AU2003231231A1 - Pyridinyl amino pyrimidine derivatives useful for treating hyper-proliferative disorders - Google Patents

Pyridinyl amino pyrimidine derivatives useful for treating hyper-proliferative disorders

Info

Publication number
AU2003231231A1
AU2003231231A1 AU2003231231A AU2003231231A AU2003231231A1 AU 2003231231 A1 AU2003231231 A1 AU 2003231231A1 AU 2003231231 A AU2003231231 A AU 2003231231A AU 2003231231 A AU2003231231 A AU 2003231231A AU 2003231231 A1 AU2003231231 A1 AU 2003231231A1
Authority
AU
Australia
Prior art keywords
proliferative disorders
pyrimidine derivatives
derivatives useful
amino pyrimidine
treating hyper
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.)
Abandoned
Application number
AU2003231231A
Other languages
English (en)
Inventor
Jianqing Chen
Yuanwei Chen
Barry Hart
Donglei Liu
Sharad K. Verma
Jill E. Wood
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer Pharmaceuticals Corp
Original Assignee
Bayer Pharmaceuticals Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Bayer Pharmaceuticals Corp filed Critical Bayer Pharmaceuticals Corp
Publication of AU2003231231A1 publication Critical patent/AU2003231231A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
AU2003231231A 2002-05-06 2003-05-02 Pyridinyl amino pyrimidine derivatives useful for treating hyper-proliferative disorders Abandoned AU2003231231A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US37832902P 2002-05-06 2002-05-06
US60/378,329 2002-05-06
PCT/US2003/013604 WO2003095448A1 (fr) 2002-05-06 2003-05-02 Derives de pyridinyl amino pyrimidine utilises dans le traitement des troubles de l'hyperproliferation

Publications (1)

Publication Number Publication Date
AU2003231231A1 true AU2003231231A1 (en) 2003-11-11

Family

ID=29420382

Family Applications (2)

Application Number Title Priority Date Filing Date
AU2003231231A Abandoned AU2003231231A1 (en) 2002-05-06 2003-05-02 Pyridinyl amino pyrimidine derivatives useful for treating hyper-proliferative disorders
AU2003299474A Abandoned AU2003299474A1 (en) 2002-05-06 2003-05-06 2-4-(di-phenyl-amino)-pyrimidine derivatives useful for treating hyper-proliferative disorders

Family Applications After (1)

Application Number Title Priority Date Filing Date
AU2003299474A Abandoned AU2003299474A1 (en) 2002-05-06 2003-05-06 2-4-(di-phenyl-amino)-pyrimidine derivatives useful for treating hyper-proliferative disorders

Country Status (2)

Country Link
AU (2) AU2003231231A1 (fr)
WO (2) WO2003095448A1 (fr)

Families Citing this family (95)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI329105B (en) 2002-02-01 2010-08-21 Rigel Pharmaceuticals Inc 2,4-pyrimidinediamine compounds and their uses
GB0206215D0 (en) 2002-03-15 2002-05-01 Novartis Ag Organic compounds
ATE451104T1 (de) 2002-07-29 2009-12-15 Rigel Pharmaceuticals Inc Verfahren zur behandlung oder pruvention von autoimmunkrankheiten mit 2,4-pyrimidindiamin- verbindungen
UA80767C2 (en) * 2002-12-20 2007-10-25 Pfizer Prod Inc Pyrimidine derivatives for the treatment of abnormal cell growth
PL379330A1 (pl) 2002-12-20 2006-08-21 Pfizer Products Inc. Pochodne pirymidyny dla leczenia nienormalnego wzrostu komórek
US7109337B2 (en) 2002-12-20 2006-09-19 Pfizer Inc Pyrimidine derivatives for the treatment of abnormal cell growth
GB0305929D0 (en) 2003-03-14 2003-04-23 Novartis Ag Organic compounds
CN1849318B (zh) 2003-07-30 2011-10-12 里格尔药品股份有限公司 用2,4-嘧啶二胺化合物预防和治疗自体免疫疾病的方法
SG145749A1 (en) * 2003-08-15 2008-09-29 Novartis Ag 2, 4-pyrimidinediamines useful in the treatment of neoplastic diseases, inflammatory and immune system disorders
BRPI0510963A (pt) 2004-05-14 2007-11-20 Pfizer Prod Inc derivados pirimidina para o tratamento do crescimento anormal de células
MXPA06013164A (es) 2004-05-14 2007-02-13 Pfizer Prod Inc Derivados de pirimidina para el tratamiento de crecimiento de celulas anormal.
WO2005111024A1 (fr) 2004-05-14 2005-11-24 Pfizer Products Inc. Derives de pyrimidine destines au traitement de croissance cellulaire anormale
WO2006004776A1 (fr) 2004-06-29 2006-01-12 Rigel Pharmaceuticals, Inc. Composés de 4-pyrimidineamine et leurs utilisations en tant qu’agent anti-prolifération
US20060051406A1 (en) * 2004-07-23 2006-03-09 Manjeet Parmar Formulation of insoluble small molecule therapeutics in lipid-based carriers
GB0419160D0 (en) * 2004-08-27 2004-09-29 Novartis Ag Organic compounds
GB0419161D0 (en) * 2004-08-27 2004-09-29 Novartis Ag Organic compounds
CA2580838A1 (fr) * 2004-09-27 2006-04-06 Amgen Inc. Composes heterocycliques substitues et procedes d'utilisation
CA2584295C (fr) 2004-11-24 2014-08-26 Rigel Pharmaceuticals, Inc. Composes de spiro-2, 4-pyrimidinediamine et leurs utilisations
BRPI0606318B8 (pt) 2005-01-19 2021-05-25 Rigel Pharmaceuticals Inc composto, composição, e, uso de um composto
US20060247263A1 (en) * 2005-04-19 2006-11-02 Amgen Inc. Substituted heterocyclic compounds and methods of use
KR100602320B1 (ko) * 2005-05-03 2006-07-18 주식회사 하이닉스반도체 프로그램 속도가 균일한 비휘발성 메모리 소자
US20070203161A1 (en) 2006-02-24 2007-08-30 Rigel Pharmaceuticals, Inc. Compositions and methods for inhibition of the jak pathway
KR101312225B1 (ko) 2005-06-08 2013-09-26 리겔 파마슈티칼스, 인크. Ｊａｋ 경로의 억제를 위한 조성물 및 방법
US8604042B2 (en) 2005-11-01 2013-12-10 Targegen, Inc. Bi-aryl meta-pyrimidine inhibitors of kinases
WO2007111720A2 (fr) 2005-12-06 2007-10-04 Rigel Pharmaceuticals, Inc. Formulation d'agents thérapeutiques à base de petites molécules insolubles dans des supports lipidiques
UA89123C2 (ru) 2005-12-21 2009-12-25 Пфайзер Продактс Инк. Производные пиримидина для лечения абнормального роста клеток
TW200736232A (en) * 2006-01-26 2007-10-01 Astrazeneca Ab Pyrimidine derivatives
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
GB2451594A (en) * 2006-03-15 2009-02-04 Csir Modulation of phosphoryl transferase activity of glutamine synthetase
BRPI0621509A2 (pt) * 2006-03-15 2011-12-13 Csir modulação da atividade de fosforil transferase de glutamina sintetase
DE602007012363D1 (de) 2006-10-19 2011-03-17 Rigel Pharmaceuticals Inc 2,4-pyridimediamon-derivate als hemmer von jak-kinasen zur behandlung von autoimmunerkrankungen
EP2684874B1 (fr) 2006-10-23 2017-05-17 Cephalon, Inc. Dérivés bicycliques fusionnés de 2,4-diaminopyrimidine utilisés comme inhibiteurs de alk et de c-met
KR101364277B1 (ko) 2006-12-08 2014-02-21 아이알엠 엘엘씨 단백질 키나제 억제제로서의 화합물
EP1939185A1 (fr) * 2006-12-20 2008-07-02 Bayer Schering Pharma Aktiengesellschaft Nouveaux hetaryl-phénylènediamine-pyrimidines en tant qu'inhibiteurs de protéine kinase pour le traitement du cancer
MX2009006454A (es) 2006-12-22 2009-06-26 Hoffmann La Roche Derivados de espiro-piperidina.
FR2911137B1 (fr) * 2007-01-05 2009-02-20 Sanofi Aventis Sa Nouveaux derives de 2,4-dianilinopyrimides, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk
KR20090129434A (ko) * 2007-03-01 2009-12-16 수퍼젠, 인크. 피리미딘-2,4-디아민 유도체 및 ｊａｋ2 키나제 억제제로서의 이의 용도
EP1969929A1 (fr) 2007-03-12 2008-09-17 Bayer CropScience AG Phénylamidine substituée et son utilisation en tant que fongicide
AU2014201847B2 (en) * 2007-04-18 2015-12-24 Pfizer Products Inc. Sulfonyl amide derivatives for the treatment of abnormal cell growth
AU2016201820B2 (en) * 2007-04-18 2018-03-08 Pfizer Products Inc. Sulfonyl amide derivatives for the treatment of abnormal cell growth
WO2008129380A1 (fr) * 2007-04-18 2008-10-30 Pfizer Products Inc. Dérivés de sulfonyle amide pour le traitement d'une croissance cellulaire anormale
CA2707653A1 (fr) * 2007-12-03 2009-06-11 Boehringer Ingelheim International Gmbh Nouveaux composes
US7923450B2 (en) 2008-01-11 2011-04-12 Hoffmann-La Roche Inc. Modulators for amyloid beta
MX2010008700A (es) * 2008-02-22 2010-08-30 Hoffmann La Roche Moduladores de beta-amiloide.
US8138339B2 (en) 2008-04-16 2012-03-20 Portola Pharmaceuticals, Inc. Inhibitors of protein kinases
WO2009136995A2 (fr) 2008-04-16 2009-11-12 Portola Pharmaceuticals, Inc. Inhibiteurs de la syk protéine kinase
NZ589315A (en) 2008-04-16 2012-11-30 Portola Pharm Inc 2,6-diamino-pyrimidin-5-yl-carboxamides as Spleen tryosine kinase (syk) or Janus kinase (JAK) inhibitors
CA2723185A1 (fr) 2008-04-22 2009-10-29 Portola Pharmaceuticals, Inc. Inhibiteurs de proteines kinases
US9273077B2 (en) 2008-05-21 2016-03-01 Ariad Pharmaceuticals, Inc. Phosphorus derivatives as kinase inhibitors
DK2300013T3 (en) 2008-05-21 2017-12-04 Ariad Pharma Inc PHOSPHORUS DERIVATIVES AS KINASE INHIBITORS
DE102008049323A1 (de) * 2008-09-29 2010-04-01 Henkel Ag & Co. Kgaa Neue Entwicklerkomponenten
BRPI0920651A2 (pt) 2008-10-09 2016-01-12 Hoffmann La Roche moduladores para amiloide beta
CN102209537A (zh) 2008-11-10 2011-10-05 弗·哈夫曼-拉罗切有限公司 杂环γ分泌酶调节剂
CA2749195C (fr) * 2009-01-15 2017-03-07 Rigel Pharmaceuticals, Inc. Inhibiteurs de la proteine kinase c et leurs utilisations
US8933227B2 (en) 2009-08-14 2015-01-13 Boehringer Ingelheim International Gmbh Selective synthesis of functionalized pyrimidines
EP2464633A1 (fr) 2009-08-14 2012-06-20 Boehringer Ingelheim International GmbH Préparation régiosélective de dérivés de 2-amino-5-trifluorométhylpyrimidine
US9180127B2 (en) 2009-12-29 2015-11-10 Dana-Farber Cancer Institute, Inc. Type II Raf kinase inhibitors
US8486967B2 (en) 2010-02-17 2013-07-16 Hoffmann-La Roche Inc. Heteroaryl substituted piperidines
CA2798578C (fr) 2010-05-21 2015-12-29 Chemilia Ab Nouveaux derives de pyrimidine
US9102625B2 (en) 2010-11-01 2015-08-11 Portola Pharmaceuticals, Inc. Nicotinamides as JAK kinase modulators
US8846928B2 (en) 2010-11-01 2014-09-30 Portola Pharmaceuticals, Inc. Benzamides and nicotinamides as Syk modulators
US20130317029A1 (en) 2010-11-01 2013-11-28 Portola Pharmaceuticals, Inc. Oxypyrimidines as syk modulators
WO2012060847A1 (fr) 2010-11-07 2012-05-10 Targegen, Inc. Compositions et procédés de traitement de la myélofibrose
CA2830129C (fr) 2011-03-24 2016-07-19 Chemilia Ab Nouveaux derives de pyrimidine
US9249124B2 (en) 2011-03-30 2016-02-02 H. Lee Moffitt Cancer Center And Research Institute, Inc. Aurora kinase inhibitors and methods of making and using thereof
CN103501612B (zh) 2011-05-04 2017-03-29 阿里亚德医药股份有限公司 抑制表皮生长因子受体导致的癌症中细胞增殖的化合物
JP6105578B2 (ja) 2011-07-21 2017-03-29 トレロ ファーマシューティカルズ， インコーポレイテッド 複素環式プロテインキナーゼ阻害剤
EP3569598A1 (fr) * 2011-11-17 2019-11-20 Dana Farber Cancer Institute, Inc. Inhibiteurs de la kinase c-jun-n-terminale (jnk)
EP2782579B1 (fr) 2011-11-23 2019-01-02 Portola Pharmaceuticals, Inc. Inhibiteurs de de la pyrazine kinase
EP2606884A1 (fr) * 2011-12-21 2013-06-26 Ecole Polytechnique Fédérale de Lausanne (EPFL) Inhibiteurs de la voie de signalisation notch et leur utilisation dans le traitement des cancers
US20150166591A1 (en) 2012-05-05 2015-06-18 Ariad Pharmaceuticals, Inc. Methods and compositions for raf kinase mediated diseases
KR101446742B1 (ko) * 2012-08-10 2014-10-01 한국화학연구원 Ｎ2,ｎ4-비스(4-(피페라진-1-일)페닐)피리미딘-2,4-디아민 유도체 또는 이의 약학적으로 허용가능한 염 및 이를 유효성분으로 함유하는 암의 예방 또는 치료용 약학적 조성물
US9676756B2 (en) 2012-10-08 2017-06-13 Portola Pharmaceuticals, Inc. Substituted pyrimidinyl kinase inhibitors
WO2014063061A1 (fr) 2012-10-19 2014-04-24 Dana-Farber Cancer Institute, Inc. Petites molécules marquées de façon hydrophobe en tant qu'inducteurs de la dégradation de protéine
TR201911151T4 (tr) * 2013-03-14 2019-08-21 Tolero Pharmaceuticals Inc Jak2 ve alk2 inhibitörleri ve bunların kullanım yöntemleri.
US9611283B1 (en) 2013-04-10 2017-04-04 Ariad Pharmaceuticals, Inc. Methods for inhibiting cell proliferation in ALK-driven cancers
ES2676734T3 (es) 2013-10-18 2018-07-24 Syros Pharmaceuticals, Inc. Compuestos heteroatómicos útiles para el tratamiento de enfermedades proliferativas
AU2014337044A1 (en) 2013-10-18 2016-05-05 Dana-Farber Cancer Institute, Inc. Polycyclic inhibitors of cyclin-dependent kinase 7 (CDK7)
WO2016022460A1 (fr) * 2014-08-03 2016-02-11 H. Lee Moffitt Cancer Center And Research Institute, Inc. Puissants doubles inhibiteurs de brd4 et de kinase à utiliser en tant qu'agents thérapeutiques anticancéreux
JP6854762B2 (ja) 2014-12-23 2021-04-07 ダナ−ファーバー キャンサー インスティテュート， インコーポレイテッド サイクリン依存性キナーゼ７（ｃｄｋ７）の阻害剤
JP6861166B2 (ja) 2015-03-27 2021-04-21 ダナ−ファーバー キャンサー インスティテュート， インコーポレイテッド サイクリン依存性キナーゼの阻害剤
CA2996978A1 (fr) 2015-09-09 2017-03-16 Dana-Farber Cancer Institute, Inc. Inhibiteurs de kinases cycline-dependantes
US10738016B2 (en) 2015-10-13 2020-08-11 H. Lee Moffitt Cancer Center And Research Institute, Inc. BRD4-kinase inhibitors as cancer therapeutics
BR112019024830A2 (pt) * 2017-05-26 2020-06-09 Cancer Research Tech Ltd inibidores de bcl6 derivados de benzimidazolona
AU2018294054B2 (en) 2017-06-30 2022-05-26 Beijing Tide Pharmaceutical Co., Ltd. Rho-associated protein kinase inhibitor, pharmaceutical composition comprising same, and preparation method and use thereof
US10329282B2 (en) 2017-06-30 2019-06-25 Beijing Tide Pharmaceutical Co., Ltd. Rho-associated protein kinase inhibitor, pharmaceutical composition comprising the same, as well as preparation method and use thereof
US10323023B2 (en) 2017-06-30 2019-06-18 Beijing Tide Pharmaceutical Co., Ltd. Rho-associated protein kinase inhibitor, pharmaceutical composition comprising the same, as well as preparation method and use thereof
CN109776522B (zh) * 2017-10-30 2020-12-29 广东东阳光药业有限公司 取代的杂芳基化合物及其组合物和用途
WO2019195753A1 (fr) 2018-04-05 2019-10-10 Tolero Pharmaceuticals, Inc. Inhibiteurs de kinases axl et leur utilisation
CA3095580A1 (fr) 2018-04-13 2019-10-17 Sumitomo Dainippon Pharma Oncology, Inc. Inhibiteurs de kinase pim pour le traitement de neoplasmes myeloproliferatifs et de fibrose associee au cancer
WO2020006724A1 (fr) * 2018-07-05 2020-01-09 清华大学 Composé de dégradation ciblée de protéine fak et utilisation associée
KR20210038906A (ko) 2018-07-26 2021-04-08 스미토모 다이니폰 파마 온콜로지, 인크. 비정상적 acvr1 발현과 연관된 질환을 치료하는 방법 및 그에 사용하기 위한 acvr1 억제제
CN111362922A (zh) * 2018-12-26 2020-07-03 上海喆邺生物科技有限公司 2,4-二氨基嘧啶衍生物及其用途
WO2020167990A1 (fr) 2019-02-12 2020-08-20 Tolero Pharmaceuticals, Inc. Formulations comprenant des inhibiteurs de protéine kinase hétérocycliques
CN114105887B (zh) * 2021-09-16 2023-12-01 沈阳药科大学 一种氨基嘧啶衍生物及其制备方法和用途

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW225528B (fr) * 1992-04-03 1994-06-21 Ciba Geigy Ag
US5543520A (en) * 1993-10-01 1996-08-06 Ciba-Geigy Corporation Pyrimidine derivatives
GB9523675D0 (en) * 1995-11-20 1996-01-24 Celltech Therapeutics Ltd Chemical compounds
GB9828511D0 (en) * 1998-12-24 1999-02-17 Zeneca Ltd Chemical compounds
GB0004890D0 (en) * 2000-03-01 2000-04-19 Astrazeneca Uk Ltd Chemical compounds
GB0004887D0 (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
WO2003040141A1 (fr) * 2001-09-28 2003-05-15 Bayer Pharmaceuticals Corporation Composes d'oxazolyl-phenyl-2,4-diamino-pyrimidine, et methodes de traitement de troubles hyperproliferatifs
WO2003031406A2 (fr) * 2001-10-12 2003-04-17 Irm Llc Squelettes d'inhibiteurs de kinase et leurs methodes de preparation
EP2090571B1 (fr) * 2001-10-17 2012-05-16 Boehringer Ingelheim Pharma GmbH & Co. KG Derivés pyrimidine, agent pharamceutique contenant ces composés, utilisation et procédé de fabrication de ces composés

Also Published As

Publication number Publication date
AU2003299474A8 (en) 2004-06-15
WO2004046118A2 (fr) 2004-06-03
WO2004046118A3 (fr) 2004-08-12
AU2003299474A1 (en) 2004-06-15
WO2003095448A1 (fr) 2003-11-20

Similar Documents

Publication Publication Date Title
AU2003231231A1 (en) Pyridinyl amino pyrimidine derivatives useful for treating hyper-proliferative disorders
AU2003259249A1 (en) Pyridazinylpiperazine derivatives for treating pain
EP1511730B8 (fr) Derives de diaryle-uree utilises pour le traitement des maladies dependant des proteines kinases
SI1487805T1 (sl) Pirimidinski derivati
AU2003216660A1 (en) N-substituted-heteroaryloxy-aryl-spiro-pyrimidine-2,4,6-trione metalloproteinase inhibitors
AU2003275632A1 (en) N-oxide compounds
PL372756A1 (en) Nicotinamide derivatives useful as pde4 inhibitors
AU2003274025A1 (en) Pyridine derivatives useful as herbicides
AU2003216290A1 (en) Secure online purchasing
AU2003219410A1 (en) Triaryl-oxy-aryl-spiro-pyrimidine-2, 4, 6-trione metalloproteinase inhibitors
AU2003237446A1 (en) Pyrazole-derivatives as p38 kinase inhibitors
ZA200501418B (en) Benzenesulfonate salts of 4-fluoro-2-cyanopyrrolidine derivatives
AU2003202116A1 (en) Nicotinamide derivatives useful as pde4 inhibitors
AU2003210597A1 (en) Methods for treating eye disorders
AU2002339185A1 (en) Pyridine and pyrimidine derivatives
AU2003216677A1 (en) Triaryl-oxy-aryloxy-pyrimidine-2,4,6-trione metalloproteinase inhibitors
AU2003205731A1 (en) Mono- and biacylphosphine derivatives
AU2003260984A1 (en) S-(-)-amlodipine nicotinate and process for the preparation thereof
AU2003244181A1 (en) Phenoxypyridine derivative or salt thereof
PL376897A1 (pl) Podstawione 6-(2-chlorowcofenylo) triazolopirymidyny
AU2003261756A1 (en) Acrylamide derivatives
AU2003264252A1 (en) Pyridine-substituted pyrazolopyridine derivative
AU2003223475A1 (en) Substituted pyrazine derivatives
AU2003231459A1 (en) Pyrimidine derivative
AU2002368112A1 (en) Pyrimidine derivatives

Legal Events

Date Code Title Description
MK6 Application lapsed section 142(2)(f)/reg. 8.3(3) - pct applic. not entering national phase
TH Corrigenda

Free format text: IN VOL 18, NO 2, PAGE(S) 494 UNDER THE HEADING APPLICATIONS OPI - NAME INDEX UNDER THE NAME CHEN, Y.; HART, B.; WOOD, J.; CHEN, J. AND BAYER PHARMACEUTICALS CORPORATION, APPLICATION NO. 2003231231, UNDER INID(43) CORRECT THE PUBLICATION DATE TO READ 24.11.2003