FR17C1031I1 - 3-((3R,4R)-4-METHYL-3-[METHYL-(7H-PYRROLO[2,3-D]PYRIMIDIN-4-YL)-AMINO]-PIPERIDINYL)-3-OXO-PROPIONITRILE AS AN INHIBITOR OF PROTEIN KINASE - Google Patents
3-((3R,4R)-4-METHYL-3-[METHYL-(7H-PYRROLO[2,3-D]PYRIMIDIN-4-YL)-AMINO]-PIPERIDINYL)-3-OXO-PROPIONITRILE AS AN INHIBITOR OF PROTEIN KINASEInfo
- Publication number
- FR17C1031I1 FR17C1031I1 FR17C1031C FR17C1031I1 FR 17C1031 I1 FR17C1031 I1 FR 17C1031I1 FR 17C1031 C FR17C1031 C FR 17C1031C FR 17C1031 I1 FR17C1031 I1 FR 17C1031I1
- Authority
- FR
- France
- Prior art keywords
- methyl
- propionitrile
- pyrrolo
- pyrimidin
- piperidinyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/56—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Dermatology (AREA)
- Oncology (AREA)
- Physical Education & Sports Medicine (AREA)
- Transplantation (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Endocrinology (AREA)
- Obesity (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Emergency Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Hydrogenated Pyridines (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US29477501P | 2001-05-31 | 2001-05-31 | |
US34104801P | 2001-12-06 | 2001-12-06 | |
EP02733058A EP1392694A1 (en) | 2001-05-31 | 2002-05-29 | Optical resolution of (1-benzyl-4-methylpiperidin-3-yl)-methylamine and the use thereof for the preparation of pyrrolo[2,3]pyrimidine derivatives as protein kinases inhibitors |
Publications (2)
Publication Number | Publication Date |
---|---|
FR17C1031I1 true FR17C1031I1 (en) | 2017-10-13 |
FR17C1031I2 FR17C1031I2 (en) | 2018-11-02 |
Family
ID=26968730
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR17C1031C Active FR17C1031I2 (en) | 2001-05-31 | 2017-09-04 | 3-((3R,4R)-4-METHYL-3-[METHYL-(7H-PYRROLO[2,3-D]PYRIMIDIN-4-YL)-AMINO]-PIPERIDINYL)-3-OXO-PROPIONITRILE AS AN INHIBITOR OF PROTEIN KINASE |
Country Status (52)
Families Citing this family (119)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PA8474101A1 (en) | 1998-06-19 | 2000-09-29 | Pfizer Prod Inc | PYROLEUM [2,3-D] PIRIMIDINE COMPOUNDS |
MXPA02005675A (en) | 1999-12-10 | 2002-09-02 | Pfizer Prod Inc | PYRROLO[2,3 d]PYRIMIDINE COMPOUNDS. |
EP1294724B1 (en) * | 2000-06-26 | 2006-04-19 | Pfizer Products Inc. | Pyrrolo¬2,3-d|pyrimidine compounds as immunosuppressive agents |
GT200200234A (en) | 2001-12-06 | 2003-06-27 | NEW CRYSTAL COMPOUNDS | |
TWI329105B (en) | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
WO2004014382A1 (en) | 2002-07-29 | 2004-02-19 | Rigel Pharmaceuticals | Methods of treating or preventing autoimmune diseases with 2,4-pyrimidinediamine compounds |
AU2003250197B2 (en) * | 2002-08-27 | 2009-11-12 | Merck Patent Gmbh | Glycinamide derivatives as raf-kinase inhibitors |
KR20050086784A (en) | 2002-11-26 | 2005-08-30 | 화이자 프로덕츠 인크. | Method of treatment of transplant rejection |
RS53109B (en) | 2003-07-30 | 2014-06-30 | Rigel Pharmaceuticals Inc. | 2,4-pyrimidinediamine compounds for use in the treatment or prevention of autoimmune diseases |
MXPA06012663A (en) * | 2004-05-03 | 2007-01-16 | Novartis Ag | Combinations comprising a s1p receptor agonist and a jak3 kinase inhibitor. |
EP1768982A2 (en) | 2004-06-29 | 2007-04-04 | Amgen Inc. | Pyrolo [2,3-d] pyrimidines that modulate ack1 and lck activity |
AR050365A1 (en) | 2004-08-02 | 2006-10-18 | Osi Pharm Inc | INHIBITING COMPOUNDS OF ARIL-AMINO PIRROLOPIRIMIDINE PULROLOPIRIMIDINE REPLACED |
US20090156602A1 (en) * | 2004-11-24 | 2009-06-18 | Nigel Graham Cooke | Organic Compounds |
AR054416A1 (en) | 2004-12-22 | 2007-06-27 | Incyte Corp | PIRROLO [2,3-B] PIRIDIN-4-IL-AMINAS AND PIRROLO [2,3-B] PIRIMIDIN-4-IL-AMINAS AS INHIBITORS OF THE JANUS KINASES. PHARMACEUTICAL COMPOSITIONS. |
CN105348203B (en) | 2005-06-08 | 2018-09-18 | 里格尔药品股份有限公司 | Inhibit the composition and method of JAK approach |
US20070203161A1 (en) | 2006-02-24 | 2007-08-30 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the jak pathway |
JP5071374B2 (en) | 2005-07-14 | 2012-11-14 | アステラス製薬株式会社 | Heterocyclic Janus Kinase 3 Inhibitor |
EP2251341A1 (en) | 2005-07-14 | 2010-11-17 | Astellas Pharma Inc. | Heterocyclic Janus kinase 3 inhibitors |
DK1913000T3 (en) | 2005-07-29 | 2012-03-12 | Pfizer Prod Inc | Pyrrolo [2,3-d] pyrimidine derivatives; their intermediates and synthesis |
CA2621261C (en) | 2005-09-22 | 2014-05-20 | Incyte Corporation | Azepine inhibitors of janus kinases |
ES2611588T3 (en) | 2005-12-13 | 2017-05-09 | Incyte Holdings Corporation | Pyrrolo [2,3-b] pyridines and pyrrolo [2,3-b] pyrimidines substituted with heteroaryl as Janus kinase inhibitors |
WO2007098507A2 (en) | 2006-02-24 | 2007-08-30 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the jak pathway |
GB0605691D0 (en) * | 2006-03-21 | 2006-05-03 | Novartis Ag | Organic Compounds |
US8513270B2 (en) | 2006-12-22 | 2013-08-20 | Incyte Corporation | Substituted heterocycles as Janus kinase inhibitors |
LT3070090T (en) | 2007-06-13 | 2019-06-25 | Incyte Holdings Corporation | Use of salts of the janus kinase inhibitor (r)-3-(4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h- pyrazol-1-yl)-3- cyclopentylpropanenitrile |
CL2008001709A1 (en) | 2007-06-13 | 2008-11-03 | Incyte Corp | Compounds derived from pyrrolo [2,3-b] pyrimidine, jak kinase modulators; pharmaceutical composition; and use in the treatment of diseases such as cancer, psoriasis, rheumatoid arthritis, among others. |
WO2009007839A1 (en) * | 2007-07-11 | 2009-01-15 | Pfizer Inc. | Pharmaceutical compositions and methods of treating dry eye disorders |
CN102007124B (en) | 2008-02-15 | 2014-06-18 | 里格尔制药公司 | Pyrimidine-2-amine compounds and their use as inhibitors of jak kinases |
US8158616B2 (en) | 2008-03-11 | 2012-04-17 | Incyte Corporation | Azetidine and cyclobutane derivatives as JAK inhibitors |
MX2010011463A (en) | 2008-04-16 | 2011-06-03 | Portola Pharm Inc | 2, 6-diamino- pyrimidin- 5-yl-carboxamides as syk or jak kinases inhibitors. |
US8138339B2 (en) | 2008-04-16 | 2012-03-20 | Portola Pharmaceuticals, Inc. | Inhibitors of protein kinases |
WO2009131687A2 (en) | 2008-04-22 | 2009-10-29 | Portola Pharmaceuticals, Inc. | Inhibitors of protein kinases |
AU2009276420A1 (en) * | 2008-08-01 | 2010-02-04 | Biocryst Pharmaceuticals, Inc. | Piperidine derivatives as JAK3 inhibitors |
PT2384326E (en) | 2008-08-20 | 2014-06-09 | Zoetis Llc | Pyrrolo[2,3-d]pyrimidine compounds |
CA2752150A1 (en) * | 2009-02-11 | 2010-08-19 | Reaction Biology Corp. | Selective kinase inhibitors |
JP5709276B2 (en) | 2009-04-20 | 2015-04-30 | オースペックス ファーマシューティカルズ,エルエルシー | Piperidine inhibitor of Janus kinase 3 |
US8604043B2 (en) | 2009-05-22 | 2013-12-10 | Incyte Corporation | 3-[4-(7H-pyrrolo[2,3-D]pyrimidin-4-yl)-1H-pyrazol-1-yl]octane- or heptane-nitrile as jak inhibitors |
WO2010135650A1 (en) | 2009-05-22 | 2010-11-25 | Incyte Corporation | N-(HETERO)ARYL-PYRROLIDINE DERIVATIVES OF PYRAZOL-4-YL-PYRROLO[2,3-d]PYRIMIDINES AND PYRROL-3-YL-PYRROLO[2,3-d]PYRIMIDINES AS JANUS KINASE INHIBITORS |
US9249145B2 (en) | 2009-09-01 | 2016-02-02 | Incyte Holdings Corporation | Heterocyclic derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines as janus kinase inhibitors |
JP5658756B2 (en) * | 2009-09-10 | 2015-01-28 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | JAK inhibitors |
EA021478B1 (en) | 2009-10-09 | 2015-06-30 | Инсайт Корпорейшн | HYDROXYL, KETO, AND GLUCURONIDE DERIVATIVES OF 3-(4-(7H-PYRROLO[2,3-d]PYRIMIDIN-4-YL)-1H-PYRAZOL-1-YL)-3-CYCLOPENTYLPROPANENITRILE |
CA2776028C (en) | 2009-10-15 | 2015-12-01 | Pfizer Inc. | Pyrrolo[2,3-d]pyrimidine compounds |
WO2011075334A1 (en) | 2009-12-18 | 2011-06-23 | Pfizer Inc. | Pyrrolo[2,3-d]pyrimidine compounds |
AR079984A1 (en) * | 2010-01-12 | 2012-03-07 | Hoffmann La Roche | TRICYCLIC HETEROCICLIC COMPOUNDS, COMPOSITIONS AND ITS USE IN THE TREATMENT OF DISEASES MEDIATED BY THE INHIBITION OF JAK1 |
JP2013518882A (en) | 2010-02-05 | 2013-05-23 | ファイザー・インク | Pyrrolo [2,3-d] pyrimidine urea compounds as JAK inhibitors |
EP4036088B1 (en) | 2010-03-10 | 2024-04-03 | Incyte Holdings Corporation | Piperidin-4-yl azetidine derivatives as jak1 inhibitors |
SG10201503983QA (en) | 2010-05-21 | 2015-06-29 | Incyte Corp | Topical Formulation for a JAK Inhibitor |
TW201300360A (en) | 2010-11-01 | 2013-01-01 | Portola Pharm Inc | Nicotinamides as JAK kinase modulators |
CA2818545C (en) | 2010-11-19 | 2019-04-16 | Incyte Corporation | Heterocyclic-substituted pyrrolopyridines and pyrrolopyrimidines as jak inhibitors |
BR112013012502A2 (en) | 2010-11-19 | 2019-03-06 | Incyte Corporation | substituted cyclobutyl pyrrolopyridine and derivative pyrrolopyrimidine derivatives as jak inhibitors |
EP2481411A1 (en) | 2011-01-27 | 2012-08-01 | Ratiopharm GmbH | Oral dosage forms for modified release comprising the JAK3 inhibitor tasocitinib |
EP2481397A1 (en) | 2011-01-27 | 2012-08-01 | Ratiopharm GmbH | Pharmaceutical compositions comprising tasocitinib |
EP2675451B9 (en) | 2011-02-18 | 2017-07-26 | Novartis Pharma AG | mTOR/JAK INHIBITOR COMBINATION THERAPY |
EP2691395B1 (en) | 2011-03-28 | 2017-08-30 | ratiopharm GmbH | Processes for preparing tofacitinib salts |
US9050342B2 (en) | 2011-03-29 | 2015-06-09 | Pfizer Inc. | Beneficial effects of combination therapy on cholesterol |
AU2012241018B2 (en) * | 2011-04-08 | 2015-11-12 | Pfizer Inc. | Crystalline and non- crystalline forms of tofacitinib, and a pharmaceutical composition comprising tofacitinib and a penetration enhancer |
EP2524688B1 (en) | 2011-05-11 | 2013-05-01 | ratiopharm GmbH | Composition for modified release comprising ranolazine |
EP2721028B1 (en) | 2011-06-20 | 2015-11-04 | Incyte Corporation | Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as jak inhibitors |
US9358229B2 (en) | 2011-08-10 | 2016-06-07 | Novartis Pharma Ag | JAK PI3K/mTOR combination therapy |
TW201313721A (en) | 2011-08-18 | 2013-04-01 | Incyte Corp | Cyclohexyl azetidine derivatives as JAK inhibitors |
UA111854C2 (en) | 2011-09-07 | 2016-06-24 | Інсайт Холдінгс Корпорейшн | METHODS AND INTERMEDIATE COMPOUNDS FOR JAK INHIBITORS |
IN2014CN04065A (en) | 2011-11-23 | 2015-09-04 | Portola Pharm Inc | |
CA2856722C (en) * | 2011-11-30 | 2022-11-22 | Emory University | Antiviral jak inhibitors useful in treating or preventing retroviral and other viral infections |
US10821111B2 (en) | 2011-11-30 | 2020-11-03 | Emory University | Antiviral JAK inhibitors useful in treating or preventing retroviral and other viral infections |
EP2791141B1 (en) | 2011-12-15 | 2017-02-08 | ratiopharm GmbH | Tofacitinib mono-tartrate salt |
WO2013173720A1 (en) | 2012-05-18 | 2013-11-21 | Incyte Corporation | Piperidinylcyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as jak inhibitors |
WO2014016338A1 (en) | 2012-07-25 | 2014-01-30 | Lek Pharmaceuticals D.D. | New synthetic route for the preparation of 3-amino-piperidine compounds |
WO2014058921A2 (en) | 2012-10-08 | 2014-04-17 | Portola Pharmaceuticals, Inc. | Substituted pyrimidinyl kinase inhibitors |
CN113384546A (en) | 2012-11-15 | 2021-09-14 | 因赛特公司 | Sustained release dosage forms of ruxolitinib |
CN104955803B (en) * | 2012-11-30 | 2017-11-28 | 斯洛文尼亚莱柯制药股份有限公司 | 3 aminopiperidines are prepared by nitro tetrahydropyridine precursor |
WO2014097150A1 (en) | 2012-12-17 | 2014-06-26 | Ranbaxy Laboratories Limited | Process for the preparation of tofacitinib and intermediates thereof |
US9670160B2 (en) | 2012-12-28 | 2017-06-06 | Glenmark Pharmaceuticals Limited | Process for the preparation of tofacitinib and intermediates thereof |
MY177476A (en) | 2013-02-22 | 2020-09-16 | Pfizer | Pyrrolo [2,3-d]pyrimidine derivatives as inhibitors of janus kinases (jak) |
AR095018A1 (en) | 2013-03-06 | 2015-09-16 | Incyte Corp | PROCESSES AND INTERMEDIATES TO MAKE A JAK INHIBITOR |
JP6041823B2 (en) | 2013-03-16 | 2016-12-14 | ファイザー・インク | Tofacitinib oral sustained release dosage form |
US20140343034A1 (en) | 2013-04-25 | 2014-11-20 | Japan Tobacco Inc. | Skin barrier function improving agent |
WO2014174073A1 (en) | 2013-04-26 | 2014-10-30 | Sandoz Ag | Sustained release formulations of tofacitinib |
US9655854B2 (en) | 2013-08-07 | 2017-05-23 | Incyte Corporation | Sustained release dosage forms for a JAK1 inhibitor |
CN104513248B (en) * | 2013-09-30 | 2019-05-24 | 重庆医药工业研究院有限责任公司 | A kind of purification process of tropsch imatinib intermediate |
AU2014358792C1 (en) | 2013-12-05 | 2021-08-26 | Pfizer Inc. | Pyrrolo[2,3-d]pyrimidinyl, pyrrolo[2,3-b]pyrazinyl and pyrrolo[2,3-d]pyridinyl acrylamides |
BR112015025543B1 (en) | 2013-12-09 | 2020-11-03 | Unichem Laboratories Limited | process for the preparation of (3r, 4r) - (1-benzyl-4-methylpiperidine-3-yl) -methylamine and intermediate compounds |
US9260438B2 (en) | 2014-02-06 | 2016-02-16 | Apotex Inc. | Solid forms of tofacitinib salts |
WO2015184305A1 (en) | 2014-05-30 | 2015-12-03 | Incyte Corporation | TREATMENT OF CHRONIC NEUTROPHILIC LEUKEMIA (CNL) AND ATYPICAL CHRONIC MYELOID LEUKEMIA (aCML) BY INHIBITORS OF JAK1 |
JP6585158B2 (en) | 2014-08-12 | 2019-10-02 | ファイザー・インク | Pyrrolo [2,3-d] pyrimidine derivatives useful for the inhibition of Janus kinase |
UA118149C2 (en) | 2015-01-20 | 2018-11-26 | Вуксі Фортуне Фармасьютікал Ко., Лтд | Jak inhibitor |
US10479763B2 (en) | 2015-02-17 | 2019-11-19 | Amorepacific Corporation | Chiral resolution method of N-[4-(1-aminoethyl)-phenyl]-sulfonamide derivatives |
CN104761556B (en) * | 2015-03-21 | 2017-06-23 | 河北国龙制药有限公司 | Support method replaces cloth impurity and its synthetic method, and support method for the quality control method of cloth for cloth intermediate impurities, support method |
EP3078665A1 (en) * | 2015-04-10 | 2016-10-12 | OLON S.p.A. | Efficient method for the preparation of tofacitinib citrate |
DK3290418T3 (en) | 2015-04-29 | 2019-07-01 | Wuxi Fortune Pharmaceutical Co Ltd | Janus Kinase (JAK) Inhibitors |
WO2016178110A1 (en) | 2015-05-01 | 2016-11-10 | Pfizer Inc. | Pyrrolo[2,3-d]pyrimidinyl, pyrrolo[2,3-b]pyrazinyl, pyrrolo[2,3-b]pyridinyl acrylamides and epoxides thereof |
PL3305788T3 (en) | 2015-05-29 | 2021-03-08 | Wuxi Fortune Pharmaceutical Co., Ltd | Janus kinase inhibitor |
JP6507272B2 (en) * | 2015-07-27 | 2019-04-24 | ユニケム ラボラトリーズ リミテッド | Tofacitinib orally disintegrating tablet |
KR101771219B1 (en) * | 2015-08-21 | 2017-09-05 | 양지화학 주식회사 | Janus kinase 1 selective inhibitors and their pharmaceutical use |
CN108472298B (en) | 2015-11-24 | 2021-04-20 | 深圳阿拉丁医疗科技有限公司 | Selective kinase inhibitors |
CN105348287A (en) * | 2015-11-30 | 2016-02-24 | 宁波立华制药有限公司 | Novel synthesis process of tofacitinib citrate |
KR102565407B1 (en) * | 2016-01-04 | 2023-08-10 | (주)아모레퍼시픽 | Method for chiral resolution of n-[4-(1-aminoethyl)-phenyl]-sulfonamide derivatives by using polar aprotic solvent |
US20190083609A1 (en) | 2016-01-18 | 2019-03-21 | Helmoltz Zentrum München - Deutsches Forschungszentrum Für Gesundheit And Umwelt (Gmbh) | Tofacitinib as vaccination immune modulator |
SG11201811470PA (en) | 2016-06-30 | 2019-01-30 | Daewoong Pharmaceutical Co Ltd | Pyrazolopyrimidine derivatives as kinase inhibitor |
CN106831538B (en) * | 2017-01-22 | 2019-06-25 | 苏州楚凯药业有限公司 | The preparation method of tropsch imatinib intermediate |
KR102398659B1 (en) | 2017-03-17 | 2022-05-16 | 주식회사 대웅제약 | Pyrrolotriazine derivatives as kinase inhibitor |
CN107602569A (en) * | 2017-10-23 | 2018-01-19 | 上海博悦生物科技有限公司 | A kind of new pyrrole simultaneously [2,3 d] pyrimidine compound and its preparation method and use |
KR102078805B1 (en) | 2017-11-30 | 2020-02-19 | 보령제약 주식회사 | Pharmaceutical Composition Comprising Tofacitinib |
WO2019113487A1 (en) | 2017-12-08 | 2019-06-13 | Incyte Corporation | Low dose combination therapy for treatment of myeloproliferative neoplasms |
RU2758370C1 (en) | 2017-12-28 | 2021-10-28 | Даевунг Фармасьютикал Ко., Лтд. | Derivatives of oxifluoropiperidine as a kinase inhibitor |
KR102577241B1 (en) | 2017-12-28 | 2023-09-11 | 주식회사 대웅제약 | Amino-fluoropiperidine derivatives as kinase inhibitor |
KR102577242B1 (en) | 2017-12-28 | 2023-09-11 | 주식회사 대웅제약 | Amino-methylpiperidine derivatives as kinase inhibitor |
WO2019152374A1 (en) | 2018-01-30 | 2019-08-08 | Incyte Corporation | Processes for preparing (1 -(3-fluoro-2-(trifluoromethyl)isonicotinyl)piperidine-4-one) |
JP7324210B2 (en) * | 2018-01-31 | 2023-08-09 | ティダブリューアイ・バイオテクノロジー・インコーポレイテッド | Topical preparations containing tofacitinib |
HUE067471T2 (en) | 2018-03-30 | 2024-10-28 | Incyte Corp | Treatment of hidradenitis suppurativa using jak inhibitors |
KR102131107B1 (en) * | 2019-01-15 | 2020-07-07 | 주식회사 다산제약 | Novel method for preparing 3-amino-piperidine |
CA3132109A1 (en) | 2019-03-13 | 2020-09-17 | Intas Pharmaceuticals Ltd. | Process for preparation of tofacitinib and pharmaceutically acceptable salt thereof |
EP3946606A1 (en) | 2019-03-27 | 2022-02-09 | Insilico Medicine IP Limited | Bicyclic jak inhibitors and uses thereof |
ES2977277T3 (en) * | 2019-04-05 | 2024-08-21 | Yuhan Corp | Processes for preparing (3R,4R)-1-benzyl-n,4-dimethylpiperidin-3-amine or a salt thereof and processes for preparing tofacitinib by using the same |
MX2022005882A (en) | 2019-11-14 | 2022-06-14 | Pfizer | 1-(((2s,3s,4s)-3-ethyl-4-fluoro-5-oxopyrrolidin-2-yl)methoxy)-7- methoxyisoquinoline-6-carboxamide combinations and oral dosage forms. |
US20220389010A1 (en) | 2019-11-25 | 2022-12-08 | Daewoong Pharmaceutical Co., Ltd. | Novel Triazolopyridine Derivatives and Pharmaceutical Composition Comprising Same |
US20230149407A1 (en) | 2020-04-04 | 2023-05-18 | Pfizer Inc. | Methods of Treating Coronavirus Disease 2019 |
US11833155B2 (en) | 2020-06-03 | 2023-12-05 | Incyte Corporation | Combination therapy for treatment of myeloproliferative neoplasms |
EP4308568A1 (en) * | 2021-03-15 | 2024-01-24 | Chiesi Farmaceutici S.p.A. | Heterocyclic derivatives as janus kinase inhibitors |
EP4180042A1 (en) | 2021-11-15 | 2023-05-17 | Sanovel Ilac Sanayi Ve Ticaret A.S. | A film coated tablet comprising micronized tofacitinib |
Family Cites Families (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL8403224A (en) | 1984-10-24 | 1986-05-16 | Oce Andeno Bv | DIOXAPHOSPHORINANS, THEIR PREPARATION AND THE USE FOR SPLITTING OF OPTICALLY ACTIVE COMPOUNDS. |
US6136595A (en) | 1993-07-29 | 2000-10-24 | St. Jude Children's Research Hospital | Jak kinases and regulations of cytokine signal transduction |
US5389509A (en) | 1993-10-04 | 1995-02-14 | Eastman Kodak Company | Ultrathin high chloride tabular grain emulsions |
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 |
DE59500788D1 (en) | 1994-05-03 | 1997-11-20 | Ciba Geigy Ag | Pyrrolopyrimidine derivatives with antiproliferative activity |
JPH07330732A (en) * | 1994-06-10 | 1995-12-19 | Kyorin Pharmaceut Co Ltd | Optically active 3-amino-1-benzylpiperidine derivative |
US6136596A (en) * | 1995-05-19 | 2000-10-24 | University Of Massachusetts | Cytokine-, stress-, and oncoprotein-activated human protein kinase kinases |
JP3290666B2 (en) | 1995-06-07 | 2002-06-10 | ファイザー・インコーポレーテッド | Heterocyclic fused-ring pyrimidine derivatives |
ES2167586T3 (en) | 1995-07-05 | 2002-05-16 | Du Pont | FUNGICIDE PYRIMIDINONES. |
BR9609617B1 (en) | 1995-07-06 | 2010-07-27 | 7h-pyrrol [2,3-d] pyrimidine derivatives, and pharmaceutical composition. | |
AR004010A1 (en) | 1995-10-11 | 1998-09-30 | Glaxo Group Ltd | HETERO CYCLIC COMPOUNDS |
CA2209598C (en) | 1995-11-14 | 2005-06-07 | Pharmacia & Upjohn Spa | Aryl and heteroaryl purine compounds |
EP0888349B1 (en) | 1996-01-23 | 2002-05-22 | Novartis AG | Pyrrolopyrimidines and processes for their preparation |
CH690773A5 (en) | 1996-02-01 | 2001-01-15 | Novartis Ag | Pyrrolo (2,3-d) pyrimides and their use. |
GB9604361D0 (en) | 1996-02-29 | 1996-05-01 | Pharmacia Spa | 4-Substituted pyrrolopyrimidine compounds as tyrosine kinase inhibitors |
AU1794697A (en) | 1996-03-06 | 1997-09-22 | Novartis Ag | 7-alkyl-pyrrolo{2,3-d}pyrimidines |
AU3176297A (en) | 1996-06-25 | 1998-01-14 | Novartis Ag | Substituted 7-amino-pyrrolo{3,2-d}pyrimidines and the use thereof |
HRP970371A2 (en) | 1996-07-13 | 1998-08-31 | Kathryn Jane Smith | Heterocyclic compounds |
CA2260058A1 (en) | 1996-07-13 | 1998-01-22 | Kathryn Jane Smith | Bicyclic heteroaromatic compounds as protein tyrosine kinase inhibitors |
DE69738468T2 (en) | 1996-08-23 | 2009-01-08 | Novartis Ag | SUBSTITUTED PYRROLOPYRIMIDINES AND METHOD FOR THE PRODUCTION THEREOF |
CA2272705C (en) | 1996-11-27 | 2003-03-18 | Pfizer Inc. | Fused bicyclic pyrimidine derivatives |
ES2301194T3 (en) | 1997-02-05 | 2008-06-16 | Warner-Lambert Company Llc | PIRIDO 2,3-D PYRIMIDINS AND 4-AMINOPIRIMIDINAS AS INHIBITORS OF THE CELL PROLIFERATION. |
WO1998043087A1 (en) | 1997-03-24 | 1998-10-01 | Pharmacia & Upjohn Company | Method for identifying inhibitors of jak2/cytokine receptor binding |
WO1999051599A1 (en) | 1998-04-02 | 1999-10-14 | Neurogen Corporation | Aminoalkyl substituted pyrrolo[2,3-b]pyridine and pyrrolo[2,3-d]pyrimidine derivatives: modulators of crf1 receptors |
EP1082311A1 (en) | 1998-05-28 | 2001-03-14 | Parker Hughes Institute | Quinazolines for treating brain tumor |
AU3951899A (en) * | 1998-06-19 | 2000-01-05 | Pfizer Products Inc. | Pyrrolo(2,3-d)pyrimidine compounds |
PA8474101A1 (en) * | 1998-06-19 | 2000-09-29 | Pfizer Prod Inc | PYROLEUM [2,3-D] PIRIMIDINE COMPOUNDS |
JP2004504259A (en) | 1998-06-30 | 2004-02-12 | パーカー ヒューズ インスティテュート | Method of inhibiting C-JUN expression using JAK-3 inhibitor |
KR20010089171A (en) | 1998-08-21 | 2001-09-29 | 추후제출 | Quinazoline derivatives |
US6080747A (en) | 1999-03-05 | 2000-06-27 | Hughes Institute | JAK-3 inhibitors for treating allergic disorders |
MXPA02005675A (en) * | 1999-12-10 | 2002-09-02 | Pfizer Prod Inc | PYRROLO[2,3 d]PYRIMIDINE COMPOUNDS. |
EP1294724B1 (en) | 2000-06-26 | 2006-04-19 | Pfizer Products Inc. | Pyrrolo¬2,3-d|pyrimidine compounds as immunosuppressive agents |
GT200200234A (en) * | 2001-12-06 | 2003-06-27 | NEW CRYSTAL COMPOUNDS | |
EP1768982A2 (en) * | 2004-06-29 | 2007-04-04 | Amgen Inc. | Pyrolo [2,3-d] pyrimidines that modulate ack1 and lck activity |
-
2002
- 2002-05-23 US US10/154,699 patent/US7301023B2/en not_active Expired - Lifetime
- 2002-05-29 EA EA200301193A patent/EA007251B1/en active Protection Beyond IP Right Term
- 2002-05-29 KR KR1020077025832A patent/KR100868814B1/en active IP Right Review Request
- 2002-05-29 ES ES05015461T patent/ES2369226T3/en not_active Expired - Lifetime
- 2002-05-29 KR KR1020067001821A patent/KR100869409B1/en active IP Right Grant
- 2002-05-29 KR KR1020067025590A patent/KR20060133117A/en not_active Application Discontinuation
- 2002-05-29 BR BR0209246-8A patent/BR0209246A/en not_active Application Discontinuation
- 2002-05-29 TW TW092133699A patent/TWI316061B/en not_active IP Right Cessation
- 2002-05-29 GE GE5361A patent/GEP20063784B/en unknown
- 2002-05-29 TN TNPCT/IB2002/001905A patent/TNSN03128A1/en unknown
- 2002-05-29 EP EP05015454.1A patent/EP1666481B9/en not_active Expired - Lifetime
- 2002-05-29 AT AT05015461T patent/ATE519741T1/en not_active IP Right Cessation
- 2002-05-29 EA EA200600575A patent/EA012666B1/en active Protection Beyond IP Right Term
- 2002-05-29 PE PE2002000452A patent/PE20030561A1/en not_active Application Discontinuation
- 2002-05-29 NZ NZ530380A patent/NZ530380A/en not_active IP Right Cessation
- 2002-05-29 PL PL409305A patent/PL228155B1/en unknown
- 2002-05-29 MX MXPA03011062A patent/MXPA03011062A/en active IP Right Grant
- 2002-05-29 JP JP2003500088A patent/JP4381137B2/en not_active Expired - Lifetime
- 2002-05-29 DK DK05015454.1T patent/DK1666481T3/en active
- 2002-05-29 CA CA002448281A patent/CA2448281C/en not_active Expired - Lifetime
- 2002-05-29 SK SK1465-2003A patent/SK288199B6/en unknown
- 2002-05-29 KR KR10-2003-7015681A patent/KR20040003037A/en not_active Application Discontinuation
- 2002-05-29 PT PT50154541T patent/PT1666481E/en unknown
- 2002-05-29 UA UA20031110841A patent/UA80093C2/en unknown
- 2002-05-29 SK SK50033-2011A patent/SK288192B6/en active Protection Beyond IP Right Term
- 2002-05-29 KR KR1020087018519A patent/KR100926875B1/en active IP Right Grant
- 2002-05-29 ES ES05015454T patent/ES2393385T3/en not_active Expired - Lifetime
- 2002-05-29 EP EP02733058A patent/EP1392694A1/en not_active Withdrawn
- 2002-05-29 EE EEP200300594A patent/EE05332B1/en active Protection Beyond IP Right Term
- 2002-05-29 AU AU2002304401A patent/AU2002304401C1/en not_active Expired
- 2002-05-29 CN CNA028108175A patent/CN1729192A/en active Pending
- 2002-05-29 CZ CZ2003-3260A patent/CZ304366B6/en not_active IP Right Cessation
- 2002-05-29 EP EP05015461A patent/EP1609781B1/en not_active Expired - Lifetime
- 2002-05-29 OA OA1200300308A patent/OA12612A/en unknown
- 2002-05-29 NZ NZ540332A patent/NZ540332A/en not_active IP Right Cessation
- 2002-05-29 WO PCT/IB2002/001905 patent/WO2002096909A1/en active Application Filing
- 2002-05-29 TW TW091111480A patent/TWI310384B/en active
- 2002-05-29 IL IL15858802A patent/IL158588A0/en active IP Right Grant
- 2002-05-29 RS YU92303A patent/RS52144B/en unknown
- 2002-05-29 SI SI200231004T patent/SI1666481T1/en unknown
- 2002-05-29 HU HU0400152A patent/HU230876B1/en active Protection Beyond IP Right Term
- 2002-05-29 PL PL02367945A patent/PL367945A1/en unknown
- 2002-05-30 UY UY27317A patent/UY27317A1/en not_active Application Discontinuation
- 2002-05-30 GT GT200200100AK patent/GT200200100AA/en unknown
- 2002-05-30 PA PA20028546301A patent/PA8546301A1/en unknown
- 2002-05-30 GT GT200200100A patent/GT200200100A/en unknown
- 2002-05-30 AR ARP020102017A patent/AR037321A1/en not_active Application Discontinuation
- 2002-05-30 MY MYPI20021988A patent/MY129649A/en unknown
- 2002-05-31 AP APAP/P/2002/002550A patent/AP1859A/en active
-
2003
- 2003-10-13 IS IS6993A patent/IS3023B/en unknown
- 2003-10-13 CU CU20030229A patent/CU23337B7/en not_active IP Right Cessation
- 2003-10-14 ZA ZA200307982A patent/ZA200307982B/en unknown
- 2003-11-19 HR HR20030943A patent/HRP20030943B1/en not_active IP Right Cessation
- 2003-11-21 MA MA27410A patent/MA27029A1/en unknown
- 2003-11-24 NO NO20035201A patent/NO328578B1/en not_active IP Right Cessation
- 2003-11-26 EC EC2003004865A patent/ECSP034865A/en unknown
- 2003-11-27 BG BG108389A patent/BG66489B1/en unknown
-
2004
- 2004-05-07 AR ARP040101561A patent/AR045680A2/en unknown
- 2004-06-16 US US10/869,101 patent/US7432370B2/en not_active Expired - Lifetime
-
2008
- 2008-03-14 CL CL200800762A patent/CL2008000762A1/en unknown
- 2008-07-16 AU AU2008203170A patent/AU2008203170B2/en active Active
- 2008-07-24 CR CR10177A patent/CR10177A/en unknown
-
2009
- 2009-10-13 NO NO20093135A patent/NO20093135L/en not_active Application Discontinuation
-
2012
- 2012-11-09 CY CY20121101069T patent/CY1113322T1/en unknown
-
2017
- 2017-08-02 NL NL300887C patent/NL300887I2/en unknown
- 2017-08-08 LT LTPA2017025C patent/LTC1666481I2/en unknown
- 2017-08-09 LU LU00031C patent/LUC00031I2/fr unknown
- 2017-08-17 BE BE2017C032C patent/BE2017C032I2/fr unknown
- 2017-09-01 CY CY2017028C patent/CY2017028I2/en unknown
- 2017-09-04 FR FR17C1031C patent/FR17C1031I2/en active Active
- 2017-09-08 NO NO2017047C patent/NO2017047I1/en unknown
-
2019
- 2019-02-19 HU HUS1900008C patent/HUS1900008I1/en unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
FR17C1031I2 (en) | 3-((3R,4R)-4-METHYL-3-[METHYL-(7H-PYRROLO[2,3-D]PYRIMIDIN-4-YL)-AMINO]-PIPERIDINYL)-3-OXO-PROPIONITRILE AS AN INHIBITOR OF PROTEIN KINASE | |
CA2469350A1 (en) | 3-{4-methyl-3[methyl-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-amino]-piperidin-1-yl}-3-oxo-propionitrile mono citrate salt | |
HUP0400300A3 (en) | Pyrrolopyrimidines as protein kinase inhibitors | |
NO20041887L (en) | Benzomidazoles useful as protein kinase inhibitors | |
PT1235830E (en) | PYRIMIDINE-2,3-D | PYRIMIDINE COMPOUNDS AS PROTEIN KINASE INHIBITORS | |
AU2002310187A1 (en) | Inhibitors of protein kinase for the treatment of disease | |
EE200200506A (en) | 5-alkylpyrido [2,3-d] pyrimidines as tyrosine kinase inhibitors | |
WO2007012953A3 (en) | Pyrrolo[2,3-d]pyrimidine derivatives; their intermediates and synthesis | |
AU2003254053A1 (en) | Pyrazolopyrimidines as protein kinase inhibitors | |
AU2002357193A1 (en) | Thienopyrimidine compounds as protein tyrosine kinase inhibitors | |
CY2008015I2 (en) | BICYCLIC ETEOAROMATIC COMPOUNDS AS PROTEIN TYROSINE KINASE INHIBITORS | |
NO20011575D0 (en) | Substituted 3-cyanoquinolines as protein tyrosine kinase inhibitors | |
NO20035728D0 (en) | Pyrrolopyrimidines as protein kinase inhibitors | |
HK1080074A1 (en) | 4,6-diaminosubstituted-2-[oxy or aminoxy]-[1,3,5]triazines as protein tyrosine kinase inhibitors | |
GB0213809D0 (en) | Dynamic shaping of laser beams | |
AU2002220630A1 (en) | Regulation of human serine-threonine protein kinase | |
ITMI20010667A0 (en) | COMPOSITION OF ODOR ABSORBERS PARTICULARLY FOR REFRIGERATORS | |
AU2002251636A1 (en) | Novel use of tyrosine kinase inhibitor | |
IL145329A0 (en) | Protein tyrosine kinase inhibitors | |
AU2002307861A1 (en) | Imidazole-2-carboxamide derivatives as raf kinase inhibitors | |
AU2002348010A1 (en) | Novel germinal center kinase proteins, compositions, and methods of use |