HUP0401052A2 - DNS-protein kináz inhibitorok - Google Patents

DNS-protein kináz inhibitorok

Info

Publication number
HUP0401052A2
HUP0401052A2 HU0401052A HUP0401052A HUP0401052A2 HU P0401052 A2 HUP0401052 A2 HU P0401052A2 HU 0401052 A HU0401052 A HU 0401052A HU P0401052 A HUP0401052 A HU P0401052A HU P0401052 A2 HUP0401052 A2 HU P0401052A2
Authority
HU
Hungary
Prior art keywords
group
ring
atom
optionally substituted
carbon atoms
Prior art date
Application number
HU0401052A
Other languages
English (en)
Inventor
Roger John Griffin
Bernard Thomas Golding
David Richard Newell
Hilary Alan Calvert
Nicola Jane Curtin
Ian Robert Hardcastle
Niall Morrison Barr Martin
Graeme Cameron Murray Smith
Laurent Jean Martin Rigoreau
Xiao-Ling Fan Cockcroft
Vincent Junior Ming-Lai Loh
Paul Workman
Florence Irene Raynaud
Bernard Paul Nutley
Original Assignee
Cancer Research Technology Ltd.
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 Cancer Research Technology Ltd. filed Critical Cancer Research Technology Ltd.
Publication of HUP0401052A2 publication Critical patent/HUP0401052A2/hu
Publication of HUP0401052A3 publication Critical patent/HUP0401052A3/hu

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • 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
    • C07D417/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • 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
    • A61P9/00Drugs for disorders of the cardiovascular system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/34Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D309/36Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms
    • C07D309/38Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms one oxygen atom in position 2 or 4, e.g. pyrones
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • C07D311/22Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/78Ring systems having three or more relevant rings
    • C07D311/92Naphthopyrans; Hydrogenated naphthopyrans
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems

Abstract

A találmány tárgya (I) általános képletű vegyületek és izomereik,sóik, szolvátjaik, kémiailag védett formáik és hatóanyag előalakjaikalkalmazása DNSPK aktivitás gátlására szolgáló gyógyszerelőállítására, ahol a képletben R1 és R2 jelentése egymástólfüggetlenül hidrogénatom, adott esetben helyettesített 1-7 szénatomosalkilcsoport, 3-20 szénatomos heterociklusos csoport vagy 5-20szénatomos arilcsoport, vagy azzal a nitrogénatommal együtt, amelyhezkapcsolódnak, egy adott esetben helyettesített, 4-8 gyűrűatomosheterociklusos gyűrűt képezhetnek, X és Y jelentése CR4 és oxigénatom,oxigénatom és CR'4, és NR<4 és nitrogénatom, ahol a telítetlen kötés agyűrűn a megfelelő helyen található és ahol az R3 és R4 vagy R'4csoportok egyikének jelentése egy adott esetben helyettesített, 3-20szénatomos heteroaril- vagy 5-20 szénatomos arilcsoport, és az R3 ésR4 vagy R'4 csoportok közül a másik jelentése hidrogénatom vagy R3 ésR4 vagy R<4 együtt -A-B- csoportot jelent, amely együttesen egykondenzált, adott esetben helyettesített aromás gyűrűt képvisel,feltéve, hogy amikor X és Y jelentése CR4 és oxigénatom, R3 és R4együttesen egy kondenzált benzol gyűrűt alkot, és R1 és R2 azzal anitrogénatommal együtt, amelyhez kapcsolódnak, egy morfolinocsoportotalkotnak, a kondenzált benzolgyűrű egyedüli szubsztituensként nemhordoz fenilszubsztituenst a 8-as helyzetben. Ó
HU0401052A 2001-08-14 2002-08-14 Dna-pk inhibitors HUP0401052A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0119865.4A GB0119865D0 (en) 2001-08-14 2001-08-14 DNA-PK inhibitors
PCT/GB2002/003781 WO2003024949A1 (en) 2001-08-14 2002-08-14 Dna-pk inhibitors

Publications (2)

Publication Number Publication Date
HUP0401052A2 true HUP0401052A2 (hu) 2004-09-28
HUP0401052A3 HUP0401052A3 (en) 2007-05-29

Family

ID=9920420

Family Applications (1)

Application Number Title Priority Date Filing Date
HU0401052A HUP0401052A3 (en) 2001-08-14 2002-08-14 Dna-pk inhibitors

Country Status (23)

Country Link
US (2) US7226918B2 (hu)
EP (1) EP1417196B1 (hu)
JP (1) JP4332032B2 (hu)
KR (1) KR100905457B1 (hu)
CN (1) CN1279034C (hu)
AT (1) ATE411987T1 (hu)
AU (1) AU2002362385B2 (hu)
BR (1) BR0211889A (hu)
CA (1) CA2454023A1 (hu)
CY (1) CY1110269T1 (hu)
DE (1) DE60229531D1 (hu)
DK (1) DK1417196T3 (hu)
ES (1) ES2315377T3 (hu)
GB (2) GB0119865D0 (hu)
HK (1) HK1070368A1 (hu)
HU (1) HUP0401052A3 (hu)
MX (1) MXPA04000804A (hu)
NO (1) NO20040636L (hu)
NZ (1) NZ530909A (hu)
PL (1) PL367081A1 (hu)
PT (1) PT1417196E (hu)
WO (1) WO2003024949A1 (hu)
ZA (1) ZA200400237B (hu)

Families Citing this family (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0119865D0 (en) 2001-08-14 2001-10-10 Cancer Res Campaign Tech DNA-PK inhibitors
GB0119863D0 (en) 2001-08-14 2001-10-10 Cancer Res Campaign Tech DNA-PK inhibitors
US7049313B2 (en) 2002-02-25 2006-05-23 Kudos Pharmaceuticals Ltd. ATM inhibitors
EA012240B1 (ru) * 2003-04-03 2009-08-28 Семафор Фармасьютикалз, Инк. Пролекарства ингибиторов киназы pi-3
CN1867566B (zh) * 2003-08-13 2010-06-16 库多斯药物有限公司 氨基吡喃酮和它们作为atm抑制剂的用途
US7402607B2 (en) * 2004-09-20 2008-07-22 Kudos Pharmaceuticals Limited DNA-PK inhibitors
TW200638938A (en) 2005-02-09 2006-11-16 Kudos Pharm Ltd ATM inhibitors
AR053358A1 (es) 2005-04-15 2007-05-02 Cancer Rec Tech Ltd Inhibidores de adn - pk
US7909830B2 (en) * 2005-08-25 2011-03-22 Synthes Usa, Llc Methods of spinal fixation and instrumentation
TW200745094A (en) * 2005-08-31 2007-12-16 Kudos Pharm Ltd ATM inhibitor
US20090326223A1 (en) * 2006-07-18 2009-12-31 Roger John Griffin Synthesis of 2-amino-substituted 4-oxo-4h-chromen-8.yl-trifluoro-methanesulfonic acid esters
ATE517868T1 (de) * 2006-08-16 2011-08-15 Boehringer Ingelheim Int Pyrazinverbindungen, ihre verwendung und herstellungsverfahren
EP2170338A2 (en) * 2007-07-06 2010-04-07 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Dna-pkcs modulates energy regulation and brain function
UY31232A1 (es) * 2007-07-19 2009-03-02 Compuestos derivados de dibenzotifenilamino-cromen-4-onas activas sustituidas y sus isomeros y aplicaciones
WO2009130469A1 (en) * 2008-04-25 2009-10-29 Kudos Pharmaceuticals Limited Dna-pk inhibitors
WO2010136778A1 (en) * 2009-05-29 2010-12-02 Kudos Pharmaceuticals Limited Dibenzothiophene derivatives as dna- pk inhibitors
RU2561130C2 (ru) 2009-07-02 2015-08-20 Санофи НОВЫЕ ПРОИЗВОДНЫЕ 1,2,3,4-ТЕТРАГИДРОПИРИМИДО{1,2-a}ПИРИМИДИН-6-ОНА, ИХ ПОЛУЧЕНИЕ И ФАРМАЦЕВТИЧЕСКОЕ ПРИМЕНЕНИЕ
SG10201403138WA (en) 2009-07-02 2014-08-28 Sanofi Sa Novel 2,3-dihydro-1h-imidazo(1,2-a)pyrimidin-5-one derivatives, preparation thereof and pharmaceutical use thereof
SI2448927T1 (sl) 2009-07-02 2014-06-30 Sanofi Novi (6-okso-1,6-dihidro-pirimidin-2-il)-amidni derivati, njihova priprava in njihova farmacevtska uporaba kot AKT fosforilacijski inhibitorji
WO2011001115A1 (fr) 2009-07-02 2011-01-06 Sanofi-Aventis Nouveaux derives de 6-morpholin-4-yl-pyrimidin-4- ( 3h ) -one, leur preparation pharmaceutique comme inhibiteurs de phos phorylat i on d ' akt ( pkb )
FR2947548B1 (fr) * 2009-07-02 2012-05-18 Sanofi Aventis Nouveaux derives de 1h-pyrimidin-2-one, leur preparation pharmaceutique comme inhibiteurs de phosphorylation d'akt(pkb)
FR2951170B1 (fr) * 2009-10-09 2011-12-02 Sanofi Aventis Nouveaux derives de 1h-pyrimidin-2-one, leur preparation et leur utilisation pharmaceutique comme inhibiteurs de phosphorylation d'akt(pkb)
WO2011137428A1 (en) * 2010-04-30 2011-11-03 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Methods of treating hiv infection: inhibition of dna dependent protein kinase
US8815853B2 (en) 2010-12-23 2014-08-26 Sanofi Pyrimidinone derivatives, preparation thereof and pharmaceutical use thereof
LT2658844T (lt) 2010-12-28 2017-02-10 Sanofi Nauji pirimidino dariniai, jų gamyba ir jų farmacinis panaudojimas kaip akt (pkb) fosforilinimo slopiklių
UY34013A (es) * 2011-04-13 2012-11-30 Astrazeneca Ab ?compuestos de cromenona con actividad anti-tumoral?.
FR2992314B1 (fr) 2012-06-22 2015-10-16 Sanofi Sa Nouveaux derives de 2,3-dihydro-1h-imidazo{1,2-a}pyrimidin-5-one et 1,2,3,4-tetrahydro-pyrimido{1,2-a}pyrimidin-6-one comportant une morpholine substituee, leur preparation et leur utilisation pharmaceutique
FR2992316A1 (fr) 2012-06-22 2013-12-27 Sanofi Sa Derives de pyrimidinones, leur preparation et leur application en therapeutique
CN102977063A (zh) * 2012-11-26 2013-03-20 盛世泰科生物医药技术(苏州)有限公司 一种2-吗啡啉-8-苯基-4-苯并吡喃-4-酮的合成方法
HRP20211855T1 (hr) * 2013-03-12 2022-03-04 Vertex Pharmaceuticals Incorporated Inhibitori dnk-pk
EP3042900B1 (en) * 2013-08-29 2020-09-23 Fujifilm Corporation Novel morpholine derivative or salt thereof
US11433047B2 (en) * 2015-10-09 2022-09-06 Neurotheryx Canada Ltd. Pharmaceutical compositions comprising one or more pyrone compounds, and their use for treating inflammatory and neurodegenerative diseases
US20200101080A1 (en) * 2017-03-31 2020-04-02 Bioventures, Llc Inhibitors of dna pk and uses thereof
US20230022146A1 (en) 2019-06-17 2023-01-26 Vertex Pharmaceuticals Incorporated Compositions and methods for editing beta-globin for treatment of hemaglobinopathies
WO2021222287A2 (en) 2020-04-28 2021-11-04 Intellia Therapeutics, Inc. Methods of in vitro cell delivery
WO2022133246A1 (en) 2020-12-17 2022-06-23 Vertex Pharmaceuticals Incorporated Compositions and methods for editing beta-globin for treatment of hemaglobinopathies
CA3216875A1 (en) 2021-04-17 2022-10-20 Intellia Therapeutics, Inc. Inhibitors of dna-dependent protein kinase and compositions and uses thereof

Family Cites Families (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1303724A (hu) 1969-05-14 1973-01-17
JPH0753725B2 (ja) 1987-10-08 1995-06-07 富山化学工業株式会社 4h―1―ベンゾピラン―4―オン誘導体およびその塩、それらの製造法並びにそれらを含有する抗炎症剤
US5284856A (en) 1988-10-28 1994-02-08 Hoechst Aktiengesellschaft Oncogene-encoded kinases inhibition using 4-H-1-benzopyran-4-one derivatives
US5703075A (en) 1988-12-21 1997-12-30 Pharmacia & Upjohn Company Antiatherosclerotic and antithrombotic 1-benzopyran-4-ones and 2-amino-1,3-benzoxazine-4-ones
HUT58310A (en) * 1988-12-21 1992-02-28 Upjohn Co Anti-atherosclerotic and anti-thrombotic 1-benzopyran-4-one- and 2-amino-1,3-benzoxazin-4-one derivatives, process for producing them and pharmaceutical compositions containing them
JPH03215423A (ja) 1990-01-18 1991-09-20 Kyowa Hakko Kogyo Co Ltd 血管拡張剤
AU7998291A (en) * 1990-06-20 1992-01-07 Upjohn Company, The Antiatherosclerotic and antithrombotic 1-benzopyran-4-ones and 2-amino-1,3-benzoxazine-4-ones
WO1992000290A1 (en) 1990-06-29 1992-01-09 The Upjohn Company Antiatherosclerotic and antithrombotic 2-amino-6-phenyl-4h-pyran-4-ones
US5302613A (en) 1990-06-29 1994-04-12 The Upjohn Company Antiatheroscleroic and antithrombotic 2-amino-6-phenyl-4H-pyran-4-ones
US5252735A (en) 1990-06-29 1993-10-12 The Upjohn Company Antiatherosclerotic and antithrombotic 2-amino-6-phenyl-4H-pyran-4-ones
WO1994005283A1 (en) 1992-09-02 1994-03-17 Kyowa Hakko Kogyo Co., Ltd. Anti-hiv drug
US5922755A (en) 1993-04-09 1999-07-13 Toyama Chemical Co., Ltd. Immunomodulator, cell adhesion inhibtor, and agent for treating, and preventing autoimmune diseases
US5378725A (en) 1993-07-19 1995-01-03 The Arizona Board Of Regents Inhibition of phosphatidylinositol 3-kinase with wortmannin and analogs thereof
US5468773A (en) 1993-08-25 1995-11-21 Eli Lilly And Company Methods for inhibiting bone loss and cartilage degradation using wortmannin and its analogs
US5504103A (en) 1993-08-25 1996-04-02 Eli Lilly And Company Inhibition of phosphatidylinositol 3-kinase with 17 β-hydroxywortmannin and analogs thereof
US5441947A (en) 1993-08-25 1995-08-15 Eli Lilly And Company Methods of inhibiting vascular restenosis
CA2133815A1 (en) 1993-10-12 1995-04-13 Jeffrey Alan Dodge Inhibition of phosphatidylinositol 3-kinase with viridin, demethoxyviridin, viridiol, demethoxyviridiol, virone, wortmannolone, and analogs thereof
US6632789B1 (en) 1994-04-29 2003-10-14 The United States Of America As Represented By The Secretary Of The Navy Methods for modulating T cell responses by manipulating intracellular signal transduction
US5480906A (en) 1994-07-01 1996-01-02 Eli Lilly And Company Stereochemical Wortmannin derivatives
GB9521987D0 (en) 1995-10-26 1996-01-03 Ludwig Inst Cancer Res Phosphoinositide 3-kinase modulators
US5733920A (en) 1995-10-31 1998-03-31 Mitotix, Inc. Inhibitors of cyclin dependent kinases
PL322876A1 (en) 1995-11-16 1998-03-02 Icos Corp Pik type kinase of cellular cycle control point: materials and methods
GB2302021A (en) 1996-10-16 1997-01-08 Lilly Co Eli Inhibiting bone loss or resorption
AU7953598A (en) 1997-06-06 1998-12-21 Mayo Foundation For Medical Education And Research Screening for phosphatidylinositol related-kinase inhibitors
WO1998056391A1 (en) 1997-06-13 1998-12-17 President And Fellows Of Harvard College Methods for treating human cancers
FR2776291B1 (fr) 1998-03-18 2000-06-16 Pf Medicament Nouveaux derives bis-benzamides, leur procede de fabrication, les compositions pharmaceutiques les contenant et leur utilisation comme medicament
US6348311B1 (en) 1999-02-10 2002-02-19 St. Jude Childre's Research Hospital ATM kinase modulation for screening and therapies
US6387640B1 (en) 1999-02-10 2002-05-14 St. Jude Children's Research Hospital ATM kinase modulation for screening and therapies
ATE363471T1 (de) * 2000-01-24 2007-06-15 Astrazeneca Ab Durch einen morpholinrest substituierte therapeutische verbindungen
WO2002000216A1 (en) * 2000-06-28 2002-01-03 Teva Pharmaceutical Industries Ltd. Carvedilol
EP1351946A2 (en) 2000-09-01 2003-10-15 Icos Corporation Materials and methods to potentiate cancer treatment
AU2002236765A1 (en) 2001-01-16 2002-07-30 Glaxo Group Limited Pharmaceutical combination for the treatment of cancer containing a 4-quinazolineamine and another anti-neoplastic agent
GB0119863D0 (en) * 2001-08-14 2001-10-10 Cancer Res Campaign Tech DNA-PK inhibitors
GB0119865D0 (en) 2001-08-14 2001-10-10 Cancer Res Campaign Tech DNA-PK inhibitors
WO2003035618A2 (en) 2001-10-24 2003-05-01 Iconix Pharmaceuticals, Inc. Modulators of phosphoinositide 3-kinase
US6894055B2 (en) 2001-10-24 2005-05-17 Iconix Pharmaceuticals Inc. Thieno-2′,3′ -5,6pyrimido[3,4-A]-1,2,4-triazole derivatives as modulators of phoshoinositide 3-kinase
DK1485377T5 (da) 2002-02-25 2010-12-06 Kudos Pharm Ltd Pyranoner egnede som ATM-inhibitorer
US7049313B2 (en) 2002-02-25 2006-05-23 Kudos Pharmaceuticals Ltd. ATM inhibitors
US7196085B2 (en) 2002-04-30 2007-03-27 Kudos Pharmaceuticals Limited Phthalazinone derivatives
CN1867566B (zh) * 2003-08-13 2010-06-16 库多斯药物有限公司 氨基吡喃酮和它们作为atm抑制剂的用途
US7402607B2 (en) * 2004-09-20 2008-07-22 Kudos Pharmaceuticals Limited DNA-PK inhibitors
TW200638938A (en) 2005-02-09 2006-11-16 Kudos Pharm Ltd ATM inhibitors
AR053358A1 (es) * 2005-04-15 2007-05-02 Cancer Rec Tech Ltd Inhibidores de adn - pk
UY31232A1 (es) * 2007-07-19 2009-03-02 Compuestos derivados de dibenzotifenilamino-cromen-4-onas activas sustituidas y sus isomeros y aplicaciones

Also Published As

Publication number Publication date
US20040192687A1 (en) 2004-09-30
US7674823B2 (en) 2010-03-09
CN1543457A (zh) 2004-11-03
AU2002362385B2 (en) 2008-07-31
CY1110269T1 (el) 2015-01-14
MXPA04000804A (es) 2004-06-03
JP4332032B2 (ja) 2009-09-16
DK1417196T3 (da) 2009-03-02
NZ530909A (en) 2005-10-28
GB2393653B (en) 2005-02-02
JP2005503414A (ja) 2005-02-03
BR0211889A (pt) 2004-09-21
EP1417196B1 (en) 2008-10-22
HK1070368A1 (en) 2005-06-17
PT1417196E (pt) 2009-01-02
ES2315377T3 (es) 2009-04-01
WO2003024949A1 (en) 2003-03-27
ATE411987T1 (de) 2008-11-15
PL367081A1 (en) 2005-02-21
NO20040636L (no) 2004-04-02
KR100905457B1 (ko) 2009-07-02
GB2393653A (en) 2004-04-07
KR20040032152A (ko) 2004-04-14
ZA200400237B (en) 2004-08-18
DE60229531D1 (de) 2008-12-04
US7226918B2 (en) 2007-06-05
HUP0401052A3 (en) 2007-05-29
EP1417196A1 (en) 2004-05-12
CN1279034C (zh) 2006-10-11
GB0119865D0 (en) 2001-10-10
GB0401411D0 (en) 2004-02-25
CA2454023A1 (en) 2003-03-27
US20070238729A1 (en) 2007-10-11

Similar Documents

Publication Publication Date Title
HUP0401052A2 (hu) DNS-protein kináz inhibitorok
UA83243C2 (ru) Соединения, которые ингибируют натриезависимый переносчик глюкозы
BR0315405A (pt) Compostos inibidores da integrase tricìclica pré-organizados
TW200611907A (en) Fused heterocyclic compound
UA84022C2 (ru) Производные (тио)карбамоилциклогексана как антагонисты d3/d2 рецептора
NO20061126L (no) Aminopyroner og deres anvendelse som ATM-inhibitorer
IL161559A0 (en) Dibenzylamine derivatives and pharmaceutical compositions containing the same
WO2003024967A3 (en) Indolizines as kinase protein inhibitors
NO972666D0 (no) Anilinderivater med nitrogenmonoksyd-synteseinhiberende aktivitet
TW200612920A (en) Novel imidazolidine derivatives
HUP0004477A2 (hu) Herbicid hatású 3-(1,2-benzizotiazol- vagy-izoxazol-5-il)-csoporttal helyettesített pirimidinszármazékok, intermedierjeik, előállításuk és alkalmazásuk
DK1204662T3 (da) Azaindoler med serotoninreceptoraffinitet
MX2010010471A (es) Derivado de tetrahidroisoquinolina novedoso.
HUP0500164A2 (hu) Heterociklussal szubsztituált benzolszulfonamidok mint HIV proteáz inhibitorok és az ezeket tartalmazó gyógyszerkészítmények
HUP0303457A2 (hu) Antimikrobiális hatású 2-piridonok, ezeket tartalmazó készítmények és alkalmazásuk
YU18404A (sh) Hemijska jedinjenja
GB0119863D0 (en) DNA-PK inhibitors
DK0640612T3 (da) Hidtil ukendte derivater af 2-(1H)-quinolinon, fremgangsmåde til deres fremstilling og farmaceutiske præparater indeholdend
TW200510350A (en) Sulfonamide derivatives having isoxazole ring

Legal Events

Date Code Title Description
FA9A Lapse of provisional patent protection due to relinquishment or protection considered relinquished