CA2165176A1
(fr)
*
|
1993-06-18 |
1995-01-05 |
Samuel L. Graham |
Inhibiteurs de la farnesyl-proteine transferase
|
US5856326A
(en)
*
|
1995-03-29 |
1999-01-05 |
Merck & Co., Inc. |
Inhibitors of farnesyl-protein transferase
|
US5712280A
(en)
*
|
1995-04-07 |
1998-01-27 |
Schering Corporation |
Tricyclic compounds useful for inhibition of G-protein function and for treatment of proliferative diseases
|
IL117798A
(en)
*
|
1995-04-07 |
2001-11-25 |
Schering Plough Corp |
Tricyclic compounds useful for inhibiting the function of protein - G and for the treatment of malignant diseases, and pharmaceutical preparations containing them
|
US5801175A
(en)
*
|
1995-04-07 |
1998-09-01 |
Schering Corporation |
Tricyclic compounds useful for inhibition of G-protein function and for treatment of proliferative diseases
|
IL117797A0
(en)
*
|
1995-04-07 |
1996-08-04 |
Pharmacopeia Inc |
Tricyclic compounds useful for inhibition of G-protein function and for treatment of proliferative diseases
|
JPH11509204A
(ja)
*
|
1995-07-13 |
1999-08-17 |
ユニバーシテイ・オブ・シンシナテイ |
神経線維腫症の治療に有用な化合物
|
BR9709773A
(pt)
*
|
1996-06-07 |
1999-08-10 |
Hoffmann La Roche |
Derivados de dibenzo-oxazepina e dioxepina e seu uso como agentes antitumorais
|
DE19624659A1
(de)
|
1996-06-20 |
1998-01-08 |
Klinge Co Chem Pharm Fab |
Neue Pyridylalken- und Pyridylalkinsäureamide
|
US6451816B1
(en)
|
1997-06-20 |
2002-09-17 |
Klinge Pharma Gmbh |
Use of pyridyl alkane, pyridyl alkene and/or pyridyl alkine acid amides in the treatment of tumors or for immunosuppression
|
DE19624704A1
(de)
|
1996-06-20 |
1998-01-08 |
Klinge Co Chem Pharm Fab |
Neue Pyridylalkansäureamide
|
US5861395A
(en)
*
|
1996-09-13 |
1999-01-19 |
Schering Corporation |
Compounds useful for inhibition of farnesyl proteins transferase
|
ATE281450T1
(de)
*
|
1996-09-13 |
2004-11-15 |
Schering Corp |
Verbindungen als inhibitoren von farnesylprotein- transferase
|
CA2266014A1
(fr)
*
|
1996-09-13 |
1998-03-19 |
Schering Corporation |
Composes servant a inhiber la farnesyl proteine transferase
|
IL128927A0
(en)
*
|
1996-09-13 |
2000-02-17 |
Schering Corp |
Substituted benzocycloheptapyridine derivatives useful for inhibition of farnesyl protein transferase
|
US5945429A
(en)
*
|
1996-09-13 |
1999-08-31 |
Schering Corporation |
Compounds useful for inhibition of farnesyl protein transferase
|
US5985879A
(en)
*
|
1996-09-13 |
1999-11-16 |
Schering Corporation |
Compounds useful for inhibition of farnesyl protein transferase
|
US6071907A
(en)
*
|
1996-09-13 |
2000-06-06 |
Schering Corporation |
Tricyclic compounds useful as FPT inhibitors
|
KR20000036120A
(ko)
*
|
1996-09-13 |
2000-06-26 |
둘락 노먼 씨. |
파르네실 단백질 트랜스퍼라제에 대한 트리사이클릭 저해제
|
US6030982A
(en)
*
|
1996-09-13 |
2000-02-29 |
Schering Corporationm |
Compounds useful for inhibition of farnesyl protein transferase
|
ID22045A
(id)
*
|
1996-09-13 |
1999-08-26 |
Schering Corp |
Senyawa-senyawa trisiklik yang berguna untuk penghambatan fungsi protein-g dan untuk pengobatan penyakit-penyakit proliferatif
|
US5958890A
(en)
*
|
1996-09-13 |
1999-09-28 |
Schering Corporation |
Tricyclic compounds useful for inhibition of G-protein function and for treatment of proliferative diseases
|
US20030060434A1
(en)
|
1997-02-18 |
2003-03-27 |
Loretta Nielsen |
Combined tumor suppressor gene therapy and chemotherapy in the treatment of neoplasms
|
ES2287974T3
(es)
*
|
1997-02-18 |
2007-12-16 |
Canji, Inc. |
Terapia genica supresora de tumor y quimioterapia combinadas en el tratamiento neoplasmas.
|
WO1998057949A1
(fr)
*
|
1997-06-17 |
1998-12-23 |
Schering Corporation |
Nouveaux sulfonamides tricycliques inhibiteurs de la farnesyle transferase
|
NZ501613A
(en)
*
|
1997-06-17 |
2001-11-30 |
Schering Corp |
Benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-4-(4-pyridinylacetyl) piperazine derivatives useful as inhibitors of farnesyl-protein transferase
|
US6689789B2
(en)
|
1997-06-17 |
2004-02-10 |
Schering Corporation |
Compounds useful for inhibition of farnesyl protein transferase
|
US6218401B1
(en)
|
1997-06-17 |
2001-04-17 |
Schering Corporation |
Phenyl-substituted tricyclic inhibitors of farnesyl-protein transferase
|
US5877177A
(en)
*
|
1997-06-17 |
1999-03-02 |
Schering Corporation |
Carboxy piperidylacetamide tricyclic compounds useful for inhibition of G-protein function and for treatment of proliferative diseases
|
US6426352B1
(en)
|
1997-06-17 |
2002-07-30 |
Schering Corporation |
Sulfonamide inhibitors of farnesyl-protein transferase
|
DE19756235A1
(de)
*
|
1997-12-17 |
1999-07-01 |
Klinge Co Chem Pharm Fab |
Neue piperidinylsubstituierte Pyridylalkan- alken- und -alkincarbonsäureamide
|
DE19756261A1
(de)
|
1997-12-17 |
1999-07-01 |
Klinge Co Chem Pharm Fab |
Neue arylsubstituierte Pyridylalkan-, alken- und alkincarbonsäureamide
|
DE19756212A1
(de)
*
|
1997-12-17 |
1999-07-01 |
Klinge Co Chem Pharm Fab |
Neue, mit einem cyclischen Imid substituierte Pyridylalkan-, alken- und -alkincarbonsäureamide
|
US6903118B1
(en)
|
1997-12-17 |
2005-06-07 |
Klinge Pharma Gmbh |
Piperazinyl-substituted pyridylalkane, alkene and alkine carboxamides
|
US6358985B1
(en)
*
|
1998-07-02 |
2002-03-19 |
Merck & Co., Inc. |
Inhibitors of prenyl-protein transferase
|
EP1031564A1
(fr)
|
1999-02-26 |
2000-08-30 |
Klinge Pharma GmbH |
Inhibiteurs de la formation du nicotinamide mononucléotide et leur utilisation dans le traitement du cancer
|
PE20020635A1
(es)
*
|
2000-11-29 |
2002-07-11 |
Schering Corp |
Compuestos triciclicos como inhibidores de la farnesil transferasa
|
US7074921B2
(en)
|
2001-11-13 |
2006-07-11 |
Bristol Myers Squibb Company |
Process for the preparation of 3,7-disubstituted-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine compounds
|
AU2002334383A1
(en)
*
|
2002-09-24 |
2004-04-19 |
Morepen Laboratories Limited |
An improved process for the production of desloratadine
|
WO2005017160A2
(fr)
|
2003-08-13 |
2005-02-24 |
Children's Hospital Medical Center |
Mobilisation de cellules hematopoietques
|
ATE550019T1
(de)
|
2005-05-17 |
2012-04-15 |
Merck Sharp & Dohme |
Cis-4-ä(4-chlorophenyl)sulfonylü-4-(2,5- difluorophenyl)cyclohexanepropansäure zur behandlug von krebs
|
GB0603041D0
(en)
|
2006-02-15 |
2006-03-29 |
Angeletti P Ist Richerche Bio |
Therapeutic compounds
|
LT2010528T
(lt)
|
2006-04-19 |
2017-12-27 |
Novartis Ag |
6-o-pakeistieji benzoksazolo junginiai bei csf-1r signalo perdavimo slopinimo būdai
|
CA2664113C
(fr)
|
2006-09-22 |
2013-05-28 |
Merck & Co., Inc. |
Utilisation de la platencine et de la platensimycine en tant qu'inhibiteurs de la synthese des acides gras pour traiter l'obesite, lediabete et le cancer
|
US20110218176A1
(en)
|
2006-11-01 |
2011-09-08 |
Barbara Brooke Jennings-Spring |
Compounds, methods, and treatments for abnormal signaling pathways for prenatal and postnatal development
|
JP4611444B2
(ja)
|
2007-01-10 |
2011-01-12 |
イステイチユート・デイ・リチエルケ・デイ・ビオロジア・モレコラーレ・ピ・アンジエレツテイ・エツセ・ピー・アー |
ポリ(adp−リボース)ポリメラーゼ(parp)阻害剤としてのアミド置換インダゾール
|
CN101679266B
(zh)
|
2007-03-01 |
2015-05-06 |
诺华股份有限公司 |
Pim激酶抑制剂及其应用方法
|
AU2008254425A1
(en)
|
2007-05-21 |
2008-11-27 |
Novartis Ag |
CSF-1R inhibitors, compositions, and methods of use
|
EP3103791B1
(fr)
|
2007-06-27 |
2018-01-31 |
Merck Sharp & Dohme Corp. |
Dérivés de 4-carboxybenzylamino utilisés comme inhibiteurs de l'histone désacétylase
|
WO2010114780A1
(fr)
|
2009-04-01 |
2010-10-07 |
Merck Sharp & Dohme Corp. |
Inhibiteurs de l'activité akt
|
JP6073677B2
(ja)
|
2009-06-12 |
2017-02-01 |
デイナ ファーバー キャンサー インスティチュート,インコーポレイテッド |
縮合複素環式化合物およびそれらの使用
|
JP5099731B1
(ja)
|
2009-10-14 |
2012-12-19 |
メルク・シャープ・アンド・ドーム・コーポレーション |
p53活性を増大する置換ピペリジン及びその使用
|
CA2784807C
(fr)
|
2009-12-29 |
2021-12-14 |
Dana-Farber Cancer Institute, Inc. |
Inhibiteurs de kinase raf de type ii
|
JP2013522292A
(ja)
|
2010-03-16 |
2013-06-13 |
デイナ ファーバー キャンサー インスティチュート,インコーポレイテッド |
インダゾール化合物およびそれらの使用
|
EP2584903B1
(fr)
|
2010-06-24 |
2018-10-24 |
Merck Sharp & Dohme Corp. |
Nouveaux composés hétérocycliques utilisés comme inhibiteurs de erk
|
US8518907B2
(en)
|
2010-08-02 |
2013-08-27 |
Merck Sharp & Dohme Corp. |
RNA interference mediated inhibition of catenin (cadherin-associated protein), beta 1 (CTNNB1) gene expression using short interfering nucleic acid (siNA)
|
DK2606134T3
(da)
|
2010-08-17 |
2019-07-22 |
Sirna Therapeutics Inc |
RNA-Interferens-formidlet inhibering af hepatitis-B-virus (HBV)-genekspression ved hjælp af kort interfererende nukleinsyre (siNA)
|
EP2608669B1
(fr)
|
2010-08-23 |
2016-06-22 |
Merck Sharp & Dohme Corp. |
Nouveaux dérivés de pyrazolo[1,5-a]pyrimidine utilisés comme inhibiteurs de mtor
|
WO2012030685A2
(fr)
|
2010-09-01 |
2012-03-08 |
Schering Corporation |
Dérivés d'indazole utilisables en tant qu'inhibiteurs de la voie erk
|
US9242981B2
(en)
|
2010-09-16 |
2016-01-26 |
Merck Sharp & Dohme Corp. |
Fused pyrazole derivatives as novel ERK inhibitors
|
DK2632472T3
(en)
|
2010-10-29 |
2018-03-19 |
Sirna Therapeutics Inc |
RNA INTERFERENCE-MEDIATED INHIBITION OF GENE EXPRESSION USING SHORT INTERFERRING NUCLEIC ACIDS (SINA)
|
EP2654748B1
(fr)
|
2010-12-21 |
2016-07-27 |
Merck Sharp & Dohme Corp. |
Dérivés d'indazole utiles en tant qu'inhibiteurs de erk
|
US20140045847A1
(en)
|
2011-04-21 |
2014-02-13 |
Piramal Enterprises Limited |
Crystalline form of a salt of a morpholino sulfonyl indole derivative and a process for its preparation
|
WO2013063214A1
(fr)
|
2011-10-27 |
2013-05-02 |
Merck Sharp & Dohme Corp. |
Nouveaux composés qui sont des inhibiteurs d'erk
|
US9382239B2
(en)
|
2011-11-17 |
2016-07-05 |
Dana-Farber Cancer Institute, Inc. |
Inhibitors of c-Jun-N-terminal kinase (JNK)
|
EP3358013B1
(fr)
|
2012-05-02 |
2020-06-24 |
Sirna Therapeutics, Inc. |
Compositions d'acide nucléique interférent court (sina)
|
RU2660429C2
(ru)
|
2012-09-28 |
2018-07-06 |
Мерк Шарп И Доум Корп. |
Новые соединения, которые являются ингибиторами erk
|
EP2909194A1
(fr)
|
2012-10-18 |
2015-08-26 |
Dana-Farber Cancer Institute, Inc. |
Inhibiteurs de cycline-dépendante kinase 7 (cdk7)
|
USRE48175E1
(en)
|
2012-10-19 |
2020-08-25 |
Dana-Farber Cancer Institute, Inc. |
Hydrophobically tagged small molecules as inducers of protein degradation
|
WO2014063054A1
(fr)
|
2012-10-19 |
2014-04-24 |
Dana-Farber Cancer Institute, Inc. |
Inhibiteurs de kinase moelle osseuse sur chromosome x (bmx) et leurs utilisations
|
CN102924430B
(zh)
*
|
2012-10-31 |
2014-10-15 |
天津药物研究院 |
地氯雷他定衍生物及其制备方法和用途
|
AU2013352568B2
(en)
|
2012-11-28 |
2019-09-19 |
Merck Sharp & Dohme Llc |
Compositions and methods for treating cancer
|
ES2707305T3
(es)
|
2012-12-20 |
2019-04-03 |
Merck Sharp & Dohme |
Imidazopiridinas sustituidas como inhibidores de HDM2
|
WO2014120748A1
(fr)
|
2013-01-30 |
2014-08-07 |
Merck Sharp & Dohme Corp. |
Purines 2,6,7,8-substituées utilisées en tant qu'inhibiteurs de hdm2
|
WO2015034925A1
(fr)
|
2013-09-03 |
2015-03-12 |
Moderna Therapeutics, Inc. |
Polynucléotides circulaires
|
US20160264551A1
(en)
|
2013-10-18 |
2016-09-15 |
Syros Pharmaceuticals, Inc. |
Heteroaromatic compounds useful for the treatment of prolferative diseases
|
EP3057956B1
(fr)
|
2013-10-18 |
2021-05-05 |
Dana-Farber Cancer Institute, Inc. |
Inhibiteurs polycycliques de la kinase cycline-dépendante 7 (cdk7)
|
WO2015164604A1
(fr)
|
2014-04-23 |
2015-10-29 |
Dana-Farber Cancer Institute, Inc. |
Inhibiteurs de janus kinase marqués de manière hydrophobe et utilisations associées
|
WO2015164614A1
(fr)
|
2014-04-23 |
2015-10-29 |
Dana-Farber Cancer Institute, Inc. |
Inhibiteurs de janus kinase et leurs utilisations
|
JO3589B1
(ar)
|
2014-08-06 |
2020-07-05 |
Novartis Ag |
مثبطات كيناز البروتين c وطرق استخداماتها
|
WO2016105528A2
(fr)
|
2014-12-23 |
2016-06-30 |
Dana-Farber Cancer Institute, Inc. |
Inhibiteurs de la kinase cycline-dépendante 7 (cdk7)
|
US10550121B2
(en)
|
2015-03-27 |
2020-02-04 |
Dana-Farber Cancer Institute, Inc. |
Inhibitors of cyclin-dependent kinases
|
AU2016276963C1
(en)
|
2015-06-12 |
2021-08-05 |
Dana-Farber Cancer Institute, Inc. |
Combination therapy of transcription inhibitors and kinase inhibitors
|
EP4019515A1
(fr)
|
2015-09-09 |
2022-06-29 |
Dana-Farber Cancer Institute, Inc. |
Inhibiteurs de kinases cycline-dépendantes
|
JOP20190055A1
(ar)
|
2016-09-26 |
2019-03-24 |
Merck Sharp & Dohme |
أجسام مضادة ضد cd27
|
EP3609922A2
(fr)
|
2017-04-13 |
2020-02-19 |
Aduro Biotech Holdings, Europe B.V. |
Anticorps anti-sirp alpha
|
EP3706742B1
(fr)
|
2017-11-08 |
2023-03-15 |
Merck Sharp & Dohme LLC |
Inhibiteurs de prmt5
|
WO2019148412A1
(fr)
|
2018-02-01 |
2019-08-08 |
Merck Sharp & Dohme Corp. |
Anticorps bispécifiques anti-pd-1/lag3
|
WO2020033282A1
(fr)
|
2018-08-07 |
2020-02-13 |
Merck Sharp & Dohme Corp. |
Inhibiteurs de prmt5
|
EP3833667B1
(fr)
|
2018-08-07 |
2024-03-13 |
Merck Sharp & Dohme LLC |
Inhibiteurs de prmt5
|