WO2004060305A3 - Anti-cancer medicaments - Google Patents

Anti-cancer medicaments Download PDF

Info

Publication number
WO2004060305A3
WO2004060305A3 PCT/US2003/041425 US0341425W WO2004060305A3 WO 2004060305 A3 WO2004060305 A3 WO 2004060305A3 US 0341425 W US0341425 W US 0341425W WO 2004060305 A3 WO2004060305 A3 WO 2004060305A3
Authority
WO
WIPO (PCT)
Prior art keywords
cancer medicaments
abl
kinase proteins
novel compounds
compounds
Prior art date
Application number
PCT/US2003/041425
Other languages
French (fr)
Other versions
WO2004060305A2 (en
Inventor
Daniel L Flynn
Peter A Petrillo
Original Assignee
Deciphera Pharmaceuticals Llc
Daniel L Flynn
Peter A Petrillo
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 Deciphera Pharmaceuticals Llc, Daniel L Flynn, Peter A Petrillo filed Critical Deciphera Pharmaceuticals Llc
Priority to JP2005508623A priority Critical patent/JP2006519765A/en
Priority to MXPA05007237A priority patent/MXPA05007237A/en
Priority to AU2003303639A priority patent/AU2003303639A1/en
Priority to EP03814980A priority patent/EP1590344A4/en
Priority to BR0317863-3A priority patent/BR0317863A/en
Priority to CA002511840A priority patent/CA2511840A1/en
Publication of WO2004060305A2 publication Critical patent/WO2004060305A2/en
Publication of WO2004060305A3 publication Critical patent/WO2004060305A3/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/32One oxygen, sulfur or nitrogen atom
    • C07D239/42One nitrogen atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/16Central respiratory analeptics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/06Antigout agents, e.g. antihyperuricemic or uricosuric agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/06Antianaemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/08Vasodilators for multiple indications
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/10Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Abstract

Novel compounds and methods of using those compounds for the treatment of oncological conditions are provided. In a preferred embodiment, modulation of the activation states of abl or bcr-abl α-kinase proteins comprises the step of contacting the kinase proteins with the novel compounds.
PCT/US2003/041425 2002-12-31 2003-12-26 Anti-cancer medicaments WO2004060305A2 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
JP2005508623A JP2006519765A (en) 2002-12-31 2003-12-26 Anticancer drug
MXPA05007237A MXPA05007237A (en) 2002-12-31 2003-12-26 Anti-cancer medicaments.
AU2003303639A AU2003303639A1 (en) 2002-12-31 2003-12-26 Anti-cancer medicaments
EP03814980A EP1590344A4 (en) 2002-12-31 2003-12-26 Anti-cancer medicaments
BR0317863-3A BR0317863A (en) 2002-12-31 2003-12-26 Anticancer Drugs
CA002511840A CA2511840A1 (en) 2002-12-31 2003-12-26 Anti-cancer medicaments

Applications Claiming Priority (11)

Application Number Priority Date Filing Date Title
US43748702P 2002-12-31 2002-12-31
US43740302P 2002-12-31 2002-12-31
US43741502P 2002-12-31 2002-12-31
US43730402P 2002-12-31 2002-12-31
US60/437,415 2002-12-31
US60/437,403 2002-12-31
US60/437,487 2002-12-31
US60/437,304 2002-12-31
US46380403P 2003-04-18 2003-04-18
US60/463,804 2003-04-18
US10/746,460 US7144911B2 (en) 2002-12-31 2003-12-24 Anti-inflammatory medicaments

Publications (2)

Publication Number Publication Date
WO2004060305A2 WO2004060305A2 (en) 2004-07-22
WO2004060305A3 true WO2004060305A3 (en) 2005-02-10

Family

ID=32719725

Family Applications (2)

Application Number Title Priority Date Filing Date
PCT/US2003/041425 WO2004060305A2 (en) 2002-12-31 2003-12-26 Anti-cancer medicaments
PCT/US2003/041449 WO2004060306A2 (en) 2002-12-31 2003-12-26 Anti-inflammatory medicaments

Family Applications After (1)

Application Number Title Priority Date Filing Date
PCT/US2003/041449 WO2004060306A2 (en) 2002-12-31 2003-12-26 Anti-inflammatory medicaments

Country Status (9)

Country Link
US (7) US7144911B2 (en)
EP (2) EP1590344A4 (en)
JP (1) JP2006514691A (en)
AU (1) AU2003303641A1 (en)
BR (1) BR0317872A (en)
CA (1) CA2513627A1 (en)
MX (1) MXPA05007236A (en)
TW (1) TW200427672A (en)
WO (2) WO2004060305A2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8372971B2 (en) 2004-08-25 2013-02-12 Targegen, Inc. Heterocyclic compounds and methods of use
US8481536B2 (en) 2004-04-08 2013-07-09 Targegen, Inc. Benzotriazine inhibitors of kinases
US8604042B2 (en) 2005-11-01 2013-12-10 Targegen, Inc. Bi-aryl meta-pyrimidine inhibitors of kinases
US9233956B2 (en) 2008-05-06 2016-01-12 Novartis Ag Benzene sulfonamide thiazole and oxazole compounds

Families Citing this family (91)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7202257B2 (en) * 2003-12-24 2007-04-10 Deciphera Pharmaceuticals, Llc Anti-inflammatory medicaments
US20080045706A1 (en) * 2002-12-31 2008-02-21 Flynn Daniel L Anti-inflammatory medicaments
US7144911B2 (en) 2002-12-31 2006-12-05 Deciphera Pharmaceuticals Llc Anti-inflammatory medicaments
JP2006518738A (en) * 2003-02-12 2006-08-17 トランス テック ファーマ,インコーポレイテッド Substituted azole derivatives as therapeutic agents
CN1798738A (en) 2003-04-03 2006-07-05 麦克公司 Biaryl substituted pyrazoles as sodium channel blockers
ES2338557T3 (en) * 2003-06-13 2010-05-10 Novartis Ag DERIVATIVES OF 2-AMINOPIRIMIDINE USED AS INHIBITORS OF RAF CINASA.
KR101204247B1 (en) 2003-07-22 2012-11-22 아스텍스 테라퓨틱스 리미티드 3,4-disubstituted 1h-pyrazole compounds and their use as cyclin dependent kinases cdk and glycogen synthase kinase-3 gsk-3 modulators
KR100854211B1 (en) 2003-12-18 2008-08-26 동아제약주식회사 Novel oxazolidinone derivatives, a process for the preparation thereof and pharmaceutical composition comprising the same for antibiotics
CA2551909C (en) * 2004-02-12 2011-10-11 Transtech Pharma, Inc. Substituted azole derivatives, compositions, and methods of use
DE602005024274D1 (en) 2004-07-16 2010-12-02 Sunesis Pharmaceuticals Inc AS AURORA KINASE INHIBITORS USEFUL THIENOPYRIMIDINE
WO2006045581A1 (en) * 2004-10-21 2006-05-04 Neuropharma, S.A. The use of 1, 2, 4-thiadiazolidine-3, 5-diones as ppar activators
US7741479B2 (en) 2004-12-07 2010-06-22 Locus Pharmaceuticals, Inc. Urea inhibitors of MAP kinases
US7612200B2 (en) 2004-12-07 2009-11-03 Locus Pharmaceuticals, Inc. Inhibitors of protein kinases
WO2006068591A1 (en) * 2004-12-20 2006-06-29 Astrazeneca Ab Novel pyrazole derivatives and their use as modulators of nicotinic acetylcholine receptors
AU2005325676A1 (en) * 2004-12-23 2006-08-03 Deciphera Pharmaceuticals, Llc Anti-inflammatory medicaments
JP5197016B2 (en) * 2004-12-23 2013-05-15 デシファラ ファーマスーティカルズ, エルエルシー Enzyme modulators and therapy
US8404718B2 (en) 2005-01-21 2013-03-26 Astex Therapeutics Limited Combinations of pyrazole kinase inhibitors
AR054425A1 (en) 2005-01-21 2007-06-27 Astex Therapeutics Ltd PIPERIDIN ADDITION SALTS 4-IL-ACID AMID 4- (2,6-DICLORO-BENZOILAMINO) 1H-PIRAZOL-3-CARBOXILICO.
DK1928454T3 (en) 2005-05-10 2014-11-03 Intermune Inc PYRIDONE DERIVATIVES FOR MODULATING STRESS-ACTIVATED PROTEINKINATION SYSTEM
WO2006137421A1 (en) * 2005-06-21 2006-12-28 Kyowa Hakko Kogyo Co., Ltd. Agent for topical administration
EA019385B1 (en) 2006-01-30 2014-03-31 ТРАНСТЕК ФАРМА ЭлЭлСи Substituted imidazole derivatives, pharmaceutical compositions containing them and use thereof as ptpase inhibitors
US8188113B2 (en) 2006-09-14 2012-05-29 Deciphera Pharmaceuticals, Inc. Dihydropyridopyrimidinyl, dihydronaphthyidinyl and related compounds useful as kinase inhibitors for the treatment of proliferative diseases
US7790756B2 (en) * 2006-10-11 2010-09-07 Deciphera Pharmaceuticals, Llc Kinase inhibitors useful for the treatment of myleoproliferative diseases and other proliferative diseases
US20110189167A1 (en) * 2007-04-20 2011-08-04 Flynn Daniel L Methods and Compositions for the Treatment of Myeloproliferative Diseases and other Proliferative Diseases
MX2009011343A (en) * 2007-04-20 2009-11-05 Deciphera Pharmaceuticals Llc Kinase inhibitors useful for the treatment of myleoproliferative diseases and other proliferative diseases.
EP2152079A4 (en) * 2007-06-04 2011-03-09 Avila Therapeutics Inc Heterocyclic compounds and uses thereof
US8367686B2 (en) * 2007-06-07 2013-02-05 Intra-Cellular Therapies, Inc. Heterocycle compounds and uses thereof
WO2009042565A2 (en) * 2007-09-26 2009-04-02 The University Of North Carolina At Chapel Hill Inhibitors of eppin/semenogelin binding as male contraceptives
PL2195312T3 (en) 2007-10-09 2013-04-30 Merck Patent Gmbh Pyridine derivatives useful as glucokinase activators
WO2009075874A1 (en) * 2007-12-13 2009-06-18 Amgen Inc. Gamma secretase modulators
ES2567283T3 (en) 2008-06-03 2016-04-21 Intermune, Inc. Compounds and methods to treat inflammatory and fibrotic disorders
AU2009299555B2 (en) 2008-10-02 2014-01-16 Respivert Limited p38 map kinase inhibitors
GB0818033D0 (en) 2008-10-02 2008-11-05 Respivert Ltd Novel compound
EP2757104B1 (en) * 2008-10-10 2019-08-14 Merck Sharp & Dohme Corp. Compounds used in the synthesis of oxazolidinones
KR20110099687A (en) * 2008-10-29 2011-09-08 데시페라 파마슈티칼스, 엘엘씨. Cyclopropane amides and analogs exhibiting anti-cancer and anti-proliferative activities
NZ593104A (en) * 2008-12-11 2012-11-30 Respivert Ltd P38 map kinase inhibitors
CU24089B1 (en) 2009-02-03 2015-04-29 Trius Therapeutics CRYSTALLINE FORM OF DIHYDROGEN PHOSPHATE R) -3- (4- (2- (2-METHYLTRETAZOL-5-IL) -3-FLUOROPHENYL) -5-HYDROXIMETHYL OXAZOLIDIN-2-ONA
GB0905955D0 (en) 2009-04-06 2009-05-20 Respivert Ltd Novel compounds
US8580767B2 (en) * 2009-05-28 2013-11-12 Trius Therapeutics, Inc. Oxazolidinone containing dimer compounds, compositions and methods to make and use
WO2011150198A1 (en) 2010-05-27 2011-12-01 Ambit Biosciences Corporation Azolyl urea compounds and methods of use thereof
AU2010363329A1 (en) 2010-11-07 2013-05-09 Targegen, Inc. Compositions and methods for treating myelofibrosis
DK2712358T3 (en) 2011-05-13 2017-02-06 Array Biopharma Inc PYRROLIDINYLUREA, PYRROLIDINYLTHIOUREA AND PYRROLIDINYLGUANIDE IN COMPOUNDS AS TRKA-KINASE INHIBITORS
NZ731797A (en) 2012-04-24 2018-08-31 Vertex Pharma Dna-pk inhibitors
US8461179B1 (en) 2012-06-07 2013-06-11 Deciphera Pharmaceuticals, Llc Dihydronaphthyridines and related compounds useful as kinase inhibitors for the treatment of proliferative diseases
AR092742A1 (en) 2012-10-02 2015-04-29 Intermune Inc ANTIFIBROTIC PYRIDINONES
US9790178B2 (en) 2012-11-13 2017-10-17 Array Biopharma Inc. Pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
WO2014078408A1 (en) 2012-11-13 2014-05-22 Array Biopharma Inc. Bicyclic heteroaryl urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors
US9969694B2 (en) 2012-11-13 2018-05-15 Array Biopharma Inc. N-(arylalkyl)-N′-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
PT2922844T (en) 2012-11-13 2018-04-02 Array Biopharma Inc N-pyrrolidinyl, n'-pyrazolyl- urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors
US9546156B2 (en) 2012-11-13 2017-01-17 Array Biopharma Inc. N-bicyclic aryl,N'-pyrazolyl urea, thiourea, guanidine cyanoguanidine compounds as TrkA kinase inhibitors
US9981959B2 (en) 2012-11-13 2018-05-29 Array Biopharma Inc. Thiazolyl and oxazolyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
WO2014078417A1 (en) 2012-11-13 2014-05-22 Array Biopharma Inc. Pyrazolyl urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors
WO2014078325A1 (en) 2012-11-13 2014-05-22 Array Biopharma Inc. N-(monocyclic aryl),n'-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors
LT2920166T (en) 2012-11-13 2016-12-12 Array Biopharma, Inc. Bicyclic urea, thiourea, guanidine and cyanoguanidine compounds useful for the treatment of pain
US9828360B2 (en) 2012-11-13 2017-11-28 Array Biopharma Inc. Pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
ES2900061T3 (en) 2013-03-12 2022-03-15 Vertex Pharma DNA-PK inhibitors
DK3424920T3 (en) 2013-10-17 2020-06-08 Vertex Pharma CO CRYSTALS OF (S) -N-METHYL-8- (1 - ((2'-METHYL- [4,5'-BIPYRIMIDIN] -6-YL) AMINO) PROPAN-2-YL) QUINOLIN-4-CARBOXAMIDE AND DEUTERATED DERIVATIVES THEREOF AS DNA-PK INHIBITORS
CN106459042B (en) 2014-04-02 2019-06-28 英特穆恩公司 Anti-fibrosis pyridinone
KR101998461B1 (en) 2014-05-15 2019-07-09 어레이 바이오파마 인크. 1-((3s,4r)-4-(3-fluorophenyl)-1-(2-methoxyethyl)pyrrolidin-3-yl)-3-(4-methyl-3-(2-methylpyrimidin-5-yl)-1-phenyl-1h-pyrazol-5-yl)urea as a trka kinase inhibitor
SG10202006053UA (en) 2014-08-04 2020-07-29 Nuevolution As Optionally fused heterocyclyl-substituted derivatives of pyrimidine useful for the treatment of inflammatory, metabolic, oncologic and autoimmune diseases
US11214565B2 (en) 2015-11-20 2022-01-04 Denali Therapeutics Inc. Compound, compositions, and methods
WO2017151409A1 (en) 2016-02-29 2017-09-08 University Of Florida Research Foundation, Incorporated Chemotherapeutic methods
US11028080B2 (en) 2016-03-11 2021-06-08 Denali Therapeutics Inc. Substituted pyrimidines as LRKK2 inhibitors
EP3472153B1 (en) 2016-06-16 2021-09-22 Denali Therapeutics Inc. Pyrimidin-2-ylamino-1h-pyrazols as lrrk2 inhibitors for use in the treatment of neurodegenerative disorders
AU2017335648B2 (en) 2016-09-27 2022-02-17 Vertex Pharmaceuticals Incorporated Method for treating cancer using a combination of DNA-damaging agents and DNA-PK inhibitors
CN108203450B (en) * 2016-12-19 2020-05-19 南京工业大学 Preparation method and application of amino phosphonate containing arylpyrazole compound
GB201721185D0 (en) 2017-12-18 2018-01-31 Nodthera Ltd Sulphonyl urea derivatives
TWI767148B (en) 2018-10-10 2022-06-11 美商弗瑪治療公司 Inhibiting fatty acid synthase (fasn)
US11066404B2 (en) 2018-10-11 2021-07-20 Incyte Corporation Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors
AU2019387370A1 (en) 2018-11-30 2021-06-10 Nuvation Bio Inc. Pyrrole and pyrazole compounds and methods of use thereof
EP4303583A3 (en) 2018-12-28 2024-03-27 Deciphera Pharmaceuticals, LLC Methods of treating disorders using csf1r inhibitors cross-reference to related applications
US11384083B2 (en) 2019-02-15 2022-07-12 Incyte Corporation Substituted spiro[cyclopropane-1,5′-pyrrolo[2,3-d]pyrimidin]-6′(7′h)-ones as CDK2 inhibitors
WO2020180959A1 (en) 2019-03-05 2020-09-10 Incyte Corporation Pyrazolyl pyrimidinylamine compounds as cdk2 inhibitors
WO2020205560A1 (en) 2019-03-29 2020-10-08 Incyte Corporation Sulfonylamide compounds as cdk2 inhibitors
WO2020223558A1 (en) 2019-05-01 2020-11-05 Incyte Corporation Tricyclic amine compounds as cdk2 inhibitors
US11440914B2 (en) 2019-05-01 2022-09-13 Incyte Corporation Tricyclic amine compounds as CDK2 inhibitors
RS64755B1 (en) 2019-05-10 2023-11-30 Deciphera Pharmaceuticals Llc Heteroarylaminopyrimidine amide autophagy inhibitors and methods of use thereof
TW202108573A (en) 2019-05-10 2021-03-01 美商迪賽孚爾製藥有限公司 Phenylaminopyrimidine amide autophagy inhibitors and methods of use thereof
EP3983081A1 (en) 2019-06-17 2022-04-20 Deciphera Pharmaceuticals, LLC Aminopyrimidine amide autophagy inhibitors and methods of use thereof
WO2021030405A1 (en) 2019-08-12 2021-02-18 Deciphera Pharmaceuticals, Llc Ripretinib for treating gastrointestinal stromal tumors
MX2022001863A (en) 2019-08-12 2022-05-30 Deciphera Pharmaceuticals Llc Ripretinib for treating gastrointestinal stromal tumors.
CN116348458A (en) 2019-08-14 2023-06-27 因赛特公司 Imidazolylpyrimidinylamine compounds as CDK2 inhibitors
WO2021072232A1 (en) 2019-10-11 2021-04-15 Incyte Corporation Bicyclic amines as cdk2 inhibitors
WO2021124277A1 (en) 2019-12-20 2021-06-24 Nuevolution A/S Compounds active towards nuclear receptors
CN114829345A (en) * 2019-12-27 2022-07-29 日本烟草产业株式会社 Acylsulfonamide compound and medicinal use thereof
KR20220123058A (en) 2019-12-30 2022-09-05 데시페라 파마슈티칼스, 엘엘씨. 1-(4-Bromo-5-(1-ethyl-7-(methylamino)-2-oxo-1,2-dihydro-1,6-naphthyridin-3-yl)-2-fluorophenyl ) -3-Phenylurea composition
RS65058B1 (en) 2019-12-30 2024-02-29 Deciphera Pharmaceuticals Llc Amorphous kinase inhibitor formulations and methods of use thereof
JP2023519603A (en) 2020-03-31 2023-05-11 ヌエヴォリューション・アクティーゼルスカブ Compounds active against nuclear receptors
AU2021249530A1 (en) 2020-03-31 2022-12-01 Nuevolution A/S Compounds active towards nuclear receptors
IL302807A (en) 2020-11-18 2023-07-01 Deciphera Pharmaceuticals Llc Gcn2 and perk kinase inhibitors and methods of use thereof
US11779572B1 (en) 2022-09-02 2023-10-10 Deciphera Pharmaceuticals, Llc Methods of treating gastrointestinal stromal tumors

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6174905B1 (en) * 1996-09-30 2001-01-16 Mitsui Chemicals, Inc. Cell differentiation inducer
US6441005B1 (en) * 1999-07-28 2002-08-27 Pharmacia & Upjohn Company Oxazolidinone compounds and compositions, and methods of using the same

Family Cites Families (121)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US181411A (en) * 1876-08-22 Improvement in frame-squaring tools
US8898A (en) * 1852-04-20 Improved device for casting circle-plates, roses
US186221A (en) * 1877-01-16 Improvement in time-locks
DE1115350B (en) 1959-04-17 1961-10-19 Siemens Ag Circuit breaker, in particular line circuit breaker, with a drive mechanism consisting of a knee joint for the switching element
GB971307A (en) 1961-03-02 1964-09-30 Wellcome Found 5-anilinopyrimidines
DE1670701A1 (en) 1966-05-23 1970-11-12 Bayer Ag Process for the preparation of thiaimidazolidines
GB1127875A (en) 1967-03-23 1968-09-18 Parke Davis & Co 4-(5-nitro-2-furyl) thiazolyl hydantoins and hydrouracils
DE2156343A1 (en) 1970-11-13 1972-05-18 Ici Ltd Heat-stable aromatic polymers - containing sulphone -or oxo-groups
US3818024A (en) * 1972-02-16 1974-06-18 Velsicol Chemical Corp Benzothiazol substituted thiadiazolidines
CH565887A5 (en) 1972-08-22 1975-08-29 Ciba Geigy Ag
US3939122A (en) * 1973-04-11 1976-02-17 Bayer Aktiengesellschaft Process for the preparation of compounds which contain hydantoin rings
FR2337554A1 (en) 1976-01-08 1977-08-05 Buzas Andre (1)-Substd. (2)-phenyl-(4)-butyl-pyrazolidine dione salts - analgesics and antiinflammatories with little ulcerogenic action
US4093624A (en) * 1977-01-31 1978-06-06 Icn Pharmaceuticals, Inc. 1,2,4-Thiadiazolidine-3,5-dione
FR2396549A2 (en) 1977-07-06 1979-02-02 Buzas Andre Antiinflammatory pyrazolidine-di:one cpds. - with reduced ulcerogenic activity
GB2036480B (en) 1977-08-02 1982-06-03 Western Electric Co Reversible analogue to digital converter with high precision
US4256758A (en) 1979-06-11 1981-03-17 Merck & Co., Inc. 4-Substituted-3-hydroxy-3-pyrroline-2,5-dione inhibitors of glycolic acid oxidase
US4298743A (en) 1979-09-11 1981-11-03 Merck & Co., Inc. 4-(Substituted phenyl thiazolyl)-3-hydroxy-3-pyrroline-2,5-diones
US4296237A (en) * 1979-09-11 1981-10-20 Merck & Co., Inc. 4-(Pyridyl, piperazinyl and thiazolyl substituted thiazolyl)-3-hydroxy-3-pyrroline-2,5-diones
US4432992A (en) * 1979-11-05 1984-02-21 Merck & Co., Inc. 4-[5(and 4)-Substituted-2-thienyl]-3-hydroxy-3-pyrroline-2,5-dione inhibitors of glycolic acid oxidase
US4366189A (en) 1979-12-21 1982-12-28 Ciba-Geigy Corporation 4-Heterocyclyl-4'-vinylstilbenes
JPS5915247A (en) 1982-07-16 1984-01-26 Mitsubishi Paper Mills Ltd Formation of image
JPS59177557A (en) 1983-03-28 1984-10-08 Fuji Photo Film Co Ltd Silver halide color photosensitive material
DE3406329A1 (en) 1984-02-22 1985-08-22 Merck Patent Gmbh, 6100 Darmstadt PYRIDONE
US4816454A (en) * 1984-09-21 1989-03-28 Cassella Aktiengesellschaft 4,5-dihydro-3(2H)-pyridazinones and their pharmacological use
US5103014A (en) * 1987-09-30 1992-04-07 American Home Products Corporation Certain 3,3'-[[[(2-phenyl-4-thiazolyl)methoxy]phenyl]methylene]dithiobis-propanoic acid derivatives
AU606808B2 (en) 1988-06-29 1991-02-14 Otsuka Pharmaceutical Factory, Inc. Arylcarboxamide substituted by alkylphosphonates, process for preparing the same and a pharmaceutical composition containing the same
US5235786A (en) * 1989-11-06 1993-08-17 Mitsubishi Jukogyo Kabushiki Kaisha Hourglass worm gear
GB9012936D0 (en) 1990-06-11 1990-08-01 Fujisawa Pharmaceutical Co Thiophene derivatives,processes for preparation thereof and pharmaceutical composition comprising the same
US5254715A (en) 1990-11-07 1993-10-19 Warner-Lambert Company Aminosulfonyl carbamates
DE69221794T2 (en) 1991-01-21 1998-03-19 Shionogi Seiyaku Kk 3-BENZYLIDEN-1-CARBAMOYL-2-PYRROLIDONE ANALOG
US5162360A (en) 1991-06-24 1992-11-10 Warner-Lambert Company 2-heteroatom containing urea and thiourea ACAT inhibitors
GB9816837D0 (en) 1998-08-04 1998-09-30 Zeneca Ltd Amide derivatives
TW225528B (en) * 1992-04-03 1994-06-21 Ciba Geigy Ag
CA2142900A1 (en) 1992-08-20 1994-03-03 Terry Russell Knapp Penile implant with triglyceride fill
DE4302702A1 (en) 1993-02-01 1994-08-04 Bayer Ag Arylaminosulfonylureas
EP0692483A1 (en) 1993-03-30 1996-01-17 Yoshitomi Pharmaceutical Industries, Ltd. Cell adhesion inhibitor and thienotriazolodiazepine compound
WO1994024095A1 (en) 1993-04-16 1994-10-27 Abbott Laboratories Immunosuppressive agents
CA2123728A1 (en) * 1993-05-21 1994-11-22 Noriyoshi Sueda Urea derivatives and their use as acat inhibitors
NO932986L (en) 1993-08-20 1995-02-21 Leiv Sandvik Headrest device
DE4337847A1 (en) 1993-11-05 1995-05-11 Bayer Ag Substituted phenylaminosulphonylureas
EP0733048A1 (en) 1993-12-07 1996-09-25 Smithkline Beecham Plc Heterocyclic biphenylylamides useful as 5ht1d antagonists
DE4343831A1 (en) 1993-12-22 1995-06-29 Magyar Tudomanyos Akademia New N-substd. N-acyloxy:methyl-N'-sulphonyl-urea cpds
FR2715155B1 (en) 1994-01-19 1996-07-26 Mayoly Spindler Monoamine oxidase B inhibitors and methods of preparing them.
DE4414840A1 (en) 1994-04-28 1995-11-02 Bayer Ag Substituted phenylaminosulfonylureas
PT1221440E (en) 1994-06-15 2007-07-20 Otsuka Pharma Co Ltd Benzoheterocyclic derivatives useful as vasopressin or oxytocin modulators
JP3117721B2 (en) 1994-11-24 2000-12-18 エフ・ホフマン−ラ ロシュ アーゲー New benzyl pyrimidines
US5494925A (en) * 1994-12-02 1996-02-27 Sterling Winthrop Inc. 2-heterocyclyloxymethyl and 2-heterocyclylthiomethyl-1,2,5-thiadiazolidin-3-one 1,1-dioxides and compositions and method of use thereof
BR9510419A (en) 1994-12-22 1998-05-19 Smithkline Beecham Plc Process tetracyclic spiro compounds for their preparation and use as 5ht1d receptor antagonists
US5716542A (en) 1995-04-24 1998-02-10 Takasago International Corporation Liquid crystal compound and liquid crystal composition containing the same
JPH09221476A (en) 1995-12-15 1997-08-26 Otsuka Pharmaceut Co Ltd Medicinal composition
GB9605945D0 (en) 1996-03-21 1996-05-22 Smithkline Beecham Plc Novel compounds
JPH107804A (en) 1996-06-25 1998-01-13 Japan Synthetic Rubber Co Ltd Thermosetting resin composition
GB9623833D0 (en) 1996-11-16 1997-01-08 Zeneca Ltd Chemical compound
US6020357A (en) * 1996-12-23 2000-02-01 Dupont Pharmaceuticals Company Nitrogen containing heteroaromatics as factor Xa inhibitors
ATE230742T1 (en) 1997-03-27 2003-01-15 Great Lakes Chemical Europ 2-(2'-HYDROXPHENYL)-BENZOTRIAZOLES AND THEIR USE AS LIGHT PROTECTIVE AGENTS FOR ORGANIC POLYMERS
JP4344960B2 (en) 1997-05-23 2009-10-14 バイエル、コーポレイション Inhibition of p38 kinase activity by arylureas
US6235786B1 (en) 1997-08-06 2001-05-22 Abbott Laboratories Reverse hydroxamate inhibitors of matrix metalloproteinases
US6294573B1 (en) * 1997-08-06 2001-09-25 Abbott Laboratories Reverse hydroxamate inhibitors of matrix metalloproteinases
AU739066B2 (en) 1997-09-23 2001-10-04 Astrazeneca Ab Amide derivatives for the treatment of diseases mediated by cytokines
IT1295933B1 (en) 1997-10-30 1999-05-28 Great Lakes Chemical Italia 2- (2'-HYDROXYPHENYL) BENZOTHRIAZOLS AND PROCEDURE FOR THEIR PREPARATION
AU1367599A (en) * 1997-11-03 1999-05-24 Boehringer Ingelheim Pharmaceuticals, Inc. Aromatic heterocyclic compounds as anti-inflammatory agents
JP2001526222A (en) 1997-12-22 2001-12-18 バイエル コーポレイション Inhibition of p38 kinase activity using aryl and heteroaryl substituted heterocyclic ureas
EP1041982B1 (en) 1997-12-22 2011-10-19 Bayer HealthCare LLC INHIBITION OF p38 KINASE ACTIVITY USING SUBSTITUTED HETEROCYCLIC UREAS
BR9814374B1 (en) 1997-12-22 2013-09-17 "Substituted heterocyclic ureas and compositions comprising them"
JP4395823B2 (en) 1997-12-22 2010-01-13 バイエル コーポレイション Inhibition of RAF kinase using aryl and heteroaryl substituted heterocyclic ureas
NZ333399A (en) 1997-12-24 2000-05-26 Sankyo Co Cyclooxygenase-2 inhibitors (COX-2) for the prevention and treatment of tumors, cachexia and tumor-metastasis
JPH11209350A (en) 1998-01-26 1999-08-03 Eisai Co Ltd Nitrogen-containing heterocyclic derivative and medicine containing the same
EP0956855B1 (en) 1998-04-24 2003-03-12 K.U. Leuven Research & Development Immunosuppressive effects of 8 substituted xanthine derivatives
ATE282590T1 (en) 1998-05-15 2004-12-15 Astrazeneca Ab BENZAMIDE DERIVATIVES FOR THE TREATMENT OF CYTOKINE-MEDIATED DISEASES
WO2000002851A1 (en) 1998-07-08 2000-01-20 Aventis Pharma Deutschland Gmbh Sulfur substituted sulfonylaminocarboxylic acid n-arylamides, their preparation, their use and pharmaceutical preparations comprising them
US6197599B1 (en) 1998-07-30 2001-03-06 Guorong Chin Method to detect proteins
US6342516B1 (en) 1998-07-31 2002-01-29 Nippon Soda Co., Ltd. Phenylazole compounds, process for producing the same and drugs for hyperlipemia
JP3602343B2 (en) * 1998-09-02 2004-12-15 アルプス電気株式会社 Display device
CA2340454A1 (en) 1998-09-25 2000-04-06 Astrazeneca Ab Benzamide derivatives and their use as cytokine derivatives
ATE284387T1 (en) 1998-10-08 2004-12-15 Smithkline Beecham Plc 3-(3-CHLORO-4-HYDROXYPHENYLAMINO)-4-(2-NITROPHENYL)-1H-PYRROL-2,5-DIONE AS A GLYCOGEN SYNTHASE KINASE-3 INHIBITOR (GSK-3)
EP2298311B1 (en) 1999-01-13 2012-05-09 Bayer HealthCare LLC w-Carboxy aryl substituted diphenyl ureas as p38 kinase inhibitors
UA73492C2 (en) * 1999-01-19 2005-08-15 Aromatic heterocyclic compounds as antiinflammatory agents
JP4820488B2 (en) * 1999-03-12 2011-11-24 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 Compounds useful as anti-inflammatory drugs
JP2000275886A (en) 1999-03-23 2000-10-06 Konica Corp Electrophotographic photoreceptor and process cartridge and image forming device using the same
US6548529B1 (en) 1999-04-05 2003-04-15 Bristol-Myers Squibb Company Heterocyclic containing biphenyl aP2 inhibitors and method
US6410254B1 (en) 1999-05-18 2002-06-25 Cytokinetics Compositions and assays utilizing ADP or phosphate for detecting protein modulators
JP3972163B2 (en) 1999-06-18 2007-09-05 株式会社大塚製薬工場 Phosphonic acid diester derivatives
CN1222520C (en) 1999-08-12 2005-10-12 沃泰克斯药物股份有限公司 Inhibitors of c-JUN N-terminal kinase (JNK) and other protein kinases
AR035016A1 (en) 1999-08-25 2004-04-14 Takeda Chemical Industries Ltd COMPOSITION OF AZOL PROMOTER OF PRODUCTION / SECRETION OF NEUROTROFINE, COMPOSITE PRODROGA OF THE SAME, PHARMACEUTICAL COMPOSITION THAT INCLUDES IT AND USE OF THE SAME TO PREPARE THIS LAST.
JP4316787B2 (en) 2000-01-11 2009-08-19 壽製薬株式会社 An ether or amide derivative, a process for producing the same, and a therapeutic agent for diabetes containing the same,
US6525046B1 (en) * 2000-01-18 2003-02-25 Boehringer Ingelheim Pharmaceuticals, Inc. Aromatic heterocyclic compounds as antiinflammatory agents
GB0008264D0 (en) 2000-04-04 2000-05-24 Smithkline Beecham Plc Novel method and compounds
US6500628B1 (en) 2000-05-25 2002-12-31 Millennium Pharmaceuticals, Inc. Nucleic acid molecules encoding human kinase and phosphatase homologues and uses therefor
MXPA02011750A (en) 2000-06-14 2003-03-27 Warner Lambert Co 1,2,4-trisubstituted benzenes as inhibitors of 15-lipoxygenase.
AU2001277723A1 (en) 2000-08-11 2002-02-25 Nippon Chemiphar Co., Ltd. Ppardelta activators
US6645990B2 (en) * 2000-08-15 2003-11-11 Amgen Inc. Thiazolyl urea compounds and methods of uses
US20020173507A1 (en) * 2000-08-15 2002-11-21 Vincent Santora Urea compounds and methods of uses
US20030181411A1 (en) 2002-03-20 2003-09-25 Elan Pharma International Ltd. Nanoparticulate compositions of mitogen-activated protein (MAP) kinase inhibitors
WO2002028835A1 (en) 2000-10-05 2002-04-11 Fujisawa Pharmaceutical Co., Ltd. Benzamide compounds as apo b secretion inhibitors
EP1337255A4 (en) 2000-10-19 2006-01-25 Smithkline Beecham Corp Use of p38 inhibitors for the treatment of inflammation-enhanced cough
PL209733B1 (en) 2000-10-27 2011-10-31 Novartis Ag Treatment of gastrointestinal stromal tumors
EP1340749A4 (en) 2000-11-17 2007-09-05 Takeda Pharmaceutical Isoxazole derivatives
JP2002226464A (en) 2001-01-30 2002-08-14 Sumitomo Pharmaceut Co Ltd Triaryl analogue and its use
EP1362037A1 (en) * 2001-02-15 2003-11-19 Boehringer Ingelheim Pharmaceuticals Inc. Process for synthesis of heteroaryl-substituted urea compounds useful as antiinflammatory agents
ATE497603T1 (en) 2001-03-02 2011-02-15 Gpc Biotech Ag THREE-HYBRID ASSAY SYSTEM
WO2003000189A2 (en) 2001-06-21 2003-01-03 Baylor College Of Medicine Prediction, diagnosis and treatment of endocrine resistant breast cancer, using p38 mapk pathway
EP1281399A3 (en) 2001-08-01 2004-02-11 Warner-Lambert Company Dual inhibitors of wax ester and cholesteryl ester synthesis for inhibiting sebum production
EP1427412A1 (en) * 2001-09-13 2004-06-16 Boehringer Ingelheim Pharmaceuticals Inc. Methods of treating cytokine mediated diseases
EP1465854A4 (en) 2001-12-19 2005-06-08 Atherogenics Inc Chalcone derivatives and their use to treat diseases
US20050090474A1 (en) 2002-01-16 2005-04-28 Zvi Naor Methods and compositions for enhancing and inhibiting fertilization
EP1480976B1 (en) 2002-02-28 2007-09-19 F.Hoffmann-La Roche Ag Thiazole derivatives as npy receptor antagonists
US20030186221A1 (en) 2002-04-02 2003-10-02 Lockhart David J. Phage display affinity filter and forward screen
US20030225089A1 (en) * 2002-04-10 2003-12-04 Boehringer Ingelheim Pharma Gmbh & Co. Kg Pharmaceutical compositions based on anticholinergics and p38 kinase inhibitors
WO2003107314A2 (en) * 2002-06-01 2003-12-24 Samsung Electronics Co., Ltd. Method of driving a shift register, a shift register, a liquid crystal display device having the shift register
US20040138216A1 (en) 2002-12-23 2004-07-15 Boehringer Ingelheim Pharma Gmbh & Co. Kg Process for the preparation of an essentially pure polymorph of an n-pyrazolyl-n'-naphthyl-urea
US7202257B2 (en) 2003-12-24 2007-04-10 Deciphera Pharmaceuticals, Llc Anti-inflammatory medicaments
US20080045706A1 (en) 2002-12-31 2008-02-21 Flynn Daniel L Anti-inflammatory medicaments
US20040171075A1 (en) 2002-12-31 2004-09-02 Flynn Daniel L Modulation of protein functionalities
US7144911B2 (en) 2002-12-31 2006-12-05 Deciphera Pharmaceuticals Llc Anti-inflammatory medicaments
KR100705617B1 (en) * 2003-03-31 2007-04-11 비오이 하이디스 테크놀로지 주식회사 Liquid crystal driving device
WO2004113352A1 (en) 2003-06-19 2004-12-29 Amedis Pharmaceuticals Ltd. Silylated heterocyclylurea derivatives as cytokine-inhibitors
US20070191336A1 (en) 2003-12-24 2007-08-16 Flynn Daniel L Anti-inflammatory medicaments
US20080220497A1 (en) 2003-12-24 2008-09-11 Flynn Daniel L Modulation of protein functionalities
JP5197016B2 (en) 2004-12-23 2013-05-15 デシファラ ファーマスーティカルズ, エルエルシー Enzyme modulators and therapy
US20080248548A1 (en) 2007-04-09 2008-10-09 Flynn Daniel L Modulation of protein functionalities
US20080248487A1 (en) 2007-04-09 2008-10-09 Flynn Daniel L Modulation of protein functionalities

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6174905B1 (en) * 1996-09-30 2001-01-16 Mitsui Chemicals, Inc. Cell differentiation inducer
US6441005B1 (en) * 1999-07-28 2002-08-27 Pharmacia & Upjohn Company Oxazolidinone compounds and compositions, and methods of using the same

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8481536B2 (en) 2004-04-08 2013-07-09 Targegen, Inc. Benzotriazine inhibitors of kinases
US8372971B2 (en) 2004-08-25 2013-02-12 Targegen, Inc. Heterocyclic compounds and methods of use
US8604042B2 (en) 2005-11-01 2013-12-10 Targegen, Inc. Bi-aryl meta-pyrimidine inhibitors of kinases
US9233956B2 (en) 2008-05-06 2016-01-12 Novartis Ag Benzene sulfonamide thiazole and oxazole compounds

Also Published As

Publication number Publication date
EP1590344A4 (en) 2007-08-29
US20080187978A1 (en) 2008-08-07
US7737283B2 (en) 2010-06-15
EP1585734A4 (en) 2007-09-19
TW200427672A (en) 2004-12-16
JP2006514691A (en) 2006-05-11
US7666895B2 (en) 2010-02-23
US20090069310A1 (en) 2009-03-12
MXPA05007236A (en) 2006-04-27
EP1585734A2 (en) 2005-10-19
BR0317872A (en) 2005-12-06
EP1590344A2 (en) 2005-11-02
US20090137021A1 (en) 2009-05-28
US20090075986A1 (en) 2009-03-19
US20040180906A1 (en) 2004-09-16
US7144911B2 (en) 2006-12-05
US20090105230A1 (en) 2009-04-23
WO2004060306A3 (en) 2005-07-28
WO2004060306A2 (en) 2004-07-22
AU2003303641A1 (en) 2004-07-29
US20080299639A1 (en) 2008-12-04
CA2513627A1 (en) 2004-07-22
WO2004060305A2 (en) 2004-07-22

Similar Documents

Publication Publication Date Title
WO2004060305A3 (en) Anti-cancer medicaments
TW200505455A (en) Anti-cancer medicaments
WO2006014290A3 (en) Anti-inflammatory medicaments
WO2006081034A3 (en) Anti-inflammatory medicaments
WO2005103076A3 (en) Erythropoietin protein variants
HK1093731A1 (en) Sulfoximine-substituted pyrimidines for use as cdk and/or vegf inhibitors, the production thereof and their use as drugs
AU2003273612A1 (en) Percutaneously introduced blood pump and related methods
AU2003218806A1 (en) Bio-disc, bio-driver apparatus, and assay method using the same
WO2007149482A3 (en) Xanthohumol based protein kinase modulation cancer treatment
HK1094044A1 (en) Diffuser disk for lcd applications, method for the production and use thereof
WO2003014303A3 (en) Molecular interactions in cells
WO2004087735A3 (en) Proteolytic and covalent antibodies
AU2003223494A1 (en) Methods for detecting bcr-abl signaling activity in tissues using phospho- specific antibodies
AU2003235307A1 (en) Crystal of glucokinase protein, and method for drug design using the crystal
IL176513A0 (en) Diarylmethyl piperazine derivatives, preparations thereof and used thereof
AU2003270149A1 (en) Akap18 delta, a novel splicing variant of a protein kinase a anchor protein and the use of the same
AU2003228634A1 (en) Dna dependent protein kinase catalytic subunit phosphorylation sites and antibodies thereto
WO2006074157A3 (en) Modified pol iii replicases and uses thereof
AU2003292761A1 (en) Modified cycloolefin copolymer, process for producing the same, and use of the polymer
WO2006017436A3 (en) Time-lapsing mirror
AU2003263435A1 (en) Method, device and input element for selecting the functional mode thereof
AU2003300262A1 (en) Phthalimidylazo dyes, processes for the preparation thereof and the use thereof
AU2003238965A1 (en) Methods for using adamts-12, an integrin and metalloprotease with thrombospondin motifs
AU2003216893A1 (en) Phenethylacrylamide, methods for the production thereof and agents containing the same
AU2003296662A1 (en) Triazolopyrimidines, methods for the production thereof, use thereof for controlling harmful fungi, and substances containing said triazolopyrimidines

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A2

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ OM PH PL PT RO RU SC SD SE SG SK SL TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A2

Designated state(s): BW GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
WWE Wipo information: entry into national phase

Ref document number: 2511840

Country of ref document: CA

WWE Wipo information: entry into national phase

Ref document number: 1433/CHENP/2005

Country of ref document: IN

WWE Wipo information: entry into national phase

Ref document number: 200505267

Country of ref document: ZA

Ref document number: 2003303639

Country of ref document: AU

Ref document number: 2005508623

Country of ref document: JP

WWE Wipo information: entry into national phase

Ref document number: PA/a/2005/007237

Country of ref document: MX

WWE Wipo information: entry into national phase

Ref document number: 2003814980

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 20038B00488

Country of ref document: CN

WWP Wipo information: published in national office

Ref document number: 2003814980

Country of ref document: EP

ENP Entry into the national phase

Ref document number: PI0317863

Country of ref document: BR

CFP Corrected version of a pamphlet front page
CR1 Correction of entry in section i

Free format text: IN PCT GAZETTE 30/2004 UNDER (71) THE NAME SHOULD READ "DECIPHERA PHARMACEUTICALS, LLC"