WO1995000497A1
(fr)
*
|
1993-06-18 |
1995-01-05 |
Merck & Co., Inc. |
Inhibiteurs de farnesyle-proteine transferase
|
US5721236A
(en)
*
|
1993-10-15 |
1998-02-24 |
Schering Corporation |
Tricyclic carbamate compounds useful for inhibition of G-protein function and for treatment of proliferative diseases
|
US6524832B1
(en)
|
1994-02-04 |
2003-02-25 |
Arch Development Corporation |
DNA damaging agents in combination with tyrosine kinase inhibitors
|
US5700806A
(en)
*
|
1995-03-24 |
1997-12-23 |
Schering Corporation |
Tricyclic amide and urea compounds useful for inhibition of G-protein function and for treatment of proliferative diseases
|
US5856326A
(en)
*
|
1995-03-29 |
1999-01-05 |
Merck & Co., Inc. |
Inhibitors of farnesyl-protein transferase
|
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
|
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
|
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
|
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
|
TW350844B
(en)
*
|
1995-12-22 |
1999-01-21 |
Schering Corp |
Tricyclic amides useful to inhibition of G-protein function and for treatment of proliferative diseases
|
US5874442A
(en)
|
1995-12-22 |
1999-02-23 |
Schering-Plough Corporation |
Tricyclic amides useful for inhibition of G-protein function and for treatment of proliferative disease
|
US6028201A
(en)
*
|
1996-01-30 |
2000-02-22 |
Merck & Co., Inc. |
Inhibitors of farnesyl-protein transferase
|
WO1997031641A1
(fr)
*
|
1996-02-29 |
1997-09-04 |
Duke University |
Methode de traitement des infections provoquees par le virus de l'hepatite delta
|
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
|
US5925757A
(en)
*
|
1996-07-26 |
1999-07-20 |
Schering Corporation |
Method for preparing carboxamides
|
PE92098A1
(es)
*
|
1996-07-31 |
1998-12-31 |
Schering Corp |
N-cianoiminas triciclicas utiles como inhibidores de transferasa de proteina farnesilo
|
NZ334342A
(en)
*
|
1996-09-13 |
2000-07-28 |
Schering Corp |
Compounds for inhibition of farnesyl protein transferase and the treatment of cancer
|
US5985879A
(en)
*
|
1996-09-13 |
1999-11-16 |
Schering Corporation |
Compounds useful for inhibition of farnesyl protein transferase
|
US5965570A
(en)
*
|
1996-09-13 |
1999-10-12 |
Schering Corporation |
Tricyclic piperidinyl compounds useful as inhibitors of farnesyl-protein transferase
|
CN1237170A
(zh)
*
|
1996-09-13 |
1999-12-01 |
先灵公司 |
用作法呢基蛋白转移酶抑制剂的新的三环哌啶基化合物
|
US5945429A
(en)
*
|
1996-09-13 |
1999-08-31 |
Schering Corporation |
Compounds useful for inhibition of farnesyl protein transferase
|
ID21577A
(id)
*
|
1996-09-13 |
1999-06-24 |
Schering Corp |
Komposisi-komposisi yang berguna untuk tranferase protein farnesil
|
KR20000036111A
(ko)
*
|
1996-09-13 |
2000-06-26 |
둘락 노먼 씨. |
파네실 단백질 트랜스페라제 억제제인 트리사이클릭 항종양성화합물
|
US6030982A
(en)
*
|
1996-09-13 |
2000-02-29 |
Schering Corporationm |
Compounds useful for inhibition of farnesyl protein transferase
|
US5994364A
(en)
|
1996-09-13 |
1999-11-30 |
Schering Corporation |
Tricyclic antitumor farnesyl protein transferase inhibitors
|
CN1237169A
(zh)
*
|
1996-09-13 |
1999-12-01 |
先灵公司 |
用于抑制g-蛋白功能并用于治疗增生性疾病的三环化合物
|
US5861395A
(en)
*
|
1996-09-13 |
1999-01-19 |
Schering Corporation |
Compounds useful for inhibition of farnesyl proteins transferase
|
US6071907A
(en)
*
|
1996-09-13 |
2000-06-06 |
Schering Corporation |
Tricyclic compounds useful as FPT inhibitors
|
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
|
BR9712831A
(pt)
*
|
1996-09-13 |
1999-11-16 |
Schering Corp |
Inibidores tricìclicos de farnesil proteìna transferase
|
ES2242232T3
(es)
*
|
1996-09-13 |
2005-11-01 |
Schering Corporation |
Benzocicloheptapiridinas sustituidas utiles como inhibidores de la farnesil-proteina-transferasa.
|
US6040305A
(en)
*
|
1996-09-13 |
2000-03-21 |
Schering Corporation |
Compounds useful for inhibition of farnesyl protein transferase
|
US6130229A
(en)
*
|
1996-10-09 |
2000-10-10 |
Schering Corporation |
Tricyclic compounds having activity as RAS-FPT inhibitors
|
ES2192671T3
(es)
*
|
1996-10-09 |
2003-10-16 |
Schering Corp |
Compuestos triciclicos que tienen actividad como inhibidores de ras-fpt.
|
US5760232A
(en)
*
|
1997-06-16 |
1998-06-02 |
Schering Corporation |
Synthesis of intermediates useful in preparing bromo-substituted tricyclic compounds
|
US6218401B1
(en)
|
1997-06-17 |
2001-04-17 |
Schering Corporation |
Phenyl-substituted tricyclic inhibitors of farnesyl-protein transferase
|
AU753658B2
(en)
*
|
1997-06-17 |
2002-10-24 |
Pharmacopeia, Inc. |
Benzpyrido cycloheptane compounds useful for inhibition of farnesyl protein transferase
|
US6576639B1
(en)
|
1997-06-17 |
2003-06-10 |
Schering Corporation |
Compounds for the inhibition of farnesyl protein transferase
|
US6051582A
(en)
*
|
1997-06-17 |
2000-04-18 |
Schering Corporation |
Compounds useful for inhibition of farnesyl protein transferase
|
US6225322B1
(en)
|
1997-06-17 |
2001-05-01 |
Schering Corporation |
Compounds useful for inhibition of farnesyl protein transferase
|
US6211193B1
(en)
|
1997-06-17 |
2001-04-03 |
Schering Corporation |
Compounds useful for inhibition of farnesyl protein transferase
|
WO1998057950A1
(fr)
*
|
1997-06-17 |
1998-12-23 |
Schering Corporation |
Nouveaux composes tricycliques de phenyle substitues inhibiteurs de farnesyl proteine transferase
|
US6689789B2
(en)
|
1997-06-17 |
2004-02-10 |
Schering Corporation |
Compounds useful for inhibition of farnesyl protein transferase
|
US5925639A
(en)
*
|
1997-06-17 |
1999-07-20 |
Schering Corporation |
Keto amide derivatives useful as farnesyl protein transferase inhibitors
|
US6159984A
(en)
|
1997-06-17 |
2000-12-12 |
Schering Corporation |
Farnesyl protein transferase inhibitors
|
NZ501418A
(en)
*
|
1997-06-17 |
2001-04-27 |
Schering Corp |
Bispyrido-cycloheptane compounds useful for inhibition of farnesyl protein transferase
|
IL133447A0
(en)
*
|
1997-06-17 |
2001-04-30 |
Schering Corp |
Compounds useful for inhibition of farnesyl protein transferase
|
US6228865B1
(en)
|
1997-06-17 |
2001-05-08 |
Schering Corporation |
Compounds useful for inhibition of farnesyl protein transferase
|
US6239140B1
(en)
|
1997-06-17 |
2001-05-29 |
Schering Corporation |
Compounds useful for inhibition 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
|
AU754066B2
(en)
*
|
1997-06-17 |
2002-11-07 |
Schering Corporation |
Benzo(5,6)cyclohepta(1,2B)pyridine derivatives useful for inhibition of farnesyl protein transferase
|
AU8253498A
(en)
*
|
1997-06-17 |
1999-01-04 |
Schering Corporation |
Tricyclic compounds useful for inhibition of g-protein function and for treatment of proliferative diseases
|
US5925648A
(en)
*
|
1997-07-29 |
1999-07-20 |
Schering Corporation |
Tricyclic N-cyanoimines useful as inhibitors of a farnesyl-protein transferase
|
US5958940A
(en)
*
|
1997-09-11 |
1999-09-28 |
Schering Corporation |
Tricyclic compounds useful as inhibitors of farnesyl-protein transferase
|
AU9683798A
(en)
*
|
1997-10-10 |
1999-05-03 |
Schering Corporation |
Ethyl 4-(8-chloro-5, 6-dihydro-11h- benzo{5,6}cyclohepta {1,2-b}pyridin -11-ylidene)-1- piperidene carboxylate polymorph
|
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
|
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
|
US6632455B2
(en)
|
1997-12-22 |
2003-10-14 |
Schering Corporation |
Molecular dispersion composition with enhanced bioavailability
|
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
|
WO2000001701A1
(fr)
|
1998-07-02 |
2000-01-13 |
Merck & Co., Inc. |
Inhibiteurs de prenyl-proteine transferase
|
US6372747B1
(en)
|
1998-12-18 |
2002-04-16 |
Schering Corporation |
Farnesyl protein transferase inhibitors
|
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
|
US6686502B1
(en)
|
1999-03-26 |
2004-02-03 |
Ucb S.A. |
Compounds and methods for treatment of asthma, allergy and inflammatory disorders
|
PE20001566A1
(es)
|
1999-03-26 |
2001-02-05 |
Ucb Sa |
Piperazinas 1,4-sustituidas, piperidinas 1,4-sustituidas y 4-alquilidenilpiperidinas 1-sustituidas
|
US6316462B1
(en)
|
1999-04-09 |
2001-11-13 |
Schering Corporation |
Methods of inducing cancer cell death and tumor regression
|
CA2384151A1
(fr)
*
|
1999-09-09 |
2001-03-15 |
Merck & Co., Inc. |
Inhibiteurs de prenyl-proteine transferase
|
EP1443936A4
(fr)
|
2001-11-13 |
2006-01-11 |
Bristol Myers Squibb Co |
Procede de preparation de composes de 3,7-disubstitue-2,3,4,5- tetrahydro-1h-1,4-benzodiazepine
|
ES2232332T3
(es)
*
|
2003-03-12 |
2007-08-16 |
Teva Pharmaceutical Industries Ltd |
Composiciones farmaceuticas estables de desloratadina.
|
US7417026B2
(en)
|
2003-08-13 |
2008-08-26 |
Children's Hospital Medical Center |
Mobilization of hematopoietic cells
|
WO2006123182A2
(fr)
|
2005-05-17 |
2006-11-23 |
Merck Sharp & Dohme Limited |
Sulfones de cyclohexyle pour le traitement du cancer
|
CA2624656A1
(fr)
*
|
2005-10-21 |
2007-05-03 |
Merck & Co., Inc. |
Inhibiteurs des tyrosine kinases
|
GB0603041D0
(en)
|
2006-02-15 |
2006-03-29 |
Angeletti P Ist Richerche Bio |
Therapeutic compounds
|
DK2010528T3
(en)
|
2006-04-19 |
2018-01-15 |
Novartis Ag |
6-O-Substituted Benzoxazole and Benzothiazole Compounds and Methods for Inhibiting CSF-1R Signaling
|
JP5489333B2
(ja)
|
2006-09-22 |
2014-05-14 |
メルク・シャープ・アンド・ドーム・コーポレーション |
脂肪酸合成阻害剤を用いた治療の方法
|
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
|
PL2336120T3
(pl)
|
2007-01-10 |
2014-12-31 |
Msd Italia Srl |
Kombinacje zawierające indazole podstawione grupą amidową jako inhibitory polimerazy poli(ADP-rybozy) (PARP)
|
MX2009009304A
(es)
|
2007-03-01 |
2009-11-18 |
Novartis Ag |
Inhibidores de cinasa pim y metodos para su uso.
|
KR20100017866A
(ko)
|
2007-05-21 |
2010-02-16 |
노파르티스 아게 |
Csf-1r 억제제, 조성물 및 사용 방법
|
AU2008269154B2
(en)
|
2007-06-27 |
2014-06-12 |
Merck Sharp & Dohme Llc |
4-carboxybenzylamino derivatives as histone deacetylase inhibitors
|
US8691825B2
(en)
|
2009-04-01 |
2014-04-08 |
Merck Sharp & Dohme Corp. |
Inhibitors of AKT activity
|
WO2010144909A1
(fr)
|
2009-06-12 |
2010-12-16 |
Novartis Ag |
Composés hétérocycliques fondus et leurs utilisations
|
WO2011046771A1
(fr)
|
2009-10-14 |
2011-04-21 |
Schering Corporation |
Pipéridines substituées qui accroissent l'activité de p53, et utilisations de ces composés
|
WO2011090738A2
(fr)
|
2009-12-29 |
2011-07-28 |
Dana-Farber Cancer Institute, Inc. |
Inhibiteurs de kinase raf de type ii
|
CN103080093A
(zh)
|
2010-03-16 |
2013-05-01 |
达纳-法伯癌症研究所公司 |
吲唑化合物及其应用
|
WO2011163330A1
(fr)
|
2010-06-24 |
2011-12-29 |
Merck Sharp & Dohme Corp. |
Nouveaux composés hétérocycliques utilisés comme inhibiteurs de erk
|
CA2805265A1
(fr)
|
2010-08-02 |
2012-02-09 |
Merck Sharp & Dohme Corp. |
Inhibition a mediation par interference arn de catenine (proteine associee a cadherine), expression du gene beta 1 (ctnnb1) a l'aide de petit acide nucleique interferent (sian)
|
CA2807307C
(fr)
|
2010-08-17 |
2021-02-09 |
Merck Sharp & Dohme Corp. |
Inhibition mediee par des arn interferents de l'expression genique du virus de l'hepatite b (vhb) a l'aide de petits acides nucleiques interferents (pani)
|
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
|
EP2615916B1
(fr)
|
2010-09-16 |
2017-01-04 |
Merck Sharp & Dohme Corp. |
Dérivés condensés de pyrazole utilisés comme nouveaux inhibiteurs erk
|
ES2663009T3
(es)
|
2010-10-29 |
2018-04-10 |
Sirna Therapeutics, Inc. |
Inhibición de la expresión génica mediada por interferencia por ARN utilizando ácidos nucleicos de interferencia cortos (ANic)
|
EP2654748B1
(fr)
|
2010-12-21 |
2016-07-27 |
Merck Sharp & Dohme Corp. |
Dérivés d'indazole utiles en tant qu'inhibiteurs de erk
|
JP2014514321A
(ja)
|
2011-04-21 |
2014-06-19 |
メルク・シャープ・アンド・ドーム・コーポレーション |
インスリン様増殖因子1受容体阻害剤
|
US9023865B2
(en)
|
2011-10-27 |
2015-05-05 |
Merck Sharp & Dohme Corp. |
Compounds that are ERK inhibitors
|
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)
|
JP6280554B2
(ja)
|
2012-09-28 |
2018-02-14 |
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. |
Erk阻害剤である新規化合物
|
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
|
BR112015012295A8
(pt)
|
2012-11-28 |
2023-03-14 |
Merck Sharp & Dohme |
Uso de um inibidor de wee1, e, kit para identificar um paciente com câncer
|
MX2015008196A
(es)
|
2012-12-20 |
2015-09-16 |
Merck Sharp & Dohme |
Imidazopiridinas sustituidas como inhibidores de doble minuto 2 humana.
|
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
|
EP3041938A1
(fr)
|
2013-09-03 |
2016-07-13 |
Moderna Therapeutics, Inc. |
Polynucléotides circulaires
|
WO2015058140A1
(fr)
|
2013-10-18 |
2015-04-23 |
Dana-Farber Cancer Institute, Inc. |
Inhibiteurs polycycliques de 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
|
US9862688B2
(en)
|
2014-04-23 |
2018-01-09 |
Dana-Farber Cancer Institute, Inc. |
Hydrophobically tagged janus kinase inhibitors and uses thereof
|
US10017477B2
(en)
|
2014-04-23 |
2018-07-10 |
Dana-Farber Cancer Institute, Inc. |
Janus kinase inhibitors and uses thereof
|
JO3589B1
(ar)
|
2014-08-06 |
2020-07-05 |
Novartis Ag |
مثبطات كيناز البروتين c وطرق استخداماتها
|
CA2972239A1
(fr)
|
2014-12-23 |
2016-06-30 |
Dana-Farber Cancer Institute, Inc. |
Inhibiteurs de la kinase cycline-dependante 7 (cdk7)
|
EP3273966B1
(fr)
|
2015-03-27 |
2023-05-03 |
Dana-Farber Cancer Institute, Inc. |
Inhibiteurs de kinases cycline-dépendantes
|
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
|
WO2018071283A1
(fr)
|
2016-10-12 |
2018-04-19 |
Merck Sharp & Dohme Corp. |
Inhibiteurs de kdm5
|
JP7160833B2
(ja)
|
2017-04-13 |
2022-10-25 |
サイロパ ビー.ブイ. |
抗sirpアルファ抗体
|
EP3706747A4
(fr)
|
2017-11-08 |
2021-08-04 |
Merck Sharp & Dohme Corp. |
Inhibiteurs de prmt5
|
WO2019094311A1
(fr)
|
2017-11-08 |
2019-05-16 |
Merck Sharp & Dohme Corp. |
Inhibiteurs de prmt5
|
WO2019148412A1
(fr)
|
2018-02-01 |
2019-08-08 |
Merck Sharp & Dohme Corp. |
Anticorps bispécifiques anti-pd-1/lag3
|
EP3833668A4
(fr)
|
2018-08-07 |
2022-05-11 |
Merck Sharp & Dohme Corp. |
Inhibiteurs de prmt5
|
EP3833667B1
(fr)
|
2018-08-07 |
2024-03-13 |
Merck Sharp & Dohme LLC |
Inhibiteurs de prmt5
|
WO2024180169A1
(fr)
|
2023-03-02 |
2024-09-06 |
Carcimun Biotech Gmbh |
Moyens et procédés de diagnostic du cancer et/ou d'une maladie inflammatoire aiguë
|
CN116496259A
(zh)
*
|
2023-04-24 |
2023-07-28 |
黑龙江珍宝岛药业股份有限公司 |
一种富马酸卢帕他定的制备方法
|