GB812366A
(en)
|
1955-08-18 |
1959-04-22 |
Wellcome Found |
Improvements in and relating to derivatives of pyrimidine and the preparation thereof
|
GB937725A
(en)
|
1960-05-11 |
1963-09-25 |
Ciba Ltd |
Pyrazolo[3:4-d]pyrimidines
|
DE2004713A1
(de)
|
1970-02-03 |
1971-08-12 |
Boehnnger Mannheim GmbH, 6800 Mann heim Waldhof |
Nitrofuryl triazolo pyrimidine und Verfahren zu ihrer Herstellung
|
US3657744A
(en)
|
1970-05-08 |
1972-04-25 |
Univ Minnesota |
Method for fixing prosthetic implants in a living body
|
IT1153216B
(it)
|
1981-10-16 |
1987-01-14 |
Schering Ag |
Procedimento per la preparazione di composti cianoeterociclici
|
DE3406533A1
(de)
|
1984-02-23 |
1985-08-29 |
Boehringer Mannheim Gmbh, 6800 Mannheim |
Verwendung von adenosin-derivaten als antiallergica und arzneimittel, die diese enthalten
|
US5310731A
(en)
|
1984-06-28 |
1994-05-10 |
Whitby Research, Inc. |
N-6 substituted-5'-(N-substitutedcarboxamido)adenosines as cardiac vasodilators and antihypertensive agents
|
JPS61109797A
(ja)
|
1984-11-01 |
1986-05-28 |
Yuki Gosei Yakuhin Kogyo Kk |
標識化ヌクレオチドおよび標識化ポリヌクレオチド
|
JPS61109797U
(xx)
|
1984-12-25 |
1986-07-11 |
|
|
US4733665C2
(en)
|
1985-11-07 |
2002-01-29 |
Expandable Grafts Partnership |
Expandable intraluminal graft and method and apparatus for implanting an expandable intraluminal graft
|
US5023252A
(en)
|
1985-12-04 |
1991-06-11 |
Conrex Pharmaceutical Corporation |
Transdermal and trans-membrane delivery of drugs
|
US5061273A
(en)
|
1989-06-01 |
1991-10-29 |
Yock Paul G |
Angioplasty apparatus facilitating rapid exchanges
|
US5350395A
(en)
|
1986-04-15 |
1994-09-27 |
Yock Paul G |
Angioplasty apparatus facilitating rapid exchanges
|
US5040548A
(en)
|
1989-06-01 |
1991-08-20 |
Yock Paul G |
Angioplasty mehtod
|
US4748982A
(en)
|
1987-01-06 |
1988-06-07 |
Advanced Cardiovascular Systems, Inc. |
Reinforced balloon dilatation catheter with slitted exchange sleeve and method
|
US5001139A
(en)
|
1987-06-12 |
1991-03-19 |
American Cyanamid Company |
Enchancers for the transdermal flux of nivadipine
|
US4992445A
(en)
|
1987-06-12 |
1991-02-12 |
American Cyanamid Co. |
Transdermal delivery of pharmaceuticals
|
WO1990003370A1
(en)
|
1988-09-28 |
1990-04-05 |
Microprobe Corporation |
DERIVATIVES OF PYRAZOLO[3,4-d]PYRIMIDINE
|
CA1322628C
(en)
|
1988-10-04 |
1993-10-05 |
Richard A. Schatz |
Expandable intraluminal graft
|
GB8827305D0
(en)
|
1988-11-23 |
1988-12-29 |
British Bio Technology |
Compounds
|
US5442039A
(en)
|
1989-07-17 |
1995-08-15 |
The Dow Chemical Company |
Mesogenic polycyanates and thermosets thereof
|
US5428125A
(en)
|
1989-07-17 |
1995-06-27 |
The Dow Chemical Company |
Mesogenic polycyanates and thermosets thereof
|
US5292331A
(en)
|
1989-08-24 |
1994-03-08 |
Applied Vascular Engineering, Inc. |
Endovascular support device
|
US6344053B1
(en)
|
1993-12-22 |
2002-02-05 |
Medtronic Ave, Inc. |
Endovascular support device and method
|
US5674278A
(en)
|
1989-08-24 |
1997-10-07 |
Arterial Vascular Engineering, Inc. |
Endovascular support device
|
US5763596A
(en)
|
1989-09-15 |
1998-06-09 |
Metabasis Therapeutics, Inc. |
C-4' modified adenosine kinase inhibitors
|
US5674998A
(en)
|
1989-09-15 |
1997-10-07 |
Gensia Inc. |
C-4' modified adenosine kinase inhibitors
|
US5646128A
(en)
|
1989-09-15 |
1997-07-08 |
Gensia, Inc. |
Methods for treating adenosine kinase related conditions
|
US5721356A
(en)
|
1989-09-15 |
1998-02-24 |
Gensia, Inc. |
Orally active adenosine kinase inhibitors
|
US5763597A
(en)
|
1989-09-15 |
1998-06-09 |
Metabasis Therapeutics, Inc. |
Orally active adenosine kinase inhibitors
|
US5795977A
(en)
|
1989-09-15 |
1998-08-18 |
Metabasis Therapeutics, Inc. |
Water soluble adenosine kinase inhibitors
|
GB9009542D0
(en)
|
1990-04-27 |
1990-06-20 |
Beecham Group Plc |
Novel compounds
|
GB9113137D0
(en)
|
1990-07-13 |
1991-08-07 |
Ici Plc |
Thioxo heterocycles
|
US5563257A
(en)
|
1990-08-20 |
1996-10-08 |
Boehringer Mannheim Gmbh |
Phospholipid derivatives of nucleosides
|
DE4026265A1
(de)
|
1990-08-20 |
1992-02-27 |
Boehringer Mannheim Gmbh |
Neue phospholipid-derivate von nucleosiden, deren herstellung sowie deren verwendung als antivirale arzneimittel
|
DE69123974T2
(de)
|
1990-09-25 |
1997-05-07 |
Rhone Poulenc Rorer Int |
Verbindungen welche antihypertensive und antiischemische eigenschaften besitzen
|
US5561134A
(en)
|
1990-09-25 |
1996-10-01 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
Compounds having antihypertensive, cardioprotective, anti-ischemic and antilipolytic properties
|
US5652366A
(en)
|
1990-09-25 |
1997-07-29 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
DI (1R)-(-)camphosulfonic acid) salt, preparation thereof and use thereof
|
GB9103839D0
(en)
|
1991-02-23 |
1991-04-10 |
Smithkline Beecham Plc |
Pharmaceuticals
|
US5916891A
(en)
|
1992-01-13 |
1999-06-29 |
Smithkline Beecham Corporation |
Pyrimidinyl imidazoles
|
IL104369A0
(en)
|
1992-01-13 |
1993-05-13 |
Smithkline Beecham Corp |
Novel compounds and compositions
|
DE4204031A1
(de)
|
1992-02-12 |
1993-08-19 |
Boehringer Mannheim Gmbh |
Neue lipidphosphonsaeure-nucleosid-konjugate sowie deren verwendung als antivirale arzneimittel
|
DE4204032A1
(de)
|
1992-02-12 |
1993-08-19 |
Boehringer Mannheim Gmbh |
Neue liponucleotide, deren herstellunmg sowie deren verwendung als antivirale arzneimittel
|
WO1993018035A1
(en)
|
1992-03-04 |
1993-09-16 |
Abbott Laboratories |
Angiotensin ii receptor antagonists
|
JP2737518B2
(ja)
|
1992-03-16 |
1998-04-08 |
富士通株式会社 |
赤外線検知器の冷却構造
|
GB9208135D0
(en)
|
1992-04-13 |
1992-05-27 |
Ludwig Inst Cancer Res |
Polypeptides having kinase activity,their preparation and use
|
AU4115693A
(en)
|
1992-04-24 |
1993-11-29 |
Sri International |
In vivo homologous sequence targeting in eukaryotic cells
|
JP3261617B2
(ja)
|
1992-06-19 |
2002-03-04 |
ハネウエル・インコーポレーテッド |
赤外線カメラ
|
US6057305A
(en)
|
1992-08-05 |
2000-05-02 |
Institute Of Organic Chemistry And Biochemistry Of The Academy Of Sciences Of The Czech Republic |
Antiretroviral enantiomeric nucleotide analogs
|
TW444018B
(en)
|
1992-12-17 |
2001-07-01 |
Pfizer |
Pyrazolopyrimidines
|
US5455258A
(en)
|
1993-01-06 |
1995-10-03 |
Ciba-Geigy Corporation |
Arylsulfonamido-substituted hydroxamic acids
|
WO1994018215A1
(en)
|
1993-02-03 |
1994-08-18 |
Gensia, Inc. |
Adenosine kinase inhibitors comprising lyxofuranosyl derivatives
|
IL108523A0
(en)
|
1993-02-03 |
1994-05-30 |
Gensia Inc |
Pharmaceutical compositions containing adenosine kinase inhibitors for preventing or treating conditions involving inflammatory responses and pain
|
AU6672794A
(en)
|
1993-11-05 |
1995-05-23 |
Biochem Pharma Inc. |
Antineoplastic heteronaphthoquinones
|
IL112249A
(en)
|
1994-01-25 |
2001-11-25 |
Warner Lambert Co |
Pharmaceutical compositions containing di and tricyclic pyrimidine derivatives for inhibiting tyrosine kinases of the epidermal growth factor receptor family and some new such compounds
|
US5679683A
(en)
|
1994-01-25 |
1997-10-21 |
Warner-Lambert Company |
Tricyclic compounds capable of inhibiting tyrosine kinases of the epidermal growth factor receptor family
|
US6632789B1
(en)
|
1994-04-29 |
2003-10-14 |
The United States Of America As Represented By The Secretary Of The Navy |
Methods for modulating T cell responses by manipulating intracellular signal transduction
|
DE4418690A1
(de)
|
1994-05-28 |
1996-01-11 |
Boehringer Mannheim Gmbh |
Neue Lipidester von Nucleosid-Monophosphaten und deren Verwendung als immunsuppressive Arzneimittel
|
US6323201B1
(en)
|
1994-12-29 |
2001-11-27 |
The Regents Of The University Of California |
Compounds for inhibition of ceramide-mediated signal transduction
|
US5863949A
(en)
|
1995-03-08 |
1999-01-26 |
Pfizer Inc |
Arylsulfonylamino hydroxamic acid derivatives
|
DK0819129T3
(da)
|
1995-04-03 |
2000-10-23 |
Novartis Ag |
Pyrazolderivater og fremgangsmåde til deres fremstilling
|
US6312894B1
(en)
|
1995-04-03 |
2001-11-06 |
Epoch Pharmaceuticals, Inc. |
Hybridization and mismatch discrimination using oligonucleotides conjugated to minor groove binders
|
US5861510A
(en)
|
1995-04-20 |
1999-01-19 |
Pfizer Inc |
Arylsulfonyl hydroxamic acid derivatives as MMP and TNF inhibitors
|
US5977061A
(en)
|
1995-04-21 |
1999-11-02 |
Institute Of Organic Chemistry And Biochemistry Of The Academy Of Sciences Of The Czech Republic |
N6 - substituted nucleotide analagues and their use
|
JPH08295667A
(ja)
|
1995-04-27 |
1996-11-12 |
Takeda Chem Ind Ltd |
複素環化合物、その製造法および剤
|
US5593997A
(en)
|
1995-05-23 |
1997-01-14 |
Pfizer Inc. |
4-aminopyrazolo(3-,4-D)pyrimidine and 4-aminopyrazolo-(3,4-D)pyridine tyrosine kinase inhibitors
|
US6403599B1
(en)
|
1995-11-08 |
2002-06-11 |
Pfizer Inc |
Corticotropin releasing factor antagonists
|
CN1192696A
(zh)
|
1995-06-07 |
1998-09-09 |
G·D·瑟尔公司 |
用于充血性心力衰竭治疗的螺甾内酯与血管紧张素ⅱ拮抗药组合疗法
|
AU5982296A
(en)
|
1995-06-07 |
1996-12-30 |
G.D. Searle & Co. |
Method to treat cardiofibrosis with a combination of an angi otensin ii antagonist and spironolactone
|
US5665721A
(en)
|
1995-06-07 |
1997-09-09 |
Abbott Laboratories |
Heterocyclic substituted cyclopentane compounds
|
CZ297975B6
(cs)
|
1995-06-07 |
2007-05-09 |
G. D. Searle & Co. |
Farmaceutická kombinace antagonisty receptoru proangiotensin II a epoxymexrenonu pro lécení kardiovaskulárních poruch
|
US5763885A
(en)
|
1995-12-19 |
1998-06-09 |
Loral Infrared & Imaging Systems, Inc. |
Method and apparatus for thermal gradient stabilization of microbolometer focal plane arrays
|
JPH09143163A
(ja)
|
1995-11-29 |
1997-06-03 |
Fuji Photo Film Co Ltd |
含窒素ヘテロ芳香族アミド類の製造方法
|
ATE225343T1
(de)
|
1995-12-20 |
2002-10-15 |
Hoffmann La Roche |
Matrix-metalloprotease inhibitoren
|
US5747235A
(en)
|
1996-01-26 |
1998-05-05 |
Eastman Kodak Company |
Silver halide light sensitive emulsion layer having enhanced photographic sensitivity
|
DE19603576A1
(de)
|
1996-02-01 |
1997-08-07 |
Bayer Ag |
Acylierte 4-Amino und 4-Hydrazinopyrimidine
|
CH690773A5
(de)
|
1996-02-01 |
2001-01-15 |
Novartis Ag |
Pyrrolo(2,3-d)pyrimide und ihre Verwendung.
|
US5914488A
(en)
|
1996-03-05 |
1999-06-22 |
Mitsubishi Denki Kabushiki Kaisha |
Infrared detector
|
GB9611460D0
(en)
|
1996-06-01 |
1996-08-07 |
Ludwig Inst Cancer Res |
Novel lipid kinase
|
EP0912549A4
(en)
|
1996-06-20 |
2002-01-02 |
Univ Texas |
CONNECTIONS AND METHOD FOR PROVIDING ACTIVE PREPARATIONS AND THE USE THEREOF
|
TR199900066T2
(xx)
|
1996-07-18 |
1999-04-21 |
Pfizer Inc. |
Matriks metalloproteazlar�n fosfinat bazl� inhibit�rleri
|
CA2264284A1
(en)
|
1996-08-23 |
1998-02-26 |
Ralph P. Robinson |
Arylsulfonylamino hydroxamic acid derivatives
|
AU720135B2
(en)
|
1996-10-02 |
2000-05-25 |
Novartis Ag |
Pyrimidine derivatives and processes for the preparation thereof
|
US5990169A
(en)
|
1996-10-23 |
1999-11-23 |
Zymogenetics, Inc. |
Compositions and methods for treating bone deficit conditions
|
US5994358A
(en)
|
1996-10-23 |
1999-11-30 |
Zymogenetics, Inc. |
Compositions and methods for treating bone deficit conditions
|
US6342514B1
(en)
|
1996-10-23 |
2002-01-29 |
Zymogenetics, Inc. |
Compositions and methods for treating bone deficit conditions
|
US6153631A
(en)
|
1996-10-23 |
2000-11-28 |
Zymogenetics, Inc. |
Compositions and methods for treating bone deficit conditions
|
US5948776A
(en)
|
1996-10-23 |
1999-09-07 |
Zymogenetic, Inc. |
Compositions and methods for treating bone deficit conditions
|
US5919808A
(en)
|
1996-10-23 |
1999-07-06 |
Zymogenetics, Inc. |
Compositions and methods for treating bone deficit conditions
|
US5965573A
(en)
|
1996-10-23 |
1999-10-12 |
Zymogenetics, Inc. |
Compositions and methods for treating bone deficit conditions
|
US6251901B1
(en)
|
1996-10-23 |
2001-06-26 |
Zymogenetics, Inc. |
Compositions and methods for treating bone deficit conditions
|
US5922753A
(en)
|
1996-10-23 |
1999-07-13 |
Zymogenetics, Inc. |
Methods for treating bone deficit conditions with benzothiazole
|
US5858753A
(en)
|
1996-11-25 |
1999-01-12 |
Icos Corporation |
Lipid kinase
|
ATE346085T1
(de)
|
1996-12-06 |
2006-12-15 |
Vertex Pharma |
Inhibitoren des interleukin-1-beta konvertierenden enzyms
|
US6093737A
(en)
|
1996-12-30 |
2000-07-25 |
Merck & Co., Inc. |
Inhibitors of farnesyl-protein transferase
|
PT950059E
(pt)
|
1997-01-06 |
2004-10-29 |
Pfizer |
Derivados de sulfona ciclicos
|
JPH10206995A
(ja)
|
1997-01-21 |
1998-08-07 |
Konica Corp |
ハロゲン化銀写真感光材料
|
PT977733E
(pt)
|
1997-02-03 |
2003-12-31 |
Pfizer Prod Inc |
Derivados de acido arilsulfonilamino-hidroxamico
|
WO1998035048A2
(en)
|
1997-02-07 |
1998-08-13 |
Princeton University |
Engineered protein kinases which can utilize modified nucleotide triphosphate substrates
|
CA2279863A1
(en)
|
1997-02-07 |
1998-08-13 |
Pfizer Inc. |
N-hydroxy-beta-sulfonyl-propionamide derivatives and their use as inhibitors of matrix metalloproteinases
|
AU722784B2
(en)
|
1997-02-11 |
2000-08-10 |
Pfizer Inc. |
Arylsulfonyl hydroxamic acid derivatives
|
US7863444B2
(en)
|
1997-03-19 |
2011-01-04 |
Abbott Laboratories |
4-aminopyrrolopyrimidines as kinase inhibitors
|
PL335685A1
(en)
|
1997-03-19 |
2000-05-08 |
Basf Ag |
Pyrrole[2,3-d]pyrimidines and their application as inhibitors of tyrosine kinase
|
WO1998043962A1
(en)
|
1997-03-28 |
1998-10-08 |
Du Pont Pharmaceuticals Company |
Heterocyclic integrin inhibitor prodrugs
|
AU7449598A
(en)
|
1997-05-23 |
1998-12-11 |
Nippon Shinyaku Co. Ltd. |
Medicinal composition for prevention or treatment of hepatopathy
|
GB9711650D0
(en)
|
1997-06-05 |
1997-07-30 |
Pfizer Ltd |
Compounds useful in therapy
|
US6207679B1
(en)
|
1997-06-19 |
2001-03-27 |
Sepracor, Inc. |
Antimicrobial agents uses and compositions related thereto
|
ATE404539T1
(de)
|
1997-10-02 |
2008-08-15 |
Eisai R&D Man Co Ltd |
Kondensierte pyridinderivate
|
US6649631B1
(en)
|
1997-10-23 |
2003-11-18 |
The Board Of Regents Of The University Of Texas System |
Compositions and methods for treating bone deficit conditions
|
ES2222614T3
(es)
|
1997-11-12 |
2005-02-01 |
Mitsubishi Chemical Corporation |
Derivados de purina y medicina que los contiene como ingrediente activo.
|
GB9725782D0
(en)
|
1997-12-05 |
1998-02-04 |
Pfizer Ltd |
Therapeutic agents
|
US6191170B1
(en)
|
1998-01-13 |
2001-02-20 |
Tularik Inc. |
Benzenesulfonamides and benzamides as therapeutic agents
|
GB9801690D0
(en)
|
1998-01-27 |
1998-03-25 |
Pfizer Ltd |
Therapeutic agents
|
US6127121A
(en)
|
1998-04-03 |
2000-10-03 |
Epoch Pharmaceuticals, Inc. |
Oligonucleotides containing pyrazolo[3,4-D]pyrimidines for hybridization and mismatch discrimination
|
US7715989B2
(en)
|
1998-04-03 |
2010-05-11 |
Elitech Holding B.V. |
Systems and methods for predicting oligonucleotide melting temperature (TmS)
|
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
|
US6251689B1
(en)
|
1998-05-14 |
2001-06-26 |
Telik, Inc. |
Methods for the solid phase synthesis of combinatorial libraries of benzimidazoles benzoxazoles benzothiazoles and derivatives thereof
|
MXPA00011889A
(es)
|
1998-06-02 |
2003-04-25 |
Osi Pharm Inc |
Composiciones de pirrolo (2,3d) piridina y su uso.
|
JP2000072773A
(ja)
|
1998-08-28 |
2000-03-07 |
Zeria Pharmaceut Co Ltd |
プリン誘導体
|
US6713474B2
(en)
|
1998-09-18 |
2004-03-30 |
Abbott Gmbh & Co. Kg |
Pyrrolopyrimidines as therapeutic agents
|
CN1326457A
(zh)
|
1998-09-18 |
2001-12-12 |
巴斯福股份公司 |
作为激酶抑制剂的4-氨基吡咯并嘧啶
|
EA200100523A1
(ru)
|
1998-11-16 |
2001-10-22 |
Басф Акциенгезельшафт |
3-[бенз(окс/ти)азол-7-ил]-1h-пиримидин-2,4-дионы
|
US6319660B1
(en)
|
1998-12-28 |
2001-11-20 |
Eastman Kodak Company |
Color photographic element containing speed improving compound
|
DE1140938T1
(de)
|
1999-01-11 |
2003-01-09 |
Princeton University Princeton |
Kinase-inhibitoren mit hoher affinität zur ziel detektion und ihre verwendung
|
CZ27399A3
(cs)
|
1999-01-26 |
2000-08-16 |
Ústav Experimentální Botaniky Av Čr |
Substituované dusíkaté heterocyklické deriváty, způsob jejich přípravy, tyto deriváty pro použití jako léčiva, farmaceutická kompozice a kombinovaný farmaceutický přípravek tyto deriváty obsahující a použití těchto derivátů pro výrobu léčiv
|
EP1040831A3
(en)
|
1999-04-02 |
2003-05-02 |
Pfizer Products Inc. |
Use of corticotropin releasing factor (CRF) antagonists to prevent sudden death
|
SE515856C2
(sv)
|
1999-05-19 |
2001-10-22 |
Ericsson Telefon Ab L M |
Bärare för elektronikkomponenter
|
CN1636005A
(zh)
|
1999-06-03 |
2005-07-06 |
克诺尔股份有限公司 |
苯并噻嗪酮和苯并噁嗪酮化合物
|
US6387894B1
(en)
|
1999-06-11 |
2002-05-14 |
Pfizer Inc. |
Use of CRF antagonists and renin-angiotensin system inhibitors
|
PE20010306A1
(es)
|
1999-07-02 |
2001-03-29 |
Agouron Pharma |
Compuestos de indazol y composiciones farmaceuticas que los contienen utiles para la inhibicion de proteina kinasa
|
TWI262914B
(en)
|
1999-07-02 |
2006-10-01 |
Agouron Pharma |
Compounds and pharmaceutical compositions for inhibiting protein kinases
|
GB9919588D0
(en)
|
1999-08-18 |
1999-10-20 |
Hoechst Schering Agrevo Gmbh |
Fungicidal compounds
|
DE60031285T2
(de)
|
1999-08-27 |
2007-08-30 |
Chemocentryx Inc., Mountain View |
Heterozyclische verbindungen und verfahren zur modulierung von cxcr3 funktion
|
ATE286033T1
(de)
|
1999-09-16 |
2005-01-15 |
Curis Inc |
Vermittler von igel signalwegen, deren zusammenstellungen und verwendungen
|
US6921763B2
(en)
|
1999-09-17 |
2005-07-26 |
Abbott Laboratories |
Pyrazolopyrimidines as therapeutic agents
|
DK1212327T3
(da)
|
1999-09-17 |
2003-12-15 |
Abbott Gmbh & Co Kg |
Pyrazolopyrimidiner som terapeutiske midler
|
US6506769B2
(en)
|
1999-10-06 |
2003-01-14 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Heterocyclic compounds useful as inhibitors of tyrosine kinases
|
JP5036112B2
(ja)
|
1999-10-06 |
2012-09-26 |
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 |
チロシンキナーゼのインヒビターとして有益な複素環化合物
|
US6472153B1
(en)
|
1999-10-26 |
2002-10-29 |
Epoch Biosciences, Inc. |
Hybridization-triggered fluorescent detection of nucleic acids
|
US6660845B1
(en)
|
1999-11-23 |
2003-12-09 |
Epoch Biosciences, Inc. |
Non-aggregating, non-quenching oligomers comprising nucleotide analogues; methods of synthesis and use thereof
|
GB0002032D0
(en)
|
2000-01-28 |
2000-03-22 |
Zeneca Ltd |
Chemical compounds
|
US7217722B2
(en)
|
2000-02-01 |
2007-05-15 |
Kirin Beer Kabushiki Kaisha |
Nitrogen-containing compounds having kinase inhibitory activity and drugs containing the same
|
US6613798B1
(en)
|
2000-03-30 |
2003-09-02 |
Curis, Inc. |
Small organic molecule regulators of cell proliferation
|
US7115653B2
(en)
|
2000-03-30 |
2006-10-03 |
Curis, Inc. |
Small organic molecule regulators of cell proliferation
|
US6667300B2
(en)
|
2000-04-25 |
2003-12-23 |
Icos Corporation |
Inhibitors of human phosphatidylinositol 3-kinase delta
|
ES2527754T3
(es)
|
2000-04-25 |
2015-01-29 |
Icos Corporation |
Inhibidores de la isoforma delta de la fosfatidilinositol 3-quinasa humana
|
JP2002037787A
(ja)
|
2000-05-16 |
2002-02-06 |
Kyowa Hakko Kogyo Co Ltd |
[1,2,4]トリアゾロ[1,5−c]ピリミジン誘導体の製造法
|
EP1289472A4
(en)
|
2000-05-30 |
2004-09-08 |
Advanced Res & Tech Inst |
COMPOSITIONS AND METHODS FOR IDENTIFYING MODULATORS OF PTEN FUNCTION AND PI-3 KINASE MECHANISMS
|
BR0112030A
(pt)
|
2000-06-27 |
2003-04-29 |
Genelabs Tech Inc |
Novos compostos que possuem atividade antibacteriana, antifúngica ou antitumor
|
US6534691B2
(en)
|
2000-07-18 |
2003-03-18 |
E. I. Du Pont De Nemours And Company |
Manufacturing process for α-olefins
|
AU2002213467A1
(en)
|
2000-10-11 |
2002-04-22 |
Chemocentryx, Inc. |
Modulation of ccr4 function
|
CA2425663C
(en)
|
2000-10-11 |
2009-12-29 |
Applera Corporation |
Fluorescent nucleobase conjugates having anionic linkers
|
JP2002131859A
(ja)
|
2000-10-19 |
2002-05-09 |
Konica Corp |
撮影用赤外感光性ハロゲン化銀写真感光材料及び赤外感光性ハロゲン化銀乳剤
|
US6890747B2
(en)
|
2000-10-23 |
2005-05-10 |
Warner-Lambert Company |
Phosphoinositide 3-kinases
|
US6964967B2
(en)
|
2000-12-11 |
2005-11-15 |
Amgen, Inc. |
Substituted pyrido[2,3-d]pyrimidines and methods for their use
|
AU2002219555B2
(en)
|
2000-12-28 |
2006-11-30 |
Daiichi Pharmaceutical Co., Ltd. |
VLA-4 Inhibitors
|
EP1355916B1
(en)
|
2001-01-22 |
2007-01-10 |
Merck & Co., Inc. |
Nucleoside derivatives as inhibitors of rna-dependent rna viral polymerase
|
US7105499B2
(en)
|
2001-01-22 |
2006-09-12 |
Merck & Co., Inc. |
Nucleoside derivatives as inhibitors of RNA-dependent RNA viral polymerase
|
MXPA03008560A
(es)
|
2001-03-22 |
2004-06-30 |
Abbot Gmbh & Co Kg |
Pirazolopirimidinas como agentes terapeuticos.
|
US7250569B2
(en)
|
2001-04-26 |
2007-07-31 |
New York University School Of Medicine |
Method for dissolving nanostructural materials
|
JP2004528376A
(ja)
|
2001-05-08 |
2004-09-16 |
クドス ファーマシューティカルズ リミテッド |
Parp阻害薬としてのイソキノリノン誘導体
|
WO2002094264A1
(en)
|
2001-05-23 |
2002-11-28 |
Tularik Inc. |
Ccr4 antagonists
|
EP1470119A4
(en)
|
2001-06-13 |
2005-10-19 |
Genesoft Pharmaceuticals Inc |
BENZOTHIOPHENE COMPOUNDS WITH ANTI-INFECTIOUS ACTIVITY
|
US20030236198A1
(en)
|
2001-06-13 |
2003-12-25 |
Genesoft, Inc. |
Antipathogenic benzamide compounds
|
EP1401817A4
(en)
|
2001-06-13 |
2005-11-02 |
Genesoft Pharmaceuticals Inc |
ISOQUINOLINE COMPOUNDS WITH ANTI-INFECTIOUS ACTIVITY
|
GB0115109D0
(en)
*
|
2001-06-21 |
2001-08-15 |
Aventis Pharma Ltd |
Chemical compounds
|
US20030114467A1
(en)
|
2001-06-21 |
2003-06-19 |
Shakespeare William C. |
Novel pyrazolo- and pyrrolo-pyrimidines and uses thereof
|
WO2003011285A1
(en)
|
2001-08-01 |
2003-02-13 |
Merck & Co., Inc. |
BENZIMIDAZO[4,5-f]ISOQUINOLINONE DERIVATIVES
|
AU2002327422A1
(en)
|
2001-08-03 |
2003-03-18 |
Abbott Laboratories |
Method of identifying inhibitors of lck
|
BR0211750A
(pt)
|
2001-08-10 |
2004-10-13 |
Shionogi & Co |
Agente antiviral
|
JP2003073357A
(ja)
|
2001-09-03 |
2003-03-12 |
Mitsubishi Pharma Corp |
アミド化合物を含有するRhoキナーゼ阻害剤
|
JP2005538183A
(ja)
|
2001-09-13 |
2005-12-15 |
ジーンソフト ファーマシューティカルズ インコーポレイテッド |
薬剤耐性細菌による感染症の治療方法
|
US7101884B2
(en)
|
2001-09-14 |
2006-09-05 |
Merck & Co., Inc. |
Tyrosine kinase inhibitors
|
AUPR769501A0
(en)
|
2001-09-14 |
2001-10-11 |
Biomolecular Research Institute Limited |
Cytokine receptor 1
|
TWI330183B
(xx)
|
2001-10-22 |
2010-09-11 |
Eisai R&D Man Co Ltd |
|
EP1440072A4
(en)
|
2001-10-30 |
2005-02-02 |
Conforma Therapeutic Corp |
PURINE ANALOGS HAVING HSP90 INHIBITORY ACTIVITY
|
US7319858B2
(en)
|
2001-11-16 |
2008-01-15 |
Cingular Wireless Ii, Llc |
System and method for querying message information
|
WO2003048081A2
(en)
|
2001-12-04 |
2003-06-12 |
Bristol-Myers Squibb Company |
Glycinamides as factor xa inhibitors
|
AU2002351412B2
(en)
|
2001-12-21 |
2010-05-20 |
Exelixis Patent Company Llc |
Modulators of LXR
|
JP4085237B2
(ja)
|
2001-12-21 |
2008-05-14 |
日本電気株式会社 |
携帯電話の利用契約システムと通信方法
|
BR0207583A
(pt)
|
2001-12-26 |
2004-04-27 |
Genelabs Tech Inc |
Derivados de poliamida possuindo atividade antibacteriana, antifungo ou antitumor
|
US7414036B2
(en)
|
2002-01-25 |
2008-08-19 |
Muscagen Limited |
Compounds useful as A3 adenosine receptor agonists
|
US20030225098A1
(en)
|
2002-03-21 |
2003-12-04 |
Hirst Gavin C. |
Kinase inhibitors
|
US20030180924A1
(en)
|
2002-03-22 |
2003-09-25 |
Desimone Robert W. |
Formulation of certain pyrazolo [3,4,-d] pyrimidines as kinase modulators
|
JP4663986B2
(ja)
|
2002-03-26 |
2011-04-06 |
ツェントファーム・ゲーエムベーハー |
フレデリカマイシン−誘導体
|
US7166293B2
(en)
|
2002-03-29 |
2007-01-23 |
Carlsbad Technology, Inc. |
Angiogenesis inhibitors
|
DE10217046A1
(de)
|
2002-04-17 |
2003-11-06 |
Bioleads Gmbh |
Fredericamycin-Derivate
|
JP2005529889A
(ja)
|
2002-04-26 |
2005-10-06 |
ファイザー・プロダクツ・インク |
ピリミジン−2,4,6−トリオンメタロ−プロテイナーゼ阻害剤
|
AU2003299517A1
(en)
|
2002-05-23 |
2004-05-25 |
Merck & Co., Inc. |
Mitotic kinesin inhibitors
|
WO2003106426A1
(en)
|
2002-06-14 |
2003-12-24 |
Cytokinetics, Inc. |
Compounds, compositions, and methods
|
US7265111B2
(en)
|
2002-06-27 |
2007-09-04 |
Sanofi-Aventis Deutschland Gmbh |
Adenosine analogues and their use as pharmaceutical agents
|
KR101124245B1
(ko)
|
2002-06-27 |
2012-07-02 |
노보 노르디스크 에이/에스 |
치료제로서 아릴 카르보닐 유도체
|
KR101116627B1
(ko)
|
2002-06-27 |
2012-10-09 |
노보 노르디스크 에이/에스 |
치료제로서 아릴 카르보닐 유도체
|
DE10230917A1
(de)
|
2002-07-09 |
2004-02-05 |
Bioleads Gmbh |
Fredericamycin-Derivate
|
WO2004006906A2
(en)
|
2002-07-15 |
2004-01-22 |
Combinatorx, Incorporated |
Methods for the treatment of neoplasms
|
WO2004014377A1
(en)
|
2002-08-13 |
2004-02-19 |
Warner-Lambert Company Llc |
4-hydroxyquinoline derivatives as matrix metalloproteinase inhibitors
|
CA2495661C
(en)
|
2002-08-16 |
2011-06-14 |
Kinacia Pty Ltd. |
Inhibition of phosphoinositide 3-kinase beta
|
US20040048853A1
(en)
|
2002-08-21 |
2004-03-11 |
Gustave Bergnes |
Compounds, compositions, and methods
|
US20030139427A1
(en)
|
2002-08-23 |
2003-07-24 |
Osi Pharmaceuticals Inc. |
Bicyclic pyrimidinyl derivatives and methods of use thereof
|
JP4487774B2
(ja)
|
2002-09-30 |
2010-06-23 |
萬有製薬株式会社 |
2−アミノベンズイミダゾール誘導体
|
US7138402B2
(en)
|
2003-09-18 |
2006-11-21 |
Conforma Therapeutics Corporation |
Pyrrolopyrimidines and related analogs as HSP90-inhibitors
|
JP2004161716A
(ja)
|
2002-11-15 |
2004-06-10 |
Takeda Chem Ind Ltd |
Jnk阻害剤
|
UA80171C2
(en)
|
2002-12-19 |
2007-08-27 |
Pfizer Prod Inc |
Pyrrolopyrimidine derivatives
|
WO2004058717A1
(en)
|
2002-12-20 |
2004-07-15 |
X-Ceptor Therapeutics, Inc. |
Isoquinolinone derivatives and their use as therapeutic agents
|
US7365094B2
(en)
|
2002-12-23 |
2008-04-29 |
4Sc Ag |
Compounds as anti-inflammatory, immunomodulatory and anti-proliferatory agents
|
US7247736B2
(en)
|
2002-12-23 |
2007-07-24 |
4Sc Ag |
Method of identifying inhibitors of DHODH
|
US7071355B2
(en)
|
2002-12-23 |
2006-07-04 |
4 Sc Ag |
Compounds as anti-inflammatory, immunomodulatory and anti-proliferatory agents
|
CA2517942A1
(en)
|
2003-03-06 |
2004-09-16 |
Dsm Ip Assets B.V. |
Process for the preparation of an .alpha.-amino carbonyl compound
|
US7550590B2
(en)
|
2003-03-25 |
2009-06-23 |
Takeda Pharmaceutical Company Limited |
Dipeptidyl peptidase inhibitors
|
GB0306907D0
(en)
|
2003-03-26 |
2003-04-30 |
Angiogene Pharm Ltd |
Boireductively-activated prodrugs
|
WO2004089297A2
(en)
|
2003-04-02 |
2004-10-21 |
Suntory Pharmaceutical Research Laboratories, Llc |
Compounds and methods for treatment of thrombosis
|
WO2004111014A1
(en)
|
2003-06-06 |
2004-12-23 |
Vertex Pharmaceuticals Incorporated |
Pyrimidine derivatives as modulators of atp-binding cassette transporters
|
US7429596B2
(en)
|
2003-06-20 |
2008-09-30 |
The Regents Of The University Of California |
1H-pyrrolo [2,3-D] pyrimidine derivatives and methods of use thereof
|
WO2005002585A1
(en)
|
2003-07-02 |
2005-01-13 |
Warner-Lambert Company Llc |
Combination of an allosteric inhibitor of matrix metalloproteinase-13 and a ligand to an alpha-2-delta receptor
|
AU2004260689B8
(en)
|
2003-07-29 |
2008-05-15 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
GB0317951D0
(en)
|
2003-07-31 |
2003-09-03 |
Trigen Ltd |
Compounds
|
US7501538B2
(en)
|
2003-08-08 |
2009-03-10 |
Transtech Pharma, Inc. |
Aryl and heteroaryl compounds, compositions and methods of use
|
US7208601B2
(en)
|
2003-08-08 |
2007-04-24 |
Mjalli Adnan M M |
Aryl and heteroaryl compounds, compositions, and methods of use
|
US20050043239A1
(en)
|
2003-08-14 |
2005-02-24 |
Jason Douangpanya |
Methods of inhibiting immune responses stimulated by an endogenous factor
|
US20050054614A1
(en)
|
2003-08-14 |
2005-03-10 |
Diacovo Thomas G. |
Methods of inhibiting leukocyte accumulation
|
JP2007502776A
(ja)
|
2003-08-15 |
2007-02-15 |
アイアールエム・リミテッド・ライアビリティ・カンパニー |
Rtk阻害剤としての6−置換アニリノプリン類
|
US7390820B2
(en)
|
2003-08-25 |
2008-06-24 |
Amgen Inc. |
Substituted quinolinone derivatives and methods of use
|
WO2005044181A2
(en)
|
2003-09-09 |
2005-05-19 |
Temple University-Of The Commonwealth System Of Higher Education |
Protection of tissues and cells from cytotoxic effects of ionizing radiation by abl inhibitors
|
GB0322409D0
(en)
|
2003-09-25 |
2003-10-29 |
Astrazeneca Ab |
Quinazoline derivatives
|
CN1863774B
(zh)
|
2003-10-08 |
2010-12-15 |
Irm责任有限公司 |
用作蛋白激酶抑制剂的化合物和组合物
|
TWI344364B
(en)
|
2003-11-10 |
2011-07-01 |
Synta Pharmaceuticals Corp |
Fused heterocyclic compounds
|
WO2005047289A1
(en)
*
|
2003-11-17 |
2005-05-26 |
Pfizer Products Inc. |
Pyrrolopyrimidine compounds useful in treatment of cancer
|
AR046845A1
(es)
|
2003-11-21 |
2005-12-28 |
Novartis Ag |
Derivados de 1h-imidazo[4,5-c]quinolina para tratamiento de enfermedades dependientes de las proteino-quinasas
|
WO2005061460A1
(en)
|
2003-12-08 |
2005-07-07 |
Cytokinetics, Inc. |
Compounds, compositions, and methods
|
MXPA06007095A
(es)
|
2003-12-22 |
2006-09-04 |
Gilead Sciences Inc |
Conjugados de fosfonato inhibidores de cinasa.
|
CA2548326A1
(en)
|
2003-12-23 |
2005-07-14 |
Novartis Ag |
Bicyclic heterocyclic p-38 kinase inhibitors
|
US20050239809A1
(en)
|
2004-01-08 |
2005-10-27 |
Watts Stephanie W |
Methods for treating and preventing hypertension and hypertension-related disorders
|
CA2553724A1
(en)
|
2004-02-03 |
2005-08-18 |
Abbott Laboratories |
Aminobenzoxazoles as therapeutic agents
|
BRPI0507629A
(pt)
|
2004-02-13 |
2007-07-03 |
Banyu Pharma Co Ltd |
composto, antagonista do receptor e agonista inverso do receptor da histamina h3, agente profilático ou terapêutico para uma doença metabólica, uma doença circulatória ou uma doença do sistema nervoso, ou um seu sal farmaceuticamente aceitável
|
US20050187418A1
(en)
|
2004-02-19 |
2005-08-25 |
Small Brooke L. |
Olefin oligomerization
|
JP2007523202A
(ja)
|
2004-02-24 |
2007-08-16 |
ビオアクソン・テラプティーク・インコーポレーテッド |
4置換ピペリジン誘導体
|
AU2005219525B2
(en)
|
2004-02-27 |
2011-08-18 |
F. Hoffmann-La Roche Ag |
Fused derivatives of pyrazole
|
KR100844864B1
(ko)
|
2004-02-27 |
2008-07-09 |
에프. 호프만-라 로슈 아게 |
헤테로아릴-융합 피라졸로 유도체
|
US20070293489A1
(en)
|
2004-04-02 |
2007-12-20 |
Jerry Adams |
Substituted Pyrazolopyrimidines
|
DK1740591T3
(da)
|
2004-04-02 |
2009-10-26 |
Osi Pharm Inc |
Heterobicykliske proteinkinaseinhibitorer substitueret med en 6,6-biocyclisk ring
|
US9212149B2
(en)
|
2004-04-30 |
2015-12-15 |
Takeda Pharmaceutical Company Limited |
Substituted 2-amidoquinazol-4-ones as matrix metalloproteinase-13 inhibitors
|
DE102004022897A1
(de)
|
2004-05-10 |
2005-12-08 |
Bayer Cropscience Ag |
Azinyl-imidazoazine
|
PL3153514T3
(pl)
|
2004-05-13 |
2022-01-10 |
Icos Corporation |
Chinazolinony jako inhibitory ludzkiej 3-kinazy fosfatydyloinozytolowej delta
|
EP1750714A1
(en)
|
2004-05-13 |
2007-02-14 |
Vanderbilt University |
Phosphoinositide 3-kinase delta selective inhibitors for inhibiting angiogenesis
|
EP1755609A1
(en)
|
2004-05-25 |
2007-02-28 |
Icos Corporation |
Methods for treating and/or preventing aberrant proliferation of hematopoietic cells
|
EP1750715A1
(en)
|
2004-06-04 |
2007-02-14 |
Icos Corporation |
Methods for treating mast cell disorders
|
GB0420722D0
(en)
|
2004-09-17 |
2004-10-20 |
Addex Pharmaceuticals Sa |
Novel allosteric modulators
|
WO2006038865A1
(en)
|
2004-10-01 |
2006-04-13 |
Betagenon Ab |
Nucleotide derivatives for the treatment of type 2 diabetes and other disorders
|
US7608594B2
(en)
|
2004-11-03 |
2009-10-27 |
University Of Kansas |
Novobiocin analogues as anticancer agents
|
US8212011B2
(en)
|
2004-11-03 |
2012-07-03 |
University Of Kansas |
Novobiocin analogues
|
US8212012B2
(en)
|
2004-11-03 |
2012-07-03 |
University Of Kansas |
Novobiocin analogues having modified sugar moieties
|
US7622451B2
(en)
|
2004-11-03 |
2009-11-24 |
University Of Kansas |
Novobiocin analogues as neuroprotective agents and in the treatment of autoimmune disorders
|
GB0425035D0
(en)
|
2004-11-12 |
2004-12-15 |
Novartis Ag |
Organic compounds
|
US9512125B2
(en)
|
2004-11-19 |
2016-12-06 |
The Regents Of The University Of California |
Substituted pyrazolo[3.4-D] pyrimidines as anti-inflammatory agents
|
CA2588607A1
(en)
|
2004-11-23 |
2006-06-01 |
Ptc Therapeutics, Inc. |
Carbazole, carboline and indole derivatives useful in the inhibition of vegf production
|
AR054321A1
(es)
|
2005-01-10 |
2007-06-20 |
Bristol Myers Squibb Co |
Derivados en fenilglicinamida utiles como anticoagulantes
|
US20060156485A1
(en)
|
2005-01-14 |
2006-07-20 |
The Procter & Gamble Company |
Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
|
PE20061119A1
(es)
|
2005-01-19 |
2006-11-27 |
Aventis Pharma Sa |
PIRAZOLO PIRIDINAS SUSTITUIDAS COMO INHIBIDORES DE CINASAS FAK, KDR Y Tie
|
GB0501999D0
(en)
|
2005-02-01 |
2005-03-09 |
Sentinel Oncology Ltd |
Pharmaceutical compounds
|
WO2006089106A2
(en)
|
2005-02-17 |
2006-08-24 |
Icos Corporation |
Phosphoinositide 3-kinase inhibitors for inhibiting leukocyte accumulation
|
US7579348B2
(en)
|
2005-02-25 |
2009-08-25 |
Pgxhealth, Llc |
Derivatives of 8-substituted xanthines
|
US20090124654A1
(en)
|
2005-03-01 |
2009-05-14 |
Mjalli Adnan M M |
Aryl and Heteroaryl Compounds, Compositions, Methods of Use
|
KR100926399B1
(ko)
|
2005-04-06 |
2009-11-12 |
아이알엠 엘엘씨 |
디아릴아민―함유 화합물 및 조성물, 및 스테로이드 호르몬핵 수용체의 조절제로서의 그들의 용도
|
KR100781704B1
(ko)
|
2005-04-20 |
2007-12-03 |
에스케이케미칼주식회사 |
피리딘 유도체와 이의 제조방법, 및 이를 포함하는약제조성물
|
US7470799B2
(en)
|
2005-04-22 |
2008-12-30 |
Wyeth |
Dihydrobenzofuran derivatives and uses thereof
|
EP1879657A2
(en)
|
2005-04-25 |
2008-01-23 |
Institute Of Organic Chemistry And Biochemistry Of The Academy Of Sciences Of The Czech Republic |
Use of compounds to enhance processivity of telomerase
|
CA2605738C
(en)
|
2005-04-25 |
2013-10-01 |
Merck Patent Gesellschaft Mit Beschraenkter Haftung |
Novel azaheterocyclic compounds as kinase inhibitors
|
MX2007015917A
(es)
|
2005-06-22 |
2008-03-10 |
Chemocentryx Inc |
Compuestos de azaindazol y metodos de uso.
|
DE602006015658D1
(de)
|
2005-06-27 |
2010-09-02 |
Amgen Inc |
Entzündungshemmende arylnitrilverbindungen
|
BRPI0615522A2
(pt)
|
2005-07-11 |
2012-04-10 |
Devgen Nv |
derivados da amida como inibidores da quinase
|
US20100168102A9
(en)
|
2005-07-11 |
2010-07-01 |
Devgen Nv |
Amide Derivatives as Kinase Inhibitors
|
GB0516723D0
(en)
|
2005-08-15 |
2005-09-21 |
Novartis Ag |
Organic compounds
|
KR101011957B1
(ko)
|
2005-08-25 |
2011-01-31 |
에프. 호프만-라 로슈 아게 |
P38 mαp 키나아제 저해제 및 이의 사용 방법
|
US20070049591A1
(en)
|
2005-08-25 |
2007-03-01 |
Kalypsys, Inc. |
Inhibitors of MAPK/Erk Kinase
|
BRPI0615272A2
(pt)
|
2005-08-25 |
2009-08-04 |
Hoffmann La Roche |
inibidores de p38 map kinase e métodos para uso dos mesmos
|
EP1919873A1
(de)
|
2005-09-01 |
2008-05-14 |
BioAgency AG |
Fredericamycin-derivate
|
TW200800887A
(en)
|
2005-09-29 |
2008-01-01 |
Wyeth Corp |
Phenylaminopropanol derivatives and methods of their use
|
PT1951724E
(pt)
|
2005-11-17 |
2011-08-02 |
Osi Pharm Inc |
Inibidores mtor fundidos bicíclicos
|
EP1954276A2
(en)
|
2005-11-22 |
2008-08-13 |
Merck & Co., Inc. |
Indole orexin receptor antagonists
|
AR057960A1
(es)
|
2005-12-02 |
2007-12-26 |
Osi Pharm Inc |
Inhibidores de proteina quinasa biciclicos
|
US20080299113A1
(en)
|
2005-12-19 |
2008-12-04 |
Arnold Lee D |
Combined treatment with and composition of 6,6-bicyclic ring substituted heterobicyclic protein kinase inhibitor and anti-cancer agents
|
JP5512975B2
(ja)
|
2005-12-29 |
2014-06-04 |
アッヴィ・インコーポレイテッド |
タンパク質キナーゼ阻害薬
|
JP5156644B2
(ja)
|
2006-01-25 |
2013-03-06 |
オーエスアイ・フアーマシユーテイカルズ・エル・エル・シー |
不飽和mTOR阻害剤
|
US20080058521A1
(en)
|
2006-01-26 |
2008-03-06 |
Wyeth |
Processes for the preparation of compounds
|
CA2641254A1
(en)
|
2006-02-14 |
2007-08-23 |
Vertex Pharmaceuticals Incorporated |
Pyrrolo(3,2-c) pyridines useful as inhibitors of protein kinases
|
JP2009529047A
(ja)
|
2006-03-07 |
2009-08-13 |
アレイ バイオファーマ、インコーポレイテッド |
ヘテロ二環系ピラゾール化合物およびその使用
|
US7651687B2
(en)
*
|
2006-03-13 |
2010-01-26 |
Osi Pharmaceuticals, Inc. |
Combined treatment with an EGFR kinase inhibitor and an agent that sensitizes tumor cells to the effects of EGFR kinase inhibitors
|
DK2004683T3
(en)
|
2006-03-24 |
2016-08-22 |
Biogen Hemophilia Inc |
PC5 AS A FACTOR IX PROPEPTID PROCESSING ENZYM
|
EP2007373A4
(en)
|
2006-03-29 |
2012-12-19 |
Foldrx Pharmaceuticals Inc |
INHIBITION OF ALPHA SYNUCLEINE TOXICITY
|
EP2557080A1
(en)
*
|
2006-04-04 |
2013-02-13 |
The Regents of The University of California |
Method for identifying pI3-kinase antagonists
|
WO2007121453A2
(en)
|
2006-04-17 |
2007-10-25 |
The Regents Of The University Of California |
2-hydroxy-1-oxo 1,2 dihydro isoquinoline chelating agents
|
GB0607948D0
(en)
|
2006-04-21 |
2006-05-31 |
Novartis Ag |
Organic compounds
|
US8258141B2
(en)
|
2006-04-21 |
2012-09-04 |
Novartis Ag |
Organic compounds
|
US7635023B2
(en)
|
2006-04-21 |
2009-12-22 |
Shell Oil Company |
Time sequenced heating of multiple layers in a hydrocarbon containing formation
|
GB0607950D0
(en)
|
2006-04-21 |
2006-05-31 |
Novartis Ag |
Organic compounds
|
US20090082370A1
(en)
|
2006-04-25 |
2009-03-26 |
Neil Thomas Thompson |
Pharmaceutical Combinations of PK Inhibitors and Other Active Agents
|
WO2007125315A2
(en)
|
2006-04-25 |
2007-11-08 |
Astex Therapeutics Limited |
Pharmaceutical compounds
|
DE102006020327A1
(de)
|
2006-04-27 |
2007-12-27 |
Bayer Healthcare Ag |
Heterocyclisch substituierte, anellierte Pyrazol-Derivate und ihre Verwendung
|
EP2029593A1
(en)
|
2006-05-22 |
2009-03-04 |
AstraZeneca AB |
Indole derivatives
|
US20080003254A1
(en)
|
2006-05-23 |
2008-01-03 |
Abbott Laboratories |
Systems and methods for delivering a rapamycin analog that do not inhibit human coronary artery endothelial cell migration
|
GB0610242D0
(en)
|
2006-05-23 |
2006-07-05 |
Novartis Ag |
Organic compounds
|
GB0610317D0
(en)
|
2006-05-24 |
2006-07-05 |
Medical Res Council |
Antiparasitic compounds and compositions
|
AU2007275682B2
(en)
|
2006-07-20 |
2012-05-17 |
Amgen Inc. |
Substituted pyridone compounds and methods of use
|
CA2657200A1
(en)
|
2006-07-28 |
2008-01-31 |
Novartis Ag |
2,4-substituted quinazolines as lipid kinase inhibitors
|
EP2589597B1
(en)
|
2006-08-22 |
2019-03-06 |
Technion Research & Development Foundation |
Heterocyclic derivatives binding to the peripheral-type benzodiazepine receptor (PBR)
|
US7678803B2
(en)
|
2006-08-24 |
2010-03-16 |
Serenex, Inc. |
Quinazoline derivatives for the treatment of cancer
|
WO2008025755A1
(de)
|
2006-09-01 |
2008-03-06 |
Basf Se |
Verwendung von n-haltigen heterozyklen in dermokosmetika
|
WO2008028168A2
(en)
|
2006-09-01 |
2008-03-06 |
Cylene Pharmaceuticals, Inc. |
Serine-threonine protein kinase and parp modulators
|
EP1903044A1
(en)
|
2006-09-14 |
2008-03-26 |
Novartis AG |
Adenosine Derivatives as A2A Receptor Agonists
|
EP1900729A1
(en)
|
2006-09-15 |
2008-03-19 |
Novartis AG |
Benzoxazoles and oxazolopyridines being useful as Janus kinases inhibitors
|
US20090286779A1
(en)
|
2006-09-29 |
2009-11-19 |
Novartis Ag |
Pyrazolopyrimidines as lipid kinase inhibitors
|
EP2298772A1
(en)
|
2006-10-18 |
2011-03-23 |
Takeda Pharmaceutical Company Limited |
Fused heterocyclic compounds
|
US7772180B2
(en)
|
2006-11-09 |
2010-08-10 |
Bristol-Myers Squibb Company |
Hepatitis C virus inhibitors
|
CN101605797A
(zh)
|
2006-11-13 |
2009-12-16 |
伊莱利利公司 |
治疗炎症疾病和癌症的噻吩并嘧啶酮
|
WO2008063625A2
(en)
|
2006-11-20 |
2008-05-29 |
Adolor Corporation |
Pyridine compounds and methods of their use
|
CN101611007A
(zh)
|
2006-12-20 |
2009-12-23 |
先灵公司 |
新颖的jnk抑制剂
|
CN101600711A
(zh)
|
2006-12-22 |
2009-12-09 |
工业研究有限公司 |
核苷酶和磷酸化酶抑制剂的氮杂环丁烷类似物
|
WO2008083070A1
(en)
|
2006-12-29 |
2008-07-10 |
Neurogen Corporation |
Crf1 receptor ligands comprising fused bicyclic heteroaryl moieties
|
CN101622001A
(zh)
|
2007-01-26 |
2010-01-06 |
Irm责任有限公司 |
作为激酶抑制剂用于治疗疟原虫相关疾病的嘌呤化合物和组合物
|
WO2008112715A2
(en)
|
2007-03-12 |
2008-09-18 |
Vm Discovery Inc. |
Novel agents of calcium ion channel modulators
|
BRPI0809141A2
(pt)
|
2007-03-23 |
2014-08-26 |
Amgen Inc |
Composto, fabricação de um medicamento, e, composição farmacêutica
|
CA2680853C
(en)
|
2007-03-23 |
2012-07-17 |
Amgen Inc. |
3- substituted quinoline or quinoxaline derivatives and their use as phosphatidylinositol 3-kinase (pi3k) inhibitors
|
WO2008118454A2
(en)
|
2007-03-23 |
2008-10-02 |
Amgen Inc. |
Derivatives of quinoline or benzopyrazine and their uses for the treatment of (inter alia) inflammatory diseases, autoimmune diseases or various kinds of cancer
|
US7867983B2
(en)
|
2007-03-29 |
2011-01-11 |
The University Of Connecticut |
Methods to protect skeletal muscle against injury
|
CN101636397B
(zh)
|
2007-04-13 |
2012-06-13 |
中国人民解放军军事医学科学院毒物药物研究所 |
脲类化合物、其制备方法及其医药用途
|
MX2009010536A
(es)
|
2007-04-13 |
2009-10-22 |
Sanofi Aventis |
Una sintesis de n-aminoindoles catalizada por un metal de transicion.
|
JP2010163361A
(ja)
|
2007-04-27 |
2010-07-29 |
Dainippon Sumitomo Pharma Co Ltd |
キノリン誘導体
|
US7960353B2
(en)
|
2007-05-10 |
2011-06-14 |
University Of Kansas |
Novobiocin analogues as neuroprotective agents and in the treatment of autoimmune disorders
|
US20090214529A9
(en)
|
2007-05-22 |
2009-08-27 |
Taigen Biotechnology Co., Ltd. |
Kinesin inhibitors
|
US9603848B2
(en)
|
2007-06-08 |
2017-03-28 |
Senomyx, Inc. |
Modulation of chemosensory receptors and ligands associated therewith
|
US7928111B2
(en)
|
2007-06-08 |
2011-04-19 |
Senomyx, Inc. |
Compounds including substituted thienopyrimidinone derivatives as ligands for modulating chemosensory receptors
|
ATE538120T1
(de)
|
2007-06-26 |
2012-01-15 |
Sanofi Sa |
Regioselektive, metallkatalysierte synthese annelierter benzimidazole und azabenzimidazole
|
US8685962B2
(en)
|
2007-07-02 |
2014-04-01 |
Technion Research & Development Foundation Limited |
Compositions, articles and methods comprising TSPO ligands for preventing or reducing tobacco-associated damage
|
RU2345996C1
(ru)
|
2007-07-17 |
2009-02-10 |
Андрей Александрович Иващенко |
Аннелированные азагетероциклические амиды, включающие пиримидиновый фрагмент, способ их получения и применения
|
EP2190466A4
(en)
|
2007-08-10 |
2011-12-21 |
Burnham Inst Medical Research |
Tissue-specific alkaline phosphatase (TNAP) activators and their use
|
CA2695583A1
(en)
|
2007-08-13 |
2009-02-19 |
Metabasis Therapeutics, Inc. |
Novel activators of glucokinase
|
AU2008288390A1
(en)
|
2007-08-14 |
2009-02-19 |
Bayer Schering Pharma Aktiengesellschaft |
Fused imidazoles for cancer treatment
|
WO2009044707A1
(ja)
|
2007-10-03 |
2009-04-09 |
Riken |
ニトロトリアゾール誘導体、およびそれを用いる化合物の製造方法
|
WO2009046448A1
(en)
|
2007-10-04 |
2009-04-09 |
Intellikine, Inc. |
Chemical entities and therapeutic uses thereof
|
CN101896180A
(zh)
|
2007-10-15 |
2010-11-24 |
阿斯利康(瑞典)有限公司 |
组合059
|
JP5256693B2
(ja)
|
2007-10-31 |
2013-08-07 |
信越化学工業株式会社 |
酸化チタン系光触媒薄膜の製造法
|
WO2009059304A2
(en)
|
2007-11-02 |
2009-05-07 |
Taiga Biotechnologies, Inc. |
Compounds for treating abnormal cellular proliferation
|
EA201070611A1
(ru)
|
2007-11-13 |
2010-12-30 |
Айкос Корпорейшн |
Ингибиторы человеческой фосфатидилинозитол-3-киназы дельта
|
AU2008338963A1
(en)
|
2007-12-13 |
2009-06-25 |
Sri International |
PPAR-delta ligands and methods of their use
|
US7960397B2
(en)
|
2007-12-28 |
2011-06-14 |
Institute Of Experimental Botany, Academy Of Sciences Of The Czech Republic |
6,9-disubstituted purine derivatives and their use as cosmetics and cosmetic compositions
|
MX2010007418A
(es)
|
2008-01-04 |
2010-11-12 |
Intellikine Inc |
Ciertas entidades quimicas, composiciones y metodos.
|
US8193182B2
(en)
|
2008-01-04 |
2012-06-05 |
Intellikine, Inc. |
Substituted isoquinolin-1(2H)-ones, and methods of use thereof
|
CA2711495A1
(en)
|
2008-01-09 |
2009-07-16 |
Pgxhealth Llc |
Intrathecal treatment of neuropathic pain with a2ar agonists
|
WO2009100406A2
(en)
|
2008-02-07 |
2009-08-13 |
Synta Pharmaceuticals Corp. |
Topical formulations for the treatment of psoriasis
|
EP2259790A1
(en)
|
2008-02-07 |
2010-12-15 |
Gilead Palo Alto, Inc. |
Abca-1 elevating compounds and the use thereof
|
TWI444384B
(zh)
|
2008-02-20 |
2014-07-11 |
Gilead Sciences Inc |
核苷酸類似物及其在治療惡性腫瘤上的用途
|
JP5547099B2
(ja)
*
|
2008-03-14 |
2014-07-09 |
インテリカイン, エルエルシー |
キナーゼ阻害剤および使用方法
|
WO2009114874A2
(en)
*
|
2008-03-14 |
2009-09-17 |
Intellikine, Inc. |
Benzothiazole kinase inhibitors and methods of use
|
CA2716856C
(en)
|
2008-03-20 |
2013-02-19 |
Amgen Inc. |
Aurora kinase modulators and method of use
|
US20090312406A1
(en)
|
2008-06-12 |
2009-12-17 |
Hsing-Pang Hsieh |
Coumarin compounds and their use for treating viral infection
|
WO2010006072A2
(en)
|
2008-07-08 |
2010-01-14 |
The Regents Of The University Of California |
Mtor modulators and uses thereof
|
JP2011528368A
(ja)
|
2008-07-16 |
2011-11-17 |
シェーリング コーポレイション |
二環式ヘテロ環誘導体およびgpcrモジュレーターとしてのその使用
|
US8450344B2
(en)
|
2008-07-25 |
2013-05-28 |
Aerie Pharmaceuticals, Inc. |
Beta- and gamma-amino-isoquinoline amide compounds and substituted benzamide compounds
|
AU2009282480B2
(en)
|
2008-08-11 |
2015-05-07 |
Children's Medical Center Corporation |
Halofuginone analogs for inhibition of tRNA synthetases and uses thereof
|
CA2738313A1
(en)
|
2008-09-23 |
2010-04-08 |
Georgetown University |
Viral and fungal inhibitors
|
JP5731978B2
(ja)
|
2008-09-26 |
2015-06-10 |
インテリカイン, エルエルシー |
複素環キナーゼ阻害剤
|
US8476282B2
(en)
|
2008-11-03 |
2013-07-02 |
Intellikine Llc |
Benzoxazole kinase inhibitors and methods of use
|
US20110269779A1
(en)
|
2008-11-18 |
2011-11-03 |
Intellikine, Inc. |
Methods and compositions for treatment of ophthalmic conditions
|
CN102282147B
(zh)
|
2009-01-28 |
2015-09-30 |
卡拉治疗学股份有限公司 |
二环吡唑并-杂环
|
US20120189641A1
(en)
|
2009-02-25 |
2012-07-26 |
OSI Pharmaceuticals, LLC |
Combination anti-cancer therapy
|
WO2010118367A2
(en)
|
2009-04-10 |
2010-10-14 |
Progenics Pharmaceuticals, Inc. |
Antiviral pyrimidines
|
JP5789252B2
(ja)
*
|
2009-05-07 |
2015-10-07 |
インテリカイン, エルエルシー |
複素環式化合物およびその使用
|
CN101602768B
(zh)
|
2009-07-17 |
2012-05-30 |
河南省农科院农副产品加工研究所 |
一种芝麻素和芝麻林素的提纯方法
|
AR085397A1
(es)
|
2011-02-23 |
2013-09-25 |
Intellikine Inc |
Combinacion de inhibidores de quinasa y sus usos
|