MX2009012832A - Inhibidor de pirazolopirimidinona quinasa. - Google Patents

Inhibidor de pirazolopirimidinona quinasa.

Info

Publication number
MX2009012832A
MX2009012832A MX2009012832A MX2009012832A MX2009012832A MX 2009012832 A MX2009012832 A MX 2009012832A MX 2009012832 A MX2009012832 A MX 2009012832A MX 2009012832 A MX2009012832 A MX 2009012832A MX 2009012832 A MX2009012832 A MX 2009012832A
Authority
MX
Mexico
Prior art keywords
kinase inhibitor
pyrazolopyrimidinone
pyrimidin
compound
pyrazolo
Prior art date
Application number
MX2009012832A
Other languages
English (en)
Inventor
Arthur F Kluge
Original Assignee
Agennix Ag
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 Agennix Ag filed Critical Agennix Ag
Publication of MX2009012832A publication Critical patent/MX2009012832A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • 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
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/10Antimycotics
    • 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
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • 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
    • 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
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/26Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
    • C07D473/28Oxygen atom
    • C07D473/30Oxygen atom attached in position 6, e.g. hypoxanthine

Abstract

La presente invención proporciona una pirazolo[3,4-d]pirimidin-4-o na novedosa, específicamente un derivado de 1-(piridin-4-il)-piraz olo[3,4-d]pirimidin-4-ona. Este compuesto es un inhibidor de quinasa que muestra actividad anti-proliferativa inesperada contra las células, incluyendo contra celular de tumor, y actividad anti-tumor en modelos de tumor de xenoinjerto. El compuesto o una sal adecuada oprofármaco del mismo es útil para el tratamiento de individuos que padecen de un cáncer u otro trastorno o enfermedad proliferativa.
MX2009012832A 2007-05-29 2008-05-28 Inhibidor de pirazolopirimidinona quinasa. MX2009012832A (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US93215507P 2007-05-29 2007-05-29
EP07113226A EP2019101A1 (en) 2007-07-26 2007-07-26 Pyrazol[3,4-d]pyrimidin-4-one useful as Kinase Inhibitor
PCT/EP2008/056569 WO2008145678A1 (en) 2007-05-29 2008-05-28 Pyrazolopyrimidinone kinase inhibitor

Publications (1)

Publication Number Publication Date
MX2009012832A true MX2009012832A (es) 2010-05-17

Family

ID=38556321

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2009012832A MX2009012832A (es) 2007-05-29 2008-05-28 Inhibidor de pirazolopirimidinona quinasa.

Country Status (19)

Country Link
US (2) US8304418B2 (es)
EP (2) EP2019101A1 (es)
JP (1) JP2010528088A (es)
KR (1) KR20100040806A (es)
CN (1) CN101765600A (es)
AR (1) AR066737A1 (es)
AT (1) ATE522533T1 (es)
AU (1) AU2008257534A1 (es)
CA (1) CA2689090A1 (es)
DK (1) DK2170891T3 (es)
EA (1) EA200901536A1 (es)
ES (1) ES2370677T3 (es)
HR (1) HRP20110768T1 (es)
IL (1) IL202375A0 (es)
MX (1) MX2009012832A (es)
SI (1) SI2170891T1 (es)
TW (1) TW200906831A (es)
WO (1) WO2008145678A1 (es)
ZA (1) ZA200908943B (es)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8586598B2 (en) * 2009-04-29 2013-11-19 Nerviano Medical Sciences S.R.L. CDK inhibitor salts
US9498471B2 (en) 2011-10-20 2016-11-22 The Regents Of The University Of California Use of CDK9 inhibitors to reduce cartilage degradation
WO2015172713A1 (zh) * 2014-05-13 2015-11-19 广东东阳光药业有限公司 一种中间体的制备方法
WO2016061144A1 (en) 2014-10-14 2016-04-21 The Regents Of The University Of California Use of cdk9 and brd4 inhibitors to inhibit inflammation

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US5073543A (en) * 1988-07-21 1991-12-17 G. D. Searle & Co. Controlled release formulations of trophic factors in ganglioside-lipsome vehicle
IT1229203B (it) * 1989-03-22 1991-07-25 Bioresearch Spa Impiego di acido 5 metiltetraidrofolico, di acido 5 formiltetraidrofolico e dei loro sali farmaceuticamente accettabili per la preparazione di composizioni farmaceutiche in forma a rilascio controllato attive nella terapia dei disturbi mentali organici e composizioni farmaceutiche relative.
US5120548A (en) * 1989-11-07 1992-06-09 Merck & Co., Inc. Swelling modulated polymeric drug delivery device
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EP0752248B1 (en) * 1992-11-13 2000-09-27 Idec Pharmaceuticals Corporation Therapeutic application of chimeric and radiolabeled antibodies to human B lymphocyte restricted differentiation antigen for treatment of B cell lymphoma
US5736137A (en) * 1992-11-13 1998-04-07 Idec Pharmaceuticals Corporation Therapeutic application of chimeric and radiolabeled antibodies to human B lymphocyte restricted differentiation antigen for treatment of B cell lymphoma
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WO2003063764A2 (en) * 2001-07-10 2003-08-07 Bristol-Myers Squibb Pharma Company 6-SUBSTITUTED PYRAZOLO [3,4-d] PYRIMIDIN-4-ONES USEFUL AS CYCLIN DEPENDENT KINASE INHIBITORS
JP2005511535A (ja) * 2001-10-15 2005-04-28 ジーピーシー バイオテック インク. サイクリン依存性キナーゼの阻害剤、組成物及びその使用
WO2004092139A2 (en) * 2003-04-07 2004-10-28 Gpc Biotech, Inc. Inhibitors of cyclin-dependent kinases, compositions and uses related thereto
WO2005026129A1 (en) 2003-09-15 2005-03-24 Gpc Biotech Ag Pharmaceutically active 4,6-disubstituted aminopyrimidine derivatives as modulators of protein kinases
WO2005063765A1 (en) 2003-12-23 2005-07-14 Gpc Biotech, Inc. Inhibitors of cyclin-dependent kinases, compositions and uses related thereto

Also Published As

Publication number Publication date
TW200906831A (en) 2009-02-16
IL202375A0 (en) 2010-06-30
ATE522533T1 (de) 2011-09-15
DK2170891T3 (da) 2011-12-12
AR066737A1 (es) 2009-09-09
AU2008257534A1 (en) 2008-12-04
KR20100040806A (ko) 2010-04-21
ES2370677T3 (es) 2011-12-21
US8304418B2 (en) 2012-11-06
SI2170891T1 (sl) 2011-12-30
EP2170891A1 (en) 2010-04-07
EA200901536A1 (ru) 2010-06-30
EP2019101A1 (en) 2009-01-28
ZA200908943B (en) 2010-08-25
JP2010528088A (ja) 2010-08-19
WO2008145678A1 (en) 2008-12-04
EP2170891B1 (en) 2011-08-31
CN101765600A (zh) 2010-06-30
HRP20110768T1 (hr) 2011-11-30
CA2689090A1 (en) 2008-12-04
US20100160350A1 (en) 2010-06-24
US20130035349A1 (en) 2013-02-07

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