FR2338043A1
(fr)
|
1976-01-13 |
1977-08-12 |
Delmar Chem |
Derives de 4-arylpiperidine et procedes de production
|
US4132710A
(en)
|
1976-12-20 |
1979-01-02 |
Ayerst, Mckenna And Harrison, Ltd. |
[2]Benzopyrano[3,4-c]pyridines and process therefor
|
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
|
US4816567A
(en)
|
1983-04-08 |
1989-03-28 |
Genentech, Inc. |
Recombinant immunoglobin preparations
|
US4676980A
(en)
|
1985-09-23 |
1987-06-30 |
The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services |
Target specific cross-linked heteroantibodies
|
US5225539A
(en)
|
1986-03-27 |
1993-07-06 |
Medical Research Council |
Recombinant altered antibodies and methods of making altered antibodies
|
IN164232B
(zh)
|
1986-04-11 |
1989-02-04 |
Hoechst India |
|
US4946778A
(en)
|
1987-09-21 |
1990-08-07 |
Genex Corporation |
Single polypeptide chain binding molecules
|
JP2691986B2
(ja)
|
1987-08-28 |
1997-12-17 |
チッソ株式会社 |
ピリジン骨格を有する光学活性化合物の製造法
|
DE3743824C2
(de)
|
1987-12-23 |
1997-03-06 |
Hoechst Ag |
Verfahren zur enzymatischen Racematspaltung von racemischen Alkoholen mit/in Vinylestern durch Umesterung
|
GB8823869D0
(en)
|
1988-10-12 |
1988-11-16 |
Medical Res Council |
Production of antibodies
|
DE3836676A1
(de)
|
1988-10-28 |
1990-05-03 |
Hoechst Ag |
Die verwendung von 4h-1-benzopyran-4-on-derivaten, neue 4h-1-benzopyran-4-on-derivate und diese enthaltende arzneimittel
|
US5284856A
(en)
|
1988-10-28 |
1994-02-08 |
Hoechst Aktiengesellschaft |
Oncogene-encoded kinases inhibition using 4-H-1-benzopyran-4-one derivatives
|
GB8827305D0
(en)
|
1988-11-23 |
1988-12-29 |
British Bio Technology |
Compounds
|
WO1991000360A1
(en)
|
1989-06-29 |
1991-01-10 |
Medarex, Inc. |
Bispecific reagents for aids therapy
|
US5804604A
(en)
|
1989-12-21 |
1998-09-08 |
Biogen, Inc. |
Tat-derived transport polypeptides and fusion proteins
|
US5670617A
(en)
|
1989-12-21 |
1997-09-23 |
Biogen Inc |
Nucleic acid conjugates of tat-derived transport polypeptides
|
WO1991010741A1
(en)
|
1990-01-12 |
1991-07-25 |
Cell Genesys, Inc. |
Generation of xenogeneic antibodies
|
US5633425A
(en)
|
1990-08-29 |
1997-05-27 |
Genpharm International, Inc. |
Transgenic non-human animals capable of producing heterologous antibodies
|
US5625126A
(en)
|
1990-08-29 |
1997-04-29 |
Genpharm International, Inc. |
Transgenic non-human animals for producing heterologous antibodies
|
US5545806A
(en)
|
1990-08-29 |
1996-08-13 |
Genpharm International, Inc. |
Ransgenic non-human animals for producing heterologous antibodies
|
CA2089661C
(en)
|
1990-08-29 |
2007-04-03 |
Nils Lonberg |
Transgenic non-human animals capable of producing heterologous antibodies
|
US5661016A
(en)
|
1990-08-29 |
1997-08-26 |
Genpharm International Inc. |
Transgenic non-human animals capable of producing heterologous antibodies of various isotypes
|
JPH0641075A
(ja)
|
1990-09-01 |
1994-02-15 |
Kazuo Achinami |
新規な1,4−ジヒドロピリジン化合物及びその製造方法
|
AU647603B2
(en)
|
1991-04-02 |
1994-03-24 |
Hoechst Aktiengesellschaft |
An immobilized biocatalyst, its preparation and use for ester synthesis in a column reactor
|
JPH06507398A
(ja)
|
1991-05-14 |
1994-08-25 |
リプリジェン コーポレーション |
Hiv感染治療のための異種複合抗体
|
US5587458A
(en)
|
1991-10-07 |
1996-12-24 |
Aronex Pharmaceuticals, Inc. |
Anti-erbB-2 antibodies, combinations thereof, and therapeutic and diagnostic uses thereof
|
WO1993008829A1
(en)
|
1991-11-04 |
1993-05-13 |
The Regents Of The University Of California |
Compositions that mediate killing of hiv-infected cells
|
DE69334351D1
(de)
|
1992-02-06 |
2011-05-12 |
Novartis Vaccines & Diagnostic |
Biosynthetisches Bindeprotein für Tumormarker
|
ES2301158T3
(es)
|
1992-07-24 |
2008-06-16 |
Amgen Fremont Inc. |
Produccion de anticuerpos xenogenicos.
|
US6177401B1
(en)
|
1992-11-13 |
2001-01-23 |
Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften |
Use of organic compounds for the inhibition of Flk-1 mediated vasculogenesis and angiogenesis
|
DE69329503T2
(de)
|
1992-11-13 |
2001-05-03 |
Idec Pharma Corp |
Therapeutische Verwendung von chimerischen und markierten Antikörpern, die gegen ein Differenzierung-Antigen gerichtet sind, dessen Expression auf menschliche B Lymphozyt beschränkt ist, für die Behandlung von B-Zell-Lymphoma
|
US5455258A
(en)
|
1993-01-06 |
1995-10-03 |
Ciba-Geigy Corporation |
Arylsulfonamido-substituted hydroxamic acids
|
IL112248A0
(en)
|
1994-01-25 |
1995-03-30 |
Warner Lambert Co |
Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them
|
GB9422836D0
(en)
|
1994-11-11 |
1995-01-04 |
Wainscoat James |
Monitoring malignant disease
|
US5731168A
(en)
|
1995-03-01 |
1998-03-24 |
Genentech, Inc. |
Method for making heteromultimeric polypeptides
|
US5863949A
(en)
|
1995-03-08 |
1999-01-26 |
Pfizer Inc |
Arylsulfonylamino hydroxamic acid derivatives
|
WO1996033172A1
(en)
|
1995-04-20 |
1996-10-24 |
Pfizer Inc. |
Arylsulfonyl hydroxamic acid derivatives as mmp and tnf inhibitors
|
CA2761116A1
(en)
|
1995-04-27 |
1996-10-31 |
Amgen Fremont Inc. |
Human antibodies derived from immunized xenomice
|
AU2466895A
(en)
|
1995-04-28 |
1996-11-18 |
Abgenix, Inc. |
Human antibodies derived from immunized xenomice
|
US5747498A
(en)
|
1996-05-28 |
1998-05-05 |
Pfizer Inc. |
Alkynyl and azido-substituted 4-anilinoquinazolines
|
US5880141A
(en)
|
1995-06-07 |
1999-03-09 |
Sugen, Inc. |
Benzylidene-Z-indoline compounds for the treatment of disease
|
CN1208438A
(zh)
|
1995-07-28 |
1999-02-17 |
玛丽·柯里癌症治疗中心 |
转运蛋白及其应用
|
GB9520822D0
(en)
|
1995-10-11 |
1995-12-13 |
Wellcome Found |
Therapeutically active compounds
|
US5733920A
(en)
|
1995-10-31 |
1998-03-31 |
Mitotix, Inc. |
Inhibitors of cyclin dependent kinases
|
GB9624482D0
(en)
|
1995-12-18 |
1997-01-15 |
Zeneca Phaema S A |
Chemical compounds
|
ATE225343T1
(de)
|
1995-12-20 |
2002-10-15 |
Hoffmann La Roche |
Matrix-metalloprotease inhibitoren
|
EP0888458A4
(en)
|
1996-02-20 |
2004-05-06 |
Sloan Kettering Institutefor C |
COMBINATION OF PROTEIN KINASE C INHIBITORS AND THERAPEUTIC AGENTS FOR THE TREATMENT OF CANCER
|
DK0885198T3
(da)
|
1996-03-05 |
2002-03-25 |
Astrazeneca Ab |
4-Anilinoquinazolinderivater
|
US6087366A
(en)
|
1996-03-07 |
2000-07-11 |
The Trustees Of Columbia University In The City Of New York |
Use of flavopiridol or a pharmaceutically acceptable salt thereof for inhibiting cell damage or cell death
|
US5849733A
(en)
|
1996-05-10 |
1998-12-15 |
Bristol-Myers Squibb Co. |
2-thio or 2-oxo flavopiridol analogs
|
EP0818442A3
(en)
|
1996-07-12 |
1998-12-30 |
Pfizer Inc. |
Cyclic sulphone derivatives as inhibitors of metalloproteinases and of the production of tumour necrosis factor
|
HRP970371A2
(en)
|
1996-07-13 |
1998-08-31 |
Kathryn Jane Smith |
Heterocyclic compounds
|
AR007857A1
(es)
|
1996-07-13 |
1999-11-24 |
Glaxo Group Ltd |
Compuestos heterociclicos fusionados como inhibidores de proteina tirosina quinasa, sus metodos de preparacion, intermediarios uso en medicina ycomposiciones farmaceuticas que los contienen.
|
DE69718472T2
(de)
|
1996-07-13 |
2003-11-06 |
Glaxo Group Ltd., Greenford |
Bicyclische heteroaromatische verbindungen als protein tyrosine kinase inhibitoren
|
KR20000067904A
(ko)
|
1996-07-18 |
2000-11-25 |
디. 제이. 우드, 스피겔 알렌 제이 |
매트릭스 메탈로프로테아제의 포스피네이트계 억제제
|
JP2000501423A
(ja)
|
1996-08-23 |
2000-02-08 |
ファイザー インク. |
アリールスルホニルアミノヒドロキサム酸誘導体
|
US5965703A
(en)
|
1996-09-20 |
1999-10-12 |
Idun Pharmaceuticals |
Human bad polypeptides, encoding nucleic acids and methods of use
|
US5908934A
(en)
|
1996-09-26 |
1999-06-01 |
Bristol-Myers Squibb Company |
Process for the preparation of chiral ketone intermediates useful for the preparation of flavopiridol and analogs
|
ID18494A
(id)
|
1996-10-02 |
1998-04-16 |
Novartis Ag |
Turunan pirazola leburan dan proses pembuatannya
|
US5916771A
(en)
|
1996-10-11 |
1999-06-29 |
Abgenix, Inc. |
Production of a multimeric protein by cell fusion method
|
CA2277100C
(en)
|
1997-01-06 |
2005-11-22 |
Pfizer Inc. |
Cyclic sulfone derivatives
|
JP3765584B2
(ja)
|
1997-02-03 |
2006-04-12 |
ファイザー・プロダクツ・インク |
アリールスルホニルアミノヒドロキサム酸誘導体
|
ES2301194T3
(es)
|
1997-02-05 |
2008-06-16 |
Warner-Lambert Company Llc |
Pirido 2,3-d pirimidinas y 4-aminopirimidinas como inhibidores de la proliferacion celular.
|
AU5493598A
(en)
|
1997-02-07 |
1998-08-26 |
Pfizer Inc. |
N-hydroxy-beta-sulfonyl-propionamide derivatives and their use as inhibitors of matrix metalloproteinases
|
ID22809A
(id)
|
1997-02-11 |
1999-12-09 |
Pfizer |
Turunan-turunan asam arilsulfonil hidroksamat
|
GB9704444D0
(en)
|
1997-03-04 |
1997-04-23 |
Isis Innovation |
Non-invasive prenatal diagnosis
|
ATE292623T1
(de)
|
1997-05-07 |
2005-04-15 |
Sugen Inc |
2-indolinonderivate als modulatoren der proteinkinase-ativität
|
CA2291709A1
(en)
|
1997-05-30 |
1998-12-03 |
Merck & Co., Inc. |
Novel angiogenesis inhibitors
|
WO1999007675A1
(en)
|
1997-08-08 |
1999-02-18 |
Pfizer Products Inc. |
Aryloxyarylsulfonylamino hydroxamic acid derivatives
|
EP1005470B1
(en)
|
1997-08-22 |
2007-08-01 |
AstraZeneca AB |
Oxindolylquinazoline derivatives as angiogenesis inhibitors
|
US7064193B1
(en)
|
1997-09-17 |
2006-06-20 |
The Walter And Eliza Hall Institute Of Medical Research |
Therapeutic molecules
|
CA2303830A1
(en)
|
1997-09-26 |
1999-04-08 |
Merck & Co., Inc. |
Novel angiogenesis inhibitors
|
AU9402898A
(en)
|
1997-09-26 |
1999-04-23 |
Washington University |
Cell death agonists
|
UA72881C2
(uk)
|
1997-11-11 |
2005-05-16 |
Пфайзер Продактс Інк. |
Похідні тієнопіридину, фармацевтична композиція з використанням таких сполук (варіанти), проміжна сполука
|
GB9725782D0
(en)
|
1997-12-05 |
1998-02-04 |
Pfizer Ltd |
Therapeutic agents
|
GB9800575D0
(en)
|
1998-01-12 |
1998-03-11 |
Glaxo Group Ltd |
Heterocyclic compounds
|
GB9800569D0
(en)
|
1998-01-12 |
1998-03-11 |
Glaxo Group Ltd |
Heterocyclic compounds
|
US6437136B2
(en)
|
1998-01-23 |
2002-08-20 |
Aventis Pharma Deutschland Gmbh |
Process for the preparation of (−)cis-3-hydroxy-1-methyl-4-(2,4,6-trimethoxyphenyl)piperidine
|
DE19802449A1
(de)
|
1998-01-23 |
1999-07-29 |
Hoechst Marion Roussel De Gmbh |
Verfahren zur Herstellung von (-)cis-3-Hydroxy-1-methyl-4-(2,4,6-trimethoxypyhenyl)-piperidin
|
GB9801690D0
(en)
|
1998-01-27 |
1998-03-25 |
Pfizer Ltd |
Therapeutic agents
|
DE19809649A1
(de)
|
1998-03-06 |
1999-09-09 |
Hoechst Marion Roussel De Gmbh |
Verfahren zur enzymatischen Enantiomeren-Trennung von 3(R)- und 3(S)-Hydroxy-1-methyl-4-(2,4,6-trimethoxyphenyl)-1,2,3,6-tetrahydro-pyridin bzw. der Carbonsäureester
|
JP4462654B2
(ja)
|
1998-03-26 |
2010-05-12 |
ソニー株式会社 |
映像素材選択装置及び映像素材選択方法
|
PA8469401A1
(es)
|
1998-04-10 |
2000-05-24 |
Pfizer Prod Inc |
Derivados biciclicos del acido hidroxamico
|
PA8469501A1
(es)
|
1998-04-10 |
2000-09-29 |
Pfizer Prod Inc |
Hidroxamidas del acido (4-arilsulfonilamino)-tetrahidropiran-4-carboxilico
|
US20020029391A1
(en)
|
1998-04-15 |
2002-03-07 |
Claude Geoffrey Davis |
Epitope-driven human antibody production and gene expression profiling
|
SK287132B6
(sk)
|
1998-05-29 |
2009-12-07 |
Sugen, Inc. |
Farmaceutická kompozícia obsahujúca pyrolom substituovaný 2-indolinón, súprava obsahujúca uvedenú kompozíciu a použitie pyrolom substituovaného 2-indolinónu
|
UA60365C2
(uk)
|
1998-06-04 |
2003-10-15 |
Пфайзер Продактс Інк. |
Похідні ізотіазолу, спосіб їх одержання, фармацевтична композиція та спосіб лікування гіперпроліферативного захворювання у ссавця
|
FR2780056B1
(fr)
|
1998-06-18 |
2000-08-04 |
Hoechst Marion Roussel Inc |
Nouveau procede de preparation de derives de la 4-phenyl-1-2 3,6-tetrahydropyridine et les produits imtermediaires mis en oeuvre
|
CA2338638C
(en)
|
1998-07-30 |
2009-03-17 |
Sigma-Tau Industrie Farmaceutiche Riunite S.P.A. |
Use of l-carnitine and its alkanoyl derivatives in the preparation of medicaments with anticancer activity
|
US6268499B1
(en)
|
1998-08-10 |
2001-07-31 |
Hoffman-La Roche Inc. |
Process and intermediates for preparation of substituted piperidine-epoxides
|
WO2000012071A2
(de)
|
1998-08-29 |
2000-03-09 |
Miklos Ghyczy |
Pharmazeutisches und/oder diätetisches produkt
|
ES2213985T3
(es)
|
1998-11-05 |
2004-09-01 |
Pfizer Products Inc. |
Derivados de hidroxiamida de acido 5-oxo-pirrolidin-2-carboxilico.
|
UA71945C2
(en)
|
1999-01-27 |
2005-01-17 |
Pfizer Prod Inc |
Substituted bicyclic derivatives being used as anticancer agents
|
US6399633B1
(en)
|
1999-02-01 |
2002-06-04 |
Aventis Pharmaceuticals Inc. |
Use of 4-H-1-benzopryan-4-one derivatives as inhibitors of smooth muscle cell proliferation
|
EP1210098A1
(en)
|
1999-04-07 |
2002-06-05 |
Thomas Jefferson University |
Enhancement of peptide cellular uptake
|
US6511993B1
(en)
|
1999-06-03 |
2003-01-28 |
Kevin Neil Dack |
Metalloprotease inhibitors
|
AU6906100A
(en)
|
1999-08-16 |
2001-03-13 |
Government of The United States of America, as represented by The Secretary Department of Health & Human Services, The National Institutes of Health, The |
Receptor-mediated uptake of an extracellular bcl-xl fusion protein inhibits apoptosis
|
US6821990B2
(en)
|
2000-01-18 |
2004-11-23 |
Aventis Pharma Deutschland Gmbh |
Ethanol solvate of (-)-cis-2-(2-chlorophenyl)-5, 7-dihydroxy-8 [4R-(3S-hydroxy-1-M ethyl) piperidinyl]-4H-1-benzopyran-4-one
|
US6576647B2
(en)
|
2000-01-18 |
2003-06-10 |
Aventis Pharmaceuticals Inc. |
Pseudopolymorph of (—)-cis-2-(2-chlorophenyl)-5,7-dihydroxy-8[4R-(3S-hydroxy -1-methyl)piperidinyl]-4H-1-benzopyran-4-one
|
UA73976C2
(uk)
|
2000-02-15 |
2005-10-17 |
Суджен, Інк. |
Заміщені піролом 2-індолінони, фармацевтична композиція, спосіб модуляції каталітичної активності протеїнкінази та спосіб лікування або профілактики захворювання, пов'язаного з протеїнкіназою
|
WO2002020568A2
(en)
|
2000-09-06 |
2002-03-14 |
Abbott Laboratories |
Mutant peptides derived from bad and their use to identify substances which bind to a member of the bcl-2 family of proteins
|
US6849631B2
(en)
|
2000-12-08 |
2005-02-01 |
Bristol Myers Squibb Pharma Company |
Semicarbazides and their uses
|
US20020115613A1
(en)
|
2001-02-16 |
2002-08-22 |
Kumar M. Vijay |
Treatment of prostate cancer
|
AU2002303164A1
(en)
|
2001-03-23 |
2002-10-08 |
Protarga, Inc. |
Fatty amine drug conjugates
|
JP4634694B2
(ja)
*
|
2001-03-23 |
2011-02-16 |
ルイトポルド・ファーマシューティカルズ・インコーポレーテッド |
脂肪アルコール薬物複合体
|
WO2003027237A2
(en)
|
2001-09-24 |
2003-04-03 |
Blood Center Research Foundation |
Method of modulating or examining ku70 levels in cells
|
KR20030026069A
(ko)
|
2001-09-24 |
2003-03-31 |
주식회사 엘지생명과학 |
티엔에프계 단백질과 플라보피리돌의 조합에 의한 암세포특이적인 세포사멸 유도용 조성물
|
WO2003040168A2
(en)
|
2001-11-06 |
2003-05-15 |
Enanta Pharmaceuticals, Inc. |
Methods and compositions for identifying peptide aptamers capable of altering a cell phenotype
|
AU2002364364A1
(en)
|
2001-12-31 |
2003-07-24 |
Dana-Farber Cancer Institute, Inc. |
Method of treating apoptosis and compositions thereof
|
PT3483183T
(pt)
|
2002-03-01 |
2021-06-02 |
Immunomedics Inc |
Imunoconjugado compreendendo anticorpos rs7 humanizados
|
US20040106647A1
(en)
|
2002-06-28 |
2004-06-03 |
Schneider Michael D. |
Modulators of Cdk9 as a therapeutic target in cardiac hypertrophy
|
AU2003267124A1
(en)
|
2002-09-09 |
2004-03-29 |
Dana-Farber Cancer Institute, Inc. |
Bh3 peptides and method of use thereof
|
WO2004058804A1
(en)
|
2002-12-24 |
2004-07-15 |
Walter And Eliza Hall Institute Of Medical Research |
Peptides and therapeutic uses thereof
|
US7452901B2
(en)
|
2003-04-25 |
2008-11-18 |
Gilead Sciences, Inc. |
Anti-cancer phosphonate analogs
|
MXPA05011296A
(es)
|
2003-04-25 |
2006-01-24 |
Gilead Sciences Inc |
Conjugados de fosfonato inhibidores de la cinasa.
|
GB0315259D0
(en)
|
2003-06-30 |
2003-08-06 |
Cyclacel Ltd |
Use
|
TW201319088A
(zh)
*
|
2003-07-18 |
2013-05-16 |
Amgen Inc |
對肝細胞生長因子具專一性之結合劑
|
CN1302004C
(zh)
|
2003-08-22 |
2007-02-28 |
浙江海正药业股份有限公司 |
一种阿糖胞苷的制备方法
|
WO2005044839A2
(en)
|
2003-11-05 |
2005-05-19 |
Dana-Farber Cancer Institute, Inc. |
Stabilized alpha helical peptides and uses thereof
|
WO2006034266A2
(en)
*
|
2004-09-21 |
2006-03-30 |
Vion Pharmaceuticals, Inc. |
Sulfonyl hydrazines as hypoxia-selective antineoplastic agents
|
WO2006069186A2
(en)
|
2004-12-22 |
2006-06-29 |
The Ohio State Research Foundation |
Small molecule bcl-xl/bcl-2 binding inhibitors
|
WO2006101846A1
(en)
*
|
2005-03-16 |
2006-09-28 |
Aventis Pharmaceuticals Inc. |
Dosing regimen of flavopiridol for treating cancer in particular cll
|
WO2006099667A1
(en)
|
2005-03-21 |
2006-09-28 |
The Walter And Eliza Hall Institute Of Medical Research |
Prophylactic and therapeutic agents and uses therefor
|
US7750000B2
(en)
|
2005-09-02 |
2010-07-06 |
Bayer Schering Pharma Ag |
Substituted imidazo[1,2b]pyridazines as kinase inhibitors, their preparation and use as medicaments
|
EP1940796A1
(en)
*
|
2005-09-09 |
2008-07-09 |
Analytecon S.A. |
Isoquinolines derivatives as igf-1r inhibitors
|
CA2645853A1
(en)
|
2006-03-31 |
2007-11-01 |
Dana-Farber Cancer Institute |
Methods of determining cellular chemosensitivity
|
WO2007129062A1
(en)
|
2006-05-08 |
2007-11-15 |
Astex Therapeutics Limited |
Pharmaceutical combinations of diazole derivatives for cancer treatment
|
WO2008021484A2
(en)
|
2006-08-16 |
2008-02-21 |
Eutropics Pharmaceuticals |
Assay system to identify therapeutic agents
|
TW200843776A
(en)
|
2007-03-01 |
2008-11-16 |
Supergen Inc |
Pyrimidine-2,4-diamine derivatives and their use as JAK2 kinase inhibitors
|
GB0706633D0
(en)
|
2007-04-04 |
2007-05-16 |
Cyclacel Ltd |
Combination
|
RU2438664C2
(ru)
|
2007-05-15 |
2012-01-10 |
Пирамал Лайф Сайнсиз Лимитед |
Синергическая фармацевтическая комбинация для лечения рака
|
CA2687204C
(en)
|
2007-05-15 |
2015-11-24 |
Piramal Life Sciences Limited |
A synergistic pharmaceutical combination for the treatment of cancer
|
WO2009014642A1
(en)
|
2007-07-19 |
2009-01-29 |
Amgen Inc. |
Combination of a de novo purine biosynthesis inhibitor and a cyclin dependent kinase inhibitor for the treatment of cancer
|
CA2700925C
(en)
|
2007-09-26 |
2016-08-23 |
Dana Farber Cancer Institute |
Methods and compositions for modulating bcl-2 family polypeptides
|
AU2008335772B2
(en)
|
2007-12-10 |
2014-11-27 |
Sunesis Pharmaceuticals, Inc. |
Methods of using (+)-1,4-dihydro-7-[(3S,4S)-3- methoxy-4-(methylamino)-1-pyrrolidinyl]-4-oxo-1- (2-thiazolyl)-1,8-naphthyridine-3-carboxylic acid for treatment of antecedent hematologic disorders
|
WO2009100335A1
(en)
*
|
2008-02-08 |
2009-08-13 |
Wyeth |
Phosphate derivatives of substituted benzoxazoles
|
EP2304047A4
(en)
|
2008-05-07 |
2012-12-26 |
Eutropics Pharmaceuticals Inc |
ANTIBODIES TAKEN UPON HETERODIMES OF THE BCL-2 FAMILY AND THEIR USES
|
KR101667641B1
(ko)
|
2008-06-09 |
2016-10-20 |
싸이클라셀 리미티드 |
데시타빈 및 프로카인과 같은 dna 메틸전이효소 저해제와 사팍시타빈 또는 cndac의 조합
|
US20100061982A1
(en)
*
|
2008-09-10 |
2010-03-11 |
Wyeth |
3-substituted-1h-indole, 3-substituted-1h-pyrrolo[2,3-b]pyridine and 3-substituted-1h-pyrrolo[3,2-b]pyridine compounds, their use as mtor kinase and pi3 kinase inhibitors, and their syntheses
|
JP2012517241A
(ja)
|
2009-02-11 |
2012-08-02 |
アボット・ラボラトリーズ |
Bcl−2ファミリー阻害剤耐性腫瘍及び癌を有する被験者を同定、分類及びモニターするための方法及び組成物
|
ES2738700T3
(es)
|
2009-02-13 |
2020-01-24 |
Immunomedics Inc |
Inmunoconjugados con un enlace escindible intracelularmente
|
WO2010147961A1
(en)
|
2009-06-15 |
2010-12-23 |
Precision Therapeutics, Inc. |
Methods and markers for predicting responses to chemotherapy
|
US20130011393A1
(en)
|
2010-01-12 |
2013-01-10 |
Johnathan Mark Lancaster |
Bad pathway gene signature
|
US8372819B2
(en)
|
2010-04-11 |
2013-02-12 |
Salk Institute For Biological Studies |
Methods and compositions for targeting skip
|
JP5935030B2
(ja)
|
2010-05-14 |
2016-06-15 |
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 |
白血病を治療するための組成物および方法
|
SG180031A1
(en)
|
2010-10-15 |
2012-05-30 |
Agency Science Tech & Res |
Combination treatment of cancer
|
EP2655334B1
(en)
|
2010-12-22 |
2018-10-03 |
Eutropics Pharmaceuticals, Inc. |
Compositions and methods useful for treating diseases
|
US9051305B2
(en)
|
2011-03-08 |
2015-06-09 |
Eutropics Pharmaceuticals, Inc. |
Compositions and methods useful for treating diseases
|
CN103608012A
(zh)
|
2011-06-14 |
2014-02-26 |
诺华股份有限公司 |
在癌症如骨髓增殖性肿瘤治疗中的帕比司他与鲁索利替尼的组合
|
EP2561867A1
(en)
|
2011-08-22 |
2013-02-27 |
Lead Discovery Center GmbH |
CDK9 inhibitors in the treatment of midline carcinoma
|
US9012215B2
(en)
|
2011-09-22 |
2015-04-21 |
The Johns Hopkins University |
Methods for identifying leukemia stem cells and distinguishing them from normal hematopietic stem cells in patients with acute myeloid leukemia: uses in diagnosis, treatment, and research
|
US20130122492A1
(en)
|
2011-11-14 |
2013-05-16 |
Kellbenx Inc. |
Detection, isolation and analysis of rare cells in biological fluids
|
WO2013082660A1
(en)
|
2011-12-09 |
2013-06-13 |
Alfred Health |
Prediction method
|
WO2013138702A2
(en)
|
2012-03-15 |
2013-09-19 |
Bristol-Myers Squibb Company |
Methods for predicting gastrointestinal immune-related adverse events (gi-irae) in patients treated with modulation of the co-stimulatory pathway
|
EP2827864B1
(en)
|
2012-03-20 |
2020-09-30 |
Dana-Farber Cancer Institute, Inc. |
Inhibition of mcl-1 and/or bfl-1/a1
|
KR102062416B1
(ko)
|
2012-05-10 |
2020-01-03 |
유트로픽스 파마슈티컬스, 인크. |
실용 가능한 암 진단 대체 법
|
WO2013182519A1
(en)
|
2012-06-04 |
2013-12-12 |
Universitaet Basel |
Combination of lysosomotropic or autophagy modulating agents and a gsk-3 inhibitor for treatment of cancer
|
WO2013188355A1
(en)
|
2012-06-12 |
2013-12-19 |
Merck Sharp & Dohme Corp. |
Cdk inhibitor for treating refractory chronic lymphocytic leukemia
|
WO2013192423A2
(en)
|
2012-06-20 |
2013-12-27 |
Eutropics Pharmaceuticals, Inc. |
Methods and compositions useful for treating diseases involving bcl-2 family proteins with quinoline derivatives
|
US20150322479A1
(en)
|
2012-06-20 |
2015-11-12 |
Cytospan Technologies Corporation |
Apparatus and method for quantification of replicative lifespan and observation of senescene
|
AU2013317985B2
(en)
|
2012-09-19 |
2019-06-13 |
Dana-Farber Cancer Institute, Inc. |
Dynamic BH3 profiling
|
US9241941B2
(en)
|
2012-09-20 |
2016-01-26 |
Memorial Sloan-Kettering Cancer Center |
Methods for treatment of lymphomas with mutations in cell cycle genes
|
SG11201502757QA
(en)
|
2012-10-09 |
2015-05-28 |
Igenica Biotherapeutics Inc |
Anti-c16orf54 antibodies and methods of use thereof
|
US20140287932A1
(en)
|
2012-10-25 |
2014-09-25 |
Whitehead Institute For Biomedical Research |
Super-enhancers and methods of use thereof
|
JP2016526892A
(ja)
|
2013-07-18 |
2016-09-08 |
ユートロピクス ファーマシューティカルズ, インコーポレイテッド |
示差的bh3ミトコンドリアプロファイリング
|
US10732182B2
(en)
|
2013-08-01 |
2020-08-04 |
Eutropics Pharmaceuticals, Inc. |
Method for predicting cancer sensitivity
|
EP3047276B1
(en)
|
2013-09-19 |
2023-06-14 |
Dana-Farber Cancer Institute, Inc. |
Methods of bh3 profiling
|
CA2920192A1
(en)
|
2013-09-27 |
2015-04-02 |
Immunomedics, Inc. |
Anti-trop-2 antibody-drug conjugates and uses thereof
|
WO2015066305A1
(en)
|
2013-10-30 |
2015-05-07 |
Eutropics Pharmaceuticals, Inc. |
Methods for determining chemosensitivity and chemotoxicity
|
MX2016005980A
(es)
|
2013-11-08 |
2016-12-09 |
Dana Farber Cancer Inst Inc |
Terapia de combinación para el cáncer usando inhibidores de la proteína bromodominio y extra-terminal.
|
WO2015130585A1
(en)
|
2014-02-28 |
2015-09-03 |
Merck Sharp & Dohme Corp. |
Method for treating cancer
|
WO2015161247A1
(en)
|
2014-04-17 |
2015-10-22 |
Igenica Biotherapeutics, Inc. |
Humanized anti-c16orf54 antibodies and methods of use thereof
|
US10577417B2
(en)
|
2014-09-17 |
2020-03-03 |
Novartis Ag |
Targeting cytotoxic cells with chimeric receptors for adoptive immunotherapy
|
JP6930913B2
(ja)
|
2014-10-14 |
2021-09-01 |
ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニアThe Regents Of The University Of California |
炎症を阻害するためのcdk9及びbrd4阻害剤の使用法
|
EP3215135B1
(en)
|
2014-11-07 |
2020-05-13 |
Tolero Pharmaceuticals, Inc. |
Methods to target transcriptional control at super-enhancer regions
|
US10793915B2
(en)
|
2015-01-12 |
2020-10-06 |
Eutropics Pharmaceuticals, Inc. |
Context dependent diagnostics test for guiding cancer treatment
|
US10052346B2
(en)
|
2015-02-17 |
2018-08-21 |
Cantex Pharmaceuticals, Inc. |
Treatment of myelodysplastic syndromes with 2-O and,or 3-O desulfated heparinoids
|
AU2016232833A1
(en)
|
2015-03-18 |
2017-10-12 |
Dana-Farber Cancer Institute, Inc. |
Selective Mcl-1 binding peptides
|
EP3274467A4
(en)
|
2015-03-24 |
2018-10-31 |
Eutropics Pharmaceuticals, Inc. |
Surrogate functional biomarker for solid tumor cancer
|
WO2016161248A1
(en)
|
2015-04-02 |
2016-10-06 |
Tolero Pharmaceuticals, Inc. |
Targeting pim kinases in combination with btk inhibition
|
RU2717829C2
(ru)
|
2015-04-20 |
2020-03-26 |
Толеро Фармасьютикалз, Инк. |
Прогнозирование ответа на альвоцидиб с помощью анализа профиля митохондрий
|
CA2983024A1
(en)
|
2015-04-27 |
2016-11-03 |
Dana-Farber Cancer Institute, Inc. |
Compositions and methods for assessing toxicity using dynamic bh3 profiling
|
MX2017014645A
(es)
*
|
2015-05-18 |
2018-01-23 |
Tolero Pharmaceuticals Inc |
Profarmacos de alvocidib que tienen una biodisponibilidad aumentada.
|
EP3331510A4
(en)
|
2015-08-03 |
2019-04-03 |
Tolero Pharmaceuticals, Inc. |
COMBINATORIAL THERAPIES FOR THE TREATMENT OF CANCER
|
WO2017075349A2
(en)
|
2015-10-30 |
2017-05-04 |
Massachusetts Institute Of Technology |
Selective mcl-1 binding peptides
|
CN105919955A
(zh)
|
2016-06-13 |
2016-09-07 |
佛山市腾瑞医药科技有限公司 |
一种鲁索利替尼制剂及其应用
|
US11279694B2
(en)
*
|
2016-11-18 |
2022-03-22 |
Sumitomo Dainippon Pharma Oncology, Inc. |
Alvocidib prodrugs and their use as protein kinase inhibitors
|
EP3362471B1
(en)
|
2016-12-19 |
2021-11-17 |
Sumitomo Dainippon Pharma Oncology, Inc. |
Profiling peptides and methods for sensitivity profiling
|
WO2019055579A1
(en)
|
2017-09-12 |
2019-03-21 |
Tolero Pharmaceuticals, Inc. |
TREATMENT REGIME FOR CANCERS THAT ARE INSENSITIVE TO BCL-2 INHIBITORS USING THE MCL-1 ALVOCIDIB INHIBITOR
|
KR20210099066A
(ko)
*
|
2018-12-04 |
2021-08-11 |
스미토모 다이니폰 파마 온콜로지, 인크. |
암의 치료를 위한 작용제로서 사용하기 위한 cdk9 억제제 및 그의 다형체
|