US2003199A
(en)
|
1930-05-31 |
1935-05-28 |
Johnson Frank James |
Automatic coal stoker
|
US2003149A
(en)
|
1931-05-22 |
1935-05-28 |
Autographic Register Co |
Manifolding
|
US2003065A
(en)
|
1931-06-20 |
1935-05-28 |
John R Ditmars |
Composition for coating sheets, fibrous stocks, and the like
|
US2004102A
(en)
|
1932-02-24 |
1935-06-11 |
Daniel A Dickey |
Hollow steel propeller construction
|
US2004138A
(en)
|
1932-11-30 |
1935-06-11 |
Byers A M Co |
Method of making wrought iron pipe
|
US2002165A
(en)
|
1933-07-08 |
1935-05-21 |
Charles A Winslow |
Air cleaner
|
US2003187A
(en)
|
1933-10-02 |
1935-05-28 |
Frederick H Shaw |
Automobile radio device
|
US2003166A
(en)
|
1933-10-26 |
1935-05-28 |
Zancan Ottavio |
Front drive for motor cars
|
US2001051A
(en)
|
1933-12-01 |
1935-05-14 |
Angelina Mariani |
Tamperproof meter box with cutout control and fuse drawer for electric meters
|
US2004092A
(en)
|
1933-12-15 |
1935-06-11 |
John L Chaney |
Device for indicating the temperature of liquids
|
US2003060A
(en)
|
1934-04-02 |
1935-05-28 |
Ernest L Heckert |
Thermostatic controlling device
|
US2667486A
(en)
|
1951-05-24 |
1954-01-26 |
Research Corp |
2,4-diamino pteridine and derivatives
|
IL44058A
(en)
|
1973-02-02 |
1978-10-31 |
Ciba Geigy Ag |
3amino-1,2,4-benzotriazine 1,4-di-noxide derivatives, their preparation and compositions for the control of microorganisms containing them
|
AU535258B2
(en)
|
1979-08-31 |
1984-03-08 |
Ici Australia Limited |
Benzotriazines
|
DE3205638A1
(de)
|
1982-02-17 |
1983-08-25 |
Hoechst Ag, 6230 Frankfurt |
Trisubstituierte pyrimidin-5-carbonsaeuren und deren derivate, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
|
US4490289A
(en)
|
1982-09-16 |
1984-12-25 |
Hoffmann-La Roche Inc. |
Homogeneous human interleukin 2
|
US5616584A
(en)
|
1986-09-25 |
1997-04-01 |
Sri International |
1,2,4-benzotriazine oxides as radiosensitizers and selective cytotoxic agents
|
JP2598100B2
(ja)
|
1988-08-31 |
1997-04-09 |
キヤノン株式会社 |
電子写真感光体
|
US5214059A
(en)
|
1989-07-03 |
1993-05-25 |
Hoechst-Roussel Pharmaceuticals Incorporated |
2-(aminoaryl) indoles and indolines as topical antiinflammatory agents for the treatment of skin disorders
|
US5776502A
(en)
|
1989-07-18 |
1998-07-07 |
Oncogene Science, Inc. |
Methods of transcriptionally modulating gene expression
|
US5665543A
(en)
|
1989-07-18 |
1997-09-09 |
Oncogene Science, Inc. |
Method of discovering chemicals capable of functioning as gene expression modulators
|
US5041430A
(en)
*
|
1989-09-18 |
1991-08-20 |
Du Pont Mereck Pharmaceutical Company |
Oral anticoagulant/platelet inhibitor low dose formulation
|
JPH03127790A
(ja)
|
1989-10-11 |
1991-05-30 |
Morishita Pharmaceut Co Ltd |
N―(1h―テトラゾール―5―イル)―2―アニリノ―5―ピリミジンカルボキシアミド類及びその合成中間体
|
GB9003553D0
(en)
|
1990-02-16 |
1990-04-11 |
Ici Plc |
Herbicidal compositions
|
JP2839106B2
(ja)
|
1990-02-19 |
1998-12-16 |
キヤノン株式会社 |
電子写真感光体
|
GB9012592D0
(en)
|
1990-06-06 |
1990-07-25 |
Smithkline Beecham Intercredit |
Compounds
|
FR2665159B1
(fr)
|
1990-07-24 |
1992-11-13 |
Rhone Poulenc Sante |
Nouveaux derives de la pyridine et de la quinoleine, leur preparation et les compositions pharmaceutiques qui les contiennent.
|
IE74711B1
(en)
|
1990-07-27 |
1997-07-30 |
Ici Plc |
Fungicides
|
GB9016800D0
(en)
|
1990-07-31 |
1990-09-12 |
Shell Int Research |
Tetrahydropyrimidine derivatives
|
DE4025891A1
(de)
|
1990-08-16 |
1992-02-20 |
Bayer Ag |
Pyrimidyl-substituierte acrylsaeureester
|
JPH05345780A
(ja)
|
1991-12-24 |
1993-12-27 |
Kumiai Chem Ind Co Ltd |
ピリミジンまたはトリアジン誘導体及び除草剤
|
HUT63941A
(en)
|
1992-05-15 |
1993-11-29 |
Hoechst Ag |
Process for producing 4-alkyl-substituted pyrimidine-5-carboxanilide derivatives, and fungicidal compositions comprising same
|
US5438130A
(en)
|
1993-01-15 |
1995-08-01 |
Cambridge Neuroscience, Inc. |
Fucosylated guanosine disulfates as excitatory amino acid antagonists
|
JPH0741461A
(ja)
|
1993-05-27 |
1995-02-10 |
Eisai Co Ltd |
スルホン酸エステル誘導体
|
JPH0782183A
(ja)
|
1993-09-09 |
1995-03-28 |
Canon Inc |
液晶中間体化合物、液晶性化合物、高分子液晶化合物、高分子液晶共重合体化合物、それらの組成物、液晶素子および記録装置
|
DE4338704A1
(de)
|
1993-11-12 |
1995-05-18 |
Hoechst Ag |
Stabilisierte Oligonucleotide und deren Verwendung
|
US5530000A
(en)
|
1993-12-22 |
1996-06-25 |
Ortho Pharmaceutical Corporation |
Substituted pyrimidinylaminothiazole derivatives useful as platelet aggreggation inhibitors
|
GB9506466D0
(en)
|
1994-08-26 |
1995-05-17 |
Prolifix Ltd |
Cell cycle regulated repressor and dna element
|
US5597826A
(en)
|
1994-09-14 |
1997-01-28 |
Pfizer Inc. |
Compositions containing sertraline and a 5-HT1D receptor agonist or antagonist
|
DE19502912A1
(de)
|
1995-01-31 |
1996-08-01 |
Hoechst Ag |
G-Cap Stabilisierte Oligonucleotide
|
US6326487B1
(en)
|
1995-06-05 |
2001-12-04 |
Aventis Pharma Deutschland Gmbh |
3 modified oligonucleotide derivatives
|
CA2230894A1
(fr)
|
1995-09-01 |
1997-03-13 |
Signal Pharmaceuticals, Inc. |
Carboxamides de pyrimidine et composes associes, et methodes de traitement d'etats inflammatoires
|
GB9523675D0
(en)
|
1995-11-20 |
1996-01-24 |
Celltech Therapeutics Ltd |
Chemical compounds
|
WO1997024122A1
(fr)
|
1995-12-29 |
1997-07-10 |
Smithkline Beecham Corporation |
Antagonistes du recepteur de vitronectine
|
JPH09274290A
(ja)
|
1996-02-07 |
1997-10-21 |
Fuji Photo Film Co Ltd |
ハロゲン化銀写真感光材料用の現像液および処理方法
|
ATE305781T1
(de)
|
1996-02-23 |
2005-10-15 |
Lilly Co Eli |
Non-peptidische vasopressin via antagonisten
|
DE59707681D1
(de)
|
1996-10-28 |
2002-08-14 |
Rolic Ag Zug |
Vernetzbare, photoaktive Silanderivate
|
AU732703B2
(en)
|
1996-11-20 |
2001-04-26 |
Crucell Holland B.V. |
An improved method for the production and purification of adenoviral vectors
|
JP3734903B2
(ja)
|
1996-11-21 |
2006-01-11 |
富士写真フイルム株式会社 |
現像処理方法
|
JPH10153838A
(ja)
|
1996-11-22 |
1998-06-09 |
Fuji Photo Film Co Ltd |
ハロゲン化銀写真感光材料の処理方法
|
JP3720931B2
(ja)
|
1996-11-26 |
2005-11-30 |
富士写真フイルム株式会社 |
ハロゲン化銀写真感光材料の処理方法
|
NZ336391A
(en)
|
1996-12-04 |
2000-09-29 |
Kimberly Clark Co |
method for making wet strength paper by adding a colourless reactive eanionic compound to the slurry
|
US5935383A
(en)
|
1996-12-04 |
1999-08-10 |
Kimberly-Clark Worldwide, Inc. |
Method for improved wet strength paper
|
ATE236890T1
(de)
|
1996-12-23 |
2003-04-15 |
Bristol Myers Squibb Pharma Co |
Sauerstoff oder schwefel enthaltende 5-gliedrige heteroaromatishe derivative als factor xa hemmer
|
JPH10207019A
(ja)
|
1997-01-22 |
1998-08-07 |
Fuji Photo Film Co Ltd |
ハロゲン化銀写真感光材料の処理方法
|
JPH10213820A
(ja)
|
1997-01-31 |
1998-08-11 |
Canon Inc |
液晶素子及び液晶装置
|
DE59807348D1
(de)
|
1997-02-05 |
2003-04-10 |
Rolic Ag Zug |
Photovernetzbare Silanderivate
|
GB9705361D0
(en)
|
1997-03-14 |
1997-04-30 |
Celltech Therapeutics Ltd |
Chemical compounds
|
JPH10260512A
(ja)
|
1997-03-19 |
1998-09-29 |
Fuji Photo Film Co Ltd |
ハロゲン化銀感光材料の処理方法
|
JPH10310583A
(ja)
|
1997-05-09 |
1998-11-24 |
Mitsubishi Chem Corp |
ピリドンアゾ系化合物、感熱転写用色素およびそれを使用した感熱転写材料
|
US6070126A
(en)
|
1997-06-13 |
2000-05-30 |
William J. Kokolus |
Immunobiologically-active linear peptides and method of identification
|
TW436485B
(en)
|
1997-08-01 |
2001-05-28 |
American Cyanamid Co |
Substituted quinazoline derivatives
|
US6635626B1
(en)
|
1997-08-25 |
2003-10-21 |
Bristol-Myers Squibb Co. |
Imidazoquinoxaline protein tyrosine kinase inhibitors
|
US6022884A
(en)
|
1997-11-07 |
2000-02-08 |
Amgen Inc. |
Substituted pyridine compounds and methods of use
|
WO1999031073A1
(fr)
|
1997-12-15 |
1999-06-24 |
Yamanouchi Pharmaceutical Co., Ltd. |
Nouveaux derives de pyrimidine-5-carboxamide
|
IL136637A0
(en)
|
1997-12-22 |
2001-06-14 |
Du Pont Pharm Co |
Nitrogen containing heteroaromatics with ortho-substituted pi's as factor xa inhibitors
|
NZ506417A
(en)
|
1998-02-17 |
2003-05-30 |
Tularik Inc |
Anti-viral pyrimidine derivatives
|
ATE232521T1
(de)
|
1998-03-27 |
2003-02-15 |
Janssen Pharmaceutica Nv |
Hiv hemmende pyrimidin derivate
|
ES2361146T3
(es)
|
1998-03-27 |
2011-06-14 |
Janssen Pharmaceutica Nv |
Derivados de la piramidina inhibitatoria de vih.
|
US6685938B1
(en)
|
1998-05-29 |
2004-02-03 |
The Scripps Research Institute |
Methods and compositions useful for modulation of angiogenesis and vascular permeability using SRC or Yes tyrosine kinases
|
DE19830181C1
(de)
|
1998-07-06 |
1999-09-30 |
Inter Control Koehler Hermann |
Mehrpolige elektrische Steckverbindung
|
US6136971A
(en)
|
1998-07-17 |
2000-10-24 |
Roche Colorado Corporation |
Preparation of sulfonamides
|
US6378526B1
(en)
|
1998-08-03 |
2002-04-30 |
Insite Vision, Incorporated |
Methods of ophthalmic administration
|
US6288082B1
(en)
|
1998-09-29 |
2001-09-11 |
American Cyanamid Company |
Substituted 3-cyanoquinolines
|
CA2344169C
(fr)
|
1998-09-29 |
2011-07-19 |
American Cyanamid Company |
Inhibiteurs de proteines de type tyrosine kinases a base de 3-cyanoquinolines substituees
|
SI2253620T1
(sl)
|
1998-09-29 |
2014-06-30 |
Wyeth Holdings Llc |
Substituirani 3-cianokinolini kot inhibitorji protein tirozin-kinaz
|
US6297258B1
(en)
|
1998-09-29 |
2001-10-02 |
American Cyanamid Company |
Substituted 3-cyanoquinolines
|
EP1058549A4
(fr)
|
1998-12-23 |
2003-11-12 |
Bristol Myers Squibb Pharma Co |
INHIBITEURS DU FACTEUR Xa OU DE LA THROMBINE
|
GB9828511D0
(en)
|
1998-12-24 |
1999-02-17 |
Zeneca Ltd |
Chemical compounds
|
CA2362401A1
(fr)
|
1999-02-04 |
2000-08-10 |
Paul Fleming |
Composes de fixation au recepteur heptahelicoidal couple a la proteine g et leurs procedes d'utilisation
|
PL215901B1
(pl)
|
1999-04-15 |
2014-02-28 |
Bristol Myers Squibb Co |
Cykliczny inhibitor bialkowych kinaz tyrozynowych, jego zastosowanie oraz kompozycja farmaceutyczna zawierajaca taki zwiazek
|
PL350920A1
(en)
|
1999-04-21 |
2003-02-10 |
American Cyanamid Co |
Substituted 3-cyano-[1.7], [1.5], and [1.8]-naphthyridine inhibitors of tyrosine kinases
|
AU5020400A
(en)
|
1999-05-20 |
2000-12-12 |
E.I. Du Pont De Nemours And Company |
Heteroaryloxypyrimidine insecticides and acaricides
|
US6710221B1
(en)
|
1999-06-15 |
2004-03-23 |
Kimberly-Clark Worldwide, Inc. |
Absorbent articles incorporating color change graphics
|
CA2377771A1
(fr)
|
1999-07-01 |
2001-01-11 |
Ajinomoto Co., Inc. |
Composes heterocycliques et leurs applications en medecine
|
WO2001007027A2
(fr)
|
1999-07-22 |
2001-02-01 |
Vertex Pharmaceuticals Incorporated |
Inhibiteurs d'helicase virale
|
AU6016000A
(en)
|
1999-07-23 |
2001-02-13 |
Shionogi & Co., Ltd. |
Tricyclic compounds and drug compositions containing the same
|
HUP0203575A3
(en)
|
1999-07-23 |
2003-11-28 |
Shionogi & Co |
Pharmaceutical compositions containing th2 differentiation inhibitors and their use
|
DE60031127T2
(de)
|
1999-08-12 |
2007-02-01 |
Wyeth Holdings Corp. |
Nsaid und egfr kinase inhibitoren enthaltende pharmazeutische formulierung zur behandlung oder inhibierung von dickdarmpolypen und kolorektalem krebs
|
US6093838A
(en)
|
1999-08-16 |
2000-07-25 |
Allergan Sales, Inc. |
Amines substituted with a dihydro-benzofuranyl or with a dihydro-isobenzofuranyl group, an aryl or heteroaryl group and an alkyl group, having retinoid-like biological activity
|
US6127382A
(en)
|
1999-08-16 |
2000-10-03 |
Allergan Sales, Inc. |
Amines substituted with a tetrahydroquinolinyl group an aryl or heteroaryl group and an alkyl group, having retinoid-like biological activity
|
KR20020027635A
(ko)
|
1999-09-10 |
2002-04-13 |
폴락 돈나 엘. |
티로신 키나제 억제제
|
GB9922171D0
(en)
|
1999-09-21 |
1999-11-17 |
Zeneca Ltd |
Chemical compounds
|
JP2001089412A
(ja)
|
1999-09-22 |
2001-04-03 |
Otsuka Pharmaceut Co Ltd |
ベンゼン誘導体またはその医薬的に許容される塩
|
US6506769B2
(en)
|
1999-10-06 |
2003-01-14 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Heterocyclic compounds useful as inhibitors of tyrosine kinases
|
US7087597B1
(en)
|
1999-10-12 |
2006-08-08 |
Takeda Pharmaceutical Company Limited |
Pyrimidine 5-carboxamide compounds, process for producing the same and use thereof
|
EP1226123A1
(fr)
|
1999-11-03 |
2002-07-31 |
Du Pont Pharmaceuticals Company |
Composes cyano utiles en tant qu'inhibiteurs du facteur xa
|
GB9929988D0
(en)
|
1999-12-17 |
2000-02-09 |
Celltech Therapeutics Ltd |
Chemical compounds
|
US6638929B2
(en)
|
1999-12-29 |
2003-10-28 |
Wyeth |
Tricyclic protein kinase inhibitors
|
ATE353320T1
(de)
|
1999-12-29 |
2007-02-15 |
Wyeth Corp |
Tricyclische proteinkinasehemmer
|
WO2001055116A2
(fr)
|
2000-01-28 |
2001-08-02 |
Astrazeneca Ab |
Composes chimiques
|
US6153752A
(en)
|
2000-01-28 |
2000-11-28 |
Creanova, Inc. |
Process for preparing heterocycles
|
US20020165244A1
(en)
|
2000-01-31 |
2002-11-07 |
Yuhong Zhou |
Mucin synthesis inhibitors
|
WO2001060816A1
(fr)
|
2000-02-17 |
2001-08-23 |
Amgen Inc. |
Inhibiteurs de kinases
|
CN1221281C
(zh)
|
2000-02-18 |
2005-10-05 |
耶达研究与开发有限公司 |
共聚物1的口服、鼻部和肺部用剂型
|
CZ20023199A3
(cs)
|
2000-02-25 |
2003-05-14 |
F. Hoffmann-La Roche Ag |
Modulátory receptoru adenosinu
|
US7105550B2
(en)
|
2000-03-01 |
2006-09-12 |
Christopher Love |
2,4-disubstituted thiazolyl derivatives
|
GB0004887D0
(en)
|
2000-03-01 |
2000-04-19 |
Astrazeneca Uk Ltd |
Chemical compounds
|
GB0004890D0
(en)
|
2000-03-01 |
2000-04-19 |
Astrazeneca Uk Ltd |
Chemical compounds
|
GB0004888D0
(en)
|
2000-03-01 |
2000-04-19 |
Astrazeneca Uk Ltd |
Chemical compounds
|
US6605615B2
(en)
|
2000-03-01 |
2003-08-12 |
Tularik Inc. |
Hydrazones and analogs as cholesterol lowering agents
|
JP2001247411A
(ja)
|
2000-03-09 |
2001-09-11 |
Tomono Agrica Co Ltd |
有害生物防除剤
|
HUP0300547A2
(hu)
|
2000-03-13 |
2003-07-28 |
American Cyanamid Co. |
Ciano-kinolin vegyületek alkalmazása vastagbél polipok kezelésére és gátlására alkalmas gyógyszerkészítmények előállítására
|
US6613917B1
(en)
|
2000-03-23 |
2003-09-02 |
Allergan, Inc. |
Amines substituted with a dihydronaphthalenyl, chromenyl, or thiochromenyl group, an aryl or heteroaryl group and an alkyl group, having retinoid-like biological activity
|
AR028261A1
(es)
|
2000-03-28 |
2003-04-30 |
Wyeth Corp |
Inhibidores triciclicos de la proteina quinasa
|
US6608048B2
(en)
|
2000-03-28 |
2003-08-19 |
Wyeth Holdings |
Tricyclic protein kinase inhibitors
|
KR20030009416A
(ko)
|
2000-04-04 |
2003-01-29 |
시오노기세이야쿠가부시키가이샤 |
고지용성 약물을 함유하는 유성 조성물
|
WO2001076582A1
(fr)
|
2000-04-05 |
2001-10-18 |
Shionogi & Co., Ltd. |
Micro-emulsions huile dans eau contenant des composes tricycliques ou des preconcentres de ceux-ci
|
US6471968B1
(en)
|
2000-05-12 |
2002-10-29 |
Regents Of The University Of Michigan |
Multifunctional nanodevice platform
|
DE10024622A1
(de)
|
2000-05-18 |
2001-11-22 |
Piesteritz Stickstoff |
N-(2-Pyrimidinyl)(thio)phosphorsäuretriamide, Verfahren zu ihrer Herstellung und deren Verwendung als Mittel zur Regulierung bzw. Hemmung der enzymatischen Harnstoff-Hydrolyse
|
DE60114518T2
(de)
|
2000-07-06 |
2006-08-10 |
Fuji Photo Film Co. Ltd., Minamiashigara |
Flüssigkristallzusammensetzung, die Flüssigkristallmoleküle und Ausrichtungsmittel enthält
|
JP5000068B2
(ja)
|
2000-08-11 |
2012-08-15 |
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用な複素環化合物
|
DE60128709T2
(de)
|
2000-09-15 |
2007-12-27 |
Vertex Pharmaceuticals Inc., Cambridge |
Triazol-verbindungen als protein-kinase-inhibitoren
|
AU2002213467A1
(en)
|
2000-10-11 |
2002-04-22 |
Chemocentryx, Inc. |
Modulation of ccr4 function
|
US7067532B2
(en)
|
2000-11-02 |
2006-06-27 |
Astrazeneca |
Substituted quinolines as antitumor agents
|
EP1337513A1
(fr)
|
2000-11-02 |
2003-08-27 |
AstraZeneca AB |
Quinoleines 4 substitues en position 4 utilisees comme agents antitumoraux
|
CA2430037A1
(fr)
|
2000-11-20 |
2002-05-30 |
Michael S. South |
Aryl-et-heteroaryl-pyridines polycycliques substituees utiles dans l'inhibition selective de la cascade de la coagulation
|
US20070026433A1
(en)
*
|
2001-03-09 |
2007-02-01 |
Hildebrand William H |
Epitope testing using soluble HLA
|
WO2002053160A1
(fr)
|
2000-12-29 |
2002-07-11 |
Alteon, Inc. |
Methode de traitement du glaucome ivb
|
EP1359911A2
(fr)
|
2000-12-29 |
2003-11-12 |
Alteon, Inc. |
Procede de traitement de troubles fibrogenes et autres symptomes de type ivc
|
JP2002221770A
(ja)
|
2001-01-24 |
2002-08-09 |
Fuji Photo Film Co Ltd |
ハロゲン化銀写真感光材料およびその処理方法
|
US20030130264A1
(en)
|
2001-02-16 |
2003-07-10 |
Tularik Inc. |
Methods of using pyrimidine-based antiviral agents
|
EA005974B1
(ru)
|
2001-02-23 |
2005-08-25 |
Мерк Энд Ко., Инк. |
N-замещенные неарильные гетероциклические антагонисты nmda/nr2b
|
AU2002247402A1
(en)
|
2001-03-23 |
2002-10-08 |
Chugai Seiyaku Kabushiki Kaisha |
Flt-1 ligands and their uses in the treatment of diseases regulatable by angiogenesis
|
JP2004535381A
(ja)
|
2001-04-13 |
2004-11-25 |
バーテックス ファーマシューティカルズ インコーポレイテッド |
c−JunN末端キナーゼ(JNK)および他のプロテインキナーゼのインヒビター
|
US20040157866A1
(en)
|
2001-04-30 |
2004-08-12 |
Hisashi Takasugi |
Amide compounds
|
JP2004536057A
(ja)
|
2001-05-11 |
2004-12-02 |
バーテックス ファーマシューティカルズ インコーポレイテッド |
p38インヒビターとして使用する2,5−二置換ピリジン、ピリミジン、ピリダジンおよび1,2,4−トリアジンの誘導体
|
WO2002094766A1
(fr)
|
2001-05-18 |
2002-11-28 |
Nihon Nohyaku Co., Ltd. |
Derive de phtalamide, insecticide agricole et horticole et son utilisation
|
WO2002096903A2
(fr)
|
2001-05-28 |
2002-12-05 |
Aventis Pharma S.A. |
Derives chimiques et leur application comme agent antitelomerase
|
IL159120A0
(en)
|
2001-05-29 |
2004-05-12 |
Schering Ag |
Cdk inhibiting pyrimidines, production thereof and their use as medicaments
|
MXPA03010893A
(es)
|
2001-05-30 |
2004-10-28 |
Univ Leland Stanford Junior |
Sistema de suministro para acidos nucleicos.
|
DE60214703T2
(de)
|
2001-06-01 |
2007-09-13 |
Vertex Pharmaceuticals Inc., Cambridge |
Thiazolverbindungen, die sich als inhibitoren von proteinkinasen eignen
|
ATE337312T1
(de)
|
2001-07-03 |
2006-09-15 |
Vertex Pharma |
Isoxazolyl-pyrimidines als inhibitoren von src- und lck-protein-kinasen
|
US6861529B2
(en)
|
2001-07-06 |
2005-03-01 |
Pfizer Inc |
Cycloalkypyrrole-3-carboxylic acid derivatives and heterocycloalkylpyrrole-3-carboxylic acid derivatives
|
JO3429B1
(ar)
|
2001-08-13 |
2019-10-20 |
Janssen Pharmaceutica Nv |
مشتقات برميدينات مثبطة فيروس الايدز
|
WO2003024448A2
(fr)
|
2001-09-14 |
2003-03-27 |
Methylgene, Inc. |
Inhibiteurs de l'histone-deacetylase
|
WO2003030909A1
(fr)
|
2001-09-25 |
2003-04-17 |
Bayer Pharmaceuticals Corporation |
2- et 4-aminopyrimidines n-substituees par un noyau bicyclique utilisees comme inhibiteurs de kinases dans le traitement du cancer
|
DE10150615A1
(de)
|
2001-10-12 |
2003-04-30 |
Clariant Gmbh |
Verfahren zur metallorganischen Herstellung organischer Zwischenprodukte
|
DE10150610A1
(de)
|
2001-10-12 |
2003-04-30 |
Clariant Gmbh |
Verfahren zur metallorganischen Herstellung organischer Zwischenprodukte über Amidbasen
|
DE10150614A1
(de)
|
2001-10-12 |
2003-04-30 |
Clariant Gmbh |
Verfahren zur metallorganischen Herstellung organischer Zwischenprodukte über Halogen-Metall-Austauschreaktionen
|
EP1453516A2
(fr)
|
2001-10-17 |
2004-09-08 |
Boehringer Ingelheim Pharma GmbH & Co.KG |
Nouvelles pyrimidines substituees, procede permettant de les produire et leur utilisation comme medicament
|
PT1442019E
(pt)
|
2001-11-01 |
2007-12-11 |
Janssen Pharmaceutica Nv |
Derivados de amida como inibidores da glicogénio sintase cinase 3-beta
|
EP1448556A1
(fr)
|
2001-11-01 |
2004-08-25 |
Janssen Pharmaceutica N.V. |
Heteroaryl amines utiles comme inhibiteurs de glycogene synthase kinase 3beta (inhibiteurs de gsk3)
|
RU2309150C2
(ru)
|
2001-11-27 |
2007-10-27 |
Уайт Холдингз Корпорейшн |
3-цианохинолины в качестве ингибиторов egf-r и her2 киназ
|
WO2003045921A1
(fr)
|
2001-11-28 |
2003-06-05 |
Fujisawa Pharmaceutical Co., Ltd. |
Composes d'amide heterocycliques en tant qu'inhibiteurs de l'apolipoproteine b
|
US20030187026A1
(en)
|
2001-12-13 |
2003-10-02 |
Qun Li |
Kinase inhibitors
|
US20030166932A1
(en)
|
2002-01-04 |
2003-09-04 |
Beard Richard L. |
Amines substituted with a dihydronaphthalenyl, chromenyl, or thiochromenyl group, an aryl or heteroaryl group and an alkyl group, having retinoid-like biological activity
|
IL162838A0
(en)
|
2002-01-04 |
2005-11-20 |
Univ Rockefeller |
Compositions and methods for prevention and treatment peptide-of amyloid- related disorders
|
TWI329105B
(en)
|
2002-02-01 |
2010-08-21 |
Rigel Pharmaceuticals Inc |
2,4-pyrimidinediamine compounds and their uses
|
CN1330627C
(zh)
|
2002-02-05 |
2007-08-08 |
惠氏公司 |
N-酰基-2-氨基-4-烷氧基-5-硝基苯甲酸类化合物的合成方法
|
AU2003209077A1
(en)
|
2002-02-08 |
2003-09-02 |
Smithkline Beecham Corporation |
Pyrimidine compounds
|
WO2003074515A1
(fr)
|
2002-03-01 |
2003-09-12 |
Smithkline Beecham Corporation |
Diamino-pyrimidines et leurs utilisations en tant qu'inhibiteurs de l'angiogenese
|
GB0206215D0
(en)
|
2002-03-15 |
2002-05-01 |
Novartis Ag |
Organic compounds
|
WO2003095448A1
(fr)
|
2002-05-06 |
2003-11-20 |
Bayer Pharmaceuticals Corporation |
Derives de pyridinyl amino pyrimidine utilises dans le traitement des troubles de l'hyperproliferation
|
TW200406374A
(en)
|
2002-05-29 |
2004-05-01 |
Novartis Ag |
Diaryl urea derivatives useful for the treatment of protein kinase dependent diseases
|
MY141867A
(en)
|
2002-06-20 |
2010-07-16 |
Vertex Pharma |
Substituted pyrimidines useful as protein kinase inhibitors
|
MXPA04011849A
(es)
|
2002-07-02 |
2005-03-31 |
Kimberly Clark Co |
Composiciones adhesivas elastomericas y laminados.
|
EP1554269A1
(fr)
|
2002-07-09 |
2005-07-20 |
Vertex Pharmaceuticals Incorporated |
Imidazoles, oxazoles et thiazoles presentant des activites d'inhibition des proteines kinases
|
AU2003265336B8
(en)
|
2002-07-29 |
2009-04-23 |
Rigel Pharmaceuticals, Inc. |
Methods of treating or preventing autoimmune diseases with 2,4-pyrimidinediamine compounds
|
EP1525200B1
(fr)
|
2002-08-02 |
2007-10-10 |
AB Science |
2-(3-aminoaryl)amino-4-aryl-thiazoles et leur utilisation en tant que inhibiteurs de c-kit
|
PL375447A1
(en)
|
2002-08-14 |
2005-11-28 |
Vertex Pharmaceuticals Incorporated |
Protein kinase inhibitors and uses thereof
|
UY27939A1
(es)
|
2002-08-21 |
2004-03-31 |
Glaxo Group Ltd |
Compuestos
|
DE10240262A1
(de)
|
2002-08-31 |
2004-03-11 |
Clariant Gmbh |
Verfahren zur metallorganischen Herstellung organischer Zwischenprodukte über Aryllithium-Basen
|
DE10240261A1
(de)
|
2002-08-31 |
2004-03-11 |
Clariant Gmbh |
Verfahren zur metallorganischen Herstellung organischer Zwischenprodukte über Halogen-Metall-Austauschreaktionen
|
EP1549614A4
(fr)
|
2002-10-03 |
2008-04-16 |
Targegen Inc |
Agents vasculo-statiques et procedes d'utilisation de ceux-ci
|
US20050282814A1
(en)
|
2002-10-03 |
2005-12-22 |
Targegen, Inc. |
Vasculostatic agents and methods of use thereof
|
CA2500368A1
(fr)
|
2002-10-04 |
2004-04-22 |
Caritas St. Elizabeth's Medical Center Of Boston, Inc. |
Inhibition de src pour le traitement de blessure par reperfusion associee a la revascularisation
|
WO2004037176A2
(fr)
|
2002-10-21 |
2004-05-06 |
Bristol-Myers Squibb Company |
Quinazolinones et derives de celles-ci comme inhibiteurs du facteur xa
|
WO2004037814A1
(fr)
|
2002-10-25 |
2004-05-06 |
Vertex Pharmaceuticals Incorporated |
Compositions indazolinones utiles en tant qu'inhibiteurs des kinases
|
DE10250708A1
(de)
|
2002-10-31 |
2004-05-19 |
Boehringer Ingelheim Pharma Gmbh & Co. Kg |
Neue Alkin-Verbindungen mit MCH-antagonistischer Wirkung und diese Verbindungen enthaltende Arzneimittel
|
US7452911B2
(en)
|
2002-10-31 |
2008-11-18 |
Boehringer Ingelheim Pharma Gmbh & Co. Kg |
Alkyne compounds with MCH antagonistic activity and medicaments comprising these compounds
|
CA2506773A1
(fr)
|
2002-11-04 |
2004-05-21 |
Vertex Pharmaceuticals Incorporated |
Derives d'heteroaryle pyrimidine utilises comme inhibiteurs de jak (janus kinase)
|
US20050101576A1
(en)
*
|
2003-11-06 |
2005-05-12 |
Novacea, Inc. |
Methods of using vitamin D compounds in the treatment of myelodysplastic syndromes
|
US8034831B2
(en)
|
2002-11-06 |
2011-10-11 |
Celgene Corporation |
Methods for the treatment and management of myeloproliferative diseases using 4-(amino)-2-(2,6-Dioxo(3-piperidyl)-isoindoline-1,3-dione in combination with other therapies
|
AU2003280188A1
(en)
|
2002-12-06 |
2004-06-30 |
Warner-Lambert Company Llc |
Benzoxazin-3-ones and derivatives thereof as inhibitors of pi3k
|
JP3837670B2
(ja)
|
2002-12-12 |
2006-10-25 |
富士通株式会社 |
データ中継装置、連想メモリデバイス、および連想メモリデバイス利用情報検索方法
|
AU2003299600A1
(en)
|
2002-12-20 |
2004-07-29 |
Pharmacia Corpration |
The r-isomer of beta amino acid compounds as integrin receptor antagonists derivatives
|
UA80767C2
(en)
|
2002-12-20 |
2007-10-25 |
Pfizer Prod Inc |
Pyrimidine derivatives for the treatment of abnormal cell growth
|
MXPA05006727A
(es)
|
2002-12-20 |
2005-09-08 |
Pharmacia Corp |
Acidos heteroarilalcanoicos como antagonistas de receptor de integrina.
|
JP2006512387A
(ja)
|
2002-12-24 |
2006-04-13 |
アストラゼネカ アクチボラグ |
化合物
|
US7144911B2
(en)
|
2002-12-31 |
2006-12-05 |
Deciphera Pharmaceuticals Llc |
Anti-inflammatory medicaments
|
AP2065A
(en)
|
2003-02-07 |
2009-11-26 |
Janssen Pharmaceutica Nv |
Pyrimidine derivatives for the prevention of HIV infection
|
CA2513123C
(fr)
|
2003-02-07 |
2013-04-23 |
Janssen Pharmaceutica N.V. |
1,2,4-triazines inhibant le vih
|
CA2515544A1
(fr)
|
2003-02-11 |
2004-08-26 |
Kemia Inc. |
Composes destines au traitement d'une infection virale
|
CL2004000303A1
(es)
|
2003-02-20 |
2005-04-08 |
Tibotec Pharm Ltd |
Compuestos derivados de pirimidinas y triazinas; proceso de preparacion; composicion farmaceutica; y su uso para inhibir la replicacion del vih.
|
GB0305929D0
(en)
|
2003-03-14 |
2003-04-23 |
Novartis Ag |
Organic compounds
|
WO2004091614A2
(fr)
|
2003-04-14 |
2004-10-28 |
Teva Pharmaceutical Industries Ltd. |
Formulations ameliorees de maleate d'amlodipine
|
US20040265375A1
(en)
|
2003-04-16 |
2004-12-30 |
Platteeuw Johannes J. |
Orally disintegrating tablets
|
JP5047613B2
(ja)
|
2003-04-24 |
2012-10-10 |
クーパーヴィジョン インターナショナル ホウルディング カンパニー リミテッド パートナーシップ |
ヒドロゲルコンタクトレンズ及び包装システム及びそれらの製造方法
|
PL1656372T3
(pl)
|
2003-07-30 |
2013-08-30 |
Rigel Pharmaceuticals Inc |
Związki 2,4-pirymidynodiaminy do stosowania w leczeniu lub zapobieganiu chorobom autoimmunologicznym
|
PT2287156E
(pt)
|
2003-08-15 |
2013-08-26 |
Novartis Ag |
2,4-di(fenilamino)-pirimidinas úteis no tratamento de doenças neoplásicas, desordens inflamatórias e do sistema imunitário
|
GB0321710D0
(en)
|
2003-09-16 |
2003-10-15 |
Novartis Ag |
Organic compounds
|
JP2007505858A
(ja)
|
2003-09-18 |
2007-03-15 |
ノバルティス アクチエンゲゼルシャフト |
増殖性障害の処置に有用な2,4−ジ(フェニルアミノ)ピリミジン
|
NZ551027A
(en)
|
2004-04-08 |
2011-01-28 |
Targegen Inc |
Benzotriazine inhibitors of kinases
|
MX2007002208A
(es)
|
2004-08-25 |
2007-05-08 |
Targegen Inc |
Compuestos hetrociclicos y metodos de uso.
|
US7210697B2
(en)
|
2004-12-16 |
2007-05-01 |
Tricam International, Inc. |
Convertible handle
|
ATE519759T1
(de)
|
2004-12-30 |
2011-08-15 |
Exelixis Inc |
Pyrimidinderivate als kinasemodulatoren und anwendungsverfahren
|
GT200600008A
(es)
*
|
2005-01-18 |
2006-08-09 |
|
Formulacion de compresion directa y proceso
|
GB0501999D0
(en)
|
2005-02-01 |
2005-03-09 |
Sentinel Oncology Ltd |
Pharmaceutical compounds
|
US20060247250A1
(en)
|
2005-03-16 |
2006-11-02 |
Targegen, Inc. |
Pyrimidine inhibitors of kinases
|
US20070032493A1
(en)
|
2005-05-26 |
2007-02-08 |
Synta Pharmaceuticals Corp. |
Method for treating B cell regulated autoimmune disorders
|
WO2006128129A2
(fr)
|
2005-05-26 |
2006-11-30 |
Synta Pharmaceuticals Corp. |
Traitement anticancereux
|
CN105348203B
(zh)
|
2005-06-08 |
2018-09-18 |
里格尔药品股份有限公司 |
抑制jak途径的组合物和方法
|
NZ563984A
(en)
|
2005-06-08 |
2011-11-25 |
Targegen Inc |
Methods and compositions for the treatment of ocular disorders
|
WO2006137658A1
(fr)
|
2005-06-20 |
2006-12-28 |
Dongbu Hitek Co., Ltd. |
Nouveaux derives thiazole 1,3 substitues ou sels pharmaceutiquement acceptables de ces derniers presentant une activite d'inhibition de l'immunosuppression ou de l'inflammation, composes intermediaires ou sels pharmaceutiquement acceptables de ces derniers, procede de preparation de ces derniers et compositions pharmaceutiq
|
JP2009500317A
(ja)
|
2005-06-29 |
2009-01-08 |
パナセア バイオテック リミテッド |
放出特性改良医薬組成物およびその製造方法
|
WO2007008541A2
(fr)
|
2005-07-08 |
2007-01-18 |
Kalypsys, Inc. |
Modificateurs d'absorption de cholesterol cellulaire
|
US7754717B2
(en)
|
2005-08-15 |
2010-07-13 |
Amgen Inc. |
Bis-aryl amide compounds and methods of use
|
US20070149506A1
(en)
|
2005-09-22 |
2007-06-28 |
Arvanitis Argyrios G |
Azepine inhibitors of Janus kinases
|
US20070072682A1
(en)
|
2005-09-29 |
2007-03-29 |
Crawford James T Iii |
Head to head electronic poker game assembly and method of operation
|
HUE028987T2
(en)
|
2005-11-01 |
2017-01-30 |
Targegen Inc |
BI-aryl-meta-pyrimidine inhibitors of kinases
|
US8133900B2
(en)
*
|
2005-11-01 |
2012-03-13 |
Targegen, Inc. |
Use of bi-aryl meta-pyrimidine inhibitors of kinases
|
US8604042B2
(en)
|
2005-11-01 |
2013-12-10 |
Targegen, Inc. |
Bi-aryl meta-pyrimidine inhibitors of kinases
|
UA99899C2
(ru)
*
|
2005-11-01 |
2012-10-25 |
Таргеджен, Инк. |
Биарил-мета-пиримидиновые ингибиторы киназ
|
WO2007056075A2
(fr)
|
2005-11-02 |
2007-05-18 |
Targegen, Inc. |
Inhibiteurs heteroaromatiques a six chainons diriges contre des mutations de kinases resistantes
|
JP2009519218A
(ja)
|
2005-11-03 |
2009-05-14 |
エスジーエックス ファーマシューティカルズ、インコーポレイテッド |
ピリミジニル−チオフェンキナーゼモジュレータ
|
US8772346B2
(en)
|
2005-11-09 |
2014-07-08 |
Torrent Pharmaceuticals Limited |
Pharmaceutical composition
|
PT1951730E
(pt)
|
2005-11-16 |
2010-08-27 |
S Bio Pte Ltd |
Derivados de pirimidina ligados a heteroalquilo
|
ES2612196T3
(es)
|
2005-12-13 |
2017-05-12 |
Incyte Holdings Corporation |
Pirrolo[2,3-b]piridinas y pirrolo[2,3-b]pirimidinas sustituidas con heteroarilo como inhibidores de quinasas Janus
|
WO2007089768A2
(fr)
*
|
2006-01-30 |
2007-08-09 |
Exelixis, Inc. |
4-aryl-2-amino-pyrimidines ou 4-aryl-2-aminoalkyl-pyrimidines utilisées comme modulateurs de la jak-2 et leurs procédés d'utilisation
|
JP2009528295A
(ja)
|
2006-02-24 |
2009-08-06 |
ライジェル ファーマシューティカルズ, インコーポレイテッド |
Jak経路の阻害のための組成物および方法
|
SG170826A1
(en)
|
2006-04-04 |
2011-05-30 |
Kg Acquisition Llc |
Oral dosage forms including an antiplatelet agent and an acid inhibitor
|
WO2007127366A2
(fr)
|
2006-04-25 |
2007-11-08 |
Targegen, Inc. |
Inhibiteurs de kinases et leurs procédés d'utilisation
|
JP2009537538A
(ja)
*
|
2006-05-15 |
2009-10-29 |
アカドイア プハルマセウチカルス インコーポレーテッド |
ピマバンセリン医薬製剤
|
WO2008008234A1
(fr)
|
2006-07-07 |
2008-01-17 |
Targegen, Inc. |
Inhibiteurs de type 2-amino-5-substituant-pyrimidines
|
AU2007276369A1
(en)
|
2006-07-21 |
2008-01-24 |
Novartis Ag |
2, 4 -di (arylaminio) -pyrimidine-5-carboxamide compounds as JAK kinases inhibitors
|
US20080021013A1
(en)
|
2006-07-21 |
2008-01-24 |
Cephalon, Inc. |
JAK inhibitors for treatment of myeloproliferative disorders
|
WO2008057233A2
(fr)
*
|
2006-10-25 |
2008-05-15 |
The Regents Of The University Of California |
Modèles d'érythropoïèse
|
EP2173752B2
(fr)
|
2007-06-13 |
2022-07-13 |
Incyte Holdings Corporation |
Sels de l'inhibiteur (r)-3-(4-(7h-pyrrolo(2,3-d)pyrimidin-4-yl)-1h-pyrazol-1-yl)-3-cyclopentylpropanenitrile de la janus kinase
|
DE102007034947B4
(de)
*
|
2007-07-26 |
2009-06-18 |
Siemens Ag |
Vorrichtung zum Entladen eines Stapels von auf ihren Schmalseiten stehenden flachen Gegenständen
|
AU2008289442A1
(en)
*
|
2007-08-21 |
2009-02-26 |
Nodality, Inc. |
Methods for diagnosis, prognosis and methods of treatment
|
WO2009046416A1
(fr)
|
2007-10-05 |
2009-04-09 |
Targegen Inc. |
Anilinopyrimidines en tant qu'inhibiteurs de kinases jak
|
US20100310563A1
(en)
*
|
2007-11-30 |
2010-12-09 |
Bumm Thomas G P |
Methods for treating induced cellular proliferative disorders
|
CA2730847A1
(fr)
*
|
2008-07-14 |
2010-01-21 |
Otonomy, Inc. |
Compositions et procedes modulant l'apoptose a liberation controlee pour le traitement de troubles otiques
|
JP2011530517A
(ja)
|
2008-08-05 |
2011-12-22 |
ターゲジェン インコーポレーティッド |
サラセミアを処置する方法
|
PL2376500T3
(pl)
|
2008-12-11 |
2015-07-31 |
Cti Biopharma Corp |
Sól maleinianowa 11-(2-pirrolidyn-1-yloetoksy)-14,19-dioksa-5,7,26 triazatetracyklo[19.3.1.1(2,6).1(8,12)]heptakosa-1(25),2(26),3,5,8,10,12(27),16,21,23-dekaenu
|
ES2382773T3
(es)
|
2009-03-13 |
2012-06-13 |
Sanovel Ilac Sanayi Ve Ticaret A.S. |
Composiciones de ezetimiba
|
US20100297194A1
(en)
|
2009-04-30 |
2010-11-25 |
Nathaniel Catron |
Formulation for oral administration of apoptosis promoter
|
US20100278921A1
(en)
*
|
2009-04-30 |
2010-11-04 |
Fischer Cristina M |
Solid oral formulation of abt-263
|
JP2013500949A
(ja)
|
2009-07-31 |
2013-01-10 |
ビーエーエスエフ ソシエタス・ヨーロピア |
イミダゾール基含有ホスフィンボラン化合物とイミダゾール基含有ホスフィンボラン化合物の製造方法
|
WO2011025685A1
(fr)
|
2009-08-24 |
2011-03-03 |
Merck Sharp & Dohme Corp. |
L'inhibition de jak bloque les toxicités associées à l'arn d'interférence
|
CA2816957A1
(fr)
|
2010-11-07 |
2012-05-10 |
Targegen, Inc. |
Compositions et procedes de traitement de la myelofibrose
|
WO2013013195A1
(fr)
|
2011-07-21 |
2013-01-24 |
Sanofi |
Compositions et méthodes de traitement de la maladie de vasquez et de la thrombocythémie essentielle
|
WO2013059548A1
(fr)
|
2011-10-19 |
2013-04-25 |
Sanofi |
Compositions et méthodes de traitement du cancer à l'aide d'un inhibiteur de jak2
|