,6-四氫吡啶作爲bace1抑制劑用於治療阿茲海默症
|
US20230190750A1
(en)
|
2014-06-13 |
2023-06-22 |
Genentech, Inc. |
Methods of treating and preventing cancer drug resistance
|
US20170204187A1
(en)
|
2014-06-13 |
2017-07-20 |
Genentech, Inc. |
Methods of treating and preventing cancer drug resistance
|
WO2016007616A1
(en)
|
2014-07-09 |
2016-01-14 |
Eip Pharma, Llc |
Methods for treating neurologic disorders
|
WO2016051186A1
(en)
|
2014-10-01 |
2016-04-07 |
Respivert Limited |
N-phenyl-3-quinazolin-6-yl-benzamide derivatives as p38 kinase inhibitors
|
MA40774A
(fr)
|
2014-10-01 |
2017-08-08 |
Respivert Ltd |
Dérivés de diaryle-urée en tant qu'inhibiteurs de kinase p38
|
WO2016049677A1
(en)
|
2014-10-03 |
2016-04-07 |
The Walter And Eliza Hall Institute Of Medical Research |
Method of treating cancer
|
WO2016066687A1
(en)
|
2014-10-30 |
2016-05-06 |
Glaxosmithkline Intellectual Property (No.2) Limited |
Losmapimod for treating copd
|
WO2016114655A1
(en)
*
|
2015-01-12 |
2016-07-21 |
Ry Pharma B.V. |
Treating neuromuscular or neurologic disease through reducing gabaergic and/or glycinergic inhibitory neurotransmitter overstimulation
|
US10538763B2
(en)
|
2015-01-16 |
2020-01-21 |
Ionis Pharmaceuticals, Inc. |
Compounds and methods for modulation of DUX4
|
ES2918975T3
(es)
|
2015-02-06 |
2022-07-21 |
Association Inst De Myologie |
Tratamiento de la distrofia facioescapulohumeral
|
TWI703138B
(zh)
|
2015-02-12 |
2020-09-01 |
義大利商吉斯藥品公司 |
具有蕈毒鹼受體拮抗劑及β2腎上腺素受體促效劑活性之化合物
|
WO2016142310A1
(en)
|
2015-03-09 |
2016-09-15 |
F. Hoffmann-La Roche Ag |
Tricyclic dlk inhibitors and uses thereof
|
US20190083470A1
(en)
*
|
2015-03-24 |
2019-03-21 |
The Trustees Of The University Of Pennsylvania |
P38 map kinase inhibitors for treating friedreich's ataxia
|
JP2016193870A
(ja)
|
2015-04-01 |
2016-11-17 |
国立大学法人広島大学 |
慢性骨髄性白血病治療剤
|
US9968604B2
(en)
|
2015-04-16 |
2018-05-15 |
Chiesi Farmaceutici S.P.A. |
Chromene derivatives as phoshoinositide 3-kinases inhibitors
|
CN107921106B
(zh)
*
|
2015-05-20 |
2023-09-08 |
住友制药株式会社 |
Wt1抗原肽和免疫调节剂的组合用途
|
WO2016198698A2
(en)
|
2015-06-12 |
2016-12-15 |
Cnic Fundación Centro Nacional De Investigaciones Cardiovasculares Carlos Iii |
P38 inhibitors for the treatment and prophylaxis of liver cancer
|
JP6873980B2
(ja)
|
2015-09-14 |
2021-05-19 |
ファイザー・インク |
LRRK2阻害薬としての新規のイミダゾ[4,5−c]キノリンおよびイミダゾ[4,5−c][1,5]ナフチリジン誘導体
|
WO2017075013A1
(en)
|
2015-10-26 |
2017-05-04 |
Eip Pharma, Llc |
Methods and compositions for recovery from stroke
|
US9427439B1
(en)
|
2015-10-26 |
2016-08-30 |
Eip Pharma, Llc |
Methods and compositions for recovery from stroke
|
EP3383867B1
(en)
|
2015-12-03 |
2021-04-14 |
Chiesi Farmaceutici S.p.A. |
Compounds having muscarinic receptor antagonist and beta2 adrenergic receptor agonist activity
|
AR107163A1
(es)
|
2015-12-23 |
2018-03-28 |
Chiesi Farm Spa |
Inhibidores de quinasa
|
EP3381472A4
(en)
|
2015-12-24 |
2019-07-31 |
The Doshisha |
MEDICINAL PRODUCTS FOR THE TREATMENT OR PREVENTION OF DISTURBANCES CAUSED BY TGF SIGNALS AND USE THEREOF
|
CN109310768A
(zh)
|
2015-12-29 |
2019-02-05 |
得克萨斯大学体系董事会 |
用于治疗癌症的p38 mapk的抑制
|
JP2019507186A
(ja)
*
|
2016-02-01 |
2019-03-14 |
プレジデント アンド フェローズ オブ ハーバード カレッジ |
マウス衛星細胞の増殖のための小分子
|
WO2017134053A1
(en)
|
2016-02-04 |
2017-08-10 |
Chiesi Farmaceutici S.P.A. |
Pyrazole derivatives as phosphoinositide 3-kinases inhibitors
|
MY195671A
(en)
|
2016-06-08 |
2023-02-03 |
Support Venture Gmbh |
Pharmaceutical Combinations for Treating Cancer
|
GB201611712D0
(en)
|
2016-07-02 |
2016-08-17 |
Hvivo Services Ltd |
Methods and compounds for the treatment or prevention of severe or persistent influenza
|
AU2018221891B2
(en)
|
2017-02-15 |
2023-05-25 |
The University Of Melbourne |
A method of treatment
|
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
|
ES2927715T3
(es)
*
|
2017-10-05 |
2022-11-10 |
Fulcrum Therapeutics Inc |
Inhibidores de la quinasa p38 reducen la expresión de dux4 y de los genes que le siguen para el tratamiento de la FSHD
|
WO2019103926A1
(en)
|
2017-11-21 |
2019-05-31 |
Saint Louis University |
P38 inhibitors for the treatment of fshd
|
CA3119781A1
(en)
|
2018-11-20 |
2020-05-28 |
Fulcrum Therapeutics, Inc. |
Compositions and methods for increasing fetal hemoglobin and treating sickle cell disease
|
WO2020132004A1
(en)
*
|
2018-12-20 |
2020-06-25 |
Saint Louis University |
Bet inhibitors for modulating dux4 expression in fshd
|
CA3133751A1
(en)
|
2019-03-15 |
2020-09-24 |
Fulcrum Therapeutics, Inc. |
Macrocyclic azolopyridine derivatives as eed and prc2 modulators
|
CA3189065A1
(en)
*
|
2020-09-11 |
2022-03-17 |
Arrowhead Pharmaceuticals, Inc. |
Rnai agents for inhibiting expression of dux4, compositions thereof, and methods of use
|