|
WO1995000497A1
(fr)
*
|
1993-06-18 |
1995-01-05 |
Merck & Co., Inc. |
Inhibiteurs de farnesyle-proteine transferase
|
|
US5856326A
(en)
*
|
1995-03-29 |
1999-01-05 |
Merck & Co., Inc. |
Inhibitors of farnesyl-protein transferase
|
|
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
|
|
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
|
|
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
|
|
CA2226623A1
(fr)
*
|
1995-07-13 |
1997-01-30 |
University Of Cincinnati |
Composes utiles dans le traitement des neurofibromatoses
|
|
KR100300152B1
(ko)
*
|
1996-06-07 |
2001-09-06 |
프리돌린 클라우스너, 롤란드 비. 보레르 |
디벤조-옥사제핀과 디벤조-디옥세핀유도체,및 항종양제로서의 이들의 용도
|
|
DE19624704A1
(de)
|
1996-06-20 |
1998-01-08 |
Klinge Co Chem Pharm Fab |
Neue Pyridylalkansäureamide
|
|
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
|
|
US5861395A
(en)
*
|
1996-09-13 |
1999-01-19 |
Schering Corporation |
Compounds useful for inhibition of farnesyl proteins transferase
|
|
HUP0000126A2
(hu)
*
|
1996-09-13 |
2001-04-28 |
Schering Corp. |
Farnezil-protein-transzferáz inhibitorként alkalmazható szubsztituált benzo-ciklohepta-piridin-származékok
|
|
BR9712819A
(pt)
*
|
1996-09-13 |
1999-11-23 |
Schering Corp |
Compostos tricìclicos úteis para inibição de função de proteìna g e para tratamento de doenças proliferativas
|
|
US6030982A
(en)
*
|
1996-09-13 |
2000-02-29 |
Schering Corporationm |
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
|
|
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
|
|
ES2235252T3
(es)
*
|
1996-09-13 |
2005-07-01 |
Schering Corporation |
Inhibidores triciclicos de la farnesil proteina transferasa.
|
|
DE69731481T2
(de)
*
|
1996-09-13 |
2005-10-27 |
Schering Corp. |
Verbindungen als inhibitoren von farnesylprotein-transferase
|
|
US6071907A
(en)
*
|
1996-09-13 |
2000-06-06 |
Schering Corporation |
Tricyclic compounds useful as FPT inhibitors
|
|
US5945429A
(en)
*
|
1996-09-13 |
1999-08-31 |
Schering Corporation |
Compounds useful for inhibition of farnesyl protein transferase
|
|
ES2234036T3
(es)
*
|
1996-09-13 |
2005-06-16 |
Schering Corporation |
Compuestos utiles para inhibir la farnesil-protein-transferasa.
|
|
US20030060434A1
(en)
|
1997-02-18 |
2003-03-27 |
Loretta Nielsen |
Combined tumor suppressor gene therapy and chemotherapy in the treatment of neoplasms
|
|
IL131447A0
(en)
*
|
1997-02-18 |
2001-01-28 |
Canji Inc |
Combined tumor supressor gene therapy and chemotherapy in the treatment of neoplasms
|
|
US6689789B2
(en)
|
1997-06-17 |
2004-02-10 |
Schering Corporation |
Compounds useful for inhibition of farnesyl protein 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
|
|
AU8253698A
(en)
*
|
1997-06-17 |
1999-01-04 |
Schering Corporation |
Novel tricyclic sulfonamide inhibitors of farnesyl-protein transferase
|
|
US6218401B1
(en)
|
1997-06-17 |
2001-04-17 |
Schering Corporation |
Phenyl-substituted tricyclic inhibitors of farnesyl-protein transferase
|
|
US6426352B1
(en)
|
1997-06-17 |
2002-07-30 |
Schering Corporation |
Sulfonamide 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
|
|
DE19756261A1
(de)
|
1997-12-17 |
1999-07-01 |
Klinge Co Chem Pharm Fab |
Neue arylsubstituierte Pyridylalkan-, alken- und alkincarbonsäureamide
|
|
US6903118B1
(en)
|
1997-12-17 |
2005-06-07 |
Klinge Pharma Gmbh |
Piperazinyl-substituted pyridylalkane, alkene and alkine carboxamides
|
|
DE19756212A1
(de)
|
1997-12-17 |
1999-07-01 |
Klinge Co Chem Pharm Fab |
Neue, mit einem cyclischen Imid substituierte Pyridylalkan-, alken- und -alkincarbonsäureamide
|
|
DE19756235A1
(de)
*
|
1997-12-17 |
1999-07-01 |
Klinge Co Chem Pharm Fab |
Neue piperidinylsubstituierte Pyridylalkan- alken- und -alkincarbonsäureamide
|
|
JP2002519376A
(ja)
*
|
1998-07-02 |
2002-07-02 |
メルク エンド カムパニー インコーポレーテッド |
プレニル蛋白トランスフェラーゼ阻害薬
|
|
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
|
|
EP1337522B1
(fr)
*
|
2000-11-29 |
2007-08-29 |
Schering Corporation |
Inhibiteurs de farnesyl proteine transferase
|
|
WO2003041658A2
(fr)
|
2001-11-13 |
2003-05-22 |
Bristol-Myers Squibb Company |
Procede de preparation de composes de 3,7-disubstitue-2,3,4,5- tetrahydro-1h-1,4-benzodiazepine
|
|
WO2004029039A1
(fr)
*
|
2002-09-24 |
2004-04-08 |
Morepen Laboratories Limited |
Procede ameliore pour la production de desloratadine
|
|
WO2005017160A2
(fr)
|
2003-08-13 |
2005-02-24 |
Children's Hospital Medical Center |
Mobilisation de cellules hematopoietques
|
|
ES2382814T3
(es)
|
2005-05-17 |
2012-06-13 |
Merck Sharp & Dohme Ltd. |
Ácido cis-4-[(4-clorofenil)sulfonil]-4-(2,5-difluorofenil)ciclohexanopropanoico para el tratamiento del cáncer
|
|
TWI387592B
(zh)
|
2005-08-30 |
2013-03-01 |
Novartis Ag |
經取代之苯并咪唑及其作為與腫瘤形成相關激酶之抑制劑之方法
|
|
GB0603041D0
(en)
|
2006-02-15 |
2006-03-29 |
Angeletti P Ist Richerche Bio |
Therapeutic compounds
|
|
CA2649288C
(fr)
|
2006-04-19 |
2015-11-24 |
Novartis Ag |
Composes a base de benzoxazole et de benzothiazole 6-0 substitues et procedes d'inhibition de signalisation csf-1r
|
|
US8173629B2
(en)
|
2006-09-22 |
2012-05-08 |
Merck Sharp & Dohme Corp. |
Method of treatment using fatty acid synthesis inhibitors
|
|
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
|
|
CA2679659C
(fr)
|
2007-03-01 |
2016-01-19 |
Novartis Ag |
Inhibiteurs de pim kinase et procedes de leur utilisation
|
|
AU2008254425A1
(en)
|
2007-05-21 |
2008-11-27 |
Novartis Ag |
CSF-1R inhibitors, compositions, and methods of use
|
|
AU2008269154B2
(en)
|
2007-06-27 |
2014-06-12 |
Merck Sharp & Dohme Llc |
4-carboxybenzylamino derivatives as histone deacetylase inhibitors
|
|
WO2010114780A1
(fr)
|
2009-04-01 |
2010-10-07 |
Merck Sharp & Dohme Corp. |
Inhibiteurs de l'activité akt
|
|
US8765747B2
(en)
|
2009-06-12 |
2014-07-01 |
Dana-Farber Cancer Institute, Inc. |
Fused 2-aminothiazole compounds
|
|
PE20121172A1
(es)
|
2009-10-14 |
2012-09-05 |
Merck Sharp & Dohme |
Piperidinas sustituidas con actividad en la hdm2
|
|
WO2011090738A2
(fr)
|
2009-12-29 |
2011-07-28 |
Dana-Farber Cancer Institute, Inc. |
Inhibiteurs de kinase raf de type ii
|
|
US8987275B2
(en)
|
2010-03-16 |
2015-03-24 |
Dana-Farber Cancer Institute, Inc. |
Indazole compounds and their uses
|
|
WO2011163330A1
(fr)
|
2010-06-24 |
2011-12-29 |
Merck Sharp & Dohme Corp. |
Nouveaux composés hétérocycliques utilisés comme inhibiteurs de erk
|
|
EP3330377A1
(fr)
|
2010-08-02 |
2018-06-06 |
Sirna Therapeutics, Inc. |
Inhibition à médiation par interférence arn de caténine (protéine associée à cadhérine), expression du gène bêta 1 (ctnnb1) à l'aide de petit acide nucléique interférent (sian)
|
|
US9029341B2
(en)
|
2010-08-17 |
2015-05-12 |
Sirna Therapeutics, Inc. |
RNA interference mediated inhibition of hepatitis B virus (HBV) gene expression using short interfering nucleic acid (siNA)
|
|
US8883801B2
(en)
|
2010-08-23 |
2014-11-11 |
Merck Sharp & Dohme Corp. |
Substituted pyrazolo[1,5-a]pyrimidines as mTOR inhibitors
|
|
EP2613782B1
(fr)
|
2010-09-01 |
2016-11-02 |
Merck Sharp & Dohme Corp. |
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
|
|
WO2012058210A1
(fr)
|
2010-10-29 |
2012-05-03 |
Merck Sharp & Dohme Corp. |
INHIBITION FACILITÉE PAR L'INTERFÉRENCE D'ARN DE L'EXPRESSION D'UN GÈNE AU MOYEN D'ACIDES NUCLÉIQUES INTERFÉRENTS COURTS (siNA)
|
|
WO2012087772A1
(fr)
|
2010-12-21 |
2012-06-28 |
Schering Corporation |
Dérivés d'indazole utiles en tant qu'inhibiteurs de erk
|
|
AU2012245971A1
(en)
|
2011-04-21 |
2013-10-17 |
Piramal Enterprises Limited |
A crystalline form of a salt of a morpholino sulfonyl indole derivative and a process for its preparation
|
|
EP2770987B1
(fr)
|
2011-10-27 |
2018-04-04 |
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)
|
|
US20150299696A1
(en)
|
2012-05-02 |
2015-10-22 |
Sirna Therapeutics, Inc. |
SHORT INTERFERING NUCLEIC ACID (siNA) COMPOSITIONS
|
|
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
|
|
RS56680B1
(sr)
|
2012-11-28 |
2018-03-30 |
Merck Sharp & Dohme |
Kompozicije i postupci za lečenje kancera
|
|
KR102196882B1
(ko)
|
2012-12-20 |
2020-12-30 |
머크 샤프 앤드 돔 코포레이션 |
Hdm2 억제제로서의 치환된 이미다조피리딘
|
|
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
|
|
EP3057956B1
(fr)
|
2013-10-18 |
2021-05-05 |
Dana-Farber Cancer Institute, Inc. |
Inhibiteurs polycycliques de la kinase cycline-dépendante 7 (cdk7)
|
|
WO2015058126A1
(fr)
|
2013-10-18 |
2015-04-23 |
Syros Pharmaceuticals, Inc. |
Composés hétéroaromatiques utiles dans le traitement de maladies prolifératives
|
|
WO2015164614A1
(fr)
|
2014-04-23 |
2015-10-29 |
Dana-Farber Cancer Institute, Inc. |
Inhibiteurs de janus kinase et leurs utilisations
|
|
US9862688B2
(en)
|
2014-04-23 |
2018-01-09 |
Dana-Farber Cancer Institute, Inc. |
Hydrophobically tagged janus kinase inhibitors and uses thereof
|
|
JO3589B1
(ar)
|
2014-08-06 |
2020-07-05 |
Novartis Ag |
مثبطات كيناز البروتين c وطرق استخداماتها
|
|
JP6854762B2
(ja)
|
2014-12-23 |
2021-04-07 |
ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド |
サイクリン依存性キナーゼ7(cdk7)の阻害剤
|
|
USRE50776E1
(en)
|
2015-03-27 |
2026-02-03 |
Dana-Farber Cancer Institute, Inc. |
Inhibitors of cyclin-dependent kinases
|
|
WO2016201370A1
(fr)
|
2015-06-12 |
2016-12-15 |
Dana-Farber Cancer Institute, Inc. |
Thérapie d'association utilisant des inhibiteurs de transcription et des inhibiteurs de kinases
|
|
AU2016319125B2
(en)
|
2015-09-09 |
2021-04-08 |
Dana-Farber Cancer Institute, Inc. |
Inhibitors of cyclin-dependent kinases
|
|
JOP20190055A1
(ar)
|
2016-09-26 |
2019-03-24 |
Merck Sharp & Dohme |
أجسام مضادة ضد cd27
|
|
EP3525785B1
(fr)
|
2016-10-12 |
2025-08-27 |
Merck Sharp & Dohme LLC |
Inhibiteurs de kdm5
|
|
KR102702926B1
(ko)
|
2017-04-13 |
2024-09-06 |
사이로파 비.브이. |
항-sirp 알파 항체
|
|
US10947234B2
(en)
|
2017-11-08 |
2021-03-16 |
Merck Sharp & Dohme Corp. |
PRMT5 inhibitors
|
|
EP3706747B1
(fr)
|
2017-11-08 |
2025-09-03 |
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
|
|
EP3810132A4
(fr)
|
2018-06-25 |
2022-06-22 |
Dana-Farber Cancer Institute, Inc. |
Inhibiteurs de kinase de la famille taire et utilisations correspondantes
|
|
US11981701B2
(en)
|
2018-08-07 |
2024-05-14 |
Merck Sharp & Dohme Llc |
PRMT5 inhibitors
|
|
US12552826B2
(en)
|
2018-08-07 |
2026-02-17 |
Merck Sharp & Dohme Llc |
PRMT5 inhibitors
|
|
EP3833668B1
(fr)
|
2018-08-07 |
2025-03-19 |
Merck Sharp & Dohme LLC |
Inhibiteurs de prmt5
|
|
US12173026B2
(en)
|
2018-08-07 |
2024-12-24 |
Merck Sharp & Dohme Llc |
PRMT5 inhibitors
|
|
US12281126B2
(en)
|
2018-12-28 |
2025-04-22 |
Dana-Farber Cancer Institute, Inc. |
Inhibitors of cyclin-dependent kinase 7 and uses thereof
|
|
AU2020372682A1
(en)
*
|
2019-10-31 |
2022-06-09 |
Jd Bioscience Inc. |
Tricyclic compound and pharmaceutical use thereof
|
|
US12441730B2
(en)
|
2019-12-17 |
2025-10-14 |
Merck Sharp & Dohme Llc |
PRMT5 inhibitors
|
|
BR112022012015A2
(pt)
|
2019-12-17 |
2022-08-30 |
Merck Sharp & Dohme Llc |
Inibidores de prmt5
|
|
EP4673747A1
(fr)
|
2023-03-02 |
2026-01-07 |
CARCIMUN BIOTECH GmbH |
Moyens et procédés de diagnostic du cancer et/ou d'une maladie inflammatoire aiguë
|
|
WO2026027944A1
(fr)
|
2024-07-30 |
2026-02-05 |
Sairopa B.V. |
Formulations d'anticorps anti-sirp alpha et leurs utilisations
|